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

PLoS One. 2016 Sep 13;11(9):e0162820. doi: 10.1371/journal.pone.0162820. eCollection 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: VP11-297, VP141-297, VP11-60, VP145-58 and VP161-297. 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. VP11-297 and VP141-297 strongly inhibited the anti-CA16 VP1 response in serum samples from both populations, while VP145-58 and VP161-297 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 VP11-60 and VP141-297) 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.

MeSH terms

  • Adult
  • Aged
  • Antibodies, Neutralizing / blood
  • Antibodies, Viral / blood*
  • Antibody Specificity
  • Antigens, Viral / genetics
  • Antigens, Viral / immunology
  • Blood Donors
  • China
  • Enterovirus A, Human / classification
  • Enterovirus A, Human / genetics
  • Enterovirus A, Human / immunology*
  • Female
  • Hand, Foot and Mouth Disease / immunology*
  • Hand, Foot and Mouth Disease / virology*
  • Humans
  • Male
  • Middle Aged
  • Peptide Fragments / genetics
  • Peptide Fragments / immunology
  • Recombinant Proteins / genetics
  • Recombinant Proteins / immunology
  • Viral Structural Proteins / genetics
  • Viral Structural Proteins / immunology*
  • Young Adult

Substances

  • Antibodies, Neutralizing
  • Antibodies, Viral
  • Antigens, Viral
  • Peptide Fragments
  • Recombinant Proteins
  • Viral Structural Proteins

Grants and funding

This work was supported by the National Natural Science Foundation of China (http://www.nsfc.gov.cn/), grant number: No.30872405 and 30972632 to WP; Chinese National Key Special Project for the Prevention and Control of Major Infectious Diseases (http://www.nmp.gov.cn/), grant number: 2009ZX10004-105 to WP; Chinese National Key Special Project for Major New Drug Discovery (http://www.nmp.gov.cn/), grant number: 2011ZX09506-001 to WP and the National 863 Project (http://program.most.gov.cn/), grant number: 2014AA021403 to WP. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.