Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/99732
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorXu, Cen_US
dc.creatorDong, Nen_US
dc.creatorChen, Ken_US
dc.creatorYang, Xen_US
dc.creatorZeng, Pen_US
dc.creatorHou, Cen_US
dc.creatorChan, EWCen_US
dc.creatorYao, Xen_US
dc.creatorChen, Sen_US
dc.date.accessioned2023-07-19T00:54:43Z-
dc.date.available2023-07-19T00:54:43Z-
dc.identifier.urihttp://hdl.handle.net/10397/99732-
dc.language.isoenen_US
dc.publisherElsevier Inc.en_US
dc.rights© 2022 The Author(s).en_US
dc.rightsThis is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Xu, C., Dong, N., Chen, K., Yang, X., Zeng, P., Hou, C., . . . Chen, S. (2022). Bactericidal, anti-biofilm, and anti-virulence activity of vitamin C against carbapenem-resistant hypervirulent klebsiella pneumoniae. IScience, 25(3), 103894 is available at https://doi.org/10.1016/j.isci.2022.103894.en_US
dc.titleBactericidal, anti-biofilm, and anti-virulence activity of vitamin C against carbapenem-resistant hypervirulent Klebsiella pneumoniaeen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume25en_US
dc.identifier.issue3en_US
dc.identifier.doi10.1016/j.isci.2022.103894en_US
dcterms.abstractThe emergence of carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKP) causing high mortality in clinical patients infers the urgent need for developing therapeutic agents. Here, we demonstrated vitamin C (VC) exhibited strong bactericidal, anti-biofilm, and virulence-suppressing effects on CR-hvKP. Our results showed such a bactericidal effect is dose-dependent both in vitro and in the mouse infection model and is associated with induction of reactive oxygen species (ROS) generation. In addition, VC inhibited biofilm formation of CR-hvKP through suppressing the production of exopolysaccharide (EPS). In addition, VC acted as an efflux pump inhibitor at subminimum inhibitory concentration (sub-MIC) to disrupt transportation of EPS and capsular polysaccharide to bacterial cell surface, thereby further inhibiting biofilm and capsule formation. Furthermore, virulence-associated genes in CR-hvKP exposed to sub-MIC of VC were downregulated. Our findings indicated VC could be an effective and safe therapeutic agent to treat CR-hvKP infections in urgent cases when all current treatment options fail.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationiScience, 18 Mar. 2022, v. 25, no. 3, 103894en_US
dcterms.isPartOfiScienceen_US
dcterms.issued2022-03-18-
dc.identifier.scopus2-s2.0-85125121337-
dc.identifier.eissn2589-0042en_US
dc.identifier.artn103894en_US
dc.description.validate202307 bcch-
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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