The role of disulfide bond isomerase A (DsbA) of Escherichia coli O157:H7 in biofilm formation and virulence

被引:33
作者
Lee, Yunho [1 ]
Kim, Younghoon [2 ]
Yeom, Sujin [1 ]
Kim, Saehun [2 ]
Park, Sungsu [3 ]
Jeon, Che Ok [4 ]
Park, Woojun [1 ,4 ]
机构
[1] Korea Univ, Div Environm Sci & Ecol Engn, Seoul, South Korea
[2] Korea Univ, Div Food Sci, Seoul, South Korea
[3] Ewha Womans Univ, Div Nanosci, Seoul, South Korea
[4] Gyeongsang Natl Univ, Environm Biotechnol Natl Res Ctr, Jinju, South Korea
关键词
biofilm; disulfide bond; virulence; Caenorhabditis elegans;
D O I
10.1111/j.1574-6968.2007.00993.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The role of periplasmic disulfide oxidoreductase DsbA in Shiga toxin-producing Escherichia coli O157:H7 (STEC) was investigated. Deletion of dsbA (Delta dsbA) significantly decreased cell motility and alkaline phosphatase activity in STEC. STEC Delta dsbA also showed greater sensitivity to menadione and under low pH conditions. Significant reductions in surface attachment to both biotic (HT-29 epithelial cells) and abiotic (polystyrene and polyvinyl chloride) surfaces were observed in STEC Delta dsbA. In addition, no biofilm formation was detected in STEC Delta dsbA compared to wild-type cells in glass capillary tubes under continuous flow-culture system conditions. In the nematode model Caenorhabditis elegans-killing assay, the deletion of dsbA in STEC resulted in attenuated virulence compared to wild-type cells. STEC Delta dsbA was also found to have a reduced ability to colonize the nematode gut. These results suggest that DsbA plays important roles in biofilm formation and virulence in STEC cells.
引用
收藏
页码:213 / 222
页数:10
相关论文
共 32 条
[1]   Paralysis and killing of Caenorhabditis elegans by enteropathogenic Escherichia coli requires the bacterial tryptophanase gene [J].
Anyanful, A ;
Dolan-Livengood, JM ;
Lewis, T ;
Sheth, S ;
DeZalia, MN ;
Sherman, MA ;
Kalman, LV ;
Benian, GM ;
Kalman, D .
MOLECULAR MICROBIOLOGY, 2005, 57 (04) :988-1007
[2]  
Ausubel F.A., 1999, CURRENT PROTOCOLS MO
[3]   Oxidative protein folding is driven by the electron transport system [J].
Bader, M ;
Muse, W ;
Ballou, DP ;
Gassner, C ;
Bardwell, JCA .
CELL, 1999, 98 (02) :217-227
[4]   A PATHWAY FOR DISULFIDE BOND FORMATION INVIVO [J].
BARDWELL, JCA ;
LEE, JO ;
JANDER, G ;
MARTIN, N ;
BELIN, D ;
BECKWITH, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (03) :1038-1042
[5]   IDENTIFICATION OF A PROTEIN REQUIRED FOR DISULFIDE BOND FORMATION INVIVO [J].
BARDWELL, JCA ;
MCGOVERN, K ;
BECKWITH, J .
CELL, 1991, 67 (03) :581-589
[6]   BUILDING BRIDGES - DISULFIDE BOND FORMATION IN THE CELL [J].
BARDWELL, JCA .
MOLECULAR MICROBIOLOGY, 1994, 14 (02) :199-205
[7]   THE ESCHERICHIA-COLI DSBA GENE IS PARTLY TRANSCRIBED FROM THE PROMOTER OF A WEAKLY EXPRESSED UPSTREAM GENE [J].
BELIN, P ;
BOQUET, PL .
MICROBIOLOGY-SGM, 1994, 140 :3337-3348
[8]  
BRENNER S, 1974, GENETICS, V77, P71
[9]   FACS-optimized mutants of the green fluorescent protein (GFP) [J].
Cormack, BP ;
Valdivia, RH ;
Falkow, S .
GENE, 1996, 173 (01) :33-38
[10]   MUTANTS IN DISULFIDE BOND FORMATION THAT DISRUPT FLAGELLAR ASSEMBLY IN ESCHERICHIA-COLI [J].
DAILEY, FE ;
BERG, HC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (03) :1043-1047