元基因组学和代谢组学分析揭示镉胁迫下Se介导的镉沉淀和养分循环调控土壤-水稻(Oryza sativa L)的微环境稳态

IF 4.5 2区 生物学 Q2 ENVIRONMENTAL SCIENCES
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引用次数: 0

摘要

外源硒(Se)的添加可动态调节微生物群落的建立,诱导特定微生物功能基因的表达,并影响土壤-植物微环境的稳态。本研究采用元基因组和代谢组分析方法研究了水稻幼苗根瘤土壤中Se介导的稳态变化和功能反应。结果表明,与镉组相比,土壤和水稻植株中的硒(1 毫克/千克)含量分别增加了 88.5 % 和 99.1 %。土壤-荧光素二乙酸酯(S-FDA)水解酶活性提高了 42.9%,水稻对镉的富集系数提高了 71.1%,但转移因子降低了 21.6%,使得大量镉离子滞留在根部,减轻了镉对植物的毒性。元基因组分析表明,Se 生物增殖改变了根圈微生物群落的结构和组成,诱导了水稻根圈微生物群落的重塑。增加了重金属抗性基因(cznA czcD、czcP、dltC 和 CREM)、养分循环功能基因(atoB tktB、aces、sdhA、accA、ppdK、NRT、narB、nifD、napA、pstS、GlpQ、poT、phoR、sucC)和重金属转运蛋白家族(P-ATPase、CDF、ABC 和 MIT)的表达。这极大地改善了根圈微环境的健康状况,缓解了重金属导致的土壤硬化和养分缺乏。同时,在代谢组学分析中,上调的差异表达代谢物(DEMs)主要集中在苷元组非核糖体肽的生物合成、硫代谢、泛醌和其他萜类-醌的生物合成、半胱氨酸和蛋氨酸代谢等方面。根瘤微生物群的介导重塑表明,营养循环中存在一种优势。同时,次生代谢和抗氧化能力也明显增强,重金属死亡造成的巨大应变是土壤贫瘠的结果。此外,重塑微生物群中的单磷酸环腺苷(CAMP)信号通路被激活,受体蛋白诱导剂上调,激活了根瘤微生物群的群体反应,导致各微生物群特定功能基因的过度表达。通过增强根圈微生物群对重金属的抗性和养分循环能力,显著降低了镉离子的迁移率和生物利用率,改善了根圈土壤微环境的健康状况,提高了水稻对镉胁迫的适应性。该研究揭示了水稻根瘤菌抗镉菌群的调控机制,为植物根瘤菌群的精准调控研究开辟了新的研究途径,为作物生产安全提供了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metagenomics and metabolomics analysis revealed that Se-mediated Cd precipitation and nutrient cycling regulated soil-rice (Oryza sativa L) microenvironmental homeostasis under cadmium stress

Exogenous selenium (Se) addition can dynamically regulate the establishment of microbial communities, induce the expression of specific microbial functional genes, and affect the homeostasis of the soil-plant microenvironment. In this study, we used metagenomic and metabolomic analyses to investigate Se-mediated homeostatic changes and functional responses in the rhizosphere soil of rice seedlings. Results show that compared with the Cd set, selenium (1 mg/kg) Se content in the Soil and rice plant increased by 88.5 % and 99.1 %, respectively. Soil-fluorescein diacetate (S-FDA) hydrolyze enzymatic activity increased by 42.9 %, Rice on Cd enrichment coefficient increased by 71.1 %, but the transfer coefficient by 21.6 %, making a lot of cadmium ion stranded in the root, easing the toxicity of cadmium to plant. Metagenomic analysis revealed that Se bioaugmentation altered the structure and composition of the rhizosphere microbial community and induced remodeling of the rice rhizosphere microbiome. Increase the heavy metal resistance genes (cznA czcD, czcP, dltC, and CREM), nutrient cycling functional genes (atoB tktB, acs, sdhA, accA, ppdK, NRT, narB, nifD, napA, pstS, GlpQ, spoT, phoR, sucC) and heavy metal transport protein family (P-ATPase, CDF, ABC, and MIT) expression. It significantly improved the health of the rhizosphere microenvironment and alleviated soil hardening and nutrient deficiency caused by heavy metals. At the same time, in metabonomics analysis, The upregulated Differentially expressed metabolites (DEMs) were mainly in the Biosynthesis of siderophore group nonribosomal peptides, Sulfur metabolism, Ubiquinone and other terpenoid-quinone Biosynthesis, Cysteine, and methionine metabolism in enrichment significantly. The mediated reshaping of rhizosphere microorganism groups indicates that there is ane an advantage in the nutrient cycle. Also, the secondary metabolism and antioxidant capacity have significantly strengthened the ed, and the large strain caused by the death of heavy metals is a result of poor Soil. In addition, the Cyclic adenosine monophosphate (CAMP) signaling pathway was activated among the remodeling microbiomes, and the receptor protein inducer was upregulated, which activated the population response among the rhizosphere microbiomes and resulted in the overexpression of specific functional genes of each microbiome. By enhancing the resistance to heavy metals and nutrient cycling ability of the rhizosphere microbiome, the mobility and bioavailability of Cd ions were significantly reduced, the rhizosphere soil microenvironment health was improved, and the adaptability of rice to Cd stress was improved. This study reveals the Se of rice rhizosphere Cd-resistant bacteria mediating mechanisms; research for precise regulation of plant rhizosphere microorganism groups opens new avenues of research and offers a new way for crop production safety.

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来源期刊
Environmental and Experimental Botany
Environmental and Experimental Botany 环境科学-环境科学
CiteScore
9.30
自引率
5.30%
发文量
342
审稿时长
26 days
期刊介绍: Environmental and Experimental Botany (EEB) publishes research papers on the physical, chemical, biological, molecular mechanisms and processes involved in the responses of plants to their environment. In addition to research papers, the journal includes review articles. Submission is in agreement with the Editors-in-Chief. The Journal also publishes special issues which are built by invited guest editors and are related to the main themes of EEB. The areas covered by the Journal include: (1) Responses of plants to heavy metals and pollutants (2) Plant/water interactions (salinity, drought, flooding) (3) Responses of plants to radiations ranging from UV-B to infrared (4) Plant/atmosphere relations (ozone, CO2 , temperature) (5) Global change impacts on plant ecophysiology (6) Biotic interactions involving environmental factors.
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