Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/112531
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dc.contributorMainland Development Office-
dc.contributorSchool of Fashion and Textiles-
dc.creatorYin, Z-
dc.creatorWang, Y-
dc.creatorFeng, X-
dc.creatorLiu, C-
dc.creatorGuan, X-
dc.creatorLiu, S-
dc.creatorLong, Z-
dc.creatorMiao, Z-
dc.creatorHe, F-
dc.creatorCheng, R-
dc.creatorHan, Y-
dc.creatorLi, K-
dc.date.accessioned2025-04-16T04:33:52Z-
dc.date.available2025-04-16T04:33:52Z-
dc.identifier.urihttp://hdl.handle.net/10397/112531-
dc.language.isoenen_US
dc.publisherWiley-Blackwell Publishing Ltd.en_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rights© 2024 The Author(s). Microbial Biotechnology published by John Wiley & Sons Ltd.en_US
dc.rightsThe following publication Yin, Z., Wang, Y., Feng, X., Liu, C., Guan, X., Liu, S. et al. (2024) Lactobacillus rhamnosus GG and Bifidobacterium animalis subsp. lactis BB-12 promote infected wound healing via regulation of the wound microenvironment. Microbial Biotechnology, 17, e70031 is available at https://doi.org/10.1111/1751-7915.70031.en_US
dc.titleLactobacillus rhamnosus GG and Bifidobacterium animalis subsp. lactis BB-12 promote infected wound healing via regulation of the wound microenvironmenten_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume17-
dc.identifier.issue10-
dc.identifier.doi10.1111/1751-7915.70031-
dcterms.abstractInfected wounds can result in complex clinical complications and delayed healing, presenting a significant global public health challenge. This study explored the effects of topical application of two probiotics, Lactobacillus rhamnosus GG (LGG) and Bifidobacterium animalis subsp. lactis BB-12, on the microenvironment of infected wounds and their impact on wound healing. LGG and BB-12 were applied separately and topically on the Staphylococcus aureus (S. aureus)-infected skin wounds of the rat model on a daily basis. Both probiotics significantly accelerated wound healing, demonstrated by enhanced granulation tissue formation and increased collagen deposition, with BB-12 showing superior efficacy. LGG and BB-12 both effectively inhibited neutrophil infiltration and decreased the expression of pro-inflammatory cytokines tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6). Notably, BB-12 markedly reduced IL-6 levels, while LGG significantly lowered TNF-α, transforming growth factor-β (TGF-β) and vascular endothelial growth factor (VEGF). Additionally, both probiotics promoted macrophage polarization towards the anti-inflammatory M2 phenotype. Microbiota analysis revealed that LGG and BB-12 significantly decreased the abundance of pathogenic bacteria (e.g. Staphylococcus and Proteus) and increased the proportion of beneficial bacteria (e.g. Corynebacterium). Particularly, BB-12 was more effective in reducing Staphylococcus abundance, whereas LGG excelled in promoting Corynebacterium growth. These findings suggest the ability of LGG and BB-12 to modulate the wound microenvironment, enhance wound healing and provide valuable insights for the management of infected wounds.-
dcterms.abstractGraphical abstract: [Figure not available: see fulltext.]-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationMicrobial biotechnology, Oct. 2024, v. 17, no. 10, e70031-
dcterms.isPartOfMicrobial biotechnology-
dcterms.issued2024-10-
dc.identifier.scopus2-s2.0-85206817195-
dc.identifier.pmid39422648-
dc.identifier.eissn1751-7915-
dc.identifier.artne70031-
dc.description.validate202504 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Sichuan University Innovative Research Project; Sichuan University Postdoctoral Interdisciplinary Innovation Fund; Sichuan Natural Science Foundation of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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