Induction of conidial traps in the nematode-trapping fungus Drechslerella dactyloides by soil microbes.

IF 4.6 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2025-03-18 Epub Date: 2025-02-13 DOI:10.1128/msystems.01291-24
Ling Zhang, Tao Zhang, Yan-Rui Xu, Jia-Mei Sun, Xue-Rong Pan, Kun-Ze Gu, Ke-Qin Zhang, Zhi-Gang Zhang, Lian-Ming Liang
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Abstract

Nematode-trapping fungi, renowned for their specialized predatory structures that ensnare nematodes, offer a promising biological approach to managing plant-parasitic nematodes. However, the efficacy of these fungi is frequently hampered by biotic and abiotic factors within the soil, which can significantly impede fungal germination (fungistasis). To counteract these environmental challenges, certain nematode-trapping fungi have evolved to produce traps from their conidia, referred to as conidial traps. This adaptation allows them to bypass the inhibitory effects of their surroundings, enhancing their predatory capabilities. In this study, we explored how soil affects conidial trap formation in Drechslerella dactyloides. Our findings revealed that Acinetobacter spp. and Pantoea spp. present in soil extracts play pivotal roles in triggering the development of these traps. Using metagenomic sequencing, we mapped the shifts in bacterial communities and their relative abundances before and after incubation for up to 24 hours to optimize soil induction effects. This analysis highlighted the enrichment of specific functional genes in soil microbes and provided insights into the mechanisms driving conidial trap formation, based on changes in soil characteristics. Furthermore, through bacterial isolation procedures, we successfully cultured and characterized the bacteria responsible for this phenomenon, confirming their potent ability to stimulate the production of conidial traps in nematode-trapping fungi. This study not only underscores the critical role of bacterial diversity in modulating the life cycle transitions of nematode-trapping fungi but also sets the stage for the development of more effective and sustainable strategies to harness these fungi in the battle against pathogenic nematodes.

Importance: Predatory nematode-trapping fungi are important microbial antagonists of nematodes and can be developed into biocontrol agents. However, microbial biocontrol agents often suffer from inconsistent efficacy, primarily due to biotic and abiotic stresses in the rhizosphere soil. Drechslerella dactyloides, a nematode-trapping fungus, produces conidial traps in soil, serving as a survival strategy to overcome these stresses. In this study, we optimized soil suspensions to efficiently induce the formation of conidial traps. We found that bacteria in the soil directly trigger this formation. Metagenomic sequencing revealed bacterial enrichment during optimization, and we isolated and purified these bacteria with inducible activity. Our research deepens the understanding of this survival strategy of nematode-trapping fungi in nature, laying the foundation for enhancing the effectiveness of nematode biocontrol using this mechanism.

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土壤微生物诱导诱捕线虫真菌芽胞杆菌分生孢子诱捕。
捕获线虫的真菌以其捕获线虫的特殊掠食性结构而闻名,为管理植物寄生线虫提供了一种有前途的生物学方法。然而,这些真菌的功效经常受到土壤中生物和非生物因素的阻碍,这些因素会严重阻碍真菌的萌发(抑菌)。为了应对这些环境挑战,某些捕获线虫的真菌已经进化到从它们的分生孢子中产生陷阱,称为分生孢子陷阱。这种适应使它们能够绕过周围环境的抑制作用,增强它们的捕食能力。在本研究中,我们探讨了土壤如何影响dactyloides drechslellella分生孢子陷阱的形成。研究结果表明,土壤提取物中存在的不动杆菌和泛菌在触发这些陷阱的形成中起着关键作用。利用宏基因组测序,我们绘制了细菌群落和相对丰度在孵育24小时前后的变化,以优化土壤诱导效果。该分析强调了土壤微生物中特定功能基因的富集,并提供了基于土壤特征变化驱动分生孢子陷阱形成的机制的见解。此外,通过细菌分离程序,我们成功地培养并鉴定了导致这种现象的细菌,证实了它们在线虫捕获真菌中刺激分生孢子陷阱产生的强大能力。这项研究不仅强调了细菌多样性在调节捕获线虫真菌生命周期转变中的关键作用,而且为开发更有效和可持续的策略来利用这些真菌对抗病原线虫奠定了基础。重要性:捕获线虫的掠食性真菌是重要的线虫微生物拮抗剂,可发展为生物防治剂。然而,由于根际土壤中的生物和非生物胁迫,微生物生物防治剂的效果往往不一致。dactyloides是一种捕获线虫的真菌,在土壤中产生分生孢子陷阱,作为克服这些压力的生存策略。在这项研究中,我们优化了土壤悬浮液,以有效地诱导分生孢子陷阱的形成。我们发现土壤中的细菌直接引发了这种形成。宏基因组测序显示优化过程中细菌富集,并分离纯化了具有诱导活性的细菌。我们的研究加深了对自然界中捕获线虫真菌这种生存策略的认识,为利用这一机制提高线虫生物防治的有效性奠定了基础。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
期刊最新文献
Urban sewage resistomes partially reflect clinical resistomes. S'Wipe: user-friendly stool collection for high-throughput gut metabolomics and multi-omics. Prediction model for periodontitis stage based on the salivary microbiome. Adaptation of Enterococcus faecalis to intestinal mucus revealed by a human colonic organoid model. Revealing transcriptomic responses in Escherichia coli during early antibiotic exposure.
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