玉米根际有益微生物的选择性招募受微生物接种剂、耕作方式和季节变化的影响。

IF 6.2 2区 环境科学与生态学 Q1 GENETICS & HEREDITY
Ioannis D Kampouris, Theresa Kuhl-Nagel, Jan Helge Behr, Loreen Sommermann, Doreen Babin, Davide Francioli, Rita Zrenner, Susanne Kublik, Michael Schloter, Uwe Ludewig, Kornelia Smalla, Günter Neumann, Rita Grosch, Joerg Geistlinger
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引用次数: 0

摘要

背景:植物有益微生物作为接种剂可以提高作物生产性能,但在田间条件下影响其对植物生产性能影响的因素尚不清楚,因此限制了它们在农业中的应用。在这里,我们研究了耕作方式(例如耕作和氮肥强度)和生长季节如何影响玉米有益微生物组合(BMc:木霉、芽孢杆菌和假单胞菌菌株)的影响,以及每种BMc菌株的根际能力。此外,我们还测试了该联合体是否影响常驻根际微生物群和作物生产性能。在两个生长季节(2020年和2021年),我们评估了不同耕作方式下BMc接种对玉米开花期生长、营养状况、基因表达和根际微生物组的影响。结果:接种菌株能独立于耕作方式成功定植玉米根际。无论耕作方式如何,接种BMc均可改善2020年植株生长和铁吸收。与2021年相比,这些影响与2020年的降水量减少同时发生。在干旱条件下,接种BMc降低了2020年玉米多个胁迫相关基因的表达。研究人员在2020年观察到接种了bmc的植株对铁的吸收增加,这与与铁吸收有关的基因ZmNAS3的上调有关。因此,接种BMc可以缓解干旱对玉米的影响。接种BMc后,两年份的根际微生物群落均发生了变化,但不同季节的响应类型有所不同。宏基因组分析显示,与2021年相比,2020年接种bmc的植株根际中富集了更多的基因(如编码生物表面活性剂和铁载体的基因)。此外,我们还发现了与玉米铁吸收呈正相关的细菌和真菌分类群。这些与铁摄取相关的细菌和真菌类群的相对丰度在2020年因接种BMc而显著增加,而在2021年,它们的相对丰度总体上较高,与接种BMc无关。我们将这些铁相关分类群的序列映射到公开可用的基因组中,并验证了在几个绘制的基因组中出现的各种植物有益性状。结论:总体而言,我们发现BMc接种对玉米植株的影响主要是通过影响玉米根际微生物组的组成和功能,而不是耕作方式。这些发现强调了在非生物胁迫条件下,微生物接种剂与常驻根际微生物之间复杂相互作用的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Selective recruitment of beneficial microbes in the rhizosphere of maize affected by microbial inoculants, farming practice, and seasonal variations.

Background: Plant beneficial microorganisms as inoculants can improve crop performance, but factors affecting their impact on plant performance under field conditions remain unclear, thereby limiting their use in farming. Here, we investigated how farming practices (e.g., tillage and N-fertilization intensity) and growing seasons influenced the impact of a beneficial microorganism consortium (BMc: Trichoderma, Bacillus, and Pseudomonas strains) in maize and affected the rhizosphere competence of each BMc strain. In addition, we tested whether the consortium affects the resident rhizosphere microbiome and crop performance. In two growing seasons (2020 and 2021), we assessed how BMc inoculation affects maize growth, nutritional status, gene expression, and rhizosphere microbiome under different farming practices at the flowering stage.

Results: Inoculated strains successfully colonized the maize rhizosphere independently of farming practice. BMc inoculation improved plant growth and iron uptake in 2020, regardless of farming practice. These effects co-occurred with lower precipitation levels in 2020 compared to 2021. BMc inoculation reduced the expression of several stress-related genes in maize in 2020 under drought. An increased iron uptake by the BMc-inoculated plants was observed in 2020 and was associated with the upregulation of the gene ZmNAS3, which is linked to iron uptake. Therefore, BMc inoculation mitigated the drought impact on maize. The microbial rhizosphere communities were altered by BMc inoculation in both years, but patterns of responder taxa differed between seasons. Metagenome analysis revealed that more genes (e.g., genes encoding biosurfactants and siderophores) were enriched in the rhizosphere of BMc-inoculated plants in 2020 than in 2021. Moreover, we identified bacterial and fungal taxa positively associated with maize iron uptake. The relative abundance of these iron uptake-associated bacterial and fungal taxa significantly increased due to BMc inoculation in 2020, while they showed overall higher relative abundances in 2021, independently of BMc inoculation. We mapped the sequences of these iron-associated taxa to publicly available genomes and verified the occurrence of various plant beneficial traits in several mapped genomes.

Conclusions: Overall, we show that the growing season determined the effect of BMc inoculation on maize plants by shaping microbiome composition and function in the maize rhizosphere more than farming practice. These findings highlight the importance of the complex interplay between microbial inoculants and the resident rhizosphere microorganisms under abiotic stress conditions.

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来源期刊
Environmental Microbiome
Environmental Microbiome Immunology and Microbiology-Microbiology
CiteScore
7.40
自引率
2.50%
发文量
55
审稿时长
13 weeks
期刊介绍: Microorganisms, omnipresent across Earth's diverse environments, play a crucial role in adapting to external changes, influencing Earth's systems and cycles, and contributing significantly to agricultural practices. Through applied microbiology, they offer solutions to various everyday needs. Environmental Microbiome recognizes the universal presence and significance of microorganisms, inviting submissions that explore the diverse facets of environmental and applied microbiological research.
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