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dc.contributor.authorKim, Wooseongen_US
dc.contributor.authorConery, Annie L.en_US
dc.contributor.authorRajamuthiah, Rajmohanen_US
dc.contributor.authorFuchs, Beth Burgwynen_US
dc.contributor.authorAusubel, Frederick M.en_US
dc.contributor.authorMylonakis, Eleftheriosen_US
dc.date.accessioned2015-07-13T18:46:48Z
dc.date.issued2015en_US
dc.identifier.citationKim, Wooseong, Annie L. Conery, Rajmohan Rajamuthiah, Beth Burgwyn Fuchs, Frederick M. Ausubel, and Eleftherios Mylonakis. 2015. “Identification of an Antimicrobial Agent Effective against Methicillin-Resistant Staphylococcus aureus Persisters Using a Fluorescence-Based Screening Strategy.” PLoS ONE 10 (6): e0127640. doi:10.1371/journal.pone.0127640. http://dx.doi.org/10.1371/journal.pone.0127640.en
dc.identifier.issn1932-6203en
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:17295611
dc.description.abstractPersisters are a subpopulation of normal bacterial cells that show tolerance to conventional antibiotics. Persister cells are responsible for recalcitrant chronic infections and new antibiotics effective against persisters would be a major development in the treatment of these infections. Using the reporter dye SYTOX Green that only stains cells with permeabilized membranes, we developed a fluorescence-based screening assay in a 384-well format for identifying compounds that can kill methicillin-resistant Staphylococcus aureus (MRSA) persisters. The assay proved robust and suitable for high throughput screening (Z`-factor: >0.7). In screening a library of hits from a previous screen, which identified compounds that had the ability to block killing of the nematode Caenorhabditis by MRSA, we discovered that the low molecular weight compound NH125, a bacterial histidine kinase inhibitor, kills MRSA persisters by causing cell membrane permeabilization, and that 5 μg/mL of the compound can kill all cells to the limit of detection in a 108 CFU/mL culture of MRSA persisters within 3h. Furthermore, NH125 disrupts 50% of established MRSA biofilms at 20 μg/mL and completely eradicates biofilms at 160 μg/mL. Our results suggest that the SYTOX Green screening assay is suitable for large-scale projects to identify small molecules effective against MRSA persisters and should be easily adaptable to a broad range of pathogens that form persisters. Since NH125 has strong bactericidal properties against MRSA persisters and high selectivity to bacteria, we believe NH125 is a good anti-MRSA candidate drug that should be further evaluated.en
dc.language.isoen_USen
dc.publisherPublic Library of Scienceen
dc.relation.isversionofdoi:10.1371/journal.pone.0127640en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454602/pdf/en
dash.licenseLAAen_US
dc.titleIdentification of an Antimicrobial Agent Effective against Methicillin-Resistant Staphylococcus aureus Persisters Using a Fluorescence-Based Screening Strategyen
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalPLoS ONEen
dash.depositing.authorConery, Annie L.en_US
dc.date.available2015-07-13T18:46:48Z
dc.identifier.doi10.1371/journal.pone.0127640*
dash.contributor.affiliatedConery, Annie
dash.contributor.affiliatedAusubel, Frederick


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