Extended virulence genotypes and phylogenetic background of Escherichia coli isolates from patients with cystitis, pyelonephritis, or prostatitis

被引:118
|
作者
Johnson, JR
Kuskowski, MA
Gajewski, A
Soto, S
Horcajada, JP
de Anta, MTJ
Vila, J
机构
[1] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Psychiat, Minneapolis, MN 55455 USA
[3] Vet Adm Med Ctr, Med Serv, Minneapolis, MN 55417 USA
[4] Vet Adm Med Ctr, Ctr Geriatr Res Educ & Clin, Minneapolis, MN 55417 USA
[5] Hosp Clin Barcelona, IDIBAPS, Inst Clin Infecciones & Inmunol, Microbiol Serv, Barcelona, Spain
来源
JOURNAL OF INFECTIOUS DISEASES | 2005年 / 191卷 / 01期
关键词
D O I
10.1086/426450
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Molecular analysis of 63 Escherichia coli urine isolates showed that pyelonephritis () and prostatitis (n = 17) isolates exhibited more virulence factors (VFs) among the 35 sought than did cystitis isolates (n = 23). Several nontraditional VFs-including bmaE (M fimbriae), gafD (G fimbriae), fyuA (yersiniabactin receptor), ireA and iroN (novel siderophore receptors), cvaC (colicin [microcin] V), traT (serum-resistance associated), ibeA (invasion of brain endothelium), ompT (outer membrane protease T), and malX (pathogenicity island marker)-either differentiated significantly between syndromes (despite small numbers of isolates and possible multiple-comparison artifacts) or were broadly prevalent. Thus, interventions that target conserved uro-VFs may be possible, despite the likely existence of syndrome-specific pathogenetic mechanisms and/or host defense systems.
引用
收藏
页码:46 / 50
页数:5
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