Quorum Sensing Interference and Structural Variation of Quorum Sensing Mimics in Australian Soft Coral

Bacterial Quorum Sensing (QS), the indirect regulation of gene expression through production and detection of small diffusible molecules, has emerged as a point of interaction between eukaryotic host organisms and their associated microbial communities. The extracellular nature of QS molecules enabl...

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Main Authors: Marnie L. Freckelton, Lone Høj, Bruce F. Bowden
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-06-01
Series:Frontiers in Marine Science
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmars.2018.00198/full
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spelling doaj-615026f8eb8242fca942637bdc5f15c42020-11-24T23:34:29ZengFrontiers Media S.A.Frontiers in Marine Science2296-77452018-06-01510.3389/fmars.2018.00198359234Quorum Sensing Interference and Structural Variation of Quorum Sensing Mimics in Australian Soft CoralMarnie L. Freckelton0Marnie L. Freckelton1Marnie L. Freckelton2Lone Høj3Lone Høj4Bruce F. Bowden5Bruce F. Bowden6College of Science and Engineering, James Cook University, Townsville, QLD, AustraliaAustralian Institute of Marine Science, Townsville, QLD, AustraliaAIMS@JCU, Division for Research and Innovation, James Cook University, Townsville, QLD, AustraliaAustralian Institute of Marine Science, Townsville, QLD, AustraliaAIMS@JCU, Division for Research and Innovation, James Cook University, Townsville, QLD, AustraliaCollege of Science and Engineering, James Cook University, Townsville, QLD, AustraliaAIMS@JCU, Division for Research and Innovation, James Cook University, Townsville, QLD, AustraliaBacterial Quorum Sensing (QS), the indirect regulation of gene expression through production and detection of small diffusible molecules, has emerged as a point of interaction between eukaryotic host organisms and their associated microbial communities. The extracellular nature of QS molecules enables interference in QS systems, in many cases via mimicry. This study targeted QS induction and inhibition in soft coral holobionts, as many soft coral species commonly contain compounds with structural similarities to the well-studied bacterial QS molecules acyl homoserine lactones. Screening with two bacterial biosensors, Agrobacterium tumefaciens A136 and Chromobacterium violaceum CV026, demonstrated that QS interference differed between the two biosensor strains and extended across the soft coral families Alcyoniidae, Clavulariidae, Nephtheidae, and Xeniidae. Bioassay-guided fractionation revealed chemical activity patterns, particularly in the induction of QS. Cembranoid diterpenes from active fractions were purified and tested for QS interference activity. Interestingly, the type of QS activity (induction or inhibition) in A. tumefaciens A136 correlated with structural variability of the secondary oxygen ring; cembranoid diterpenes with a furan ring or five-membered lactone induced QS, while compounds with larger (six or seven membered) lactone rings inhibited QS. Addition of the dominant cembranoid diterpene in the soft coral Lobophytum compactum, isolobophytolide, to bacterial culture media increased the number and morphological diversity of bacteria recovered from the mucosal layer of this soft coral, demonstrating a selective effect on certain members of the soft coral bacterial community. The identity and QS activity of recovered isolates differed between the mucosal layers of L. compactum and Sinularia flexibilis. In conclusion, this study provides information on the complexity of the interaction between soft corals and their associated bacteria, as well as, a structural understanding of how QS mimic compounds are able to interfere with a bacterial communication system.https://www.frontiersin.org/article/10.3389/fmars.2018.00198/fullquorum sensingsoft coralbacterial isolatescembrenolidequorum sensing mimic
collection DOAJ
language English
format Article
sources DOAJ
author Marnie L. Freckelton
Marnie L. Freckelton
Marnie L. Freckelton
Lone Høj
Lone Høj
Bruce F. Bowden
Bruce F. Bowden
spellingShingle Marnie L. Freckelton
Marnie L. Freckelton
Marnie L. Freckelton
Lone Høj
Lone Høj
Bruce F. Bowden
Bruce F. Bowden
Quorum Sensing Interference and Structural Variation of Quorum Sensing Mimics in Australian Soft Coral
Frontiers in Marine Science
quorum sensing
soft coral
bacterial isolates
cembrenolide
quorum sensing mimic
author_facet Marnie L. Freckelton
Marnie L. Freckelton
Marnie L. Freckelton
Lone Høj
Lone Høj
Bruce F. Bowden
Bruce F. Bowden
author_sort Marnie L. Freckelton
title Quorum Sensing Interference and Structural Variation of Quorum Sensing Mimics in Australian Soft Coral
title_short Quorum Sensing Interference and Structural Variation of Quorum Sensing Mimics in Australian Soft Coral
title_full Quorum Sensing Interference and Structural Variation of Quorum Sensing Mimics in Australian Soft Coral
title_fullStr Quorum Sensing Interference and Structural Variation of Quorum Sensing Mimics in Australian Soft Coral
title_full_unstemmed Quorum Sensing Interference and Structural Variation of Quorum Sensing Mimics in Australian Soft Coral
title_sort quorum sensing interference and structural variation of quorum sensing mimics in australian soft coral
publisher Frontiers Media S.A.
series Frontiers in Marine Science
issn 2296-7745
publishDate 2018-06-01
description Bacterial Quorum Sensing (QS), the indirect regulation of gene expression through production and detection of small diffusible molecules, has emerged as a point of interaction between eukaryotic host organisms and their associated microbial communities. The extracellular nature of QS molecules enables interference in QS systems, in many cases via mimicry. This study targeted QS induction and inhibition in soft coral holobionts, as many soft coral species commonly contain compounds with structural similarities to the well-studied bacterial QS molecules acyl homoserine lactones. Screening with two bacterial biosensors, Agrobacterium tumefaciens A136 and Chromobacterium violaceum CV026, demonstrated that QS interference differed between the two biosensor strains and extended across the soft coral families Alcyoniidae, Clavulariidae, Nephtheidae, and Xeniidae. Bioassay-guided fractionation revealed chemical activity patterns, particularly in the induction of QS. Cembranoid diterpenes from active fractions were purified and tested for QS interference activity. Interestingly, the type of QS activity (induction or inhibition) in A. tumefaciens A136 correlated with structural variability of the secondary oxygen ring; cembranoid diterpenes with a furan ring or five-membered lactone induced QS, while compounds with larger (six or seven membered) lactone rings inhibited QS. Addition of the dominant cembranoid diterpene in the soft coral Lobophytum compactum, isolobophytolide, to bacterial culture media increased the number and morphological diversity of bacteria recovered from the mucosal layer of this soft coral, demonstrating a selective effect on certain members of the soft coral bacterial community. The identity and QS activity of recovered isolates differed between the mucosal layers of L. compactum and Sinularia flexibilis. In conclusion, this study provides information on the complexity of the interaction between soft corals and their associated bacteria, as well as, a structural understanding of how QS mimic compounds are able to interfere with a bacterial communication system.
topic quorum sensing
soft coral
bacterial isolates
cembrenolide
quorum sensing mimic
url https://www.frontiersin.org/article/10.3389/fmars.2018.00198/full
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