The long range goal of the proposed work is to define the molecular components and mechanisms mediating Vibrio cholerae colonization and virulence protein secretion to the point where there is sufficient knowledge to intelligently incorporate this information into improved cholera vaccine strategies and antimicrobial therapies designed to inhibit these events. Most of the proposal involves analysis of the molecular mechanisms by which toxin coregulated pilus (TCP) is formed and mediates intestinal colonization. Some steps in the process by which TCP and other type 4 pili are built are linked and/or related to the process of toxin and other virulence determinant secretion by type II secretion systems. Thus further understanding of the mechanisms of type 4 pilus biogenesis should lead to the characterization of potential antimicrobial targets involved in multiple virulence pathways. We will examine the aspects of pilus biogenesis in detail. These experiments will be facilitated by our currently available collections of tcp genetic constructs and immunoreagents. Regarding the mechanism of TCP function, we will utilize the technique of field emission scanning electron microscopy in combination with specifically engineered tcpA missense mutations to address the biophysical mechanisms that lead to pilus supertwist formation, promoting the bacterial associations that represent the basis of microcolony formation in the intestine. Further characterization of TcpF and its role in colonization will be undertaken. TcpF has become even more interesting with the identification by other labs of genes in two other pilus operons that are located in the same position as tcpF and that encode secreted proteins that have no homology amongst themselves. Lastly we will build upon our identification of a new V. cholerae colonization factor that links the epithelial steps of intestinal colonization with environmental persistence and quorum sensing to understand the mechanism by which the new factor, GbpA, functions and is modulated by the quorum sensing system. Additional steps in the epithelial interaction with V. cholerae will be defined. Taken together, the results of the proposed studies will provide detailed information regarding the mechanisms of V. cholerae colonization from the levels of defining the components, understanding how they are elaborated to the cell surface and beyond, and even addressing the biophysical nature of pilus interactions that are essential for microcolony formation and disease. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37AI025096-23
Application #
7385017
Study Section
Special Emphasis Panel (ZRG1-IDM-H (02))
Program Officer
Hall, Robert H
Project Start
1987-07-01
Project End
2012-04-30
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
23
Fiscal Year
2008
Total Cost
$473,312
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
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
Gao, Yang; Hauke, Caitlyn A; Marles, Jarrad M et al. (2016) Effects of tcpB Mutations on Biogenesis and Function of the Toxin-Coregulated Pilus, the Type IVb Pilus of Vibrio cholerae. J Bacteriol 198:2818-28
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:
Megli, Christina J; Taylor, Ronald K (2013) Secretion of TcpF by the Vibrio cholerae toxin-coregulated pilus biogenesis apparatus requires an N-terminal determinant. J Bacteriol 195:2718-27
Son, Mike S; Taylor, Ronald K (2012) Growth and maintenance of Escherichia coli laboratory strains. Curr Protoc Microbiol Chapter 5:Unit 5A.4.
Son, Mike S; Taylor, Ronald K (2011) Preparing DNA libraries for multiplexed paired-end deep sequencing for Illumina GA sequencers. Curr Protoc Microbiol Chapter 1:Unit 1E.4
Krebs, Shelly J; Taylor, Ronald K (2011) Protection and attachment of Vibrio cholerae mediated by the toxin-coregulated pilus in the infant mouse model. J Bacteriol 193:5260-70
Megli, Christina J; Yuen, Alex S W; Kolappan, Subramaniapillai et al. (2011) Crystal structure of the Vibrio cholerae colonization factor TcpF and identification of a functional immunogenic site. J Mol Biol 409:146-58
Krebs, Shelly J; Taylor, Ronald K (2011) Nutrient-dependent, rapid transition of Vibrio cholerae to coccoid morphology and expression of the toxin co-regulated pilus in this form. Microbiology 157:2942-53

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