Persistent colonization is a key facet of microbe-host interactions. Little is known about the mechanisms that allow a bacterium to persistently colonize its host. We have developed a mouse model for dissecting bacterial and host determinants of persistent colonization. It pairs a commensal of wild mice, Neisseria musculi, with the lab mouse, which is not naturally colonized with Neisseria. N. musculi is closely related to commensal and pathogenic species of Neisseria, and encode many host interaction factors and vaccine candidates of these pathogens. A single oral dose of N. musculi results in persistent, asymptomatic colonization of the oral cavity and gut of the mouse for at least 1 year. Colonization requires not only the Type IV pilus (Tfp) fiber but also retraction of the fiber. ?pilE, which does not express the pilus fiber subunit and ?pilT, which does not express the pilus retraction motor, both fail to colonize mice. Here, we will use our newly developed model to examine the role of Tfp retraction on N. musculi colonization and persistence. We will also use spectral imaging Fluorescence In Situ Hybridization (FISH) to locate and characterize the biofilms formed by N. musculi and its Tfp retraction mutant in the mouse alimentary tract.

Public Health Relevance

Persistent colonization is a key facet of microbe-host interactions. Little is known about the mechanisms that mediate persistent colonization by commensal and pathogenic Neisseria, due to the absence of an animal model that recapitulates these events in their cognate hosts. We have developed a powerful mouse model that avoids barriers imposed by host restriction, allowing identification of neisserial and host determinants of persistent colonization. We will use this model to dissect the role of Type IV pilus retraction in colonzation and persistence. We will also use the powerful new technique of spectral imaging Fluorescence In Situ Hybridation (FISH) to characterize the biogeography of Neisseria in the mouse alimentary tract.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21AI144763-02
Application #
9884734
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Vincent, Leah Rebecca
Project Start
2019-03-05
Project End
2021-02-28
Budget Start
2020-03-01
Budget End
2021-02-28
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Arizona
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721