Teleosts Flashcards

1
Q

What are the three forms of iodine in seawater and which is not biologically available for uptake across the gills?

What other environmental factors contribute to iodine bioavailability?

A

A CLUSTER OF CASES OF THYROID HYPERPLASIA IN AQUARIUM-HOUSED TROPICAL MARINE TELEOSTS FOLLOWING A CHANGE OF SALT MIX BRAND
Marion Jalenques, Claire Vergneau-Grosset, Noémie Summa, Wahiba Ait Youcef, Jean-Francois St-Cyr, Stéphane Lair
J. of Zoo and Wildlife Medicine, 51(3):725-728 (2020).

Key Points:
Large goiter may lead to inhibition pharyngeal region → difficulty respiring eating → death

Iodine exists as iodate (IO3-), iodine (I2), and iodide (I–); Iodate is not available for absorption across gills/GI

Iodate (IO3-) = 96% of it, not available

Iodide (I-) = Biologically active, thyroid hormone synthesis

Iodine (I2) meas by spectrophotometry - May significantly underestimate the biologically available forms of iodine in the system

Measuring total water iodine does not differentiate the forms (I- vs IO3-)

Ozone (O3) - converts iodide (I-) to iodate (IO3-)

High nitrate concentrations competitively inhibit thyroid utilization of iodine

Tx - Can add potassium iodide or Lugol’s to water; iodine dietary supplementation; maintain nitrate concentrations

Conclusions: Check the iodine concentrations in the water! Thyroid hyperplasia - iodine deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What was observed in gold fish anesthetized by propofol immersion at 5 and 10 mg/L?

Did propofol affect MAC following repeated exposure? Does MS-222?

A

PROPOFOL AS AN IMMERSION ANESTHETIC AND IN A MINIMUM ANESTHETIC CONCENTRATION (MAC) REDUCTION MODEL IN GOLDFISH (CARASSIUS AURATUS)
Julie A. Balko, V.M.D., Sarah K. Wilson, B.A., Gregory A. Lewbart, M.S., V.M.D., Dipl. A.C.Z.M., Brian R. Gaines, B.A., M.S., and Lysa P. Posner, D.V.M., Dipl. A.C.V.A.A.
Journal of Zoo and Wildlife Medicine 48(1): 48–54, 2017

Background:
MAC: the alveolar concentration of an anesthetic agent at which 50% of the population will not respond to supramaximal stimulus with gross purposeful movement
Allows for the comparison of analgesic potency
MAC model was recently validated in goldfish with MS-222
MS-222 repeat exposure requires increasing doses

Key Points:
Propofol immersion at 5 and 10mg/L → consistent anesthesia with rapid, dose-dependent induction (<5 min)
Opercular rates dropped to almost zero in most (70%) in both groups
Physiologic parameters were otherwise normal
MAC did not change following repeated exposure (in contrast to MS-222)
MAC ws reduced with dexmedetomidine at 0.04mg/kg, but not butorphanol, morphine, ketoprofen, or lower dexmed
No deaths in phase I of anesthesia, only deaths in phase IV. Propofol is safe for goldfish.

Conclusions: In goldfish, propofol immersion with 5 and 10 mg/L produces anesthesia and MAC does not change with repeated exposures. MAC was decreased with dexmedetomidine 0.04 mg/kg.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the only anesthetic approved for use in fish by the FDA?

What was observed regarding the effect of ax time on physiologic status of koi?

A

THE EFFECT OF ANESTHETIC TIME AND CONCENTRATION ON BLOOD GASES, ACID-BASE STATUS, AND ELECTROLYTES IN KOI (CYPRINUS CARPIO) ANESTHETIZED WITH BUFFERED TRICAINE METHANESULFONATE (MS-222)
Parker-Graham CA, Lima KM, Soto E.
Journal of Zoo and Wildlife Medicine. 2020 Mar;51(1):102-9.

Key Points:
MS-222 at 100 and 150 mg/L induced Stage III anesthesia in all fish within 5 min

Dose- and time-depending increases in pCO2 and hyperglycemia and decrease in potassium

Time-dependent decrease in pO2 with increased anesthetic time

Decrease in pH and tCO2, more in 150mg/L group; lactate decreased in both groups

Conclusions: MS-222 at 100-150 mg/L increases pCO2, hyperglycemia and decreases potassium and pO2.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What type of virus is carp edema virus?

Clinical signs?

A

OUTBREAK AND TREATMENT OF CARP EDEMA VIRUS IN KOI (CYPRINUS CARPIO) FROM NORTHERN CALIFORNIA
Stevens BN, Michel A, Liepnieks ML, Kenelty K, Gardhouse SM, Groff JM, Waltzek TB, Soto E.
Journal of zoo and wildlife medicine. 2018 Sep;49(3):755-64.

Poxvirus aka sleepy koi dz

Most significant histo findings in gills - necrotizing branchitis, intranuclear inclusion bodies; PCR gill and kidney tissue positive

Extensive erosions, edema of underlying tissue, inflammation of vent.

Dx - Virus most abundant in gill; light microscopy, TEM, PCR; severe epithelial hyperplasia and edematous changes

Outbreak management:

0.5% salt water holding following stress

Reduced proliferation of CEV

Avoid harvest of koi when water temps are permissive

Management and control:
No treatment
Prevent introduction
Source fish from reputable suppliers
Disease-free broodstocks
Biosecurity, disease surveillance

Quarantine and testing
30 days between 15-25C
Fish returning from koi shows
Avoid crowding, stress
Water quality, nutrition

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How does anesthesia and lead toxicity affect voltage in electric eels?

A

CLINICAL SIGNS, DIAGNOSIS, AND TREATMENT OF LEAD INTOXICATION IN AN ELECTRIC EEL (ELECTROPHORUS ELECTRICUS)
Sandra Wenger, Helene Pendl, Stamatios Tahas, Monika Bochmann, Jean-Michel Hatt
J Zoo Wildl Med. 2018 Dec 13;49(4):1029-1031. doi: 10.1638/018-0006.1.

Case: Electric eel ate lead wire and developed lead toxicity
Signs: Bilateral swellings behind the pectoral fins (distended, flaccid stomach), lethargy, anorexia
Elevated blood lead values
Treated with CaEDTA injections, then dimercaptosuccinic acid (DMSA) orally

Key Points:
Electric eels are obligate air breathers, majority of O2 absorption occurs in oral cavity

Voltage in eels is voluntary and can be used to monitor depth of anesthesia

Had a decreased voltage response with lead poisoning compared to other measurements

Voltage normalized once lead treated

Conclusions: An electric eel suffering lead poisoning had a flaccid, distended stomach and was treated successfully with chelating agents.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What organs could be visualized well during cranial or caudal celioscopy of koi?

Which organs were not visualized?

A

Evaluation of diagnostic coelioscopy in koi (Cyprinus carpio).
Stevens BN, Guzman DS, Phillips KL, Camus AC, Soto E.
Am J Vet Res. 2019 Mar;80(3):221-229.

Key Points:
Approach: Incision on ventral midline cranial or caudal to the pelvic girdle

For both approaches (no diff):

Good visualization of anterior kidney, gonads, intestines, and liver

Difficult visualization of swim bladder and posterior kidney

Unable to view spleen and gallbladder

Occasional hemorrhage and ruptured gonad capsule

Two week post op: Incomplete healing, redness,and swelling but good reepithelialization
Eight weeks post op: half of the koi were not fully healed
Approach caudal to the pelvic girdle was easier to view structures

Conclusions: Celioscopy with an cranial or caudal to the pelvic girdle in koi can view anterior kidney, gonads, intestines, and liver +/- swim bladder, posterior kidney. Spleen and gallbladder were not visualized. Caudal approach was recommended as more comfortable. Definitely take sutures out of fish by like 7-10 days unless you want a horrible inflammatory reaction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What was observed in evaluating KCl as a second step for euthanasia of koi via IC, ICe, and topical application to the gills?

A

EVALUATION OF POTASSIUM CHLORIDE ADMINISTERED VIA THREE ROUTES FOR EUTHANASIA OF ANESTHETIZED KOI (CYPRINUS CARPIO)
Meghan M. Louis, Emma L. Houck, Gregory A. Lewbart, Lysa P. Posner, Julie A. Balko
J. of Zoo and Wildlife Medicine, 51(3):485-489 (2020).

Intracardiac KCl at 10 mEq/kg rapidly ceases Doppler sounds and is a successful technique for euthanasia of anesthetized koi.

Intracoelomic and topical KCl at 10 mEq/kg were not effective for euthanasia of koi.

Conclusions: KCl administered intracardiac after MS222 immobilization resulted in cessation of heart rate and opercular movement, but intracoelomic and topical routes did not.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How do teleost fish IOPs compare vs mammals and birds? How did IOP differ in trout when immobilized with electronarcosis vs MS-222?

A

A PRELIMINARY STUDY OF INTRINSIC AND EXTRINSIC FACTORS INFLUENCING INTRAOCULAR PRESSURE IN BROOK TROUT (SALVELINUS FONTINALIS)
Lamglait B, Jalenques M, Summa N, Youcef WA, Vergneau-Grosset C.
Journal of Zoo and Wildlife Medicine. 2021 Jan;51(4):1012-6.

IOP in fish measured in ventral recumbency with rebound tonometry
Fish IOPs are lower than mammals and birds
Fish anesthetized with electronarcosis had higher IOPs than those in MS-222
Causes electrotetany

Conclusions: IOP significantly higher in brook trout when immobilized with electronarcosis vs. MS-222.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What was observed following enrofloxacin IM injections in striped bass?

A

Evaluation of localized inflammatory reactions secondary to intramuscular injections of enrofloxacin in striped bass (Morone saxatilis)
Scott G, Law M, Christiansen EF, Lewbart GA, Harms CA.
Journal of Zoo and Wildlife Medicine. 2020 Mar;51(1):46-52.

Key Points:
Enrofloxacin 2.27% is basic (pH 11.5) and causes tissue site reactions in mammals

Fish injected with enrofloxacin 2.27% IM had:

Darkened skin that resolved within 24 hours

Severe, hemorrhage, necrosis, and inflammation that increased for at least 96 hours

Conclusions: IM enrofloxacin in striped bass causes tissue necrosis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Describe pharmacokinetics of danofloxacin when administered 10 mg/kg IM in koi.

How does this differ from enrofloxacin?

A

Pharmacokinetics of danofloxacin following intramuscular administration of a single dose in koi (Cyprinus carpio)
Christine A. Parker-Graham, Wesley C. Siniard, Barbara A. Byrne, Heather K. Knych, Esteban Soto
(Am J Vet Res 2020;81:708–713)

Introduction:
Danofloxacin = broad spectrum (Gram +, -, Mycoplasma), bactericidal, concentration-dependent fluoroquinolone

MOA: Inhibits bacterial DNA gyrase

Key Points:
IM danofloxacin at 10 mg/kg was rapidly absorbed (detected within 15 min)

Above MIC90 for common bacteria (Vibrio, Pseudomonas, Aeromonas) for at least 96 h post-injection

No inflammation or myodegeneration at injection sites

Conclusions: Danofloxacin 10 mg/kg IM in koi is rapidly absorbed (15 min), above MIC90 for >96 hrs (4d), and has no injection site reactions.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How can mortalities during copper treatment be reduced?

A

Retrospective review of copper sulfate immersion treatment in marine teleosts during quarantine at the National Aquarium of Baltimore from 2004 to 2016.
Zec S, Hadfield C, Hungerford L.
Journal of Zoo and Wildlife Medicine. 2021 Apr;52(1):97-102.

FW system - Copper tx based on alkalinity (low alkalinity more toxic copper).

SW system - Ionic form Cu2+ is active, dependent on alkalinity, pH, salinity.

Tx is generally slowly increased over 3-5 days, maintained for 21 days, and then removed with activated carbon and water changes.

This study recommended slowly increasing copper over 7 days and starting 1 wk after fish have been in quarantine to reduce mortality.

Overall 4% mortality rate, but some species were more susceptible. Mortality was more likely to occur in the subtherapeutic period.

System volume did not have an impact

Still recommend copper treatment over introducing C. irritans

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How did vertebral lesions for discus receiving a beef heart diet compare to commercial discus feed?

A

Lewisch, E., Gumpenberger, M., Amesberger-Freitag, A., & El-Matbouli, M. (2018). Preliminary radiographic observations of vertebral changes in discus (symphysodon discus). Journal of Zoo and Wildlife Medicine, 49(4), 1016-1020.

  • Beef heart, low water calcium group and commercial food, moderate water calcium group had the most vertebral alterations, but alterations were seen in all groups including controls.
  • May suggest the unbalanced diets have aggravated an underlying condition.

Takeaway: Unsupplemented beef-heart diet not appropriate for discus, but commercial discus feed did not appear much better. Overall further nutritional investigations needed for this and other commonly kept fish spp.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How does tumor type affect cryotherapy effectiveness in cutaneous neoplasms of fish?

A

LIQUID NITROGEN CRYOSURGERY FOR CUTANEOUS AND OCULAR NEOPLASMS IN KOI (CYPRINUS CARPIO) AND GOLDFISH (CARASSIUS AURATUS): EIGHT CASES (2018–2019)
Journal of Zoo and Wildlife Medicine 52(2): 763–773, 2021

This report suggests that the use of cryosurgery for the treatment of cutaneous tumors may be curative for certain sarcomas, but appears to be ineffective in case of melanophoroma
· Besides tumor type, the response to treatment and prognosis appears to be heavily dependent on the progression or stage of the neoplasm at the time of diagnosis (ie depth of invasiveness and completeness of surgical margins)
· Tumors appeared to become MORE invasive when they recurred after cryotherapy, causes of this is unknown
· Cutaneous and corneal tumors, despite their similar histologic appearance, respond differently to cryotherapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What was observed at the IM injection site following injection of meloxicam in goldfish? How did this compare to saline control?

A

Larouche, C. B., Limoges, M. J., & Lair, S. (2018). Absence of acute toxicity of a single intramuscular injection of meloxicam in goldfish (carassius auratus auratus): a randomized controlled trial. Journal of Zoo and Wildlife Medicine, 49(3), 617-622.

