Ruminant and Camelid Diarrhea Differential Diagnoses Flashcards

1
Q

describe salmonella

A

background:
1. similar to horses BUT
2. host adapted (endemic) serotype in cattle: salmonella dublin
3. additional common serotypes: S. typhimurium, S. cerro, S. montivedo, S. heidelberg, S. newport

clinical findings:
1. similar to horses, wide spectrum of disease possible
2. complications of endotoxemia/SIRS seems less likely in ruminants, but still very possible

diagnosis:
1. fecal culture or PCR: repeated or pooled samples
2. rectal biopsy culture/mesenteric LN culture
3. serology (ELISA): salmonella Dublin
-diff from horses!

prognosis:
1. variable like in horses, but rum have better prognosis overall
2. ZOONOTIC and REPORTABLE in GA
3. cattle vaccines DO exist, questionable efficacy

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2
Q

describe C. perfringens

A
  1. anaerobic gram positive rod-shaped bacteria
    -present in environment and part of normal microbiota
    -presence DOES NOT equal disease
  2. RARE cause of diarrhea in adult ruminants overall
    -more common in neonates/juveniles
  3. biotypes based on toxin production
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3
Q

describe diagnosis and prognosis of C. perfringens

A

diagnosis:
1. isolation of C. perfringens alone does NOT = diagnosis
2. must demonstrate toxin production: fecal ELISA or PCR

prognosis:
1. poor
2. vaccines available: type C and D pretty effective
3. prevent excessive or sudden starch/sugar/digestible protein ingestions

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4
Q

describe bovine coronavirus

A
  1. winter dysentery; betacoronavirus
  2. fecal-oral and respiratory transmission
  3. outbreaks most common in:
    -housed dairy cattle
    -wintertime: november-april
    -northern states
  4. short incubation
  5. destroys colonic crypt epithelial cells
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5
Q

describe bovine coronarvirus clinical signs

A
  1. fever and mild respiratory signs: sometimes be present before diarrhea
  2. lethargy
  3. acute, severe diarrhea +/- blood
  4. decreased appetite, dehydration possible
  5. significant drop in milk production
  6. typically spontaneously resolve within 24-36 hours
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6
Q

describe diagnosis and prognosis of bovine coronavirus

A

dx: often presumptive, fecal ELISA or PCR

prognosis: good to excellent (self resolve), vaccine available but not widely used

control: mgmt and vaccines

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7
Q

describe bovine viral diarrhea virus (BVDV)

A
  1. pestivirus
  2. type biotypes:
    -cytopathic
    -non-cytopathic
  3. two genotypes: type 1 and type 2
  4. mutates: often and random!
  5. transmission:
    -horizontal: ingestion/inhalation after direct contact, contam vectors, semen, or embryos

-vertical: transplacental

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8
Q

describe BVDV acute infection

A
  1. complex spectrum of clinical manifestations
    -subclin to severe
    -GI, resp, repro, immunosuppression
  2. transient viremia
  3. transient viral shedding
    -duration dependent on strain
  4. subclinical = majority (70%) of infections
    -mild fever, leukopenia, decreased milk production
  5. acute clinical disease:
    -damage to epithelial surfaces of GI, resp, integument = widespread clinical signs
    -hemorrhagic syndrome in most cases: TCP, petechiation and ecchymoses mucosal surfaces, epistaxis, blood diarrhea, bleeding from injection sites/trauma, death
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9
Q

describe BVDV reproductive disease

A
  1. infertility/early embryonic death: before and during 1st 60d of gestation
  2. abortion: typically 60+ days but can be any stage
  3. persistent infection: from 0-125d of gestation
    -non-cytopathic phenotypes only!
  4. congenital defects: from 80-150d of gestation
  5. acute infection: from 150+ days of gestation through adulthood
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10
Q

describe BVDV persistent infection

A
  1. in utero infection at <125d gestation
  2. immune system does not recognize virus as foreign so does not mount immune response
  3. always associated with non-cytopathic strains
  4. mostly poor doers clinically but not all!
  5. continuously shedding the virus
    -major source of infection for everyone else on farm
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11
Q

