Difference between revisions of "Feline Infectious Peritonitis"
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− | == | + | {| cellpadding="10" cellspacing="0" border="1" |
− | A progressive disease of the cat caused by feline [[Coronaviridae|coronavirus]]. FIP arises from a mutation of | + | | Also known as: |
+ | | '''FIP''' | ||
+ | |- | ||
+ | |} | ||
+ | |||
+ | ==Description== | ||
+ | A progressive disease of the cat caused by feline [[Coronaviridae|coronavirus]]. The disease is characterised by a variety of clinical signs, including weight loss, fever and vasculitis. FIP arises from a mutation of Feline Enteric Coronavirus (FECoV) in 5-10% of chronically infected cats and not directly from cat to cat.Two forms of the disease exist the wet form and the dry form. | ||
==Signalment== | ==Signalment== | ||
Domestic and wild cats. | Domestic and wild cats. | ||
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==Diagnosis== | ==Diagnosis== | ||
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Simple serology is impossible as most cats will have antibody to FECoV. | Simple serology is impossible as most cats will have antibody to FECoV. | ||
− | + | However, 4 indicators can be used to cross reference: | |
− | + | *High FECoV Ab titres | |
− | *High FECoV | ||
*Low albumin:globulin ratio in plasma/ascites (globulin levels rise in FIP) | *Low albumin:globulin ratio in plasma/ascites (globulin levels rise in FIP) | ||
*High levels of glycoprotein alpha 1-acid glycoprotein (AGP) | *High levels of glycoprotein alpha 1-acid glycoprotein (AGP) | ||
*Low white cell counts | *Low white cell counts | ||
− | FIP antigen detection by immunofluorescence in macrophages gives a definite positive diagnosis | + | FIP antigen detection by '''immunofluorescence''' in macrophages gives a definite positive diagnosis |
+ | |||
==Pathogenesis== | ==Pathogenesis== | ||
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− | + | Weeks, months or years may intervene between localized primary FECoV infection and FIP development. FECoV replicates in the gut, but FIP spreads systemically in the circulation. FIP then gains the ability to replicate in [[Monocytes|monocytes]] and macrophages | |
+ | |||
+ | *Failure of the immune system to clear antibody-antigen complexes leads to '''immune-mediated disease''' | ||
+ | **Deposited complexes cause '''inflammation''' and '''exudation''' | ||
+ | **This leads to characteristic '''oedema''' as fibrin-rich serum escapes to intercellular spaces | ||
+ | ** '''Pyogranulomas''' can develop in major organs as a result of the immune response and the body's failure to clear away excess [[Neutrophils|neutrophils]] | ||
+ | *Cats previously exposed to coronavirus (and therefore with circulating antibody) may be at greater risk as they are more susceptible to taking up virus into mononuclear cells | ||
+ | *Cats making a biased Th-1 response are more likely to evade infection, whereas cats making a balanced response are at moderate risk and cats making a biased Th-2 response are at greater risk, as the virus is best tackled by cell mediation and not antibody | ||
+ | *Cats compromised by '''immunosuppression''' (either iatrogenic or disease-related) are at a greater risk of developing FIP | ||
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− | + | ==History and Clinical signs== | |
+ | FECoV may cause mild respiratory symptoms and diarrhoea but is often asymptomatic | ||
+ | |||
+ | Signs of FIP include, chronic weight loss, anorexia, pyrexia and depression. | ||
+ | Fluid in the abdomen, thorax or pericardium are symptomatic of '''wet, or exudative FIP'''. | ||
+ | Granulomatous change in the organs are symptomatic of '''dry, or nonexudative FIP'''. | ||
+ | FIP has been documented to cause: | ||
+ | Uveitis, hydrocephalus, neurological symptoms, such as ataxia or seizures and chronic diarrhoea. | ||
− | + | ====Epidemiology==== | |
+ | *FECoV is '''endemic worldwide''', with the majority of cats showing a subclinical seroconversion | ||
+ | *'''Orofecal, aerosol, and contact''' transmission | ||
+ | *Particular concern for '''catteries''' and homes with '''multiple cats''' | ||
+ | * | ||
==Pathology== | ==Pathology== | ||
====Gross==== | ====Gross==== | ||
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− | ''' | + | ==='''Wet form'''=== |
+ | Widespread miliary, white, pinhead granulomas and fibrin deposition, particularly in the serosa of the intestine. | ||
+ | High-protein exudates can be found in [[Peritoneal cavity - Anatomy & Physiology|peritoneal cavity]]. | ||
− | Larger, grey granulomatous masses | + | ==='''Dry form'''=== |
+ | Larger, grey granulomatous masses causing thickening of the wall of the [[Small Intestine - Anatomy & Physiology|small]] and [[Large Intestine - Anatomy & Physiology|large intestine]]. | ||
====Histological==== | ====Histological==== | ||
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− | + | Multifocal pyogranulomas on serosa and throughout gut wall. Infiltration by mononuclear cells, lymphocytes, plasma cells, macrophages and a few[[Neutrophils|neutrophils]]. Necrosis and vasculitis will also be seen. | |
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+ | ==Treatment== | ||
+ | Almost invariably fatal. | ||
