DNA immunization against the clumping factor A (ClfA) of Staphylococcus aureus

被引:62
作者
Brouillette, E
Lacasse, P
Shkreta, L
Bélanger, J
Grondin, G
Diarra, MS
Fournier, S
Talbot, BG
机构
[1] Agr & Agri Food Canada, Dairy & Swine Res & Dev Ctr, Lennoxville, PQ J1M 1Z3, Canada
[2] Univ Sherbrooke, Fac Sci, Dept Biol, Sherbrooke, PQ J1K 2R1, Canada
[3] CHU Sherbrooke, Ctr Rech Clin, Fleurimont, PQ J1H 5N4, Canada
关键词
DNA vaccine; mastitis; fibrinogen-binding protein;
D O I
10.1016/S0264-410X(02)00100-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Adhesins are considered the most important virulence factors during early phases Staphylococcus aureus infection. Antibodies induced by vaccination toward an adhesin should reduce the adherence of the pathogen and augment its phagocytosis. The present report describes the immune response of mice to a DNA vaccine directed against one of these adhesins, clumping factor A (ClfA). Injection of plasmids expressing the fibrinogen-binding region A of ClfA induced a strong and specific antibody response to ClfA in mice. In addition, splenocyte proliferation was provoked by in vitro stimulation with recombinant ClfA, thus, indicating direct implication of these cells in the immune response. 0 p Pre-incubation of S. aureus with sera of vaccinated mice reduced the pathogen's ability to bind fibrinogen by up to 92%. These pre-incubated bacteria were phagocytosed by macrophages at an increased level in vitro and were less virulent in vivo in a mouse mastitis model. However, DNA-immunized mice were not protected against an intraperitoneal challenge. Overall, the results suggest that DNA immunization against adhesins represents a new and valuable approach to combat S. aureus infections. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2348 / 2357
页数:10
相关论文
共 39 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]   DNA vaccines: Technology and application as anti-parasite and anti-microbial agents [J].
Alarcon, JB ;
Waine, GW ;
McManus, DP .
ADVANCES IN PARASITOLOGY, VOL 42, 1999, 42 :343-410
[3]   Enhanced response to a DNA vaccine encoding a fusion antigen that is directed to sites of immune induction [J].
Boyle, JS ;
Brady, JL ;
Lew, AM .
NATURE, 1998, 392 (6674) :408-411
[4]   A NEW MEMBER OF THE IMMUNOGLOBULIN SUPERFAMILY - CTLA-4 [J].
BRUNET, JF ;
DENIZOT, F ;
LUCIANI, MF ;
ROUXDOSSETO, M ;
SUZAN, M ;
MATTEI, MG ;
GOLSTEIN, P .
NATURE, 1987, 328 (6127) :267-270
[5]   EXPERIMENTAL BACTERIAL MASTITIS IN MOUSE [J].
CHANDLER, RL .
JOURNAL OF MEDICAL MICROBIOLOGY, 1970, 3 (02) :273-&
[6]  
DAVIS HL, 1999, DNA VACCINES METHODS, P71
[7]   QUANTITATIVE COMPARISON OF CLUMPING FACTOR-MEDIATED AND COAGULASE-MEDIATED STAPHYLOCOCCUS-AUREUS ADHESION TO SURFACE-BOUND FIBRINOGEN UNDER FLOW [J].
DICKINSON, RB ;
NAGEL, JA ;
MCDEVITT, D ;
FOSTER, TJ ;
PROCTOR, RA ;
COUPER, SL .
INFECTION AND IMMUNITY, 1995, 63 (08) :3143-3150
[8]   Contribution of clumping factor B to pathogenesis of experimental endocarditis due to Staphylococcus aureus [J].
Entenza, JM ;
Foster, TJ ;
Eidhin, DN ;
Vaudaux, P ;
Francioli, P ;
Moreillon, P .
INFECTION AND IMMUNITY, 2000, 68 (09) :5443-5446
[9]   Molecular weights of CTLA-4 and CD80 by sedimentation equilibrium ultracentrifugation [J].
Fairman, R ;
Fenderson, W ;
Hail, ME ;
Wu, YL ;
Shaw, SY .
ANALYTICAL BIOCHEMISTRY, 1999, 270 (02) :286-295
[10]   Priming by DNA immunization augments protective efficacy of Mycobacterium bovis bacille Calmette-Guerin against tuberculosis [J].
Feng, CG ;
Palendira, U ;
Demangel, C ;
Spratt, JM ;
Malin, AS ;
Britton, WJ .
INFECTION AND IMMUNITY, 2001, 69 (06) :4174-4176