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细菌分泌 D-精氨酸控制环境微生物生物多样性。

Bacterial secretion of D-arginine controls environmental microbial biodiversity.

机构信息

Department of Molecular Biology, Laboratory for Molecular Infection Medicine Sweden, Umeå Centre for Microbial Research, Umeå University, Umeå, Sweden.

Centro de Biología Molecular 'Severo Ochoa', Universidad Autónoma de Madrid-Consejo Superior de Investigaciones Científicas, Madrid, Spain.

出版信息

ISME J. 2018 Feb;12(2):438-450. doi: 10.1038/ismej.2017.176. Epub 2017 Oct 13.

Abstract

Bacteria face tough competition in polymicrobial communities. To persist in a specific niche, many species produce toxic extracellular effectors to interfere with the growth of nearby microbes. These effectors include the recently reported non-canonical D-amino acids (NCDAAs). In Vibrio cholerae, the causative agent of cholera, NCDAAs control cell wall integrity in stationary phase. Here, an analysis of the composition of the extracellular medium of V. cholerae revealed the unprecedented presence of D-Arg. Compared with other D-amino acids, D-Arg displayed higher potency and broader toxicity in terms of the number of bacterial species affected. Tolerance to D-Arg was associated with mutations in the phosphate transport and chaperone systems, whereas D-Met lethality was suppressed by mutations in cell wall determinants. These observations suggest that NCDAAs target different cellular processes. Finally, even though virtually all Vibrio species are tolerant to D-Arg, only a few can produce this D-amino acid. Indeed, we demonstrate that D-Arg may function as part of a cooperative strategy in vibrio communities to protect non-producing members from competing bacteria. Because NCDAA production is widespread in bacteria, we anticipate that D-Arg is a relevant modulator of microbial subpopulations in diverse ecosystems.

摘要

细菌在多微生物群落中面临着激烈的竞争。为了在特定的小生境中生存,许多物种会产生有毒的细胞外效应物来干扰附近微生物的生长。这些效应物包括最近报道的非典型 D-氨基酸 (NCDAAs)。在霍乱弧菌中,霍乱的病原体,NCDAAs 在静止期控制细胞壁的完整性。在这里,对霍乱弧菌细胞外培养基成分的分析揭示了 D-Arg 的前所未有的存在。与其他 D-氨基酸相比,D-Arg 在受影响的细菌种类数量方面表现出更高的效力和更广泛的毒性。对 D-Arg 的耐受性与磷酸盐转运和伴侣系统的突变有关,而 D-Met 的致死性则被细胞壁决定因素的突变所抑制。这些观察结果表明,NCDAAs 针对不同的细胞过程。最后,尽管几乎所有的弧菌都能耐受 D-Arg,但只有少数能产生这种 D-氨基酸。事实上,我们证明 D-Arg 可能作为弧菌群落中一种合作策略的一部分,以保护非产生成员免受竞争细菌的侵害。由于 NCDAA 的产生在细菌中广泛存在,我们预计 D-Arg 是不同生态系统中微生物亚群的一个相关调节剂。

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