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Two Component Regulatory Systems and Antibiotic Resistance in Gram-Negative Pathogens

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2019 Apr 13
PMID 30974906
Citations 66
Authors
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Abstract

Gram-negative pathogens such as , , and are the leading cause of nosocomial infections throughout the world. One commonality shared among these pathogens is their ubiquitous presence, robust host-colonization and most importantly, resistance to antibiotics. A significant number of two-component systems (TCSs) exist in these pathogens, which are involved in regulation of gene expression in response to environmental signals such as antibiotic exposure. While the development of antimicrobial resistance is a complex phenomenon, it has been shown that TCSs are involved in sensing antibiotics and regulating genes associated with antibiotic resistance. In this review, we aim to interpret current knowledge about the signaling mechanisms of TCSs in these three pathogenic bacteria. We further attempt to answer questions about the role of TCSs in antimicrobial resistance. We will also briefly discuss how specific two-component systems present in , , and may serve as potential therapeutic targets.

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References
1.
Lopez-Rojas R, Garcia-Quintanilla M, Labrador-Herrera G, Pachon J, McConnell M . Impaired growth under iron-limiting conditions associated with the acquisition of colistin resistance in Acinetobacter baumannii. Int J Antimicrob Agents. 2016; 47(6):473-7. DOI: 10.1016/j.ijantimicag.2016.03.010. View

2.
da Silva G, Domingues S . Interplay between Colistin Resistance, Virulence and Fitness in Acinetobacter baumannii. Antibiotics (Basel). 2017; 6(4). PMC: 5745471. DOI: 10.3390/antibiotics6040028. View

3.
Mah T, OToole G . Mechanisms of biofilm resistance to antimicrobial agents. Trends Microbiol. 2001; 9(1):34-9. DOI: 10.1016/s0966-842x(00)01913-2. View

4.
Yoon E, Nait Chabane Y, Goussard S, Snesrud E, Courvalin P, De E . Contribution of resistance-nodulation-cell division efflux systems to antibiotic resistance and biofilm formation in Acinetobacter baumannii. mBio. 2015; 6(2). PMC: 4453527. DOI: 10.1128/mBio.00309-15. View

5.
Tsakiridou E, Makris D, Daniil Z, Manoulakas E, Chatzipantazi V, Vlachos O . Acinetobacter baumannii infection in prior ICU bed occupants is an independent risk factor for subsequent cases of ventilator-associated pneumonia. Biomed Res Int. 2014; 2014:193516. PMC: 4101956. DOI: 10.1155/2014/193516. View