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Metabolite transfer with the fermentation product 2,3-butanediol enhances virulence by Pseudomonas aeruginosa

机译:发酵产物2,3-丁二醇的代谢物转移增强了铜绿假单胞菌的毒力

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The respiratory tract of cystic fibrosis (CF) patients harbor persistent microbial communities (CF airway microbiome) with Pseudomonas aeruginosa emerging as a dominant pathogen. Within a polymicrobial infection, interactions between co-habitant microbes can be important for pathogenesis, but even when considered, these interactions are not well understood. Here, we show with in vitro experiments that, compared with glucose, common fermentation products from co-habitant bacteria significantly increase virulence factor production, antimicrobial activity and biofilm formation of P. aeruginosa. The maximum stimulating effect was produced with the fermentation product 2,3-butanediol, which is a substrate for P. aeruginosa, resulting in a metabolic relationship between fermenters and this pathogen. The global transcription regulator LasI LasR, which controls quorum sensing, was upregulated threefold with 2,3-butanediol, resulting in higher phenazine and exotoxin concentrations and improved biofilm formation. This indicates that the success of P. aeruginosa in CF airway microbiomes could be governed by the location within the food web with fermenting bacteria. Our findings suggest that interbacterial metabolite transfer in polymicrobial infections stimulates virulence of P. aeruginosa and could have a considerable impact on disease progression.
机译:囊性纤维化(CF)患者的呼吸道具有持久性微生物群落(CF气道微生物组),其中铜绿假单胞菌(Pseudomonas aeruginosa)成为主要病原体。在多微生物感染中,同居微生物之间的相互作用对于发病机理可能很重要,但是即使考虑到这些相互作用,人们对此也知之甚少。在这里,我们通过体外实验表明,与葡萄糖相比,来自同居细菌的常见发酵产物显着提高了铜绿假单胞菌的毒力因子产生,抗菌活性和生物膜形成。发酵产物2,3-丁二醇是铜绿假单胞菌的底物,产生了最大的刺激作用,导致了发酵罐和该病原体之间的代谢关系。控制群体感应的全局转录调节剂LasI LasR被2,3-丁二醇上调了三倍,从而导致吩嗪和外毒素浓度更高,生物膜形成也得到改善。这表明铜绿假单胞菌在CF气道微生物群中的成功可能受发酵细菌在食物网中的位置控制。我们的发现表明,细菌在多种微生物感染中的代谢物转移会刺激铜绿假单胞菌的毒性,并且可能对疾病的发展产生重大影响。

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