4.5 Article

Antibody response to the central unglycosylated region of the respiratory syncytial virus attachment protein in mice

Journal

VACCINE
Volume 30, Issue 36, Pages 5382-5388

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2012.06.016

Keywords

Respiratory syncytial virus; Attachment protein; Humoral immune response; Viral subtype

Funding

  1. Public Health Service from the National Institutes of Allergy and Infectious Diseases [R21 AI076781, R56 AI091731]
  2. Rochester General Hospital Kidd Foundation

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We examined the humoral immune response to the unglycosylated central region of the respiratory syncytial virus (RSV) attachment (G) protein in mice following intranasal challenge at day 0 (primary) and day 21 (secondary) with subtype A (A2 strain) or B (B1 strain) RSV preparations. Our serological screening reagents included bacterially derived glutathione S-transferase (GST) fusion proteins, each bearing a portion of the RSV G central core (CC; residues 151-190), proximal central core (PCC; residues 151-172), and the distal central core (DCC; residues 173-190) and purified RSV G proteins from subtype A and B viruses. Convalescent sera collected on day 21 following primary RSV infection bore robust IgG response primarily against the homosubtypic RSV G DCC with relatively modest antigen affinity/avidity as demonstrated by brief incubation with 6 M urea. In contrast, sera collected on day 42 following secondary homosubtypic RSV infection bore IgG titers of higher magnitudes and antigen affinity/avidity against the homosubtypic RSV G CC, PCC, and/or the DCC regions and full-length RSV G protein but not against the heterosubtypic RSV G protein or recombinant CC subdomains. In contrast, heterosubtypic secondary RSV infection elicits a broad array of IgG responses with titers of varying magnitudes to homo- and heterosubtypic RSV G CC regions as well as to purified F, Ga. and Gb proteins with the notable exception of minimal response to the RSV G DCC domain associated with the secondary RSV challenge. Our results have implications for RSV G-based serological assays as well as prophylactic immunotherapy and RSV vaccine development. (C) 2012 Elsevier Ltd. All rights reserved.

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