Harrington Patrick R, Vinjé Jan, Moe Christine L, Baric Ralph S
Department of Microbiology and Immunology, School of Medicine, School of Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.
J Virol. 2004 Mar;78(6):3035-45. doi: 10.1128/jvi.78.6.3035-3045.2004.
Noroviruses are genetically diverse, uncultivable, positive-sense RNA viruses and are the most common cause of epidemic acute gastroenteritis in humans in the United States. Recent studies of norovirus attachment in vitro by using recombinant virus-like particles (VLPs) suggest that various norovirus strains exhibit different patterns of attachment to ABH histo-blood group antigens, which are carbohydrate epitopes present in high concentrations on mucosal cell surfaces of the gut. However, attachment of live norovirus strains to histo-blood group antigens has not been investigated to date. Utilizing a newly designed magnetic bead-virus capture method, we characterized histo-blood group antigen attachment properties of various norovirus strains obtained from clinical stool specimens to compare the attachment properties of wild-type virus and VLPs and to further map norovirus attachment. Consistent with previous reports using VLPs, various strains of noroviruses exhibited different patterns of attachment to histo- blood group antigens. Norwalk virus bound specifically to H type 1, H type 3, and Le(b). Two genogroup II noroviruses, one representing the Toronto genotype and the other from a novel genotype, bound specifically to Le(b). A Desert Shield-like strain did not attach to H types 1, 2, or 3, H type 1 and 3 precursors, Le(a), or Le(b). Surprisingly, wild-type Snow Mountain virus (SMV) attached specifically to H type 3, which contradicted previous findings with SMV VLPs. On further investigation, we found that stool components promote this attachment, providing the first known observation that one or more components of human feces could promote and enhance norovirus attachment to histo-blood group antigens.
诺如病毒是基因多样、不可培养的正链RNA病毒,是美国人类流行性急性胃肠炎最常见的病因。最近利用重组病毒样颗粒(VLP)对诺如病毒体外附着的研究表明,各种诺如病毒株对ABH组织血型抗原表现出不同的附着模式,ABH组织血型抗原是肠道粘膜细胞表面高浓度存在的碳水化合物表位。然而,迄今为止尚未研究活诺如病毒株与组织血型抗原的附着情况。利用一种新设计的磁珠-病毒捕获方法,我们对从临床粪便标本中获得的各种诺如病毒株的组织血型抗原附着特性进行了表征,以比较野生型病毒和VLP的附着特性,并进一步绘制诺如病毒附着图谱。与先前使用VLP的报告一致,各种诺如病毒株对组织血型抗原表现出不同的附着模式。诺沃克病毒特异性结合1型H、3型H和Le(b)。两种基因II型诺如病毒,一种代表多伦多基因型,另一种来自新基因型,特异性结合Le(b)。一种类沙漠盾牌毒株不附着于1型H、2型H或3型H、1型H和3型H前体、Le(a)或Le(b)。令人惊讶的是,野生型雪山病毒(SMV)特异性附着于3型H,这与先前关于SMV VLP的研究结果相矛盾。进一步研究发现,粪便成分促进了这种附着,这是首次观察到人类粪便中的一种或多种成分可以促进和增强诺如病毒与组织血型抗原的附着。