Epidemic typhus, one of the most deadly bacterial diseases affecting humans, is caused by the louse-borne pathogen, Rickettsia prowazekii. Due to the high mortality rate of this disease, the lack of an effective vaccine, and the possibility o aerosol dissemination, R. prowazekii is designated as a select agent and has the potential to pose a severe threat to public health and safety. R. prowazekii is an obligate intracellular, parasitic bacterium that only grows within the cytosol of the host cell, unbounded by a vacuolar membrane. This ability to exploit the intracytoplasmic environment and cause serious human disease provides the basis for our continuing studies to elucidate the mechanisms underlying R. prowazekii virulence and how they impact obligate intracellular growth. This proposal builds upon our success in developing new methods to genetically manipulate R. prowazekii and isolate mutants for characterization.
In Specific Aim 1 we will employ these techniques to delete a defined subset of genes hypothesized to affect R. prowazekii virulence including enzymes with membranolytic activities, surface-exposed proteins, and protein modifying enzymes. Gene deletions will be generated using proven homologous recombination methods. Mutants will be assessed for gene-specific phenotypes, alterations in growth and morphology, as well as for virulence-associated phenotypes, such as efficient replication in macrophages and the ability to cause fever and weight loss in an animal infection model. These studies will contribute to the identification of new targets for antimicrobial therapy and vaccines.
In Specific Aim 2 we will build upon our recent advances to develop and apply new genetic tools fundamentally important for dissecting rickettsial gene function. We have successfully introduced a new recombinant plasmid into R. prowazekii that provides an extrachromosomal platform for recombinant gene expression and allows us to assign phenotypes to specific genes, as well as characterize essential genes. In addition, this platform will be used to develop regulated gene expression systems in R. prowazekii by examining the expression of a fluorescent protein placed under the control of a variety of potential control elements. Our proven ability to overcome the roadblocks in the genetic manipulation of R. prowazekii and the development of new detection and isolation techniques will accelerate our gene-by-gene dissection of systems that dictate rickettsial virulence and intracellular growth.

Public Health Relevance

Rickettsia prowazekii is the louse-borne agent of epidemic typhus. The potential for aerosol transmission coupled with the severity of the disease and lack of an approved vaccine make this select agent a potential bioweapon. The goal of this proposal is to dissect the mechanisms this human pathogen uses to cause disease and to identify novel targets for new antimicrobial or vaccine therapies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI020384-30
Application #
8899398
Study Section
Bacterial Pathogenesis Study Section (BACP)
Program Officer
Perdue, Samuel S
Project Start
1983-07-01
Project End
2017-08-31
Budget Start
2015-09-01
Budget End
2017-08-31
Support Year
30
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of South Alabama
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
172750234
City
Mobile
State
AL
Country
United States
Zip Code
36688
McClure, Erin E; Chávez, Adela S Oliva; Shaw, Dana K et al. (2017) Engineering of obligate intracellular bacteria: progress, challenges and paradigms. Nat Rev Microbiol 15:544-558
Driskell, Lonnie O; Tucker, Aimee M; Woodard, Andrew et al. (2016) Fluorescence Activated Cell Sorting of Rickettsia prowazekii-Infected Host Cells Based on Bacterial Burden and Early Detection of Fluorescent Rickettsial Transformants. PLoS One 11:e0152365
Wood, David O; Wood, Raphael R; Tucker, Aimee M (2014) Genetic systems for studying obligate intracellular pathogens: an update. Curr Opin Microbiol 17:11-6
Wood, David O; Hines, Andria; Tucker, Aimee M et al. (2012) Establishment of a replicating plasmid in Rickettsia prowazekii. PLoS One 7:e34715
Clark, Tina R; Lackey, Amanda M; Kleba, Betsy et al. (2011) Transformation frequency of a mariner-based transposon in Rickettsia rickettsii. J Bacteriol 193:4993-5
Woodard, Andrew; Wood, David O (2011) Analysis of convergent gene transcripts in the obligate intracellular bacterium Rickettsia prowazekii. PLoS One 6:e16537
Tucker, Aimee M; Driskell, Lonnie O; Pannell, Lewis K et al. (2011) Differential proteomic analysis of Rickettsia prowazekii propagated in diverse host backgrounds. Appl Environ Microbiol 77:4712-8
Driskell, Lonnie O; Yu, Xue-jie; Zhang, Lihong et al. (2009) Directed mutagenesis of the Rickettsia prowazekii pld gene encoding phospholipase D. Infect Immun 77:3244-8
Liu, Zhi-Mei; Tucker, Aimee M; Driskell, Lonnie O et al. (2007) Mariner-based transposon mutagenesis of Rickettsia prowazekii. Appl Environ Microbiol 73:6644-9
Tucker, Aimee M; Pannell, Lewis K; Wood, David O (2005) Dissecting the Rickettsia prowazekii genome: genetic and proteomic approaches. Ann N Y Acad Sci 1063:35-46

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