1887

Abstract

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 Δ mutant of El Tor biotype . 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 Δ mutant produced more cholera toxin and enhanced biofilm. Expression of flagellar genes, reported to be affected in Δ mutants, was diminished in the Δ mutant. However, an epistasis analysis indicated that cAMP–CRP affects motility by a mechanism independent of HapR. Inactivation of inhibited the expression of multiple genes reported to be strongly induced and to affect the ability of to colonize the small intestine and cause disease. These genes included , and encoding outer-membrane proteins, the alternative sigma factor required for intestinal colonization, and genes involved in anaerobic energy metabolism. Our results indicate that CRP plays a crucial role in the life cycle by affecting quorum sensing and multiple genes required for survival of in the human host and the environment.

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2007-09-01
2019-08-23
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vol. , part 9, pp. 2964 - 2975

complete list of differentially expressed genes in the Βcrp mutant [ .xls file] (624 kb)



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