| Literature DB >> 31650901 |
Chunyan Jiang1,2, Haijian He1,2, Chaoying Zhang1,2, Xiaoju Zhang1,2, Jianfeng Han1,2, Hongbing Zhang1,2, Yu Luo1,2, Yuan Wu1,2, Yanli Wang1,2, Bingqian Ge1,2, Jia Xu1,2.
Abstract
Swine diarrhea can be caused by multiple agents, including porcine epidemic diarrhea virus (PEDV), porcine sapelovirus (PSV), and porcine sapovirus (SaV). We designed a one-step triplex reverse-transcription PCR (RT-PCR) detection method including 3 pairs of primers that focused on the S1 gene of PEDV, a conserved gene of PSV, and the VP1 gene of SaV. The optimal concentrations of upstream and downstream primers in the triplex RT-PCR were 0.24 μM for PEDV, 0.15 μM for PSV, and 0.2 μM for SaV, and the optimal annealing temperature was 55.5°C. Triplex RT-PCR assessment of 402 piglet diarrhea samples was compared with conventional individual RT-PCR. Concordance rates in both tests for individual viruses were 100%, 97.6%, and 94.4% for PEDV, PSV, and SaV, respectively. PEDV, PSV, and SaV were detected in 57.2%, 10.4%, and 9.0% of the samples, respectively. The high sensitivity and specificity of this triplex RT-PCR-based detection method for PEDV, PSV, and SaV could allow rapid detection and analysis of mixed infections by these 3 viruses.Entities:
Keywords: porcine epidemic diarrhea virus; porcine sapelovirus; porcine sapovirus; triplex RT-PCR
Mesh:
Year: 2019 PMID: 31650901 PMCID: PMC6900713 DOI: 10.1177/1040638719883834
Source DB: PubMed Journal: J Vet Diagn Invest ISSN: 1040-6387 Impact factor: 1.279