Bordetella pertussis causes one of the most important human diseases, Pertussis or Whooping Cough, infecting tens of millions and killing hundreds of thousands of children annually. Although vaccines available in most industrialized countries are reasonably effective in preventing death and the most severe forms of disease, there is growing appreciation that the current acellular vaccines fail to prevent colonization, bacterial shedding and transmission between hosts, which allows B. pertussis to continue to circulate and cause disease and death in the most susceptible groups. There is little understanding of the mechanistic basis for transmission, either in terms of bacterial factors or host immune functions involved, and consequently, there is no agreed upon strategy to interfere with its ongoing circulation. Excitingly, recent work in our group now allows detailed analysis of the initial and highly contagious ?catarrhal phase? of the infection that is crucial for transmission of the pathogen and spread of the disease. Based on our novel mouse model of B. pertussis infection, that reproduces the catarrhal phase in mice, we will identify the bacterial factors that trigger host inflammatory response, mucus secretion and bacterial shedding and the factors required for the colonization of a new host. We will evaluate these factors for their potential to stimulate a robust host immune response and assess these proteins or epitopes thereof as vaccine components to prevent bacterial transmission. Supplementation of the currently used pertussis vaccines with these newly identified bacterial ?transmission factors? will not only protect against the disease but also block the rampant spread of the pathogen.

Public Health Relevance

We have developed a novel and innovative mouse model of infection that replicates most aspects of the catarrhal phase of B. pertussis infection, including inflammation of host mucosa, mucus production, profuse bacterial shedding from the nose of an infected host, and transmission between hosts. In the proposed study we will identify the bacterial factors involved in these important aspects of the infection process and examine candidates as vaccine components to prevent this stage that is critical for the ongoing transmission of this important reemerging pathogen.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56AI149787-01A1
Application #
10230869
Study Section
Host Interactions with Bacterial Pathogens Study Section (HIBP)
Program Officer
GU, Xin-Xing
Project Start
2020-09-01
Project End
2021-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Georgia
Department
Microbiology/Immun/Virology
Type
Schools of Veterinary Medicine
DUNS #
004315578
City
Athens
State
GA
Country
United States
Zip Code
30602