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DSM 2243通过胆汁酸转化减轻[具体物种]的胆汁酸应激反应。 (注:原文中“in and by”之间缺少具体内容,这里是根据已有信息尽量完整翻译)

DSM 2243 Alleviates Bile Acid Stress Response in and by Transformation of Bile Acids.

作者信息

Pedersen Kristian Jensen, Haange Sven-Bastiaan, Žížalová Kateřina, Viehof Alina, Clavel Thomas, Leniček Martin, Engelmann Beatrice, Wick Lukas Y, Schaap Frank G, Jehmlich Nico, Rolle-Kampczyk Ulrike, von Bergen Martin

机构信息

Helmholtz-Centre for Environmental Research-UFZ GmbH, Department of Molecular Systems Biology, 04318 Leipzig, Germany.

Institute of Medical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine and General University Hospital in Prague, Charles University, Kateřinská 32, 12108 Prague, Czech Republic.

出版信息

Microorganisms. 2022 Oct 13;10(10):2025. doi: 10.3390/microorganisms10102025.

Abstract

Bile acids are crucial for the uptake of dietary lipids and can shape the gut-microbiome composition. This latter function is associated with the toxicity of bile acids and can be modulated by bile acid modifying bacteria such as , but the molecular details of the interaction of bacteria depending on bile acid modifications are not well understood. In order to unravel the molecular response to bile acids and their metabolites, we cultivated eight strains from a human intestinal microbiome model alone and in co-culture with in the presence of cholic acid (CA) and deoxycholic acid (DCA). We observed growth inhibition of particularly gram-positive strains such as and the gram-variable Anaerostipes cacae by CA and DCA stress. was alleviated through co-culturing with . We approached effects on the membrane by zeta potential and genotoxic and metabolic effects by (meta)proteomic and metabolomic analyses. Co-culturing with decreased both CA and DCA by the formation of oxidized and epimerized bile acids. also produces microbial bile salt conjugates in a co-cultured species-specific manner. This study highlights how the interaction with other bacteria can influence the functionality of bacteria.

摘要

胆汁酸对于膳食脂质的吸收至关重要,并且能够塑造肠道微生物群的组成。后一种功能与胆汁酸的毒性相关,并且可以被诸如[未提及具体细菌名称]等胆汁酸修饰细菌所调节,但是依赖于胆汁酸修饰的细菌相互作用的分子细节尚未得到充分理解。为了阐明对胆汁酸及其代谢物的分子反应,我们单独培养了来自人类肠道微生物群模型的八株菌株,并在胆酸(CA)和脱氧胆酸(DCA)存在的情况下与[未提及具体细菌名称]进行共培养。我们观察到,特别是革兰氏阳性菌株如[未提及具体细菌名称]和革兰氏可变的粪厌氧棒状菌在CA和DCA胁迫下生长受到抑制。通过与[未提及具体细菌名称]共培养,这种抑制作用得到缓解。我们通过zeta电位研究对膜的影响,并通过(元)蛋白质组学和代谢组学分析研究遗传毒性和代谢影响。与[未提及具体细菌名称]共培养通过形成氧化和差向异构化的胆汁酸降低了CA和DCA的水平。[未提及具体细菌名称]还以共培养物种特异性的方式产生微生物胆汁盐缀合物。这项研究突出了与其他细菌的相互作用如何能够影响细菌的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10c6/9607062/15e10be3eedf/microorganisms-10-02025-g001.jpg

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