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1,8-桉叶素通过抑制[具体对象]中的基因表达来抑制生物膜形成和细菌致病性。

1,8-Cineole inhibits biofilm formation and bacterial pathogenicity by suppressing gene expression in .

作者信息

Wang Yiming, Zhang Yu, Song Xu, Fang Chunlin, Xing Rui, Liu Lu, Zhao Xinghong, Zou Yuanfeng, Li Lixia, Jia Renyong, Ye Gang, Shi Fei, Zhou Xun, Zhang Yingying, Wan Hongping, Wei Qin, Yin Zhongqiong

机构信息

Natural Medicine Research Center, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.

Chengdu Agricultural College, Chengdu, China.

出版信息

Front Pharmacol. 2022 Oct 14;13:988245. doi: 10.3389/fphar.2022.988245. eCollection 2022.

Abstract

In recent years, with frequent reports of multi-drug resistant strains, bacteria antibiotic resistance has become an increasingly serious health problem worldwide. One of the most promising ways for combating bacterial infections and antibiotic resistance is development of quorum-sensing (QS) interfering drugs. In this study, the results show that 1,8-cineole inhibited the expression of QS as well as the virulence genes in O101 O101 with a 65% inhibition rate against gene. Therefore, we hypothesized that 1,8-cineole may inhibit the biofilm formation and reduce the pathogenicity of O101 by inhibiting the expression of gene. To confirm our hypotheses, a gene deleted O101 was constructed. The results show that the biofilm formation, motility, structure and pathogenicity of O101 were significantly inhibited following deletion of the gene. In addition, the transcript levels of QS and virulence genes of O101 were also significantly down-regulated. Interestingly, 1,8-cineole no longer had a significant inhibitory effect on the related phenotype and gene expression of O101 without gene. In conclusion, the results show that 1,8-cineole can affect bacterial biofilm formation and pathogenicity by suppressing the expression of gene in O101, which could provide a new perspective for dealing with the biofilm problem of pathogenic bacteria.

摘要

近年来,随着多重耐药菌株的报道频繁出现,细菌抗生素耐药性已成为全球范围内日益严重的健康问题。对抗细菌感染和抗生素耐药性最有前景的方法之一是开发群体感应(QS)干扰药物。在本研究中,结果表明1,8-桉叶素抑制了QS的表达以及O101中致病基因的表达,对基因的抑制率为65%。因此,我们推测1,8-桉叶素可能通过抑制基因的表达来抑制O101的生物膜形成并降低其致病性。为了证实我们的假设,构建了一个缺失基因的O101。结果表明,缺失基因后,O101的生物膜形成、运动性、结构和致病性均受到显著抑制。此外,O101的QS和致病基因的转录水平也显著下调。有趣的是,1,8-桉叶素对无基因的O101的相关表型和基因表达不再有显著抑制作用。总之,结果表明1,8-桉叶素可通过抑制O101中基因的表达来影响细菌生物膜形成和致病性,这可为解决病原菌的生物膜问题提供新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e86f/9624193/ae0660d5b90b/fphar-13-988245-g001.jpg

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