Bikaverin作为分子武器:通过根际微生物组调控提高香蕉尖孢镰刀菌的致病性。

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Honglin Lu, Suxia Guo, Yongbao Yang, Zhihao Zhao, Qingbiao Xie, Qiong Wu, Changjun Sun, Hongli Luo, Bang An, Qiannan Wang
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引用次数: 0

摘要

背景:香蕉枯萎病(Fusarium oxysporum f. sp. cubense Tropical Race 4, Foc TR4)引起的枯萎病对全球香蕉生产构成严重威胁。次生代谢物是病原体与其环境相互作用和调节宿主-病原体动力学的关键工具。镰刀菌素(Bikaverin)是几种镰刀菌属植物生产的一种红色聚酮色素,其药理特性已被研究,但其生态作用和致病性的影响尚不清楚。结果:本研究研究了比卡维林在Foc TR4中的作用,重点研究了其对致病性的贡献及其与根际微生物群的相互作用。在无菌和高压灭菌条件下进行的致病性试验表明,比卡维林不会通过影响感染过程或损害宿主组织直接促进致病性。相反,比卡维林通过重塑根际微生物群间接增强了Foc TR4的致病性。它抑制有益植物生长的根杆菌,如芽孢杆菌,同时促进真菌属的优势,从而创造一个有利于病原体定植和感染的微生物环境。值得注意的是,bikaverin的生物合成被发现受到环境因素的严格调节,包括酸性pH值、氮稀缺和微生物竞争。与velezensis和Botrytis cinerea等微生物共培养强烈诱导bikaverin的产生,并上调bikaverin关键生物合成基因FocBik1的表达。此外,具有广谱抗真菌活性的抗比卡维林芽孢杆菌BR160的鉴定,突出了其作为香蕉枯萎病生物防治剂的潜力,尽管其在田间条件下的稳定性和效率有待进一步验证。结论:比卡维林通过调控根际微生物群在Foc TR4致病性中起间接但重要的作用。这种生态功能强调了其作为可持续疾病管理战略目标的潜力。未来的研究应集中于阐明比卡维林介导的微生物相互作用的分子机制,利用转录组学和代谢组学等综合方法。总之,这些发现为对抗香蕉枯萎病和提高作物抗性的新方法提供了基础。视频摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bikaverin as a molecular weapon: enhancing Fusarium oxysporum pathogenicity in bananas via rhizosphere microbiome manipulation.

Background: Fusarium wilt, caused by Fusarium oxysporum f. sp. cubense Tropical Race 4 (Foc TR4), poses a severe threat to global banana production. Secondary metabolites are critical tools employed by pathogens to interact with their environment and modulate host-pathogen dynamics. Bikaverin, a red-colored polyketide pigment produced by several Fusarium species, has been studied for its pharmacological properties, but its ecological roles and impact on pathogenicity remain unclear.

Results: This study investigated the role of bikaverin in Foc TR4, focusing on its contribution to pathogenicity and its interaction with the rhizosphere microbiome. Pathogenicity assays under sterile and autoclaved conditions demonstrated that bikaverin does not directly contribute to pathogenicity by affecting the infection process or damaging host tissues. Instead, bikaverin indirectly enhances Foc TR4's pathogenicity by reshaping the rhizosphere microbiome. It suppresses beneficial plant growth-promoting rhizobacteria, such as Bacillus, while promoting the dominance of fungal genera, thereby creating a microbial environment beneficial for pathogen colonization and infection. Notably, bikaverin biosynthesis was found to be tightly regulated by environmental cues, including acidic pH, nitrogen scarcity, and microbial competition. Co-culture with microbes such as Bacillus velezensis and Botrytis cinerea strongly induced bikaverin production and upregulated expression of the key bikaverin biosynthetic gene FocBik1. In addition, the identification of bikaverin-resistant Bacillus BR160, a strain with broad-spectrum antifungal activity, highlights its potential as a biocontrol agent for banana wilt management, although its stability and efficiency under field conditions require further validation.

Conclusions: Bikaverin plays an indirect yet important role in the pathogenicity of Foc TR4 by manipulating the rhizosphere microbiome. This ecological function underscores its potential as a target for sustainable disease management strategies. Future research should focus on elucidating the molecular mechanisms underlying bikaverin-mediated microbial interactions, using integrated approaches such as transcriptomics and metabolomics. Together, these findings provide a foundation for novel approaches to combat banana wilt disease and enhance crop resistance. Video Abstract.

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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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