Key Points:
• Meloxicam – preferential COX-2 selective NSAID
• PK study in Nile tilapia showed 1 mg/kg only lasts for 4-6 hours
• This study
• Gave 5 mg/kg (1 mL/kg) meloxicam or 1 mL/kg saline
• Necropsy – no obvious signs of toxicity, various other pathologies identified
• Significant IM hemorrhage at injection site for both

Take home: Meloxicam 5 mg/kg produces local muscle necrosis but so does IM injection of saline and acute toxicity otherwise was not observed.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the causative agent of bacterial kidney disease?

A

Richards, C. A., Abdel-Latif, H. M., Loch, T. P., & Faisal, M. (2021). High prevalence of circulating antibodies to renibacterium salmoninarum in spawning oncorhynchus spp. from lake michigan, usa. Journal of Wildlife Diseases, 57(1), 19-26.

  • Renibacterium salmoninarum – Causative agent of bacterial kidney disease BKD.
    o Salmonids, FW and SW. Wild, feral, and farmed in Great Lakes Basin.
    o BKD prevalence declined in trout following implementation of strict biosecurity measures in egg collection facilities and culling of infected fish. Still high in other salmonids.

Takeaways: High number of seropositive Oncorhynchus spp means R. salmoninarum still prevalent in Lake Michigan and continues to constitute a potential risk for other nonmanaged susceptible salmonids likely exposed. Modified Ab ELISA useful tool for screening seropositive salmonids. Chinook salmon > steelhead trout > Coho salmon.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How did immersion in MS222, 2PE, and clove oil impact anesthesia and cessation of physiologic measures (caudal fin stroke, reaction to stimuli, righting reflex, swimming, operculation) and HR in cichlids?

What was the most economically viable option? Which was most expensive?

A

Bradley, S., Sparrow, S., Rowden, L. J., & Guthrie, A. (2021). USE OF TRICAINE METHANESULFONATE, CLOVE OIL AND 2-PHENOXYETHANOL FOR IMMERSION EUTHANASIA OF UNGA CICHLIDS (SAROTHERODON LINELLII). Journal of Zoo and Wildlife Medicine, 52(3), 893-900.

After a 60-min immersion in the euthanasia solution, the presence of an audible heartbeat was identified in 100% of the cichlids immersed in 2-PE, 100% immersed in CO, and 90% in MS-222, indicating that they were not reliably euthanized. Therefore, a two-step protocol is recommended in cichlids for euthanasia: heavy anesthesia via immersion followed by an intravenous or intracardiac injection of euthanasia solution, or other secondary method of euthanasia.

The cost of euthanasia per cichlid was calculated, with the most economically viable option being 2-PE; MS-222 was the most expensive.

Time to all CPM significantly longer in 2PE vs MS-222.

IV injection of pentobarb was required in 97% to ensure HR stopped.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Which organ was most contrast enhancing on contrast CT of koi?

How did the delayed parenchymal phase compare to the timeline in mammals?

A

Brust, K., Phillips, K., Kaufman, M., Stevens, B., Camus, A., Camus, M. S., & Soto, E. (2021). INTRAVENOUS CONTRAST-ENHANCED COMPUTED TOMOGRAPHY IN ADULT KOI (CYPRINUS CARPIO). Journal of Zoo and Wildlife Medicine, 52(2), 460-469.

The caudal kidney was the most contrast-enhancing organ. Both doses produced good vascular enhancement and similar distribution. The delayed postcontrast scans showed repeatable parenchymal enhancement of organs. No mortality was encountered. No abnormalities were detected on blood smears, necropsies, or histopathology. Results suggest IV contrast administration is feasible, both contrast doses provided valuable anatomical information in the study with CT of coelomic organs, and no contraindications of contrast administration were detected.

o Initial vascular phase, delayed parenchymal phase (similar to mammals but was slower overall – 5 min later). Fish have lower BP.
o Caudal kidney most strongly contrast-enhancing organ.
o Spleen only organ not readily identified as separate from adjacent liver parenchyma.
- Ecchymosis at the injection site in some fish 24h after injection, no other side effects.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Describe a nociceptive model that could be used in fish?

A

Journal of Zoo and Wildlife Medicine 52(2): 529-537, 2021
PHARMACOKINETIC, PHARMACODYNAMIC, AND TOXICOLOGY STUDY OF ROBENACOXIB IN RAINBOW TROUT (ONCORHYNCHUS MYKISS)
Juliette Raulic, Dr méd vet, IPSAV, Francis Beaudry, PhD, Guy Beauchamp, PhD…

• Used previous nociception models in rainbow trout - intralabial acetic acid injection causes lip rubbing, rocking, increased opercular rate; hyporexia is also reliable pain indicator in postoperative koi

  • PK study: 6 trout robenacoxib 2 mg/kg IM, venipuncture at 5 timepoints up to 72h post; 2 controls given saline
  • Analgesic concentrations (10 ng/mL, based on cats) measured for 3-4d in trout kept at 12°C with average Cmax of 2.1h postinjection
  • PD study: 10 trout injected w/ intralabial acetic acid, 6 treated w/ robenacoxib, 4 controls given saline
  • Significant decrease in rocking behavior in robenacoxib fish.
  • No difference in opercular frequency; could not analyze rubbing behavior (infrequent)

Take-Home Message: Robenacoxib 2 mg/kg IM may give 3-4 days of analgesia in rainbow trout. No adverse effects of histopathologic lesions seen with this drug but difficult to monitor antemortem renal lesions in fish

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Describe evidence-based treatment of lateral line depigmentation of individual fish.

What are four broad categories of causes of LLD?

A

AN INTEGRATIVE REVIEW OF LATERAL LINE DEPIGMENTATION IN MARINE AND FRESHWATER FISH Dannemiller, O’connor, Van Bonn; JAVMA

Infectious agents (least likely): diplomonad flagellates (Spironucleus) and reovirus-like agent from angelfish; Aeromonas hydrophila isolated from one fish
• May be secondary invaders

Water quality:
• Poor water quality—groundwater pools
• Heavy metals likely most causative factor (copper, zinc, cadmium) and damaged skin of mummichog
• Low pH and high CO2 could also be a potential factor

Nutrition:
• Vitamin deficiency (especially tangs and surgeonfish)
• Blue tangs fed dry flake diet developed LLD after 3 weeks, but animals fed the same but grazed were unaffected.

  • Resolved when fed green algae supplemented with vitamin C.
  • Low vitamin A may cause HLLE in captive tangs

Activated carbon:
• Activated carbon filtered in led to LLD in tangs in 2 studies, typically in 14 days
• Severity varied among investigations

CONCLUSIONS AND CLINICAL RELEVANCE LLD should be considered a clinical observation indicative of a dermatologic response of fish to suboptimal conditions; LLD should continue to be adopted as the preferred term to describe the classic signs. Whereas gross findings are similar among species, histologic findings can vary.

Evidence-based treatment of LLD for individual fish consists of source control (changing tanks or systems), topical treatment with 0.01% becaplermin gel, supportive care, and antimicrobial treatment when warranted. For schools of fish, treatment and prevention of LLD should be focused on improving suboptimal environmental and physiologic conditions.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Meloxicam PK in tilapia?

A

PHARMACOKINETIC EVALUATION OF MELOXICAM AFTER INTRAVENOUS AND INTRAMUSCULAR ADMINISTRATION IN NILE TILAPIA (OREOCHROMIS NILOTICUS)
Daniel V. Fredholm, Natalie D. Mylniczenko, Butch KuKanich
J. of Zoo and Wildlife Medicine, 47(3):736-742 (2016).

Take Home Message: Meloxicam 1mg/kg IM or IVgiven to Nile tilapia leads to appropriate Cmax but a very short half-life short, requiring q4-6h dosing interval. Bioavailability of IM half that of IV.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Name 3 cyprinid herpesviruses

What family are fish herpesviruses in?

A

Alloherpesviridae

CyHV1 – “Carp Pox”

  • Epidermal hyperplasia, cosmetic

CyHV2 – Goldfish Herpesvirual Hematopoetic Necrosis Virus

  • Targets anterior kidney. Juvenile goldfish, high mortality.

CyHV3 – Koi Herpesvirus; REPORTABLE

  • All ages, high mortality. Goldfish and grass carp asymptomatic.
  • Targets gills.
  • Permissive temp 23-28 C (60-82F). Incubation 7-21 days, so hold fish at permissive temp at least 4 wks in quarantine.
  • Test ELISA or VN for antibodies, persiste for years. PCR gill, kidney, spleen. Cell culture kidney, spleen.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What type of virus is Spring Viremia of Carp Virus?

When are outbreaks?

Dx?

Response to active outbreak?

How can you declare a population virus free?

A

Spring Viremia of Carp Virus* OIE

Rhabdovirus carpio (carp spivivirus RNA)

Outbreaks in winter - Hemorrhages of skin/organs, edema, ascites, bloody mucoid discharge from vent.

Immunosuppression is triggered by the cold - Peak mortality 15-17C, most fish survive > 20 C.

Dx - Viral isolation (spleen, caudal kidney), viral neut, PCR

Pos results from IF, ELISA sufficient to initiate control measures

Active outbreak – Depopulation; mandatory (unlike KHV).

Inactivation:
Formalin, ozone, sodium hypochlorite, organic iodophors, gamma and UV radiation, pH extremes (<4 or >10)
Heating at 60C for 15 minutes

Incoming water should be treated with sand filtration and UV

To declare virus free:

Test negative for at least 2 years

Water supply only from spring, well, or borehole free of wild fish

Incoming water should not be connected to a watercourse, or natural barrier should prevent upstream migration of fish

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Which cyprinid herpesvirus is reportable to the OIE?

Which other cyprinid virus is reportable to the OIE?

A

Cyprinid herpes 3 (koi herpes)

Spring viremia of carp virus (rhabdovirus/spivivirus)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What are your quarantine recommendations for a koi hobbyist interested in adding three new koi to their established koi pond?

A

Minimum 4-6 weeks at permissive temp for KHV (18-28C or 60-82F)
Consider serology to aid in detection of carrier fish
Avoid mixing susceptible species (goldfish, grass carp carriers)
Consider source/disease free fish

Baseline diagnostics (skin/gill biopsy), general health assessment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

What type of parasite is amyloodinium? Life cycle? Tx?

A

Amyloodiniosis aka Marine Velvet Dz (SW)

Warm water marine fish and elasmos

Dinoflagellate

Trophont (lesions on fish) -> tomont (free swim) -> dinospores (floating spores that enter new host); LC can be completed in 3-6 days.

Division limited to 61-86F but can return to dividing when warms up even after 4 mos

Tx copper, chloroquine diphosphate, FW; (formalin resistant)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

What type of virus is red seabream iridovirus? Is this virus reportable?

A

Red seabream iridovirus:

Megalocytivirus, family iridoviridae

Characterized by presence of cytomegalic inclusion body bearing cells IBCs, often occupy entire cell cytoplasms, typically in spleen but can be systemic

RSIV is reportable to the OIE

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

What is the causative agent of whirling dz in hartchery-reared salmonids?

A

Myxobolus cerebralis

Myxozoan parasite, whirling dz

Requires oligochaete worm Tubifex tubifex and salmonid host to complete LC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

Life cycle of ichthyopthirius multifilis?

A

Trophont (feeds on fish) -> tomont (encysts onto substrate, divides) -> theront (fish-infective stage)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

Describe how pH, temp, salinity influence % ionized vs unionized ammonia

A

o Primary protein waste product from fish is ammonia
o Passively excreted across gills, lesser extent in urine and feces

o Two forms:
- Ionized ammonium NH4+
- Unionized ammonia NH3 – 100x more toxic to fish
o As pH and temp increase and salinity decreases, greater percentage becomes unionized and more toxic

(fresh, basic, hot water = toxicity)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

Describe how temp and salinity affects dissolved oxygen

A

Higher temp = Lower DO

SW holds less O2 vs FW at the same temp

Higher temp, SW = lower total O2 dissolved in water

Cold, FW = highest total O2 dissolved in water

Cold freshwater has high oxygen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

Describe two methods for measuring ammonia and compare/contrast

A

Ammonia assays
- Spectrophotometer
 Preferred – ammonia salicylate test
• No false reactions with SW
• No interference caused by ammonia-locking compounds – chemical ammonia binders on market

  • Nessler method
    • Requires complexing minerals (esp magnesium in SW)
    • Sensitivity is decreased ~30% in SW due to chloride ions
    • Reagent contains mercury and hazardous waste
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

Describe relationship between alkalinity and copper toxicity

A

Copper sulfate tx is contraindicated in low alkalinity because of the possibility of rapid pH changes (generally an issue in FW systems).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

How can nitrite toxicity be prevented in Channel Catfish?

A

Cl competitively inhibits nitrite uptake across gill; maintain at low level of salt

Nitrite toxicity is a FW fish thing - 1 ppt SW contains over 500 mg/L chloride, prevents toxicity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

Describe water quality parameter changes in pond over the course of the day

A

DAWN - Low O2, high CO2, low pH; Over course of day, photosynthesis uses CO2/produces O2, results in increase in pH and dissolved O2

DUSK - High DO, high pH, low CO2

Chronically high diurnal pH in ponds almost always caused by excessive phytoplankton or photosynthesis as CO2 is consumed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
35
Q

List OIE reportable viral fish diseases (8)

A

Koi herpes (cyprinid herpes 3)

Spring viremia of carp (rhabdovirus)

Viral hemorrhagic septicemia virus (rhabdovirus)

Infectious hematopoietic necrosis (rhabdovirus)

Epizootic hematopoietic necrosis (iridovirus/ranavirus)

Red seabream iridivorus

Infectious salmon anemia (orthomyxoviridae)

Salmonid alphavirus (togaviridae)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
36
Q

What is the causative agent of furunculosis in salmonids and what treatments are approved by the FDA?

A

Aeromonas salmonicida subsp. salmonicida
- Nonmotile, gram neg

Oxytetracycline dihydrate (Terramycin 200), sulfadimethoxine and ormetoprim (Romet 30), Florfenicol (Aquaflor) PO

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
37
Q

What drug is FDA approved for tx of motile aeromonad septicemia in catfish and salmonids?

A

Aeromonas hydrophila and friends
Oxytetracycline PO

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
38
Q

What is the causative agent of enteric septicemia of catfish?

