Vibrio cholerae causes the disease cholera and is a natural inhabitant of aquatic environments. Seasonal cholera outbreaks occur where the disease is endemic and can spread worldwide. V. cholerae?s ability to form biofilms, extracellular matrix-enclosed, surface-associated microbial communities, is crucial for its survival in aquatic habitats between epidemics and is advantageous for host-to-host transmission during epidemics. The objective of this proposal is to elucidate the molecular mechanisms of biofilm formation and biofilm-mediated hyperinfectivity.
In Aim 1, we will focus on understanding the mechanisms of V. cholerae biofilm matrix biogenesis. We recently characterized the V. cholerae biofilm matrix proteome and will determine the role of a prioritized set of the newly identified proteins in matrix biogenesis and function. We will also specifically analyze how biofilm biogenesis is impacted by bacterial outer membrane vesicles, which we found to be associated with the biofilm matrix, and identify the molecular determinants and the consequences of interactions between the identified exopolysaccharides, proteins, and lipid constituents of the biofilm matrix.
In Aim 2, we will determine the impact of environmental and host surfaces on biofilm formation and biofilm hyperinfectivity. Specifically, we will determine how newly identified V. cholerae adhesins impact biofilm formation on chitinous surfaces, and identify the molecular determinants of biofilm formation on chitinous surfaces. To gain insight into biofilm hyperinfectivity, we will analyze the molecular mechanisms underlying V. cholerae interaction with intestinal mucin, determine the spatial and temporal colonization dynamics of planktonic versus biofilm-grown cells, and evaluate the impact of biofilm matrix components on the colonization of the small intestine. A better understanding of the molecular principles of matrix biogenesis and biofilm hyperinfectivity will allow us to identify targets for the development of inhibitors of V. cholerae infection and transmission.

Public Health Relevance

Surface attached microbial communities, called biofilms, cause significant problems in environmental, industrial, and clinical settings. Vibrio cholerae, which causes the disease cholera, forms biofilms that are critical to its environmental survival, transmission, and infectivity. This research will improve our understanding of biofilm formation and biofilm-mediated hyperinfectivity, define targets to combat this deadly pathogen in both intestinal and aquatic ecosystems, and help develop tools for prediction and control of cholera epidemics.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
2R01AI114261-06
Application #
10053197
Study Section
Bacterial Pathogenesis Study Section (BACP)
Program Officer
Hall, Robert H
Project Start
2014-07-01
Project End
2025-05-31
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
6
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of California Santa Cruz
Department
Public Health & Prev Medicine
Type
Schools of Arts and Sciences
DUNS #
125084723
City
Santa Cruz
State
CA
Country
United States
Zip Code
95064
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Conner, Jenna G; Zamorano-Sánchez, David; Park, Jin Hwan et al. (2017) The ins and outs of cyclic di-GMP signaling in Vibrio cholerae. Curr Opin Microbiol 36:20-29
Joshi, Avatar; Kostiuk, Benjamin; Rogers, Andrew et al. (2017) Rules of Engagement: The Type VI Secretion System in Vibrio cholerae. Trends Microbiol 25:267-279
Fong, Jiunn Cn; Rogers, Andrew; Michael, Alicia K et al. (2017) Structural dynamics of RbmA governs plasticity of Vibrio cholerae biofilms. Elife 6:
Conner, Jenna G; Teschler, Jennifer K; Jones, Christopher J et al. (2016) Staying Alive: Vibrio cholerae's Cycle of Environmental Survival, Transmission, and Dissemination. Microbiol Spectr 4:
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Ruhe, Zachary C; Townsley, Loni; Wallace, Adam B et al. (2015) CdiA promotes receptor-independent intercellular adhesion. Mol Microbiol 98:175-92