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dc.contributor.authorReen, F.
dc.contributor.authorMcGlacken, G.
dc.contributor.authorO'Gara, Fergal
dc.date.accessioned2018-08-08T04:43:50Z
dc.date.available2018-08-08T04:43:50Z
dc.date.created2018-08-08T03:50:37Z
dc.date.issued2018
dc.identifier.citationReen, F. and McGlacken, G. and O'Gara, F. 2018. The expanding horizon of alkyl quinolone signalling and communication in polycellular interactomes. FEMS Microbiology Letters. 365 (9): Article number fny076.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/70194
dc.identifier.doi10.1093/femsle/fny076
dc.description.abstract

Population dynamics within natural ecosystems is underpinned by microbial diversity and the heterogeneity of host-microbe and microbe-microbe interactions. Small molecule signals that intersperse between species have been shown to govern many virulence-related processes in established and emerging pathogens. Understanding the capacity of microbes to decode diverse languages and adapt to the presence of 'non-self' cells will provide an important new direction to the understanding of the 'polycellular' interactome. Alkyl quinolones (AQs) have been described in the ESKAPE pathogen Pseudomonas aeruginosa, the primary agent associated with mortality in patients with cystic fibrosis and the third most prevalent nosocomial pathogen worldwide. The role of these molecules in governing the physiology and virulence of P. aeruginosa and other pathogens has received considerable attention, while a role in interspecies and interkingdom communication has recently emerged. Herein we discuss recent advances in our understanding of AQ signalling and communication in the context of microbe-microbe and microbe-host interactions. The integrated knowledge from these systems-based investigations will facilitate the development of new therapeutics based on the AQ framework that serves to disarm the pathogenesis of P. aeruginosa and competing pathogens.

dc.publisherOxford University Press
dc.titleThe expanding horizon of alkyl quinolone signalling and communication in polycellular interactomes
dc.typeJournal Article
dcterms.source.volume365
dcterms.source.number9
dcterms.source.issn1574-6968
dcterms.source.titleFEMS Microbiology Letters
curtin.departmentSchool of Pharmacy and Biomedical Sciences
curtin.accessStatusFulltext not available


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