Disease transmission is a multifaceted process mediated by the interactions between the pathogen and host. Salmonella enterica serovars are important human pathogens that cause disease ranging from self-limiting gastroenteritis to persistent systemic infections, such as typhoid fever. Transmission occurs via the fecal-oral route, and epidemiological analyses have revealed heterogeneity in host transmission capabilities. However, relatively little is known about the factors that dictate pathogen shedding and transmission. A number of studies have described mechanisms of Salmonella enterica serovar Typhimurium expansion in mice postantibiotic treatment. However, these mechanisms have not been explored in the absence of antibiotic treatment. Although antibiotic treatment in humans enhances susceptibility to enteric pathogens such as S. Typhimurium and Clostridium difficile, Salmonella colonizes the gut in the absence of antibiotic treatment. Thus, it is important to study the mechanisms of S. Typhimurium emergence and expansion in non-antibiotic treated hosts. We use a mouse model to study molecular mechanisms of S. Typhimurium expansion in the mammalian gut in which ~20-30% of these mice shed ?108 CFU/g feces and readily transmit to nave cage mates. We hypothesized that alterations in the diet could influence pathogen shedding. To test this, we fed mice a high cholesterol diet at the time of infection. We have preliminary data demonstrating that high cholesterol diet increases S. Typhimurium shedding levels very rapidly. The long-term goal of this research proposal is to understand how S. Typhimurium usurps and manipulates the gut microbiome and host immune responses during colonization of the mammalian gut.
In Aim 1, we will identify host factors that promote cholesterol-dependent expansion of Salmonella in the distal gut.
In Aim 2, we will identify and characterize Salmonella factors required for expansion in the distal gut, and determine whether they are specific for expansion in mice fed a high cholesterol diet. These studies are aimed at gaining a better understanding of the molecular mechanisms of host-pathogen interactions during S. Typhimurium infections in the gut, and influence pathogen transmission. The expected results will lead to new methods of transmission control and to the rational design of therapeutics that will benefit public health.

Public Health Relevance

Many enteric pathogens that cause high levels of morbidity and mortality are spread via the fecal oral route. Thus, an increased understanding of the molecular mechanisms that influence fecal shedding and host-to-host transmission of infectious diseases will have a large impact on human health. !

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI131249-01A1
Application #
9455196
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Alexander, William A
Project Start
2018-06-01
Project End
2023-05-31
Budget Start
2018-06-01
Budget End
2019-05-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Stanford University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94304