Motility influences biofilm architecture in Escherichia coli

被引:283
作者
Wood, Thomas K. [1 ]
Barrios, Andres F. Gonzalez
Herzberg, Moshe
Lee, Jintae
机构
[1] Texas A&M Univ, Dept Chem Engn, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Biol, College Stn, TX 77843 USA
关键词
D O I
10.1007/s00253-005-0263-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Eight Escherichia coli strains were studied in minimal medium with a continuous flow system using confocal microscopy. K12 wild-type strains ATCC 25404 and MG1655 formed the best biofilms (similar to 43 mu m thick, 21 to 34% surface coverage). JM109, DH5 alpha, and MG1655 motA formed intermediate biofilms (similar to 13 mu m thick, 41 to 58% surface coverage). BW25113, MG1655 qseB, and MG1655 fliA had poor biofilms (surface coverage less than 5%). The best biofilm-formers, ATCC 25404 and MG1655, displayed the highest motility, whereas the worst biofilm former, BW25113, was motility-impaired. The differences in motility were due to differences in expression of the motility loci qseB, flhD, fliA, fliC, and motA (e.g., qseB expression in MG1655 was 139-fold higher than BW25113 and 209-fold higher than JM109). Motility affected the biofilm architecture as those strains which had poor motility (E. coli JM109, E. coli MG1655 motA, and DH5 alpha) formed flatter microcolonies compared with MG1655 and ATCC 25404, which had more dramatic vertical structures as a result of their enhanced motility. The presence of flagella was also found to be important as qseB and fliA mutants (which lack flagella) had less biofilm than the isogenic paralyzed motA strain (threefold less thickness and 15-fold less surface coverage).
引用
收藏
页码:361 / 367
页数:7
相关论文
共 35 条
[31]   Adaptive responses to antimicrobial agents in biofilms [J].
Szomolay, B ;
Klapper, I ;
Dockery, J ;
Stewart, PS .
ENVIRONMENTAL MICROBIOLOGY, 2005, 7 (08) :1186-1191
[32]   Stratified growth in Pseudomonas aeruginosa biofilms [J].
Werner, E ;
Roe, F ;
Bugnicourt, A ;
Franklin, MJ ;
Heydorn, A ;
Molin, S ;
Pitts, B ;
Stewart, PS .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (10) :6188-6196
[33]   Gene expression in Pseudomonas aeruginosa biofilms [J].
Whiteley, M ;
Bangera, MG ;
Bumgarner, RE ;
Parsek, MR ;
Teitzel, GM ;
Lory, S ;
Greenberg, EP .
NATURE, 2001, 413 (6858) :860-864
[34]   EFFECT OF CHEMICALLY-INDUCED, CLONED-GENE EXPRESSION ON PROTEIN-SYNTHESIS IN ESCHERICHIA-COLI [J].
WOOD, TK ;
PERETTI, SW .
BIOTECHNOLOGY AND BIOENGINEERING, 1991, 38 (04) :397-412
[35]   IMPROVED M13 PHAGE CLONING VECTORS AND HOST STRAINS - NUCLEOTIDE-SEQUENCES OF THE M13MP18 AND PUC19 VECTORS [J].
YANISCHPERRON, C ;
VIEIRA, J ;
MESSING, J .
GENE, 1985, 33 (01) :103-119