A Quadruplex Reverse Transcription Quantitative Polymerase Chain Reaction for Detecting Canine Coronavirus, Canine Rotavirus, Canine Parvovirus, and Canine Distemper Virus

被引:2
|
作者
Shi, Yandi [1 ]
Long, Feng [2 ]
Shi, Kaichuang [1 ,2 ]
He, Mengyi [1 ]
Shi, Yuwen [1 ]
Feng, Shuping [2 ]
Yin, Yanwen [2 ]
Wei, Xiankai [2 ]
Li, Zongqiang [1 ]
机构
[1] Guangxi Univ, Coll Anim Sci & Technol, Nanning 530005, Peoples R China
[2] Guangxi Ctr Anim Dis Control & Prevent, Nanning 530001, Peoples R China
关键词
canine coronavirus (CCoV); canine rotavirus (CRV); canine parvovirus (CPV); canine distemper virus (CDV); multiplex RT-qPCR; ANTIGENIC TYPES; DOGS; RNA; PCR;
D O I
10.3390/microbiolres15020049
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Canine coronavirus (CCoV), canine rotavirus (CRV), canine parvovirus (CPV), and canine distemper virus (CDV) cause gastroenteritis in dogs, and co-infections of these pathogens are common in China. In particular, CCoV and CRV are confirmed to have important zoonotic potential and cause public health issues. It is difficult to diagnose these diseases based only on clinical manifestations and pathological damage. Methods: In this study, four pairs of specific primers and probes targeting the CCoV M, CRV VP7, CPV VP2, and CDV N genes were designed. The reaction conditions, including the primer and probe concentrations, annealing temperatures, and reaction cycles, were optimized for the development of a quadruplex RT-qPCR for the detection of CCoV, CRV, CPV, and CDV. The assay was used to test 1028 clinical samples to validate its application. Results: A quadruplex RT-qPCR was successfully established for the differential detection of CCoV, CRV, CPV, and CDV, with good specificity, high sensitivity, and excellent repeatability. The assay could specifically detect CCoV, CRV, CPV, and CDV without cross-reactivity with the other canine viruses tested. It showed high sensitivity with limits of detection (LOD) of 1.1 x 102 copies/reaction for all four plasmid constructs. It showed excellent repeatability, with 0.05-0.90% intra-assay variation and 0.02-0.94% inter-assay variation. The 1028 clinical samples were tested using the quadruplex RT-qPCR and a reported reference RT-qPCR. The positivity rates of CCoV, CRV, CPV, and CDV were 9.53%, 0.97%, 25.68%, and 5.06% using the developed assay, and 9.05%, 0.88%, 25.68%, and 4.86% using the reference assay, with agreements higher than 99.32%. Conclusion: The results indicated that a rapid and accurate quadruplex RT-qPCR was developed for the detection and differentiation of CCoV, CRV, CPV, and CDV.
引用
收藏
页码:746 / 761
页数:16
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