Regulation of Staphylococcus aureus type 5 capsular polysaccharides by agr and sarA in vitro and in an experimental endocarditis model

被引:34
作者
van Wamel, W
Xiong, YQ
Bayer, AS
Yeaman, MR
Nast, CC
Cheung, AL [1 ]
机构
[1] Dartmouth Coll Sch Med, Dept Microbiol & Immunol, Hanover, NH 03755 USA
[2] Harbor UCLA Res & Educ Inst, Div Infect Dis, Torrance, CA 90509 USA
[3] Univ Calif Los Angeles, Sch Med, Los Angeles, CA 90024 USA
[4] Cedars Sinai Med Ctr, Dept Pathol, Los Angeles, CA 90048 USA
关键词
capsular type 5; agr; sarA; S; aureus; endocarditis;
D O I
10.1006/mpat.2002.0513
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The expression of antiphagocytic polysaccharide capsules is an important pathogenetic step in establishing Staphylococcus aureus infections. Using a green fluorescent protein reporter gene (gfp) system, we examined the expression and genetic regulation of the caP5 promoter (capsular polysaccharide 5 genes) by two major global regulators of S. aureus (agr and sarA) in vitro and in a rabbit endocarditis model. In vitro, cap5 expression substantially increased during the post-exponential phase in parental, as well as sarA mutant constructs. However, cap5 expression was greatly reduced in agr and agr/sarA double mutants. In the endocarditis model, the extent of cap5 expression in vegetations infected with the parental strain was substantially higher than that observed with the agr/sarA double mutants (P < 0.05). Similar trends were noted in renal, but not splenic abscesses. Collectively, these data suggest that agr positively regulates cap5 expression both in vitro and in vivo, while the contribution of sarA to cap5 regulation, although modest, is readily discerned in vivo in agr minus background. In addition, the regulation of cap5 expression by these global regulators may vary in distinct anatomic niches in vivo. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:73 / 79
页数:7
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