Proteomic analysis of Staphylococcus aureus biofilm cells grown under physiologically relevant fluid shear stress conditions

dc.contributor.authorIslam, Nazrul
dc.contributor.authorKim, Yonghyun
dc.contributor.authorRoss, Julia M.
dc.contributor.authorMarten, Mark
dc.date.accessioned2019-02-11T16:30:03Z
dc.date.available2019-02-11T16:30:03Z
dc.date.issued2014-04-30
dc.description.abstractBackground: The biofilm forming bacterium Staphylococcus aureus is responsible for maladies ranging from severe skin infection to major diseases such as bacteremia, endocarditis and osteomyelitis. A flow displacement system was used to grow S. aureus biofilms in four physiologically relevant fluid shear rates (50, 100, 500 and 1000 s−1) to identify proteins that are associated with biofilm. Results: Global protein expressions from the membrane and cytosolic fractions of S. aureus biofilm cells grown under the above shear rate conditions are reported. Sixteen proteins in the membrane-enriched fraction and eight proteins in the cytosolic fraction showed significantly altered expression (p < 0.05) under increasing fluid shear. These 24 proteins were identified using nano-LC-ESI-MS/MS. They were found to be associated with various metabolic functions such as glycolysis / TCA pathways, protein synthesis and stress tolerance. Increased fluid shear stress did not influence the expression of two important surface binding proteins: fibronectin-binding and collagen-binding proteins. Conclusions: The reported data suggest that while the general metabolic function of the sessile bacteria is minimal under high fluid shear stress conditions, they seem to retain the binding capacity to initiate new infections.en_US
dc.description.sponsorshipThis research was supported by Grant R01-AI059369 from the National Institutes of Health (NIH), USA, and by Grant EEC-1342388 from the National Science Foundation (NSF), USA. We thank Drs. Bin Guan and Alexei Gapeev for their help with nano-LC-ESI-MS/MS, and special thanks to Dr. Pyong Kyun Shin for helping NI in setting up the biofilm experimenten_US
dc.description.urihttps://proteomesci.biomedcentral.com/articles/10.1186/1477-5956-12-21en_US
dc.format.extent12 pagesen_US
dc.genrejournal articlesen_US
dc.identifierdoi:10.13016/m20ndn-ux0v
dc.identifier.citationNazrul Islam, Yonghyun Kim, Julia M Ross and Mark R Marten, Proteomic analysis of Staphylococcus aureus biofilm cells grown under physiologically relevant fluid shear stress conditions, Proteome Science 2014 , https://doi.org/10.1186/1477-5956-12-21en_US
dc.identifier.urihttps://doi.org/10.1186/1477-5956-12-21
dc.identifier.urihttp://hdl.handle.net/11603/12763
dc.language.isoen_USen_US
dc.publisherBioMed Central Ltden_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Chemical, Biochemical & Environmental Engineering Department Collection
dc.relation.ispartofUMBC College of Engineering and Information Technology Dean's Office
dc.relation.ispartofUMBC Faculty Collection
dc.rightsThis item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.
dc.rightsAttribution 2.0 Generic (CC BY 2.0)*
dc.rights.urihttps://creativecommons.org/licenses/by/2.0/*
dc.subjectbiofilmen_US
dc.subjectstaphylococcus aureusen_US
dc.subjectflow chamberen_US
dc.subjectshear stressen_US
dc.subjectproteomicsen_US
dc.titleProteomic analysis of Staphylococcus aureus biofilm cells grown under physiologically relevant fluid shear stress conditionsen_US
dc.typeTexten_US
dcterms.creatorhttps://orcid.org/0000-0002-1863-8956

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