A

Edwardsiella ictaluri
Causes economic losses of channel catfish (Ictalurus punctatus)

Acute enteric form, chronic neurologic form

Sulfadimethoxine and ormetoprim, florfenicol PO approved

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
39
Q

What is the causative agent of columnaris disease?

How does this appear on light microscopy?

What drugs are approved by the FDA for tx?

A

Flavobacterium columnare - FW
Marine counterpart is Tenacibaculum maritinum

Long thin, gram negative bacilli grouped in ‘haystacks’

Florfenicol, FW finfish

Oxytet, FW rainbow trout

Chloramine T immersion, walleye, salmonids, warm water finfish

Hydrogen peroxide - finfish

40
Q

What is the causative agent of bacterial cold water dz (BCWD) and rainbow trout fry syndrome (RTFS) in salmonids?

A

Flavobacterium psychrophilum

FW teleosts, cold water only

Florfenicol and oxytetracycline approved for salmonids with BCWD

41
Q

What are the two most common streptococcal spp most commonly reported to cause dz in fish?

A

Streptococcus agalactiae
Streptococcus iniae

Gram pos, chains

Survives well in organics and suspended solids, feed can remain a source of infection after >6 mos of freezing.

Florfenicol PO approved for finfish in warm-water

42
Q

What is the causative agent of bacterial kidney disease BKD in salmonids?

A

Renibacterium salmoninarum

Nonmotile, small gram pos diplobacilli

Causes granulomatous renomegaly with gram pos diplobacilli

Macrolide abx i.e. erythromycin commonly used, not FDA approved

43
Q

What are the three predominant mycobacterium spp in fish?

A

M. fortuitum - FW
M. marinum - SW but also sometimes FW
M. chelonae - Zebrafish

44
Q

What bacteria is grouped with chlamydia-like organisms in fish and is an obligate intracellular, gram negative bacteria?

A

Epitheliocystis; often causes gill nodules

45
Q

Name two piscirickettsial-like organisms that cause septicemic granulomatous disease in fish and what spp they commonly affect.

A

Francisella noatunensis - Marine, cold water i.e. cod, salmon

Francisella orientalis - Nile tilapia, aquaculture

46
Q

What is the causative agent of piscirickettsiosis aka salmon rickettsia syndrome?

What are some risk factors?

A

Piscirickettsia salmonis

Risk factors - transfer to salt water within prev 6 mos, season (fall or spring), high prevalence of infected stock within 7-10 km radius

47
Q

What two treatments are FDA approved for treatment of fish and eggs with saprolegniaceae?

A

Formalin, hydrogen peroxide immersion

48
Q

What disease shows cytology with characteristic large, sickle-shaped macroconidia with numerous septa?

A

Fusarium; Fusarium solani most common

49
Q

What cystic lesions are associated with microsporidial infection in fish?

A

Xenomas - Usually grossly visible, smears of ruptured xenomas or histology typically sufficient to confirm presence of microsporidian infection.

Fumagillin orally is the most effective tx in comprative studies

50
Q

What is the life cycle of ichthyophthirius multifiliis and which life stage is susceptible to treatment? What are some management strategies?

A

Trophont - Feeding stage, burrows under epithelium, resistant. This is the stage observed on skin scrapes. C-shaped nucleus.

Trophonts mature and grow, leave host and attach to solid surface, encyst as tomonts containing developing tomites.

The tomonts rupture, release the tomites that differentiate into free swimming theronts.

Theronts are most sensitive to immersion treatments and are immediately infectious, must find a host within 48h.

Little to no development > 86F, increasing temp will speed up the life cycle.

Formalin immersion 37% is the most commonly reported treatment.

51
Q

What is the life cycle of cryptocaryon irritans? Which life stage is observed on the fish? Which life stage is targetted with treatment?

What are some management strategies?

A

Trophont - Feeding stage, burrows under epithelium, resistant. This is the stage observed on skin scrapes. Large, round clear to tan slowly rolling ciliates. Seeing one is significant.

Trophonts mature and grow, leave host and attach to solid surface, encyst as tomonts containing developing tomites.

The tomonts rupture, release the tomites that differentiate into free swimming theronts.

Theronts are most sensitive to immersion treatments. Do not swim well, infections are likely acquired when fish are near substrate.

Little to no development > 86F, increasing temp will speed up the life cycle. LC is slower than ichthyophthirius multifillis.

Copper sulfate immersion is the most common treatment. Using ionized copper sulfate, slow increase over 5-7 days to 0.16-0.21 mg/L target for 21 days. Narrow safety margin, allkalinity should be > 50 mg/L of CaCO3 (not really an issue in SW).

Formalin immersion 37% and chloroquine diphosphate immersion other common treatments.

Hyposalinity can be effective where tolerated (18-20 g/L).

In reef systems, remove the teleosts and treat them in an isolated system. Also remove elasmos if a system is being treated.

52
Q

What type of parasites are chilodonella and brooklynella? Which is FW and which is SW?

A

Brooklynella (SW)
Chilodonella (FW)

Ciliated protozoan ectoparasites

Direct LC

The ciliates are oval or heart-shaped, dorsoventrally flattened, some show a notched anterior end.

Formalin tx

Brooklynella is NOT susceptible to copper sulfate immersion

53
Q

Name two scutociliates (one FW, one SW).

Diagnosis?

Treatment?

A

SW - Uronema/Miamiensis
FW - Tetrahymena

Holotrich ciliates

Small, teardrop (pyriform) to oval in shape. Fast, forward spinning movements.

Formalin immersion 37% commonly used; metronidazole immersion can be used

Prognosis is poor when muscles, organs are invaded

54
Q

Treatment options for trichodinid ciliates?

A

Formalin immersion 37%

Long-term hypersalinity

Copper sulfate immersion is common in pond systems

Usually improving the environment will resolve the problem

LC is direct, SW and FW

55
Q

Apiosoma sessile ciliate characteristics on light microscopy.

A

Apiosoma - Solitary or colonial, long vase with wide stalk and only oral cilia.

56
Q

Ambiphyra sessile ciliate characteristics on light microscopy.

A

Ambiphyra - Solitary, barrel shapped with cilia along oral and mid-body. No stalk.

57
Q

Capriniana sessile ciliate characteristics on light microscopy.

A

Capriniana - Solitary, straight feeding tentacles look like pins, usually only found on gills. Sea urchin vibes.

58
Q

Parasite commonly found in the GI of discus and other cichlids, causes granulomatous gastritis.

A

Cryptobia iubilans (flagellate, gastritis in cichlids).

Cryptobia salmositica aka trypanoplasma is a hematozoic cyptobia spp that can cause high mortality in salmonids. Dx on blood smear.

59
Q

Characteristics of ichthyobodo on light microscopy, tx options.

A

Small flagellates, often shaped like a comma or tear drop, flickering tumbling motion. SW and FW.

Tx formalin immersion 37% or copper sulfate immersion.

60
Q

Diplomonad flagellates often found in the caudal intestinal tract of cichlids, cyprinids, salmonids.

A

Spironucleus, Hexamita spp
Internal flagellates, fish are chronic poor-doers; FW and SW.

Usually more caudal in GI vs cryptobia

Small, elongated, pear-shaped, fast, jerky movements

Unlike cryptobia, easier to control medically. Metronidazole orally most effective followed by immersion.

61
Q

Ectoparasitic dinoflagellates found on skill and gills of SW and FW fish and corresponding parasite spp.

Cause of ‘marine velvet dz’

A

Amyloodinium ocellatum - SW
Piscinoodinium spp - FW

Life cycle - direct, 3 stages
Nonmotile trophonts feed on fish. Encyst in environment and become tomonts. Tomonts produce a free-swimming dinospore that is susceptible to immersion tx.

Dx - Trophonts on skin scrape, nonmotile, golden brown, round, oval or hexagonal shape.

Tx - Copper sulfate immersion for SW fish, chloroquine diphosphate immersion, FW dips or long term hypersalinity.

62
Q

Lifecycle of capsalid monogenes i.e. Neobenedenia spp?

General appearance?

Tx?

A

All monogeneans have a direct LC

Capsalids are oviparous, produce large numbers of eggs. Eggs hatch into ciliated larvae (oncomiracidium) which infect new host. Larvae attach and migrate to tissue sites.

Adults are large, oval, unsegmented flatworms that move by stretching and jerking. White, gray, or translucent. Four large black eye spots. Eggs triangular with trailing filaments.

Praziquantel immersion most common, can also treat orally. FW dips, long-term hyposalinity, trichlorfon (adverse effects).

63
Q

Capsalid monogene on ventral skin of cownose rays?

Capsalid monogene on gills of southern stingrays?

A

Capsalid monogene on ventral skin of cownose rays = Benedeniella posterocolpa

Capsalid monogene on gills of southern stingrays = Entobdella bumpusii

64
Q

Differentiation between dactylogyrids, gyrodactylids?

A

Dactylogyrus spp - Adults have four small eye spots, scallop-shaped head. FW gills most common, also SW. Lay eggs. Tx prazi.

Gyrodactylus spp - Viviparous. FW and SW. Adults have no eye spots, two pairs of large central hooks and a V-shaped head. Treatment easier since they do not produce eggs. Tx prazi or formalin.

65
Q

Species of gyrodactylid that is reportable to the OIE.

A

Gyrodactylus salaris - Reportable OIE. Viviparous, no eye spots, salmonids in Europe.

66
Q

What are some of the common body shapes of teleost fish?

What is unique about the endothelium of teleosts?

What are the Corpuscles of Stannius?

What are rodlet cells?

A

Introduction

● Bony fish (Osteichthyes) 🡪 flesh-finned fish (lungfish, coelacanths) + ray-finned fish (teleosts, sturgeon, gar)

● Cartilaginous fish (Chondrichthyes) 🡪 elasmobranchs + chimaeras

Anatomy of Bony Fish

Body Plan

● Body shapes 🡪 fusiform, laterally flattened, ventrally flattened, eel-like, ribbon-like, spheroid

● Laterally flattened - coelom toward R or L - ipsilateral to operculum (if assist feeding, orient tube toward side, not midline)

● Electric eels, rainbowfish - anus cranially b/w opercula

  • Unique features (ZPP)
  • Endothelium lining chambers of heart in teleosts is phagocytic.
    • May undergo hypertrophy when processing endogenous and exogenous molecules in circulation.
  • Corpuscles of Stannius
    • Nodular endocrine organs along lateral kidney, normal in toleosts, often mistaken for granulomas or encysted parasites.
  • Rodlet cells
    • Normal cell in immune-active fish; historically believed to be a parasite.
67
Q

Describe the integumentary anatomy of teleosts.

What is the outermost layer? What is its function?

What cells make up the epidermis? Is the epidermis keratinized?

Describe the anatomy of the dermis.

How can chromatophores be used to localize lesions?

What are the various scale types in teleosts? Which are teh most common?

What fish are scaleless? What have very fine scales? How does being scaleless affect a fish?

What fish taxa produce excessive mucous?

What is the lateral line?

What fish have bacterial luminescence?

A

Integument

  • External mucus layer
    • Rich in mucopolysaccharides, immunoglobulins, lysozymes, free fatty acids 🡪 mucosal defense system
  • Epidermis = epithelial cells, mucous glands
    • Thicker in fish w/ no scales
    • Unlike mammals - lacks keratin, all layers capable of mitosis (including squamous)
  • Dermis = scales, chromatophores, mast cells
    • Chromatophores - color change can imply different physiologic states
      • Generalized dark color - stress, disease
      • If only on one side - may indicate visual problem
      • If only caudal, may localize spinal problem
    • Scales embedded w/in pockets of dermal tissue, oriented toward tail
      • Scale types - placoid, cosmoid, ganoid, cycloid, ctenoid
        • Cycloid, ctenoid most common in teleosts
      • Some large & thick like ganoid scales of arowana/arapaima/sturgeon/tarpon
      • Avoid puncturing w/ needles - removal of scale can lead to osmoregulatory problems, infection (esp. 2º like oomycetes, scuticociliates)
      • For surgery - can remove along incision
      • Some have very fine scales (jacks, tuna), others scaleless (jacks, eels, catfish, elephantfish)
        • Scaleless - may be more vulnerable to toxins, medications, direct trauma
      • Some have deciduous scales & shed regularly (herring, anchovies)
    • Some have segmented bony plates w/in dermis (seahorses, pipefish, shrimpfish, trunkfish, boxfish, armored catfish, Plecostomus)
      • Injection, incision in soft areas; if must be cut - seal w/ wax
    • Pufferfish - erectable spines from scales w/ overlapping roots - must be cut for coelomic incision
  • Some produce copious mucus - eels, catfish, rays
    • Slippery, use chamois or flannel cloth to help
  • Parrotfish create mucoid casting (cocoon) at night - hand-net catches easier at night
  • Epithelial hyperplasia - common, nonspecific response to irritants; can be MF
  • Some fancy goldfish - overgrowth of head epithelium (wen, hoof) - consists of non-ciliated epithelium w/ goblet cells covering mucinous stroma
  • Lateral line - canal w/in integument w/ pores - in canal are neuromasts w/ sensory hairs surrounded by gel material 🡪sensitive to water displacement and vibration
    • Depigmentation common problem
  • Transparency feature in some - d/t arrangement of collagen fibers allowing passage of light (glass catfish)
  • Bacterial luminescence - Beryciformes group (pinecone fish, flashlight fish)
    • Have single species of bioluminescent bacteria (Photobacterium fischeri) in organ under eye
    • Bacteria may be observed by pulling into or covering w/ fold of skin
    • Antibacterial Tx can damage the bioluminescent bacteria

Integumentary system (ZP)

  • Epidermis, dermis, and hypodermis.
  • Epidermis lacks keratinization except the reproductive tubercles of male cyprinids.
  • Outer layer of goblet cell mucus and protoplasma aka glycocaylx or cuticle contains immunoglobulins, lysozyme, and antipathogen effector molecules for defense.
  • Alarm or club cells present in Cypriniformes, Characiformes, Gymnotiformes, Siluriformes.
  • Dermis divided into vascularized stratum spongiosum and dense stratum compactum.
  • Also contains scales, chromatophores, and lateral line system.
  • Scale loss represents a true ulcer and potential for microbial invasion.
  • Cycloid scales – Salmonids, cyprinids; oval.
  • Ctenoid scales – Spiny fish i.e. perchids; posterior spines (ctenii) and anterior radii directed from a central focus.
  • Hypodermis composed of connective tissue and adipose.
68
Q

Describe the MS anatomy of teleost fish.

