Chen Xuyan, Qin Bo, Shi Min, Zhu Longying, Sun Menglin, Liu Xufeng, Zhang Jianhua
1 Department of Laboratory Medicine, School of Medicine, Shaoxing University , Shaoxing, Zhejiang, People's Republic of China .
2 Clinical Laboratory Center , Shaoxing People's Hospital, Shaoxing, Zhejiang, People's Republic of China .
Viral Immunol. 2017 Mar;30(2):106-110. doi: 10.1089/vim.2016.0110. Epub 2016 Nov 21.
Human enterovirus 71 (EV-A71) is one of the main etiological agents of hand, foot, and mouth disease (HFMD), which has been prevalent mainly in the Asia-Pacific region in the past several decades. The nonstructural proteins of EV-A71 will be expressed significantly during viral replication in host cells after EV-A71 infection. For the determination of the antibodies response against nonstructural proteins of EV-A71, in this study, the complete 2ABC, 3ABC, and 3D proteins were expressed in Escherichia coli and were then studied for their immunoreactivity by immunoblot assay and indirect enzyme-linked immunosorbent assay (ELISA), respectively. Three His-tagged fusion proteins were expressed effectively in E. coli, which were in agreement with the expected molecular mass. The results from immunoblot assay and indirect ELISA showed that all three purified fusion proteins can react with IgG antibodies from EV-A71-infected patients, but can hardly be recognized by IgG antibodies derived from mice or rabbits immunized by inactivated EV-A71 virus particles. The IgG antibody response against nonstructural proteins of EV-A71 is associated with viral infection or replication, which indicate that these nonstructural proteins could be used as candidate antigen for early diagnosis of EV-A71 infection, or to distinguish the EV-A71-specific antibodies after viral infection from inactivated vaccine immunization.
人肠道病毒71型(EV - A71)是手足口病(HFMD)的主要病原体之一,在过去几十年中主要在亚太地区流行。EV - A71感染宿主细胞后,其非结构蛋白在病毒复制过程中会大量表达。为了检测针对EV - A71非结构蛋白的抗体反应,本研究在大肠杆菌中表达了完整的2ABC、3ABC和3D蛋白,然后分别通过免疫印迹分析和间接酶联免疫吸附测定(ELISA)研究它们的免疫反应性。三种带有His标签的融合蛋白在大肠杆菌中有效表达,其分子量与预期一致。免疫印迹分析和间接ELISA结果表明,所有三种纯化的融合蛋白都能与EV - A71感染患者的IgG抗体发生反应,但几乎不能被用灭活的EV - A71病毒颗粒免疫的小鼠或兔的IgG抗体识别。针对EV - A71非结构蛋白的IgG抗体反应与病毒感染或复制有关,这表明这些非结构蛋白可作为早期诊断EV - A71感染的候选抗原,或用于区分病毒感染后产生的EV - A71特异性抗体与灭活疫苗免疫产生的抗体。