Interventions Flashcards

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1
Q

Methods of diagnosis/detection of tuberculosis infection in non-human primates

A
  1. Tranquilise animal
  2. Inject 0.1ml containing 1250 iu mammalian PPD tuberculin in sterile water i/d into upper lid of left eye (or i/d in mid abdomen or thigh) with 27 or 25G needle (PPD = precipitated fractions of culture filtrates)
  3. Check for swelling at 8, 24, 48, 72 hours and score.

0 No reaction Negative
1 Bruise Negative
2 Erythema of palpebrum and no swelling Negative
3 Erythema of palpebrum and slight swelling ?
4 Swelling of palpebrum, drooped eyelid and erythema Positive
5 Swelling and/or necrosis, eyelid closed Positive

No true gold standard, except finding disease lesions

  • tuberculin testing
  • BLOOD γ- INTERFERON (PRIMAGAM ASSAY)
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2
Q

Reasons for unreliability of tuberculosis detection and dealing with false positives and false negative results.

A

False positives:
• Use of buffered diluents instead of sterile water for diluting the tuberculin
• Impurities in the Tuberculin - especially
Koch’s old TB (= unfractionated heated concentrates of Mycob. culture filtrates)
• Trauma due to poor injection technique
• Previous BCG vaccination
• Cross reaction with atypical or saprophytic mycobacteria which share some antigens

False negatives
• Anergy due to overwhelming pulmonary tuberculosis
• Testing early in infection before development of hypersensitivity
• Systemic fungal disease
• Concurrent measles infection or vaccination
• Immunosuppressive drugs
• Technical errors
• Localized desensitization if the test is repeated in the same site

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3
Q

Use of tuberculosis diagnostic methods

A

Prevention

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4
Q

Differential diagnosis of enteric disease in non-human primates and methods of detection of shigella infection

A
Collection and transport of samples:
• Rectal swabs vs. faecal samples
• Transport time to lab
• Transport media
• Temperature

Differential diagnoses:

  • Bacteria (shigella, salmonella, e.coli, campylobacter, yersinia)
  • Environmental factors (diet)
  • Parasites (entamoeba, balantidium, nematodes, cestodes)
  • Viruses (rotavirus)

Frequency of sampling:
• Detection rate from known clinical cases = 44% on any one sample
• Sample on three consecutive days = 82% (P = 1-(1-x)n, x = detection rate, n = no. of days)
• Probability = 90% for 4 days sampling and 94.5% for 5 days

Poor detection due to:
• intracellular maintenance
• dilute/bloody sample
• faeces not fresh
• insufficient selective media – overgrowth especially by E.coli
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5
Q

Control of endemic shigellosis in non-human primate colonies

A
Consider:
• number of animals involved
• type of housing
• number of staff
• in vitro sensitivity of bacterium to antibiotics
• stress factors for the animals

What to do:
• Monitor all cases of diarrhoea
• Dose adequately
• Monitor staff
• Oral vs. injectable medication
• Good sampling methodology
• Good hygiene
• Good clinical monitoring
• Elimination of carrier state or reduction of bacteria below detectable level?
• Vaccination – oral vaccines have been tried but high doses are needed and cause shedding of bacteria (protect against disease but do not prevent carrier state)
Control depends on breaking the cycles of infection and transmission by 1) improving hygiene by:
• restricted entry to units to prevent cross infection
• protective clothing which is disposed of when soiled.
• disinfectant footbaths, used correctly.
• uncontaminated water supply
• washing fruit in chlorinated water
• barriers between areas to limit contact
• power washing with hot water and disinfection

2) detecting and treating carriers. Include the following groups when screening:
• all clinical cases of diarrhoea
• new arrivals: no animals should be moved to another unit until the entire batch is free from infection (all in, all out)
• post weaning
• following any period of stress, e.g. surgery, movement
• random sampling of all animals on a regular basis

And 3) reducing stress by:

  • Enrichment
  • socialisation
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6
Q

Risk assessment and considerations of endemic enteritis in non-human primates

A
Assessment of the problem:
• Number of clinical cases - correct diagnosis
• Routine screening results
• Number of carriers
• Health and safety assessment
• Staff:animal proximity
• Stress levels in animals
• Use of animals
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7
Q

Recognise that human-mediated translocations of wild animals occur for many reasons, such as trade, rehabilitation and conservation.

