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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Antigenic site variation in foot-and-mouth disease virus serotype O grown under vaccinal serum antibodies in vitro
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Antigenic site variation in foot-and-mouth disease virus serotype O grown under vaccinal serum antibodies in vitro

机译:在疫苗血清抗体的体外培养的O型口蹄疫病毒血清中的抗原位点变化

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摘要

Foot-and-mouth disease virus (FMDV) is constantly evolving under neutralizing antibody pressure in either naturally infected or vaccinated animals. This study was carried out to understand the dynamics of evolution of antigenic sites. Neutralizing antibody-resistant populations of three strains of FMDV serotype O (INDR2/1975, IND120/2002 and IND271/2001) were isolated by serial propagation in BHK-21 cells in the presence of sub-neutralizing level of bovine vaccinal sera (BVS). In the partial neutralization escape variants, fixation of aa substitutions were observed at critical residues of all established antigenic sites of serotype O {144 of VP1 (site 1), 45 and 48 of VP1 (site 3), 72 and 134 of VP2 (Site 2)} except site 4 and 5. In majority of the variant populations, site 3 was found to be substituted and therefore immunodominance may not be associated with a particular site, rather it appears to be a virus strain and infected host specific affair. Substitutions were also observed in proximity to the identified residues {41 and 51 (βB-βC loop), 133, 140 and 143 (βG-βH loop), 201, 204 and 209 (C terminus) of VP1, 71 and 75 (βB-βC loop), 131 (βE-αB region), 174 and 179 (βG-βH loop) and 219 (C terminus) of VP3} within antigenic sites of serotype O or other serotypes which could be significant in terms of neutralizing antibody binding and immune escape. Presence of similar residues in the Indian field viruses as selected in the variants supports the importance of these sites in antigenic diversification of serotype O FMD virus.
机译:口蹄疫病毒(FMDV)在自然感染或接种疫苗的动物中,在中和抗体压力下不断进化。进行这项研究是为了了解抗原位点进化的动力学。在亚中和水平的牛疫苗血清(BVS)存在下,通过在BHK-21细胞中连续繁殖,分离了三种FMDV O型血清型(INDR2 / 1975,IND120 / 2002和IND271 / 2001)的中和抗体耐药群。 。在部分中和逃逸变体中,在所有已建立的血清型O抗原位点(VP1的144个(位点1),VP1的45和48个位点(位点3),VP2的72和134个位点)的关键残基上观察到了aa置换的固定。 2)}位点4和5除外。在大多数变异群体中,位点3被发现被取代,因此免疫优势可能与特定位点不相关,而是似乎是病毒株和受感染的宿主特异性事件。在VP1、71和75(βB)的残基{41和51(βB-βC环),133、140和143(βG-βH环),201、204和209(C端)附近也观察到了取代在血清型O或其他血清型的抗原位点内,VP3的-βC环),131(βE-αB区域),174和179(βG-βH环)和219(C末端)(在中和抗体结合方面可能很重要)和免疫逃逸。在变种中选择的印度田间病毒中相似残基的存在支持了这些位点在血清型O FMD病毒的抗原多样化中的重要性。

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