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Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage

BACKGROUND: Since bacteria embedded in biofilms are far more difficult to eradicate than planktonic infections, it would be useful to know whether certain Staphylococcus aureus lineages are especially involved in strong biofilm formation. For this reason, in vitro biofilm formation of 228 clinical S...

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Autores principales: Croes, Sander, Deurenberg, Ruud H, Boumans, Marie-Louise L, Beisser, Patrick S, Neef, Cees, Stobberingh, Ellen E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774858/
https://www.ncbi.nlm.nih.gov/pubmed/19863820
http://dx.doi.org/10.1186/1471-2180-9-229
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author Croes, Sander
Deurenberg, Ruud H
Boumans, Marie-Louise L
Beisser, Patrick S
Neef, Cees
Stobberingh, Ellen E
author_facet Croes, Sander
Deurenberg, Ruud H
Boumans, Marie-Louise L
Beisser, Patrick S
Neef, Cees
Stobberingh, Ellen E
author_sort Croes, Sander
collection PubMed
description BACKGROUND: Since bacteria embedded in biofilms are far more difficult to eradicate than planktonic infections, it would be useful to know whether certain Staphylococcus aureus lineages are especially involved in strong biofilm formation. For this reason, in vitro biofilm formation of 228 clinical S. aureus isolates of distinct clonal lineages was investigated. RESULTS: At 0.1% glucose, more than 60% of the S. aureus strains associated with multilocus sequence typing (MLST) clonal complex (CC)8 produced large amounts of biomass, compared to 0-7% for various other clonal lineages. Additionally, S. aureus bloodstream isolates associated with MLST CC8 and CC7 had similar biofilm forming capacities as their commensal counterparts. Furthermore, strong biofilm formation could not be attributed to a specific accessory gene regulator (agr) genotype, as suggested previously. The agr genotypes were strictly associated with the clonal lineages. Moreover, strong biofilm formation was not related to slime formation. Congo red agar (CRA) screening is therefore not useful as a qualitative screening method for biofilm formation. CONCLUSION: The adherence to polystyrene surfaces under physiologic glucose concentration (0.1%) was dependent on the clonal lineage. Strains associated with MLST CC8 were markedly more often classified as strong biofilm former at glucose concentrations of 0%, 0.1% and 0.25%. The present study reveals that the MLST CC8 associated genetic background was a predisposing factor for strong biofilm formation in vitro, under all tested glucose concentrations.
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spelling pubmed-27748582009-11-10 Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage Croes, Sander Deurenberg, Ruud H Boumans, Marie-Louise L Beisser, Patrick S Neef, Cees Stobberingh, Ellen E BMC Microbiol Research article BACKGROUND: Since bacteria embedded in biofilms are far more difficult to eradicate than planktonic infections, it would be useful to know whether certain Staphylococcus aureus lineages are especially involved in strong biofilm formation. For this reason, in vitro biofilm formation of 228 clinical S. aureus isolates of distinct clonal lineages was investigated. RESULTS: At 0.1% glucose, more than 60% of the S. aureus strains associated with multilocus sequence typing (MLST) clonal complex (CC)8 produced large amounts of biomass, compared to 0-7% for various other clonal lineages. Additionally, S. aureus bloodstream isolates associated with MLST CC8 and CC7 had similar biofilm forming capacities as their commensal counterparts. Furthermore, strong biofilm formation could not be attributed to a specific accessory gene regulator (agr) genotype, as suggested previously. The agr genotypes were strictly associated with the clonal lineages. Moreover, strong biofilm formation was not related to slime formation. Congo red agar (CRA) screening is therefore not useful as a qualitative screening method for biofilm formation. CONCLUSION: The adherence to polystyrene surfaces under physiologic glucose concentration (0.1%) was dependent on the clonal lineage. Strains associated with MLST CC8 were markedly more often classified as strong biofilm former at glucose concentrations of 0%, 0.1% and 0.25%. The present study reveals that the MLST CC8 associated genetic background was a predisposing factor for strong biofilm formation in vitro, under all tested glucose concentrations. BioMed Central 2009-10-28 /pmc/articles/PMC2774858/ /pubmed/19863820 http://dx.doi.org/10.1186/1471-2180-9-229 Text en Copyright ©2009 Croes et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Croes, Sander
Deurenberg, Ruud H
Boumans, Marie-Louise L
Beisser, Patrick S
Neef, Cees
Stobberingh, Ellen E
Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage
title Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage
title_full Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage
title_fullStr Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage
title_full_unstemmed Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage
title_short Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage
title_sort staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the s. aureus lineage
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774858/
https://www.ncbi.nlm.nih.gov/pubmed/19863820
http://dx.doi.org/10.1186/1471-2180-9-229
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