Bacterial wilt disease alters the structure and function of fungal communities around plant roots

Abstract Background Fungal communities around plant roots play crucial roles in maintaining plant health. Nonetheless, the responses of fungal communities to bacterial wilt disease remain poorly understood. Here, the structure and function of fungal communities across four consecutive compartments (...

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Main Authors: Jiemeng Tao, Jingjing Jin, Peng Lu, Shizhou Yu, Mengli Gu, Jinbang Wang, Jianfeng Zhang, Peijian Cao
Format: Article
Language:English
Published: BMC 2025-01-01
Series:BMC Plant Biology
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Online Access:https://doi.org/10.1186/s12870-025-06056-1
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author Jiemeng Tao
Jingjing Jin
Peng Lu
Shizhou Yu
Mengli Gu
Jinbang Wang
Jianfeng Zhang
Peijian Cao
author_facet Jiemeng Tao
Jingjing Jin
Peng Lu
Shizhou Yu
Mengli Gu
Jinbang Wang
Jianfeng Zhang
Peijian Cao
author_sort Jiemeng Tao
collection DOAJ
description Abstract Background Fungal communities around plant roots play crucial roles in maintaining plant health. Nonetheless, the responses of fungal communities to bacterial wilt disease remain poorly understood. Here, the structure and function of fungal communities across four consecutive compartments (bulk soil, rhizosphere, rhizoplane and root endosphere) were investigated under the influence of bacterial wilt disease. Results The results showed that bacterial wilt disease caused different assembly patterns of fungal communities in the bulk soil, rhizosphere, rhizoplane and endosphere. Under the influence of bacterial wilt disease, a decreased fungal diversity was observed in the rhizoplane and endosphere, and completely different kinds of fungal genera were enriched in the four compartments. The complexity and stability of fungal networks were less affected, but the number of key fungal members in networks were significantly reduced in diseased samples. Functional predictions based on FUNGuild suggested that with the pathogen infection, saprotrophic fungi were increased in the bulk soil, but pathotrophic fungi (potential plant and animal pathogens) were increased in the rhizosphere, rhizoplane and endosphere. Conclusion This work provides a deep insight into the effects of bacterial wilt disease on fungal communities along the soil-root continuum, and is helpful to identify plant-associated beneficial fungi to resist plant disease. Clinical trial number Not applicable.
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id doaj-art-9f8a03a21d6e40a7bbe5492037f1b3f7
institution Kabale University
issn 1471-2229
language English
publishDate 2025-01-01
publisher BMC
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series BMC Plant Biology
spelling doaj-art-9f8a03a21d6e40a7bbe5492037f1b3f72025-01-12T12:14:09ZengBMCBMC Plant Biology1471-22292025-01-0125111110.1186/s12870-025-06056-1Bacterial wilt disease alters the structure and function of fungal communities around plant rootsJiemeng Tao0Jingjing Jin1Peng Lu2Shizhou Yu3Mengli Gu4Jinbang Wang5Jianfeng Zhang6Peijian Cao7Beijing Life Science AcademyBeijing Life Science AcademyBeijing Life Science AcademyMolecular Genetics Key Laboratory of China Tobacco, Guizhou Academy of Tobacco ScienceChina Tobacco Gene Research Center, Zhengzhou Tobacco Research Institute of CNTCChina Tobacco Gene Research Center, Zhengzhou Tobacco Research Institute of CNTCBeijing Life Science AcademyBeijing Life Science AcademyAbstract Background Fungal communities around plant roots play crucial roles in maintaining plant health. Nonetheless, the responses of fungal communities to bacterial wilt disease remain poorly understood. Here, the structure and function of fungal communities across four consecutive compartments (bulk soil, rhizosphere, rhizoplane and root endosphere) were investigated under the influence of bacterial wilt disease. Results The results showed that bacterial wilt disease caused different assembly patterns of fungal communities in the bulk soil, rhizosphere, rhizoplane and endosphere. Under the influence of bacterial wilt disease, a decreased fungal diversity was observed in the rhizoplane and endosphere, and completely different kinds of fungal genera were enriched in the four compartments. The complexity and stability of fungal networks were less affected, but the number of key fungal members in networks were significantly reduced in diseased samples. Functional predictions based on FUNGuild suggested that with the pathogen infection, saprotrophic fungi were increased in the bulk soil, but pathotrophic fungi (potential plant and animal pathogens) were increased in the rhizosphere, rhizoplane and endosphere. Conclusion This work provides a deep insight into the effects of bacterial wilt disease on fungal communities along the soil-root continuum, and is helpful to identify plant-associated beneficial fungi to resist plant disease. Clinical trial number Not applicable.https://doi.org/10.1186/s12870-025-06056-1Bacterial wilt diseaseFungal communityCommunity assemblyCo-occurrence network
spellingShingle Jiemeng Tao
Jingjing Jin
Peng Lu
Shizhou Yu
Mengli Gu
Jinbang Wang
Jianfeng Zhang
Peijian Cao
Bacterial wilt disease alters the structure and function of fungal communities around plant roots
BMC Plant Biology
Bacterial wilt disease
Fungal community
Community assembly
Co-occurrence network
title Bacterial wilt disease alters the structure and function of fungal communities around plant roots
title_full Bacterial wilt disease alters the structure and function of fungal communities around plant roots
title_fullStr Bacterial wilt disease alters the structure and function of fungal communities around plant roots
title_full_unstemmed Bacterial wilt disease alters the structure and function of fungal communities around plant roots
title_short Bacterial wilt disease alters the structure and function of fungal communities around plant roots
title_sort bacterial wilt disease alters the structure and function of fungal communities around plant roots
topic Bacterial wilt disease
Fungal community
Community assembly
Co-occurrence network
url https://doi.org/10.1186/s12870-025-06056-1
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AT shizhouyu bacterialwiltdiseasealtersthestructureandfunctionoffungalcommunitiesaroundplantroots
AT mengligu bacterialwiltdiseasealtersthestructureandfunctionoffungalcommunitiesaroundplantroots
AT jinbangwang bacterialwiltdiseasealtersthestructureandfunctionoffungalcommunitiesaroundplantroots
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