describe congenital defects associated with BVDV

A
  1. CNS: cerebellar hypoplasia, microencephaly, hydrocephalus, hydranencephaly, porencephaly, hypomyelination
  2. ocular system: cataracts, microopthalmia, retinal degeneration, optic neuritis
  3. others:
    -thymic hypoplasia
    -hypotrichosis/alopecia
    -deranged osteogenesis
    -mandibular brachygnathism
    -growth reduction
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12
Q

describe BVDV diagnostics

A
  1. virus isolation in cell culture
  2. antigen detection:
    -antigen capture ELISA (ACE)
    -IHC
    -acute and PI calves
  3. nucleic acid detection
    -RT-PCR
    -acute and PI calves
  4. antibody detection: serum
    -only for acute cases, PI calves never made antibodies

most important aspect for herd surveillance is to detect PI animals!

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13
Q

describe BVDV client education/prognosis

A
  1. prognosis variable for acute disease
    -dep on severity
  2. grave for mucosal disease
  3. control/prevention rely on:
    -ID and culling PI animals
    -biosecurity and surveillance
    -vaccination: may reduce severity of signs
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14
Q

describe paratuberculosis (chronic)

A
  1. Johne’s disease
    -mycobacterium avium subspp. paratuberculosis (MAP)
  2. transmission:
    -fecal oral most common
    -colostrum or milk
    -transplacental
  3. susceptibility to infection is greatest in young animals
  4. long incubation period:
    -infected when young but no clinical signs until older
  5. pathophysiology:
    -incites a chronic inflammatory response
    -granulomatous inflammation causes intestinal thickening, clubbing of villi, and marked lympahgiectasia which causes maldigestion and PLE
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15
Q

describe paratuberculosis phases of infection

A
  1. eclipse phase:
    -no shedding
    -no clinical signs
  2. asymptomatic shedder phase
    -detectable fecal shedding
    -spread to extra-intestinal sites can allow for shedding in colostrum, milk, and infection through the placenta
  3. clinical disease phase:
    -pipestream diarrhea (cattle only)
    -rapid weight loss progressing to emaciation/cachexia
    -hypoproteinemia leading to edema: brisket and jaw

-animals typically afebrile and still have very good appetite (until very late in course of disease)

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16
Q

describe paratuberculosis diagnosis and prognosis

A
  1. immune-based tests:
    -ELISA on serum or milk preferred
    -drawback is that infected animals will start fecal shedding prior to producing detectable antibodies
  2. organism detection tests:
    -Fecal PCR preferred
    -allows earlier detection of fecal shedding!!!
    -more expensive though

NOTE: no test works perfectly for screening due to eclipse phase!!

prognosis: grave, control is the focus

17
Q

describe trichistrongyles

A
  1. group of parasites that includes:
    -Haemonchus: caprine, ovine, camelids
    -ostertagia: bovine
    -trichostrongyles
    -cooperia
18
Q

describe haemonchus

A
  1. parasitic nematode lives in abomasum
  2. feeds on blood: anemia and hypoproteinemia
  3. resulting decreased oncotic pressure leads to intestinal edema and loss of fluid into lumen, sometimes enough to cause secondary diarrhea
  4. routine FAMACHA scoring, FEC surveillance, judicious use of anthelmintics and ancillary mgmt = important
19
Q

describe ostertagia

A
  1. parasitic nematode in abomasum
  2. clinical signs:
    -difficulty gaining wt or wt loss
    -diarrhea
    -hypoproteinemia and edema that can lead to diarrhea
    -ill thrift
  3. routine FEC surveillance, judicious anthelmintics, ancillary mgmt
20
Q

describe coccidia

A
  1. rare cause of diarrhea in adults unless immunocompromised
  2. only exception in Eimeria macusaniensis:
    -can occur in camelids of any age (as young as 21d)
    -risk factors and pathophys similar to other coccidia apart from ability to infect adults and longer prepatent period of 35d

-clinical findings: lethargy, wt loss, diarrhea (+/- bloody), hypoproteinemia without anemia

