The goal of this research is to discern mechanisms by which the environment within the human host are responsible for inducing expression of specific genes of infecting bacteria. The model system to be analyzed is the Vibrio cholerae ToxR regulon, for which a number of parameters that induce gene expression as well as many of the genes involved have been identified. ToxR can be thought of as an integral membrane protein positioned centrally in a regulatory scheme where it receives signals perhaps via small molecules and through protein-protein interactions that allow ultimate control of gene expression through a regulatory cascade. ToxR spans the bacterial cytoplasmic membrane and in this configuration is able to directly activate expression of a number of host specific genes. Some of these gene products are directly involved in allowing the bacteria to colonize and express an ADP-ribosylating exotoxin that stimulates the activity of host membrane adenylate cyclase. Another gene that ToxR activates, toxT, also encodes an activator protein of the AraC family that is cytoplasmically located. In turn, this protein activates additional genes including itself and colonization factors required for maintenance of an infected state. Thus, there is a hierarchy of gene expression that responds to the host to initiate and maintain infection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI039654-02
Application #
2429501
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Project Start
1996-06-01
Project End
2001-05-31
Budget Start
1997-06-01
Budget End
1998-05-31
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Dartmouth College
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
Kovacikova, Gabriela; Lin, Wei; Taylor, Ronald K et al. (2017) The Fatty Acid Regulator FadR Influences the Expression of the Virulence Cascade in the El Tor Biotype of Vibrio cholerae by Modulating the Levels of ToxT via Two Different Mechanisms. J Bacteriol 199:
Privett, Britney R; Pellegrini, Maria; Kovacikova, Gabriela et al. (2017) Identification of a Small Molecule Activator for AphB, a LysR-Type Virulence Transcriptional Regulator in Vibrio cholerae. Biochemistry 56:3840-3849
Midgett, Charles R; Almagro-Moreno, Salvador; Pellegrini, Maria et al. (2017) Bile salts and alkaline pH reciprocally modulate the interaction between the periplasmic domains of Vibrio cholerae ToxR and ToxS. Mol Microbiol 105:258-272
Shi, Wei; Kovacikova, Gabriela; Lin, Wei et al. (2015) The 40-residue insertion in Vibrio cholerae FadR facilitates binding of an additional fatty acyl-CoA ligand. Nat Commun 6:6032
Almagro-Moreno, Salvador; Kim, Tae K; Skorupski, Karen et al. (2015) Proteolysis of virulence regulator ToxR is associated with entry of Vibrio cholerae into a dormant state. PLoS Genet 11:e1005145
Almagro-Moreno, Salvador; Pruss, Kali; Taylor, Ronald K (2015) Intestinal Colonization Dynamics of Vibrio cholerae. PLoS Pathog 11:e1004787
Almagro-Moreno, Salvador; Root, Michael Z; Taylor, Ronald K (2015) Role of ToxS in the proteolytic cascade of virulence regulator ToxR in Vibrio cholerae. Mol Microbiol 98:963-76
Almagro-Moreno, Salvador; Taylor, Ronald K (2013) Cholera: Environmental Reservoirs and Impact on Disease Transmission. Microbiol Spectr 1:
Cerda-Maira, Francisca A; Kovacikova, Gabriela; Jude, Brooke A et al. (2013) Characterization of BreR interaction with the bile response promoters breAB and breR in Vibrio cholerae. J Bacteriol 195:307-17
Taylor, Jennifer L; De Silva, Rukman S; Kovacikova, Gabriela et al. (2012) The crystal structure of AphB, a virulence gene activator from Vibrio cholerae, reveals residues that influence its response to oxygen and pH. Mol Microbiol 83:457-70

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