Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/114961
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dc.contributorDepartment of Food Science and Nutrition-
dc.contributorMainland Affairs Office-
dc.creatorLiu, XX-
dc.creatorXu, Q-
dc.creatorYang, XM-
dc.creatorHeng, H-
dc.creatorYang, C-
dc.creatorYang, G-
dc.creatorPeng, MX-
dc.creatorChan, EWC-
dc.creatorChen, S-
dc.date.accessioned2025-09-02T00:31:44Z-
dc.date.available2025-09-02T00:31:44Z-
dc.identifier.issn2161-2129-
dc.identifier.urihttp://hdl.handle.net/10397/114961-
dc.language.isoenen_US
dc.publisherAmerican Society for Microbiologyen_US
dc.rightsCopyright © 2025 Liu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Liu X, Xu Q, Yang X, Heng H, Yang C, Yang G, Peng M, Chan EW, Chen S. 2025. Capsular polysaccharide enables Klebsiella pneumoniae to evade phagocytosis by blocking host-bacteria interactions. mBio 16:e03838-24 is available at https://dx.doi.org/10.1128/mbio.03838-24.en_US
dc.subjectKlebsiella pneumoniaeen_US
dc.subjectVirulence mechanismsen_US
dc.subjectCapsular polysaccharideen_US
dc.subjectHost recognitionen_US
dc.subjectHost responseen_US
dc.titleCapsular polysaccharide enables Klebsiella pneumoniae to evade phagocytosis by blocking host-bacteria interactionsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume16-
dc.identifier.issue3-
dc.identifier.doi10.1128/mbio.03838-24-
dcterms.abstractCapsule polysaccharide (CPS) is among the most important virulence factors of Klebsiella pneumoniae. Previous studies demonstrated that CPS plays multiple functional roles, but the mechanism by which this virulence factor enhances the survival fitness of K. pneumoniae remains unclear. In this work, we demonstrate that CPS is the main cellular component that not only elicits the host immune response to K. pneumoniae but also enables this pathogen to survive for a prolonged period under adverse environmental conditions. Consistently, our in vitro experiments suggest that CPS prevents K. pneumoniae from phagocytosis, rendering the encapsulated strain more difficult to be eradicated by the host. We also found that phagocytosis of K. pneumoniae is partially mediated by LOX-1, a scavenger receptor of the host, and that CPS may impede interaction between LOX-1 and this pathogenic bacteria, therefore reducing the phagocytosis process. These findings provide insights into the pathogenic mechanisms of this important clinical pathogen and should facilitate the design of new strategies to combat K. pneumoniae infections.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationmBio, Mar. 2025, v. 16, no. 3, e03838-24-
dcterms.issued2025-03-
dc.identifier.isiWOS:001421868900001-
dc.identifier.pmid39950808-
dc.identifier.eissn2150-7511-
dc.identifier.artne03838-24-
dc.description.validate202509 bcrc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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