-dx: fecal float or fecal PCR

-prog: good overall with tx

21
Q

describe E. coli

A
  1. colibacillosis
  2. may strains:
    -ETEC: enterotoxigenic
  3. septicemia
  4. localized non-enteric (coliform mastitis)
22
Q

describe pathophysiology of E. coli ETEC

A
  1. fimbriae (pili) mediate attachment to cells
  2. adhesion of bacteria to enterocytes is age dependent
    -decreases as calf ages
    -primarily affects calves 1-4 d old
  3. enterotoxins produces: cause hypersecretion of fluids and electrolytes (Na, Cl, K, bicarb)
    -heat stable toxin
    -heat labile toxin
23
Q

describe clinical signs of E. coli

A
  1. severe watery diarrhea: pineapple juice appearance
  2. lethargy progressing to dullness/stupor/coma
  3. decreased milk intake
  4. dehydration progressing to hypovolemia
  5. tachycardia, hypothermia, acute death
24
Q

describe diagnosis of E. coli

A
  1. bacterial culture
  2. E. coli pilus antigen ID
    -ELISA
    -multiplex PCR
  3. histopathology post mortem
25
Q

describe prognosis and control of E. coli

A

prognosis variable

control: biosecurity, dam vaccination, calf passive immunization

26
Q

describe salmonella in calves

A
  1. usually calves approx 10d old and older
  2. can also cause septicemia
  3. S. dublin and typhimurium most common
27
Q

describe clostridium in calves

A
  1. usually calves less than 2 weeks
  2. often the healthiest, quickly growing calves, from dams with high milk supply
  3. type C most common: segmental enteritis
28
Q

describe rotavirus

A
  1. most frequent pathogen isolated from calves with diarrhea
  2. primarily affects calves 3-21 d old
  3. fairly short incubation: 15-96 hr
  4. damages/denudes SI microvilli
    -loss of lactase causes maldigestion of lactose and osmotic diarrhea

clinical signs:
1. diarrhea: yellow, watery, voluminous
2. dehydration
3. anorexia

diagnosis:
-ELISA and fecal latex agglutination most common

prognosis: good to guarded, vx avail

29
Q

describe coronavirus in calves

A
  1. affects calves 5-30d
  2. typically more severe diarrhea than rotavirus
30
Q

describe cryptosporidium in calves

A
  1. cryptosporidium parvum
  2. second most frequent pathogen in calves with diarrhea
  3. fecal oral transmission of thick walled oocysts
    -very hard in environment
  4. 5-12d incubation period
  5. colonizes a unique place within enterocyte plasma membrane
    -intracellular by extracytoplasmic
    -causes villous atrophy and fusion leading to malabsorption
    -autoinfection of neighboring enterocytes
31
Q

describe cryptosporidium clinical signs, diagnosis, and prognosis in calves

A

clinical signs:
1. most common in 1-4wk old calves
2. anorexia
3. yellow, watery, malodorous diarrhea for 6-1 days

dx:
1. fecal float: sheather’s solution (sucrose); will see small thick walled cryptosporidium

  1. dried fecal smears: oocysts staining with acid fast stains

prognosis: good to guarded
-ZOONOTIC AND WILL INFECT HUMANS!!!!
-control: good biosecurity, resistant to many disinfectants, requires ammonia or peroxide based products to disinfect

32
Q

describe coccidia in cattle, small ruminants, and camelids

A

cattle:
-eimeria bovis and eimeria zuernii most pathogenic
-3-6months of age

small rum:
-eimeria caprina/ovinoidalis most pathogenic
-1-4 months of age

camelids:
-eimeria macusaniensis most pathogenic, E. alpacae, E. lamae
-1-6 months (E. mac can infect adults)

most often associated with changes in feed, weaning stress, and/or overcrowding/confinement

33
Q

describe coccidia pathophysiology

A
  1. 15-20 day prepatent period (except E. mac 35d)
  2. fecal oral transmission
  3. replicate within cells, rupturing the cell to be released
    -localized primarily to lower ileum, cecum, and LI
34
Q

describe coccidia clinical signs

A
  1. diarrhea +/- blood/mucus
  2. tenesmus
  3. anorexia, dehydration, weakness
  4. chronic subclinical infections can lead to juveniles with ill thrift
  5. rarely, nervous coccidiosis occurs and leads to neuro signs
    -muscle fasciculations, hyperesthesia, nystagmus, tonic-clonic convulsions, ventroflexion of head/neck
35
Q

describe diagnosis and client education for coccidia

A

diagnosis:
1. fecal float: large numbers in clinical disease

  1. McMaster
  2. modified Stoll

education:
-prognosis is good with treatment
-control/prevention: biosecurity/minimize stress