Edwardsiella tarda mutants defective in siderophore production, motility, serum resistance and catalase activity

被引:58
作者
Mathew, JA [1 ]
Tan, YP [1 ]
Rao, PSS [1 ]
Lim, TM [1 ]
Leung, KY [1 ]
机构
[1] Natl Univ Singapore, Fac Sci, Dept Biol Sci, Singapore 119260, Singapore
来源
MICROBIOLOGY-UK | 2001年 / 147卷
关键词
fish pathogen; transposon mutagenesis; virulence genes;
D O I
10.1099/00221287-147-2-449
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Edwardsiella tarda is a Cram-negative bacterium that causes a systemic infection, edwardsiellosis, in fish. The virulence factors of this pathogen and its genetic determinants have not been systematically examined. In this study, TnphoA transposon mutagenesis was used to construct a library of 440 alkaline phosphatase (PhoA(+)) fusion mutants from a total of 400000 transconjugants derived from Ed. tarda 000130/91. This library included genes for secreted and membrane-associated proteins normally involved in virulence. The library was screened for four virulence factors: siderophore production, motility, serum resistance and catalase production. Eight mutants deficient in one or more of these phenotypes were grouped into four classes. They were further characterized for their stimulation of reactive oxygen intermediate production by fish phagocytes, for their adhesion to and internalization into EPC (epithelioma papillosum of carp) cells, and for attenuation of virulence in blue gourami. Mutants 2A and 34 were highly attenuated in fish, with LD50 values about 10 times higher than for the wild-type. These strains had mutations in the genes encoding arylsulfate sulfotransferase (mutant 2A) and a catalase precursor protein (mutant 34). One hyperinvasive/adhesive mutant and four pst mutants that were pleiotropic and slightly attenuated in fish were also isolated.
引用
收藏
页码:449 / 457
页数:9
相关论文
共 61 条
[1]  
AINSWORTH AJ, 1990, DEV COMP IMMUNOL, V14, P201, DOI 10.1016/0145-305X(90)90091-R
[2]   NUCLEOTIDE-SEQUENCE OF THE GENES INVOLVED IN PHOSPHATE-TRANSPORT AND REGULATION OF THE PHOSPHATE REGULON IN ESCHERICHIA-COLI [J].
AMEMURA, M ;
MAKINO, K ;
SHINAGAWA, H ;
KOBAYASHI, A ;
NAKATA, A .
JOURNAL OF MOLECULAR BIOLOGY, 1985, 184 (02) :241-250
[3]   Cloning and sequencing of the Klebsiella K-36 astA gene, encoding an arylsulfate sulfotransferase [J].
Baek, MC ;
Kim, SK ;
Kim, DH ;
Kim, BK ;
Choi, EC .
MICROBIOLOGY AND IMMUNOLOGY, 1996, 40 (08) :531-537
[4]  
BERG CM, 1996, CELLULAR MOL BIOL, V2, P2588
[5]   Utilization of alkaline phosphatase fusions to identify secreted proteins, including potential efflux proteins and virulence factors from Helicobacter pylori [J].
Bina, JE ;
Nano, F ;
Hancock, REW .
FEMS MICROBIOLOGY LETTERS, 1997, 148 (01) :63-68
[6]   CLONING AND CHARACTERIZATION OF THE KATB GENE OF PSEUDOMONAS-AERUGINOSA ENCODING A HYDROGEN PEROXIDE-INDUCIBLE CATALASE - PURIFICATION OF KATB, CELLULAR-LOCALIZATION, AND DEMONSTRATION THAT IT IS ESSENTIAL FOR OPTIMAL RESISTANCE TO HYDROGEN-PEROXIDE [J].
BROWN, SM ;
HOWELL, ML ;
VASIL, ML ;
ANDERSON, AJ ;
HASSETT, DJ .
JOURNAL OF BACTERIOLOGY, 1995, 177 (22) :6536-6544
[7]   Molecular cloning, characterization, and sequencing of the hemolysin gene from Edwardsiella tarda [J].
Chen, JD ;
Lai, SY ;
Huang, SL .
ARCHIVES OF MICROBIOLOGY, 1996, 165 (01) :9-17
[8]   Development of a defined minimal medium for the growth of Edwardsiella ictaluri [J].
Collins, LA ;
Thune, RL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (03) :848-852
[9]   Pseudomonas aeruginosa gene products PilT and PilU are required for cytotoxicity in vitro and virulence in a mouse model of acute pneumonia [J].
Comolli, JC ;
Hauser, AR ;
Waite, L ;
Whitchurch, CB ;
Mattick, JS ;
Engel, JN .
INFECTION AND IMMUNITY, 1999, 67 (07) :3625-3630
[10]   IDENTIFICATION OF A MUTATION IN THE PST-PHOU OPERON THAT REDUCES PATHOGENICITY OF AN ESCHERICHIA-COLI STRAIN CAUSING SEPTICEMIA IN PIGS [J].
DAIGLE, F ;
FAIRBROTHER, JM ;
HAREL, J .
INFECTION AND IMMUNITY, 1995, 63 (12) :4924-4927