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Detection of Feline Coronavirus Variants in Cats without Feline Infectious Peritonitis.
Jähne, Stéphanie; Felten, Sandra; Bergmann, Michèle; Erber, Katharina; Matiasek, Kaspar; Meli, Marina L; Hofmann-Lehmann, Regina; Hartmann, Katrin.
Afiliación
  • Jähne S; Clinic of Small Animal Medicine, Centre for Clinical Veterinary Medicine, LMU Munich, Veterinärstraße 13, 80539 Munich, Germany.
  • Felten S; Clinic of Small Animal Medicine, Centre for Clinical Veterinary Medicine, LMU Munich, Veterinärstraße 13, 80539 Munich, Germany.
  • Bergmann M; Clinic of Small Animal Medicine, Centre for Clinical Veterinary Medicine, LMU Munich, Veterinärstraße 13, 80539 Munich, Germany.
  • Erber K; Section of Clinical and Comparative Neuropathology, Institute of Veterinary Pathology, Centre for Clinical Veterinary Medicine, LMU Munich, Veterinärstraße 13, 80539 Munich, Germany.
  • Matiasek K; Section of Clinical and Comparative Neuropathology, Institute of Veterinary Pathology, Centre for Clinical Veterinary Medicine, LMU Munich, Veterinärstraße 13, 80539 Munich, Germany.
  • Meli ML; Clinical Laboratory, Department of Clinical Diagnostics and Services, Center for Clinical Studies, Vetsuisse Faculty, University of Zurich, Winterthurerstrasse 260, 8057 Zurich, Switzerland.
  • Hofmann-Lehmann R; Clinical Laboratory, Department of Clinical Diagnostics and Services, Center for Clinical Studies, Vetsuisse Faculty, University of Zurich, Winterthurerstrasse 260, 8057 Zurich, Switzerland.
  • Hartmann K; Clinic of Small Animal Medicine, Centre for Clinical Veterinary Medicine, LMU Munich, Veterinärstraße 13, 80539 Munich, Germany.
Viruses ; 14(8)2022 07 29.
Article en En | MEDLINE | ID: mdl-36016293
(1) Background: This study aimed to detect feline coronavirus (FCoV) and characterize spike (S) gene mutation profiles in cats suffering from diseases other than feline infectious peritonitis (FIP) using commercial real-time reverse transcription polymerase chain reaction (RT-qPCR) and reevaluating results by sequencing. (2) Methods: In 87 cats in which FIP was excluded by histopathology and immunohistochemistry, FCoV 7b gene and S gene mutation RT-qPCR was performed prospectively on incisional biopsies and fine-needle aspirates of different organs, body fluids, and feces. Samples positive for S gene mutations or mixed FCoV underwent sequencing. (3) Results: In 21/87 cats, FCoV RNA was detectable. S gene mutations were detected by commercial RT-qPCR (and a diagnostic algorithm that was used at the time of sample submission) in at least one sample in 14/21 cats (66.7%), with only mutated FCoV in 2/21, only mixed in 1/21, and different results in 11/21 cats; in the remaining 7/21 cats, RNA load was too low to differentiate. However, sequencing of 8 tissue samples and 8 fecal samples of 9 cats did not confirm mutated FCoV in any of the FCoV RNA-positive cats without FIP. (4) Conclusions: Sequencing results did not confirm results of the commercial S gene mutation RT-qPCR.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Peritonitis Infecciosa Felina / Coronavirus Felino Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: Viruses Año: 2022 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Peritonitis Infecciosa Felina / Coronavirus Felino Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: Viruses Año: 2022 Tipo del documento: Article País de afiliación: Alemania