Development of a novel reverse transcription PCR and its application to field sample testing for feline calicivirus prevalence in healthy stray cats in Korea

• Published in: Journal of veterinary science (Suwŏn-si, Korea) Vol. 21; no. 5; p. e71
• Main Authors: Kim, Sung Jae, Park, Yong Ho, Park, Kun Taek
• Format: Journal Article
• Language: English
• Published: The Korean Society of Veterinary Science 01.09.2020; 대한수의학회
• Subjects: Original; 수의학
• ISSN: 1229-845X; 1976-555X
• DOI: 10.4142/jvs.2020.21.e71

BACKGROUNDFeline calicivirus (FCV) is a major and highly infectious pathogen in cats worldwide. However, there have been limited studies about the status of FCV infections in Korea. OBJECTIVESTo investigate the current status of FCV infections in stray cats in Korea. METHODSA novel reverse transcription polymerase chain reaction (RT-PCR) assay was developed based on the conserved nucleotide sequences of reported FCV strains. Field swab samples were collected from 122 cats (2 hospital admitted cats and 120 stray cats) in 2016 and 2017. All the samples were tested by virus isolation and 2 different RT-PCRs, including the novel RT-PCR, for the detection of FCV. RESULTSThe novel RT-PCR assay showed no cross-reactivity to the nucleic acids of the other feline pathogens tested, and the limit of detection was calculated as 10⁰ TCID50/mL based on an in vitro assessment. The novel RT-PCR assay detected 5 positive samples from the 122 field samples, which showed perfect agreement with the results of the virus isolation method. In contrast, another RT-PCR assay used in a previous study in Korea detected no positive samples. The prevalence of FCV infection in stray cats was 2.5% (3/120) based on the results of virus isolation and the novel RT-PCR assays. CONCLUSIONSThe current study is the first report of the detection and prevalence of FCV in stray cats in Korea. The novel RT-PCR assay developed in this study showed high sensitivity and specificity, which indicates a useful diagnostic assay to identify FCV infection in cats.