Clostridium difficile is a major nosocomial pathogen that causes severe diarrheal disease that is highly infectious and difficult to treat. C. difficileis easily transmitted due to the formation and expulsion of contagious spores from infected hosts. The spore form of C. difficile is resistant to most disinfectants and is critical for the survival f the bacterium outside of the host. The only natural environment known to support C. difficile spore formation is the gastrointestinal tract, yet we know very little about how spore formation occurs. We hypothesize that sporulation of C. difficile is initiated in response to signals found within the host intestine, through unknown and unique genetic mechanisms. The long-term goal of this project is to uncover the intestinal environment triggers C. difficile sporulation. The specific objectives of this application are to identify the genetic mechanisms required for spore initiation and determine how sporulation is initiated in the host. Capitalizing on our previous experience with Bacillus subtilis sporulation, Gram-positive intestinal pathogenesis and C. difficile molecular genetics, we will meet these objectives through the experiments detailed in two specific aims. First, we will reveal the genetic mechanisms of spore initiation in C. difficile through genetic analysis of sporulation-defective mutants and newly identified early sporulation regulators. In parallel, we will evaluate the effects of identified and suspected sporulation-inducing compounds on the timing and frequency of spore formation. The research proposed in this application is innovative because it represents a departure from the model sporulation paradigm as the archetypal standard for spore initiation by C. difficile and seeks to uncover the unique mechanisms that regulate sporulation in this pathogen. The expected contribution of the proposed research is a detailed understanding of the genes required for spore initiation and the development of spores within the host. This contribution is significant because it is the first ste in the development of strategies to prevent spore formation by C. difficile.

Public Health Relevance

The experiments in this application are designed to uncover the mechanisms used by Clostridium difficile to form an infectious spore. The project is relevant to the NIH's mission of understanding and preventing bacterial infections and digestive diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI116933-03
Application #
9315097
Study Section
Host Interactions with Bacterial Pathogens Study Section (HIBP)
Program Officer
Ranallo, Ryan
Project Start
2015-08-01
Project End
2020-07-31
Budget Start
2017-08-01
Budget End
2018-07-31
Support Year
3
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Emory University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Nawrocki, Kathryn L; Wetzel, Daniela; Jones, Joshua B et al. (2018) Ethanolamine is a valuable nutrient source that impacts Clostridium difficile pathogenesis. Environ Microbiol 20:1419-1435
Woods, Emily C; Wetzel, Daniela; Mukerjee, Monjori et al. (2018) Examination of the Clostridioides (Clostridium) difficile VanZ ortholog, CD1240. Anaerobe :
Etienne-Mesmin, Lucie; Chassaing, Benoit; Adekunle, Oluwaseyi et al. (2017) Genome Sequence of a Toxin-PositiveClostridium difficileStrain Isolated from Murine Feces. Genome Announc 5:
Woods, Emily C; McBride, Shonna M (2017) Regulation of antimicrobial resistance by extracytoplasmic function (ECF) sigma factors. Microbes Infect 19:238-248
Edwards, Adrianne N; McBride, Shonna M (2017) Determination of the in vitro Sporulation Frequency of Clostridium difficile. Bio Protoc 7:
Edwards, Adrianne N; Tamayo, Rita; McBride, Shonna M (2016) A novel regulator controls Clostridium difficile sporulation, motility and toxin production. Mol Microbiol 100:954-71
Childress, Kevin O; Edwards, Adrianne N; Nawrocki, Kathryn L et al. (2016) The Phosphotransfer Protein CD1492 Represses Sporulation Initiation in Clostridium difficile. Infect Immun 84:3434-3444
Edwards, Adrianne N; McBride, Shonna M (2016) Isolating and Purifying Clostridium difficile Spores. Methods Mol Biol 1476:117-28
Woods, Emily C; Nawrocki, Kathryn L; Suárez, Jose M et al. (2016) The Clostridium difficile Dlt Pathway Is Controlled by the Extracytoplasmic Function Sigma Factor ?V in Response to Lysozyme. Infect Immun 84:1902-1916
Nawrocki, Kathryn L; Edwards, Adrianne N; Daou, Nadine et al. (2016) CodY-Dependent Regulation of Sporulation in Clostridium difficile. J Bacteriol 198:2113-30

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