Clinical, pathological, immunohistochemical and molecular characterization of feline chronic gingivostomatitis

Author:

Rolim Veronica Machado1,Pavarini Saulo Petinatti1,Campos Fabrício Souza2,Pignone Viviam3,Faraco Cláudia3,Muccillo Marcelo de Souza3,Roehe Paulo Michel2,da Costa Fernanda Viera Amorim4,Driemeier David1

Affiliation:

1. Department of Veterinary Pathology of the Federal University of Rio Grande do Sul, Porto Alegre, Brazil

2. Laboratory of Virology, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences of the Federal University of Rio Grande do Sul, Porto Alegre, Brazil

3. Hospital Veterinary Clinics of the Federal University of Rio Grande do Sul, Porto Alegre, Brazil

4. Department of Animal Medicine of the Federal University of Rio Grande do Sul, Porto Alegre, Brazil

Abstract

Objectives This study presents the clinical, pathological, immunohistochemical and molecular characterization of 26 cats with feline chronic gingivostomatitis (FCG). Methods Oral mucosal biopsies, blood and swabs were collected from cats presenting with oral lesions. The tissue sections were submitted for histopathology and immunohistochemical analysis for feline calicivirus (FCV), feline leukemia virus (FeLV) and feline immunodeficiency virus (FIV). The swabs were subjected to PCR analysis for FCV, and blood for FeLV and FIV. Results The main clinical findings were dysphagia (88.2%), halitosis (76.5%), sialorrhea (47.1%), weight loss (41.2%), intense oral discomfort (35.3%), oral hemorrhage (17.6%), and lackluster and fragile coat (11.8%). Gross inspection revealed bilateral lesions across the palatoglossal fold to the lateral tongue base. The lesions were diffuse, proliferative, intensely red and friable, and bled easily upon examination in 80.8% of cases. In 23.1% of cases, the lesions were multifocal to coalescent, at times forming multiple vesicles on a reddened, edematous palatoglossal fold. Microscopic examination showed that 15.4% of lesions had moderate (grade 2) and 84.6% had severe (grade 3) inflammation. Immunohistochemistry revealed the presence of FeLV antigens in the epithelium and the inflammatory infiltrate of 30.8% of the cats with FCG. FCV antigens were not detected in the FCG lesions. Conclusions and relevance The FCG cases analyzed could not be correlated with FCV. It is possible that FeLV plays a role as a causal agent of lesions in cases where the presence of the virus has been confirmed by immunohistochemistry in epithelial samples.

Publisher

SAGE Publications

Subject

Small Animals

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