Yiming Zhang , Ye Cui , Qixiu Cheng , Zishan Li , Yiming Dai , Keqing Lin , Xiaoyu Li , Jin Chen
{"title":"丛枝菌根真菌介导了葱根际和内生细菌群落中罕见的分类群和网络复杂性","authors":"Yiming Zhang , Ye Cui , Qixiu Cheng , Zishan Li , Yiming Dai , Keqing Lin , Xiaoyu Li , Jin Chen","doi":"10.1016/j.rhisph.2025.101146","DOIUrl":null,"url":null,"abstract":"<div><div>Arbuscular mycorrhizal fungi (AMF) play a crucial role in enhancing plant growth and regulating rhizospheric microbial composition. However, their influence on rare bacterial taxa in both the rhizospheric and endophytic environments of <em>Allium schoenoprasum</em> L. remains largely unknown. To address this gap, we conducted a randomized experiment with four treatment groups: three inoculated with 30 g of <em>Rhizophagus irregularis</em>, <em>Diversispora epigaea</em>, or <em>Funneliformis mosseae</em>, and one uninoculated control group with sterilized inoculum (20 replicates each), using real-time quantitative PCR and Illumina MiSeq sequencing to analyze microbial communities. Results showed that AMF-inoculated plants exhibited significantly superior phenotypic traits compared to the control, with plant heights of 26.05 ± 2.88 cm (<em>R. irregularis</em>), 28.63 ± 2.09 cm (<em>D. epigaea</em>), and 24.92 ± 2.86 cm (<em>F. mosseae</em>) versus 8.59 ± 1.60 cm in the control, alongside significant differences in other traits. Among AMF treatments, <em>R. irregularis</em> strain notably promoted growth effectively with a high infection rate but lower infection intensity than <em>D. epigaea</em> and <em>F. mosseae</em> strains. Rhizospheric communities had more unique amplified sequence variants among rare bacterial taxa, while endophytic communities showed increased abundances of key taxa. Furthermore, inoculation with AMF leads to alterations in the expression of functional genes associated with the carbon, nitrogen, and phosphorus cycles. Specifically, the expression of the <em>cbbLR</em> and <em>phoD</em> genes was significantly elevated, while the expression of the <em>amoA</em> gene remained stable. Additionally, the complexity of the rhizospheric bacterial network was notably greater compared to the endophytic environment. These findings highlight the different roles of AMF in shaping microbial communities and promoting plant health.</div></div>","PeriodicalId":48589,"journal":{"name":"Rhizosphere","volume":"35 ","pages":"Article 101146"},"PeriodicalIF":3.5000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Arbuscular mycorrhizal fungi mediate rare taxa and network complexity in rhizospheric and endophytic bacterial communities of Allium schoenoprasum L\",\"authors\":\"Yiming Zhang , Ye Cui , Qixiu Cheng , Zishan Li , Yiming Dai , Keqing Lin , Xiaoyu Li , Jin Chen\",\"doi\":\"10.1016/j.rhisph.2025.101146\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Arbuscular mycorrhizal fungi (AMF) play a crucial role in enhancing plant growth and regulating rhizospheric microbial composition. However, their influence on rare bacterial taxa in both the rhizospheric and endophytic environments of <em>Allium schoenoprasum</em> L. remains largely unknown. To address this gap, we conducted a randomized experiment with four treatment groups: three inoculated with 30 g of <em>Rhizophagus irregularis</em>, <em>Diversispora epigaea</em>, or <em>Funneliformis mosseae</em>, and one uninoculated control group with sterilized inoculum (20 replicates each), using real-time quantitative PCR and Illumina MiSeq sequencing to analyze microbial communities. Results showed that AMF-inoculated plants exhibited significantly superior phenotypic traits compared to the control, with plant heights of 26.05 ± 2.88 cm (<em>R. irregularis</em>), 28.63 ± 2.09 cm (<em>D. epigaea</em>), and 24.92 ± 2.86 cm (<em>F. mosseae</em>) versus 8.59 ± 1.60 cm in the control, alongside significant differences in other traits. Among AMF treatments, <em>R. irregularis</em> strain notably promoted growth effectively with a high infection rate but lower infection intensity than <em>D. epigaea</em> and <em>F. mosseae</em> strains. Rhizospheric communities had more unique amplified sequence variants among rare bacterial taxa, while endophytic communities showed increased abundances of key taxa. Furthermore, inoculation with AMF leads to alterations in the expression of functional genes associated with the carbon, nitrogen, and phosphorus cycles. Specifically, the expression of the <em>cbbLR</em> and <em>phoD</em> genes was significantly elevated, while the expression of the <em>amoA</em> gene remained stable. Additionally, the complexity of the rhizospheric bacterial network was notably greater compared to the endophytic environment. These findings highlight the different roles of AMF in shaping microbial communities and promoting plant health.</div></div>\",\"PeriodicalId\":48589,\"journal\":{\"name\":\"Rhizosphere\",\"volume\":\"35 \",\"pages\":\"Article 101146\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-07-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Rhizosphere\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2452219825001314\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rhizosphere","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452219825001314","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Arbuscular mycorrhizal fungi mediate rare taxa and network complexity in rhizospheric and endophytic bacterial communities of Allium schoenoprasum L
Arbuscular mycorrhizal fungi (AMF) play a crucial role in enhancing plant growth and regulating rhizospheric microbial composition. However, their influence on rare bacterial taxa in both the rhizospheric and endophytic environments of Allium schoenoprasum L. remains largely unknown. To address this gap, we conducted a randomized experiment with four treatment groups: three inoculated with 30 g of Rhizophagus irregularis, Diversispora epigaea, or Funneliformis mosseae, and one uninoculated control group with sterilized inoculum (20 replicates each), using real-time quantitative PCR and Illumina MiSeq sequencing to analyze microbial communities. Results showed that AMF-inoculated plants exhibited significantly superior phenotypic traits compared to the control, with plant heights of 26.05 ± 2.88 cm (R. irregularis), 28.63 ± 2.09 cm (D. epigaea), and 24.92 ± 2.86 cm (F. mosseae) versus 8.59 ± 1.60 cm in the control, alongside significant differences in other traits. Among AMF treatments, R. irregularis strain notably promoted growth effectively with a high infection rate but lower infection intensity than D. epigaea and F. mosseae strains. Rhizospheric communities had more unique amplified sequence variants among rare bacterial taxa, while endophytic communities showed increased abundances of key taxa. Furthermore, inoculation with AMF leads to alterations in the expression of functional genes associated with the carbon, nitrogen, and phosphorus cycles. Specifically, the expression of the cbbLR and phoD genes was significantly elevated, while the expression of the amoA gene remained stable. Additionally, the complexity of the rhizospheric bacterial network was notably greater compared to the endophytic environment. These findings highlight the different roles of AMF in shaping microbial communities and promoting plant health.
RhizosphereAgricultural 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.