» Articles » PMID: 26991085

Toxin-antitoxin Systems in Bacterial Growth Arrest and Persistence

Overview
Journal Nat Chem Biol
Date 2016 Mar 19
PMID 26991085
Citations 333
Authors
Affiliations
Soon will be listed here.
Abstract

Bacterial persister cells constitute a subpopulation of genetically identical, metabolically slow-growing cells that are highly tolerant of antibiotics and other environmental stresses. Recent studies have demonstrated that gene loci known as toxin-antitoxin (TA) modules play a central role in the persister state. Under normal growth conditions, antitoxins potently inhibit the activities of the toxins. In contrast, under conditions of stress, the antitoxins are selectively degraded, freeing the toxins to inhibit essential cellular processes, such as DNA replication and protein translation. This inhibition results in rapid growth arrest. In this Review, we highlight recent discoveries of these multifaceted TA systems with a focus on the newly uncovered mechanisms, especially conditional cooperativity, that are used to regulate cell growth and persistence. We also discuss the potential for targeting TA systems for antimicrobial drug discovery.

Citing Articles

Understanding the physiological role and cross-interaction network of VapBC35 toxin-antitoxin system from Mycobacterium tuberculosis.

Singh N, Chattopadhyay G, Sundaramoorthy N, Varadarajan R, Singh R Commun Biol. 2025; 8(1):327.

PMID: 40016306 PMC: 11868609. DOI: 10.1038/s42003-025-07663-2.


Prophage dynamics in gastric and enterohepatic environments: unraveling ecological barriers and adaptive transitions.

Proenca M, Tanoeiro L, Fox J, Vale F ISME Commun. 2025; 5(1):ycaf017.

PMID: 39981300 PMC: 11840440. DOI: 10.1093/ismeco/ycaf017.


Dormancy in the origin, evolution and persistence of life on Earth.

Webster K, Lennon J Proc Biol Sci. 2025; 292(2038):20242035.

PMID: 39772956 PMC: 11706647. DOI: 10.1098/rspb.2024.2035.


Overview of Phage Defense Systems in Bacteria and Their Applications.

Xu X, Gu P Int J Mol Sci. 2025; 25(24.

PMID: 39769080 PMC: 11676413. DOI: 10.3390/ijms252413316.


Microalgae for bioremediation: advances, challenges, and public perception on genetic engineering.

Calatrava V, Ballester D, Gonzalez-Ballester D, Dubini A BMC Plant Biol. 2024; 24(1):1261.

PMID: 39731038 PMC: 11674212. DOI: 10.1186/s12870-024-05995-5.


References
1.
Balaban N, Merrin J, Chait R, Kowalik L, Leibler S . Bacterial persistence as a phenotypic switch. Science. 2004; 305(5690):1622-5. DOI: 10.1126/science.1099390. View

2.
Kamada K, Hanaoka F . Conformational change in the catalytic site of the ribonuclease YoeB toxin by YefM antitoxin. Mol Cell. 2005; 19(4):497-509. DOI: 10.1016/j.molcel.2005.07.004. View

3.
De Jonge N, Garcia-Pino A, Buts L, Haesaerts S, Charlier D, Zangger K . Rejuvenation of CcdB-poisoned gyrase by an intrinsically disordered protein domain. Mol Cell. 2009; 35(2):154-63. DOI: 10.1016/j.molcel.2009.05.025. View

4.
Christensen S, Pedersen K, Hansen F, Gerdes K . Toxin-antitoxin loci as stress-response-elements: ChpAK/MazF and ChpBK cleave translated RNAs and are counteracted by tmRNA. J Mol Biol. 2003; 332(4):809-19. DOI: 10.1016/s0022-2836(03)00922-7. View

5.
Shah D, Zhang Z, Khodursky A, Kaldalu N, Kurg K, Lewis K . Persisters: a distinct physiological state of E. coli. BMC Microbiol. 2006; 6:53. PMC: 1557402. DOI: 10.1186/1471-2180-6-53. View