What type of bone do teleosts have?

How does calcium absorption differ from other vertebrates?

What is hyperostosis?

Do fish have bone marrow?

What are the two types of muscle in fish?

What gives scup muscle its pink color and icefish muscle its yello color?

What teleosts have regional endothermy?

A

Musculoskeletal System

  • Skeleton
  • Cellular bone more common in bony fish
    • Acellular bone in perch-like fish, bass, sunfish
  • Bone solid and Ca absorption cannot occur locally (fracturs lack Ca reserve for repair)
  • Lack bone marrow - may be some vascular canals, spaces
  • Hyperostosis (aka pachyostosis, Tilly bones) - known in 22 families, most common Atlantic spadefish - not typically pathologic but if large can form sequestrate 🡪 skin ulcerations
    • Removal or rongeuring bone underneath can help resolve skin signs
  • Teleost skulls - complex series of bones w/ spp. variability
  • Vertebrae vary across spp.; radiographically have prominent cross representing conical recesses enclosing intervertebral pad, a neural spine, hemal arch, and hemal spine
  • Ribes either pleural (attached to vertebrae) or intermuscular (w/in muscle; salmonids)
  • Fins may be embedded in muscle or bone
    • Firm fin spines common, esp. along dorsal fin
    • Some contain venom (lionfish, stonefish)
    • Some fins modified into suckers (lumpfish)
    • Lobe-finned fish - lungfish and coelacanths - muscular fins w/ articulating bone in pectoral fin
  • Muscle
    • White (fast, twitch) predominates - anaerobic bursts, spring swimming
    • Red (slow) - aerobic swimming, more blood supply - typ. thin band under skin along lateral line and/or dorsal midline
    • Pelagic and more active fish 🡪 more red muscle
    • Drug PK likely affected by muscle type - but impact not well-known
    • Scup - pink muscle 🡪 less myoglobin; Icefish –< yellow muscle d/t lack of hemoglobin
    • Muscle and skin generally in elastic 🡪 injection volume and depth imp. to consider
      • IM meds may be more likely to cause lesions, volumes should be small
      • Leakage from injections common
    • Most poikilothermic but few have regional endothermy (tunas, billfish, mackerel spp.)
      • Endothermy d/t retes in brain, muscle, viscera 🡪 using red muscle located near vertebral column 🡪improves digestion, nerve, and muscle activity - important for large predators chasing fast prey in cold waters
    • Electrogeneration possible d/t modified skeletal muscles in FW elephantfish, S. American knifefish, electric catfish
  • Musculoskeletal system (ZP)
    • Unlike mammals, numbers of muscle fibers not fixed and increase throughout life.
    • Segregation of white and red muscle fibers.
      • White muscle – Short bursts of high speed swimming.
      • Red muscle – Pelagic, long distance migrators i.e. tuna.
      • Pink muscle intermediate.
    • Fish bone lacks the ordered canalicular systems found in mammals and does not appear to serve as a reservoir for regulation of blood calcium.
69
Q

What is the primary function of the teleost swim bladder? Are there any secondary funcitons?

What is the gas composed of?

What are the two types and list some taxa that have each?

What fish have one lobe? What about 2? What about 3?

Which have swim bladders that extend down the vertebrae?

Which are modified into lung-like tissue?

A

Buoyancy Organs

● Swim (gas) bladder - extensive spp. variations

● 1º function - buoyancy; but also sound production, pressure reception

● Absent in cartilaginous fish, some bottom-dwelling teleosts, weather loaches, some highly pelagic teleosts

● Filled w/ oil or fat in some bathypelagic spp. (laternfish, orange roughy)

● Volume to BW typically <5% in SW and <7% in FW

● Gas composed of CO2, O2, N - not in same %s as air

● Types of swim bladders -

o Physostomous - pneumatic duct connect swim bladder to esophagus; gas maintained by swallowing air (FB or gavaged food can enter swim bladder); some have rete mirabile for some gas absorption

▪ Salmon, trout, catfish, koi, goldfish, tetras

o Physoclistous - lack connecting duct; inflation via blood gases diffusion along one or more rete mirabile (gas glands) or vessels (typ. cranial and ventral); some also have capillary plexus caudodorsally (oval or oval window) to help resorb gases

▪ Most marine teleosts, cichlids, bass, sunfish

● Must know normal swim bladder appearance d/t species differences

o Abnormalities - hyperinflation, hypoinflation, displacement, fluid, parasites

o One lobe - most common - may be U-shaped (some pufferfish)

o Two lobes in several spp. (goldfish, carp, koi - some goldfish breeds lost Cd. lobe)

o Three lobes - cod, channel catfish, some pufferfish

o Extension common - may connect to inner ear (herring, anchovies), extend into vertebrae (FW angelfish), extend down the tail (electric eel, arowana)

o May be modified into lungs/lung-like tissues (garfish, tarpon, arapaima, lungfish)

70
Q

Where do fish put their adipose tissue?

Does location affect how easily it is used?

A

Adipose Tissue

  • Lipid deposited 🡪 muscle, liver and in some species brain, under skin
  • Coelomic fat 🡪 long-term storage vs. Liver/muscle fat 🡪 easier mobilization
  • In active bony fish - tend to be stored in skeletal muscle vs. bottom dwellers 🡪 liver
  • Red muscle stores more lipids than white
  • Deposits fluctuate seasonally 🡪 less likely to vary under human care
  • Over-conditioning common in human care - esp. large, mixed spp. habitats 🡪 use diets, targeted feeding, suitable fasting to help
71
Q

Describe the ocular anatomy of teleosts.

What fish have rudimentary eyes or eyespots? What fish have large eyes? How does that affect them clinically?

Do FW or SW fish have thicker corneas?

What is unique about the moray eel’s cornea?

Do fish have a PLR?

What are their lenses like?

What is the relationship between the vascular rete of the choroid and the pseudobranch?

A

Ocular Anatomy

  • Eyes vary greatly by spp.
  • Rudimentary eye/eyespot 🡪 hagfish; Eyeless fish 🡪 cavefish
  • Large eyes 🡪 squirrelfish, rockfish; seem more prone to issues like gas bubble disease, inflammation
  • Do not have opposable eyelids - many have membrane (aka epidermal conjunctiva) covering cornea or tissue around eye
  • Some have static eyelids to protect eyes (salmonids, jacks)
  • FW fish corneas are thicker than SQ and some have 2-layered corneas
  • Green moray eel cornea - dermal layer + scleral layer; common abnormal lipid deposition in dermal layer
  • Microanatomical features - epidermal conjunctiva, basement membrane (Bowman’s membrane), and endothelial layer (Descemet’s membrane)
  • Some spp. - normal corneal iridescence or pigmentation (pufferfish)
  • Most have fixed pupil 🡪 no PLR (some exceptions 🡪 true eels, turbot, flounder, African lungfish)
  • Iris - can be round, pear-shaped, elliptical, slit-like
    • Deep sea fish lack an iris
  • Amphibious fish (mudskippers) - flattened cornea, two pupils in each eye
  • Suckermouth catfish 🡪 modified iris called “omega iris” - loop at top can expand and contract
  • Lenses - dense, spherical (compensate for lack of refraction underwater), protrude slightly from iris
  • No mechanical separation of vitreous and aqueous humor
  • Ciliary bodies absent or rudimentary; ciliary processes absent; vitreal fluid production not understood
  • Sclera is cartilaginous, orbit is bony - some fish have tenacular ligament anchoring globe to orbit
  • Some spp. have scleral ossicles (sturgeon)
  • Retina variable; rods and cone present - more cones in diurnal spp.; fovea and tapetum lucidum present
  • European eel - only teleost w/ intraretinal vascular circulation
  • Other teleosts - organ w/ vascular rete (choroidal gland) that wraps around optic nerve & communicates w/ pseudobranch
    • Important in O2 secretion, implicated in intraocular gas bubble formation and potential source of hemorrhage during enucleation
72
Q

What is the function of the otoliths in the fish ear? How are these used in field research?

How do fish use their swim bladders to conduct sound?

What are three methods of sound production used by fish?

How do fish use olfaction and taste?

Where are taste buds located?

A

Auditory Anatomy

  • Acoustic organs - info on acoustic stimuli, gravity forces, linear and angular acceleration
  • Labyrinth 🡪 semicircular canals, inner ear ampullae, otoliths or otoconia
    • Otoliths - calcified stones overlay sensory epithelium, surrounded by endolymph - facilitates their movement for sound perception and equilibrium
      • Most ray-finned - single otolith per chamber, but can be several
      • Can be used for age and bony fish ID
    • Pathology of inner ear can lead to loss of equilibrium
  • Swim bladder and other gas cavities - conduct sound w/ bones known as Weberian apparatus (carp, bowfin, tetras, etc.)
  • If direct/indirect connect from swim bladder to perilymphatic system (inner ear) allows high frequency perception (carp, catfish > cod)
  • Three methods of sound production
    • Stridulatory (teeth, fins, spines, bones)
    • Hydrodynamic (swimming movements)
    • Muscle vibrations around swim bladder
  • Clinically - difficult to evaluate these structures
    • Swim bladder, otoliths - XR, CT, MRI
    • Swim bladder disease may result in reduced functional hearing (catfish - reduced freq. range)

Olfactory and Gustatory Anatomy

  • Water-soluble chemicals detected by olfaction (smell) or gustation (taste)
  • Paired nares on rostrum w/ olfactory epithelium; hagfish + lampreys have only single naris
    • Water 🡪 nares 🡪 stimulates receptors 🡪 signal 🡪 olfactory bulbs w/in forebrain (telencephalon)
      • Some have nasal sacs/accessory nasal sacs 🡪 actively pump water over epithelium
    • Some rely heavily on olfaction w/ large olfactory pits (moray eels, true eels)
  • Some visual reliant, lack nasal sacs (pufferfish)
  • Some species - males have more developed olfaction
  • Taste buds - epidermal, in oral cavity, lips, head, barbels, body all, fins, esophagus
    • In some, external outnumber internal by as much as 90%
    • Up to 3 anatomically different taste buds - amino, nucleic and organic acid reception
    • Do have aversive and preferential responses but extensive research has not been done
73
Q

Describe the oral anatomy of teleosts.

What type of glands are present in the mouth?

What type of teeth do fish have?

What forms can teeth take?

What species lack teeth?

Describe the esophagus of teleosts. How does the angle of the esophagus matter clinically?

A

Oral/Pharyngeal Cavity

  • Lining of oral cavity - thick epithelium and dermis bound to bone or muscle
  • Some have ornate, protruding maxillary rostrums or telescopic mouth
  • Some have pharyngeal jaws (moray eels)
  • Fish tongues - limited mobility, simply propel food into esophagus
    • Some have teeth on tongue to hold prey
  • Buccal glands - produce mucus; no salivary glands
  • Thyroid hyperplasia (goiter) - typically presents as mass along gill arches in bony fish
  • Dentition varies - acrodont teeth w/ ankyloses (fibrous attachment) to jaw
    • Tooth types - canine, molariform, incisor, plate-like (lungfish, gar)
      • Hinged pointed backwards (pike); front teeth grow continuously in parrotfish, pufferfish and may require trimming
      • Some lack teeth - filter feeders, seahorses, pipefish, sturgeon
      • Pharyngeal teeth - holding, masticating, grinding food (if present, often lack muscular stomach)
  • Esophagus - short, muscular tube; straight in most spp. but know differences/angularity when gavaging
    • Angle into stomach can be dramatic (lookdowns), misplaced tube can perforate
    • In some spp., has blind diverticular lined w/ calcified esophageal teeth
    • Folds present in sturgeon; epithelium may have abundant mucus, esp. in carnivores
74
Q

Describe the GI and hepatobiliary systems of teleost fish.

What fish lack a stomach? What fish have grinding organs?

What are the two regions of the stomach?

What are the pyloric ceca?

What is the intestinal anatomy like?

What role does the stomach play in pufferfish inflation?

What fish have a separate anus and reproductive opening? Which have a cloaca?

How does the liver differ from the structure of mammals?

What fish lack a gallbladder?

A

Gastrointestinal System

  • Stomach size varies; some agastric (goldfish, koi, zebrafish), grinding organ (gizzard shad, sturgeon, mullet)
  • Striated muscle (cardia) transitions to smooth (pyloric) and mucosa contains numerous mucus glands
  • Pyloric ceca (diverticula off stomach) - present in salmonids, many other teleosts
    • Increase absorptive surface, not fermentative like in birds, mammals
  • Variable intestinal length - fairly simple; colon minimal or not distinguishable; rectum present
    • Spiral-shaped in lungfish, sturgeon
  • GI emptying times vary w/ both temp and volume
  • Pufferfish can inflate w/ water or air - pump mouthfuls to stomach via modifications of pectoral girdle and head; skin distensible, ribs absent - in some spp. spines stand erect w/ inflation
  • External intestinal and urogenital openings differ among spp. - most separate anus and repro opening/urogenital pore
    • Some fish have cloaca - lungfish, coelacanths
  • Alimentary system (ZP)
  • Cyprinids and many herbivores lack a stomach.
  • Intestinal length varies to reflect feeding habits.
  • Pyloric ceca in many spp – can range from few to hundreds.
  • Swim bladder – Derived from outpouching of esophageal wall.
    • Phsysostomous – Pneumatic duct communicates with esophagus.
    • Physoclistous – No pneumatic duct as adults, rely on vascular structures/gas gland to fill and empty the bladder.

Liver and Gallbladder

  • Liver fairly large (single or bilobed), typ. L side - orange to brown - if yellow/tan 🡪 fatty (r/o normal seasonal vs. abnormal high fat diet)
    • Separated from pericardial cavity by a septum
  • Gallbladder - most spp. have (except burbot, others); b/w liver lobes in most, caudal coelom in rockfish
  • Bile duct enters stomach or small intestine; most bile = bile salts and taurine conjugates of bile acids (except in carp - principal bile salt = alcohol sulfates)
  • Hepatobiliary system (ZP)
  • Liver – Usually lacks classic hexagonal pattern of lobule organization of mammals.
  • Most (except cod) have a gallbladder.
  • Proportions of glycogen and lipid may be species and diet dependent, caution in making diagnosis of hepatic lipidosis.
75
Q

Describe the respiratory anatomy of teleost fish.

