Role of the K2 Capsule in Escherichia coli Urinary Tract Infection and Serum Resistance

被引:64
作者
Buckles, Eric L. [1 ]
Wang, Xiaolin [1 ]
Lane, M. Chelsea [4 ]
Lockatell, C. Virginia [1 ]
Johnson, David E. [1 ,3 ]
Rasko, David A. [2 ]
Mobley, Harry L. T. [4 ]
Donnenberg, Michael S. [1 ]
机构
[1] Univ Maryland, Sch Med, Dept Med, Div Infect Dis, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Inst Genome Sci, Baltimore, MD 21201 USA
[3] Dept Vet Affairs, Baltimore, MD USA
[4] Univ Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
MICROBIAL PATHOGENICITY; BACTERIAL VIRULENCE; GENES; STRAINS; POLYSACCHARIDE; IDENTIFICATION; DETERMINANT; EXPRESSION; ANTIGEN; LIPOPOLYSACCHARIDE;
D O I
10.1086/598524
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Capsule expression may be important during ascending Escherichia coli urinary tract infections (UTIs). Methods. An isogenic ksl(k2) ABCDE mutant of extraintestinal pathogenic E. coli (ExPEC) strain CFT073 that could not synthesize the K2 capsule was compared with wild-type CFT073, to determine virulence in a murine model of ascending UTI and in vitro killing assays. Results. No significant differences were observed regarding the abilities of the mutant and the wild-type CFT073 strains to colonize the murine urinary tract in single-challenge infection experiments. However, in competitive-colonization experiments, the mutant was significantly outcompeted by the wild-type strain in urine and the kidneys. The mutant strain was also more susceptible to human serum. Complementation of the mutant with a plasmid containing the ksl(k2) ABCDE genes restored capsule expression, enhanced survival in the murine urinary tract, and restored serum resistance. Conclusion. These results indicate that expression of the K2 capsule is important for the pathogenesis of UTI and provides protection against complement-mediated killing. To our knowledge, this is the first study in which the E. coli capsule has been proven to play a role in infection by use of isogenic mutants and genetic complementation.
引用
收藏
页码:1689 / 1697
页数:9
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