Bacterial and host heterogeneity in TB latency, persistence and progression

Active Cooperative Agreement Awarded Last action

Award ID
U19AI162598
Recipient
Awarding agency
Obligated
$39,258,838

Award facts

Assistance listing
93.855 Allergy and Infectious Diseases Research
Completion date 88% complete
Originally
Funding
  • $36,507,304.00 Federal
  • $2,751,534.00 Non-federal
Place of performance
Newark, NJ 07103, USA

Award details come from USAspending.gov.

Description

Abstract
Overall until recently, tuberculosis (TB) has been viewed as a disease that progresses over several discrete stages, principally consisting of a period of infection followed by either active TB disease or a latent state with the potential for reactivation. Similarly, mycobacterium tuberculosis (MTB), the causative agent of TB, has been viewed as a relatively stable bacterium with little genomic diversity, predictable causes of antibiotic resistance, and phenotypic uniformity both during culture and within its infected host. However, recent findings, many spearheaded by the members of this application, have begun to discover unexpected heterogeneity in TB disease states, host responses, the genotypes and phenotypes of the bacteria, and among the apparently clonal infecting population of MTB. The premise for this program is that the heterogenous outcomes of TB infections and treatments are determined by the interplay between heterogeneous host-bacteria transcriptional and metabolic programs. Host and bacteria may be pre-programmed phenotypically or genetically to progress from TB infection to TB disease; and to do so rapidly or slowly; and, with or without extensive inflammation and lung damage. Immune tolerance, evasion or subversion may be another result of these interactions, which could lead to worsening disease and adverse treatment outcomes including relapse. Drug tolerance or resistance is another result of these interactions that may have widespread effects on treatment responses. Although MTB-host and MTB-drug interactions would seem to be unrelated, we will also study the possibility that immune and drug tolerant MTB share a number of transcriptional and metabolic programs; and thus, also share some of the same vulnerabilities that could provide therapeutic targets. Consisting of 4 projects and 3 cores, this program will be accomplished in the following specific aims: 1) to determine the effects of bacterial and host heterogeneity on the manifestations, progression and consequences of close exposure to TB in the household, and of active TB. Addressed in project 1: bacterial and host determinants of progression, manifestations and consequences of TB. 2) to uncover the immunological mechanisms underlying the diverse clinical outcomes in hosts infected with high and low transmission strains of MTB. Addressed in project 2: immune determinants of the course of MTB infection and disease. 3) to define the host immune pathways that induce drug tolerance and identify potential routes to therapeutic intervention. Addressed in project 3: minimizing in vivo drug tolerance induction in TB. 4) to define bacterial factors that contribute to the heterogeneous expression of drug tolerance and characterize links with adverse treatment outcomes. Addressed in project 4. Drug tolerance, bacterial heterogeneity and adverse TB treatment outcomes.

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Original award $2,751,534 $2,751,534
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Subawards

Subrecipient Amount Awarded
Irmandade DA Santa Casa De Misericordia De Vitoria Bacterial and Host Heterogeneity in TB latency, persistence and progression $38,013
University Of Georgia Research Foundation, Inc. $29,543
Weill Medical College Of Cornell University $101,700
Cornell University $349,311
University Of Washington $298,823
Frontier Science & Technology Research Foundation, Inc. $16,680
University Of Massachusetts Medical School $21,750
Seattle Children's Hospital $139,500
University Of Massachusetts Medical School $351,793
Makerere University College Of Health Sciences $128,382
Weill Medical College Of Cornell University $101,700
Irmandade DA Santa Casa De Misericordia De Vitoria $47,565
University Of Georgia Research Foundation, Inc. $29,543
University Of Washington $292,558
Cornell University $349,311
Makerere University College Of Health Sciences $40,799
University Of Massachusetts Medical School $351,792
Seattle Children's Hospital $139,500
Frontier Science & Technology Research Foundation, Inc. $16,195
University Of Massachusetts Medical School $21,750
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Quick answers

Who received award U19AI162598?

U19AI162598 was awarded to Rutgers The State University Of New Jersey by National Institute of Allergy and Infectious Diseases (National Institutes of Health) on September 23, 2021.

How much is award U19AI162598 worth?

$39,258,838 has been obligated on U19AI162598: $36,507,304 in federal funding and $2,751,534 in non-federal funding.

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