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Emergence of Two different recombinant PRRSV strains with low neutralizing antibody susceptibility in China

PRRSV causes major economic loss in global swine industry. 41 of 131 (31.29%) tissue samples collected from pig farms in central and east China from 2016 to 2017 were confirmed as PRRSV positive in RT-PCR. Base on phylogenetic analysis for ORF5 and ORF6, 3 isolates closely related to QYYZ strain for...

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Autores principales: Han, Guangwei, Xu, Huiling, Wang, Kexiong, He, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385303/
https://www.ncbi.nlm.nih.gov/pubmed/30792441
http://dx.doi.org/10.1038/s41598-019-39059-8
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author Han, Guangwei
Xu, Huiling
Wang, Kexiong
He, Fang
author_facet Han, Guangwei
Xu, Huiling
Wang, Kexiong
He, Fang
author_sort Han, Guangwei
collection PubMed
description PRRSV causes major economic loss in global swine industry. 41 of 131 (31.29%) tissue samples collected from pig farms in central and east China from 2016 to 2017 were confirmed as PRRSV positive in RT-PCR. Base on phylogenetic analysis for ORF5 and ORF6, 3 isolates closely related to QYYZ strain form a new subgroup IV, while 3 other ones were clustered into subgroup III, represented by NADC30. Numerous amino acid substitutions involved in viral neutralization susceptibility were identified in GP5 among these isolates. Two emerging PRRSV strains (ZJnb16-2, SDbz16-2) were successfully isolated and sequenced. ZJnb16-2 was identified as a recombinant virus between strain QYYZ and JXA1 while SDbz16-2 was an inter-subgenotype recombinant virus of strains NADC30 and JXA1. As shown in the pathogenicity evaluation in piglets, ZJnb16-2 is highly pathogenic while SDbz16-2 is mild. Hyper-immune sera against major vaccine strains HUN4-F112 and JK-100 failed to neutralize either ZJnb16-2 or SDbz16-2. Only 0.8–2.0% of pig serum samples which were confirmed as PRRSV-positive with commercial ELISA kits presented neutralization reactivity against either ZJnb16-2 or SDbz16-2. The study confirmed that the viral genomic recombination contributes to the emergence of new pathogenic PRRSVs in China, which may escape from the protective immunity elicited by the conventional vaccines, highlighting the necessity in updates of vaccine strains and the need for a universal vaccine against PRRSV.
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spelling pubmed-63853032019-02-27 Emergence of Two different recombinant PRRSV strains with low neutralizing antibody susceptibility in China Han, Guangwei Xu, Huiling Wang, Kexiong He, Fang Sci Rep Article PRRSV causes major economic loss in global swine industry. 41 of 131 (31.29%) tissue samples collected from pig farms in central and east China from 2016 to 2017 were confirmed as PRRSV positive in RT-PCR. Base on phylogenetic analysis for ORF5 and ORF6, 3 isolates closely related to QYYZ strain form a new subgroup IV, while 3 other ones were clustered into subgroup III, represented by NADC30. Numerous amino acid substitutions involved in viral neutralization susceptibility were identified in GP5 among these isolates. Two emerging PRRSV strains (ZJnb16-2, SDbz16-2) were successfully isolated and sequenced. ZJnb16-2 was identified as a recombinant virus between strain QYYZ and JXA1 while SDbz16-2 was an inter-subgenotype recombinant virus of strains NADC30 and JXA1. As shown in the pathogenicity evaluation in piglets, ZJnb16-2 is highly pathogenic while SDbz16-2 is mild. Hyper-immune sera against major vaccine strains HUN4-F112 and JK-100 failed to neutralize either ZJnb16-2 or SDbz16-2. Only 0.8–2.0% of pig serum samples which were confirmed as PRRSV-positive with commercial ELISA kits presented neutralization reactivity against either ZJnb16-2 or SDbz16-2. The study confirmed that the viral genomic recombination contributes to the emergence of new pathogenic PRRSVs in China, which may escape from the protective immunity elicited by the conventional vaccines, highlighting the necessity in updates of vaccine strains and the need for a universal vaccine against PRRSV. Nature Publishing Group UK 2019-02-21 /pmc/articles/PMC6385303/ /pubmed/30792441 http://dx.doi.org/10.1038/s41598-019-39059-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Han, Guangwei
Xu, Huiling
Wang, Kexiong
He, Fang
Emergence of Two different recombinant PRRSV strains with low neutralizing antibody susceptibility in China
title Emergence of Two different recombinant PRRSV strains with low neutralizing antibody susceptibility in China
title_full Emergence of Two different recombinant PRRSV strains with low neutralizing antibody susceptibility in China
title_fullStr Emergence of Two different recombinant PRRSV strains with low neutralizing antibody susceptibility in China
title_full_unstemmed Emergence of Two different recombinant PRRSV strains with low neutralizing antibody susceptibility in China
title_short Emergence of Two different recombinant PRRSV strains with low neutralizing antibody susceptibility in China
title_sort emergence of two different recombinant prrsv strains with low neutralizing antibody susceptibility in china
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385303/
https://www.ncbi.nlm.nih.gov/pubmed/30792441
http://dx.doi.org/10.1038/s41598-019-39059-8
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