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柯萨奇病毒A9的抗原位点。

Antigenic sites of coxsackievirus A9.

作者信息

Pulli T, Lankinen H, Roivainen M, Hyypiä T

机构信息

Enterovirus Laboratory, National Public Health Institute, Helsinki, Finland.

出版信息

Virology. 1998 Jan 20;240(2):202-12. doi: 10.1006/viro.1997.8908.

DOI:10.1006/viro.1997.8908
PMID:9454693
Abstract

Antigenic analysis of coxsackievirus A9 (CAV9) was carried out by using a peptide scanning method. Immunogenic regions in the capsid proteins VP1, VP2, and VP3 were recognized by antibodies in the sera of virus-immunized rabbits. The peptide sequences were scanned using a 12-amino-acid window and three-residue shift. Three immunogenic regions, located in the N- and C-terminal parts of VP1 and in the N-terminus of VP3, were identified. Trypsin treatment of the virus, known to cleave off the C-terminus of VP1 containing a functional RGD motif, completely abolished the reactivity against this region but did not have any other significant effect on antigenicity. In further studies, it was found that the RGD motif itself was poorly immunogenic whereas antibody-binding sites were located at both sides of the motif. New antigenic sites emerged after heat treatment of CAV9 at 56 or 100 degrees C prior to immunization; in particular, loop structures between beta strands in VP2 exhibited increased immunogenicity. New antigenic sites in VP1 and VP3 also appeared after the treatments. In spite of the markedly altered reactivity in peptide scanning, the virus treated at 56 degrees C elicited high titers of neutralizing antibodies. To reveal cross-reactive antigenic sites, antisera raised against coxsackievirus B3 and echovirus 11 were also tested. The cross-reactive antigenic sites were located mainly in the N-terminal parts of VP1 and VP3.

摘要

采用肽扫描法对柯萨奇病毒A9(CAV9)进行了抗原分析。病毒免疫兔血清中的抗体识别衣壳蛋白VP1、VP2和VP3中的免疫原性区域。使用12个氨基酸的窗口和三个残基的移动对肽序列进行扫描。确定了三个免疫原性区域,分别位于VP1的N端和C端部分以及VP3的N端。已知胰蛋白酶处理病毒可切割掉含有功能性RGD基序的VP1的C端,这完全消除了针对该区域的反应性,但对抗原性没有任何其他显著影响。在进一步的研究中,发现RGD基序本身免疫原性较差,而抗体结合位点位于该基序的两侧。在免疫前将CAV9在56或100℃下热处理后出现了新的抗原位点;特别是,VP2中β链之间的环结构表现出增强的免疫原性。处理后VP1和VP3中也出现了新的抗原位点。尽管在肽扫描中反应性明显改变,但在56℃下处理的病毒仍能诱导出高滴度的中和抗体。为了揭示交叉反应性抗原位点,还检测了针对柯萨奇病毒B3和埃可病毒11产生的抗血清。交叉反应性抗原位点主要位于VP1和VP3的N端部分。

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