Chapter 279 Coronaviruses causing disease in cats include feline infectious peritonitis virus (FIPV) and feline enteric coronavirus (FECV). Enteric infection generally results in mild gastrointestinal signs; systemic infection can induce a clinical syndrome with diverse manifestations commonly referred to as feline infectious peritonitis (FIP) (Pedersen, 2009). FIP-inducing strains may arise from enteric strains by mutation (called the “in vivo mutation transition hypothesis”), or distinctive benign and pathogenic strains may circulate in a population with the pathogenic strains inducing disease in exposed cats with the appropriate predisposition (called the “circulating virulent-avirulent FCoV hypothesis”) (O’Brien et al, 2012). Diagnostic tests for diagnosis of FIP have been reviewed (Giori et al, 2011; Hartmann et al, 2003). Cats with effusion disease are usually easy to confirm because the fluid is fairly characteristic. The fluid is sterile, appears colorless to straw colored, may contain fibrin strands, and may clot when exposed to air. The protein concentration on fluid analysis commonly ranges from 3.5 g/dl to 12 g/dl and is generally higher than that associated with other diseases. Mixed inflammatory cell populations of lymphocytes, macrophages, and neutrophils occur most commonly; neutrophils predominate in most cases, but in some cats macrophages are the primary cell type seen. In some cats the coronavirus antibody titers are greater in the effusion than in serum. Measurement of protein concentrations in effusions and calculation of the albumin/globulin ratio can aid in the diagnosis of effusive FIP. In one study an albumin/globulin ratio of 0.5 had a positive predictive value of 89%, and an albumin/globulin ratio of 1.0 had a negative predictive value of 91% (Hartmann et al, 2003). Coronavirus antigens commonly are detected by direct immunofluorescence in the effusions of cats with FIP but not in the effusions of cats with other diseases. In addition, viral RNA can be amplified detected by reverse transcriptase polymerase chain reaction (RT-PCR) in effusions and is unlikely to be in effusions from other causes. Multiple hematologic, serum biochemical, urinalysis, diagnostic imaging, and CSF abnormalities develop in cats with noneffusive FIP. Several authors have assessed the predictive values of individual and combinations of tests (Giori et al, 2011; Hartmann et al, 2003). Other than histopathology, the positive predictive values of tests used to aid in the diagnosis of FIP are less than 100%, including the amplification of mRNA from blood. A presumptive diagnosis of noneffusive FIP usually is based on the combination of clinical and clinicopathologic findings and excluding other causes of the presenting clinical syndromes. Definitive diagnosis can be made by documenting appropriate histopathologic findings and coronavirus in tissues with immunohistochemistry.
Feline Infectious Peritonitis Virus Infections
Diagnosis
Feline Infectious Peritonitis
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Feline Infectious Peritonitis Virus Infections
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