• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

印度新德里新生儿院内急性腹泻暴发中罕见 G12P[11]轮状病毒的全基因组分析。

Complete genomic analysis of uncommon G12P[11] rotavirus causing a nosocomial outbreak of acute diarrhea in the newborns in New Delhi, India.

机构信息

Enteric Viruses Group, ICMR-National Institute of Virology, Pune, India.

Maulana Azad Medical College and Lok Nayak Hospital, New Delhi, India.

出版信息

J Med Virol. 2022 Jun;94(6):2613-2623. doi: 10.1002/jmv.27468. Epub 2021 Dec 2.

DOI:10.1002/jmv.27468
PMID:34811775
Abstract

Rotaviruses (RVs) are the major causative agents of acute gastroenteritis in children, but in neonates, RV infections are generally nosocomial in origin and mostly asymptomatic. However, there have been infrequent reports of nosocomial outbreaks of clinical disease in this population. In this study, we describe uncommon RV genotype; G12P[11] associated with an outbreak of acute gastroenteritis in the neonatal ward and neonatal intensive care unit (NICU) in New Delhi, North India. Full-genome analyses of the pathogenic G12P[11] strain was carried out to map the genotype constellation and further to explore the variations in the antigenic epitopes on the immunodominant VP7 and VP4 proteins, the amino acid sequences were compared with neonatal strains; ROTAVAC® (G9P[11]) and asymptomatic G12P[11] and also other G/P-type matched strains. The study revealed G12-P[11]-I1-R1-C1-M1-A1-N1-T1-E1-H1 human Wa-like genotype constellation and highlights evidence of gene reassortment. No significant differences were observed in the sequences of structural (except VP3) and nonstructural encoding genes of G12P[11] strains recovered from symptomatic and asymptomatic neonates. Presence of additional N-linked glycosylation site was noted in the G12 strains, as a consequence of a change from Asp→Asn at amino acid position 238. Interestingly, only two and four amino acids substitution within the 7-1a and 8-1 antigenic epitope were observed, respectively, compared with asymptomatic G12P[11] strain. The study emphasizes the importance of close monitoring of RV outbreaks in neonates for early alarming of novel strain.

摘要

轮状病毒(RV)是导致儿童急性肠胃炎的主要病原体,但在新生儿中,RV 感染通常为医院感染,且大多无症状。然而,在该人群中,偶有医院感染爆发临床疾病的报道。在本研究中,我们描述了一种不常见的 RV 基因型;G12P[11]与印度北部新德里新生儿病房和新生儿重症监护病房(NICU)爆发的急性肠胃炎有关。对致病性 G12P[11]株进行了全基因组分析,以绘制基因型图谱,并进一步探索免疫显性 VP7 和 VP4 蛋白上抗原表位的变异,将氨基酸序列与新生儿株;ROTAVAC®(G9P[11])和无症状 G12P[11]以及其他 G/P 型匹配株进行比较。研究揭示了 G12-P[11]-I1-R1-C1-M1-A1-N1-T1-E1-H1 人 Wa 样基因型图谱,并强调了基因重配的证据。从有症状和无症状新生儿中分离出的 G12P[11]菌株的结构(VP3 除外)和非结构编码基因的序列没有观察到显著差异。在 G12 株中,由于在氨基酸位置 238 处从天冬氨酸(Asp)变为天冬酰胺(Asn),观察到额外的 N 连接糖基化位点。有趣的是,与无症状 G12P[11]株相比,在 7-1a 和 8-1 抗原表位内分别仅观察到两个和四个氨基酸取代。本研究强调了密切监测新生儿中 RV 爆发的重要性,以便早期预警新菌株。

