Dai Ying-Chun, Zhang Xu-Fu, Xia Ming, Tan Ming, Quigley Christina, Lei Wen, Fang Hao, Zhong Weiming, Lee Bonita, Pang Xiaoli, Nie Jun, Jiang Xi
Department of Epidemiology, School of Public Health and Tropical Medicine, Southern Medical University, Guangzhou, Guangdong, China; Divisions of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou, Guangdong, China; Divisions of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
PLoS One. 2015 Apr 27;10(4):e0124945. doi: 10.1371/journal.pone.0124945. eCollection 2015.
The GII.4 noroviruses (NoVs) are a single genotype that is responsible for over 50% of NoV gastroenteritis epidemics worldwide. However, GII.4 NoVs have been found to undergo antigenic drifts, likely selected by host herd immunity, which raises an issue for vaccine strategies against NoVs. We previously characterized GII.4 NoV antigenic variations and found significant levels of antigenic relatedness among different GII.4 variants. Further characterization of the genetic and antigenic relatedness of recent GII.4 variants (2008b and 2010 cluster) was performed in this study. The amino acid sequences of the receptor binding interfaces were highly conserved among all GII.4 variants from the past two decades. Using serum samples from patients enrolled in a GII.4 virus challenge study, significant cross-reactivity between major GII.4 variants from 1998 to 2012 was observed using enzyme-linked immunosorbent assays and HBGA receptor blocking assays. The overall abilities of GII.4 NoVs to bind to the A/B/H HBGAs were maintained while their binding affinities to individual ABH antigens varied. These results highlight the importance of human HBGAs in NoV evolution and how conserved antigenic types impact vaccine development against GII.4 variants.
GII.4型诺如病毒(NoVs)是单一基因型,在全球范围内超过50%的诺如病毒肠胃炎流行疫情都由其引起。然而,已发现GII.4型诺如病毒会发生抗原漂移,这可能是由宿主群体免疫选择导致的,这给针对诺如病毒的疫苗策略带来了问题。我们之前对GII.4型诺如病毒的抗原变异进行了表征,发现不同的GII.4变异株之间存在显著水平的抗原相关性。本研究对近期的GII.4变异株(2008b和2010簇)的遗传和抗原相关性进行了进一步表征。在过去二十年的所有GII.4变异株中,受体结合界面的氨基酸序列高度保守。使用参与GII.4病毒攻击研究的患者的血清样本,通过酶联免疫吸附测定和HBGA受体阻断测定,观察到1998年至2012年主要GII.4变异株之间存在显著的交叉反应性。GII.4型诺如病毒与A/B/H HBGAs结合的总体能力得以维持,但其与各个ABH抗原的结合亲和力有所不同。这些结果突出了人HBGAs在诺如病毒进化中的重要性,以及保守抗原类型对针对GII.4变异株的疫苗开发的影响。