Listeria monocytogenes physiology and host pathogen interactions
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Principal Investigator: Joshua Woodward Organization: UNIVERSITY OF WASHINGTON Fiscal Year: 2019 Award: $389,875 Funding agency: National Institute of Allergy and Infectious Diseases DESCRIPTION (provided by applicant): Listeria monocytogenes is a gram-positive, opportunistic, intracellular bacterial pathogen that causes food borne illness. Given its well-characterized infection cycle and genetic amenability, L. monocytogenes provides a powerful tool to interrogate the fundamental aspects of intracellular bacterial pathogenesis and the host immune response to invasion by intracellular pathogens. It has previously been demonstrated that L. monocytogenes that enter into the host cell cytosol secrete a signaling nucleotide, c-di-AMP, resulting in stimulation of host IFN-ß production. Our preliminary studies have uncovered important roles for c-di-AMP signaling in the ability of the bacterium to grow in broth and within the host. Furthermore, evidence suggests c-di-AMP may have functional consequences beyond IFN-ß induction by the infected host cell. Using proteomics and genetic studies we have identified novel bacterial and host pathways that may mediate the numerous phenotypes associated with this unique bacterial signaling molecule. In Aim I, we propose to explore the role of a bacterial small RNA regulated by c-di-AMP and required for Listeria virulence. In Aim II, we will characterize the role of three c-di-AMP binding proteins in mediating signal transduction. In the final aim, we will characterize the effects of c-di-AMP binding to a novel host protein and elucidate the effects of these interactions on the outcome of infection. Together these studies will define the molecular mechanisms of c-di-AMP signaling that mediate host pathogen interactions during infection by this intracellular bacterium. Terms: <5'-Adenylic acid><Address><Adenosine Monophosphate><Adenylic Acid><Affect><Affinity><Antibiotic susceptibility><Attenuated><Autoregulation><Bacteria><Bacterial Infections><Bacterial Physiology><Behavior><Binding><Binding Proteins><Bio-Informatics><Biochemical><Bioinformatics><Biological Function><Biological Process><C trachomatis><C. trachomatis><Cell Body><Cell Communication and Signaling><Cell Signaling><Cell Wall><Cells><Chemicals><Chlamydia trachomatis><Computer Models><Computer Simulation><Computer based Simulation><Computerized Models><Cyclicity><Cytosol><Detection><Disease><Disorder><Endogenous Interferon Beta><Exhibits><Face><Family><Fibroblast Interferon><Gene Expression Monitoring><Gene Expression Pattern Analysis><Gene Expression Profiling><Gene Transcription><Generalized Growth><Genetic><Genetic Transcription><Genetic study><Growth><Health><Homeostasis><Human><IFN-Beta><IFN-β><IFNb><IMiD><Immune><Immune response><Immune system><Immunes><Immunity><Immunologic Receptors><Immunological Receptors><Immunological response><Immunomodulators><Infection><Innate Immune Response><Innate Immune System><Interferon-beta><Interferon-β><Intermediary Metabolism><Intracellular Communication and Signaling><Intracellular Second Messenger><L monocytogenes><L. monocytogenes><Ligand Binding Protein><Ligand Binding Protein Gene><Listeria><Listeria Infections><Listeria monocytogenes><Listeriosis><Liver><M tb><M tuberculosis><M. tb><M. tuberculosis><M.tb><M.tuberculosis><Mathematical Model Simulation><Mathematical Models and Simulations><Mediating><Messenger RNA><Metabolic><Metabolic Processes><Metabolism><Modeling><Modern Man><Molecular><Molecular Interaction><Molecular Target><Mycobacterium tuberculosis><Natural Interferon Beta><Natural human interferon beta><Nucleotides><Organism><Outcome><Pathogenesis><Pathogenicity Factors><Pathway interactions><Periodicity><Phenotype><Physiological Homeostasis><Physiology><Production><Protein Binding><Proteins><Proteomics><Public Health><Quantitative RTPCR><Quantitative Reverse Transcriptase PCR><RNA Expression><Regulation><Rhythmicity><Rickettsia trachomae><Role><Second Messenger Systems><Second Messengers><Signal Transduction><Signal Transduction Pathway><Signal Transduction Systems><Signaling><Signaling Molecule><Small RNA><Structure><System><Testing><Tissue Growth><Transcript><Transcript Expression Analyses><Transcript Expression Analysis><Transcription><Virulence><Virulence Factors><allergic/immunologic body system><allergic/immunologic organ system><anti-microbial><antimicrobial><bacteria infection><bacterial disease><bacterial pathogen><biological signal transduction><bound protein><cellular development><computational modeling><computational models><computational simulation><computer based models><computerized modeling><computerized simulation><develop a vaccine><development of a vaccine><faces><facial><food-born><food-born illness><food-borne><food-borne disease><food-borne illness><foodborn><foodborn illness><foodborne><foodborne disease><foodborne illness><gene expression analysis><gene expression assay><hepatic body system><hepatic organ system><host response><human pathogen><immune modulating agents><immune modulating drug><immune modulating therapeutics><immune modulatory agents><immune modulatory drugs><immune receptor><immunomodulating agents><immunomodulatory agents><immunomodulatory drugs><immunomodulatory therapeutics><immunoresponse><in silico><in vivo Model><living system><mRNA><macrophage><member><molecular recognition><mtb><novel><ontogeny><pathogen><pathogenic bacteria><pathway><protein function><public health relevance><qRTPCR><response><signal transduction second messengers><social role><tissue culture><tool><transcriptional profiling><vaccine development><vaccine formulation><virtual simulation>