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FELASA Module 5 Animal Health

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FELASA function ABD course notes for module 5 concerning animal health

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FELASA Module 5: Laboratory Animal Health
 Disease in laboratory animals usually refers to infectious diseases
 Microorganisms in laboratory animals may be zoonotic (cause disease
in humans)
 They may cause disease in the animals
 They may interfere with the research
 Some bacteria may be important for the models you want to induce
in animals
 Fulminant disease- the infection causes clinical symptoms that we can
observe
 Latent infection- an infection without a clinical expression
 Infections can cause disease but don’t always cause disease
 Impact of latent infection on animal research
 Direct effects on research
 Immune modulation (can change the immune system)
 Physiological modulation (change the physiology)
 Oncological modulation (change the sensitivity to cancer)
 Fertility modulation (may impact the fertility of an animal)
 Microbiological competition (may compete with experimental
infections you want to induce)
 Indirect effects on research
 Contamination of biological products
 When animals are stressed due to experiments the direct effects
may be activated
 Zoonoses are not a huge problem in laboratory rodents
 They can be easily purchased though
 Rodent diseases
 Nude mouse no thymus (and thus no T-cells which means it is
immune deficient)
 It can be infected with mouse hepatitis virus that is a coronavirus
 Symptoms include wasting, cachexia (thin + muscle loss),
diarrhea and jaundice
 Infection with mouse hepatitis impacts liver function
 This infection is serious in an animal like the nude mouse that
has no immune system
 Infection will cause the mouse to die
 B6 mice are sensitive to clinical disease rom mouse hepatitis
 B6 mice from hepatitis infected colonies are paretic (partial
paralysis) and have problems walking
 The coronavirus will also effect the central nervous system
 Rats can also have similar coronaviruses
 The clinical symptoms include sneezing, corneal ulcerations and
porphyrin rings around the eyes
 Tyzzer’s disease in mice
 Bacterial disease caused by Clostidium pilliforme

,  Causes high fatality in mice
 Can see white spots on the liver where it is infected
 Slightly different presentation in rats
 Often latent and no clinical expression
 Sprague-Dawley rats may have whirls on abdominal surface
 Small intestine (ileum) is usually enlarged (megaloileitis)
 In mice with fulminant Tyzzer’s disease the half life of the antibiotic
Trimethoprim is increased
 However when mice recover from Tyzzer’s disease the half life of
the antibiotic returns to normal
 In mice with fulminant Tyzzer’s disease the half life of the anti-
coagulant warfarin is also increased
 However upon recovery, mice still have long half-lives for this
drug
 This shows there is permanent damage to the liver function
 Disease in non-rodent species
 Different species experience different infections but they have
similar outcomes
 Glasser’s disease in pigs (Haemophilus parasuis)
 At death you can see that connective tissue adheres all surfaces
of the organs to each other
 Mouse norovirus (MNV)
 Non-enveloped RNA virus
 Most prevalent viral infection in mouse
 Four described strains (MNV-1, MNV-2, MNV-3, MNV-4)
 Causes enteric infections and can also exit the gut to effect
macrophages and dendritic cells in lymph nodes and liver
 Transmission through fecal oral route- virus is shed in feces
 Symptoms include weight loss, hunched posture, ruffled fur and
death
 No clinical symptoms have been reported in immunocompetent
mice or immunocompromised mice with intact innate immunity
 Pathology: no pathology with natural infection
 Following experimental inoculation mice have mortality with
lesions including encephalitis, cerebral vasculitis, pneumonia,
meningitis and hepatitis
 Diagnosis: Serological assays to detect all strains, PCR of feces
useful for screening

 Heliobacter infections
 Caused by gram negative bacteria (heliobacters)
 Common in mice
 Species include: Helicobacter hepaticus, H. bilis, H. rodentiumH.
trogontum, H. ganmani and H. typhlonius
 Transmission through fecal-oral route
 Normally colonize the lower intestine tract

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Number of pages
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Written in
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Felasa abd
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