A
  • Organised sport hunting
  • Rehabilitation
  • Trade
  • Conservation
  • Human-wildlife conflict
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8
Q

Critically analyse the potential changes in host-parasite interactions as a consequence of wild animal translocations, and the effect of these changes on risk from disease.

A

Translocation cause changes in host-parasite interactions as a result of:
• Introduction of an alien parasite
• Aggregation of hosts – amplification parasites (R0 changes)
• Host loses parasites (enemy release)
• Released animals contract destination parasite
• Gain parasite during transport
• Stressors influence immunity / parasite interactions
• Altered parasite communities

Alien parasites more likely to become established at release sites if they have:
• a widespread geographic distribution
• a direct transmission life cycle
• high prevalence and intensity of infection
• infective for other species at the release site
(No evidence - guesses based on epidemiological principles)

  • Translocated animals affected by endemic infectious disease
  • Stressor-induced disease
  • Translocated animals affected by non-infectious disease
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9
Q

Be able to list methods available for wild mammal capture and translocation

A

Physical capture and restraint:
• Cage, pit traps, plastic corrals or nets.
• Animals restrained for sampling, treatment, or translocation with or without tranquilisation

Chemical immobilisation:
• Restrained chemically using remote injection systems - inject anaesthetics into a muscle mass with subsequent immobilisation.
• Once induced manipulated as required – require close monitoring to avoid anaesthetic emergencies

Remote injection approach method:
Foot:
•	low cost
•	low efficiency.
•	Low stress on animal
•	Dangerous with certain species and habitats.
•	Exhausting on operators.
•	Requires aircraft support usually.
Vehicle:
•	efficient in open habitats
•	moderate stress
•	dangerous in certain habitats
•	vehicle damage a concern
•	requires aircraft support usually
Helicopter:
•	highly efficient & effective
•	moderate stress animals low stress operators
•	dangerous
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10
Q

Be able to describe which equipment and drugs should optimally be used in different groups of mammals and circumstances

A
  • Corrals (Funnels)
  • Drive nets
  • Fixed nets (Drop nets, Mist nets, Cannon nets, Net guns)
  • Snag poles
  • Kick boards
  • Crates
  • Transport
  • Bomas or holding pens
Remote Injection System:
•	Rifles
•	Darts, Rubbers, internal charges (all sizes_
•	Dart Push Rod
•	Cartridge holder and spares, charge loads (3 wts)
•	Silicon gel
•	Gun oil
•	Gun Rod and cleaning wads
•	Spare seals (Gas)

Immobilisation Agents, Drugs and Miscellaneous:
• Immobilising agent, sedatives, tranquilisers
• Adrenaline, respiratory stimulants, reversal drugs
• Antibiotics, wound spray, eye ointment, clean water.
• Knife, pliers, head cover, cotton rope, absorbent paper.
• GPS, binoculars, range finder

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11
Q

Be able to give safety advice on immobilisation of wild mammals

A
Human Safety Aspects:
Use of rifles:
•	Cleaning, emptying, handling, AD.
Use of dangerous anaesthetic agents:
•	Antidotes and Narcotic emergencies
•	Dangerous animals and Bush craft:
•	High risk species
•	Tracking & animal signs
•	Clothing, footware
•	Safety guns
Handling injuries:
•	Head
•	Kick
•	Crush

Animal Safety & welfare:
Use of dart rifles:
• Correct charge for distance & dart type
• Use of dangerous anaesthetic agents:
• Appropriate dose for immobilisation.
• Appropriate management of dose effects.
• Antidotes & anaesthetic emergencies
Capture injuries:
• Hypoxia, hyperthermia, acidosis, capture myopathy
• Trauma, wounds, drowning.
• Posture; ischaemia, airway obstruction, bloat
Handling injuries:
• Netted animals: over-restraint
• Rope injuries, strangulation
• Crate injuries

Principles of wildlife capture and immobilisation:
• Use recognised methods for each species
• Have experienced veterinarians & capture team
• Ensure careful planning & preparation
• Keep equipment & drugs in secure containers & in good condition, cool & in date.
• Have at least 2 persons per animal for drug safety, to manipulate, administer & monitor anaesthesia.
• For large animals have cotton ropes, head covers.
• Have correct combinations & adequate amount of drugs
• Ensure continuous monitoring of anaesthesia & emergency drugs to hand. Ensure animal welfare.

