Toxin-antitoxin systems: reversible toxicity
File(s)Hall review revised.docx (115.48 KB)
Accepted version
Author(s)
Hall, A
Gollan, B
Helaine, S
Type
Journal Article
Abstract
Toxin–antitoxin (TA) systems encoded on the plasmids and chromosomes of bacteria are emerging as key players in stress adaptation. In particular, they have been implicated in the induction of persisters non-growing cells that can evade antibiotic exposure. TA toxins operate by a diverse range of mechanisms, either destructive or conservative, leading to the reversible growth arrest of bacterial cells. Whilst the molecular mechanisms of intoxication are now well understood, we still have very little information on how corrupted cells reawaken. Alongside the phenomenon of conditional cooperativity, new evidence suggests that the effects of some TA toxins can be reversed, allowing non-growing cells to be detoxified and growth to resume.
Date Issued
2017-04-01
Date Acceptance
2017-02-21
Citation
Current Opinion in Microbiology, 2017, 36, pp.102-110
ISSN
1879-0364
Publisher
Elsevier
Start Page
102
End Page
110
Journal / Book Title
Current Opinion in Microbiology
Volume
36
Copyright Statement
© 2017 Elsevier Ltd. All rights reserved. This manuscript is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Licence http://creativecommons.org/licenses/by-nc-nd/4.0/
Sponsor
Medical Research Council (MRC)
Medical Research Council (MRC)
Medical Research Council (MRC)
MRC
Grant Number
MR/J006874/1B
MR/M009629/1
MR/M009629/1
MRC
Subjects
Science & Technology
Life Sciences & Biomedicine
Microbiology
MESSENGER-RNA INTERFERASE
INITIATOR TRANSFER-RNA
PLASMID CCDB PROTEIN
ESCHERICHIA-COLI
TRANSCRIPTIONAL REPRESSION
CONDITIONAL COOPERATIVITY
BACTERIAL TOXIN
INHIBITS TRANSLATION
DNA GYRASE
CELL-DEATH
Anti-Bacterial Agents
Bacteria
Bacterial Physiological Phenomena
Bacterial Proteins
Bacterial Toxins
Chromosomes, Bacterial
Plasmids
Stress, Physiological
Toxin-Antitoxin Systems
0605 Microbiology
1108 Medical Microbiology
Publication Status
Published
Date Publish Online
2017-03-06