Identification of in vivo-expressed antigens of Staphylococcus aureus and their use in vaccinations for protection against nasal carriage

被引:164
作者
Clarke, SR
Brummell, KJ
Horsburgh, MJ
McDowell, PW
Mohamad, SAS
Stapleton, MR
Acevedo, J
Read, RC
Day, NPJ
Peacock, SJ
Mond, JJ
Kokai-Kun, JF
Foster, SJ
机构
[1] Univ Sheffield, Dept Mol Biol & Biotechnol, Western Bank, Sheffield S10 2TN, S Yorkshire, England
[2] Univ Sheffield, Div Genom Med, Sheffield S10 2TN, S Yorkshire, England
[3] Biosynexus, Gaithersburg, MD USA
[4] Mahidol Univ, Fac Trop Med, Wellcome Trust, Oxford Trop Med Res Programme, Bangkok 10700, Thailand
基金
英国惠康基金;
关键词
D O I
10.1086/501471
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A spectrum of in vivo-expressed Staphylococcus aureus antigens was identified by probing bacteriophage expression libraries of S. aureus with serum samples from infected and uninfected individuals. Eleven recombinant antigenic proteins were produced, and specific antibody titers in a large collection of human serum samples were determined. Significantly increased concentrations of reactive immunoglobulin G (IgG) to 7 antigens were found in serum samples from ill individuals, compared with those in healthy individuals. Significantly higher concentrations of reactive IgG to 4 antigens, including iron-responsive surface determinant (Isd) A and IsdH, were found in serum samples from healthy individuals who were not nasal carriers of S. aureus, compared with those in healthy carriers. Vaccination of cotton rats with IsdA or IsdH protected against nasal carriage. Also, IsdA is involved in adherence of S. aureus to human desquamated nasal epithelial cells and is required for nasal colonization in the cotton rat model. Thus, vaccination with these antigens may prevent S. aureus carriage and reduce the prevalence of human disease.
引用
收藏
页码:1098 / 1108
页数:11
相关论文
共 47 条
  • [1] BACTERIAL ADHERENCE TO NASAL MUCOSAL CELLS
    ALY, R
    SHINEFIELD, HI
    STRAUSS, WG
    MAIBACH, HI
    [J]. INFECTION AND IMMUNITY, 1977, 17 (03) : 546 - 549
  • [2] Bacterial iron homeostasis
    Andrews, SC
    Robinson, AK
    Rodríguez-Quiñones, F
    [J]. FEMS MICROBIOLOGY REVIEWS, 2003, 27 (2-3) : 215 - 237
  • [3] IMPORTANCE OF THE KERATINIZED EPITHELIAL-CELL IN BACTERIAL ADHERENCE
    BIBEL, DJ
    ALY, R
    SHINEFIELD, HR
    MAIBACH, HI
    STRAUSS, WG
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1982, 79 (04) : 250 - 253
  • [4] BREDIUS RGM, 1993, J IMMUNOL, V151, P1463
  • [5] IsdA of Staphylococcus aureus is a broad spectrum, iron-regulated adhesin
    Clarke, SR
    Wiltshire, MD
    Foster, SJ
    [J]. MOLECULAR MICROBIOLOGY, 2004, 51 (05) : 1509 - 1519
  • [6] Analysis of Ebh, a 1.1-megadalton cell wall-associated fibronectin-binding protein of Staphylococcus aureus
    Clarke, SR
    Harris, LG
    Richards, RG
    Foster, SJ
    [J]. INFECTION AND IMMUNITY, 2002, 70 (12) : 6680 - 6687
  • [7] Determinants of Staphylococcus aureus nasal carriage
    Cole, AM
    Tahk, S
    Oren, A
    Yoshioka, D
    Kim, YH
    Park, A
    Ganz, T
    [J]. CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2001, 8 (06) : 1064 - 1069
  • [8] Comparison of antibody repertoires against Staphylococcus aureus in healthy individuals and in acutely infected patients
    Dryla, A
    Prustomersky, S
    Gelbmann, D
    Hanner, M
    Bettinger, E
    Kocsis, B
    Kustos, T
    Henics, T
    Meinke, A
    Nagy, E
    [J]. CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2005, 12 (03) : 387 - 398
  • [9] Identification of a novel iron regulated staphylococcal surface protein with haptoglobin-haemoglobin binding activity
    Dryla, A
    Gelbmann, D
    von Gabain, A
    Nagy, E
    [J]. MOLECULAR MICROBIOLOGY, 2003, 49 (01) : 37 - 53
  • [10] STAPHYLOCOCCAL COAGULASE - MODE OF ACTION AND ANTIGENICITY
    DUTHIE, ES
    LORENZ, LL
    [J]. JOURNAL OF GENERAL MICROBIOLOGY, 1952, 6 (1-2): : 95 - 107