What makes up the gill arch, filaments, and lamellae?

What is the function of gill rakers?

What is the function of the pseudobranch? What are the three types of pseudobranchs?

What fish are obligate air breathers?

What are some facultative air breathers?

A

Respiratory System

  • Not inspiration/expiration 🡪 continuous flow; rate determined by muscular/opercular pumping
  • Gills primary organ in most fish - covered by operculum or skin w/ slits
    • Two sets made up of gill arches (holobranchs)w/ paired rows of 1º gill filaments (hemobranchs)
    • Each 1º filament has perpendicular 2º filaments
    • Most bony fish have 4 gill arches; uniform dark red (pink to white w/ anemia, fades after death, brown w/ methemoglobinemia)
    • Some have gill rakers - sieve to collect food
    • Gill epithelium thin to allow gas exchange - but also vulnerable to pathogens, toxins
    • Have metabolic, excretory functions - damage can subject o respiratory and osmoregulatory challenges
    • Have some capacity to regenerate (w/in 1-2 wks after insult then ~2 wk growth)
  • Bilateral pseudobranchs - dorsocranial to gill arches in most (except catfish, some eels, African knifefish, spiny loaches)
    • 3 types - free (exposed - look like partial gill arch, direct contact w/ water - some perch-like fish, many marine spp.), covered (w/ subtypes - resemble gill arch but have membrane covering -cyprinids, salmonids), glandular (deep w/in connective tissue - some gouramis, snakeheads, featherbacks)
    • Delivers O2 to choroid of eye via carbonic anhydrase pathway, suspected of regulating intraocular O2 and pressure - depends on hydrostatic and osmotic pressure, pH, pCO2
    • Some also deliver O2 to vascular rete of swim bladder
    • Proposed osmoregulatory and glandular function not understood
    • Surgery (removal, ablation, cautery) when ocular gas nonresponsive to medical management
  • Most have opercula - appearance varies; sturgeon doesn’t completely cover gill, marine angelfish - spike
    • Opercular flaring - egg incubation temps, genetics, trauma, nutritional issues
      • Consequences vary from cosmetic to gill damage
    • Some lack opercula (triggerfish, eels, frogfish, lumpfish, seahorses, sea dragons, pipefish)
  • Use pressure change to move water over gills; some swim to do this (must ventilate these under manual or chemical restraint!)
  • Air-breathing can occur - if low DO or survive brief periods out of water
    • Obligate air-breathers
      • Rudimentary gills, do not do enough gas exchange over gills for respiration, so if air access restricted unable to ventilate
      • Gourami, betta, snakeheads (labyrinth organ), African reedfish, arapaima, non-Australian lungfish (lung), African knifefish, FW butterflyfish (swim bladder), electric eel, mudskippers, swamp eel (pharynx), mudskippers (skin), weather loach (intestine)
  • Facultative air-breathers
    • Maintain gas exchange across gills and use air when DO is low
    • Australian lungfish (lung), arowana, Atlantic tarpon, gar, various catfish (swim bladder), Alaska blackfish (esophagus), various catfish (GI tract, labyrinth organ)
  • Organs can include buccal/pharyngeal cavity surface, GI tract, swim bladder, lungs
  • Skin respiratory in many fish, including larval stages - directly observed
  • Many FW teleosts able to do aquatic surface respiration (ASR) - when DO is low - surface to skim air/water interface d/t higher DO content

● Respiratory system

  • Gills – respiration, osmoregulation, excretion.
  • Respiratory efficiency complicated by higher density of water, lower availability of DO, variable osmolality of aquatic environments.
  • Four pairs of bony arches extend from roof to floor of pharynx.
    • Two diverging rows of filaments extend posteriorly and laterally.
    • From filaments, plate-like lamellae (site of gas exchange).
      • Oriented parallel to flow of water.
  • Pseudobranch – High in carbonic anhydrase, believed to increase O2 delivery to retina via choroid rete.
76
Q

Describe the cardiovascular anatomy of teleost fish

Trace the flow of blood through the heart. How many chambers are there?

What portal systems do they have?

What is the secondary vascular system?

What are some commonly used venipuncture sites?

What makes the blood of humphead wrasses and Japanese eels blue-green?

What makes the blood of icefish clear?

If blood is pale tan to brown, what environemental condition should you be concerned about?

A

Cardiovascular System

  • All bony fish have 2-chambered heart w/ 4 distinct regions
    • Sinus venosus 🡪 atrium 🡪 ventricle 🡪 bulbus arteriosus 🡪 ventral aorta, gills, dorsal aorta, organs
    • Atrium and ventricle partitions in lungfish and coelacanth
    • Pericardial sac filled w/ serous fluid
    • Renal and hepatic portal systems in most fish - proportion of blood passing through varies by spp.
      • May impact PK, toxicity of drugs
    • Curious lymphatic system - in some fluid system separate from 1º circulation (lymphatic system)
    • Secondary vascular system (SVS - not lymphatic system) well-described too
      • Larger in volume, similar constituent to plasma, lacks most cellular components
      • Lower circulation rates (sometimes by hours)
      • Has role in gas and ion exchange
    • Stress, hypoxia, exercise alter volume + cellularity in each system, esp. PCV of 1º system
    • 1º and 2º connected by anastomoses (unlike other vertebrates)
  • Venipuncture sites - typically ventral tail; others - gill arch, peduncular notch, retro-orbital sinus via oral cavity, cardiac; in elasmobranchs - cloacal superficial vessels, dorsal fin sinus, pectoral fin/radial vessels, mesopterygial vein
  • Blood and serum blue-green (biliverdin) in humphead wrasse, Japanese eels
  • Icefish blood clear (lack hemoglobin)
  • Pale tan to brown blood can be d/t methemoglobinemia (often d/t high nitrites)
    • Cardiovascular system (ZP)
  • Low systemic pressure.
  • Inelastic pericardial chamber, separated from coelomic cavity by transverse septum.
  • Atrium, ventricle -> aortic valve -> bulbus arteriosis.
  • Hepatic and renal portal systems.
77
Q

What parts of the lymphomyeloid system do fish lack?

Where does hematopoiesis occur?

Where is their lymphatic tissue located?

What tissues have local white blood cell populations?

What are melanomacrophages?

What are the immune functions of the kidneys and the thymus?

A

Lymphomyeloid System

  • Lack lymph nodes, Peyer’s patches, and bone marrow
  • Hematopoiesis - 1º in spleen, cranial kidney +/- liver, thymus, pericardium (spp. dependent)
  • Other lymphoid activity - mucosa-associated lymphoid tissues (MALT)
  • GI tract, gills, and skin - pathogen barriers, have local WBC populations
  • Melanomacrophages - ubiquitous, increase w/ antigenic stimulation; pigmented macrophage aggregates (PMA; aka melanomacrophage centers MMC) - high numbers in liver, spleen, Cr. kidney - seen on wet mounts, can increase w/ chronic inflammatory diseases
  • Spleen - dark red to black, sharp edges; multiple in some, no distinct spleen in hagfish, lampreys
  • Thymus - hard to find, doesn’t follow mammalian involution pattern, may be SQ at dorsal edge of operculum, base of gill arches, assoc. w/ pharyngeal epithelium, or w/in Cr. kidney
    • One pair of organs typical, but some have two pairs (clingfish)
  • Hematopoietic and lymphoid systems (ZP)
    • Bones lack hematopoietic tissue.
    • Primarily spleen and kidney.
  • Sturgeons have epicardial and meningeal hematopoietic tissues.
  • Lymph nodes absent in all spp of teleosts.
  • Thymus, spleen, kidney major lymphoid organs.
  • Mucosa-associated lymphoid tissue, also within skin and gills.
  • Anterior kidney – First site of B-lymphocyte production.
  • Posterior kidney is excretory with variable amounts of lymphoid tissue.
  • Thymus site of T-cell maturation.
78
Q

Describe the endocrine system of teleosts.

What is the saccus vasculosus associated with? What is its function?

What is the urophysis? What is its function?

Where is the thyroid gland located? What disorders are common? How does it differ from mammalian thyroids?

Where is the pancreas? What do the endocrine cells produce?

What are the equivalent tissues to the mammalian adrenal? Do any fish have a discrete adrenal gland?

What are the corpuscles of Stannius? What is their function?

What is the function of the ultimobrachial bodies? Where are they located?

A

Endocrine System

  • Resembles other verts. - some features w/ no mamm. counterparts (urophysis, corpuscles of Stannius)
  • Pituitary (hypophysis) - many endocrine functions
  • Saccus vasculosus assoc. w/ hypothalamus, helps detect seasonal changes
  • Pineal organ (epiphysis) - light-sensitive, lies b/w midbrain and dorsal forebrain; can be seen through cartilage in young fish
  • Urophysis - thickening of Cd. spinal cord, neurosecretory cells w/ osmoregulatory function
  • Thyroid gland - usually diffuse, follicles along ventral aorta, branchial arteries, pharyngeal cavity retro-orbital tissues
    • Goiter common - can cause oral or respiratory obstruction
  • Pancreatic tissue - typically diffuse throughout adipose or along portal veins
    • Occasionally seen as white nodules in mesentery
    • In some, assoc. w/ venous system or capsule of spleen; discrete organ in lungfish, some catfish
  • Interrenal tissue (equiv. to mammal adrenal cortex) - Cr. kidney or around posterior cardinal veins
  • Suprarenal tissue (equiv. to mammal adrenal medulla) - scattered chromaffin tissues w/in Cr. kidney
    • In sculpin - tissues combined into distinct adrenal organ
  • Corpuscles of Stannius - endocrine cells in Cd. kidney
    • Act like parathyroid glands and secrete teleocalcin (aka hypocalcin) - blocks Ca absorption across gills
  • Ultimobranchial bodies - endocrine cells in ventral esophagus or in septum separating heart and coelom
    • Act like parathyroid glands and secrete calcitonin for Ca regulation
  • Pseudobranch may have some endocrine functions; gonads secrete androgens and estrogens
  • Endocrine system (ZP)
  • Pineal gland.
  • Pituitary gland.
    • Most prominent cell is the acidophil, growth hormone producing cell of the proximal pars distalis.
  • Urophysis – Exclusive to fish.
    • Neuroendocrine and hemal complex that forms a ventral extension of the terminal SC.
      • Composed of neurosecretory Dahlgren cells within SC and a neurohemal complex on its ventral surface.
      • Axons secrete vasoactive peptide hormones (urotensis) with hypertensive and osmoregulatory effects.
  • Thyroid gland – Contains no C cells, no assoc parathyroid glands.
  • Ultimobranchial gland – Synonymous with calcitonin-secreting parafollicular C cells.
  • Interrenal tissue and chromaffin cells (lack discrete adrenal gland).
  • Corpuscles of Stannius – Small, nodular organs on lateral margins of kidneys of holostean and teleostean fish.
    • May accidentally be mistaken for granumolas or encysted parasites.
    • Produce Ca channel blocker stanniocalciun, prevents influx of environmental Ca across gills; dominant calcium regulatory hormone of fish.
  • Islets of Langerhans scattered throughout exocrine pancreatic tissues.
    • Alpha cells produce glucagon-like peptide, beta cells produce insulin, delta cells produce somatostatin.
79
Q

Describe the urinary system of teleost fish.

What are the multiple functions of this system?

Where are the kidneys located? How do the two kidneys differ in function?

Do FW or SW fish have larger kidneys? How do SW fish kidneys differ from FW fish?

How does the osmoregulation of SW & FW fish differ?

What is the term for FW to SW migration? What about SW to FW migration?

A

Urinary System

  • Hemopoietic, reticuloendothelial, endocrine and excretory functions
  • Located retrocoelomically, vary from parallel, paired to fused single structure
  • FW fish - larger kidneys; SW fish - fewer glomeruli (some have none), missing distal segments of nephron and loop of Henle, cannot concentrate urine above blood osmolality, prone to dehydration
  • Euryhaline sp. - urinary bladder changes permeability based on enviro osmolality, regulates Na, Cl removal
  • Cr. (head) kidney - lymphoid tissue predominates, may also have thyroid tissue
  • Cd. (excretory) kidney - predominantly excretory
  • Ureters move urine from collecting ducts 🡪 urinary papilla or urinary bladder 🡪 water resorption
  • Bladder not homologous to mammalian bladder - develops from distal ureter, not mesodermal origin
  • Internal bod fluid composition/maintenance complex; enviro circumstances play huge role
  • Fluid exchange at gill, GI tract, kidney
  • FW - large influx of water, large volume dilute urine, Na intake by gills (pH dependent)
  • SW - do drink water but do not absorb water via GI tract, Na and Cl diffuse into fish (salt overload), salt excrete by gills, kidneys more involved in Mg, sulfate excretion
  • Some migrate - FW to SW = catadromous (true eels); SW to FW = anadromous (salmonids)
  • Urine collection possible but not easy due to low, continuous flow
  • Urinary system (ZP)
  • Anterior/cranial/head – Mostly hematopoietic and lymphoid tissues, few nephrons, corpuscles of Stannius.
  • Posterior/trunk – Dominated by nephrons, variable interstitial hematopoietic tissue.
    • Nephron has a glomerulus and tubular system.
    • Do not have a significant role in excretion of nitrogenous wastes (gills via ammonia).
    • Marine teleosts have fewer, smaller, relatively avascular glomeruli.
    • FW teleosts have more numerous, large glomeruli.
    • Distal segment of the tubular system is lacking in most marine species.
    • Fish retain the capacity to generate nephrons de novo throughout life.
80
Q

Describe the reproductive anatomy of teleost fish.

What forms of hermaphroditism are common?

What is the term for sequential hermaphroditism where males become females? What species exhibit this?

What is the term for sequential hermaphroditism where females become males? What species exhibit that?

What are the two basic ovarian arrangements? How big are the ovaries?

What is the functional unit of the testis? What are the three varietis of spermatogenic organization in teleosts?

Is fertilization external or internal?

Where do livebearing fish develop?

What are some of the reproductive modalities of bony fish?

