Host selection shapes structure and network of microbial community of Epimedium plants along the soil–rhizosphere–plant continuum

IF 3.5 3区 生物学 Q1 PLANT SCIENCES Rhizosphere Pub Date : 2025-03-01 Epub Date: 2024-12-20 DOI:10.1016/j.rhisph.2024.101010
Zhaoyu Zhang , Ziying Huang , Xiao Chen , Guozhuang Zhang , Mengzhi Li , Anning Li , Xiaolin Lin , Yuxin Zhou , Yu Zhang , Shilin Chen , Linlin Dong , Guangfei Wei
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Abstract

Background and aims

Microbiota inhabiting plants are essential for plant productivity and health. Microbes in various plant compartment niches perform distinct ecological functions. However, the microbial characteristics in different niches of Epimedium plants, one of the most promising tonic herbs in traditional Chinese medicine, remain largely unknown.

Methods

Here, microbial composition, diversity and co-occurrence network in the five ecological niches (bulk soil, rhizosphere soil, root, stem, and leaf) of three Epimedium plant cultivars were investigated using high-throughput sequencing.

Results

The microbial composition were predominately imprinted by compartment niches than by host cultivars. Bacterial diversity and network complexity incrementally decreased from the soils to the root to the leaf; however, fungal diversity and network complexity gradually decreased from the soils to the root to the stem but increased from the stem to the leaf. Cyanobacteria, Proteobacteria, Arthrobacter, Sphingomonas, and Gemmatimonas were bacterial keystone taxa, while Ascomycota, Davidiella, and Hymenoscyphus were fungal keystone taxa. These taxa exhibited significant compartment-specific properties and performed distinct ecological functions.

Conclusion

The microbial communities are mostly originated from bulk soil, and subsequently filtered and enriched in various compartment niches through host selection. Compartment niches profoundly imprinted the plant-associated microbiota, which provided valuable insights into harnessing beneficial communities for Epimedium plants in sustainable agriculture and the improvement of herbal quality.
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寄主选择决定了淫羊藿植物沿土壤-根际-植物连续体的微生物群落结构和网络
背景与目的植物微生物群对植物的生产力和健康至关重要。微生物在不同的植物隔间生态位中发挥着不同的生态功能。然而,淫羊藿(Epimedium)作为中药中最有潜力的滋补药材之一,其不同生态位的微生物特征仍不为人所知。方法采用高通量测序技术对3个淫羊藿品种土壤、根际土壤、根、茎、叶5个生态位(土壤、根、茎、叶)的生态位、微生物组成、多样性和共生网络进行研究。结果微生物组成主要是由菌室生态位而非寄主品种印记。细菌多样性和网络复杂性从土壤到根再到叶逐渐降低;真菌多样性和网络复杂性从土壤到根到茎逐渐降低,而从茎到叶逐渐增加。蓝藻门、变形菌门、节杆菌门、鞘单胞菌门和双胞菌门是细菌的重点分类群,子囊菌门、大维菌门和膜隐菌门是真菌的重点分类群。这些分类群表现出明显的区室特征,并具有不同的生态功能。结论微生物群落主要来源于散装土壤,通过寄主选择在不同的隔间生态位中进行过滤和富集。隔间生态位深刻地影响着植物相关的微生物群,为利用淫羊藿植物的有益群落进行可持续农业和提高草药质量提供了有价值的见解。
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来源期刊
Rhizosphere
Rhizosphere Agricultural and Biological Sciences-Agronomy and Crop Science
CiteScore
5.70
自引率
8.10%
发文量
155
审稿时长
29 days
期刊介绍: Rhizosphere aims to advance the frontier of our understanding of plant-soil interactions. Rhizosphere is a multidisciplinary journal that publishes research on the interactions between plant roots, soil organisms, nutrients, and water. Except carbon fixation by photosynthesis, plants obtain all other elements primarily from soil through roots. We are beginning to understand how communications at the rhizosphere, with soil organisms and other plant species, affect root exudates and nutrient uptake. This rapidly evolving subject utilizes molecular biology and genomic tools, food web or community structure manipulations, high performance liquid chromatography, isotopic analysis, diverse spectroscopic analytics, tomography and other microscopy, complex statistical and modeling tools.
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