R01HL155547
Project Grant
Overview
Grant Description
MYCOBACTERIAL LUNG DISEASES IN VIRGINIA: SEQUENCING AND CLINICAL DETERMINANTS OF RELAPSE AND OUTCOME - PROJECT SUMMARY / ABSTRACT
NONTUBERCULOUS MYCOBACTERIAL LUNG DISEASES, PRIMARILY DUE TO M. AVIUM COMPLEX (MAC), IS AN INCREASING CLINICAL PROBLEM NATIONWIDE AND NOW OVERTAKES DOMESTIC TB IN TERMS OF MORBIDITY AND MORTALITY. IT IS ALSO HARDER TO TREAT AND RESULTS IN POORER OUTCOMES DESPITE LONGER DRUG REGIMENS.
IN THIS CONTEXT NIH ISSUED A NOTICE AI-17-016 TO REQUEST APPLICATIONS FOR NTM DISEASES. HERE WE PRESENT A PROPOSAL FROM THE UNIVERSITY OF VIRGINIA, WITH COLLABORATORS AT THE VIRGINIA DEPARTMENT OF HEALTH AND VIRGINIA TECH, THAT ADDRESSES MANY OF THE NEEDS THAT WERE CITED.
FIRST, WE WILL PERFORM WHOLE GENOME SEQUENCING OF MAC ISOLATES FROM ALL OF OUR STATE'S MAC LUNG DISEASE PATIENTS TO DISCERN RELAPSE VERSUS REINFECTION AND THE ENVIRONMENTAL SOURCES OF ACQUISITION. SECOND WE WILL UTILIZE A STATE-WIDE COHORT OF NEW MAC LUNG DISEASE PATIENTS TO CORRELATE CLINICAL OUTCOMES WITH MAC SPECIES, DRUG SUSCEPTIBILITY, SERUM DRUG LEVELS, AND BIOFILM BIOASSAY.
INNOVATION INCLUDES THE USE OF A STATE-WIDE EPIDEMIOLOGICAL COHORT, EXQUISITE RESOLUTION WITH EXTENSIVE PRELIMINARY DATA OF WHOLE GENOME SEQUENCING TO DISCERN SPECIES AND MIXED INFECTIONS, A COMPREHENSIVE STATE-WIDE SERUM DRUG MONITORING PROGRAM (AS WE HAVE DONE ALREADY FOR TB), AND EXPERTISE IN MOLECULAR DIAGNOSTICS AND GENOTYPIC-PHENOTYPIC CORRELATIONS.
IN SUM, FOR THIS MOST VEXING CLINICAL PROBLEM OF MAC LUNG DISEASE WE BRING TO BEAR EXTENSIVE PRELIMINARY DATA, UNIQUE EXPERTISE, INNOVATIVE TECHNOLOGY, COHESIVE COLLABORATIONS, AND SYNERGISTIC AIMS.
NONTUBERCULOUS MYCOBACTERIAL LUNG DISEASES, PRIMARILY DUE TO M. AVIUM COMPLEX (MAC), IS AN INCREASING CLINICAL PROBLEM NATIONWIDE AND NOW OVERTAKES DOMESTIC TB IN TERMS OF MORBIDITY AND MORTALITY. IT IS ALSO HARDER TO TREAT AND RESULTS IN POORER OUTCOMES DESPITE LONGER DRUG REGIMENS.
IN THIS CONTEXT NIH ISSUED A NOTICE AI-17-016 TO REQUEST APPLICATIONS FOR NTM DISEASES. HERE WE PRESENT A PROPOSAL FROM THE UNIVERSITY OF VIRGINIA, WITH COLLABORATORS AT THE VIRGINIA DEPARTMENT OF HEALTH AND VIRGINIA TECH, THAT ADDRESSES MANY OF THE NEEDS THAT WERE CITED.
FIRST, WE WILL PERFORM WHOLE GENOME SEQUENCING OF MAC ISOLATES FROM ALL OF OUR STATE'S MAC LUNG DISEASE PATIENTS TO DISCERN RELAPSE VERSUS REINFECTION AND THE ENVIRONMENTAL SOURCES OF ACQUISITION. SECOND WE WILL UTILIZE A STATE-WIDE COHORT OF NEW MAC LUNG DISEASE PATIENTS TO CORRELATE CLINICAL OUTCOMES WITH MAC SPECIES, DRUG SUSCEPTIBILITY, SERUM DRUG LEVELS, AND BIOFILM BIOASSAY.
