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PEG-8 月桂酸酯发酵降低克林霉素对 的所需剂量。

PEG-8 Laurate Fermentation of Reduces the Required Dose of Clindamycin Against .

机构信息

Department of Biomedical Sciences and Engineering, National Central University, Taoyuan 32001, Taiwan.

Department of Life Sciences, National Central University, Taoyuan 32001, Taiwan.

出版信息

Int J Mol Sci. 2020 Jul 19;21(14):5103. doi: 10.3390/ijms21145103.

Abstract

The probiotic activity of skin () bacteria can elicit diverse biological functions via the fermentation of various carbon sources. Here, we found that polyethylene glycol (PEG)-8 Laurate, a carbon-rich molecule, can selectively induce the fermentation of , not (), a bacterium associated with acne vulgaris. The PEG-8 Laurate fermentation of remarkably diminished the growth of and the -induced production of pro-inflammatory macrophage-inflammatory protein 2 (MIP-2) cytokines in mice. Fermentation media enhanced the anti- activity of a low dose (0.1%) clindamycin, a prescription antibiotic commonly used to treat acne vulgaris, in terms of the suppression of colonization and MIP-2 production. Furthermore, PEG-8 Laurate fermentation of boosted the activity of 0.1% clindamycin to reduce the sizes of colonies. Our results demonstrated, for the first time, that the PEG-8 Laurate fermentation of displayed the adjuvant effect on promoting the efficacy of low-dose clindamycin against . Targeting by lowering the required doses of antibiotics may avoid the risk of creating drug-resistant and maintain the bacterial homeostasis in the skin microbiome, leading to a novel modality for the antibiotic treatment of acne vulgaris.

摘要

皮肤()细菌的益生菌活性可以通过各种碳源的发酵来引发多种生物学功能。在这里,我们发现聚乙二醇(PEG)-8 月桂酸酯,一种富含碳的分子,可以选择性地诱导而不是()发酵,一种与寻常痤疮相关的细菌。PEG-8 月桂酸酯发酵显著减少了和 -诱导的促炎巨噬细胞炎症蛋白 2(MIP-2)细胞因子在小鼠中的产生。发酵培养基增强了低剂量(0.1%)克林霉素的抗活性,克林霉素是一种常用于治疗寻常痤疮的处方抗生素,可抑制定植和 MIP-2 的产生。此外,发酵的 PEG-8 月桂酸酯增强了 0.1%克林霉素的活性,从而减少了的菌落大小。我们的研究结果首次表明,发酵显示出佐剂作用,可促进低剂量克林霉素对的疗效。通过降低抗生素的剂量来靶向,可以避免产生耐药性的风险,并维持皮肤微生物组中细菌的内稳态,为寻常痤疮的抗生素治疗提供新的模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ec/7404057/5b293ce8bcb8/ijms-21-05103-g001.jpg

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