Detection of Feline Coronavirus in Feline Effusions by Immunofluorescence Staining and Reverse Transcription Polymerase Chain Reaction

Feline coronavirus (FCoV), the pathogen for feline infectious peritonitis, is a lethal infectious agent that can cause effusions in the pleural and abdominal cavities in domestic cats. To study the epidemiology of FCoV in Taiwan, 81 FIP-suspected sick cats with effusive specimens were recruited to t...

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Main Authors: Yi-Chen Luo, I-Li Liu, Yu-Tan Chen, Hui-Wen Chen
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Pathogens
Subjects:
Online Access:https://www.mdpi.com/2076-0817/9/9/698
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author Yi-Chen Luo
I-Li Liu
Yu-Tan Chen
Hui-Wen Chen
author_facet Yi-Chen Luo
I-Li Liu
Yu-Tan Chen
Hui-Wen Chen
author_sort Yi-Chen Luo
collection DOAJ
description Feline coronavirus (FCoV), the pathogen for feline infectious peritonitis, is a lethal infectious agent that can cause effusions in the pleural and abdominal cavities in domestic cats. To study the epidemiology of FCoV in Taiwan, 81 FIP-suspected sick cats with effusive specimens were recruited to test for FCoV infection using immunofluorescence staining and reverse transcription-polymerase chain reaction as detection methods, and viral RNAs were recovered from the specimens to conduct genotyping and phylogenetic analysis based on the spike (S) protein gene. The results revealed that a total of 47 (47/81, 58%) of the sick cats were positive for FCoV in the effusion samples, of which 39 were successfully sequenced and comprised of 21 type I strains, 9 type II strains, and 9 co-infections. The signalment analysis of these sick cats revealed that only the sex of cats showed a significant association (odds ratio = 2.74, 95% confidence interval = 1.06–7.07, <i>p</i> = 0.03) with the infection of FCoV, while age and breed showed no association. FCoV-positive cats demonstrated a significantly lower albumin to globulin ratio than negative individuals (<i>p</i> = 0.0004). The partial S gene-based phylogenetic analysis revealed that the type I strains demonstrated genetic diversity forming several clades, while the type II strains were more conserved. This study demonstrates the latest epidemiological status of FCoV infection in the northern part of Taiwan among sick cats and presents comparisons of Taiwan and other countries.
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spelling doaj.art-77159015662f4de19e9c3be9310d81d72023-11-20T11:18:57ZengMDPI AGPathogens2076-08172020-08-019969810.3390/pathogens9090698Detection of Feline Coronavirus in Feline Effusions by Immunofluorescence Staining and Reverse Transcription Polymerase Chain ReactionYi-Chen Luo0I-Li Liu1Yu-Tan Chen2Hui-Wen Chen3Department of Veterinary Medicine, National Taiwan University, 10617 Taipei, TaiwanInstitute of Veterinary Clinical Science, School of Veterinary Medicine, National Taiwan University, 10617 Taipei, TaiwanDepartment of Veterinary Medicine, National Taiwan University, 10617 Taipei, TaiwanDepartment of Veterinary Medicine, National Taiwan University, 10617 Taipei, TaiwanFeline coronavirus (FCoV), the pathogen for feline infectious peritonitis, is a lethal infectious agent that can cause effusions in the pleural and abdominal cavities in domestic cats. To study the epidemiology of FCoV in Taiwan, 81 FIP-suspected sick cats with effusive specimens were recruited to test for FCoV infection using immunofluorescence staining and reverse transcription-polymerase chain reaction as detection methods, and viral RNAs were recovered from the specimens to conduct genotyping and phylogenetic analysis based on the spike (S) protein gene. The results revealed that a total of 47 (47/81, 58%) of the sick cats were positive for FCoV in the effusion samples, of which 39 were successfully sequenced and comprised of 21 type I strains, 9 type II strains, and 9 co-infections. The signalment analysis of these sick cats revealed that only the sex of cats showed a significant association (odds ratio = 2.74, 95% confidence interval = 1.06–7.07, <i>p</i> = 0.03) with the infection of FCoV, while age and breed showed no association. FCoV-positive cats demonstrated a significantly lower albumin to globulin ratio than negative individuals (<i>p</i> = 0.0004). The partial S gene-based phylogenetic analysis revealed that the type I strains demonstrated genetic diversity forming several clades, while the type II strains were more conserved. This study demonstrates the latest epidemiological status of FCoV infection in the northern part of Taiwan among sick cats and presents comparisons of Taiwan and other countries.https://www.mdpi.com/2076-0817/9/9/698feline coronavirusimmunofluorescence staininggenotypingspike protein genephylogenetic analysis
spellingShingle Yi-Chen Luo
I-Li Liu
Yu-Tan Chen
Hui-Wen Chen
Detection of Feline Coronavirus in Feline Effusions by Immunofluorescence Staining and Reverse Transcription Polymerase Chain Reaction
Pathogens
feline coronavirus
immunofluorescence staining
genotyping
spike protein gene
phylogenetic analysis
title Detection of Feline Coronavirus in Feline Effusions by Immunofluorescence Staining and Reverse Transcription Polymerase Chain Reaction
title_full Detection of Feline Coronavirus in Feline Effusions by Immunofluorescence Staining and Reverse Transcription Polymerase Chain Reaction
title_fullStr Detection of Feline Coronavirus in Feline Effusions by Immunofluorescence Staining and Reverse Transcription Polymerase Chain Reaction
title_full_unstemmed Detection of Feline Coronavirus in Feline Effusions by Immunofluorescence Staining and Reverse Transcription Polymerase Chain Reaction
title_short Detection of Feline Coronavirus in Feline Effusions by Immunofluorescence Staining and Reverse Transcription Polymerase Chain Reaction
title_sort detection of feline coronavirus in feline effusions by immunofluorescence staining and reverse transcription polymerase chain reaction
topic feline coronavirus
immunofluorescence staining
genotyping
spike protein gene
phylogenetic analysis
url https://www.mdpi.com/2076-0817/9/9/698
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AT yutanchen detectionoffelinecoronavirusinfelineeffusionsbyimmunofluorescencestainingandreversetranscriptionpolymerasechainreaction
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