Novel antibiofilm chemotherapies target nitrogen from glutamate and glutamine.

Novel antibiofilm chemotherapies target nitrogen from glutamate and glutamine.
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DOI:
10.1038/s41598-018-25401-z
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发表时间:
2018-05-08
期刊:
影响因子:
4.6
通讯作者:
Kolodkin-Gal I
Kolodkin-Gal I
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Hassanov T;Karunker I;Steinberg N;Erez A;Kolodkin-Gal I

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自然界中的细菌通常存在于称为生物膜的分化群落中,生物膜是细菌单细胞和多细胞生命状态之间的活跃界面。在这里,我们证明枯草芽孢杆菌生物膜的发育依赖于谷氨酰胺或谷氨酸作为氮源的使用。我们展示了生物膜内不同的代谢需求;虽然谷氨酰胺对于边缘的分裂细胞是必需的,但内部细胞团利用乳酸。我们的结果表明生物膜细胞保留了谷氨酸代谢的短期记忆。最后,我们确定针对谷氨酰胺和谷氨酸盐利用的药物限制生物膜的形成。总的来说,我们的工作揭示了生物膜内氮和碳代谢的空间调节,这有助于细菌复合群落的适应性。生物膜内这种获得性代谢分工可以作为新型抗生物膜化疗的目标
Bacteria in nature often reside in differentiated communities termed biofilms, which are an active interphase between uni-cellular and multicellular life states for bacteria. Here we demonstrate that the development of B. subtilis biofilms is dependent on the use of glutamine or glutamate as a nitrogen source. We show a differential metabolic requirement within the biofilm; while glutamine is necessary for the dividing cells at the edges, the inner cell mass utilizes lactic acid. Our results indicate that biofilm cells preserve a short-term memory of glutamate metabolism. Finally, we establish that drugs that target glutamine and glutamate utilization restrict biofilm development. Overall, our work reveals a spatial regulation of nitrogen and carbon metabolism within the biofilm, which contributes to the fitness of bacterial complex communities. This acquired metabolic division of labor within biofilm can serve as a target for novel anti-biofilm chemotherapies
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