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12
Q

Resolution of human-wildlife conflict requires a detailed understanding of the ecology and population dynamics of the conflict-species and how human development and activities influence these.

A

Need to reduce impacts of wildlife and offset the costs of wildlife
Fencing is associated with reduced carrying capacity – some species can’t be fenced in
Direct payments – difficult large scale

  • separation
  • reducing impacts
  • offsetting the costs (direct payment, ecotourism, sport hunting)
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13
Q

Novel methods for conflict resolution require scientific investigation before they are recommended.

A

Elephants - Coordinated guarding of crops (lights, noises, chasing, natural repellents e.g. chilli grease)
Wild dogs - Conservation areas that increase food opportunities for predators by restoring prey populations
Wolves – Yellowstone profited from ecotourism because of the reintroduction

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14
Q

Compare and contrast primate pathogen issues between wild and captive housed primates

A

Dysbiosis:

  1. Loss of beneficial organisms
  2. Expansion of pathobiomes of potentially harmful microorganisms
  3. Loss of overall microbial biodiversity

Langur is folivorous and has a multi-chambered stomach = issues in captivity:
• Shift in gut microbiome in captivity compared to the wild
• Reduction in microbiome diversity associated with reduction in diet diversity
Captive microbiomes cause large weight gains
Overall effects of Langur captivity:
• Reduced microbiome diversity
• Humanises the microbiome
• Reduces amount of dietary fibre – major risk factor

Human pathogens detected in wild primates: TB in captive, and anthrax increasing in free-living primates
URTI can lead to sinusitis, air sacculitis and pneumonia. It can also cause anatomical variation (pneumatised superior turbinate)
Severe sinusitis = swollen mucosal membranes and blocked ostium
Air sacculitis = often clinically silent, chronic suppurative infection, and via inhalation of respiratory secretions of faeces

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15
Q

Develop an understanding of the practicalities, availability, and difficulties of use in a variety of primate pathogen diagnostics

A
e.g. difficulty with tuberculin testing
false positives due to:
-	Buffered diluents
-	Impurities in the tuberculin
-	Trauma due to injection technique
-	Previous BCG vaccination
-	Cross reaction with atypical or saprophytic mycobacteria

False negatives due to:

  • Anergy
  • Testing too early
  • Fungal disease
  • Measles
  • Immunosuppressive drugs
  • Technical errors
  • Local desensitization if test is repeated in the same site
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16
Q

Begin to critically assess the peer reviewed literature as groundwork for when developing a primate health programme for a perspective employer

A

Disease outbreak risk management set up:
• Focussed on risk communication
• Surveillance - especially for zoonotic diseases
• Disease fact sheet to analyse situation
• Hygienic measures
• Staff communication
• Public health advisory cmmunication

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17
Q

Have an appreciation of what DRA is, and why it is relevant to wildlife medicine in general

A

In a captive situation a health system tries to:
• Be Science/ Evidence Based.
• Be able to Highlight Data Gaps.
• Accurately assess Cost-benefit
• Improve communication = improve understanding = improve compliance

What do we ask?
• What question(s) are we trying to answer? (Problem Description)
• Can we interpret the data we get? (Assessment)
• How are we going to manage health situations? (Management)
• How are we going to learn from what we find to improve the situation into the future? (Review and change Problem Description)

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18
Q

Be able to set up a basic primate preventative health programme using DRA principles (Hazard ID thru Risk communication) – relates to learning objective 3 of lecture 1. Main resource: Manual of Procedures for Wildlife DRA.

A
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19
Q

Infection with retroviruses is irreversible since the viral genome integrates into host DNA.

A

The virus replicates using reverse transcriptase and its genome is incorporated into the host’s DNA making the infection irreversible

20
Q

For anyone handling primates it is, therefore, important to know what these retroviral infections are.

