近代 GI.1 沙巴病毒的流行病学和分子进化

IF 6.8 3区 医学 Q1 VIROLOGY
Sheikh A. Hoque, Yuki Akari, Pattara Khamrin, Tung Phan, Yuko Onda, Shoko Okitsu, Satoshi Komoto, Satoshi Hayakawa, Shihoko Komine- Aizawa, Yoshikazu Yuki, Hiroshi Kiyono, Hiroshi Ushijima
{"title":"近代 GI.1 沙巴病毒的流行病学和分子进化","authors":"Sheikh A. Hoque,&nbsp;Yuki Akari,&nbsp;Pattara Khamrin,&nbsp;Tung Phan,&nbsp;Yuko Onda,&nbsp;Shoko Okitsu,&nbsp;Satoshi Komoto,&nbsp;Satoshi Hayakawa,&nbsp;Shihoko Komine- Aizawa,&nbsp;Yoshikazu Yuki,&nbsp;Hiroshi Kiyono,&nbsp;Hiroshi Ushijima","doi":"10.1002/jmv.29904","DOIUrl":null,"url":null,"abstract":"<p>Sapovirus (SaV) infection is increasing worldwide. Herein, we provided evidence of a significant increase in SaV infection in Japan during 2010–2022, primarily due to the considerable (<i>p</i> = 0.0003) rise of the GI.1 genotype. Furthermore, we found that all major and minor SaV outbreaks in Japan, including the largest SaV outbreak in 2021–2022, were caused by the GI.1 genotype. Therefore, to get insight into the underlying molecular mechanism behind this rising trend of the SaV GI.1 type, we selected 15 SaV GI.1 outbreak strains for complete genome analysis through next-generation sequencing. Phylogenetically, our strains remained clustered in different branches in lineages I and II among the GI.1 genotype. We showed all amino acid (aa) substitutions in different open reading frames (ORFs) in these strains. Importantly, we have demonstrated that the strains involved in the largest SaV outbreak in Japan in 2021–2022 belonged to lineage II and possessed the third ORF. We have identified some unique aa mutations in these major outbreak strains in the NS1 and NS6-NS7 regions that are thought to be associated with viral pathogenicity, cell tropism, and epidemiological competence. Thus, in addition to enriching the database of SaV's complete sequences, this study provides insights into its important mutations.</p>","PeriodicalId":16354,"journal":{"name":"Journal of Medical Virology","volume":null,"pages":null},"PeriodicalIF":6.8000,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Epidemiology and molecular evolution of GI.1 sapovirus in the recent era\",\"authors\":\"Sheikh A. Hoque,&nbsp;Yuki Akari,&nbsp;Pattara Khamrin,&nbsp;Tung Phan,&nbsp;Yuko Onda,&nbsp;Shoko Okitsu,&nbsp;Satoshi Komoto,&nbsp;Satoshi Hayakawa,&nbsp;Shihoko Komine- Aizawa,&nbsp;Yoshikazu Yuki,&nbsp;Hiroshi Kiyono,&nbsp;Hiroshi Ushijima\",\"doi\":\"10.1002/jmv.29904\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Sapovirus (SaV) infection is increasing worldwide. Herein, we provided evidence of a significant increase in SaV infection in Japan during 2010–2022, primarily due to the considerable (<i>p</i> = 0.0003) rise of the GI.1 genotype. Furthermore, we found that all major and minor SaV outbreaks in Japan, including the largest SaV outbreak in 2021–2022, were caused by the GI.1 genotype. Therefore, to get insight into the underlying molecular mechanism behind this rising trend of the SaV GI.1 type, we selected 15 SaV GI.1 outbreak strains for complete genome analysis through next-generation sequencing. Phylogenetically, our strains remained clustered in different branches in lineages I and II among the GI.1 genotype. We showed all amino acid (aa) substitutions in different open reading frames (ORFs) in these strains. Importantly, we have demonstrated that the strains involved in the largest SaV outbreak in Japan in 2021–2022 belonged to lineage II and possessed the third ORF. We have identified some unique aa mutations in these major outbreak strains in the NS1 and NS6-NS7 regions that are thought to be associated with viral pathogenicity, cell tropism, and epidemiological competence. Thus, in addition to enriching the database of SaV's complete sequences, this study provides insights into its important mutations.</p>\",\"PeriodicalId\":16354,\"journal\":{\"name\":\"Journal of Medical Virology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":6.8000,\"publicationDate\":\"2024-09-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Medical Virology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jmv.29904\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"VIROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medical Virology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jmv.29904","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"VIROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

