Hierarchy and interconnected networks in the WhiB7 mediated transcriptional response to antibiotic stress in Mycobacterium abscessus.

Mycobacterium abscessus is intrinsically resistant to antibiotics effective against other pathogenic mycobacteria largely due to the drug-induced expression of genes that confer resistance. WhiB7 is a major hub controlling the induction of resistance to ribosome-targeting antibiotics. It activates t...

Full description

Saved in:
Bibliographic Details
Main Authors: Kelley Hurst-Hess, Charity McManaman, Yong Yang, Shamba Gupta, Pallavi Ghosh
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-12-01
Series:PLoS Genetics
Online Access:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1011060&type=printable
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850182611835551744
author Kelley Hurst-Hess
Charity McManaman
Yong Yang
Shamba Gupta
Pallavi Ghosh
author_facet Kelley Hurst-Hess
Charity McManaman
Yong Yang
Shamba Gupta
Pallavi Ghosh
author_sort Kelley Hurst-Hess
collection DOAJ
description Mycobacterium abscessus is intrinsically resistant to antibiotics effective against other pathogenic mycobacteria largely due to the drug-induced expression of genes that confer resistance. WhiB7 is a major hub controlling the induction of resistance to ribosome-targeting antibiotics. It activates the expression of >100 genes, 7 of which are known determinants of drug resistance; the function of most genes within the regulon is however unknown, but some conceivably encode additional mechanisms of resistance. Furthermore, the hierarchy of gene expression within the regulon, if any, is poorly understood. In the present work we have identified 56 WhiB7 binding sites using chromatin immunoprecipitation sequencing (CHIP-Seq) which accounts for the WhiB7-dependent upregulation of 72 genes, and find that M. abscessus WhiB7 functions exclusively as a transcriptional activator at promoters recognized by σA/σB. We have investigated the role of 18 WhiB7 regulated genes in drug resistance. Our results suggest that while some genes within the regulon (eg. erm41, hflX, eis2 and the ABCFs) play a major role in resistance, others make smaller contributions (eg. MAB_4324c and MAB_1409c) and the observed hypersensitivity ΔMabwhiB7 is a cumulative effect of these individual contributions. Moreover, our CHIP-Seq data implicate additional roles of WhiB7 induced genes beyond antibiotic resistance. Finally, we identify a σH-dependent network in aminoglycoside and tigecycline resistance which is induced upon drug exposure and is further activated by WhiB7 demonstrating the existence of a crosstalk between components of the WhiB7-dependent and -independent circuits.
format Article
id doaj-art-aff055563a2e4e5bad87d4437393d0f7
institution OA Journals
issn 1553-7390
1553-7404
language English
publishDate 2023-12-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Genetics
spelling doaj-art-aff055563a2e4e5bad87d4437393d0f72025-08-20T02:17:35ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042023-12-011912e101106010.1371/journal.pgen.1011060Hierarchy and interconnected networks in the WhiB7 mediated transcriptional response to antibiotic stress in Mycobacterium abscessus.Kelley Hurst-HessCharity McManamanYong YangShamba GuptaPallavi GhoshMycobacterium abscessus is intrinsically resistant to antibiotics effective against other pathogenic mycobacteria largely due to the drug-induced expression of genes that confer resistance. WhiB7 is a major hub controlling the induction of resistance to ribosome-targeting antibiotics. It activates the expression of >100 genes, 7 of which are known determinants of drug resistance; the function of most genes within the regulon is however unknown, but some conceivably encode additional mechanisms of resistance. Furthermore, the hierarchy of gene expression within the regulon, if any, is poorly understood. In the present work we have identified 56 WhiB7 binding sites using chromatin immunoprecipitation sequencing (CHIP-Seq) which accounts for the WhiB7-dependent upregulation of 72 genes, and find that M. abscessus WhiB7 functions exclusively as a transcriptional activator at promoters recognized by σA/σB. We have investigated the role of 18 WhiB7 regulated genes in drug resistance. Our results suggest that while some genes within the regulon (eg. erm41, hflX, eis2 and the ABCFs) play a major role in resistance, others make smaller contributions (eg. MAB_4324c and MAB_1409c) and the observed hypersensitivity ΔMabwhiB7 is a cumulative effect of these individual contributions. Moreover, our CHIP-Seq data implicate additional roles of WhiB7 induced genes beyond antibiotic resistance. Finally, we identify a σH-dependent network in aminoglycoside and tigecycline resistance which is induced upon drug exposure and is further activated by WhiB7 demonstrating the existence of a crosstalk between components of the WhiB7-dependent and -independent circuits.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1011060&type=printable
spellingShingle Kelley Hurst-Hess
Charity McManaman
Yong Yang
Shamba Gupta
Pallavi Ghosh
Hierarchy and interconnected networks in the WhiB7 mediated transcriptional response to antibiotic stress in Mycobacterium abscessus.
PLoS Genetics
title Hierarchy and interconnected networks in the WhiB7 mediated transcriptional response to antibiotic stress in Mycobacterium abscessus.
title_full Hierarchy and interconnected networks in the WhiB7 mediated transcriptional response to antibiotic stress in Mycobacterium abscessus.
title_fullStr Hierarchy and interconnected networks in the WhiB7 mediated transcriptional response to antibiotic stress in Mycobacterium abscessus.
title_full_unstemmed Hierarchy and interconnected networks in the WhiB7 mediated transcriptional response to antibiotic stress in Mycobacterium abscessus.
title_short Hierarchy and interconnected networks in the WhiB7 mediated transcriptional response to antibiotic stress in Mycobacterium abscessus.
title_sort hierarchy and interconnected networks in the whib7 mediated transcriptional response to antibiotic stress in mycobacterium abscessus
url https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1011060&type=printable
work_keys_str_mv AT kelleyhursthess hierarchyandinterconnectednetworksinthewhib7mediatedtranscriptionalresponsetoantibioticstressinmycobacteriumabscessus
AT charitymcmanaman hierarchyandinterconnectednetworksinthewhib7mediatedtranscriptionalresponsetoantibioticstressinmycobacteriumabscessus
AT yongyang hierarchyandinterconnectednetworksinthewhib7mediatedtranscriptionalresponsetoantibioticstressinmycobacteriumabscessus
AT shambagupta hierarchyandinterconnectednetworksinthewhib7mediatedtranscriptionalresponsetoantibioticstressinmycobacteriumabscessus
AT pallavighosh hierarchyandinterconnectednetworksinthewhib7mediatedtranscriptionalresponsetoantibioticstressinmycobacteriumabscessus