Molecular Evolution of Human Norovirus GII.2 Clusters

被引:11
作者
Li, Xingguang [1 ]
Liu, Haizhou [2 ]
Rife Magalis, Brittany [3 ]
Pond, Sergei L. Kosakovsky [3 ]
Volz, Erik M. [4 ]
机构
[1] First Peoples Hosp Fangchenggang, Dept Hosp Off, Fangchenggang, Peoples R China
[2] Univ Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Ctr Emerging Infect Dis, Wuhan, Peoples R China
[3] Temple Univ, Inst Genom & Evolutionary Med, Philadelphia, PA 19122 USA
[4] Imperial Coll London, Sch Publ Hlth, MRC Ctr Global Infect Dis Anal, London, England
基金
英国医学研究理事会;
关键词
human norovirus; genetic diversity; positive selection; virus evolution; phylogenetic analyses; MAXIMUM-LIKELIHOOD; LARGE PHYLOGENIES; GASTROENTERITIS;
D O I
10.3389/fmicb.2021.655567
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background The human norovirus GII.2 outbreak during the 2016-2017 winter season was of unprecedented scale and geographic distribution. Methods We analyzed 519 complete VP1 gene sequences of the human norovirus GII.2 genotype sampled during the 2016-2017 winter season, as well as prior (dating back to 1976) from 7 countries. Phylodynamic analyses of these sequences were performed using maximum likelihood and Bayesian statistical frameworks in order to estimate viral evolutionary and population dynamics associated with the outbreak. Results Our results revealed an increase in the genetic diversity of human norovirus GII.2 during the recent Asian outbreak and diversification was characterized by at least eight distinct clusters. Bayesian estimation of viral population dynamics revealed a highly fluctuating effective population size, increasing in frequency during the past 15 years. Conclusion Despite an increasing viral diversity, we found no evidence of an elevated evolutionary rate or significant selection pressure in human norovirus GII.2, indicating viral evolutionary adaptation was not responsible for the volatility of or spread of the virus during this time.
引用
收藏
页数:10
相关论文
共 39 条
[31]  
THANUSUWANNASAK T, 2018, MOL BIOL EVOL, V61, P108, DOI DOI 10.1016/J.MEEGID.2018.03.021
[32]  
TO TH, 2016, J VIROL, V65, P82, DOI DOI 10.1093/SYSBIO/SYV068
[33]   Phylogenetic Analyses Suggest that Factors Other Than the Capsid Protein Play a Role in the Epidemic Potential of GII.2 Norovirus [J].
Tohma, Kentaro ;
Lepore, Cara J. ;
Ford-Siltz, Lauren A. ;
Parra, Gabriel I. .
MSPHERE, 2017, 2 (03)
[34]  
VINJE J, 2015, SYST BIOL, V53, P373, DOI DOI 10.1128/JCM.01535-14
[35]   Scalable relaxed clock phylogenetic dating [J].
Volz, E. M. ;
Frost, S. D. W. .
VIRUS EVOLUTION, 2017, 3 (02)
[36]  
VOLZ EM, 2018, MSPHERE, V67, P719, DOI DOI 10.1093/SYSBIO/SYY007
[37]  
WERTHEIM JO, 2015, SYST BIOL, V32, P820, DOI DOI 10.1093/MOLBEV/MSU400
[38]   Metagenomic Analysis of Bacteria, Fungi, Bacteriophages, and Helminths in the Gut of Giant Pandas [J].
Yang, Shengzhi ;
Gao, Xin ;
Meng, Jianghong ;
Zhang, Anyun ;
Zhou, Yingmin ;
Long, Mei ;
Li, Bei ;
Deng, Wenwen ;
Jin, Lei ;
Zhao, Siyue ;
Wu, Daifu ;
He, Yongguo ;
Li, Caiwu ;
Liu, Shuliang ;
Huang, Yan ;
Zhang, Hemin ;
Zou, Likou .
FRONTIERS IN MICROBIOLOGY, 2018, 9
[39]   Norovirus classification and proposed strain nomenclature [J].
Zheng, DP ;
Ando, T ;
Fankhauser, RL ;
Beard, RS ;
Glass, RI ;
Monroe, SS .
VIROLOGY, 2006, 346 (02) :312-323