Proteomic analysis of Staphylococcus aureus biofilm cells grown under physiologically relevant fluid shear stress conditions
dc.contributor.author | Islam, Nazrul | |
dc.contributor.author | Kim, Yonghyun | |
dc.contributor.author | Ross, Julia M. | |
dc.contributor.author | Marten, Mark | |
dc.date.accessioned | 2019-02-11T16:30:03Z | |
dc.date.available | 2019-02-11T16:30:03Z | |
dc.date.issued | 2014-04-30 | |
dc.description.abstract | Background: 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.sponsorship | This 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 experiment | en_US |
dc.description.uri | https://proteomesci.biomedcentral.com/articles/10.1186/1477-5956-12-21 | en_US |
dc.format.extent | 12 pages | en_US |
dc.genre | journal articles | en_US |
dc.identifier | doi:10.13016/m20ndn-ux0v | |
dc.identifier.citation | Nazrul 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/10.1186/1477-5956-12-21 | en_US |
dc.identifier.uri | https://doi.org/10.1186/1477-5956-12-21 | |
dc.identifier.uri | http://hdl.handle.net/11603/12763 | |
dc.language.iso | en_US | en_US |
dc.publisher | BioMed Central Ltd | en_US |
dc.relation.isAvailableAt | The University of Maryland, Baltimore County (UMBC) | |
dc.relation.ispartof | UMBC Chemical, Biochemical & Environmental Engineering Department Collection | |
dc.relation.ispartof | UMBC College of Engineering and Information Technology Dean's Office | |
dc.relation.ispartof | UMBC Faculty Collection | |
dc.rights | This 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.rights | Attribution 2.0 Generic (CC BY 2.0) | * |
dc.rights.uri | https://creativecommons.org/licenses/by/2.0/ | * |
dc.subject | biofilm | en_US |
dc.subject | staphylococcus aureus | en_US |
dc.subject | flow chamber | en_US |
dc.subject | shear stress | en_US |
dc.subject | proteomics | en_US |
dc.title | Proteomic analysis of Staphylococcus aureus biofilm cells grown under physiologically relevant fluid shear stress conditions | en_US |
dc.type | Text | en_US |
dcterms.creator | https://orcid.org/0000-0002-1863-8956 |