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Different Antibody Response against the Coxsackievirus A16 VP1 Capsid Protein: Specific or Non-Specific.

Authors :
Ding, Yingying
Wang, Zhihong
Zhang, Xi
Teng, Zheng
Gao, Caixia
Qian, Baohua
Wang, Lili
Feng, Jiaojiao
Wang, Jinhong
Zhao, Chunyan
Guo, Cunjiu
Pan, Wei
Source :
PLoS ONE; 9/13/2016, Vol. 11 Issue 9, p1-17, 17p
Publication Year :
2016

Abstract

Coxsackievirus A16 (CA16) is one of the major causative agents of hand, foot, and mouth disease worldwide. The non-neutralizing antibody response that targets CA16 VP1 remains poorly elucidated. In the present study, antibody responses against CA16 VP1 in Shanghai blood donors and Shanxi individuals were analyzed by ELISA and inhibitory ELISA using five CA16 VP1 antigens: VP1<subscript>1-297</subscript>, VP1<subscript>41-297</subscript>, VP1<subscript>1-60</subscript>, VP1<subscript>45-58</subscript> and VP1<subscript>61-297</subscript>. The correlation coefficients for most of the reactions against each of the five antigens and the inhibition of the anti-CA16 VP1 antibody response produced by the various antigens were higher in Shanghai blood donors compared to those in Shanxi individuals. VP1<subscript>1-297</subscript> and VP1<subscript>41-297</subscript> strongly inhibited the anti-CA16 VP1 response in serum samples from both populations, while VP1<subscript>45-58</subscript> and VP1<subscript>61-297</subscript> intermediately and weakly inhibited the anti-CA16 VP1 response, respectively, in only Shanghai group. A specific type of inhibition (anti-CA16 VP1 was completely inhibited by both VP1<subscript>1-60</subscript> and VP1<subscript>41-297</subscript>) characterized by high neutralizing antibody titers was identified and accounted for 71.4% of the strongly reactive samples from the Shanghai group. These results indicate that the Shanghai blood donors exhibited a consistent and specific antibody response, while the Shanxi individuals showed an inconsistent and non-specific antibody response. These findings may improve the understanding of host humoral immunity against CA16 and help to identify an effective approach for seroepidemiological surveillance and specific diagnosis of CA16 infection based on normal and competitive ELISA. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19326203
Volume :
11
Issue :
9
Database :
Complementary Index
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
118050756
Full Text :
https://doi.org/10.1371/journal.pone.0162820