盐胁迫下高粱-花生间作通过影响土壤糖代谢途径介导高粱根际微生物群落的形成。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-05-01 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1589415
Xia Shao, Chunmei Yang, Yuxuan Chen, Chang Liu, Chunjuan Liu, Xiaolong Shi, Yufei Zhou
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引用次数: 0

摘要

土壤盐碱化是农业生产的重大障碍,研究可持续的缓解措施对于解决粮食安全问题至关重要。通过2年盆栽试验,研究盐胁迫下高粱-花生间作制度下高粱根际微生物群落的形成机制。试验分为正常土壤条件下单作高粱(NSS)、正常土壤条件下间作高粱(NIS)、盐胁迫条件下单作高粱(SSS)和盐胁迫条件下间作高粱(SIS) 4个处理。采用GC-MS检测了高粱根际土壤代谢物,并通过代谢组测序对根际微生物群落进行了表征。我们在不同处理中鉴定出123种代谢物,在正常和盐胁迫土壤条件下存在显著差异。主要的代谢物种类包括碳水化合物、醇和酸。与SSS、NSS和NIS处理相比,SIS组的关键碳水化合物(包括果糖和蔗糖)显著减少。代谢途径分析显示,这些差异主要与“果糖和甘露糖代谢”、“淀粉和蔗糖代谢”和“ABC转运蛋白”有关。代谢组学分析显示,不同土壤条件和不同种植方式的微生物群落结构存在显著差异。在门水平上,Proteobacteria、gemmatimonadees和Verrucomicrobia占主导地位,它们的相对丰度在盐胁迫下发生了实质性的变化。SIS促进了特定属(罗丹诺杆菌)的富集,这些属与土壤健康和耐受性有关。此外,稀有微生物类群对盐胁迫和间作的响应也存在差异,个别稀有微生物类群(根霉)在盐胁迫下表现出相对丰度。代谢物与微生物类群的相关性分析显示,某些碳水化合物与特定微生物门(蓝藻门和硝基螺旋藻门)呈显著正相关,而与植物菌门和拟杆菌门呈显著负相关。这些相关性表明,花生间作高粱可以促进盐胁迫下微生物类群的富集,从而通过优化根际微生物群落来增强土壤代谢功能和抗逆性。本研究揭示了盐胁迫下高粱-花生间作通过调节土壤糖代谢途径影响高粱根际微生物群落组成的机制。这一发现为盐渍土壤的可持续农业实践提供了新的视角,并强调了植物-代谢物-微生物相互作用在缓解非生物胁迫中的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sorghum-peanut intercropping under salt stress mediates rhizosphere microbial community shaping in sorghum by affecting soil sugar metabolism pathways.

Soil salinization is a substantial impediment to agricultural production, and investigating sustainable mitigation measures is essential for addressing food security. We conducted a two-year pot experiment to investigate the shaping mechanism of sorghum rhizosphere microbial community in sorghum-peanut intercropping system under salt stress. The experiment comprised four treatments: sole-cropped sorghum under normal soil conditions (NSS), intercropped sorghum under normal soil conditions (NIS), sole-cropped sorghum under salt-stress conditions (SSS), and intercropped sorghum under salt-stress conditions (SIS). The sorghum rhizosphere soil metabolites were examined using GC-MS, and the rhizosphere microbial community was characterized through metabolome sequencing. We identified 123 metabolites across treatments, with significant differences between normal and salt-stress soil conditions. The major metabolite classes included carbohydrates, alcohols, and acids. Key carbohydrates, including fructose and sucrose, were significantly reduced in the SIS than in SSS, NSS, and NIS treatments. Metabolic pathway analyses revealed that these differences were primarily associated with "Fructose and mannose metabolism," "Starch and sucrose metabolism" and "ABC transporter." Metabolome analyses revealed significant differences in microbial community structure across diverse soil conditions and cropping patterns. At phylum level, Proteobacteria, Gemmatimonadetes, and Verrucomicrobia predominated, with their relative abundance experiencing substantial changes under salt stress. SIS facilitated the enrichment of specific genera (Rhodanobacter), which were associated with soil health and stress tolerance. Additionally, the responses of rare microbial taxa to salt stress and intercropping varied, with specific rare microbial taxa (Rhizopus) exhibiting relative abundance under salt stress. Correlation analysis of metabolites and microbial taxa revealed that certain carbohydrates were significantly positively correlated with specific microbial phyla (Cyanobacteria and Nitrospirae) while demonstrating a significant negative correlation with Planctomycetota and Bacteroidota. These correlations indicate that sorghum intercropped with peanuts can promote the enrichment of microbial taxa under salt stress, thereby enhancing soil metabolic functions and stress tolerance by optimizing the rhizosphere microbial community. This study reveals the mechanism through which sorghum-peanut intercropping under salt stress influences the composition of sorghum's rhizosphere microbial community by modulating soil sugar metabolism pathways. This finding provides a new perspective on sustainable agricultural practices in saline soils and emphasizes the pivotal role of plant-metabolite-microbe interactions in abiotic stress mitigation.

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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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