Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX 77030, USA.
Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX 77030, USA.
Viruses. 2021 Oct 14;13(10):2066. doi: 10.3390/v13102066.
Recognition of cell-surface glycans is an important step in the attachment of several viruses to susceptible host cells. The molecular basis of glycan interactions and their functional consequences are well studied for human norovirus (HuNoV), an important gastrointestinal pathogen. Histo-blood group antigens (HBGAs), a family of fucosylated carbohydrate structures that are present on the cell surface, are utilized by HuNoVs to initially bind to cells. In this review, we describe the discovery of HBGAs as genetic susceptibility factors for HuNoV infection and review biochemical and structural studies investigating HuNoV binding to different HBGA glycans. Recently, human intestinal enteroids (HIEs) were developed as a laboratory cultivation system for HuNoV. We review how the use of this novel culture system has confirmed that fucosylated HBGAs are necessary and sufficient for infection by several HuNoV strains, describe mechanisms of antibody-mediated neutralization of infection that involve blocking of HuNoV binding to HBGAs, and discuss the potential for using the HIE model to answer unresolved questions on viral interactions with HBGAs and other glycans.
细胞表面糖链的识别是几种病毒附着于易感宿主细胞的重要步骤。人诺如病毒(HuNoV)是一种重要的胃肠道病原体,其糖链相互作用的分子基础及其功能后果已得到深入研究。组织血型抗原(HBGA)是一类存在于细胞表面的岩藻糖基化碳水化合物结构,被 HuNoVs 用于初始结合细胞。在这篇综述中,我们描述了 HBGA 作为 HuNoV 感染遗传易感性因素的发现,并综述了研究 HuNoV 与不同 HBGA 糖链结合的生化和结构研究。最近,人类肠道类器官(HIEs)被开发为 HuNoV 的实验室培养系统。我们回顾了该新型培养系统的使用如何证实了几种 HuNoV 株系的感染需要并足以利用岩藻糖基化 HBGA,描述了抗体介导的中和感染的机制,该机制涉及阻止 HuNoV 与 HBGA 的结合,并讨论了利用 HIE 模型回答关于病毒与 HBGA 和其他糖链相互作用的未解决问题的潜力。