Identification of a potent indigoid persister antimicrobial by screening dormant cells

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dc.contributor.authorS Song-
dc.contributor.authorT Gong-
dc.contributor.authorR Yamasaki-
dc.contributor.authorJun Seob Kim-
dc.contributor.authorT K Wood-
dc.date.accessioned2019-10-28T16:30:17Z-
dc.date.available2019-10-28T16:30:17Z-
dc.date.issued2019-
dc.identifier.issn0006-3592-
dc.identifier.uri10.1002/bit.27078ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18908-
dc.description.abstractThe subpopulation of bacterial cells that survive myriad stress conditions (e.g., nutrient deprivation and antimicrobials) by ceasing metabolism, revive by activating ribosomes. These resuscitated cells can reconstitute infections; hence, it is imperative to discover compounds which eradicate persister cells. By screening 10,000 compounds directly for persister cell killing, we identified 5-nitro-3-phenyl-1H-indol-2-yl-methylamine hydrochloride (NPIMA) kills Escherichia coli persister cells more effectively than the best indigoid found to date, 5-iodoindole, and better than the DNA-crosslinker cisplatin. In addition, NPIMA eradicated Pseudomonas aeruginosa persister cells in a manner comparable to cisplatin. NPIMA also eradicated Staphylococcus aureus persister cells but was less effective than cisplatin. Critically, NPIMA kills Gram-positive and Gram-negative bacteria by damaging membranes and causing lysis as demonstrated by microscopy and release of extracellular DNA and protein. Furthermore, NPIMA was effective in reducing P. aeruginosa and S. aureus cell numbers in a wound model, and no resistance was found after 1 week. Hence, we identified a potent indigoid that kills persister cells by damaging their membranes.-
dc.publisherWiley-
dc.titleIdentification of a potent indigoid persister antimicrobial by screening dormant cells-
dc.title.alternativeIdentification of a potent indigoid persister antimicrobial by screening dormant cells-
dc.typeArticle-
dc.citation.titleBiotechnology and Bioengineering-
dc.citation.number0-
dc.citation.endPage2274-
dc.citation.startPage2263-
dc.citation.volume116-
dc.contributor.affiliatedAuthorJun Seob Kim-
dc.contributor.alternativeName송수연-
dc.contributor.alternativeNameGong-
dc.contributor.alternativeNameYamasaki-
dc.contributor.alternativeName김준섭-
dc.contributor.alternativeNameWood-
dc.identifier.bibliographicCitationBiotechnology and Bioengineering, vol. 116, pp. 2263-2274-
dc.identifier.doi10.1002/bit.27078-
dc.subject.keywordindole-
dc.subject.keywordpersisters-
dc.subject.localindole-
dc.subject.localIndole-
dc.subject.localpersisters-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Infectious Disease Research Center > 1. Journal Articles
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