Altered Mycobacterium tuberculosis Cell Wall Metabolism and Physiology Associated With RpoB Mutation H526D

Background:Mycobacterium tuberculosis (Mtb) rpoB mutations are associated with global metabolic remodeling. However, the net effects of rpoB mutations on Mtb physiology, metabolism and function are not completely understood. Based on previous work, we hypothesized that changes in the expression of c...

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Main Authors: Victoria L. Campodónico, Dalin Rifat, Yu-Min Chuang, Thomas R. Ioerger, Petros C. Karakousis
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-03-01
Series:Frontiers in Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fmicb.2018.00494/full
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spelling doaj-b0b9792abfea48479b74628e8c46937e2020-11-24T23:22:53ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2018-03-01910.3389/fmicb.2018.00494350770Altered Mycobacterium tuberculosis Cell Wall Metabolism and Physiology Associated With RpoB Mutation H526DVictoria L. Campodónico0Dalin Rifat1Yu-Min Chuang2Thomas R. Ioerger3Petros C. Karakousis4Petros C. Karakousis5Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, United StatesDepartment of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, United StatesDepartment of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, United StatesDepartment of Computer Science and Engineering, Texas A&M University, College Station, TX, United StatesDepartment of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, United StatesDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United StatesBackground:Mycobacterium tuberculosis (Mtb) rpoB mutations are associated with global metabolic remodeling. However, the net effects of rpoB mutations on Mtb physiology, metabolism and function are not completely understood. Based on previous work, we hypothesized that changes in the expression of cell wall molecules in Mtb mutant RpoB 526D lead to changes in cell wall permeability and to altered resistance to environmental stresses and drugs.Methods: The phenotypes of a fully drug-susceptible clinical strain of Mtb and its paired rifampin-monoresistant, RpoB H526D mutant progeny strain were compared.Results: The rpoB mutant showed altered colony morphology, bacillary length and cell wall thickness, which were associated with increased cell wall permeability and susceptibility to the cell wall detergent sodium dodecyl sulfate (SDS) after exposure to nutrient starvation. Relative to the isogenic rifampin-susceptible strain, the RpoB H526D mutant showed altered bacterial cellular metabolic activity and an eightfold increase in susceptibility to the cell-wall acting drug vancomycin.Conclusion: Our data suggest that RpoB mutation H526D is associated with altered cell wall physiology and resistance to cell wall-related stress. These findings are expected to contribute to an improved understanding of the pathogenesis of drug-resistant M. tuberculosis infections.http://journal.frontiersin.org/article/10.3389/fmicb.2018.00494/fullMycobacterium tuberculosisrpoB mutationrifampincell wallvancomycin
collection DOAJ
language English
format Article
sources DOAJ
author Victoria L. Campodónico
Dalin Rifat
Yu-Min Chuang
Thomas R. Ioerger
Petros C. Karakousis
Petros C. Karakousis
spellingShingle Victoria L. Campodónico
Dalin Rifat
Yu-Min Chuang
Thomas R. Ioerger
Petros C. Karakousis
Petros C. Karakousis
Altered Mycobacterium tuberculosis Cell Wall Metabolism and Physiology Associated With RpoB Mutation H526D
Frontiers in Microbiology
Mycobacterium tuberculosis
rpoB mutation
rifampin
cell wall
vancomycin
author_facet Victoria L. Campodónico
Dalin Rifat
Yu-Min Chuang
Thomas R. Ioerger
Petros C. Karakousis
Petros C. Karakousis
author_sort Victoria L. Campodónico
title Altered Mycobacterium tuberculosis Cell Wall Metabolism and Physiology Associated With RpoB Mutation H526D
title_short Altered Mycobacterium tuberculosis Cell Wall Metabolism and Physiology Associated With RpoB Mutation H526D
title_full Altered Mycobacterium tuberculosis Cell Wall Metabolism and Physiology Associated With RpoB Mutation H526D
title_fullStr Altered Mycobacterium tuberculosis Cell Wall Metabolism and Physiology Associated With RpoB Mutation H526D
title_full_unstemmed Altered Mycobacterium tuberculosis Cell Wall Metabolism and Physiology Associated With RpoB Mutation H526D
title_sort altered mycobacterium tuberculosis cell wall metabolism and physiology associated with rpob mutation h526d
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2018-03-01
description Background:Mycobacterium tuberculosis (Mtb) rpoB mutations are associated with global metabolic remodeling. However, the net effects of rpoB mutations on Mtb physiology, metabolism and function are not completely understood. Based on previous work, we hypothesized that changes in the expression of cell wall molecules in Mtb mutant RpoB 526D lead to changes in cell wall permeability and to altered resistance to environmental stresses and drugs.Methods: The phenotypes of a fully drug-susceptible clinical strain of Mtb and its paired rifampin-monoresistant, RpoB H526D mutant progeny strain were compared.Results: The rpoB mutant showed altered colony morphology, bacillary length and cell wall thickness, which were associated with increased cell wall permeability and susceptibility to the cell wall detergent sodium dodecyl sulfate (SDS) after exposure to nutrient starvation. Relative to the isogenic rifampin-susceptible strain, the RpoB H526D mutant showed altered bacterial cellular metabolic activity and an eightfold increase in susceptibility to the cell-wall acting drug vancomycin.Conclusion: Our data suggest that RpoB mutation H526D is associated with altered cell wall physiology and resistance to cell wall-related stress. These findings are expected to contribute to an improved understanding of the pathogenesis of drug-resistant M. tuberculosis infections.
topic Mycobacterium tuberculosis
rpoB mutation
rifampin
cell wall
vancomycin
url http://journal.frontiersin.org/article/10.3389/fmicb.2018.00494/full
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