INNOVATION INCLUDES THE USE OF A STATE-WIDE EPIDEMIOLOGICAL COHORT, EXQUISITE RESOLUTION WITH EXTENSIVE PRELIMINARY DATA OF WHOLE GENOME SEQUENCING TO DISCERN SPECIES AND MIXED INFECTIONS, A COMPREHENSIVE STATE-WIDE SERUM DRUG MONITORING PROGRAM (AS WE HAVE DONE ALREADY FOR TB), AND EXPERTISE IN MOLECULAR DIAGNOSTICS AND GENOTYPIC-PHENOTYPIC CORRELATIONS.
IN SUM, FOR THIS MOST VEXING CLINICAL PROBLEM OF MAC LUNG DISEASE WE BRING TO BEAR EXTENSIVE PRELIMINARY DATA, UNIQUE EXPERTISE, INNOVATIVE TECHNOLOGY, COHESIVE COLLABORATIONS, AND SYNERGISTIC AIMS.
Funding Goals
THE DIVISION OF LUNG DISEASES SUPPORTS RESEARCH AND RESEARCH TRAINING ON THE CAUSES, DIAGNOSIS, PREVENTION, AND TREATMENT OF LUNG DISEASES AND SLEEP DISORDERS. RESEARCH IS FUNDED THROUGH INVESTIGATOR-INITIATED AND INSTITUTE-INITIATED GRANT PROGRAMS AND THROUGH CONTRACT PROGRAMS IN AREAS INCLUDING ASTHMA, BRONCHOPULMONARY DYSPLASIA, CHRONIC OBSTRUCTIVE PULMONARY DISEASE, CYSTIC FIBROSIS, RESPIRATORY NEUROBIOLOGY, SLEEP AND CIRCADIAN BIOLOGY, SLEEP-DISORDERED BREATHING, CRITICAL CARE AND ACUTE LUNG INJURY, DEVELOPMENTAL BIOLOGY AND PEDIATRIC PULMONARY DISEASES, IMMUNOLOGIC AND FIBROTIC PULMONARY DISEASE, RARE LUNG DISORDERS, PULMONARY VASCULAR DISEASE, AND PULMONARY COMPLICATIONS OF AIDS AND TUBERCULOSIS. THE DIVISION IS RESPONSIBLE FOR MONITORING THE LATEST RESEARCH DEVELOPMENTS IN THE EXTRAMURAL SCIENTIFIC COMMUNITY AS WELL AS IDENTIFYING RESEARCH GAPS AND NEEDS, OBTAINING ADVICE FROM EXPERTS IN THE FIELD, AND IMPLEMENTING PROGRAMS TO ADDRESS NEW OPPORTUNITIES. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, USE SMALL BUSINESS TO MEET FEDERAL RESEARCH AND DEVELOPMENT NEEDS, FOSTER AND ENCOURAGE PARTICIPATION IN INNOVATION AND ENTREPRENEURSHIP BY SOCIALLY AND ECONOMICALLY DISADVANTAGED PERSONS, AND INCREASE PRIVATE-SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT FUNDING. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, FOSTER TECHNOLOGY TRANSFER THROUGH COOPERATIVE R&D BETWEEN SMALL BUSINESSES AND RESEARCH INSTITUTIONS, AND INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL R&D.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Virginia
United States
Geographic Scope
State-Wide
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 349% from $721,114 to $3,237,702.
Rector & Visitors Of The University Of Virginia was awarded
Genomic Analysis of MAC Lung Disease in Virginia
Project Grant R01HL155547
worth $3,237,702
from National Heart Lung and Blood Institute in January 2020 with work to be completed primarily in Virginia United States.
The grant
has a duration of 5 years and
was awarded through assistance program 93.837 Cardiovascular Diseases Research.
The Project Grant was awarded through grant opportunity Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 8/20/25
Period of Performance
1/1/21
Start Date
12/31/25
End Date
Funding Split
$3.2M
Federal Obligation
$0.0
Non-Federal Obligation
$3.2M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01HL155547
Transaction History
Modifications to R01HL155547
Additional Detail
Award ID FAIN
R01HL155547
SAI Number
R01HL155547-2132820912
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Funding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Awardee UEI
JJG6HU8PA4S5
Awardee CAGE
9B982
Performance District
VA-90
Senators
Mark Warner
Timothy Kaine
Timothy Kaine
Budget Funding
Federal Account | Budget Subfunction | Object Class | Total | Percentage |
---|---|---|---|---|
National Heart, Lung, and Blood Institute, National Institutes of Health, Health and Human Services (075-0872) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,349,070 | 100% |
Modified: 8/20/25