期刊
JOURNAL OF VIROLOGICAL METHODS
卷 310, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.jviromet.2022.114613
关键词
Avian orthoreovirus; Real-time RT-PCR; TaqMan; Sensitivity; Specificity; Wide -range detection
A real-time reverse transcription polymerase chain reaction (RT-qPCR) assay for the detection of avian reovirus (ARV) was developed in this study. The assay showed simplicity, convenience, high sensitivity, and specificity, making it a potential alternative diagnostic method for detecting ARVs in veterinary diagnostic laboratories.
Avian reovirus (ARV) is a common pathogen in chickens and other birds causing a variety of clinical symptoms such as arthritis and tenosynovitis but also enteric and respiratory symptoms. A rapid method that detects as many ARV genotypes as possible, will contribute to the early identification and control of the virus infection that causes high economic damage to the poultry industry worldwide. In this study, a real-time reverse transcription polymerase chain reaction (RT-qPCR) assay for the detection of ARV was developed. The RT-qPCR detection threshold for ARV genomic RNA standard cases was 10 copies/mu L. Reproducibility of the RT-qPCR was confirmed by intra- and inter-assays. When the nucleic acids of different ARV genotypes and other common avian pathogens (IBDV, AIV, NDV, and IBV) were subjected to that RT-qPCR test, only ARV samples tested positive while all other pathogens tested negative. Due to the simplicity, convenience, high sensitivity, and specificity of the assay, the probe-based RT-qPCR is proposed to be used as an alternative diagnostic assay for the detection of ARVs in veterinary diagnostic laboratories.
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