SigE: A master regulator of Mycobacterium tuberculosis

The Extracellular function (ECF) sigma factor SigE is one of the best characterized out of the 13 sigma factors encoded in the Mycobacterium tuberculosis chromosome. SigE is required for blocking phagosome maturation and full virulence in both mice and guinea pigs. Moreover, it is involved in the re...

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Main Authors: Riccardo Manganelli, Laura Cioetto-Mazzabò, Greta Segafreddo, Francesca Boldrin, Davide Sorze, Marta Conflitti, Agnese Serafini, Roberta Provvedi
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-03-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2023.1075143/full
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author Riccardo Manganelli
Laura Cioetto-Mazzabò
Greta Segafreddo
Francesca Boldrin
Davide Sorze
Marta Conflitti
Agnese Serafini
Roberta Provvedi
author_facet Riccardo Manganelli
Laura Cioetto-Mazzabò
Greta Segafreddo
Francesca Boldrin
Davide Sorze
Marta Conflitti
Agnese Serafini
Roberta Provvedi
author_sort Riccardo Manganelli
collection DOAJ
description The Extracellular function (ECF) sigma factor SigE is one of the best characterized out of the 13 sigma factors encoded in the Mycobacterium tuberculosis chromosome. SigE is required for blocking phagosome maturation and full virulence in both mice and guinea pigs. Moreover, it is involved in the response to several environmental stresses as surface stress, oxidative stress, acidic pH, and phosphate starvation. Underscoring its importance in M. tuberculosis physiology, SigE is subjected to a very complex regulatory system: depending on the environmental conditions, its expression is regulated by three different sigma factors (SigA, SigE, and SigH) and a two-component system (MprAB). SigE is also regulated at the post-translational level by an anti-sigma factor (RseA) which is regulated by the intracellular redox potential and by proteolysis following phosphorylation from PknB upon surface stress. The set of genes under its direct control includes other regulators, as SigB, ClgR, and MprAB, and genes involved in surface remodeling and stabilization. Recently SigE has been shown to interact with PhoP to activate a subset of genes in conditions of acidic pH. The complex structure of its regulatory network has been suggested to result in a bistable switch leading to the development of heterogeneous bacterial populations. This hypothesis has been recently reinforced by the finding of its involvement in the development of persister cells able to survive to the killing activity of several drugs.
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spelling doaj.art-1302d970cc554718848eba18398f94d52023-03-07T05:15:53ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2023-03-011410.3389/fmicb.2023.10751431075143SigE: A master regulator of Mycobacterium tuberculosisRiccardo Manganelli0Laura Cioetto-Mazzabò1Greta Segafreddo2Francesca Boldrin3Davide Sorze4Marta Conflitti5Agnese Serafini6Roberta Provvedi7Department of Molecular Medicine, University of Padova, Padova, ItalyDepartment of Molecular Medicine, University of Padova, Padova, ItalyDepartment of Molecular Medicine, University of Padova, Padova, ItalyDepartment of Molecular Medicine, University of Padova, Padova, ItalyDepartment of Molecular Medicine, University of Padova, Padova, ItalyDepartment of Molecular Medicine, University of Padova, Padova, ItalyDepartment of Molecular Medicine, University of Padova, Padova, ItalyDepartment of Biology, University of Padova, Padova, ItalyThe Extracellular function (ECF) sigma factor SigE is one of the best characterized out of the 13 sigma factors encoded in the Mycobacterium tuberculosis chromosome. SigE is required for blocking phagosome maturation and full virulence in both mice and guinea pigs. Moreover, it is involved in the response to several environmental stresses as surface stress, oxidative stress, acidic pH, and phosphate starvation. Underscoring its importance in M. tuberculosis physiology, SigE is subjected to a very complex regulatory system: depending on the environmental conditions, its expression is regulated by three different sigma factors (SigA, SigE, and SigH) and a two-component system (MprAB). SigE is also regulated at the post-translational level by an anti-sigma factor (RseA) which is regulated by the intracellular redox potential and by proteolysis following phosphorylation from PknB upon surface stress. The set of genes under its direct control includes other regulators, as SigB, ClgR, and MprAB, and genes involved in surface remodeling and stabilization. Recently SigE has been shown to interact with PhoP to activate a subset of genes in conditions of acidic pH. The complex structure of its regulatory network has been suggested to result in a bistable switch leading to the development of heterogeneous bacterial populations. This hypothesis has been recently reinforced by the finding of its involvement in the development of persister cells able to survive to the killing activity of several drugs.https://www.frontiersin.org/articles/10.3389/fmicb.2023.1075143/fullMycobacterium tuberculosissigma factorstress responseregulatory networkpathogenesis
spellingShingle Riccardo Manganelli
Laura Cioetto-Mazzabò
Greta Segafreddo
Francesca Boldrin
Davide Sorze
Marta Conflitti
Agnese Serafini
Roberta Provvedi
SigE: A master regulator of Mycobacterium tuberculosis
Frontiers in Microbiology
Mycobacterium tuberculosis
sigma factor
stress response
regulatory network
pathogenesis
title SigE: A master regulator of Mycobacterium tuberculosis
title_full SigE: A master regulator of Mycobacterium tuberculosis
title_fullStr SigE: A master regulator of Mycobacterium tuberculosis
title_full_unstemmed SigE: A master regulator of Mycobacterium tuberculosis
title_short SigE: A master regulator of Mycobacterium tuberculosis
title_sort sige a master regulator of mycobacterium tuberculosis
topic Mycobacterium tuberculosis
sigma factor
stress response
regulatory network
pathogenesis
url https://www.frontiersin.org/articles/10.3389/fmicb.2023.1075143/full
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