Preadaptation of pandemic GII.4 noroviruses in unsampled virus reservoirs years before emergence

被引:22
作者
Ruis, Christopher [1 ]
Lindesmith, Lisa C. [2 ]
Mallory, Michael L. [2 ]
Brewer-Jensen, Paul D. [2 ]
Bryant, Josephine M. [1 ]
Costantini, Veronica [3 ]
Monit, Christopher [1 ]
Vinje, Jan [3 ]
Baric, Ralph S. [2 ]
Goldstein, Richard A. [1 ]
Breuer, Judith [1 ,4 ]
机构
[1] UCL, Div Infect & Immun, London WC1E 6BT, England
[2] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27515 USA
[3] Ctr Dis Control & Prevent, Div Viral Dis, Atlanta, GA USA
[4] Great Ormond St Hosp Sick Children, Dept Microbiol Virol & Infect Control, London, England
基金
英国医学研究理事会; 英国惠康基金; 美国国家卫生研究院; 英国生物技术与生命科学研究理事会;
关键词
phylogenetics; phylodynamics; antigenic change; serology; PHYLOGENETIC ANALYSIS; EVOLUTION; INFECTION; RECOMBINATION; PROTECTION; OUTBREAKS; CORRELATE; IMMUNITY; NETWORK; TOOL;
D O I
10.1093/ve/veaa067
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The control of re-occurring pandemic pathogens requires understanding the origins of new pandemic variants and the factors that drive their global spread. This is especially important for GII.4 norovirus, where vaccines under development offer promise to prevent hundreds of millions of annual gastroenteritis cases. Previous studies have hypothesized that new GII.4 pandemic viruses arise when previously circulating pandemic or pre-pandemic variants undergo substitutions in antigenic regions that enable evasion of host population immunity, as described by conventional models of antigenic drift. In contrast, we show here that the acquisition of new genetic and antigenic characteristics cannot be the proximal driver of new pandemics. Pandemic GII.4 viruses diversify and spread over wide geographical areas over several years prior to simultaneous pandemic emergence of multiple lineages, indicating that the necessary sequence changes must have occurred before diversification, years prior to pandemic emergence. We confirm this result through serological assays of reconstructed ancestral virus capsids, demonstrating that by 2003, the ancestral 2012 pandemic strain had already acquired the antigenic characteristics that allowed it to evade prevailing population immunity against the previous 2009 pandemic variant. These results provide strong evidence that viral genetic changes are necessary but not sufficient for GII.4 pandemic spread. Instead, we suggest that it is changes in host population immunity that enable pandemic spread of an antigenically preadapted GII.4 variant. These results indicate that predicting future GII.4 pandemic variants will require surveillance of currently unsampled reservoir populations. Furthermore, a broadly acting GII.4 vaccine will be critical to prevent future pandemics.
引用
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页数:11
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