Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface

Biofilm formation in Staphylococcus aureus is usually associated with the production of the poly-N-acetylglucosamine (PNAG) exopolysaccharide, synthesized by proteins encoded by the icaADBC operon. PNAG is a linear beta-(1-6)-linked N-acetylglucosaminoglycan that has to be partially deacetylated and...

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Autores principales: Vergara-Irigaray, Marta, Maira-Litran, Tomas, Merino, Nekane, Pier, Gerald B., Penadés, José R., Lasa, Inigo
Formato: Artículo
Lenguaje:Inglés
Publicado: 2017
Acceso en línea:http://hdl.handle.net/20.500.11939/4700
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author Vergara-Irigaray, Marta
Maira-Litran, Tomas
Merino, Nekane
Pier, Gerald B.
Penadés, José R.
Lasa, Inigo
author_browse Lasa, Inigo
Maira-Litran, Tomas
Merino, Nekane
Penadés, José R.
Pier, Gerald B.
Vergara-Irigaray, Marta
author_facet Vergara-Irigaray, Marta
Maira-Litran, Tomas
Merino, Nekane
Pier, Gerald B.
Penadés, José R.
Lasa, Inigo
author_sort Vergara-Irigaray, Marta
collection ReDivia
description Biofilm formation in Staphylococcus aureus is usually associated with the production of the poly-N-acetylglucosamine (PNAG) exopolysaccharide, synthesized by proteins encoded by the icaADBC operon. PNAG is a linear beta-(1-6)-linked N-acetylglucosaminoglycan that has to be partially deacetylated and consequently positively charged in order to be associated with bacterial cell surfaces. Here, we investigated whether attachment of PNAG to bacterial surfaces is mediated by ionic interactions with the negative charge of wall teichoic acids (WTAs), which represent the most abundant polyanions of the Gram-positive bacterial envelope. We generated WTA-deficient mutants by in-frame deletion of the tagO gene in two genetically unrelated S. aureus strains. The Delta tagO mutants were more sensitive to high temperatures, showed a higher degree of cell aggregation, had reduced initial adherence to abiotic surfaces and had a reduced capacity to form biofilms under both steady-state and flow conditions. However, the levels as well as the strength of the PNAG interaction with the bacterial cell surface were similar between AtagO mutants and their corresponding wild-type strains. Furthermore, double Delta tagO Delta icaADBC mutants displayed a similar aggregative phenotype to that of single Delta tagO mutants, indicating that PNAG is not responsible for the aggregative behaviour observed in Delta tagO mutants. Overall, the absence of WTAs in S. aureus had little effect on PNAG production or anchoring to the cell surface, but did affect the biofilm-forming capacity, cell aggregative behaviour and the temperature sensitivity/stability of S. aureus.
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spelling ReDivia47002025-04-25T14:44:11Z Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface Vergara-Irigaray, Marta Maira-Litran, Tomas Merino, Nekane Pier, Gerald B. Penadés, José R. Lasa, Inigo Biofilm formation in Staphylococcus aureus is usually associated with the production of the poly-N-acetylglucosamine (PNAG) exopolysaccharide, synthesized by proteins encoded by the icaADBC operon. PNAG is a linear beta-(1-6)-linked N-acetylglucosaminoglycan that has to be partially deacetylated and consequently positively charged in order to be associated with bacterial cell surfaces. Here, we investigated whether attachment of PNAG to bacterial surfaces is mediated by ionic interactions with the negative charge of wall teichoic acids (WTAs), which represent the most abundant polyanions of the Gram-positive bacterial envelope. We generated WTA-deficient mutants by in-frame deletion of the tagO gene in two genetically unrelated S. aureus strains. The Delta tagO mutants were more sensitive to high temperatures, showed a higher degree of cell aggregation, had reduced initial adherence to abiotic surfaces and had a reduced capacity to form biofilms under both steady-state and flow conditions. However, the levels as well as the strength of the PNAG interaction with the bacterial cell surface were similar between AtagO mutants and their corresponding wild-type strains. Furthermore, double Delta tagO Delta icaADBC mutants displayed a similar aggregative phenotype to that of single Delta tagO mutants, indicating that PNAG is not responsible for the aggregative behaviour observed in Delta tagO mutants. Overall, the absence of WTAs in S. aureus had little effect on PNAG production or anchoring to the cell surface, but did affect the biofilm-forming capacity, cell aggregative behaviour and the temperature sensitivity/stability of S. aureus. 2017-06-01T10:10:47Z 2017-06-01T10:10:47Z 2008 MAR 2008 article Vergara-Irigaray, Marta, Maira-Litran, Tomas, Merino, Nekane, Pier, Gerald B., Penades, J.R., Lasa, Inigo (2008). Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface. Microbiology-Sgm, 154, 865-877. 1350-0872 http://hdl.handle.net/20.500.11939/4700 10.1099/mic.0.2007/013292-0 en openAccess Impreso
spellingShingle Vergara-Irigaray, Marta
Maira-Litran, Tomas
Merino, Nekane
Pier, Gerald B.
Penadés, José R.
Lasa, Inigo
Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface
title Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface
title_full Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface
title_fullStr Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface
title_full_unstemmed Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface
title_short Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface
title_sort wall teichoic acids are dispensable for anchoring the pnag exopolysaccharide to the staphylococcus aureus cell surface
url http://hdl.handle.net/20.500.11939/4700
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