Planktonic aggregates of Staphylococcus aureus protect against common antibiotics.

Bacterial cells are mostly studied during planktonic growth although in their natural habitats they are often found in communities such as biofilms with dramatically different physiological properties. We have examined another type of community namely cellular aggregates observed in strains of the h...

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Autores principales: Jakob Haaber, Marianne Thorup Cohn, Dorte Frees, Thorbjørn Joest Andersen, Hanne Ingmer
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:6475b8bf526946aaba559f61787996422021-11-18T07:12:00ZPlanktonic aggregates of Staphylococcus aureus protect against common antibiotics.1932-620310.1371/journal.pone.0041075https://doaj.org/article/6475b8bf526946aaba559f61787996422012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22815921/?tool=EBIhttps://doaj.org/toc/1932-6203Bacterial cells are mostly studied during planktonic growth although in their natural habitats they are often found in communities such as biofilms with dramatically different physiological properties. We have examined another type of community namely cellular aggregates observed in strains of the human pathogen Staphylococcus aureus. By laser-diffraction particle-size analysis (LDA) we show, for strains forming visible aggregates, that the aggregation starts already in the early exponential growth phase and proceeds until post-exponential phase where more than 90% of the population is part of the aggregate community. Similar to some types of biofilm, the structural component of S. aureus aggregates is the polysaccharide intercellular adhesin (PIA). Importantly, PIA production correlates with the level of aggregation whether altered through mutations or exposure to sub-inhibitory concentrations of selected antibiotics. While some properties of aggregates resemble those of biofilms including increased mutation frequency and survival during antibiotic treatment, aggregated cells displayed higher metabolic activity than planktonic cells or cells in biofilm. Thus, our data indicate that the properties of cells in aggregates differ in some aspects from those in biofilms. It is generally accepted that the biofilm life style protects pathogens against antibiotics and the hostile environment of the host. We speculate that in aggregate communities S. aureus increases its tolerance to hazardous environments and that the combination of a biofilm-like environment with mobility has substantial practical and clinical importance.Jakob HaaberMarianne Thorup CohnDorte FreesThorbjørn Joest AndersenHanne IngmerPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 7, p e41075 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Jakob Haaber
Marianne Thorup Cohn
Dorte Frees
Thorbjørn Joest Andersen
Hanne Ingmer
Planktonic aggregates of Staphylococcus aureus protect against common antibiotics.
description Bacterial cells are mostly studied during planktonic growth although in their natural habitats they are often found in communities such as biofilms with dramatically different physiological properties. We have examined another type of community namely cellular aggregates observed in strains of the human pathogen Staphylococcus aureus. By laser-diffraction particle-size analysis (LDA) we show, for strains forming visible aggregates, that the aggregation starts already in the early exponential growth phase and proceeds until post-exponential phase where more than 90% of the population is part of the aggregate community. Similar to some types of biofilm, the structural component of S. aureus aggregates is the polysaccharide intercellular adhesin (PIA). Importantly, PIA production correlates with the level of aggregation whether altered through mutations or exposure to sub-inhibitory concentrations of selected antibiotics. While some properties of aggregates resemble those of biofilms including increased mutation frequency and survival during antibiotic treatment, aggregated cells displayed higher metabolic activity than planktonic cells or cells in biofilm. Thus, our data indicate that the properties of cells in aggregates differ in some aspects from those in biofilms. It is generally accepted that the biofilm life style protects pathogens against antibiotics and the hostile environment of the host. We speculate that in aggregate communities S. aureus increases its tolerance to hazardous environments and that the combination of a biofilm-like environment with mobility has substantial practical and clinical importance.
format article
author Jakob Haaber
Marianne Thorup Cohn
Dorte Frees
Thorbjørn Joest Andersen
Hanne Ingmer
author_facet Jakob Haaber
Marianne Thorup Cohn
Dorte Frees
Thorbjørn Joest Andersen
Hanne Ingmer
author_sort Jakob Haaber
title Planktonic aggregates of Staphylococcus aureus protect against common antibiotics.
title_short Planktonic aggregates of Staphylococcus aureus protect against common antibiotics.
title_full Planktonic aggregates of Staphylococcus aureus protect against common antibiotics.
title_fullStr Planktonic aggregates of Staphylococcus aureus protect against common antibiotics.
title_full_unstemmed Planktonic aggregates of Staphylococcus aureus protect against common antibiotics.
title_sort planktonic aggregates of staphylococcus aureus protect against common antibiotics.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/6475b8bf526946aaba559f6178799642
work_keys_str_mv AT jakobhaaber planktonicaggregatesofstaphylococcusaureusprotectagainstcommonantibiotics
AT mariannethorupcohn planktonicaggregatesofstaphylococcusaureusprotectagainstcommonantibiotics
AT dortefrees planktonicaggregatesofstaphylococcusaureusprotectagainstcommonantibiotics
AT thorbjørnjoestandersen planktonicaggregatesofstaphylococcusaureusprotectagainstcommonantibiotics
AT hanneingmer planktonicaggregatesofstaphylococcusaureusprotectagainstcommonantibiotics
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