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利迪霉素在放线菌相互作用中诱导形态分化。

Lydicamycins induce morphological differentiation in actinobacterial interactions.

作者信息

Jarmusch Scott A, Schostag Morten D, Yang Zhijie, Wang Jinglin, Andersen Aaron J C, Weber Tilmann, Ding Ling

机构信息

Department of Biotechnology and Biomedicine, Technical University of Denmark, Kongens Lyngby, Denmark.

The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kongens Lyngby, Denmark.

出版信息

Appl Environ Microbiol. 2025 Jun 18;91(6):e0029525. doi: 10.1128/aem.00295-25. Epub 2025 May 13.

Abstract

UNLABELLED

are major players in soil microbiomes; however, their interactions with other actinobacteria remain largely unexplored. Given the complex developmental cycle of actinobacteria, a multi-omics approach is essential to unravel the interactions. This study originated from the observation of induced morphogenesis between two environmental isolates from the same site, sp. P9-2B1 and sp. P9-2B2. When co-cultivated on potato dextrose agar, P9-2B2 triggered a wave-like sporulation pattern in strain P9-2B1. Mass pectrometry imaging revealed that a suite of lydicamycins accumulated in the induced sporulation zone. Using CRISPR base editing, lydicamycin-deficient mutants were generated, and the inducible sporulation was ceased, confirming the role of lydicamycin in triggering morphological differentiation. In agar diffusion assays, pure lydicamycin was inhibitory when added concurrently with bacterial inoculation but induced sporulation when added later. The same inducible sporulation wave phenomenon was also observed in additional environmental isolates and M145 and M1146. Transcriptomics analysis revealed differential gene expression linked to early aerial mycelium development at 4 days into co-culture, the transitional genes responsible for the development of spores at day 9, together with numerous genes for overall stress responses, particularly cell envelope stress responses. These findings highlight previously unrecognized actinobacteria interactions mediated by lydicamycins, suggesting a broader ecological role of bioactive metabolites in microbiomes.

IMPORTANCE

Moving beyond an antibiotic discovery mindset, exploring the chemical ecology of secondary metabolites is key to maximizing their biotechnological potential. Dual cultures offer reduced complexity, enabling an in-depth analysis of these interactions via multi-omics, which provides complementary data for more robust conclusions. This study sheds light on the role of lydicamycins in dual cultures with other actinobacteria and establishes an integral roadmap for future chemical ecology work between microorganisms, particularly through mass spectrometry imaging.

摘要

未标记

是土壤微生物群落中的主要参与者;然而,它们与其他放线菌的相互作用在很大程度上仍未得到探索。鉴于放线菌复杂的发育周期,多组学方法对于揭示这些相互作用至关重要。本研究源于对来自同一地点的两种环境分离株(链霉菌属P9 - 2B1和链霉菌属P9 - 2B2)之间诱导形态发生的观察。当在马铃薯葡萄糖琼脂上共培养时,P9 - 2B2在菌株P9 - 2B1中引发了波浪状的孢子形成模式。质谱成像显示,一组利迪霉素在诱导的孢子形成区域积累。使用CRISPR碱基编辑,产生了利迪霉素缺陷型突变体,诱导的孢子形成停止,证实了利迪霉素在触发形态分化中的作用。在琼脂扩散试验中,纯利迪霉素在与细菌接种同时添加时具有抑制作用,但在稍后添加时诱导孢子形成。在其他环境分离株以及M145和M1146中也观察到了相同的诱导孢子形成波现象。转录组学分析揭示了与共培养4天时早期气生菌丝发育相关的差异基因表达、在第9天负责孢子发育的过渡基因,以及许多与整体应激反应相关的基因,特别是细胞壁应激反应基因。这些发现突出了以前未被认识的由利迪霉素介导的放线菌相互作用,表明生物活性代谢物在微生物群落中具有更广泛的生态作用。

重要性

超越抗生素发现的思维模式,探索次生代谢物的化学生态学是最大化其生物技术潜力的关键。双重培养降低了复杂性,能够通过多组学对这些相互作用进行深入分析,为得出更可靠的结论提供补充数据。本研究揭示了利迪霉素在与其他放线菌的双重培养中的作用,并为未来微生物之间的化学生态学工作建立了一个完整的路线图,特别是通过质谱成像。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e83a/12175524/dd0d9c6503af/aem.00295-25.f001.jpg

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