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The Two-Component System ZraPSR Is a Novel ESR that Contributes to Intrinsic Antibiotic Tolerance in Escherichia coli.
- Source :
-
Journal of molecular biology [J Mol Biol] 2018 Dec 07; Vol. 430 (24), pp. 4971-4985. Date of Electronic Publication: 2018 Oct 30. - Publication Year :
- 2018
-
Abstract
- During their lifecycle, bacteria are exposed to continuous changes in their environment, some of which are stressful and can be harmful. The cell envelope is the first line of defense against a hostile environment, but it is also the first target for damage. To deal with this problem, bacteria have evolved systems collectively called "envelope stress response," or ESR, dedicated to the detection and repair of damaged components. Here we decided to investigate whether the atypical two-component system ZraP-SR is a novel ESR. Based on the screening of more than 240 drugs using the Biolog technology, we show that the deletion of zraP or zraR confers increased susceptibility to five classes of antibiotics and to some environmental stress targeting the envelope. Using a microscopy approach, we also establish that ZraP and ZraR are required to maintain envelope integrity. So far, the ZraR regulator was only known to activate the transcription of zraP and zraSR. Using chromatin immunoprecipitation followed by sequencing and RT-qPCR, we have now identified 25 additional genes regulated by ZraR, the majority of which are involved in the response against stress. Taken together, our results demonstrate that ZraP-SR is a novel ESR.<br /> (Copyright © 2018 Elsevier Ltd. All rights reserved.)
- Subjects :
- Chromatin Immunoprecipitation
Drug Resistance, Bacterial
Escherichia coli drug effects
Escherichia coli metabolism
Escherichia coli Proteins metabolism
Gene Deletion
Gene Expression Regulation, Bacterial
Sequence Analysis, RNA
Stress, Physiological
Trans-Activators metabolism
Anti-Bacterial Agents pharmacology
Escherichia coli genetics
Escherichia coli Proteins genetics
Trans-Activators genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1089-8638
- Volume :
- 430
- Issue :
- 24
- Database :
- MEDLINE
- Journal :
- Journal of molecular biology
- Publication Type :
- Academic Journal
- Accession number :
- 30389436
- Full Text :
- https://doi.org/10.1016/j.jmb.2018.10.021