Loading…

Loading grant details…

Active NON-SBIR/STTR RPGS NIH (US)

Mtb strain-dependent mechanisms of pathogenesis in mouse models


Funder NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
Recipient Organization University of Washington
Country United States
Start Date Aug 01, 2021
End Date May 31, 2026
Duration 1,764 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10845583
Grant Description

Tuberculosis (TB) is a highly heterogeneous human disease that develops in some, but not all, individuals who inhale 1-3 infectious bacilli of Mycobacterium tuberculosis (Mtb). TB disease can range from pulmonary disease that is mild and self-resolving, to severe, or can disseminate to extrapulmonary sites. Understanding the complexity of TB pathogenesis requires a holistic

approach that integrates human and animal model studies. Although there is growing evidence that Mtb strain-dependent factors drive different infection outcomes, the in vivo mechanisms that govern these outcomes are poorly understood. In this project, we start with clinical Mtb strains associated with different pathogenic outcomes (e.g., high transmission or disseminated disease)

or mutant strains harboring modifications in gene candidates, identified in Core A and Project 1, to identify polymorphisms in Mtb strains associated with distinct human clinical outcomes. Mice infected with these clinical or mutant Mtb strains will be used to investigate how they govern three distinct stages of pathogenesis: 1) establishing infection at the site of aerosol

inhalation, 2) dissemination to distant sites, and 3) interactions with host immunity in distinct lung macrophage populations. These studies will leverage our group’s recent advances in mouse TB models, including identifying the earliest cellular events after aerosol Mtb infection, tracking Mtb dissemination using a physiologic, ultra low-dose (ULD) infection model in which

mice are infected with 1-3 CFUs of aerosolized Mtb, and assessing paired host and Mtb transcriptomes in distinct pulmonary macrophage types. Multiparameter confocal microscopy and advanced quantitative image analysis will be used to determine how these Mtb strain- dependent factors shape immune cell interactions at infection sites. The overall goal of the

proposed experiments is to gain insight into molecular and cellular mechanisms of pathogenesis at distinct stages of Mtb infection to inform development of novel host- and pathogen-directed interventions.

All Grantees

University of Washington

Advertisement
Apply for grants with GrantFunds
Advertisement
Browse Grants on GrantFunds
Interested in applying for this grant?

Complete our application form to express your interest and we'll guide you through the process.

Apply for This Grant