Zhang Dongsheng, Huang Pengwei, Zou Lu, Lowary Todd L, Tan Ming, Jiang Xi
Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Department of Chemistry and Alberta Glycomics Centre, University of Alberta, Edmonton, Alberta, Canada.
J Virol. 2015 Jan 15;89(2):1419-27. doi: 10.1128/JVI.02595-14. Epub 2014 Nov 12.
Tulane virus (TV), the prototype of the Recovirus genus in the calicivirus family, was isolated from the stools of rhesus monkeys and can be cultivated in vitro in monkey kidney cells. TV is genetically closely related to the genus Norovirus and recognizes the histo-blood group antigens (HBGAs), similarly to human noroviruses (NoVs), making it a valuable surrogate for human NoVs. However, the precise structures of HBGAs recognized by TV remain elusive. In this study, we performed binding and blocking experiments on TV with extended HBGA types and showed that, while TV binds all four types (types 1 to 4) of the B antigens, it recognizes only the A type 3 antigen among four types of A antigens tested. The requirements for HBGAs in TV replication were demonstrated by blocking of TV replication in cell culture using the A type 3/4 and B saliva samples. Similar results were also observed in oligosaccharide-based blocking assays. Importantly, the previously reported, unexplained increase in TV replication by oligosaccharide in cell-based blocking assays has been clarified, which will facilitate the application of TV as a surrogate for human NoVs.
Our understanding of the role of HBGAs in NoV infection has been significantly advanced in the past decade, but direct evidence for HBGAs as receptors for human NoVs remains lacking due to a lack of a cell culture method. TV recognizes HBGAs and can replicate in vitro, providing a valuable surrogate for human NoVs. However, TV binds to some but not all saliva samples from A-positive individuals, and an unexplained observation of synthetic oligosaccharide blocking of TV binding has been reported. These issues have been resolved in this study.
杜兰病毒(TV)是杯状病毒科Recovirus属的原型,从恒河猴粪便中分离得到,可在猴肾细胞中进行体外培养。TV在基因上与诺如病毒属密切相关,并且与人类诺如病毒(NoV)类似,能够识别组织血型抗原(HBGA),这使其成为人类NoV的有价值替代物。然而,TV识别的HBGA的确切结构仍然不清楚。在本研究中,我们对TV与扩展的HBGA类型进行了结合和阻断实验,结果表明,虽然TV能结合所有四种类型(1至4型)的B抗原,但在测试的四种类型的A抗原中,它仅识别A3型抗原。使用A3/4型和B型唾液样本在细胞培养中阻断TV复制,证明了HBGA对TV复制的需求。在基于寡糖的阻断试验中也观察到了类似结果。重要的是,此前报道的在基于细胞的阻断试验中寡糖导致TV复制出现无法解释的增加这一现象已得到澄清,这将有助于TV作为人类NoV替代物的应用。
在过去十年中,我们对HBGA在NoV感染中的作用的理解有了显著进展,但由于缺乏细胞培养方法,仍缺乏HBGA作为人类NoV受体的直接证据。TV能识别HBGA并可在体外复制,为人类NoV提供了有价值的替代物。然而,TV与A阳性个体的部分而非全部唾液样本结合,并且有报道称合成寡糖对TV结合的阻断存在无法解释的现象。这些问题在本研究中得到了解决。