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Development and Clinical Applications of a 5-Plex Real-Time RT-PCR for Swine Enteric Coronaviruses

A PEDV/PDCoV/TGEV/SADS-CoV/XIPC 5-plex real-time RT-PCR was developed and validated for the simultaneous detection and differentiation of four swine enteric coronaviruses (PEDV, PDCoV, TGEV and SADS-CoV) in one PCR reaction (XIPC serves as an exogenous internal positive control). The 5-plex PCR had...

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Autores principales: Zhu, Jin-Hui, Rawal, Gaurav, Aljets, Ethan, Yim-Im, Wannarat, Yang, Yong-Le, Huang, Yao-Wei, Krueger, Karen, Gauger, Phillip, Main, Rodger, Zhang, Jianqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324624/
https://www.ncbi.nlm.nih.gov/pubmed/35891517
http://dx.doi.org/10.3390/v14071536
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author Zhu, Jin-Hui
Rawal, Gaurav
Aljets, Ethan
Yim-Im, Wannarat
Yang, Yong-Le
Huang, Yao-Wei
Krueger, Karen
Gauger, Phillip
Main, Rodger
Zhang, Jianqiang
author_facet Zhu, Jin-Hui
Rawal, Gaurav
Aljets, Ethan
Yim-Im, Wannarat
Yang, Yong-Le
Huang, Yao-Wei
Krueger, Karen
Gauger, Phillip
Main, Rodger
Zhang, Jianqiang
author_sort Zhu, Jin-Hui
collection PubMed
description A PEDV/PDCoV/TGEV/SADS-CoV/XIPC 5-plex real-time RT-PCR was developed and validated for the simultaneous detection and differentiation of four swine enteric coronaviruses (PEDV, PDCoV, TGEV and SADS-CoV) in one PCR reaction (XIPC serves as an exogenous internal positive control). The 5-plex PCR had excellent analytical specificity, analytical sensitivity, and repeatability based on the testing of various viral and bacterial pathogens, serial dilutions of virus isolates, and in vitro transcribed RNAs. The 5-plex PCR had comparable diagnostic performance to a commercial PEDV/TGEV/PDCoV reference PCR, based on the testing of 219 clinical samples. Subsequently, 1807 clinical samples collected from various U.S. states during 2019–2021 were tested by the 5-plex PCR to investigate the presence of SADS-CoV in U.S. swine and the frequency of detecting swine enteric CoVs. All 1807 samples tested negative for SADS-CoV. Among the samples positive for swine enteric CoVs, there was a low frequency of detecting TGEV, an intermediate frequency of detecting PDCoV, and a high frequency of detecting PEDV. Although there is no evidence of SADS-CoV presence in the U.S. at present, the availability of the 5-plex PCR will enable us to conduct ongoing surveillance to detect and differentiate these viruses in swine samples and other host species samples as some of these coronaviruses can cause cross-species infection.
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spelling pubmed-93246242022-07-27 Development and Clinical Applications of a 5-Plex Real-Time RT-PCR for Swine Enteric Coronaviruses Zhu, Jin-Hui Rawal, Gaurav Aljets, Ethan Yim-Im, Wannarat Yang, Yong-Le Huang, Yao-Wei Krueger, Karen Gauger, Phillip Main, Rodger Zhang, Jianqiang Viruses Article A PEDV/PDCoV/TGEV/SADS-CoV/XIPC 5-plex real-time RT-PCR was developed and validated for the simultaneous detection and differentiation of four swine enteric coronaviruses (PEDV, PDCoV, TGEV and SADS-CoV) in one PCR reaction (XIPC serves as an exogenous internal positive control). The 5-plex PCR had excellent analytical specificity, analytical sensitivity, and repeatability based on the testing of various viral and bacterial pathogens, serial dilutions of virus isolates, and in vitro transcribed RNAs. The 5-plex PCR had comparable diagnostic performance to a commercial PEDV/TGEV/PDCoV reference PCR, based on the testing of 219 clinical samples. Subsequently, 1807 clinical samples collected from various U.S. states during 2019–2021 were tested by the 5-plex PCR to investigate the presence of SADS-CoV in U.S. swine and the frequency of detecting swine enteric CoVs. All 1807 samples tested negative for SADS-CoV. Among the samples positive for swine enteric CoVs, there was a low frequency of detecting TGEV, an intermediate frequency of detecting PDCoV, and a high frequency of detecting PEDV. Although there is no evidence of SADS-CoV presence in the U.S. at present, the availability of the 5-plex PCR will enable us to conduct ongoing surveillance to detect and differentiate these viruses in swine samples and other host species samples as some of these coronaviruses can cause cross-species infection. MDPI 2022-07-14 /pmc/articles/PMC9324624/ /pubmed/35891517 http://dx.doi.org/10.3390/v14071536 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhu, Jin-Hui
Rawal, Gaurav
Aljets, Ethan
Yim-Im, Wannarat
Yang, Yong-Le
Huang, Yao-Wei
Krueger, Karen
Gauger, Phillip
Main, Rodger
Zhang, Jianqiang
Development and Clinical Applications of a 5-Plex Real-Time RT-PCR for Swine Enteric Coronaviruses
title Development and Clinical Applications of a 5-Plex Real-Time RT-PCR for Swine Enteric Coronaviruses
title_full Development and Clinical Applications of a 5-Plex Real-Time RT-PCR for Swine Enteric Coronaviruses
title_fullStr Development and Clinical Applications of a 5-Plex Real-Time RT-PCR for Swine Enteric Coronaviruses
title_full_unstemmed Development and Clinical Applications of a 5-Plex Real-Time RT-PCR for Swine Enteric Coronaviruses
title_short Development and Clinical Applications of a 5-Plex Real-Time RT-PCR for Swine Enteric Coronaviruses
title_sort development and clinical applications of a 5-plex real-time rt-pcr for swine enteric coronaviruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324624/
https://www.ncbi.nlm.nih.gov/pubmed/35891517
http://dx.doi.org/10.3390/v14071536
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