Cargando…

Staphylococcus aureus biofilm removal by targeting biofilm-associated extracellular proteins

BACKGROUND & OBJECTIVES: Among cell surface proteins, biofilm-associated protein (Bap) promotes biofilm development in Staphylococcus aureus strains. The aim of this study was to investigate proteinase-mediated biofilm dispersion in different isolates of S. aureus. METHODS: Biofilm assay was don...

Descripción completa

Detalles Bibliográficos
Autores principales: Shukla, Sudhir K., Rao, T. Subba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735565/
https://www.ncbi.nlm.nih.gov/pubmed/29205189
http://dx.doi.org/10.4103/ijmr.IJMR_410_15
_version_ 1783287233609990144
author Shukla, Sudhir K.
Rao, T. Subba
author_facet Shukla, Sudhir K.
Rao, T. Subba
author_sort Shukla, Sudhir K.
collection PubMed
description BACKGROUND & OBJECTIVES: Among cell surface proteins, biofilm-associated protein (Bap) promotes biofilm development in Staphylococcus aureus strains. The aim of this study was to investigate proteinase-mediated biofilm dispersion in different isolates of S. aureus. METHODS: Biofilm assay was done in 96-well microtitre plate to evaluate the effect of proteinase K on biofilms of bovine mastitis S. Aureus isolates. Extracellular polymeric substances were extracted and evaluated for their composition (protein, polysaccharides and extracellular DNA), before and after the proteinase K treatment. RESULTS: Biofilm assay showed that 2 µg/ml proteinase K significantly inhibited biofilm development in bap-positive S. aureus V329 as well as other S. aureus isolates (SA7, SA10, SA33, SA352), but not in bap-mutant M556 and SA392 (a weak biofilm-producing strain). Proteinase K treatment on S. aureus planktonic cells showed that there was no inhibition of planktonic growth up to 32 µg/ml of proteinase K. Proteinase K treatment on 24 h old preformed biofilms showed an enhanced dispersion of bap-positive V329 and SA7, SA10, SA33 and SA352 biofilms; however, proteinase K did not affect the bap-mutant S. aureus M556 and SA392 biofilms. Biofilm compositions study before and after proteinase K treatment indicated that Bap might also be involved in eDNA retention in the biofilm matrix that aids in biofilm stability. When proteinase K was used in combination with antibiotics, a synergistic effect in antibiotic efficacy was observed against all biofilm-forming S. aureus isolates. INTERPRETATION & CONCLUSIONS: Proteinase K inhibited biofilms growth in S. aureus bovine mastitis isolates but did not affect their planktonic growth. An enhanced dispersion of preformed S. aureus biofilms was observed on proteinase K treatment. Proteinase K treatment with antibiotics showed a synergistic effect against S. aureus biofilms. The study suggests that dispersing S. aureus by protease can be of use while devising strategies against S. aureus biofilms.
format Online
Article
Text
id pubmed-5735565
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-57355652017-12-28 Staphylococcus aureus biofilm removal by targeting biofilm-associated extracellular proteins Shukla, Sudhir K. Rao, T. Subba Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Among cell surface proteins, biofilm-associated protein (Bap) promotes biofilm development in Staphylococcus aureus strains. The aim of this study was to investigate proteinase-mediated biofilm dispersion in different isolates of S. aureus. METHODS: Biofilm assay was done in 96-well microtitre plate to evaluate the effect of proteinase K on biofilms of bovine mastitis S. Aureus isolates. Extracellular polymeric substances were extracted and evaluated for their composition (protein, polysaccharides and extracellular DNA), before and after the proteinase K treatment. RESULTS: Biofilm assay showed that 2 µg/ml proteinase K significantly inhibited biofilm development in bap-positive S. aureus V329 as well as other S. aureus isolates (SA7, SA10, SA33, SA352), but not in bap-mutant M556 and SA392 (a weak biofilm-producing strain). Proteinase K treatment on S. aureus planktonic cells showed that there was no inhibition of planktonic growth up to 32 µg/ml of proteinase K. Proteinase K treatment on 24 h old preformed biofilms showed an enhanced dispersion of bap-positive V329 and SA7, SA10, SA33 and SA352 biofilms; however, proteinase K did not affect the bap-mutant S. aureus M556 and SA392 biofilms. Biofilm compositions study before and after proteinase K treatment indicated that Bap might also be involved in eDNA retention in the biofilm matrix that aids in biofilm stability. When proteinase K was used in combination with antibiotics, a synergistic effect in antibiotic efficacy was observed against all biofilm-forming S. aureus isolates. INTERPRETATION & CONCLUSIONS: Proteinase K inhibited biofilms growth in S. aureus bovine mastitis isolates but did not affect their planktonic growth. An enhanced dispersion of preformed S. aureus biofilms was observed on proteinase K treatment. Proteinase K treatment with antibiotics showed a synergistic effect against S. aureus biofilms. The study suggests that dispersing S. aureus by protease can be of use while devising strategies against S. aureus biofilms. Medknow Publications & Media Pvt Ltd 2017-07 /pmc/articles/PMC5735565/ /pubmed/29205189 http://dx.doi.org/10.4103/ijmr.IJMR_410_15 Text en Copyright: © 2017 Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Shukla, Sudhir K.
Rao, T. Subba
Staphylococcus aureus biofilm removal by targeting biofilm-associated extracellular proteins
title Staphylococcus aureus biofilm removal by targeting biofilm-associated extracellular proteins
title_full Staphylococcus aureus biofilm removal by targeting biofilm-associated extracellular proteins
title_fullStr Staphylococcus aureus biofilm removal by targeting biofilm-associated extracellular proteins
title_full_unstemmed Staphylococcus aureus biofilm removal by targeting biofilm-associated extracellular proteins
title_short Staphylococcus aureus biofilm removal by targeting biofilm-associated extracellular proteins
title_sort staphylococcus aureus biofilm removal by targeting biofilm-associated extracellular proteins
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735565/
https://www.ncbi.nlm.nih.gov/pubmed/29205189
http://dx.doi.org/10.4103/ijmr.IJMR_410_15
work_keys_str_mv AT shuklasudhirk staphylococcusaureusbiofilmremovalbytargetingbiofilmassociatedextracellularproteins
AT raotsubba staphylococcusaureusbiofilmremovalbytargetingbiofilmassociatedextracellularproteins