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利用诺如病毒感染患者的血清样本和小鼠血清对GI型诺如病毒基因型之间的抗原相关性进行表征。

Characterization of Antigenic Relatedness Among GI Norovirus Genotypes Using Serum Samples From Norovirus-Infected Patients and Mouse Sera.

作者信息

Xie Dongjie, Chen Junrui, Yu Jingrong, Pei Fuyu, Koroma Mark Momoh, Wang Lu, Qiu Mengsi, Hou Yuzhen, Yu Dexian, Zhang Xu-Fu, Dai Ying-Chun

机构信息

School of Traditional Chinese Medicine, Southern Medical University, Guangzhou, China.

Guangdong Provincial Key Laboratory of Tropical Disease Research, Department of Epidemiology, School of Public Health, Southern Medical University, Guangzhou, China.

出版信息

Front Microbiol. 2020 Dec 8;11:607723. doi: 10.3389/fmicb.2020.607723. eCollection 2020.

DOI:10.3389/fmicb.2020.607723
PMID:33363528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7752868/
Abstract

Characterizing diversity and the antigenic relatedness of norovirus remains a primary focus in understanding its biological properties and vaccine designs. The precise antigenic and serological features of GI genotypes have not been studied. The study represented an investigation on a gastroenteritis outbreak related to GI.3 norovirus and the three most detected GI genotypes, GI.2 (belonging to immunotype B), GI.3 and GI.9 (belonging to immunotype C), were selected to characterize their phylogenetic relationship, HBGA binding profiles and antigenic relatedness within (intra-immunotype), and between (inter-immunotypes) genotypes using mouse sera and patient's serum samples from the GI.3 related outbreak. Wide HBGA binding profiles and evolution of binding affinity were observed in the three GI genotypes studied. A low specific blockade antibody to GI.3 in the population generated the pool of susceptible individuals and supported virus spread in the outbreak. We found strong blockade immune response in homologous strains, moderate intra-immunotype blockade but weak inter-immunotypes blockade in humans following GI.3 norovirus infections. These findings further support the immunotypes grouping and will be valuable for optimizing the design of norovirus vaccine.

摘要

确定诺如病毒的多样性及其抗原相关性仍然是理解其生物学特性和疫苗设计的主要重点。目前尚未对GI基因型的确切抗原和血清学特征进行研究。该研究针对一次与GI.3诺如病毒相关的胃肠炎暴发展开调查,并选取了三种检测频率最高的GI基因型,即GI.2(属于免疫型B)、GI.3和GI.9(属于免疫型C),利用小鼠血清和来自GI.3相关暴发的患者血清样本,来表征它们在基因型内部(免疫型内)以及不同基因型之间(免疫型间)的系统发育关系、HBGA结合谱和抗原相关性。在所研究的三种GI基因型中观察到了广泛的HBGA结合谱和结合亲和力的演变。人群中针对GI.3的低特异性阻断抗体产生了易感个体库,并促进了病毒在暴发中的传播。我们发现,在感染GI.3诺如病毒后,人体对同源毒株有强烈的阻断免疫反应,免疫型内阻断反应中等,但免疫型间阻断反应较弱。这些发现进一步支持了免疫型分组,对优化诺如病毒疫苗设计具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/27762597e518/fmicb-11-607723-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/e7c28d4be7c9/fmicb-11-607723-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/fa38cde56c04/fmicb-11-607723-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/3fba7fe180d4/fmicb-11-607723-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/d2a1dd51c8e5/fmicb-11-607723-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/c4e976c3e024/fmicb-11-607723-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/27762597e518/fmicb-11-607723-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/e7c28d4be7c9/fmicb-11-607723-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/fa38cde56c04/fmicb-11-607723-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/3fba7fe180d4/fmicb-11-607723-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/d2a1dd51c8e5/fmicb-11-607723-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/c4e976c3e024/fmicb-11-607723-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e34/7752868/27762597e518/fmicb-11-607723-g006.jpg

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