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Impact of phenolic compounds in the acyl homoserine lactone-mediated quorum sensing regulatory pathways
Quorum sensing (QS) is a cell density-dependent regulation of virulent bacterial gene expression by autoinducers that potentially pertains in the epidemic of bacterial virulence. This study was initially designed to evaluate the effect of 5 phenolic compounds in the modulation of QS and virulence fa...
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Published in: | Scientific reports 2017-09, Vol.7 (1), p.10618-16, Article 10618 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Quorum sensing (QS) is a cell density-dependent regulation of virulent bacterial gene expression by autoinducers that potentially pertains in the epidemic of bacterial virulence. This study was initially designed to evaluate the effect of 5 phenolic compounds in the modulation of QS and virulence factors of
Chromobacterium violaceum
and
Pseudomonas aeruginosa
, and to determine the mechanisms of their effects. Biosensor strains were used to assess antibacterial and anti-QS effect of these compounds. Only methyl gallate (MG) among these compounds demonstrated profound anti-QS effect in the preliminary study, and thus only MG was utilized further to evaluate the effects on the synthesis and activity of acyl homoserine lactone (AHL) in
C. violaceum
and on the modulation of biofilm, motility, proteolytic, elastase, pyocyanin, and rhamnolipid activity in
P. aeruginosa
. Finally, the effect of MG on the expression of QS-regulated genes of
P. aeruginosa
was verified. MG suppressed both the synthesis and activity of AHL in
C. violaceum
. It also restricted the biofilm formation and other QS-associated virulence factor of
P. aeruginosa
. MG concentration-dependently suppressed the expression of
lasI
/
R
,
rhlI
/
R
, and
pqsA
of
P. aeruginosa
and was non-toxic in
in vitro
study. This is the first report of the anti-QS mechanism of MG. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-017-10997-5 |