A

SIV (simian immunodeficiency viruses, incl chimp)
STLV (simian T-leukaemia viruses)
SRV (simian retroviruses / D-types)
PFV (primate foamy viruses)
Transmitted like HIV, bodily fluids, sexual intercourse, bites etc.

21
Q

Zoonosis by retro- (and other) viruses is a concern as human contact with non-human primates increases.

A

SIV is morphologically very similar to HIV

STLV closely related to HTLV

22
Q

Recognise that disease risk analysis can be used to predict the magnitude and probability of adverse consequences associated with wildlife conservation translocation.

A
  • a formal assessment of the health risks
  • reduce credible health risks by altering translocation protocols
  • Reasoned, logical, referenced
  • identify probability of occurrence
  • identify magnitude of any negative consequences
  • Qualitative or quantitative
23
Q

Describe the difficulty with assessing the risk of disease with translocation because of the number of parasites involved, and the limited information on pathogenicity, distribution and identity of those parasites.

A
24
Q

Critically evaluate the role of post-release health surveillance in improving our understanding of the risks from disease and to detect unpredictable disease outbreaks.

A
25
Q

Have an overview of paramyxoviruses detected in reptiles and their clinical significance

A
  • Most commonly involve the respiratory system and CNS
  • Gaping of the mouth
  • Mucus or blood in the oral cavity
  • Gagging, regurgitation
  • Convultions, abnormal behavior, loss of equilibrium, opisthotonos
  • Congested, thickened and oedematous lungs
  • Serous exudate to caseous necrotic cellular debris within the lumen of the lungs and air sacs
  • Changes in liver also possible

Found in:
- Snakes (generally viperids): respiratory system and CNS
o Congested, thickened and oedematous lungs
o Serous exudate to caseous necrotic cellular debris in lumen of lungs
o Secondary bacterial infection

  • Lizards
  • Chelonians: quite rare, associated with dermatitis and glossitis
26
Q

Understand the diagnostic methods used for the detection of ferlavirus infections in reptiles

A
Serological tests:
•	HI, virus neutralization
•	Positive titre only indicates exposure to ferlavirus, presence of virus and shedding requires additional tests
Virus detection:
•	Immunohistochemistry
•	in situ hybridization
•	Virus isolation
•	RT-PCR
27
Q

Understand treatment and prevention strategies for ferlavirus infections of reptiles

A
  • Vaccines – but unclear on whether antibodies protect against infection; seroconversion was variable and transient
  • No treatment known – antibiotic therapy may be useful in reducing secondary bacterial infection
  • In case of outbreak reduce contact, divide large collections into groups and disinfect cages of dead animals
  • Quarantine of at least 90 days
28
Q

Have an overview of herpesviruses detected in reptiles

A

All those found in reptiles are alpha-herpesviruses
most common viral infection in tortoises
Found in:
- Lizards: tongue lesions

  • Snakes: various species
  • Crocodilians
  • Tortoises: upper digestive tract mostly affected showing stomatitis and glossitis. There are at least 4 tortoise HVs (TeHV1-4)
    Clinical signs:
    • Ulcerative to diphtheroid-necrotizing stomatitis and glossitis
    • Lethargy and anorexia
    • Rhinitis
    • CNS signs
    • Upper digestive tract most typically affected
    • Diphtheroid-necrotizing stomatitis and glossitis
29
Q

Understand the diagnostic methods used for the detection of herpesvirus infections in tortoises

A

Direct virus detection (virus or parts of the virus found in clinical samples)
• Mainly via PCR - Can be done using oral swabs and biopsies from live animals or tissues from dead animal - Tongue, esophagus, trachea, small intestine
• Latently infected animals may not be shedding the virus leading to false negatives
- DNA from formalin-fixed tissues:
• Pan-herpesvirus PCR often used for the detection of herpesviruses in reptiles

Indirectly via immune response:
-	Serology – main issues:
o	Existence of different serotypes
o	Difference in titres among species
o	Titres can shrink below detectable levels in positive animals
30
Q

Be able to plan quarantine and contingency plans to prevent or deal with herpesvirus infection in tortoise collections

