Huang Pengwei, Farkas Tibor, Zhong Weiming, Tan Ming, Thornton Scott, Morrow Ardythe L, Jiang Xi
Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229-3039, USA.
J Virol. 2005 Jun;79(11):6714-22. doi: 10.1128/JVI.79.11.6714-6722.2005.
Noroviruses, an important cause of acute gastroenteritis, have been found to recognize human histo-blood group antigens (HBGAs) as receptors. Four strain-specific binding patterns to HBGAs have been described in our previous report. In this study, we have extended the binding patterns to seven based on 14 noroviruses examined. The oligosaccharide-based assays revealed additional epitopes that were not detected by the saliva-based assays. The seven patterns have been classified into two groups according to their interactions with three major epitopes (A/B, H, and Lewis) of human HBGAs: the A/B-binding group and the Lewis-binding group. Strains in the A/B binding group recognize the A and/or B and H antigens, but not the Lewis antigens, while strains in the Lewis-binding group react only to the Lewis and/or H antigens. This classification also resulted in a model of the norovirus/HBGA interaction. Phylogenetic analyses showed that strains with identical or closely related binding patterns tend to be clustered, but strains in both binding group can be found in both genogroups I and II. Our results suggest that noroviruses have a wide spectrum of host range and that human HBGAs play an important role in norovirus evolution. The high polymorphism of the human HBGA system, the involvement of multiple epitopes, and the typical protein/carbohydrate interaction between norovirus VLPs and HBGAs provide an explanation for the virus-ligand binding diversities.
诺如病毒是急性肠胃炎的一个重要病因,已发现其将人类组织血型抗原(HBGAs)识别为受体。我们之前的报告中描述了诺如病毒与HBGAs的四种菌株特异性结合模式。在本研究中,基于检测的14种诺如病毒,我们将结合模式扩展至七种。基于寡糖的检测揭示了基于唾液的检测未检测到的额外表位。根据它们与人类HBGAs的三个主要表位(A/B、H和Lewis)的相互作用,这七种模式已被分为两组:A/B结合组和Lewis结合组。A/B结合组中的菌株识别A和/或B以及H抗原,但不识别Lewis抗原,而Lewis结合组中的菌株仅对Lewis和/或H抗原产生反应。这种分类还得出了诺如病毒/HBGA相互作用的模型。系统发育分析表明,具有相同或密切相关结合模式的菌株倾向于聚类,但两个结合组中的菌株在基因组I和II中均有发现。我们的结果表明,诺如病毒具有广泛的宿主范围,并且人类HBGAs在诺如病毒进化中起重要作用。人类HBGA系统的高度多态性、多个表位的参与以及诺如病毒病毒样颗粒(VLPs)与HBGAs之间典型的蛋白质/碳水化合物相互作用为病毒-配体结合多样性提供了解释。