枯草芽孢杆菌和边缘假单胞菌对铁的竞争形成了代谢拮抗。

IF 10.8 1区 环境科学与生态学 Q1 ECOLOGY
Mark Lyng, Johan P B Jørgensen, Morten D Schostag, Scott A Jarmusch, Diana K C Aguilar, Carlos N Lozano-Andrade, Ákos T Kovács
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引用次数: 0

摘要

长期以来,嗜苷酸盐作为细菌相互关系的决定因素一直与社会微生物学有关。对于与植物相关的菌属,如芽孢杆菌和假单胞菌,嗜苷酸盐因其生物防治功能而广为人知。在这里,我们探讨了枯草芽孢杆菌嗜苷酸盐巴氏杆菌素(BB)在与边缘假单胞菌(Pseudomonas marginalis)的拮抗作用中的功能作用。BB 的存在以铁依赖的方式强烈影响了相互作用的结果。BB 生产者 B. subtilis 通过抑制组氨酸激酶编码基因 gacS 的转录,限制了边缘假单胞菌的菌落扩散,从而抑制了次生代谢物(如吡咯烷和粘菌素)的产生。相比之下,缺乏 BB 会限制枯草杆菌菌落的生长。为了探索这种拮抗作用的特异性,我们将枯草杆菌与一系列荧光假单胞菌进行了共培养,结果发现枯草杆菌与假单胞菌之间的相互作用是保守的,这拓展了我们对土壤细菌中两个研究最深入的菌属之间相互作用的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Competition for iron shapes metabolic antagonism between Bacillus subtilis and Pseudomonas marginalis.

Siderophores have long been implicated in sociomicrobiology as determinants of bacterial interrelations. For plant-associated genera, like Bacillus and Pseudomonas, siderophores are well known for their biocontrol functions. Here, we explored the functional role of the Bacillus subtilis siderophore bacillibactin (BB) in an antagonistic interaction with Pseudomonas marginalis. The presence of BB strongly influenced the outcome of the interaction in an iron-dependent manner. The BB producer B. subtilis restricts colony spreading of P. marginalis by repressing the transcription of histidine kinase-encoding gene gacS, thereby abolishing production of secondary metabolites such as pyoverdine and viscosin. By contrast, lack of BB restricted B. subtilis colony growth. To explore the specificity of the antagonism, we cocultured B. subtilis with a collection of fluorescent Pseudomonas spp. and found that the Bacillus-Pseudomonas interaction is conserved, expanding our understanding of the interplay between two of the most well-studied genera of soil bacteria.

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来源期刊
ISME Journal
ISME Journal 环境科学-生态学
CiteScore
22.10
自引率
2.70%
发文量
171
审稿时长
2.6 months
期刊介绍: The ISME Journal covers the diverse and integrated areas of microbial ecology. We encourage contributions that represent major advances for the study of microbial ecosystems, communities, and interactions of microorganisms in the environment. Articles in The ISME Journal describe pioneering discoveries of wide appeal that enhance our understanding of functional and mechanistic relationships among microorganisms, their communities, and their habitats.
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