有鼻病毒(SaV)感染在全球范围内呈上升趋势。在此,我们提供了 2010-2022 年间日本 SaV 感染显著增加的证据,这主要是由于 GI.1 基因型的显著增加(p = 0.0003)。此外,我们还发现,日本所有大小规模的 SaV 爆发,包括 2021-2022 年最大的 SaV 爆发,都是由 GI.1 基因型引起的。因此,为了深入了解SaV GI.1型呈上升趋势背后的分子机制,我们选择了15株SaV GI.1型爆发株,通过新一代测序进行全基因组分析。从系统发育上看,我们的菌株仍然聚集在 GI.1 基因型的 I 系和 II 系的不同分支中。我们显示了这些菌株中不同开放阅读框(ORF)中的所有氨基酸(aa)置换。重要的是,我们证明了 2021-2022 年日本爆发的最大规模 SaV 所涉及的菌株属于 II 系,并拥有第三个 ORF。我们在这些主要疫情毒株的 NS1 和 NS6-NS7 区域发现了一些独特的 aa 突变,这些突变被认为与病毒的致病性、细胞滋养性和流行病学能力有关。因此,本研究除了丰富了 SaV 完整序列数据库之外,还提供了对其重要突变的深入了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epidemiology and molecular evolution of GI.1 sapovirus in the recent era

Sapovirus (SaV) infection is increasing worldwide. Herein, we provided evidence of a significant increase in SaV infection in Japan during 2010–2022, primarily due to the considerable (p = 0.0003) rise of the GI.1 genotype. Furthermore, we found that all major and minor SaV outbreaks in Japan, including the largest SaV outbreak in 2021–2022, were caused by the GI.1 genotype. Therefore, to get insight into the underlying molecular mechanism behind this rising trend of the SaV GI.1 type, we selected 15 SaV GI.1 outbreak strains for complete genome analysis through next-generation sequencing. Phylogenetically, our strains remained clustered in different branches in lineages I and II among the GI.1 genotype. We showed all amino acid (aa) substitutions in different open reading frames (ORFs) in these strains. Importantly, we have demonstrated that the strains involved in the largest SaV outbreak in Japan in 2021–2022 belonged to lineage II and possessed the third ORF. We have identified some unique aa mutations in these major outbreak strains in the NS1 and NS6-NS7 regions that are thought to be associated with viral pathogenicity, cell tropism, and epidemiological competence. Thus, in addition to enriching the database of SaV's complete sequences, this study provides insights into its important mutations.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Medical Virology
Journal of Medical Virology 医学-病毒学
CiteScore
23.20
自引率
2.40%
发文量
777
审稿时长
1 months
期刊介绍: The Journal of Medical Virology focuses on publishing original scientific papers on both basic and applied research related to viruses that affect humans. The journal publishes reports covering a wide range of topics, including the characterization, diagnosis, epidemiology, immunology, and pathogenesis of human virus infections. It also includes studies on virus morphology, genetics, replication, and interactions with host cells. The intended readership of the journal includes virologists, microbiologists, immunologists, infectious disease specialists, diagnostic laboratory technologists, epidemiologists, hematologists, and cell biologists. The Journal of Medical Virology is indexed and abstracted in various databases, including Abstracts in Anthropology (Sage), CABI, AgBiotech News & Information, National Agricultural Library, Biological Abstracts, Embase, Global Health, Web of Science, Veterinary Bulletin, and others.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信