A

Reproductive System

  • Highly variable, complex; typically separate sexes but hermaphroditism, parthenogenesis occur
    • Hermaphroditism esp. common w/in Perciformes (parrotfish, wrasses, damsels, gobies)
      • Protandry (sequential; males become females) - gilthead seabream, clownfish
      • Protogyny (sequential; females become males) - Indo-Pacific cleaner wrasse
    • Simultaneous hermaphroditism - can release viable eggs or sperm in same spawning - hamlets
    • Parthenogenesis - less common but happens (Amazon mollies - all female)
  • Some show sexual dimorphism and some assoc. skin changes can be mistaken for pathology
  • Testis - typ. elongated, paired, lobular (common) or tubular;
    • Assoc. connective mesorchium; surrounded by tunica albuginea
    • Can look like ovaries in young fish 🡪 wet mount to differentiate
    • Ducts can both store and transport sperm
  • Ovaries - vary from cultures of follicles to organized organs (paired, fused, or coiled)
    • Assoc. connective mesovarium
    • Mature ovaries can take up to 70% of the coelom
    • Typ. paired - fused in some spp. (lampreys, hagfish, mollies, guppies, medaka)
    • Types of ovaries
      • Cystovarian - ova released into oviduct; (most bony fish, gar)
      • Gymnovarian - ova released into coelom 🡪 ostium 🡪 oviduct (lungfish, sturgeon, bowfin, cartilaginous fish)
      • Semicystovarian (2º gymnovarian) - ova released into coelom 🡪 urogenital pore (salmonids)
  • Live-bearing species - embryos develop in either oviduct or the uterus
  • Fertilization can be internal or external
  • Reproductive system
  • Gonads, efferent ducts (oviduct or ductus deferens), genital papilla.
  • Two basic ovarian arrangements – Cystovarian, gymnovarian.
    • Most are cystovarian – eggs released into central ovarian cavity contiguous with the oviduct.
      • Some spp, eggs release into coelomic cavity and are expressed through an elongated or short oviduct segment.
      • Functional unit of ovary is the follicle.
        • Oocyte surrounded by sheaths of theca and granulosa cells.
      • Primordial germ cells/oogonia -> ovarian germ cells (oocytes/follicles) -> ovulation -> post-ovulatory follicle, rapidly resorbed by resident macrophages.
      • Synchronous spawners – all eggs spawned simultaneously.
        • Female dies or spawns again next year.
      • Asynchronous spawners – Spawn multiple times, only expel some follicles at each cycle, different folliculogenic phases may be evident continuously.
  • Functional germinative unit of testis – spermatocyst.
    • Three major varieties of spermatogenic organization – Tubular, unrestricted spermatogonial, restricted spermatogonial.
      • Tubular – Spermatocysts develop throughout entire length of each seminiferous tubule.
      • Unrestricted spermatogonial – Most common, lobules originate blindly at periphery of testis.
      • Restricted – Spermatocysts initially form only at blind ends of tubules at periphery of testis, maturation progressive within spermatocysts as they migrate toward a central duct to be expelled.
      • Male germ cells become smaller as they occur.
81
Q

Discuss megalocytiviruses in Teleosts.

What family of viruses does this belong to?
- What other genera are in this family?

What are some of the megalocytiviruses that affect fish?
- Which one is reportable?

What are the clinical signs of this disease?

What findings are seen on necropsy?
- What are the findings on histology?

What is morbidity and mortality like with this disease?

How is it diagnosed?

How is it treated and prevented?

A

Megalocytivirus (MCV) in Teleosts
* Global with wide host range
* Icosahedral, double-stranded DNA virus, one of 6 genera within iridoviridae

Iridoviridae
* Iridovirus
* Chloriridovirus
* Decapodiridovirus (insects and crustaceans)
* Ranavirus (herptiles and fish)
* Lymphocystivirus
* Megalocytivirus (freshwater and marine finfish)

Megalocytivirus
* Infectious spleen and kidney necrosis virus (ISKNV)
- Red seabream iridovirus (RSIV)
– Caused by genotypes RSIV and ISKNV
– Reportable
* Turbot reddish body iridovirus (TRBIV)
* Scale drop disease virus
* Clinical signs: abnormal swimming/position, anorexia, lethargy, ascites, ulceration, hemorrhages, anemia, white feces
– Can have no external lesions OR color change
* Necropsy: enlarged spleen with petechiae, amber/hemorrhagic fluid
– Inclusion body-bearing cells (IBCs)
– Hypertrophied cells (thought to be monocytes or macrophages) with large foamy or granular basophilic inclusions in cytoplasm
– Commonly found in spleen, kidney, liver, intestine
* Morbidity and mortality rates vary from low, chronic to acute, to as high as 100%
– Subclinical carrier states exist in some spp
* Diagnosis via PCR and IFAT for confirmation and typing
* Transmission
– Warmer temps increase outbreaks
– Spread via cohabitation, contaminated water, consumption of infected fish/tissues
* Treatment
– None, depop and disinfect
– 15 min exposure to potassium permanganate, formalin, sodium hypochlorite
– Raise pH to 11 for 30 min
* Prevention
– Commercial vaccine available, but appears to only prevent for a certain period of time then eventually break with disease

82
Q

Discuss betanodaviral infection in teleost fish.

What family and genus do these viruses belong to?

Which viruses affect what species?
- What is the warm water generalist?
- What is the cold water generalist?
- What are the two known species specific viruses?

What are the clinical signs these viruses cause?
- What demographic is typically affected?
- What is mortality like?

How is this diagnosed?

How are these viruses transmitted?
- What are the known vectors?

How is this treated and prevented?

A

Betanodavirus in Teleost Fish
Family: Nodaviridae, Genus: Betanodavirus

Species
* Red-spotted grouper nervous necrosis virus (RGNNV)
– Warm water fish, wide host range
* Barfin flounder nervous necrosis virus (BFNNV)
– Cold water fish, wide host range
* Striped jack nervous necrosis virus (SJNNV)
– Narrow host range (striped jack)
* Tiger puffer nervous necrosis virus (TPNNV)
– Narrow host range (tiger puffer)

Global, wide host range (marine and freshwater finfish)
* Small, spherical, nonenveloped, two single strand positive sense RNA
* Targets CNS → neuro signs
* Affects younger stages > older
* Higher temps → increased incidence in older stages

Mortality high
* Incubation 2-7d with death 1-2d after onset of CS

Diagnosis
* Presumptive with CS + histo evidence of vacuolation and neural degeneration in CNS
* Confirmatory: PCR, IFAT, IHC, culture

Transmission
* Horizontal and vertical, exposure to contaminated water/feces/vectors
* Vectors = wild marine crustaceans, zooplankton, frozen fish/mollusks

Treatment - none

Prevention
* Good husbandry/biosecurity including quarantine and screening measures
* Stress increases severity so optimize tank with ideal temp/stocking density
* Vaccines exist but impractical for early life stages which typically have most severe disease

83
Q

Discuss picornaviral infections in teleosts.

How does bluegill picornavirus present?

How does Europen eel picornavirus present?

How does clownfish picornavirus present?

A

Picornaviruses
* Small nonenveloped, relatively newly discovered in fish with limited info on pathogenicity, host specificity, control, and prevention but evidence there is a wide host range with many asymptomatic cases detected in unrelated spp

Bluegill picornavirus
* inflammation/erythema at fin base, hemorrhage, exophthalmia, ascites

European eel picornavirus
* All cases to date have had concurrent Aeromonas infection, so CS may be mixed

Challenge studies with just virus resulted in mortalities without over external signs
* Chronic mortalities in clownfish production facilities linked to novel picornavirus (related to bluegill picornavirus in genus Limnipivirus) - termed clownfish picornavirus (CFPV)
* Nonspecific CS
* Histo - cell necrosis, mononuclear cell inflammation

84
Q

Discuss tilapia lake viral infections in teleosts.

What species are affected?

What are the clinical signs?

What are the histological findings?
- What types of inclusion bodies are noted?

How is the virus transmitted?
- How is it shed?

How is it prevented?

A

Tilapia Lake Virus (TiLV)
* Reported in N and S America, Africa, and Asia
* Affects tilapia (Oreochromis spp) and mango tilapia (Saratherodon galilaeus)
* CS - darkening, skin erosions, ocular lesions, ascites, lepidorthosis, pale gills, hemorrhage

Causative agent = Tilapia tilapinevirus - Orthomyxo-like virus

Histo
- focal hemorrhage in leptomeninges
- vascular congestion and perivascular cuffing of lymphocytes,
- hepatocellular necrosis
- eosinophilic intracytoplasmic IB in hepatocytes and splenic lymphocytes

Transmission - horizontal via direct contact or ingestion and vertical transmission
* Virus sheds in mucus, feces, and fertilized eggs
* Risk of transmission less if frozen filets of tilapia stored 14d at -20C in SUBCLINICALLY infected tilapia, and 90d at -20C if clinically affected tilapia

Diagnosis
* Presumptive with CS and histo
* Confirmatory - PCR, viral isolation, in situ hybridization

Prevention
* Disinfection with chlorine, iodine, hydrogen peroxide, Virkon
* Experimental vaccine only, promising

Treatment - none

85
Q

Discuss erysipelas in Teleost Fish.

What is the main species of zoonotic concern?
- What stressors contribute to mortality?

What fish have been affected by E. piscisicarius?
- What lesions were seen?

How is this disease managed?

A

Erysipelothrix in Teleosts

E. rhusiopathiae important pathogen in fish and mammals, zoonotic
* Ubiquitous - associated with decomp of nitrogenous substances
* Causative agent in several outbreaks in fish
* Short-fin and long-fin eels in Australia
* High temps and transport stressors likely impacted mortality rate
* Barramundi in N. America

E. piscisicarius sp. Nov.
* Cyprinidae (bars) and Characidae (tetras)
* Recently isolated from western mosquitofish (Poeciliidae)
* Necrotizing facial dermatitis

Management
* Lesion severity and rapid progression/spread make management difficult
* Antibiotics limited success
* Autogenous oral vaccine → reduced incidence but did not prevent
* Disinfection - important to clean and remove biofilm prior to disinfection

86
Q

What is the causative agent of tetra disseminated microsporidiosis?

What lesions are seen on histology?

How is this disease diagnosed?

How is it treated?

A

Fusasporis stethaprioni
* Microsporidium
* Causative agent of tetra disseminated microsporidiosis (TDM)
* Identified in 2 tetra spp: black tetra (Gymnocorymbus ternetzi) and cardinal tetra (Paracheirodon axelrodi)
* Histo - microsporidium spores in cells on H&E stain, macrophages preferred cell type
* Diagnosis
– Presumptive diagnosis if nonxenoma forming microsporidium seen in liver and intestine
– Definitive diagnosis with genetic characterization of DNA of spores
* Treatment - varying success
– Fumagillin, benzamidazole derivatives, toltrazuril
– Disinfection - chlorine, ethanol, sodium hypochlorite, Virkon
– No vaccine available

87
Q

Discuss antibiotic resistance in public aquaria.

What is the difference between innate and acquired antimicrobial resistance?

What are these standard definitions for antimicrobial resistance?
- Multidrug resistant
- Extensively drug resistant
- Pandrug resistant

How does assessing resistance differ between a clinical and an epidemiological standpoint?

Describe the public aquaria AMR cycle
- How does chlorination affect AMD?
- How does UV affect AMD?
- How does ozone affect AMD?
- How can AMR elements be introduced into aquarium systems?

What are the four classes of drugs based on the European Medicine’s Agency of AMR?

What are some of the common bacterial pathogens affecting taxa in public aquaria?
- Which are the most resistant?
- What antibiotics show the most promise for use?
- How does it vary by taxa - fish, amphibians, birds?

A

Antibiotic Resistance in Public Aquariums
Fowler 10 Ch. 59

Resistance Mechanisms
* Despite different mechanisms of action, all AMD (antimicrobial drug) classes have strains with AMR (antimicrobial resistance)
* Innate AMR, distinctive in a species or genus, is a slow adaptive evolutionary process in response to environmental pressure
* Acquired AMR is a quick adaptive process to an abrupt selective AMD pressure
* Mutation in the bacteria’s genome or acquisition of foreign DNA material encoding AMR-resistant genes through horizontal gene transfer are the two main genetic strategies for a bacterium to gain AMR

Multidrug Resistance Organisms
* Multiple drug resistance (MDR) occurs in multidrug-resistant organisms that show in vitro resistance to more than one AMD
* Extensively drug resistant - at least one agent in all but one or two antimicrobial classes
* Pandrug resistance - nonsucuscebtility to all agents in all antimicrobial categories

Testing
* Veterinary AMD prescriptions should be backed by antimicrobial susceptibility tests (AST)
– The most common methods for these ASTs are disk diffusion and minimum inhibitory concentration (MIC) tests
– The reliability of disc diffusion test results decreases at lower incubation temperature, so MIC, performed by broth dilution, is preferable in cultures done at less than 28°C
* In a clinical perspective, a bacterial clinical breakpoint is the MIC or disc zone size value utilized to classify a bacterial strain as susceptible, intermediate, nonsusceptible, or resistant
– These definitions are established by breakpoints which are based on AST values for the isolate, in the AMD pharmacokinetics and pharmacodynamics (PK/PD) in the animal species, and in the clinical outcome based on previous data, so they are pathogen, AMD dose, and host-specific
- An epidemiological perspective will be centered on the distribution of susceptibility to an AMD from different isolates of a specific bacteria species, regardless of the animal species affected
– These definitions use epidemiological cut-off values (ECOFFs=ECV), which define bacteria species, using statistically determined MIC or disc diffusion values, as wild type (WT), as opposite to nonwild type (NWT), by the absence of acquired and mutational mechanisms of resistance to a specific AMD
- Few ECVs are determined for bacteria isolated from aquatic animals (e.g., A. salmonicida, A. hydrophila, Flavobacterium columnare, F. psychrophilum, and Edwardsiella ictaluri)

Antimicrobial Stewardship
- The European Medicines Agency’s (EMA) Antimicrobial Advice ad hoc Expert Group (AMEG) divided AMD classes (and subclasses) into four categories, taking into consideration if they are licensed for veterinary use in the European Union, importance to human medicine according to World Health Organization (WHO), the possibility of transferring AMR from animals to humans, and availability of other veterinary antibiotics with lower AMR risk

Public Aquarium Antimicrobial Resistance Cycle
* Water supply (e.g., municipal/tap water and seawater) may be a source of resistant elements, and to mitigate this biological contamination, water may be treated (e.g., ozone or ultraviolets [UVs]) before being in contact with the animals
– Water treatments and disinfection methods (WTDM) commonly used in public aquariums (e.g., activated carbon, chlorination, UV, or ozone) will significantly decrease the presence of ARBs, ARGs, and AMD residues
– Chlorination eliminates AMD as ampicillin, tetracycline, cephalexin, and cefotaxime
– Macrolides are poorly removed by UV, while flumequine is effectively removed by UV/ H2 O2 or by activated carbon fixed-bed columns
– Ozone may significantly reduce ofloxacin, trimethoprim, sulfamethoxazole, sulfapyridine, and clarithromycin levels
* Wild animals, even from pristine ecosystems, may also harbor ARBs/ARGs
* Food may also carry resistant elements in live animals, raw fish feed, dry pelleted food, and in vegetables
* The risk of staff being a source of ARBs and ARGs for the animal collection, and vice versa, could be mitigated by biosecurity measures (e.g., footbaths, handwashing, and disinfection protocols, general disinfection protocols, wearing working clothes and shoes, baths prior to and after diving, etc.) which may also be applied to public interactions with animals (e.g., touch pools and diving with animals).
* Routine bacterial cultures and ASTs should be part of the diagnostic testing performed under the health control program

88
Q

A recent study investigated the efficacy of acyclovir against cyprinid herpesvirus 3 infection in Koi.

