Effect of the crp mutation on the utilization of transferrin-bound iron by Vibrio vulnificus

被引:20
作者
Choi, MH
Sun, HY
Park, RY
Kim, CM
Bai, YH
Kim, YR
Rhee, JH
Shin, SH
机构
[1] Chosun Univ, Sch Med, Res Ctr Resistant Cells, Kwangju 501759, South Korea
[2] Chosun Univ, Sch Med, Dept Biol, Kwangju 501759, South Korea
[3] Chonnam Natl Univ, Sch Med, Dept Microbiol, Kwangju, South Korea
[4] Chonnam Natl Univ, Sch Med, Clin Vaccine R&D Ctr,Res Inst Vibrio Infect, Natl Res Lab Mol Microbial Pathogenesis, Kwangju, South Korea
[5] Chonnam Natl Univ, Sch Med, Genome Res Ctr Enteropathogen Bacteria, Kwangju, South Korea
关键词
Vibrio vulnificus; cAMP-CRP; vulnibactin; transferrin; ascites;
D O I
10.1111/j.1574-6968.2006.00183.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Cyclic AMP-cAMP receptor protein (CRP) complex plays an essential role in the global regulation of Vibrio vulnificus virulence. We found that growth retardation of V. vulnificus caused by mutation of the crp gene encoding CRP was exacerbated under iron-limited conditions. Accordingly, we investigated the effect of crp mutation on the expression of the vulnibactin-mediated iron-uptake system and the ability of V. vulnificus to utilize transferrin-bound iron, and thus to grow in cirrhotic ascites, a human ex vivo system. The production of vulnibactin was suppressed, and the transcription of the vis and vuuA genes, which encode an enzyme required for vulnibactin synthesis and vulnibactin receptor protein, was also suppressed in the crp mutant. Moreover, the crp mutant could not utilize transferrin-bound iron, and its growth was severely suppressed both on transferrin-bound iron and in cirrhotic ascites. All the defects in the crp mutant were recovered by the in trans complementation of the wild-type crp gene. Putative CRP-binding sequences were found in the regulatory regions of the fur, vis and vuuA genes. These results indicate that crp mutation attenuates the ability to grow on transferrin-bound iron and in a human body fluid by down-regulating the vulnibactin-mediated iron-uptake system.
引用
收藏
页码:285 / 292
页数:8
相关论文
共 23 条
[1]  
Arnow LE, 1937, J BIOL CHEM, V118, P531
[2]   Immunization with components of two iron uptake ABC transporters protects mice against systemic Streptococcus pneumoniae infection [J].
Brown, JS ;
Ogunniyi, AD ;
Woodrow, MC ;
Holden, DW ;
Paton, JC .
INFECTION AND IMMUNITY, 2001, 69 (11) :6702-6706
[3]   Promoter analysis and regulatory characteristics of vvhBA encoding cytolytic hemolysin of Vibrio vulnificus [J].
Choi, HK ;
Park, NY ;
Kim, DI ;
Chung, HJ ;
Ryu, S ;
Choi, SH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (49) :47292-47299
[4]  
DELORENZO V, 1988, EUR J BIOCHEM, V173, P537
[5]  
DITTA DW, 1980, P NATL ACAD SCI USA, V27, P7347
[6]  
Gulig PA, 2005, J MICROBIOL, V43, P118
[7]   The putative iron transport system SitABCD encoded on SPI1 is required for full virulence of Salmonella typhimurium [J].
Janakiraman, A ;
Slauch, JM .
MOLECULAR MICROBIOLOGY, 2000, 35 (05) :1146-1155
[8]   SmcR and cyclic AMP receptor protein coactivate Vibrio vulnificus vvpE encoding elastase through the RpoS-dependent promoter in a synergistic manner [J].
Jeong, HS ;
Lee, MH ;
Lee, KH ;
Park, SJ ;
Choi, SH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (46) :45072-45081
[9]   Regulation of Vibrio vulnificus virulence by the LuxS quorum-sensing system [J].
Kim, SY ;
Lee, SE ;
Kim, YR ;
Kim, CM ;
Ryu, PY ;
Choy, HE ;
Chung, SS ;
Rhee, JH .
MOLECULAR MICROBIOLOGY, 2003, 48 (06) :1647-1664
[10]   Essential role of an adenylate cyclase in regulating Vibrio vulnificus virulence [J].
Kim, YR ;
Kim, SY ;
Kim, CM ;
Lee, SE ;
Rhee, JH .
FEMS MICROBIOLOGY LETTERS, 2005, 243 (02) :497-503