Transmission Networks and Population Turnover of Echovirus 30

Author:

Leitch E. C. McWilliam1,Bendig J.2,Cabrerizo M.3,Cardosa J.4,Hyypiä T.5,Ivanova O. E.6,Kelly A.7,Kroes A. C. M.8,Lukashev A.6,MacAdam A.9,McMinn P.10,Roivainen M.11,Trallero G.3,Evans D. J.12,Simmonds P.1

Affiliation:

1. Centre for Infectious Diseases, University of Edinburgh, Summerhall, Edinburgh EH9 1QH, United Kingdom

2. PHLS Coxsackievirus Reference Unit, Department of Medical Microbiology, West Park Hospital, Epsom, Surrey, United Kingdom

3. Enterovirus Laboratory, National Centre for Microbiology, Carlos III Institute of Health, Majadahonda, Madrid, Spain

4. Institute of Health and Community Medicine, University Sarawak Malaysia, Sarawak, Malaysia

5. Department of Virology, University of Turku, Finland

6. M. P. Chumakov Institute of Poliomyelitis and Viral Encephalitides, Moscow, Russia

7. National Virus Reference Laboratory, Dublin, Ireland

8. Department of Medical Microbiology, Leiden University Medical Centre, Leiden, The Netherlands

9. National Institute for Biological Standards and Controls, London, United Kingdom

10. Discipline of Immunology and Infectious Diseases, University of Sydney, Australia

11. Enterovirus Laboratory, National Public Health Institute, Helsinki, Finland

12. Department of Biological Sciences, University of Warwick, United Kingdom

Abstract

ABSTRACT Globally, echovirus 30 (E30) is one of the most frequently identified enteroviruses and a major cause of meningitis. Despite its wide distribution, little is known about its transmission networks or the dynamics of its recombination and geographical spread. To address this, we have conducted an extensive molecular epidemiology and evolutionary study of E30 isolates collected over 8 years from a geographically wide sample base (11 European countries, Asia, and Australia). 3Dpol sequences fell into several distinct phylogenetic groups, interspersed with other species B serotypes, enabling E30 isolates to be classified into 38 recombinant forms (RFs). Substitutions in VP1 and 3Dpol regions occurred predominantly at synonymous sites (ratio of nonsynonymous to synonymous substitutions, 0.05) with VP1 showing a rapid substitution rate of 8.3 × 10 −3 substitutions per site per year. Recombination frequency was tightly correlated with VP1 divergence; viruses differing by evolutionary distances of >0.1 (or 6 years divergent evolution) almost invariably (>97%) had different 3Dpol groups. Frequencies of shared 3Dpol groups additionally correlated with geographical distances, with Europe and South Asia showing turnover of entirely distinct virus populations. Population turnover of E30 was characterized by repeated cycles of emergence, dominance, and disappearance of individual RFs over periods of 3 to 5 years, although the existence and nature of evolutionary selection underlying these population replacements remain unclear. The occurrence of frequent “sporadic” recombinants embedded within VP1 groupings of other RFs and the much greater number of 3Dpol groups than separately identifiable VP1 lineages suggest frequent recombination with an external diverse reservoir of non-E30 viruses.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Cited by 94 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3