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Isolation and characterization of a variant subgroup GII-a porcine epidemic diarrhea virus strain in China

BACKGROUND: Highly virulent variants of porcine epidemic diarrhea virus (PEDV) have been closely associated with recent outbreaks of porcine epidemic diarrhea (PED) in China, which have resulted in severe economic losses to the pork industry. METHODS: In the current study, the variant PEDV strain HM...

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Autores principales: Yang, Dan, Su, Mingjun, Li, Chunqiu, Zhang, Bei, Qi, Shanshan, Sun, Dongbo, Yin, Baishuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126716/
https://www.ncbi.nlm.nih.gov/pubmed/31838173
http://dx.doi.org/10.1016/j.micpath.2019.103922
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author Yang, Dan
Su, Mingjun
Li, Chunqiu
Zhang, Bei
Qi, Shanshan
Sun, Dongbo
Yin, Baishuang
author_facet Yang, Dan
Su, Mingjun
Li, Chunqiu
Zhang, Bei
Qi, Shanshan
Sun, Dongbo
Yin, Baishuang
author_sort Yang, Dan
collection PubMed
description BACKGROUND: Highly virulent variants of porcine epidemic diarrhea virus (PEDV) have been closely associated with recent outbreaks of porcine epidemic diarrhea (PED) in China, which have resulted in severe economic losses to the pork industry. METHODS: In the current study, the variant PEDV strain HM2017 was isolated and purified and a viral growth curve was constructed according to the median tissue culture infective dose (TCID50). HM2017 were amplify with RT-PCR and analyzed by phylogeny analysis. Animal pathogenicity experiment was carried to evaluate the HM2017 clinical assessment. RESULTS: Genome-based phylogenetic analysis revealed that PEDV strain HM2017 was clustered into the variant subgroup GII-a that is currently circulating in pig populations in China. The highest median tissue culture infectious dose of strain HM2017 after 15 passages in Vero cells was 1.33 × 10(7) viral particles/mL. Strain HM2017 was highly virulent to suckling piglets, which exhibited clinical symptoms at 12 h post-infection (hpi) (i.e., weight loss at 12–84 hpi, increased body temperatures at 24–48 hpi, high viral loads in the jejunum and ileum, and 100% mortality by 84 hpi). CONCLUSION: The present study reports a variant subgroup GII-a PEDV HM2017 strain in China and characterize its pathogenicity. PEDV strain HM2017 of subgroup GII-a presents a promising vaccine candidate for the control of PED outbreaks in China.
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spelling pubmed-71267162020-04-08 Isolation and characterization of a variant subgroup GII-a porcine epidemic diarrhea virus strain in China Yang, Dan Su, Mingjun Li, Chunqiu Zhang, Bei Qi, Shanshan Sun, Dongbo Yin, Baishuang Microb Pathog Article BACKGROUND: Highly virulent variants of porcine epidemic diarrhea virus (PEDV) have been closely associated with recent outbreaks of porcine epidemic diarrhea (PED) in China, which have resulted in severe economic losses to the pork industry. METHODS: In the current study, the variant PEDV strain HM2017 was isolated and purified and a viral growth curve was constructed according to the median tissue culture infective dose (TCID50). HM2017 were amplify with RT-PCR and analyzed by phylogeny analysis. Animal pathogenicity experiment was carried to evaluate the HM2017 clinical assessment. RESULTS: Genome-based phylogenetic analysis revealed that PEDV strain HM2017 was clustered into the variant subgroup GII-a that is currently circulating in pig populations in China. The highest median tissue culture infectious dose of strain HM2017 after 15 passages in Vero cells was 1.33 × 10(7) viral particles/mL. Strain HM2017 was highly virulent to suckling piglets, which exhibited clinical symptoms at 12 h post-infection (hpi) (i.e., weight loss at 12–84 hpi, increased body temperatures at 24–48 hpi, high viral loads in the jejunum and ileum, and 100% mortality by 84 hpi). CONCLUSION: The present study reports a variant subgroup GII-a PEDV HM2017 strain in China and characterize its pathogenicity. PEDV strain HM2017 of subgroup GII-a presents a promising vaccine candidate for the control of PED outbreaks in China. Elsevier Ltd. 2020-03 2019-12-12 /pmc/articles/PMC7126716/ /pubmed/31838173 http://dx.doi.org/10.1016/j.micpath.2019.103922 Text en © 2019 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Yang, Dan
Su, Mingjun
Li, Chunqiu
Zhang, Bei
Qi, Shanshan
Sun, Dongbo
Yin, Baishuang
Isolation and characterization of a variant subgroup GII-a porcine epidemic diarrhea virus strain in China
title Isolation and characterization of a variant subgroup GII-a porcine epidemic diarrhea virus strain in China
title_full Isolation and characterization of a variant subgroup GII-a porcine epidemic diarrhea virus strain in China
title_fullStr Isolation and characterization of a variant subgroup GII-a porcine epidemic diarrhea virus strain in China
title_full_unstemmed Isolation and characterization of a variant subgroup GII-a porcine epidemic diarrhea virus strain in China
title_short Isolation and characterization of a variant subgroup GII-a porcine epidemic diarrhea virus strain in China
title_sort isolation and characterization of a variant subgroup gii-a porcine epidemic diarrhea virus strain in china
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126716/
https://www.ncbi.nlm.nih.gov/pubmed/31838173
http://dx.doi.org/10.1016/j.micpath.2019.103922
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