Vesicle self-assembly of amphiphilic siderophores produced by bacterial isolates from Soap Lake, Washington
dc.contributor.author | Figueroa, L. O. | |
dc.contributor.author | Pitts, Betsey | |
dc.contributor.author | Uchida, M. | |
dc.contributor.author | Richards, Abigail M. | |
dc.date.accessioned | 2016-11-29T18:06:40Z | |
dc.date.available | 2016-11-29T18:06:40Z | |
dc.date.issued | 2016-01 | |
dc.description.abstract | Due to the emergence of staphylococcal biofilm infections, the need for advanced antibiotics is crucial. The aim of this investigation was to evaluate the potency and penetration of telavancin against staphylococcal biofilms using two different biofilm models. Multiple staphylococcal strains, including meticillin-sensitive Staphylococcus aureus ATCC 29213, vancomycin-intermediate S. aureus ATCC 700787, heterogeneously vancomycin-intermediate S. aureus ATCC 700698 and meticillin-sensitive Staphylococcus epidermidis ATCC 12228, were grown and treated in drip-flow reactors to determine log reductions due to telavancin treatment. After 3 days of biofilm growth and 24 h of treatment, mean log reductions for telavancin ranged from 1.65 to 2.17 depending on the bacterial strain tested. Penetration was evaluated qualitatively using confocal scanning laser microscopy to image the infiltration of fluorescently labelled antibiotic into a staphylococcal biofilm grown in a flow cell. Fluorescently labelled telavancin rapidly penetrated the biofilms with no alteration in the biofilm structure. | en_US |
dc.identifier.citation | Figueroa LO, Pitts B, Uchida M, Richards AM, "Vesicle self-assembly of amphiphilic siderophores produced by bacterial isolates from Soap Lake, Washington," Can. J. Chem. 2016 94(1):35-43. | en_US |
dc.identifier.uri | https://scholarworks.montana.edu/handle/1/12263 | |
dc.title | Vesicle self-assembly of amphiphilic siderophores produced by bacterial isolates from Soap Lake, Washington | en_US |
dc.type | Article | en_US |
mus.citation.extentfirstpage | 35 | en_US |
mus.citation.extentlastpage | 43 | en_US |
mus.citation.issue | 1 | en_US |
mus.citation.journaltitle | Canadian Journal of Chemistry | en_US |
mus.citation.volume | 94 | en_US |
mus.data.thumbpage | 3 | en_US |
mus.identifier.category | Chemical & Material Sciences | en_US |
mus.identifier.category | Engineering & Computer Science | en_US |
mus.identifier.category | Life Sciences & Earth Sciences | en_US |
mus.identifier.doi | 10.1139/cjc-2015-0173 | en_US |
mus.relation.college | College of Agriculture | en_US |
mus.relation.college | College of Engineering | en_US |
mus.relation.college | College of Letters & Science | en_US |
mus.relation.department | Cell Biology & Neuroscience. | en_US |
mus.relation.department | Center for Biofilm Engineering. | en_US |
mus.relation.department | Chemical & Biological Engineering. | en_US |
mus.relation.department | Chemistry & Biochemistry. | en_US |
mus.relation.department | Microbiology & Immunology. | en_US |
mus.relation.researchgroup | Center for Biofilm Engineering. | en_US |
mus.relation.university | Montana State University - Bozeman | en_US |
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