Phylogenetic and pathotypic comparison of concurrent urine and rectal Escherichia coli isolates from men with febrile urinary tract infection

被引:50
作者
Johnson, JR
Scheutz, F
Ulleryd, P
Kuskowski, MA
O'Bryan, TT
Sandberg, T
机构
[1] Minneapolis VA Med Ctr, Mucosal & Vaccine Res Ctr, Minneapolis, MN 55417 USA
[2] Minneapolis VA Med Ctr, Geriatr Res Educ & Clin Ctr, Minneapolis, MN 55417 USA
[3] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Dept Psychiat, Minneapolis, MN 55455 USA
[5] Int Escherichia & Klebsiella Ctr, Statens Seruminst, Copenhagen, Denmark
[6] Univ Gothenburg, Dept Infect Dis, Gothenburg, Sweden
关键词
D O I
10.1128/JCM.43.8.3895-3900.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Among men with febrile urinary tract infection (FUTI), whether the host's fecal flora is the source for the urine strain ("fecal-urethral" hypothesis), and whether pathogenesis is driven by prevalence versus special pathogenicity, are unknown. Accordingly, pretherapy urine isolates from 65 men with FUTI were compared with concurrent rectal isolates from the same hosts according to serotype, genomic profile, phylogenetic group, and virulence genotype. The host's multiple rectal colonies included only the urine clone in 25% of subjects, the urine clone plus additional clones in 22%, and only nonurine clones in 54%. Compared with the 67 unique rectal clones, the 65 urine isolates were significantly enriched for phylogenetic group B2, virulence-associated serotypes, and specific virulence genes and contained more virulence genes (median, 10 versus 6: P < 0.001). In multivariable models, phylogenetic group B2, hlyD (hemolysin), cnf1 (cytotoxic necrotizing factor), iroN (siderophore receptor), ompT (outer membrane protease), and malX (pathogenicity island marker) most strongly predicted urine source. These findings challenge the fecal-urethral and prevalence hypotheses for FUTI pathogenesis and instead strongly support the possibility of alternate infection routes in some men and the special pathogenicity hypothesis. They also identify specific bacterial traits as potential targets for anti-FUTI interventions.
引用
收藏
页码:3895 / 3900
页数:6
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