Type 1 Fimbriae Contribute to Catheter-Associated Urinary Tract Infections Caused by Escherichia coli

被引:59
作者
Reisner, Andreas [1 ]
Maierl, Mario [1 ]
Joerger, Michael [1 ]
Krause, Robert [2 ]
Berger, Daniela [1 ]
Haid, Andrea [1 ]
Tesic, Dijana [1 ]
Zechner, Ellen L. [3 ]
机构
[1] Univ Appl Sci, Graz, Austria
[2] Med Univ Graz, Dept Internal Med, Sect Infect Dis & Trop Med, Graz, Austria
[3] Graz Univ, Inst Mol Biosci, Graz, Austria
基金
奥地利科学基金会;
关键词
COMPLETE GENOME SEQUENCE; TAMM-HORSFALL PROTEIN; BIOFILM FORMATION; PHASE VARIATION; IN-VITRO; E.-COLI; EXPRESSION; MODEL; VIRULENCE; GROWTH;
D O I
10.1128/JB.00985-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Biofilm formation on catheters is thought to contribute to persistence of catheter-associated urinary tract infections (CAUTI),which represent the most frequent nosocomial infections. Knowledge of genetic factors for catheter colonization is limited, since their role has not been assessed using physicochemical conditions prevailing in a catheterized human bladder. The current study aimed to combine data from a dynamic catheterized bladder model in vitro with in vivo expression analysis for understanding molecular factors relevant for CAUTI caused by Escherichia coli. By application of the in vitro model that mirrors the physicochemical environment during human infection, we found that an E. coli K-12 mutant defective in type 1 fimbriae, but not isogenic mutants lacking flagella or antigen 43, was outcompeted by the wild-type strain during prolonged catheter colonization. The importance of type 1 fimbriae for catheter colonization was verified using a fimA mutant of uropathogenic E. coli strain CFT073 with human and artificial urine. Orientation of the invertible element (IE) controlling type 1 fimbrial expression in bacterial populations harvested from the colonized catheterized bladder in vitro suggested that the vast majority of catheter-colonizing cells (up to 88%) express type 1 fimbriae. Analysis of IE orientation in E. coli populations harvested from patient catheters revealed that a median level of similar to 73% of cells from nine samples have switched on type 1 fimbrial expression. This study supports the utility of the dynamic catheterized bladder model for analyzing catheter colonization factors and highlights a role for type 1 fimbriae during CAUTI.
引用
收藏
页码:931 / 939
页数:9
相关论文
共 62 条
  • [21] Antigen-43-mediated autoaggregation of Escherichia coli is blocked by fimbriation
    Hasman, H
    Chakraborty, T
    Klemm, P
    [J]. JOURNAL OF BACTERIOLOGY, 1999, 181 (16) : 4834 - 4841
  • [22] Complicated catheter-associated urinary tract infections due to Escherichia coli and Proteus mirabilis
    Jacobsen, S. M.
    Stickler, D. J.
    Mobley, H. L. T.
    Shirtliff, M. E.
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 2008, 21 (01) : 26 - +
  • [23] INVIVO EXPRESSION AND VARIATION OF ESCHERICHIA-COLI TYPE-1 AND P-PILI IN THE URINE OF ADULTS WITH ACUTE URINARY-TRACT INFECTIONS
    KISIELIUS, PV
    SCHWAN, WR
    AMUNDSEN, SK
    DUNCAN, JL
    SCHAEFFER, AJ
    [J]. INFECTION AND IMMUNITY, 1989, 57 (06) : 1656 - 1662
  • [24] Antigen 43 facilitates formation of multispecies biofilms
    Kjærgaard, K
    Schembri, MA
    Ramos, C
    Molin, S
    Klemm, P
    [J]. ENVIRONMENTAL MICROBIOLOGY, 2000, 2 (06) : 695 - 702
  • [25] Oxygen-Limiting Conditions Enrich for Fimbriate Cells of Uropathogenic Proteus mirabilis and Escherichia coli
    Lane, M. Chelsea
    Li, Xin
    Pearson, Melanie M.
    Simms, Amy N.
    Mobley, Harry L. T.
    [J]. JOURNAL OF BACTERIOLOGY, 2009, 191 (05) : 1382 - 1392
  • [26] LICHODZIEJEWSKA M, 1989, LANCET, V1, P1414
  • [27] In vivo phase variation of Escherichia coli type 1 fimbrial genes in women with urinary tract infection
    Lim, JK
    Gunther, NW
    Zhao, H
    Johnson, DE
    Keay, SK
    Mobley, HLT
    [J]. INFECTION AND IMMUNITY, 1998, 66 (07) : 3303 - 3310
  • [28] Species interactions in mixed-community crystalline biofilms on urinary catheters
    Macleod, Sarah M.
    Stickler, David J.
    [J]. JOURNAL OF MEDICAL MICROBIOLOGY, 2007, 56 (11) : 1549 - 1557
  • [29] McBain AJ., 2009, ADV APPL MICROBIOL, V69, P99, DOI DOI 10.1016/S0065-2164(09)69004-3
  • [30] Merritt Judith H, 2005, Curr Protoc Microbiol, VChapter 1, DOI 10.1002/9780471729259.mc01b01s00