One-step triplex reverse-transcription PCR detection of porcine epidemic diarrhea virus, porcine sapelovirus, and porcine sapovirus

Author:

Jiang Chunyan12ORCID,He Haijian12,Zhang Chaoying12,Zhang Xiaoju12,Han Jianfeng12,Zhang Hongbing12,Luo Yu12,Wu Yuan12,Wang Yanli12,Ge Bingqian12,Xu Jia12

Affiliation:

1. Department of Animal Production, Faculty of Agriculture and Bioengineering, Jinhua Polytechnic, Jinhua, Zhejiang, China (Jiang, He, C. Zhang, X. Zhang, H. Zhang, Luo, Wu, Wang, Ge, Xu)

2. Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing, China (Han)

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.

Funder

Jinhua Science and Technology Research Project

Publisher

SAGE Publications

Subject

General Veterinary

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