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dc.contributor.authorFux, C. A.
dc.contributor.authorWilson, Suzanne
dc.contributor.authorStoodley, Paul
dc.date.accessioned2017-07-20T17:54:49Z
dc.date.available2017-07-20T17:54:49Z
dc.date.issued2004-07
dc.identifier.citationFux CA, Wilson S, Stoodley P, "Detachment characteristics and oxacillin resistance of Staphyloccocus aureus biofilm emboli in an in vitro catheter infection model," J Bacteriol, 2004 186(14):4486-4491en_US
dc.identifier.issn0021-9193
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/13375
dc.description.abstractCatheter-related bloodstream infections due to Staphylococcus aureus are of increasing clinical importance. The pathophysiological steps leading to colonization and infection, however, are still incompletely defined. We observed growth and detachment of S. aureus biofilms in an in vitro catheter-infection model by using time-lapse microscopy. Biofilm emboli were characterized by their size and their susceptibility for oxacillin. Biofilm dispersal was found to be a dynamic process in which clumps of a wide range of diameters detach. Large detached clumps were highly tolerant to oxacillin compared with exponential-phase planktonic cultures. Interestingly, the degree of antibiotic tolerance in stationary-phase planktonic cultures was equal to that in the large clumps. The mechanical disruption of large clumps reduced the minimal bactericidal concentration (MBC) by more than 1,000 times. The MBC for whole biofilm effluent, consisting of particles with an average number of 20 bacteria was 3.5 times higher than the MBC for planktonic cultures. We conclude that the antibiotic resistance of detached biofilm particles depends on the embolus size and could be attributed to nutrient-limited stationary-phase physiology of cells within the clumps. We hypothesize that the detachment of multicellular clumps may explain the high rate of symptomatic metastatic infections seen with S. aureus.en_US
dc.titleDetachment characteristics and oxacillin resistance of Staphyloccocus aureus biofilm emboli in an in vitro catheter infection modelen_US
dc.typeArticleen_US
mus.citation.extentfirstpage4486en_US
mus.citation.extentlastpage4491en_US
mus.citation.issue14en_US
mus.citation.journaltitleJournal of Bacteriologyen_US
mus.citation.volume186en_US
mus.identifier.categoryEngineering & Computer Scienceen_US
mus.identifier.doi10.1128/jb.186.14.4486-4491.2004en_US
mus.relation.collegeCollege of Engineeringen_US
mus.relation.departmentCenter for Biofilm Engineering.en_US
mus.relation.departmentChemical & Biological Engineering.en_US
mus.relation.departmentChemical Engineering.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.relation.researchgroupCenter for Biofilm Engineering.en_US
mus.data.thumbpage4en_US
mus.contributor.orcidStoodley, Paul|0000-0001-6069-273Xen_US


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