相似文献

1
Complete genomic analysis of uncommon G12P[11] rotavirus causing a nosocomial outbreak of acute diarrhea in the newborns in New Delhi, India.印度新德里新生儿院内急性腹泻暴发中罕见 G12P[11]轮状病毒的全基因组分析。
J Med Virol. 2022 Jun;94(6):2613-2623. doi: 10.1002/jmv.27468. Epub 2021 Dec 2.
2
Complete genotyping of unusual species A rotavirus G12P[11] and G10P[14] isolates and evidence of frequent in vivo reassortment among the rotaviruses detected in children with diarrhea in Kolkata, India, during 2014.2014年印度加尔各答腹泻儿童中检测到的A组轮状病毒G12P[11]和G10P[14]不寻常毒株的全基因分型以及轮状病毒频繁体内重配的证据
Arch Virol. 2016 Oct;161(10):2773-85. doi: 10.1007/s00705-016-2969-6. Epub 2016 Jul 22.
3
Whole genomic analysis of human G12P[6] and G12P[8] rotavirus strains that have emerged in Kenya: identification of porcine-like NSP4 genes.对肯尼亚出现的人类G12P[6]和G12P[8]轮状病毒株进行全基因组分析:鉴定猪样NSP4基因。
Infect Genet Evol. 2014 Oct;27:277-93. doi: 10.1016/j.meegid.2014.08.002. Epub 2014 Aug 8.
4
Phylogenetic analysis of VP7 and VP4 genes of the most predominant human group A rotavirus G12 identified in children with acute gastroenteritis in Himachal Pradesh, India during 2013-2016.对2013年至2016年期间在印度喜马偕尔邦急性胃肠炎儿童中鉴定出的最主要的人A组轮状病毒G12的VP7和VP4基因进行系统发育分析。
J Med Virol. 2021 Nov;93(11):6200-6209. doi: 10.1002/jmv.27142. Epub 2021 Jun 24.
5
Whole Genomic Analysis of Human G12P[6] and G12P[8] Rotavirus Strains that Have Emerged in Myanmar.对缅甸出现的人G12P[6]和G12P[8]轮状病毒株的全基因组分析。
PLoS One. 2015 May 4;10(5):e0124965. doi: 10.1371/journal.pone.0124965. eCollection 2015.
6
Complete genome analyses of G12P[8] rotavirus strains from hospitalized children in Surabaya, Indonesia, 2017-2018.2017-2018 年印度尼西亚泗水住院儿童中 G12P[8]轮状病毒株的全基因组分析。
J Med Virol. 2023 Feb;95(2):e28485. doi: 10.1002/jmv.28485.
7
Whole-genome characterisation of G12P[6] rotavirus strains possessing two distinct genotype constellations co-circulating in Blantyre, Malawi, 2008.2008年在马拉维布兰太尔共同流行的具有两种不同基因型组合的G12P[6]轮状病毒株的全基因组特征分析
Arch Virol. 2017 Jan;162(1):213-226. doi: 10.1007/s00705-016-3103-5. Epub 2016 Oct 7.
8
Upsurge and spread of G3 rotaviruses in Eastern India (2014-2016): Full genome analyses reveals heterogeneity within Wa-like genomic constellation.东印度(2014-2016 年)G3 轮状病毒的爆发和传播:全基因组分析显示 Wa 样基因组构成内的异质性。
Infect Genet Evol. 2018 Sep;63:158-174. doi: 10.1016/j.meegid.2018.05.026. Epub 2018 May 26.
9
Full genome analysis of rotavirus G9P[8] strains identified in acute gastroenteritis cases reveals genetic diversity: Pune, western India.在急性肠胃炎病例中鉴定出的轮状病毒 G9P[8] 株的全基因组分析显示遗传多样性:印度西部浦那。
J Med Virol. 2017 Aug;89(8):1354-1363. doi: 10.1002/jmv.24799. Epub 2017 Mar 14.
10
Clinical and genetic characteristics of unusual G12P[11] rotavirus strains recovered from neonates: A study from Pune, Western India.从印度西部浦那地区新生儿中分离出的不常见 G12P[11]轮状病毒株的临床和遗传特征:一项研究。
Infect Genet Evol. 2019 Jun;70:45-52. doi: 10.1016/j.meegid.2019.02.014. Epub 2019 Feb 20.

引用本文的文献

1
Rotavirus outbreaks in China, 1982-2021: a systematic review.中国轮状病毒疫情,1982-2021:系统评价。
Front Public Health. 2024 Aug 8;12:1423573. doi: 10.3389/fpubh.2024.1423573. eCollection 2024.