In vitro Biofilm formation of commensal and pathogenic Escherichia coli strains:: Impact of environmental and genetic factors

被引:182
作者
Reisner, Andreas
Krogfelt, Karen A.
Klein, Bjarke M.
Zechner, Ellen L.
Molin, Soren
机构
[1] Karl Frazens Univ Graz, Inst Mol Biowissensch, A-8010 Graz, Austria
[2] Tech Univ Denmark, BioCentrum DTU, Mol Microbial Ecol Grp, DK-2800 Lyngby, Denmark
[3] Statens Serum Inst, Dept Gastrointestinal Infect, DK-2300 Copenhagen, Denmark
[4] Statens Serum Inst, Biostat Unit, DK-2300 Copenhagen 5, Denmark
关键词
D O I
10.1128/JB.188.10.3572-3581.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
Our understanding of Escherichia coli biofilm formation in vitro is based on studies of laboratory K-12 strains grown in standard media. However, pathogenic E. coli isolates differ substantially in their genetic repertoire from E. coli K-12 and are subject to heterogeneous environmental conditions. In this study, in vitro biofilm formation of 331 nondomesticated E. coli strains isolated from healthy (n = 105) and diarrhea-afflicted children (n = 68), bacteremia patients (n = 90), and male patients with urinary tract infections (n = 68) was monitored using a variety of growth conditions and compared to in vitro biofilm formation of prototypic pathogenic and laboratory strains. Our results revealed remarkable variation among the capacities of diverse E. coli isolates to form biofilms in vitro. Notably, we could not identify an association of increased biofilm formation in vitro with a specific strain collection that represented pathogenic E. coli strains. Instead, analysis of biofilm data revealed a significant dependence on growth medium composition (P < 0.05). Poor correlation between biofilm formation in the various media suggests that diverse E. coli isolates respond very differently to changing environmental conditions. The data demonstrate that prevalence and expression of three factors known to strongly promote biofilm formation in E. coli K-12 (F-like conjugative pili, aggregative adherence fimbriae, and curli) cannot adequately account for the increased biofilm formation of nondomesticated E. coli isolates in vitro. This study highlights the complexity of genetic and environmental effectors of the biofilm phenotype within the species E. coli.
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页码:3572 / 3581
页数:10
相关论文
共 52 条
[1]
6 WIDESPREAD BACTERIAL CLONES AMONG ESCHERICHIA-COLI K1 ISOLATES [J].
ACHTMAN, M ;
MERCER, A ;
KUSECEK, B ;
POHL, A ;
HEUZENROEDER, M ;
AARONSON, W ;
SUTTON, A ;
SILVER, RP .
INFECTION AND IMMUNITY, 1983, 39 (01) :315-335
[2]
Finding gene-expression patterns in bacterial biofilms [J].
Beloin, C ;
Ghigo, JM .
TRENDS IN MICROBIOLOGY, 2005, 13 (01) :16-19
[3]
BERGER H, 1982, J BACTERIOL, V152, P1241
[5]
The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+
[6]
PIGLET ILEAL MUCUS CONTAINS PROTEIN AND GLYCOLIPID (GALACTOSYLCERAMIDE) RECEPTORS SPECIFIC FOR ESCHERICHIA-COLI K88 FIMBRIAE [J].
BLOMBERG, L ;
KRIVAN, HC ;
COHEN, PS ;
CONWAY, PL .
INFECTION AND IMMUNITY, 1993, 61 (06) :2526-2531
[7]
Bollinger RR, 2003, IMMUNOLOGY, V109, P580
[8]
Boyd EF, 1996, GENETICS, V143, P1091
[9]
Multiplex PCR for detection of three plasmid-borne genes of enteroaggregative Escherichia coli strains [J].
Cerna, JF ;
Nataro, JP ;
Estrada-Garcia, T .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (05) :2138-2140
[10]
Christensen BB, 1999, METHOD ENZYMOL, V310, P20