Listeria monocytogenes is one of the most problematic causative agents of foodborne illness. Despite a relatively low number of cases, listeriosis is ranked as the deadliest and the fourth costliest foodborne disease in the USA among all diseases caused by bacterial, parasitic and viral foodborne pathogens. We have characterized a major regulatory system involving the second messenger, c-di-GMP, in L. monocytogenes and found that it plays unexpectedly important roles at the interface between the saprophitic and the pathogenic lifestyles of this bacterium. One of the consequences of elevated intracellular c-di-GMP levels is severe inhibition of mammalian cell invasion. This project is aimed at (i) deciphering the mechanism of c-di-GMP- dependent inhibition of cell invasion, which appears to involve key regulators of biosynthesis and virulence, and (ii) identifying natural compounds that strongly affect intracellular c-di-GMP levels in L. monocytogenes. This project is expected to shed light onto the interplay between c-di-GMP signaling, metabolism and virulence in L. monocytogenes that is emerging as a novel regulatory paradigm. Results of this project may also lead to identifying natural compounds that inhibit listerial invasiveness and therefore may be used to reduce frequency of listerial infections.

Public Health Relevance

Gomelsky, M, PI NARRATIVE Foodborne illnesses caused by the pathogenic bacterium, Listeria monocytogenes, result in thousands of hospitalizations, hundreds of deaths, and billions of dollars in financial losses. The proposed research is important to the public health mission of the NIH because it will uncover novel mechanisms linking signaling pathways to metabolism and virulence and because it may lead to identification of natural products that inhibit listerial virulence.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI135683-01
Application #
9437451
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Mills, Melody
Project Start
2018-01-01
Project End
2019-12-31
Budget Start
2018-01-01
Budget End
2018-12-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Wyoming
Department
Biochemistry
Type
Earth Sciences/Resources
DUNS #
069690956
City
Laramie
State
WY
Country
United States
Zip Code
82071
Xu, Gaoge; Han, Sen; Huo, Cuimei et al. (2018) Signaling specificity in the c-di-GMP-dependent network regulating antibiotic synthesis in Lysobacter. Nucleic Acids Res 46:9276-9288
Elbakush, Ahmed M; Miller, Kurt W; Gomelsky, Mark (2018) CodY-Mediated c-di-GMP-Dependent Inhibition of Mammalian Cell Invasion in Listeria monocytogenes. J Bacteriol 200: