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dc.contributor.authorKourtesi, Christina
dc.contributor.authorBall, Anthony R.
dc.contributor.authorHuang, Ying-Ying
dc.contributor.authorJachak, Sanjay M.
dc.contributor.authorVera, D. Mariano A.
dc.contributor.authorKhondkar, Proma
dc.contributor.authorGibbons, Simon
dc.contributor.authorHamblin, Michael R.
dc.contributor.authorTegos, George P.
dc.date.accessioned2013-11-15T18:38:37Z
dc.date.available2013-11-15T18:38:37Z
dc.date.issued2013-03
dc.date.submitted2013-01
dc.identifier.issn18742858
dc.identifier.urihttp://hdl.handle.net/1721.1/82136
dc.description.abstractConventional antimicrobials are increasingly ineffective due to the emergence of multidrug-resistance among pathogenic microorganisms. The need to overcome these deficiencies has triggered exploration for novel and unconven-tional approaches to controlling microbial infections. Multidrug efflux systems (MES) have been a profound obstacle in the successful deployment of antimicrobials. The discovery of small molecule efflux system blockers has been an active and rapidly expanding research discipline. A major theme in this platform involves efflux pump inhibitors (EPIs) from natural sources. The discovery methodologies and the available number of natural EPI-chemotypes are increasing. Advances in our understanding of microbial physiology have shed light on a series of pathways and phenotypes where the role of efflux systems is pivotal. Complementing existing antimicrobial discovery platforms such as photodynamic therapy (PDT) with efflux inhibition is a subject under investigation. This core information is a stepping stone in the challenge of highlighting an effective drug development path for EPIs since the puzzle of clinical implementation remains unsolved. This review summarizes advances in the path of EPI discovery, discusses potential avenues of EPI implementation and development, and underlines the need for highly informative and comprehensive translational approaches.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (R01AI050875)en_US
dc.description.sponsorshipUnited States. Air Force (MFEL Program FA9550-04-1-0079)en_US
dc.language.isoen_US
dc.publisherBentham Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.2174/1874285801307010034en_US
dc.rights.urihttp://creativecommons.org/licenses/ by-nc/3.0/en_US
dc.sourcePMCen_US
dc.titleMicrobial Efflux Systems and Inhibitors: Approaches to Drug Discovery and the Challenge of Clinical Implementationen_US
dc.typeArticleen_US
dc.identifier.citationKourtesi, Christina. “Microbial Efflux Systems and Inhibitors: Approaches to Drug Discovery and the Challenge of Clinical Implementation.” The Open Microbiology Journal 7, no. 1 (March 29, 2013): 34-52.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.mitauthorHamblin, Michael R.en_US
dc.relation.journalThe Open Microbiology Journalen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsKourtesi, Christina; Ball, Anthony R.; Huang, Ying-Ying; Jachak, Sanjay M.; Vera, D. Mariano A.; Khondkar, Proma; Hamblin, Michael R.; Tegos, George P.en_US
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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