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Changes in the Expression of Biofilm-Associated Surface Proteins in Staphylococcus aureus Food-Environmental Isolates Subjected to Sublethal Concentrations of Disinfectants
L. Cincarova, O. Polansky, V. Babak, P. Kulich, P. Kralik,
Language English Country United States
Document type Journal Article
NLK
Free Medical Journals
from 2013
PubMed Central
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ProQuest Central
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Open Access Digital Library
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CINAHL Plus with Full Text (EBSCOhost)
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PubMed
27868063
DOI
10.1155/2016/4034517
Knihovny.cz E-resources
- MeSH
- Bacterial Proteins metabolism MeSH
- Biofilms drug effects growth & development MeSH
- Disinfectants administration & dosage MeSH
- Species Specificity MeSH
- Membrane Proteins metabolism MeSH
- Food Microbiology * MeSH
- Gene Expression Regulation, Bacterial drug effects physiology MeSH
- Staphylococcus aureus classification drug effects metabolism MeSH
- Cell Survival drug effects MeSH
- Dose-Response Relationship, Drug MeSH
- Publication type
- Journal Article MeSH
Sublethal concentrations (sub-MICs) of certain disinfectants are no longer effective in removing biofilms from abiotic surfaces and can even promote the formation of biofilms. Bacterial cells can probably adapt to these low concentrations of disinfectants and defend themselves by way of biofilm formation. In this paper, we report on three Staphylococcus aureus biofilm formers (strong B+++, moderate B++, and weak B+) that were cultivated with sub-MICs of commonly used disinfectants, ethanol or chloramine T, and quantified using Syto9 green fluorogenic nucleic acid stain. We demonstrate that 1.25-2.5% ethanol and 2500 μg/mL chloramine T significantly enhanced S. aureus biofilm formation. To visualize differences in biofilm compactness between S. aureus biofilms in control medium, 1.25% ethanol, or 2500 μg/mL chloramine T, scanning electron microscopy was used. To describe changes in abundance of surface-exposed proteins in ethanol- or chloramine T-treated biofilms, surface proteins were prepared using a novel trypsin shaving approach and quantified after dimethyl labeling by LC-LTQ/Orbitrap MS. Our data show that some proteins with adhesive functions and others with cell maintenance functions and virulence factor EsxA were significantly upregulated by both treatments. In contrast, immunoglobulin-binding protein A was significantly downregulated for both disinfectants. Significant differences were observed in the effect of the two disinfectants on the expression of surface proteins including some adhesins, foldase protein PrsA, and two virulence factors.
Department of Chemistry and Toxicology Veterinary Research Institute Brno Czech Republic
Department of Food and Feed Safety Veterinary Research Institute Hudcova 70 Brno Czech Republic
Department of Immunology Veterinary Research Institute Hudcova 70 Brno Czech Republic
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