What is the scientific name of this species?

Describe koi herpes viral disease
- What is the temperature range of this disease?
- What role do latent infections play?
- What are the clinical signs?
- How is this disease managed?

What is the mechanism of acyclovir?
- How has it been used in this disease in the past
- What pharmacokinetic data is available in this species?

What was this study design?
- What clinical signs were seen in this study?
- Was there a difference in survival?
- What was a potential additional cause of mortality in this study?

A

Efficacy of a multidose acyclovir protocol against cyprinid herpesvirus 3 infection in koi (Cyprinus carpio)
AJVR 2022 - Mariana Sosa-Higareda, ONE DACVM

OBJECTIVE To evaluate the effect of a multidose acyclovir protocol on koi herpesvirus (KHV) viral load and mortality in a cohabitation challenge.
ANIMALS 180 koi fish.
PROCEDURES Forty fish (shedders) were immersed in a 0.5 KHV plaque-forming units/mL static bath for 8 hours. Mock shedders were treated similarly but exposed to cell culture media. KHV shedders were then transferred into 8 tanks (5 shedders per tank) containing 10 naïve fish (cohabitants) each.** Fish in the acyclovir group (AT) received a 10 mg/kg acyclovir intracoelomic injection 1, 3, and 6 days after the first confirmed KHV mortality**. Positive controls (PC) were treated similarly but received sterile saline injections. Negative controls (NC) were exposed to mock shedders. Morbidity and mortality were evaluated daily for 50 days post-challenge. Quantitative PCR was used to determine viral load in the gill biopsies of shedders and cohabitants collected at days 19 (T1), 22 (T2), 25 (T3), 34 (T4), and 50 (T5) post-challenge.
RESULTS Survival curves analyzed by the Gehan-Breslow-Wilcoxon method revealed a delayed onset of mortalities and a significantly lower KHV load at T2 and T3 detected in AT cohabitant fish (P = .042) compared to positive control group. However, there were no significant differences in overall mortality or viral loads at T5.
CLINICAL RELEVANCE The acyclovir protocol used in this study did not control viral infection or mortality at the end of the 50-day trial. Shorter intervals between injections could improve outcomes, but the additional stress inflicted by handling should be considered. Exploring other therapeutic alternatives and doses is warranted.

Basics:
- KHVD – temperature dependent = disease between 16-28 degrees C
- Latency infections: Stress 🡪 viral replication and shedding 🡪 outbreaks
- CS: nonspecific and include lethargy, hyporexia, pale and necrotic gills, enophthalmos, reduced skin mucous production sometimes leading to sandpaper texture, and ulcerative hemorrhagic skin lesions
- Strict biosecurity is only method of prevention and there is no effective treatment
- Temp manipulation and prolonged salting can disrupt replication and provide palliative tx
- Acyclovir = synthetic 20-deoxyguanosine (guanine) nucleoside analog capable of selectively inhibiting the activity of viral DNA polymerase, thus preventing viral replication
– Reported to decrease KHV cytopathic effects, viral load, and viral gene expression in vitro using common carp brain cells
– PK study – 10 mg/kg in koi fingerlings reached MIC for >24 hrs
–Reduction in mortality and showed safety via ICe route

Details:
- Clinical signs and gross changes in KHV-infected fish were evident in shedders and cohabitants and included anorexia, lethargy, hemorrhagic and ulcerative skin lesions, hyphema, exophthalmia, and pale gills
- highest number of mortalities occurred at days 25 for + control and 36 postexposure in treated groups
- No significant difference in survival between groups results suggest that there is a positive effect on survivability while receiving acyclovir
effect decreases with time after the last dose
- frequently repeated administration is required to achieve adequate therapeutic effects.
- highest mortalities seen immediately after handling and injection – consider diff. routes
- Viral loads measured from gill tissue (gills is a main target tissue for KHV, along w/ spleen and kidney)

Take-away:
- The 3-dose acyclovir protocol in this study was not effective in controlling KHVD long-term as similar viral loads and mortality were observed between treated and positive control groups at the end of the trial.
- There was a significant increase in survival in AT group after 2 doses of acyclovir and after fish had received 3 doses of acyclovir

89
Q

A recent study (Perret-Thiry) investigated prolonged immersion in MS-222 for euthanasia of goldfish.

What is the scientific name of the goldfish?

A previous study (Balko et al) also investigated MS-222 for euthanasia.
- What were their findings? What doses and formulations did they use?

What doses and formulations were used in this study?
- Was euthanasia succesful in this study?
- What factors may account for the differenceds in the two studies?

A

JAVMA 2022 260(8):911-915
Evaluation of prolonged immersion in tricaine methanesulfonate for juvenile goldfish (Carassius auratus) euthanasia
Perret-Thiry C, Raulic J, Vergneau-Grosset C

ABSTRACT:
Objective: Doses of buffered tricaine methanesulfonate (MS-222) up to 1000 mg/L for 15 minutes are reported inefficient to produce euthanasia in goldfish. The goal of this study was to determine if goldfish can be euthanized by more prolonged immersion in MS-222.
Animals: 24 healthy goldfish (weight range: 1 to 10 g) were randomly assigned to 4 groups of 6 fish.
Procedures: The first group (G1) was exposed to 500 mg/L buffered MS-222 for 15 minutes then placed in freshwater for 3 hours. The second (G2) and third groups (G3) were exposed to 1000 mg/L of buffered MS-222 for 15 minutes then placed in freshwater for 3 hours and 18 hours respectively. The fourth group (G4) was exposed to 1000 mg/L of buffered MS-222 for 60 minutes then placed in freshwater for 3 hours. Time to cessation and return of operculation were recorded. If the goldfish did not resume operculation, heart rate was evaluated by Doppler ultrasonic flow detector.
Results: Median times to apnea were 35 seconds at 1000 mg/L and 65 seconds at 500 mg/L. Re-operculation occurred only in G1 in 5 out of 6 individuals. All fish from G1, 3 fish from G2, 0 fish from G3, 1 fish from G4 had remaining heartbeats at the end of the observation period.
Clinical relevance: Overall, a dose of 1000 mg/L of buffered MS-222 for 15 minutes was efficient to euthanize juvenile goldfish at 20 °C. Different fish body mass and water quality parameters might explain different results compared to previous studies.

Key Points:
* 250-500 mg/L buffered MS-222 for ≥ 10 min historically recommended for fish euthanasia
– Due to its 21-day withdrawal time, MS-222 is not adapted to euthanize food fish species
– Balko et al 2018 found this method inefficient to euthanize goldfish
– Suggests 1000 mg/L buffered MS-222 for 15 min AND pithing or KCl injection
– At temp close to 0 °C, cyprinidae can survive in anoxic condition for months
* In present study, no goldfish in buffered 1000 mg/L MS-222 for 15 min resumed operculation
– After 18 hours in freshwater at 20 °C, no goldfish had remaining heart beats
- Result of Balko et al 2018 was not repeatable
– Different age & body mass of goldfish could explain why buffered 1000 mg/L MS-222 for 15 min worked in juveniles but not adults
– Water quality parameters from Balko et al 2018 were unknown
– MS-222 more efficient when buffered, at higher temp, and at lower hardness
– Powdered MS-222 was used while a MS-222 stock solution was used in Balko et al 2018
– Stock solutions shown stable for 3 months in a dark/cool environment

TLDR: 1000 mg/L of buffered MS-222 for 15 minutes was efficient to euthanize juvenile goldfish at 20 °C

90
Q

A recent study investigated Aqua-Sed for euthanasia fo butterly splitfin.

What is the active ingredient in Aqua-Sed?
- How is it absorbed?
- What is its mechanism?
- What are the advantages and disadvantages of its use?

What concentrations were used in this study?
- What were the results of the study?

What is the recommended concentration for euthanasia in this species?

A

JZWM 2022 53(2):241-248
Comparison Of Three Concentrations Of Aqua-Sedtm For Immersion Euthanasia Of Butterfly Splitfin (Ameca splendens)
Bradley S, Sparrow S, Rowden LJ, Guthrie A

ABSTRACT: The efficacies of three concentrations of 2-phenoxyethanol from Aqua-sedTM were examined to determine the suitability for euthanasia of butterfly splitfin (Ameca splendens). Thirty fish were randomly assigned to be immersed in one of three Aqua-SedTM concentrations: 0.5, 2, and 6 ml/L. Opercular rates and caudal fin stroke rates were quantified, and time to the cessation of physiological measures including heartbeat, caudal fin strokes, reaction to external stimuli, righting reflex, swimming, and operculation were recorded. To test for the effects of concentration of Aqua-sedTM on all times to cessation of physiological measures, a linear mixed model was performed followed by pairwise comparisons with a Bonferroni correction. A proportions test compared the number of fish that lost their heartbeat across Aqua-sedTM concentrations. Varying anesthetic induction times were observed for all three Aqua-sedTM concentrations; time to cessation of physiological measures was fastest with 6 ml/L, followed by 2 then 0.5 ml/L, but only concentrations of 2 and 6 ml/L induced anesthesia in less than the recommended 180 s. Aqua-sedTM concentration had a significant effect on time to cessation of physiological measures (P < 0.01), but not on time to cessation of a heartbeat (P > 0.05). Pairwise comparisons indicate time to cessation of caudal fin strokes, reaction to external stimuli, righting reflex, and swimming significantly decreased as concentration increased (P < 0.01). After 60 min of immersion in Aqua-sedTM the number of fish without a heartbeat differed significantly across concentrations (P < 0.01); 20% of fish immersed in 0.5 ml/L, 90% of fish immersed in 2 ml/L, and 90% of fish immersed in 6 ml/L had no heartbeat. A minimum dose of 2 ml/L of Aqua-sedTM, and an immersion time of 60 min for euthanasia of butterfly splitfin is recommended, with a secondary euthanasia measure to confirm death when the heartbeat remains.

Key Points:
* Aqua-SedTM is a 2-phenoxyethanol–based product
– 2-PE is absorbed via gills and transported by arterial blood to CNS
– MOA is unknown but thought to involve hypoxia secondary to CNS depression
- Advantages: inexpensive, more water soluble than clove oil, no additions are required to buffer or emulsify 2-PE given its more neutral pH
* Disadvantages reported include:
– Prolonged induction times
– Species-specific dosing
– Hyperactivity before loss of consciousness
– Aversive nature (e.g., zebrafish)
– Not suitable for euthanasia of fish intended for consumption
* Current AVMA guidelines recommend fish should be left in an anesthetic solution for a minimum of 30 min after cessation of opercular movement
* Doses recommended for 2-PE are 0.5–0.6 ml/L for finfish
* Study found 2-PE no more aversive to butterfly splitfin than being transferred to a different tank
* All three Aqua-sedTM concentrations induced anesthesia, but at varying rates
– Only 2 and 6 ml/L induced anesthesia within the 180s recommended induction time
* The number of butterfly splitfin that lost their heart beat at 2 ml/L (90%) contrasts with a previous study in unga cichlids in which none at 2 ml/L lost their heart beat
– Cessation of physiological measures were ~3x slower in cichlids, indicating species-specific responses
* Temperature is known to affect the solubility of 2-PE which may influence uptake
– Water solubility of 2-PE decreases as water temperature decreases
– Research also suggests that increased temperature increases the metabolic rate in fish

TLDR: A minimum dose of 2 ml/L of 2-PE and immersion time of 60 min for euthanasia of butterfly splitfin is recommended with a secondary euthanasia measure to confirm death

91
Q

A recent study investigated the oral and IM pharmacokinetics of meloxicam in China rockfish.

Are COX-2 enzymes in fish similar to mammals?

What doses were used in this study?

How did the two routes compare?

A

Journal of Zoo and Wildlife Medicine, 54(1): 8-15
PHARMACOKINETICS OF MELOXICAM AFTER SINGLE ORAL AND INTRAMUSCULAR ADMINISTRATION IN CHINA ROCKFISH (SEBASTES NEBULOSUS)
Colin C. Berg, DVM, Sherry Cox, DVM, PhD, Lauren Mulreany, DVM, Karen Wolf, DVM, DACZM, and Kadie Anderson, DVM, DACZM – Rev AJC

Abstract: Fish species are important for various purposes including aquaculture stock and display animals, but there are significant gaps in the medical knowledge regarding pharmacological parameters and effective pain management. Meloxicam is a nonsteroidal anti-inflammatory drug (NSAID) that has been studied in few teleost species and with several administration routes. However, these species were typically freshwater or euryhaline fish, and evaluation in marine species is lacking. The pharmacokinetic properties of meloxicam were determined in nine adult China rockfish (Sebastes nebulosus), presumed healthy based on physical examination and benign medical histories. Based on a pilot study, China rockfish were given 1 mg/kg meloxicam via IM injection in the epaxial musculature, and, after a 48-h washout period, 1 mg/kg meloxicam was given by PO gavage. Blood samples were collected from the caudal vein at baseline and at nine time intervals over a 48-h time period following administration of meloxicam. Plasma meloxicam concentrations were determined by reverse phase high-performance liquid chromatography, and noncompartmental analysis was performed. The mean peak plasma concentration after IM injection was 4.9 ug/ml, and the mean terminal half-life was 5.0 h. The mean peak plasma concentration after PO administration was 0.07 ug/ml. Based on these findings, IM injected meloxicam reaches plasma levels consistent with therapeutic concentrations in select mammals, and peak levels were maintained for less than 12 h. Single-dose PO administration failed to achieve similar concentrations, and clinical practicality is unknown. Further studies evaluating NSAID multidose regimes and their pharmacodynamic effects may provide additional dosing information.

