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Visual detection of porcine epidemic diarrhea virus using a novel reverse transcription polymerase spiral reaction method

BACKGROUND: Porcine epidemic diarrhea virus (PEDV) is a major etiological agent of porcine epidemic diarrhea around the world. Point-of-care testing in the field is lacking owing to the requirement for a simple, robust field applicable test that does not require professional laboratory equipment. Th...

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Autores principales: Wang, Xueyu, Xu, Xin, Hu, Wen, Zuo, Kejing, Li, Zhili, Kan, Yunchao, Yao, Lunguang, Ji, Jun, Bi, Yingzuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466714/
https://www.ncbi.nlm.nih.gov/pubmed/30987635
http://dx.doi.org/10.1186/s12917-019-1851-7
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author Wang, Xueyu
Xu, Xin
Hu, Wen
Zuo, Kejing
Li, Zhili
Kan, Yunchao
Yao, Lunguang
Ji, Jun
Bi, Yingzuo
author_facet Wang, Xueyu
Xu, Xin
Hu, Wen
Zuo, Kejing
Li, Zhili
Kan, Yunchao
Yao, Lunguang
Ji, Jun
Bi, Yingzuo
author_sort Wang, Xueyu
collection PubMed
description BACKGROUND: Porcine epidemic diarrhea virus (PEDV) is a major etiological agent of porcine epidemic diarrhea around the world. Point-of-care testing in the field is lacking owing to the requirement for a simple, robust field applicable test that does not require professional laboratory equipment. The aim of this study was to establish a novel reverse transcription polymerase spiral reaction (RT-PSR) assay for the rapid detection of porcine epidemic diarrhea virus (PEDV). For the assay, a specific RT-PSR primer pair was designed against a conserved region in PEDV ORF3. RESULTS: The RT-PSR was optimized, and PEDV could be detected after a 50 min incubation at 62 °C, in addition to the 15 min required for reverse transcription. No cross-reaction with other porcine infectious viruses was observed. This new method for PEDV detection was 10 times more sensitive than the conventional reverse transcription-polymerase chain reaction (RT-PCR) assay. The positive rates for 65 clinical samples using the new RT-PSR assay and the conventional RT-PCR assay were 58.46% (38/65) and 53.84% (35/65), respectively. In the RT-PSR assay, the addition of a mixture of dyes allowed a positive reaction to be directly observed by the naked eye. CONCLUSIONS: These results indicate that this RT-PSR assay is capable of accurately detecting PEDV, and has the advantages of high specificity and sensitivity for the detection of PEDV.
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spelling pubmed-64667142019-04-22 Visual detection of porcine epidemic diarrhea virus using a novel reverse transcription polymerase spiral reaction method Wang, Xueyu Xu, Xin Hu, Wen Zuo, Kejing Li, Zhili Kan, Yunchao Yao, Lunguang Ji, Jun Bi, Yingzuo BMC Vet Res Research Article BACKGROUND: Porcine epidemic diarrhea virus (PEDV) is a major etiological agent of porcine epidemic diarrhea around the world. Point-of-care testing in the field is lacking owing to the requirement for a simple, robust field applicable test that does not require professional laboratory equipment. The aim of this study was to establish a novel reverse transcription polymerase spiral reaction (RT-PSR) assay for the rapid detection of porcine epidemic diarrhea virus (PEDV). For the assay, a specific RT-PSR primer pair was designed against a conserved region in PEDV ORF3. RESULTS: The RT-PSR was optimized, and PEDV could be detected after a 50 min incubation at 62 °C, in addition to the 15 min required for reverse transcription. No cross-reaction with other porcine infectious viruses was observed. This new method for PEDV detection was 10 times more sensitive than the conventional reverse transcription-polymerase chain reaction (RT-PCR) assay. The positive rates for 65 clinical samples using the new RT-PSR assay and the conventional RT-PCR assay were 58.46% (38/65) and 53.84% (35/65), respectively. In the RT-PSR assay, the addition of a mixture of dyes allowed a positive reaction to be directly observed by the naked eye. CONCLUSIONS: These results indicate that this RT-PSR assay is capable of accurately detecting PEDV, and has the advantages of high specificity and sensitivity for the detection of PEDV. BioMed Central 2019-04-15 /pmc/articles/PMC6466714/ /pubmed/30987635 http://dx.doi.org/10.1186/s12917-019-1851-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wang, Xueyu
Xu, Xin
Hu, Wen
Zuo, Kejing
Li, Zhili
Kan, Yunchao
Yao, Lunguang
Ji, Jun
Bi, Yingzuo
Visual detection of porcine epidemic diarrhea virus using a novel reverse transcription polymerase spiral reaction method
title Visual detection of porcine epidemic diarrhea virus using a novel reverse transcription polymerase spiral reaction method
title_full Visual detection of porcine epidemic diarrhea virus using a novel reverse transcription polymerase spiral reaction method
title_fullStr Visual detection of porcine epidemic diarrhea virus using a novel reverse transcription polymerase spiral reaction method
title_full_unstemmed Visual detection of porcine epidemic diarrhea virus using a novel reverse transcription polymerase spiral reaction method
title_short Visual detection of porcine epidemic diarrhea virus using a novel reverse transcription polymerase spiral reaction method
title_sort visual detection of porcine epidemic diarrhea virus using a novel reverse transcription polymerase spiral reaction method
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466714/
https://www.ncbi.nlm.nih.gov/pubmed/30987635
http://dx.doi.org/10.1186/s12917-019-1851-7
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