New locus controlling suscept. to TB: genetics & funct.
Project Number5R01AI049421-04
Contact PI/Project LeaderKRAMNIK, IGOR
Awardee OrganizationHARVARD SCHOOL OF PUBLIC HEALTH
Description
Abstract Text
DESCRIPTION (provided by the applicant): It is projected that a total of 225
million new cases of tuberculosis will occur between 1998 and 2030. The outcome
of primary infection with Mycobacterium tuberculosis (MTB) varies and, in
immunocompetent hosts, imparts only a 10 percent lifetime risk of developing
clinical disease. The significant variation in tuberculosis susceptibility
among immunocompetent individuals remains unexplained. Differences in the
outcome of tuberculosis infection in the setting of similar risk factors
support a significant role of the host genetic background in predisposition to
progression towards clinical disease. Therefore, identification of genetic
factors associated with susceptibility to tuberculosis will have important
implications for controlling the disease.
We use a mouse experimental model of infection with virulent strain of MTB to
characterize genes that are responsible for control of tuberculosis infection
in immunocompetent hosts. We have identified and mapped to a 2 cM interval on
mouse chromosome 1 a novel locus (sst1) that significantly contributes to
control of growth of virulent MTB primarily in the lungs. Observations on its
phenotypic expression demonstrate that genetic mechanisms controlling infection
with virulent MTB are distinct from those that control an avirulent vaccine
strain of M bovis BCG. Having generated a set of sst1-congenic inbred strains
of mice, we propose to use them (1) to isolate the sst1-candidate genes by
positional cloning; (2) to identify genetic polymorphism responsible for
tuberculosis susceptibility; (3) to identify cells and functional pathways
affected by the sst1 polymorphism.
The proposed project will identify the nature and mechanism of action of the
sst1 in mice, which in the future should permit isolation of its human
homologue and the analysis of its role in tuberculosis susceptibility in
humans. The understanding of genetically determined mechanisms that operate
during the course of tuberculosis infection in the lung will provide new
insights into the pathogenesis of tuberculosis and suggest improved strategies
for treatment and prevention of the disease.
National Institute of Allergy and Infectious Diseases
CFDA Code
856
DUNS Number
149617367
UEI
UNVDZNFA8R29
Project Start Date
30-September-2001
Project End Date
30-June-2006
Budget Start Date
01-July-2004
Budget End Date
30-June-2005
Project Funding Information for 2004
Total Funding
$404,500
Direct Costs
$250,000
Indirect Costs
$154,500
Year
Funding IC
FY Total Cost by IC
2004
National Institute of Allergy and Infectious Diseases
$404,500
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01AI049421-04
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