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dc.contributor.authorNeto, Catherine C.
dc.contributor.authorMacLean, Jason
dc.contributor.authorSong, Biqin
dc.contributor.authorDovell, Anthony
dc.contributor.authorKwasny, Steven
dc.contributor.authorOpperman, Timothy
dc.date2022-08-11T08:08:14.000
dc.date.accessioned2022-08-23T15:47:31Z
dc.date.available2022-08-23T15:47:31Z
dc.date.issued2014-05-20
dc.date.submitted2014-10-10
dc.identifier.doi10.13028/18k6-w430
dc.identifier.urihttp://hdl.handle.net/20.500.14038/28003
dc.description<p>Abstract of poster presented at the 2014 UMass Center for Clinical and Translational Science Research Retreat, held on May 20, 2014 at the University of Massachusetts Medical School, Worcester, Mass.</p>
dc.description.abstractCranberry (Vaccinium macrocarpon) is known for urinary tract health benefits associated with reducing the adhesion of E. coli bacteria. This property has been linked to cranberry polyphenols known as proanthocyanidins. Staphylococcus bacteria are a growing public health concern due to development of resistant strains. Identification of agents that inhibit biofilm formation by these bacteria may provide a new route to reduce infection in clinical settings. Fruit and leaves of North American cranberry (Vaccinium macrocarpon) and cranberry juice were fractionated and screened for their ability to prevent biofilm formation by several strains of S. aureus and S. epidermidis bacteria. MALDI-TOF MS analysis of the most bioactive fractions identified the major constituents as proanthocyanidin oligomers (PACs) with A-type linkages, ranging in size from 2-12 degrees of polymerization. Further characterization by NMR is underway. The polyphenol-rich fractions from cranberry leaf, fruit and juice inhibited biofilm formation by strains of S. aureus and S. epidermidis, with MBIC as low as 3.1 μg/mL, and without significant bacteriocidal activity. Thus, compounds from cranberry fruit, plant material and juice may be useful in reducing Staphylococcus biofilms without promoting resistance.
dc.formatyoutube
dc.language.isoen_US
dc.rightsCopyright the Author(s)
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/
dc.subjectBacterial Infections and Mycoses
dc.subjectBacteriology
dc.subjectBiochemistry
dc.subjectOrganic Chemicals
dc.subjectPlant Sciences
dc.subjectPublic Health
dc.subjectTranslational Medical Research
dc.titleCranberry Fruit and Leaf Polyphenols Inhibit Staphylococcus Bacterial Biofilms
dc.typePoster Abstract
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1306&amp;context=cts_retreat&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/cts_retreat/2014/posters/86
dc.identifier.contextkey6226131
refterms.dateFOA2022-08-23T15:47:31Z
html.description.abstract<p>Cranberry (Vaccinium macrocarpon) is known for urinary tract health benefits associated with reducing the adhesion of E. coli bacteria. This property has been linked to cranberry polyphenols known as proanthocyanidins. Staphylococcus bacteria are a growing public health concern due to development of resistant strains. Identification of agents that inhibit biofilm formation by these bacteria may provide a new route to reduce infection in clinical settings. Fruit and leaves of North American cranberry (Vaccinium macrocarpon) and cranberry juice were fractionated and screened for their ability to prevent biofilm formation by several strains of S. aureus and S. epidermidis bacteria. MALDI-TOF MS analysis of the most bioactive fractions identified the major constituents as proanthocyanidin oligomers (PACs) with A-type linkages, ranging in size from 2-12 degrees of polymerization. Further characterization by NMR is underway. The polyphenol-rich fractions from cranberry leaf, fruit and juice inhibited biofilm formation by strains of S. aureus and S. epidermidis, with MBIC as low as 3.1 μg/mL, and without significant bacteriocidal activity. Thus, compounds from cranberry fruit, plant material and juice may be useful in reducing Staphylococcus biofilms without promoting resistance.</p>
dc.identifier.submissionpathcts_retreat/2014/posters/86


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