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Antigenic characteristics and genomic analysis of novel EV-A90 enteroviruses isolated in Xinjiang, China

Enterovirus A90 (EV-A90) is a novel serotype of enterovirus A species that is rarely reported. Here, we isolated five enteroviruses from patients with acute flaccid paralysis in Hotan and Kashgar cities in Xinjiang, China that were identified as EV-A90 by molecular typing. The VP1 sequences of these...

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Autores principales: Huang, Keqiang, Zhang, Yong, Song, Yang, Cui, Hui, Yan, Dongmei, Zhu, Shuangli, Sun, Qiang, Tang, Haishu, Wang, Dongyan, Xu, Wenbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035207/
https://www.ncbi.nlm.nih.gov/pubmed/29980696
http://dx.doi.org/10.1038/s41598-018-28469-9
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author Huang, Keqiang
Zhang, Yong
Song, Yang
Cui, Hui
Yan, Dongmei
Zhu, Shuangli
Sun, Qiang
Tang, Haishu
Wang, Dongyan
Xu, Wenbo
author_facet Huang, Keqiang
Zhang, Yong
Song, Yang
Cui, Hui
Yan, Dongmei
Zhu, Shuangli
Sun, Qiang
Tang, Haishu
Wang, Dongyan
Xu, Wenbo
author_sort Huang, Keqiang
collection PubMed
description Enterovirus A90 (EV-A90) is a novel serotype of enterovirus A species that is rarely reported. Here, we isolated five enteroviruses from patients with acute flaccid paralysis in Hotan and Kashgar cities in Xinjiang, China that were identified as EV-A90 by molecular typing. The VP1 sequences of these Xinjiang EV-A90 strains showed 88.4–89% nucleotide sequence identity to the prototype EV-A90 strain; however, genome analysis indicated complex recombination events in P2 and P3 regions. Next, the seroprevalence of EV-A90 was examined in 49 serum specimens collected in Hotan and Kashgar, and 37.5% were EV-A90 antibody positive (>1:8), with a geometric mean titre (GMT) of 1:10.47. The low positive rate and GMT suggest a low-level EV-A90 epidemic in Xinjiang. Two of the five Xinjiang EV-A90 strains were temperature sensitive, and three were temperature resistant, and a comparative genomics analysis suggested that an amino acid substitution (H1799Y) in the 3D(pol) region was related to temperature sensitivity. Although the epidemic strength is low, some EV-A90 strains were temperature resistant, which is suggestive of strong virulence and transmission capacity. This study expanded the number of EV-A90 in GenBank and provided basic data that may be useful for studying the molecular epidemiology of EV-A90.
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spelling pubmed-60352072018-07-12 Antigenic characteristics and genomic analysis of novel EV-A90 enteroviruses isolated in Xinjiang, China Huang, Keqiang Zhang, Yong Song, Yang Cui, Hui Yan, Dongmei Zhu, Shuangli Sun, Qiang Tang, Haishu Wang, Dongyan Xu, Wenbo Sci Rep Article Enterovirus A90 (EV-A90) is a novel serotype of enterovirus A species that is rarely reported. Here, we isolated five enteroviruses from patients with acute flaccid paralysis in Hotan and Kashgar cities in Xinjiang, China that were identified as EV-A90 by molecular typing. The VP1 sequences of these Xinjiang EV-A90 strains showed 88.4–89% nucleotide sequence identity to the prototype EV-A90 strain; however, genome analysis indicated complex recombination events in P2 and P3 regions. Next, the seroprevalence of EV-A90 was examined in 49 serum specimens collected in Hotan and Kashgar, and 37.5% were EV-A90 antibody positive (>1:8), with a geometric mean titre (GMT) of 1:10.47. The low positive rate and GMT suggest a low-level EV-A90 epidemic in Xinjiang. Two of the five Xinjiang EV-A90 strains were temperature sensitive, and three were temperature resistant, and a comparative genomics analysis suggested that an amino acid substitution (H1799Y) in the 3D(pol) region was related to temperature sensitivity. Although the epidemic strength is low, some EV-A90 strains were temperature resistant, which is suggestive of strong virulence and transmission capacity. This study expanded the number of EV-A90 in GenBank and provided basic data that may be useful for studying the molecular epidemiology of EV-A90. Nature Publishing Group UK 2018-07-06 /pmc/articles/PMC6035207/ /pubmed/29980696 http://dx.doi.org/10.1038/s41598-018-28469-9 Text en © The Author(s) 2018 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
Huang, Keqiang
Zhang, Yong
Song, Yang
Cui, Hui
Yan, Dongmei
Zhu, Shuangli
Sun, Qiang
Tang, Haishu
Wang, Dongyan
Xu, Wenbo
Antigenic characteristics and genomic analysis of novel EV-A90 enteroviruses isolated in Xinjiang, China
title Antigenic characteristics and genomic analysis of novel EV-A90 enteroviruses isolated in Xinjiang, China
title_full Antigenic characteristics and genomic analysis of novel EV-A90 enteroviruses isolated in Xinjiang, China
title_fullStr Antigenic characteristics and genomic analysis of novel EV-A90 enteroviruses isolated in Xinjiang, China
title_full_unstemmed Antigenic characteristics and genomic analysis of novel EV-A90 enteroviruses isolated in Xinjiang, China
title_short Antigenic characteristics and genomic analysis of novel EV-A90 enteroviruses isolated in Xinjiang, China
title_sort antigenic characteristics and genomic analysis of novel ev-a90 enteroviruses isolated in xinjiang, china
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035207/
https://www.ncbi.nlm.nih.gov/pubmed/29980696
http://dx.doi.org/10.1038/s41598-018-28469-9
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