Antibodies to the iron uptake ABC transporter lipoproteins PiaA and PiuA promote opsonophagocytosis of Streptococcus pneumoniae

被引:75
作者
Jomaa, M
Yuste, J
Paton, JC
Jones, C
Dougan, G
Brown, JS
机构
[1] UCL Royal Free & Univ Coll Med Sch, Rayne Inst, Dept Med, Ctr Resp Res, London WC1E 6JJ, England
[2] Univ London Imperial Coll Sci Technol & Med, Ctr Biol Sci, London SW7 2AZ, England
[3] Univ Adelaide, Sch Mol & Biomed Sci, Adelaide, SA, Australia
[4] Microsci Ltd, Wokingham RG41 5TU, Berks, England
[5] Wellcome Trust Sanger Inst, Pathogen Sequencing Unit, Cambridge CB10 1SA, England
关键词
D O I
10.1128/IAI.73.10.6852-6859.2005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
PiaA and PiuA are the lipoprotein components of the Pia and Piu Streptococcus pneumoniae iron uptake ABC transporters and are required for full virulence in mouse models of infection. Active or passive vaccination with recombinant PiuA and PiaA protects mice against invasive S. pneumoniae disease. In this study we have analyzed the antibody responses and mechanism of protection induced by PiuA and PiaA in more detail. For both proteins, two booster vaccinations induced stronger antibody responses in mice than a single or no booster vaccinations, and 5 jig of protein induced similar levels of antibody responses as 20 mu g. Inmmnoglobulin G (IgG) subclass-specific enzyme-linked immunosorbent assays demonstrated that the antibody response to PiuA and PiaA was predominantly IgG1, with induction of only low levels of IgG2a. Anti-PiaA and anti-PiuA polyclonal rabbit antibodies bound to the surface of live S. pneumoniae when assessed by flow cytometry but did not inhibit growth of S. pneumoniae in cation-depleted medium or bacterial susceptibility to the iron-dependent antibiotic streptonigrin. However, anti-PiaA and anti-PiuA did increase complement-independent and -dependent opsonophagocytosis of different serotypes of S. pneumoniae by the human neutrophil cell line HL60. Hence, vaccination with PiaA and PiuA protects against S. pneumoniae infection by inducing antibodies that promote bacterial opsonophagocytosis rather than inhibiting iron transport.
引用
收藏
页码:6852 / 6859
页数:8
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