Role of Cyclic Di-GMP during El Tor Biotype Vibrio cholerae Infection: Characterization of the In Vivo-Induced Cyclic Di-GMP Phosphodiesterase CdpA

• Published in: Infection and Immunity Vol. 76; no. 4; pp. 1617 - 1627
• Main Authors: Tamayo, Rita, Schild, Stefan, Pratt, Jason T, Camilli, Andrew
• Format: Journal Article
• Language: English
• Published: Washington, DC American Society for Microbiology 01.04.2008; American Society for Microbiology (ASM)
• Subjects: Animals; Bacterial Proteins - chemistry; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Bacterial Typing Techniques; Bacteriology; Biofilms; Biological and medical sciences; Cholera - microbiology; Cyclic GMP - analogs & derivatives; Cyclic GMP - metabolism; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation, Bacterial - physiology; Mice; Microbiology; Miscellaneous; Molecular Pathogenesis; Phosphoric Diester Hydrolases - chemistry; Phosphoric Diester Hydrolases - genetics; Phosphoric Diester Hydrolases - metabolism; Protein Structure, Tertiary; Vibrio cholerae; Vibrio cholerae - classification; Vibrio cholerae - enzymology; Bacteria; Vibrionaceae; Vibrio cholerae elTor
• ISSN: 0019-9567; 1098-5522
• DOI: 10.1128/IAI.01337-07

In Vibrio cholerae, the second messenger cyclic di-GMP (c-di-GMP) positively regulates biofilm formation and negatively regulates virulence and is proposed to play an important role in the transition from persistence in the environment to survival in the host. Herein we describe a characterization of the infection-induced gene cdpA, which encodes both GGDEF and EAL domains, which are known to mediate diguanylate cyclase and c-di-GMP phosphodiesterase (PDE) activities, respectively. CdpA is shown to possess PDE activity, and this activity is regulated by its inactive degenerate GGDEF domain. CdpA inhibits biofilm formation but has no effect on colonization of the infant mouse small intestine. Consistent with these observations, cdpA is expressed during in vitro growth in a biofilm but is not expressed in vivo until the late stage of infection, after colonization has occurred. To test for a role of c-di-GMP in the early stages of infection, we artificially increased c-di-GMP and observed reduced colonization. This was attributed to a significant reduction in toxT transcription during infection. Cumulatively, these results support a model of the V. cholerae life cycle in which c-di-GMP must be down-regulated early after entering the small intestine and maintained at a low level to allow virulence gene expression, colonization, and motility at appropriate stages of infection.