==Control== | ==Control== | ||
− | Conventional | + | Conventional vaccination is counterproductive as antibody worsens infection however a non-systemic vaccine (Primucell) is available outside the UK |
− | + | **Temperature-sensitive mutant | |
− | Antibody tests are available to certify FECoV-free cat houses | + | **Replication confined to nasal mucosa, providing local immunity and cell-mediated immunity |
− | + | **Cannot protect cats already infected with FECoV | |
− | + | **Kittens must be isolated until old enough to vaccinate at 16 weeks | |
− | + | Antibody tests are available to certify "FECoV-free" cat houses | |
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==Prognosis== | ==Prognosis== | ||
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==References== | ==References== | ||
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− | [[Category:Coronaviridae]][[Category:Cat | + | [[Category:Coronaviridae]][[Category:Cat]] |
[[Category:Enteritis, Granulomatous]] | [[Category:Enteritis, Granulomatous]] | ||
[[Category:Enteritis,_Viral]] | [[Category:Enteritis,_Viral]] | ||
[[Category:Hepatitis,_Viral]] | [[Category:Hepatitis,_Viral]] | ||
− | [[Category: | + | [[Category:To_Do_-_Viruses]][[ |
− | [[ | + | [[Category:To_Do_-_Caz]] |
− | [[Category: |
Revision as of 10:43, 27 July 2010
This article is still under construction. |
Also known as: | FIP |
Description
A progressive disease of the cat caused by feline coronavirus. The disease is characterised by a variety of clinical signs, including weight loss, fever and vasculitis. FIP arises from a mutation of Feline Enteric Coronavirus (FECoV) in 5-10% of chronically infected cats and not directly from cat to cat.Two forms of the disease exist the wet form and the dry form.
Signalment
Domestic and wild cats.
Diagnosis
FIP should be suspected in all cases of chronic weight loss or recurrent fever unresponsive to antibiotics, particularly in multiple cat situations. Simple serology is impossible as most cats will have antibody to FECoV.
However, 4 indicators can be used to cross reference:
- High FECoV Ab titres
- Low albumin:globulin ratio in plasma/ascites (globulin levels rise in FIP)
- High levels of glycoprotein alpha 1-acid glycoprotein (AGP)
- Low white cell counts
FIP antigen detection by immunofluorescence in macrophages gives a definite positive diagnosis
Pathogenesis
Weeks, months or years may intervene between localized primary FECoV infection and FIP development. FECoV replicates in the gut, but FIP spreads systemically in the circulation. FIP then gains the ability to replicate in monocytes and macrophages
- Failure of the immune system to clear antibody-antigen complexes leads to immune-mediated disease
- Deposited complexes cause inflammation and exudation
- This leads to characteristic oedema as fibrin-rich serum escapes to intercellular spaces
- Pyogranulomas can develop in major organs as a result of the immune response and the body's failure to clear away excess neutrophils
- Cats previously exposed to coronavirus (and therefore with circulating antibody) may be at greater risk as they are more susceptible to taking up virus into mononuclear cells
- Cats making a biased Th-1 response are more likely to evade infection, whereas cats making a balanced response are at moderate risk and cats making a biased Th-2 response are at greater risk, as the virus is best tackled by cell mediation and not antibody
- Cats compromised by immunosuppression (either iatrogenic or disease-related) are at a greater risk of developing FIP
History and Clinical signs
FECoV may cause mild respiratory symptoms and diarrhoea but is often asymptomatic
Signs of FIP include, chronic weight loss, anorexia, pyrexia and depression. Fluid in the abdomen, thorax or pericardium are symptomatic of wet, or exudative FIP. Granulomatous change in the organs are symptomatic of dry, or nonexudative FIP. FIP has been documented to cause: Uveitis, hydrocephalus, neurological symptoms, such as ataxia or seizures and chronic diarrhoea.
Epidemiology
- FECoV is endemic worldwide, with the majority of cats showing a subclinical seroconversion
- Orofecal, aerosol, and contact transmission
- Particular concern for catteries and homes with multiple cats
Pathology
Gross
Wet form
Widespread miliary, white, pinhead granulomas and fibrin deposition, particularly in the serosa of the intestine. High-protein exudates can be found in peritoneal cavity.
Dry form
Larger, grey granulomatous masses causing thickening of the wall of the small and large intestine.
Histological
Multifocal pyogranulomas on serosa and throughout gut wall. Infiltration by mononuclear cells, lymphocytes, plasma cells, macrophages and a fewneutrophils. Necrosis and vasculitis will also be seen.
Treatment
Almost invariably fatal.
Control
Conventional vaccination is counterproductive as antibody worsens infection however a non-systemic vaccine (Primucell) is available outside the UK
- Temperature-sensitive mutant
- Replication confined to nasal mucosa, providing local immunity and cell-mediated immunity
- Cannot protect cats already infected with FECoV
- Kittens must be isolated until old enough to vaccinate at 16 weeks
Antibody tests are available to certify "FECoV-free" cat houses
Prognosis
References
[[