Key Points:
* Teleost fish possess COX-2 enzymes similar to mammals
* Study eval 1 mg/kg IM and PO injection to China rockfish (cold-water marine species)
* Leakage from IM injection not observed and no regurg seen following PO gavage; no side effects
* Cmax achieved after 1hr for IM, T ½ of ~5 hr
– Therapeutic plasma levels for IM achieved for ~12hr
* Limited detectable level of meloxicam when given PO
– Therapeutic plasma levels not achieved for PO administration
* They sampled a single diff rockfish spp that was given meloxicam q48hr for 4wk which had therapeutic plasma levels, thus therapeutic conc may be achieved with a PO multidose schedule

Take-Home Message:
- IM meloxicam in China rockfish provided transient clinically relevant plasma concentrations (~12hr) and may not be suitable for clinical use.
- Single 1 mg/kg PO meloxicam failed to reach presumed therapeutic plasma concentrations and likely has minimal clinical use

92
Q

A recent study evaluated the placement of PIT tags in teleosts and elasmobranchs in a public aquarium.

What sites were used to place PIT tags in teleosts, sharks, and rays?

Were any adverse effects noted?

A

ZB 2022 41(6) 576-581
Observations on the use of passive integrated transponder (PIT) tags in teleosts and elasmobranchs at a public aquarium, 728 cases, 2007–2020

Abstract
Between 2007 and 2020 at New England Aquarium, Boston, MA, USA, we implanted passive integrated transponder (PIT) tags into 728 fish representing 105 teleost and elasmobranch species to identify animals as individuals. At the time of retrospective data analysis, mean longevity interval (median, range) after tag placement for animals that remained alive (n = 236) was 4.7 years (4.5, 0.3-13.8). Mean interval (median, range) between tag placement and death (n = 317) was 2.1 years (1.6, 0-11.2); and mean interval (median, range) between tag placement and transfer to other facilities (n = 175) was 2.5 years (3.1, 0.1-9.3). Possible adverse effects of tagging were extremely rare. Using the described methods, the equipment cost for every 10 PIT tag implantations was $2.83. PIT tag implantation in fishes is a safe and cost effective method to identify individuals, providing an opportunity to accumulate valuable data regarding individual longevity, welfare, basic demographics, and outcome of medical management. PIT tag implantation is recommended as a routine aspect of acquisition, quarantine, and medical management of fish under human care.

Key points
* Individual ID of fish is often impossible
* Fin notching, fin tags and elastomer tags are other methods to ID fish. However, external identfiers are often undesirable in aquarium setting.
* PIT tag: small glass capsule containing an integrated circuit chip, capacitor, and antenna coil injected into the animal
* In this study, they described observations for PIT tags used over a 14 yr period
* Inserted PIT tags in the left epaxial muscle (most teleosts and sharks), dorsal surface of left pectoral fin (batoidea, rays) or the left lateral base of the tail (Ostraciidae i.e. cowfish, burrfish due to their large armored bodies). Placed tags under sedation in most instances.
* 26 fish died within 4wk of tag implantation. Only 1 fish out of 728 appeared to be adversely affected by the tag (nx showed diffuse ventral dermatitis, mild hemorrhage and purulent exudate at the insertion site). Histo on that animal showed diffuse G(-) bacterial dermatitis with vascular necrosis and gram negative bacterial branchial vasculitis consistent with sepsis.
* Majority of animals survived for years after the tag implant.
* Low incidence of tag failure and tag loss. Retention rate was 99.6%.

Take home message
- PIT tagging is generally safe and effective for fish with low mortality and high rates of tag retention.
- The sites described were effective sites for tagging.

References: none

93
Q

A recent study investigated the effects of UV treatments on aquarium water microbial communities.

What changes in the microbial community were seen with UV exposure?
- What were the predominant taxa that were decreased?
- What effect was there on cyanobacteria?
- What effect was there on Aeromona and mycobacteria?

A

ZB 2023 42(1):133-141
Ultraviolet light alters experimental aquarium water microbial communities
Van Bonn W, Oliaro FJ, Pinnell LJ

ABSTRACT: The effect of ultraviolet (UV) light exposure, alone and in combination with CO2 exposure, on the water microbial community composition was tested in replicate experimental aquaria using source water from an established Amazon-themed exhibit housing mixed species of fishes. Total bacterial abundance, α-diversity metrics, and β-diversity metrics were determined 3 weeks and 1 week before, and weekly during 8 weeks of continuous treatment. The UV treatment significantly lowered the overall bacterial abundance while CO2 treatment had no effect. However, the UV exposure effect was variable across phyla. Some phyla were decreased while others were increased, including some of potential clinical significance. At the genus level, there were no significant differences in the relative abundance of Mycobacteria between treatments and an increase in the relative abundance of Aeromonas spp. with UV light treatment. Further work is needed to determine if the observed effects are dose-dependent or if different exposure doses produce different results.

Background:
* A growing number of studies have examined microbiomes w/ aquarium life support systems
* Relatively few have investigated how common life support methods alter the microbial community structure and subsequently animal health within aquaria
* UV radiation is used to control the proliferation of pathogens in aquarium systems
– However, there are no broadly accepted industry engineering standards for UV use
* Aquarists sometimes infuse aquarium water with CO2 to:
– Provide a carbon source for plants
– Aid in pH control

Key Points:
* Experimental setup was intentionally designed to evaluate the influence of UV radiation and CO2 gas infusion on microbial communities in the water of an Amazon-themed exhibit
* Microbial community richness and diversity increased w/ UV radiation but not CO2
– May be the result of ecological niches previously occupied by dominant community members (i.e., Bacteroidetes and Actinobacteria) being made available to a wider variety of taxa after UV radiation reduced the abundance of the predominant taxa
– However, this increased richness and diversity may also be the result of a reduced abundance of 16S rRNA gene sequences from predominant taxa within amplicon libraries, which resulted in the sequencing of a greater number of rare taxa within these samples
* Absolute microbial abundance decreased significantly w/ UV (CO2 had no effect)
– Driven by decreases in Bacteroidetes and Actinobacteria
* Bacteroidetes & Actinobacteria relative abundance decreased w/ UV
– Concurrently relative abundance of other microbial taxa increased
– Including Cyanobacteria, a potentially harmful toxin-producing phyla
– UV exposure may provide Cyanobacteria with an advantage vs. other taxa
* UV displayed mixed results in decreasing the relative abundance of taxa of clinical interest
– The relative abundance of Enterobacteriaceae was higher when treated with UV
– The genus Aeromonas had higher relative abundance following UV exposure
– No significant treatment effect on Mycobacterium following UV exposure

TLDR:
- UV exposure treatment significantly lowered the overall bacterial abundance in test aquaria, but this was largely the result of decreases in Bacteroidetes and Actinobacteria.
- There was no evidence of UV decreasing the relative abundance of clinically relevant microbial taxa

94
Q

A recent literature review evaluated the psychological and social well-being of bony fishes in zoos and aquariums.

How well-represented were teleost and elasmobranch fish on welfare publications across traditional zoo journals?

What findings have been associated with decreased welfare in fish?

A

ZB 2023 42(2):185-193
Psychological and social well-being of bony fishes in zoos and aquariums
Oldfield RG, Bonano PE

ABSTRACT: Research on the behavior of animals in zoos has been conducted for decades and observations have provided information that has improved the psychological and social well-being of animals. However, research on fishes in zoos and aquariums seems to be lacking. Here we assess the current state of research on fishes in zoos and aquariums by surveying peer-reviewed literature. Our assessment differs from previous surveys in that we examine the taxonomic classes Chondrichthyes (sharks and rays) and Osteichthyes (bony fishes) separately. Our survey finds that bony fishes have been drastically underrepresented in zoo journals, more so than chondrichthyans, revealing an urgent need for zoos and aquariums to conduct research on the behavior of the bony fishes in their care, to ensure a positive state of psychological and social well-being. To plot a course for the future, we discuss the few studies that have been conducted on the behavior of bony fishes in zoos and aquariums, and we discuss research conducted on bony fishes in food-fish aquaculture and biomedicine to identify the types of studies that could be conducted in zoos and aquariums. We conclude that data-driven analyses of fish behavior could aid in development of evidence-based practices that enhance the well-being of bony fishes in zoos and aquariums, just as they already do for terrestrial animals.

Background:
* AZA definition of animal welfare: “an animal’s collective physical, mental, and emotional states over a period of time, and is measured on a continuum from good to poor”
* Bony fish have been drastically underrepresented in zoo and aquarium research
* Bony fishes are now recognized to be complex individuals of advanced cognitive ability
* Recent consensus is that they can feel pain, fear, and emotions

Key Points:
* This lit review surveyed three zoo-oriented research journals: Zoo Biology, Journal of Zoo and Aquarium Research, and International Zoo Yearbook
– Did not survey Journal of Zoo and Wildlife Medicine or Drum and Croaker
– Also surveyed two additional journals: Animal Behaviour and Conservation Biology
– All three zoo journals overrepresented mammals, but only slightly underrepresented birds
– Largely underrepresented reptiles and bony fishes
- Across the biological sciences researchers over-represent mammals and underrepresent fishes
- In zoo and aquarium research sharks and rays receive a proportionate amount of attention and bony fishes are particularly overlooked
- Changes in feeding behavior are well known indicators of welfare in bony fishes
- Latency to start feeding and daily food intake are often reduced as a result of stress

95
Q

A recent study investigated ntopical naltrexone as a treatment for lateral line depigmentation.

What is lateral line disease?
- What families are particularly susceptible?
- What are suspected etiologies?
- What treatments are traditionally used?

What are the effects of naltrexone on wound healing?

How did naltrexone treated fish heal compared to Ilex treated or control fish?

A

Journal of Zoo and Wildlife Medicine 54(1): 137–142, 2023
NALTREXONE AS A PROMISING TREATMENT FOR CLINICAL SIGNS OF LATERAL LINE DEPIGMENTATION IN PALETTE SURGEONFISH (PARACANTHURUS HEPATUS)
Megan M. Strobel, DVM, Kendra C. Baker, DVM, Aimee L. Berliner, DVM, Karisa N. Tang, DVM, MS, Dipl ACZM, Caitlin M. Hepps Keeney, DVM, and Gregory A. Lewbart, MS, VMD, Dipl ACZM, Dipl ECZM (ZHM) – rev by AJC

Abstract: Lateral line depigmentation (LLD) is a common condition in managed tropical saltwater fish, and treatment is somewhat elusive. Naltrexone, an opioid receptor antagonist, enhances epithelial cell replication, cytokine production, and angiogenesis to stimulate wound healing in mice. A treatment trial with 11 palette surgeonfish with LLD was performed. Seven fish underwent a single topical treatment of a mixture of 4 mg naltrexone and 10 g iLEX petroleum paste applied topically to LLD lesions. Four additional fish served as controls: two received only topical iLEX and two received no treatment. Severity of disease was scored on a 0–3 scale. Inflammatory response was gauged on a separate 0–3 scale for 5 d after treatment based on severity of erythema, as seen in a clinical case performed prior to this study. After 11 days, four affected animals that lacked an inflammatory response after naltrexone topical treatment were administered a single dose of intralesional 0.04% naltrexone (4 mg diluted into 10 ml saline). Lesions on all fish were photographed and measured at day 33. Clinical improvements in lesion size and pigmentation were apparent following topical naltrexone therapy in fish with severe lesions. Although these cases are promising, more data are needed to further evaluate the effectiveness of naltrexone 0.04% in treating LLD lesions in palette surgeonfish.

Key Points
* Lateral line depigmentation – focally depigmented to ulcerated skin along the lateral line of the head and flank, typically systemically unaffected though lesions can become secondarily infected
– SW surgeonfish and tangs (Acanthuridae) and anglefish (pomacanthidae) are particularly susceptible
– Postulated etiologies – environmental (activated carbon, ozone, high Cu, poor water quality, stray electricity, overcrowding), nutritional (inadeq Vit A or C in surgeonfish), and infectious (diplomonad flagellates or reoviruses)
– Treatment options include resolve inciting parameters & topical becaplermin
* Naltrexone – opioid receptor antagonist; topical low dose enhances wound healing via temporary intermittent blockade of the opioid growth factor to promote angiogenesis, and stimulate fibroblasts, epithelial cells, mast cells and collagen to create a granulation layer and have anti-inflamm effects on B and T immune cells
– Study investigated use of naltrexone for the treatment of clinical appearance of LLD
– Surgeonfish w/ LLD had greater improvement 33d after naltrexone tx compared to ilex only and control
– Fish w/ more severe initial LLD lesions had the greatest percentage of improvement
– Naltrexone treated fish had a greater reduction in wound size than illex or control fish
– Fish treated w/ naltrexone displayed normal blue pigmentation by day 33 vs one from the illex group had irreg black pigmentation in the treated region
- Differences in clinical response seen in animals w/ varying dz severities
* Inversely proportion relationship btwn inflammation score and percent change in LLD lesion
– Fish w/ higher inflammation scores had more notable clinical improvement, but were also more signif affected by LLD
* Red coloration of the skin seen w/ treatment 🡪 suspected to be due to inflammation
– Fish that did not have red coloration to the skin ( no signs of inflammation) were considered to have received an inadequate dose and were re-dosed with an injectable form of naltrexone
– Do NOT recommend injectable naltrexone application 🡪 carried addtl risk of iatrogenic complications and did not improve efficacy

Take Home
- Clinical improvements in lesion size and pigmentation was apparent following topical naltrexone therapy in fish with LLD, with the most with severe lesions showing the greatest improvement.