12/111phiA Prophage Domestication Is Associated with Autoaggregation and Increased Ability to Produce Biofilm in <i>Streptococcus agalactiae</i>

CC17 <i>Streptococcus agalactiae</i> carrying group-A prophages is increasingly responsible for neonatal infections. To investigate the impact of the genetic features of a group-A prophage, we first conducted an in silico analysis of the genome of 12/111phiA, a group-A prophage carried b...

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Main Authors: Adélaïde Renard, Seydina M. Diene, Luka Courtier-Martinez, Julien Burlaud Gaillard, Houssein Gbaguidi-Haore, Laurent Mereghetti, Roland Quentin, Patrice Francois, Nathalie Van Der Mee-Marquet
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/9/6/1112
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spelling doaj-ca772fca6d6d4931a775c426ad1c56812021-06-01T00:41:48ZengMDPI AGMicroorganisms2076-26072021-05-0191112111210.3390/microorganisms906111212/111phiA Prophage Domestication Is Associated with Autoaggregation and Increased Ability to Produce Biofilm in <i>Streptococcus agalactiae</i>Adélaïde Renard0Seydina M. Diene1Luka Courtier-Martinez2Julien Burlaud Gaillard3Houssein Gbaguidi-Haore4Laurent Mereghetti5Roland Quentin6Patrice Francois7Nathalie Van Der Mee-Marquet8UMR INRAE 1282 Infectiologie et Santé Publique, Bactéries et Risque Materno-Foetal, Université de Tours, 37000 Tours, FranceAix-Marseille Université, MEPHI, IRD, APHM, IHU-Méditerranée Infection, Faculté de Pharmacie, 13000 Marseille, FranceUMR INRAE 1282 Infectiologie et Santé Publique, Bactéries et Risque Materno-Foetal, Université de Tours, 37000 Tours, FrancePlateforme IBiSA Microscopie Electronique, Faculté de Médecine, Université de Tours, 37000 Tours, FranceService d’Hygiène Hospitalière, CHRU, 25056 Besançon, FranceUMR INRAE 1282 Infectiologie et Santé Publique, Bactéries et Risque Materno-Foetal, Université de Tours, 37000 Tours, FranceUMR INRAE 1282 Infectiologie et Santé Publique, Bactéries et Risque Materno-Foetal, Université de Tours, 37000 Tours, FranceLaboratoire de Recherche Génomique, Service des Maladies Infectieuses, Centre Médical Universitaire, Hôpitaux Universitaire de Genève, 1205 Geneva, SwitzerlandUMR INRAE 1282 Infectiologie et Santé Publique, Bactéries et Risque Materno-Foetal, Université de Tours, 37000 Tours, FranceCC17 <i>Streptococcus agalactiae</i> carrying group-A prophages is increasingly responsible for neonatal infections. To investigate the impact of the genetic features of a group-A prophage, we first conducted an in silico analysis of the genome of 12/111phiA, a group-A prophage carried by a strain responsible for a bloodstream infection in a parturient. This revealed a Restriction Modification system, suggesting a prophage maintenance strategy and five ORFs of interest for the host and encoding a type II toxin antitoxin system RelB/YafQ, an endonuclease, an S-adenosylmethionine synthetase MetK, and an StrP-like adhesin. Using the WT strain cured from 12/111phiA and constructing deleted mutants for the ORFs of interest, and their complemented mutants, we demonstrated an impact of prophage features on growth characteristics, cell morphology and biofilm formation. Our findings argue in favor of 12/111phiA domestication by the host and a role of prophage features in cell autoaggregation, glycocalyx and biofilm formation. We suggest that lysogeny may promote GBS adaptation to the acid environment of the vagina, consequently colonizing and infecting neonates.https://www.mdpi.com/2076-2607/9/6/1112<i>Streptococcus agalactiae</i>phageautoaggregationbiofilmpathogenicityneonate
collection DOAJ
language English
format Article
sources DOAJ
author Adélaïde Renard
Seydina M. Diene
Luka Courtier-Martinez
Julien Burlaud Gaillard
Houssein Gbaguidi-Haore
Laurent Mereghetti
Roland Quentin
Patrice Francois
Nathalie Van Der Mee-Marquet
spellingShingle Adélaïde Renard
Seydina M. Diene
Luka Courtier-Martinez
Julien Burlaud Gaillard
Houssein Gbaguidi-Haore
Laurent Mereghetti
Roland Quentin
Patrice Francois
Nathalie Van Der Mee-Marquet
12/111phiA Prophage Domestication Is Associated with Autoaggregation and Increased Ability to Produce Biofilm in <i>Streptococcus agalactiae</i>
Microorganisms
<i>Streptococcus agalactiae</i>
phage
autoaggregation
biofilm
pathogenicity
neonate
author_facet Adélaïde Renard
Seydina M. Diene
Luka Courtier-Martinez
Julien Burlaud Gaillard
Houssein Gbaguidi-Haore
Laurent Mereghetti
Roland Quentin
Patrice Francois
Nathalie Van Der Mee-Marquet
author_sort Adélaïde Renard
title 12/111phiA Prophage Domestication Is Associated with Autoaggregation and Increased Ability to Produce Biofilm in <i>Streptococcus agalactiae</i>
title_short 12/111phiA Prophage Domestication Is Associated with Autoaggregation and Increased Ability to Produce Biofilm in <i>Streptococcus agalactiae</i>
title_full 12/111phiA Prophage Domestication Is Associated with Autoaggregation and Increased Ability to Produce Biofilm in <i>Streptococcus agalactiae</i>
title_fullStr 12/111phiA Prophage Domestication Is Associated with Autoaggregation and Increased Ability to Produce Biofilm in <i>Streptococcus agalactiae</i>
title_full_unstemmed 12/111phiA Prophage Domestication Is Associated with Autoaggregation and Increased Ability to Produce Biofilm in <i>Streptococcus agalactiae</i>
title_sort 12/111phia prophage domestication is associated with autoaggregation and increased ability to produce biofilm in <i>streptococcus agalactiae</i>
publisher MDPI AG
series Microorganisms
issn 2076-2607
publishDate 2021-05-01
description CC17 <i>Streptococcus agalactiae</i> carrying group-A prophages is increasingly responsible for neonatal infections. To investigate the impact of the genetic features of a group-A prophage, we first conducted an in silico analysis of the genome of 12/111phiA, a group-A prophage carried by a strain responsible for a bloodstream infection in a parturient. This revealed a Restriction Modification system, suggesting a prophage maintenance strategy and five ORFs of interest for the host and encoding a type II toxin antitoxin system RelB/YafQ, an endonuclease, an S-adenosylmethionine synthetase MetK, and an StrP-like adhesin. Using the WT strain cured from 12/111phiA and constructing deleted mutants for the ORFs of interest, and their complemented mutants, we demonstrated an impact of prophage features on growth characteristics, cell morphology and biofilm formation. Our findings argue in favor of 12/111phiA domestication by the host and a role of prophage features in cell autoaggregation, glycocalyx and biofilm formation. We suggest that lysogeny may promote GBS adaptation to the acid environment of the vagina, consequently colonizing and infecting neonates.
topic <i>Streptococcus agalactiae</i>
phage
autoaggregation
biofilm
pathogenicity
neonate
url https://www.mdpi.com/2076-2607/9/6/1112
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