Friday, September 29, 2023 9/29/2023

Supplement Request: Investigating the role of prophage encoded gene products on mycobacterial gene expression and intrinsic antibiotic resistance

Award Number: R15GM148943
ORGANIZATION: NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
OPDIV: NIH
AWARD CLASS: DISCRETIONARY
AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

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PROJECT SUMMARY - No updates from original submission The goal of the proposed research is to understand how prophages regulate mycobacterial antibiotic resistance and alter gene expression in mycobacteria. Drug-resistant infections caused by clinically important mycobacteria continue to be a significant public health burden. Mycobacterium abscessus is an emerging pathogen in cystic fibrosis patients with a treatment success rate of only 45%, and is considered one of the most drug-resistant mycobacteria. Resistant isolates commonly display increased expression of intrinsic antibiotic resistance genes, making drug treatment challenging. M. abscessus isolates are typically lysogens, meaning their genomes carry one or more prophages, integrated viral genomes, that have the potential to regulate intrinsic antibiotic resistance. The mechanism by which prophage alter gene expression and antibiotic resistance in mycobacteria is not yet understood and is the focus of this grant. Expression of the transcriptional regulator whiB7 increases in response to stresses, such as sub- inhibitory concentrations of antibiotics and the intracellular environment of macrophages and plays a critical role in mycobacterial intrinsic antibiotic resistance and survival in macrophages (8). Our lab showed for the first time that prophage contribute to intrinsic antibiotic resistance and increased expression of whiB7, which in turn positively regulates a large set of intrinsic antibiotic resistance genes (8-10). We identified a novel group of prophages found in the genomes of M. abscessus and M. chelonae that belong to cluster MabR (7, 11) and determined that the MabR prophage, McProf, increases M. chelonae resistance to aminoglycosides, cornerstone antibiotic treatments for M. abscessus/chelonae infections (9). We found that mycobacteria carrying McProf have an enhanced whiB7 response particularly when superinfected by a second phage. It is not understood how the prophage McProf interacts with the second prophage to drive changes in whiB7 expression and intrinsic resistance. We hypothesize that genes expressed from the McProf genome detect stress and regulate antibiotic resistance in mycobacteria through the induction of whiB7. To understand the mechanisms of whiB7 regulation in mycobacterial lysogens, we propose characterizing the cellular stresses that enhance the whiB7 response in bacterial lysogens carrying the McProf prophage and identify and characterize McProf genes that upregulate whiB7 in response to stress.


Issue Date FY	Funding FY	Legal Entity Name	Legal Entity Address	Legal Entity City	Legal Entity State	Legal Entity Zip Code	Legal Entity COUNTY	Legal Entity COUNTRY	Assistance Listing	Award Code	Budget Year	Action Date	Action Type	Action Amount

Issue Date FY: 2023 ( Subtotal = $29,038 )
2023	2023	UNIVERSITY OF MAINE SYSTEM	5717 CORBETT HALL RM 422	ORONO	ME	04469	PENOBSCOT	USA	Biomedical Research and Research Training	000	1	7/24/2023	SUPPLEMENT FOR EXPANSION	$29,038


Issue Date FY: 2022 ( Subtotal = $432,274 )
2022	2022	UNIVERSITY OF MAINE SYSTEM	5717 CORBETT HALL RM 422	ORONO	ME	04469	PENOBSCOT	USA	Biomedical Research and Research Training	000	1	9/19/2022	NEW	$432,274


Grand Total All Awards = $461,312

Sum of Action Amount is $461,312;

Grand Total = $461,312

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Supplement Request: Investigating the role of prophage encoded gene products on mycobacterial gene expression and intrinsic antibiotic resistance

Award Number: R15GM148943

ORGANIZATION: NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES

OPDIV: NIH

AWARD CLASS: DISCRETIONARY

AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

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