A
  • Quarantine procedures:
    ○ At least 6 months
    ○ Serological testing at least twice (beginning and end)
    Virological testing at least once at the beginningKeep different species separate
    • Keep animals in small groups
    • Use a strict quarantine procedure
    • Herpesviruses can cause latent infections
    • Diagnostic tests carried out on latently infected animals may be negative
31
Q

Understanding the clinical significance of boid inclusion body disease (BIBD) and its etiology

A
IBD is a slow, progressive disease of boas and pythons
Defined by the presence of intracytoplasmic inclusion bodies in cells of various tissues
•	Immunosuppression
•	CNS disease
•	Regurgitation
•	Anorexia
•	Lethargy
•	Pneumonia

Transmission route is unknown but possibly via horizontal transmission (direct contact or via mites) or also vertical transmission

32
Q

Knowing how to diagnose BIBD in boas and pythons

A

Inclusions in:
• Biopsies from the liver, kidney, and esophageal tonsils
• Blood cells (erythrocytes and lymphocytes)

33
Q

Understanding the significance of viruses in the order Nidovirales in reptiles

A

Enveloped, largest RNA viruses
Detected most commonly in python species
Main clinical signs: mucus in oral cavity
Diagnosis via virus detection through PCR
Some infected animals remain clinically healthy

34
Q

Understand the implications of rehabilitating wild animals and why post release monitoring is important

A

Animal welfare – will the animal suffer? Animal welfare act 2006
Legal – permit? Legal to release? Need to register?
Ethics – Is it right to interfere? How should we interfere?
Conservation – population effects?
Ecological – individuals within population effected?
Evolutionary – interference with natural selection?

35
Q

The RSPCA’s policies and ethos regarding wildlife rehabilitation

A
  • Reduce or eliminate suffering
  • Release back to the wild
  • Integration
  • Normal behaviour
  • Minimise stress
  • Veterinary care
  • Euthanasia
36
Q

Techniques that can be used to monitor animals post release from the case studies presented

A

The RSPCA assesses the effects of any attachment in captivity before releasing the
Animals – rings, GPS devices

37
Q

knowledge of the legislation most likely to be applicable in the course of practising wild animal health and wild animal biology

A

Animals: health, welfare, conservation. environment, import/export, CITES, medicines.
Humans: Work, movement, professional recognition, health & safety.

38
Q

understanding of the significance of the relevant legislation and the necessity of assessing its implications in the planning and in the course of study and work involving non-domesticated animals in the wild and in captivity.

A

Many levels: international, regional treaties and agreements, national, and local

39
Q

Role of wild birds in epidemiology of influenza

A

Waterbirds are the main reservoir for low pathogenic avian influenza A viruses (LPAIV), from which occasional spillover to poultry occurs. When circulating among poultry, LPAIV may become highly pathogenic avian influenza A viruses (HPAIV).

40
Q

Role of wild birds in epidemiology of influenza

A

Waterbirds are the main reservoir for low pathogenic avian influenza A viruses (LPAIV), from which occasional spillover to poultry occurs. When circulating among poultry, LPAIV may become highly pathogenic avian influenza A viruses (HPAIV).

41
Q

Difference between low pathogenic and high pathogenic avian influenza virus: Tissue tropism; Pathogenicity; Transmission

A

Ubiquitous proteases VS Proteases localised in respiratory and intestinal organs

42
Q

Unusual aspects of HPAIV H5N1:

A
  • Pathogenicity for wild birds
  • Potential role of wild birds in spread
  • “Sentinel” vs. “vector” species
  • Adaptation of HPAIV to wild bird populations
  • Wild birds as a novel source of HPAIV for poultry farms
43
Q

Host species barrier

A

“The interaction of factors that collectively limit the transmission of an infection from a donor host species to a recipient host species”
• A: Donor species requires contact with recipient species
• B: Virus needs to enter and replicate in recipient species
• C: Virus needs be excreted from and spread in recipient species

44
Q

Receptor specificity of viral attachment proteins

A

Avian and human influenza viruses differ in specificity of haemagglutinin

45
Q

Pathogenesis of HPAIV H5N1 infection in cats and other carnivores

A

HPAIV H5 highly pathogenic for many carnivorous species

46
Q

How HPAIV H5N1 enters the mammalian host

A

Olfactory mucosa new portal of entry for HPAIV H5 in mammals