Contribution of the Pseudomonas fluorescens MFE01 Type VI Secretion System to Biofilm Formation.

Type VI secretion systems (T6SSs) are widespread in Gram-negative bacteria, including Pseudomonas. These macromolecular machineries inject toxins directly into prokaryotic or eukaryotic prey cells. Hcp proteins are structural components of the extracellular part of this machinery. We recently report...

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Main Authors: Mathias Gallique, Victorien Decoin, Corinne Barbey, Thibaut Rosay, Marc G J Feuilloley, Nicole Orange, Annabelle Merieau
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5256989?pdf=render
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spelling doaj-3d68203fc259493e98c2898bdc24c10a2020-11-24T22:03:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01121e017077010.1371/journal.pone.0170770Contribution of the Pseudomonas fluorescens MFE01 Type VI Secretion System to Biofilm Formation.Mathias GalliqueVictorien DecoinCorinne BarbeyThibaut RosayMarc G J FeuilloleyNicole OrangeAnnabelle MerieauType VI secretion systems (T6SSs) are widespread in Gram-negative bacteria, including Pseudomonas. These macromolecular machineries inject toxins directly into prokaryotic or eukaryotic prey cells. Hcp proteins are structural components of the extracellular part of this machinery. We recently reported that MFE01, an avirulent strain of Pseudomonas fluorescens, possesses at least two hcp genes, hcp1 and hcp2, encoding proteins playing important roles in interbacterial interactions. Indeed, P. fluorescens MFE01 can immobilise and kill diverse bacteria of various origins through the action of the Hcp1 or Hcp2 proteins of the T6SS. We show here that another Hcp protein, Hcp3, is involved in killing prey cells during co-culture on solid medium. Even after the mutation of hcp1, hcp2, or hcp3, MFE01 impaired biofilm formation by MFP05, a P. fluorescens strain isolated from human skin. These mutations did not reduce P. fluorescens MFE01 biofilm formation, but the three Hcp proteins were required for the completion of biofilm maturation. Moreover, a mutant with a disruption of one of the unique core component genes, MFE01ΔtssC, was unable to produce its own biofilm or inhibit MFP05 biofilm formation. Finally, MFE01 did not produce detectable N-acyl-homoserine lactones for quorum sensing, a phenomenon reported for many other P. fluorescens strains. Our results suggest a role for the T6SS in communication between bacterial cells, in this strain, under biofilm conditions.http://europepmc.org/articles/PMC5256989?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mathias Gallique
Victorien Decoin
Corinne Barbey
Thibaut Rosay
Marc G J Feuilloley
Nicole Orange
Annabelle Merieau
spellingShingle Mathias Gallique
Victorien Decoin
Corinne Barbey
Thibaut Rosay
Marc G J Feuilloley
Nicole Orange
Annabelle Merieau
Contribution of the Pseudomonas fluorescens MFE01 Type VI Secretion System to Biofilm Formation.
PLoS ONE
author_facet Mathias Gallique
Victorien Decoin
Corinne Barbey
Thibaut Rosay
Marc G J Feuilloley
Nicole Orange
Annabelle Merieau
author_sort Mathias Gallique
title Contribution of the Pseudomonas fluorescens MFE01 Type VI Secretion System to Biofilm Formation.
title_short Contribution of the Pseudomonas fluorescens MFE01 Type VI Secretion System to Biofilm Formation.
title_full Contribution of the Pseudomonas fluorescens MFE01 Type VI Secretion System to Biofilm Formation.
title_fullStr Contribution of the Pseudomonas fluorescens MFE01 Type VI Secretion System to Biofilm Formation.
title_full_unstemmed Contribution of the Pseudomonas fluorescens MFE01 Type VI Secretion System to Biofilm Formation.
title_sort contribution of the pseudomonas fluorescens mfe01 type vi secretion system to biofilm formation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Type VI secretion systems (T6SSs) are widespread in Gram-negative bacteria, including Pseudomonas. These macromolecular machineries inject toxins directly into prokaryotic or eukaryotic prey cells. Hcp proteins are structural components of the extracellular part of this machinery. We recently reported that MFE01, an avirulent strain of Pseudomonas fluorescens, possesses at least two hcp genes, hcp1 and hcp2, encoding proteins playing important roles in interbacterial interactions. Indeed, P. fluorescens MFE01 can immobilise and kill diverse bacteria of various origins through the action of the Hcp1 or Hcp2 proteins of the T6SS. We show here that another Hcp protein, Hcp3, is involved in killing prey cells during co-culture on solid medium. Even after the mutation of hcp1, hcp2, or hcp3, MFE01 impaired biofilm formation by MFP05, a P. fluorescens strain isolated from human skin. These mutations did not reduce P. fluorescens MFE01 biofilm formation, but the three Hcp proteins were required for the completion of biofilm maturation. Moreover, a mutant with a disruption of one of the unique core component genes, MFE01ΔtssC, was unable to produce its own biofilm or inhibit MFP05 biofilm formation. Finally, MFE01 did not produce detectable N-acyl-homoserine lactones for quorum sensing, a phenomenon reported for many other P. fluorescens strains. Our results suggest a role for the T6SS in communication between bacterial cells, in this strain, under biofilm conditions.
url http://europepmc.org/articles/PMC5256989?pdf=render
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