Liang Weili, Pascual-Montano Alberto, Silva Anisia J, Benitez Jorge A
Morehouse School of Medicine, Department of Microbiology, Biochemistry and Immunology, 720 Westview Dr. SW, Atlanta, GA, USA.
Computer Architecture Department, Facultad de Ciencias Físicas, Universidad Complutense de Madrid, Madrid 28040, Spain.
Microbiology (Reading). 2007 Sep;153(Pt 9):2964-2975. doi: 10.1099/mic.0.2007/006668-0.
Vibrio cholerae is the causative agent of cholera, which continues to be a major public health concern in Asia, Africa and Latin America. The bacterium can persist outside the human host and alternates between planktonic and biofilm community lifestyles. Transition between the different lifestyles is mediated by multiple signal transduction pathways including quorum sensing. Expression of the Zn-metalloprotease haemagglutinin (HA)/protease is subject to a dual regulation which involves the quorum-sensing regulator HapR and the cAMP receptor protein. In a previous study, we observed that a mutant defective in the cAMP-receptor protein (CRP) expressed lower levels of HapR. To further investigate the role of CRP in modulating HapR and other signal transduction pathways, we performed global gene expression profiling of a Deltacrp mutant of El Tor biotype V. cholerae. Here we show that CRP is required for the biosynthesis of cholera autoinducer 1 (CAI-1) and affects the expression of multiple HapR-regulated genes. As expected, the Deltacrp mutant produced more cholera toxin and enhanced biofilm. Expression of flagellar genes, reported to be affected in DeltahapR mutants, was diminished in the Deltacrp mutant. However, an epistasis analysis indicated that cAMP-CRP affects motility by a mechanism independent of HapR. Inactivation of crp inhibited the expression of multiple genes reported to be strongly induced in vivo and to affect the ability of V. cholerae to colonize the small intestine and cause disease. These genes included ompU, ompT and ompW encoding outer-membrane proteins, the alternative sigma factor sigma(E) required for intestinal colonization, and genes involved in anaerobic energy metabolism. Our results indicate that CRP plays a crucial role in the V. cholerae life cycle by affecting quorum sensing and multiple genes required for survival of V. cholerae in the human host and the environment.
霍乱弧菌是霍乱的病原体,在亚洲、非洲和拉丁美洲仍是一个主要的公共卫生问题。这种细菌可以在人类宿主之外存活,并在浮游生物和生物膜群落生活方式之间交替。不同生活方式之间的转变由包括群体感应在内的多种信号转导途径介导。锌金属蛋白酶血凝素(HA)/蛋白酶的表达受到双重调控,这涉及群体感应调节因子HapR和环磷酸腺苷(cAMP)受体蛋白。在之前的一项研究中,我们观察到cAMP受体蛋白(CRP)缺陷的突变体表达的HapR水平较低。为了进一步研究CRP在调节HapR和其他信号转导途径中的作用,我们对埃尔托生物型霍乱弧菌的Δcrp突变体进行了全基因表达谱分析。我们在此表明,CRP是霍乱自诱导物1(CAI-1)生物合成所必需的,并影响多个受HapR调控基因的表达。正如预期那样,Δcrp突变体产生了更多的霍乱毒素并增强了生物膜形成。据报道,鞭毛基因的表达在ΔhapR突变体中受到影响,在Δcrp突变体中也减少了。然而,上位性分析表明,cAMP-CRP通过一种独立于HapR的机制影响运动性。crp的失活抑制了多个据报道在体内被强烈诱导并影响霍乱弧菌在小肠定植和致病能力的基因的表达。这些基因包括编码外膜蛋白的ompU、ompT和ompW、肠道定植所需的替代sigma因子sigma(E),以及参与厌氧能量代谢的基因。我们的结果表明,CRP通过影响群体感应以及霍乱弧菌在人类宿主和环境中生存所需的多个基因,在霍乱弧菌的生命周期中发挥关键作用。