Kambhampati Anita, Payne Daniel C, Costantini Veronica, Lopman Benjamin A
Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, US Centers for Disease Control and Prevention, Atlanta, Georgia.
Oak Ridge Institute for Science and Education, Tennessee.
Clin Infect Dis. 2016 Jan 1;62(1):11-18. doi: 10.1093/cid/civ873. Epub 2015 Oct 26.
Norovirus and rotavirus are prominent enteric viruses responsible for severe acute gastroenteritis disease burden around the world. Both viruses recognize and bind to histo-blood group antigens, which are expressed by the fucosyltransferase 2 (FUT2) gene. Individuals with a functional FUT2 gene are termed "secretors." FUT2 polymorphisms may influence viral binding patterns and, therefore, may influence host susceptibility to infection by these viruses.
We performed a systematic review of the published literature on this topic. Data were abstracted and compiled for descriptive analyses and metaanalyses. We estimated pooled odds ratios (ORs) for infection using random-effects models.
We found that secretors were 9.9 times (95% confidence interval [CI], 3.9-24.8) as likely to be infected with genogroup II.4 noroviruses and 2.2 times as likely to be infected with genogroup II non-4 noroviruses (95% CI, 1.2-4.2) compared with nonsecretors. Secretors were also 26.6 times more susceptible to infections from P[8]-type rotaviruses compared with nonsecretors (95% CI, 8.3-85.0).
Our analyses indicate that host genetic susceptibility to norovirus and rotavirus infection may be strain specific. As strain distribution and the proportion of genetic phenotypes vary in different countries, future studies should focus on differences in susceptibility among various ethnicities. Knowledge of innate susceptibility to rotavirus and norovirus can lead to improved understanding of both vaccine performance and individual risk of disease.
诺如病毒和轮状病毒是引起全球严重急性胃肠炎疾病负担的主要肠道病毒。这两种病毒都能识别并结合组织血型抗原,该抗原由岩藻糖基转移酶2(FUT2)基因表达。具有功能性FUT2基因的个体被称为“分泌型者”。FUT2基因多态性可能影响病毒结合模式,因此可能影响宿主对这些病毒感染的易感性。
我们对关于该主题的已发表文献进行了系统综述。提取并汇总数据用于描述性分析和荟萃分析。我们使用随机效应模型估计感染的合并比值比(OR)。
我们发现,与非分泌型者相比,分泌型者感染II.4基因型诺如病毒的可能性高9.9倍(95%置信区间[CI],3.9 - 24.8),感染非4型II基因型诺如病毒的可能性高2.2倍(95%CI,1.2 - 4.2)。与非分泌型者相比,分泌型者感染P[8]型轮状病毒的易感性也高26.6倍(95%CI,8.3 - 85.0)。
我们的分析表明,宿主对诺如病毒和轮状病毒感染的遗传易感性可能具有毒株特异性。由于不同国家的毒株分布和遗传表型比例不同,未来的研究应关注不同种族间易感性的差异。了解对轮状病毒和诺如病毒的先天易感性有助于更好地理解疫苗效果和个体患病风险。