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Developments in strategies for Quorum Sensing virulence factor inhibition to combat bacterial drug resistance
- Source :
- Microbial Pathogenesis. 121:293-302
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- Quorum sensing (QS) is a complex bacterial intercellular communication system. It is mediated by molecules called auto-inducers (AIs) and allows coordinated responses to a variety of environmental signals by inducing alterations in gene expression. Communication through QS can tremendously stimulate the pathogenicity and virulence via multiple mechanisms in pathogenic bacteria. The present review explores the major types of multitudinous QS systems known in Gram-positive and Gram-negative bacteria and their roles in bacterial pathogenesis and drug resistance. Because bacterial resistance to antibiotics is increasingly becoming a significant clinical challenge to human health; alternate strategies to combat drug resistance are warranted. Targeting bacterial pathogenicity by interruptions in QS using natural QS inhibitors and synthetic quorum-quenching analogs are being increasingly considered for development of next generation antimicrobials. The review highlights the recent advancements in discovery of promising new QS modulators and their efficiency in controlling infections caused by multidrug-resistant bacterial pathogens.
- Subjects :
- 0301 basic medicine
Virulence Factors
030106 microbiology
Quorum Sensing
Virulence
Pathogenic bacteria
Drug resistance
Computational biology
Biology
Gram-Positive Bacteria
medicine.disease_cause
Microbiology
Virulence factor
Anti-Bacterial Agents
03 medical and health sciences
Quorum sensing
030104 developmental biology
Infectious Diseases
Antibiotic resistance
Quorum Quenching
Drug Resistance, Multiple, Bacterial
Gram-Negative Bacteria
medicine
Humans
Autoinducer
Subjects
Details
- ISSN :
- 08824010
- Volume :
- 121
- Database :
- OpenAIRE
- Journal :
- Microbial Pathogenesis
- Accession number :
- edsair.doi.dedup.....1132a86f45a0f7c0879ae1d89c928289
- Full Text :
- https://doi.org/10.1016/j.micpath.2018.05.046