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Genome-wide linear B-cell epitopes of enterovirus 71 in a hand, foot and mouth disease (HFMD) population.

Authors :
Zhang, Huiying
Song, Zhigang
Yu, Huiju
Zhang, Xiaoling
Xu, Shanshan
Li, Zhong
Li, Jingzhi
Xu, Hongke
Yuan, Zhenghong
Ma, Hongwei
Yi, Zhigang
Hu, Yunwen
Source :
Journal of Clinical Virology. Aug2018, Vol. 105, p41-48. 8p.
Publication Year :
2018

Abstract

Background Enteroviruses cause hand, foot and mouth disease (HFMD). The host B-cells recognize the viral proteins and provoke humoral responses. Deciphering the B-cell responses to the viral epitopes helps diagnosis and vaccine development. Objectives The objective of the present study was to investigate for the first time the landscape of genome-wide linear B-cell epitopes of enterovirus 71 in HFMD population. Study design The peptides encompassing the entire coding region of EV71 were chemically synthesized and displayed on a microarray. The peptide microarray was used to screen serum samples from an HFMD population, including EV71-, CAV10-, CAV16- and CAV6-infected patients. We identified the dominant epitope-containing-peptides (DECPs) that react with the sera of more than 20% of the HFMD population and the common DECPs that cross-react with the sera from other enteroviruses-infected population. Results Ten DECPs reacting with IgM and 9 DECPs reacting with IgG antibodies were identified, of which, 6 IgM and 5 IgG common DECPs cross-reacted with the sera from other enteroviruses. Some DECPs preferentially reacted with IgG or IgM antibodies and some epitope-antibody interactions correlated with the severity of HFMD. Conclusions We uncovered the DECPs and the common DECPs among a group of enteroviruses in HFMD population and found that some epitope-antibody reactions were associated with the outcome of HFMD. These data may guide developing vaccines against the enteroviruses and help the diagnosis and prognosis of HFMD. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13866532
Volume :
105
Database :
Academic Search Index
Journal :
Journal of Clinical Virology
Publication Type :
Academic Journal
Accession number :
130744923
Full Text :
https://doi.org/10.1016/j.jcv.2018.06.001