Protective immune responses to a multi-gene DNA vaccine against Staphylococcus aureus

被引:41
作者
Gaudreau, Marie-Claude
Lacasse, Pierre
Talbot, Brian G. [1 ]
机构
[1] Fac Sci, Dept Biol, Ctr Etud & Valorisat Diversite Microbienne, Sherbrooke, PQ J1K 2R1, Canada
[2] Agr & Agri Food Canada, Dairy & Swine Res & Dev Ctr, Lennoxville, PQ J1M 1Z3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
DNA vaccine; Th1 and Th2; Staphylococcus aureus; arthritis; septicemia;
D O I
10.1016/j.vaccine.2006.09.043
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To investigate the strategy of using a multivalent polyprotein DNA vaccine against Staphylococcus aureus, a series of plasmids was used to immunize mice followed by infectious challenge. The plasmid vaccines expressed Clumping factor A (Clfa), fibronectin binding protein A (FnBPA) and the enzyme Sortase (Srt) as single proteins or combined as a polyprotein. All animals produced a mixed Th1 and Th2 response including functional antigen-specific, mostly IgG2a antibodies, sustained production of IFN-gamma and a predominantly CD8+ T-cell response. Upon challenge with a virulent S. aureus isolate (Sa042), after 21 days, 55% of the multi-gene vaccinated mice survived infection compared to only 15% of the control groups. Vaccinated mice showed no signs of arthritis when challenged with the less virulent "Newman" strain that caused reactive arthritis in the controls. The results suggest that a multi-gene polyprotein-expressing nucleic acid vaccine alone produces a combined Th1 and Th2 response that can contribute to protection against the complex pathogenesis of S. aureus. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:814 / 824
页数:11
相关论文
共 51 条
[41]   Protective immune response against methicillin resistant Staphylococcus aureus in a murine model using a DNA vaccine approach [J].
Senna, JPM ;
Roth, DM ;
Oliveira, JS ;
Machado, DC ;
Santos, DS .
VACCINE, 2003, 21 (19-20) :2661-2666
[42]   Use of a conjugate polysaccharide vaccine in the prevention of invasive staphylococcal disease: Is an additional vaccine needed or possible? [J].
Shinefield, HR .
VACCINE, 2006, 24 :S65-S69
[43]   Immune responses to a DNA/protein vaccination strategy against Staphylococcus aureus induced mastitis in dairy cows [J].
Shkreta, L ;
Talbot, BG ;
Diarra, MS ;
Lacasse, P .
VACCINE, 2004, 23 (01) :114-126
[44]   Optimization of DNA vaccination immune responses in dairy cows: effect of injection site and the targeting efficacy of antigen-bCTLA-4 complex [J].
Shkreta, L ;
Talbot, BG ;
Lacasse, P .
VACCINE, 2003, 21 (19-20) :2372-2382
[45]   Protection of mice with a divalent tuberculosis DNA vaccine encoding antigens Ag85B and MPT64 [J].
Tian, X ;
Cai, H ;
Zhu, YX .
ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2004, 36 (04) :269-276
[46]  
VONEIFF C, 2006, J ARTICLE INJURY S2, V37, pS26
[47]   The fibronectin-binding MSCRAMM FnbpA of Staphylococcus aureus is a bifunctional protein that also binds to fibrinogen [J].
Wann, ER ;
Gurusiddappa, S ;
Höök, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (18) :13863-13871
[48]   Functional selection of vaccine candidate peptides from Staphylococcus aureus whole-genome expression libraries in vitro [J].
Weichhart, T ;
Horky, M ;
Söllner, J ;
Gangl, S ;
Henics, T ;
Nagy, E ;
Meinke, A ;
von Gabain, A ;
Fraser, CM ;
Gill, SR ;
Hafner, M ;
von Ahsen, U .
INFECTION AND IMMUNITY, 2003, 71 (08) :4633-4641
[49]   Vancomycin-resistant Staphylococcus aureus in the absence of vancomycin exposure [J].
Whitener, CJ ;
Park, SY ;
Browne, FA ;
Parent, LJ ;
Julian, K ;
Bozdogan, B ;
Appelbaum, PC ;
Chaitram, J ;
Weigel, LM ;
Jernigan, J ;
McDougal, LK ;
Tenover, FC ;
Fridkin, SK .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (08) :1049-1055
[50]  
Zhao YX, 1998, IMMUNOLOGY, V93, P80