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一种表达人诺如病毒可裂解衣壳蛋白的细菌表面展示系统:一种发现候选受体的新系统。

A Bacterial Surface Display System Expressing Cleavable Capsid Proteins of Human Norovirus: A Novel System to Discover Candidate Receptors.

作者信息

Xu Qian, Ni Pei'en, Liu Danlei, Yin Yujie, Li Qianqian, Zhang Jvmei, Wu Qingping, Tian Peng, Shi Xianming, Wang Dapeng

机构信息

MOST-USDA Joint Research Center for Food Safety, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, China.

Department of Bioengineering, Shanghai Institute of Technology, Shanghai, China.

出版信息

Front Microbiol. 2017 Dec 6;8:2405. doi: 10.3389/fmicb.2017.02405. eCollection 2017.

Abstract

Human noroviruses (HuNoVs) are the dominant cause of food-borne outbreaks of acute gastroenteritis. However, fundamental researches on HuNoVs, such as identification of viral receptors have been limited by the currently immature system to culture HuNoVs and the lack of efficient small animal models. Previously, we demonstrated that the recombinant protruding domain (P domain) of HuNoVs capsid proteins were successfully anchored on the surface of BL21 cells after the bacteria were transformed with a plasmid expressing HuNoVs P protein fused with bacterial transmembrane anchor protein. The cell-surface-displayed P proteins could specifically recognize and bind to histo-blood group antigens (HBGAs, receptors of HuNoVs). In this study, an upgraded bacterial surface displayed system was developed as a new platform to discover candidate receptors of HuNoVs. A thrombin-susceptible "linker" sequence was added between the sequences of bacterial transmembrane anchor protein and P domain of HuNoV (GII.4) capsid protein in a plasmid that displays the functional P proteins on the surface of bacteria. In this new system, the surface-displayed HuNoV P proteins could be released by thrombin treatment. The released P proteins self-assembled into small particles, which were visualized by electron microscopy. The bacteria with the surface-displayed P proteins were incubated with pig stomach mucin which contained HBGAs. The bacteria-HuNoV P proteins-HBGAs complex could be collected by low speed centrifugation. The HuNoV P proteins-HBGAs complex was then separated from the recombinant bacterial surface by thrombin treatment. The released viral receptor was confirmed by using the monoclonal antibody against type A HBGA. It demonstrated that the new system was able to capture and easily isolate receptors of HuNoVs. This new strategy provides an alternative, easier approach for isolating unknown receptors/ligands of HuNoVs from different samples including mammalian cell lines, oysters, and fresh produce.

摘要

人诺如病毒(HuNoVs)是食源性急性胃肠炎暴发的主要原因。然而,由于目前培养HuNoVs的系统尚不成熟以及缺乏有效的小动物模型,对HuNoVs的基础研究,如病毒受体的鉴定受到了限制。此前,我们证明,在用表达与细菌跨膜锚定蛋白融合的HuNoVs P蛋白的质粒转化细菌后,HuNoVs衣壳蛋白的重组突出结构域(P结构域)成功锚定在BL21细胞表面。细胞表面展示的P蛋白可以特异性识别并结合组织血型抗原(HBGAs,HuNoVs的受体)。在本研究中,开发了一种升级的细菌表面展示系统,作为发现HuNoVs候选受体的新平台。在一个能在细菌表面展示功能性P蛋白的质粒中,在细菌跨膜锚定蛋白序列和HuNoV(GII.4)衣壳蛋白的P结构域序列之间添加了一个凝血酶敏感的“接头”序列。在这个新系统中,表面展示的HuNoV P蛋白可以通过凝血酶处理释放出来。释放的P蛋白自组装成小颗粒,通过电子显微镜可以观察到。将带有表面展示P蛋白的细菌与含有HBGAs的猪胃粘蛋白一起孵育。细菌-HuNoV P蛋白-HBGAs复合物可以通过低速离心收集。然后通过凝血酶处理将HuNoV P蛋白-HBGAs复合物与重组细菌表面分离。使用抗A型HBGA的单克隆抗体确认了释放的病毒受体。结果表明,新系统能够捕获并轻松分离HuNoVs的受体。这种新策略为从包括哺乳动物细胞系、牡蛎和新鲜农产品在内的不同样品中分离HuNoVs未知受体/配体提供了一种替代的、更简便的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43cf/5723664/ceac117c31da/fmicb-08-02405-g001.jpg

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