Biofilm Structures in a Mono-Associated Mouse Model of Clostridium difficile Infection

Clostridium difficile infection (CDI) is a major healthcare-associated disease with high recurrence rates. Host colonization is critical for the infectious process, both in first episodes and in recurrent disease, with biofilm formation playing a key role. The ability of C. difficile to form a biofi...

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Main Authors: Anna P. Soavelomandroso, Françoise Gaudin, Sandra Hoys, Valérie Nicolas, Gayatri Vedantam, Claire Janoir, Sylvie Bouttier
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-10-01
Series:Frontiers in Microbiology
Subjects:
gut
Online Access:http://journal.frontiersin.org/article/10.3389/fmicb.2017.02086/full
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spelling doaj-69d15acc22274c05b865d2f30e2baacb2020-11-24T22:39:47ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2017-10-01810.3389/fmicb.2017.02086267342Biofilm Structures in a Mono-Associated Mouse Model of Clostridium difficile InfectionAnna P. Soavelomandroso0Françoise Gaudin1Sandra Hoys2Valérie Nicolas3Gayatri Vedantam4Claire Janoir5Sylvie Bouttier6EA4043, Unité Bactéries Pathogènes et Santé (UBaPS), Univ. Paris-Sud, Université Paris-Saclay, Châtenay-Malabry, FranceInstitut Paris Saclay d’Innovation Thérapeutique (IPSIT), UMS IPSIT Université Paris-Sud – US 31 INSERM – UMS 3679 CNRS, Plateforme d’Histologie souris Immunopathologie de Clamart – PHIC, Clamart, FranceEA4043, Unité Bactéries Pathogènes et Santé (UBaPS), Univ. Paris-Sud, Université Paris-Saclay, Châtenay-Malabry, FranceInstitut Paris Saclay d’Innovation Thérapeutique (IPSIT), UMS IPSIT Université Paris-Sud – US 31 INSERM – UMS 3679 CNRS, Plateforme d’Imagerie cellulaire – MIPSIT, Châtenay-Malabry, FranceSchool of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, AZ, United StatesEA4043, Unité Bactéries Pathogènes et Santé (UBaPS), Univ. Paris-Sud, Université Paris-Saclay, Châtenay-Malabry, FranceEA4043, Unité Bactéries Pathogènes et Santé (UBaPS), Univ. Paris-Sud, Université Paris-Saclay, Châtenay-Malabry, FranceClostridium difficile infection (CDI) is a major healthcare-associated disease with high recurrence rates. Host colonization is critical for the infectious process, both in first episodes and in recurrent disease, with biofilm formation playing a key role. The ability of C. difficile to form a biofilm on abiotic surfaces is established, but has not yet been confirmed in the intestinal tract. Here, four different isolates of C. difficile, which are in vitro biofilm producers, were studied for their ability to colonize germ-free mice. The level of colonization achieved was similar for all isolates in the different parts of the murine gastrointestinal tract, but pathogen burden was higher in the cecum and colon. Confocal laser scanning microscopy revealed that C. difficile bacteria were distributed heterogeneously over the intestinal tissue, without contact with epithelial cells. The R20291 strain, which belongs to the Ribotype 027 lineage, displayed a unique behavior compared to the other strains by forming numerous aggregates. By immunochemistry analyses, we showed that bacteria were localized inside and outside the mucus layer, irrespective of the strains tested. Most bacteria were entrapped in 3-D structures overlaying the mucus layer. For the R20291 strain, the cell-wall associated polysaccharide PS-II was detected in large amounts in the 3-D structure. As this component has been detected in the extrapolymeric matrix of in vitro C. difficile biofilms, our data suggest strongly that at least the R20291 strain is organized in the mono-associated mouse model in glycan-rich biofilm architecture, which sustainably maintains bacteria outside the mucus layer.http://journal.frontiersin.org/article/10.3389/fmicb.2017.02086/fullC. difficilebiofilmmono-associated mouse modelcolonizationgutmucus
collection DOAJ
language English
format Article
sources DOAJ
author Anna P. Soavelomandroso
Françoise Gaudin
Sandra Hoys
Valérie Nicolas
Gayatri Vedantam
Claire Janoir
Sylvie Bouttier
spellingShingle Anna P. Soavelomandroso
Françoise Gaudin
Sandra Hoys
Valérie Nicolas
Gayatri Vedantam
Claire Janoir
Sylvie Bouttier
Biofilm Structures in a Mono-Associated Mouse Model of Clostridium difficile Infection
Frontiers in Microbiology
C. difficile
biofilm
mono-associated mouse model
colonization
gut
mucus
author_facet Anna P. Soavelomandroso
Françoise Gaudin
Sandra Hoys
Valérie Nicolas
Gayatri Vedantam
Claire Janoir
Sylvie Bouttier
author_sort Anna P. Soavelomandroso
title Biofilm Structures in a Mono-Associated Mouse Model of Clostridium difficile Infection
title_short Biofilm Structures in a Mono-Associated Mouse Model of Clostridium difficile Infection
title_full Biofilm Structures in a Mono-Associated Mouse Model of Clostridium difficile Infection
title_fullStr Biofilm Structures in a Mono-Associated Mouse Model of Clostridium difficile Infection
title_full_unstemmed Biofilm Structures in a Mono-Associated Mouse Model of Clostridium difficile Infection
title_sort biofilm structures in a mono-associated mouse model of clostridium difficile infection
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2017-10-01
description Clostridium difficile infection (CDI) is a major healthcare-associated disease with high recurrence rates. Host colonization is critical for the infectious process, both in first episodes and in recurrent disease, with biofilm formation playing a key role. The ability of C. difficile to form a biofilm on abiotic surfaces is established, but has not yet been confirmed in the intestinal tract. Here, four different isolates of C. difficile, which are in vitro biofilm producers, were studied for their ability to colonize germ-free mice. The level of colonization achieved was similar for all isolates in the different parts of the murine gastrointestinal tract, but pathogen burden was higher in the cecum and colon. Confocal laser scanning microscopy revealed that C. difficile bacteria were distributed heterogeneously over the intestinal tissue, without contact with epithelial cells. The R20291 strain, which belongs to the Ribotype 027 lineage, displayed a unique behavior compared to the other strains by forming numerous aggregates. By immunochemistry analyses, we showed that bacteria were localized inside and outside the mucus layer, irrespective of the strains tested. Most bacteria were entrapped in 3-D structures overlaying the mucus layer. For the R20291 strain, the cell-wall associated polysaccharide PS-II was detected in large amounts in the 3-D structure. As this component has been detected in the extrapolymeric matrix of in vitro C. difficile biofilms, our data suggest strongly that at least the R20291 strain is organized in the mono-associated mouse model in glycan-rich biofilm architecture, which sustainably maintains bacteria outside the mucus layer.
topic C. difficile
biofilm
mono-associated mouse model
colonization
gut
mucus
url http://journal.frontiersin.org/article/10.3389/fmicb.2017.02086/full
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