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比卡维林作为一种分子武器:通过根际微生物群落调控增强尖孢镰刀菌对香蕉的致病性

Bikaverin as a molecular weapon: enhancing Fusarium oxysporum pathogenicity in bananas via rhizosphere microbiome manipulation.

作者信息

Lu Honglin, Guo Suxia, Yang Yongbao, Zhao Zhihao, Xie Qingbiao, Wu Qiong, Sun Changjun, Luo Hongli, An Bang, Wang Qiannan

机构信息

National Key Laboratory for Tropical Crop Breeding, School of Breeding and Multiplication (Sanya Institute of Breeding and Multiplication), School of Tropical Agriculture and Forestry (School of Agriculture and Rural Affairs & School of Rural Revitalization), Hainan University, Sanya, Hainan Province, People's Republic of China.

Key Laboratory of Banana Genetic Improvement of Hainan Province, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, Hainan Province, 571101, People's Republic of China.

出版信息

Microbiome. 2025 Apr 29;13(1):107. doi: 10.1186/s40168-025-02109-7.

Abstract

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.

摘要

背景

由尖孢镰刀菌古巴专化型热带4号小种(Foc TR4)引起的香蕉枯萎病对全球香蕉生产构成严重威胁。次生代谢产物是病原体与环境相互作用并调节宿主 - 病原体动态的关键工具。比卡维林是几种镰刀菌产生的一种红色聚酮类色素,其药理特性已得到研究,但其生态作用和对致病性的影响仍不清楚。

结果

本研究调查了比卡维林在Foc TR4中的作用,重点关注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导致致病性。相反,比卡维林通过重塑根际微生物群间接增强Foc TR4的致病性。它抑制有益的植物促生根际细菌,如芽孢杆菌,同时促进真菌属的优势地位,从而创造一个有利于病原体定殖和感染的微生物环境。值得注意的是,发现比卡维林的生物合成受到环境线索的严格调控,包括酸性pH值、氮缺乏和微生物竞争。与诸如贝莱斯芽孢杆菌和灰葡萄孢等微生物共培养强烈诱导比卡维林的产生并上调关键的比卡维林生物合成基因FocBik1的表达。此外,鉴定出具有广谱抗真菌活性的抗比卡维林芽孢杆菌BR160,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需要进一步验证。

结论

比卡维林通过操纵根际微生物群在Foc TR4的致病性中发挥间接但重要的作用。这种生态功能强调了其作为可持续疾病管理策略靶点的潜力。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,采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增强作物抗性的新方法提供了基础。视频摘要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f7e/12042607/09907ec21fc9/40168_2025_2109_Fig1_HTML.jpg

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