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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorXu, Cen_US
dc.creatorLiu, Cen_US
dc.creatorChen, Ken_US
dc.creatorZeng, Pen_US
dc.creatorChan, EWCen_US
dc.creatorChen, Sen_US
dc.date.accessioned2023-05-10T02:04:04Z-
dc.date.available2023-05-10T02:04:04Z-
dc.identifier.urihttp://hdl.handle.net/10397/98684-
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.rights© The Author(s) 2022en_US
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en_US
dc.rightsThe following publication Xu, C., Liu, C., Chen, K., Zeng, P., Chan, E. W. C., & Chen, S. (2022). Otilonium bromide boosts antimicrobial activities of colistin against Gram-negative pathogens and their persisters. Communications Biology, 5(1), 613 is available at https://doi.org/10.1038/s42003-022-03561-z.en_US
dc.titleOtilonium bromide boosts antimicrobial activities of colistin against gram-negative pathogens and their persistersen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume5en_US
dc.identifier.doi10.1038/s42003-022-03561-zen_US
dcterms.abstractColistin is the last-line antibiotic against Gram-negative pathogens. Here we identify an FDA-approved drug, Otilonium bromide (Ob), which restores the activity of colistin against colistin-resistant Gram-negative bacteria in vitro and in a mouse infection model. Ob also reduces the colistin dosage required for effective treatment of infections caused by colistin-susceptible bacteria, thereby reducing the toxicity of the drug regimen. Furthermore, Ob acts synergistically with colistin in eradicating multidrug-tolerant persisters of Gram-negative bacteria in vitro. Functional studies and microscopy assays confirm that the synergistic antimicrobial effect exhibited by the Ob and colistin involves permeabilizing the bacterial cell membrane, dissipating proton motive force and suppressing efflux pumps, resulting in membrane damages, cytosol leakage and eventually bacterial cell death. Our findings suggest that Ob is a colistin adjuvant which can restore the clinical value of colistin in combating life-threatening, multidrug resistant Gram-negative pathogens.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationCommunications biology, 2022, v. 5, 613en_US
dcterms.isPartOfCommunications biologyen_US
dcterms.issued2022-
dc.identifier.isiWOS:000814262700001-
dc.identifier.scopus2-s2.0-85132296215-
dc.identifier.eissn2399-3642en_US
dc.identifier.artn613en_US
dc.description.validate202305 bcvcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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