Small sample amounts from rhizosphere of barley maintain microbial community structure and diversity revealed by total RNA sequencing.

IF 4.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Nikolaj L Kindtler, Sanea Sheikh, Athanasios Zervas, Lea Ellegaard-Jensen, Louise Feld, Maria Scheel, Francisco Campuzano Jiménez, Rute R da Fonseca, Kristian H Laursen, Carsten S Jacobsen, Flemming Ekelund
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Abstract

Total RNA sequencing is a crucial technique in microbial ecology for profiling active microbial communities in various environments, including the rhizosphere. Since total RNA sequencing yields both 16 S and 18 S ribosomal RNA (rRNA), it is effective for taxonomic profiling of the full microbial community in a sample. However, the effectiveness of this approach with limited initial sample amounts remains unclear. In this study, we grew barley in a growth system designed for highly controlled plant experiments using an inert growth medium inoculated with a soil microbiome. Our objectives were two-fold: firstly, to test the feasibility of extracting total RNA from the rhizosphere of barley grown in an inert growth medium consisting of sand and perlite. Secondly, we aimed to address the challenge of extracting comprehensive taxonomic information from minimal amounts of rhizosphere samples from barley plants, using three different amounts of freeze-dried rhizosphere material: 10, 40, and 200 mg. We showed that although smaller sample amounts yielded lower concentrations of extracted RNA, this did not significantly influence the diversity or composition of the rhizosphere microbiome as indicated by SSU rRNA. Our results demonstrate that total RNA sequencing, focusing on SSU rRNA, robustly captures the taxonomic diversity of active rhizosphere microbial communities, even in small initial sample amounts. Effective use of smaller samples opens new possibilities for detailed studies in environments where sample quantity is limited. We also conclude that the growth system applied in this experiment is suitable for highly controlled plant experiments focusing on total RNA extraction from the rhizosphere.

总RNA测序结果显示,大麦根际少量样品维持了微生物群落结构和多样性。
总RNA测序是微生物生态学中的一项关键技术,用于分析包括根际在内的各种环境中的活跃微生物群落。由于总RNA测序可产生16s和18s核糖体RNA (rRNA),因此对样品中整个微生物群落的分类分析是有效的。然而,在有限的初始样本量下,这种方法的有效性尚不清楚。在这项研究中,我们在一个为高度控制的植物实验设计的生长系统中种植大麦,使用接种了土壤微生物组的惰性生长培养基。我们的目的有两个:首先,测试从大麦根际提取总RNA的可行性,大麦根际生长在由沙子和珍珠岩组成的惰性生长介质中。其次,利用10、40和200 mg三种不同量的冻干根际物质,从大麦植株的最少量根际样品中提取全面的分类信息。我们发现,虽然较小的样本量产生较低浓度的提取RNA,但这并没有显着影响根际微生物组的多样性或组成,如SSU rRNA所示。我们的研究结果表明,以SSU rRNA为重点的总RNA测序,即使在很小的初始样本量下,也能强有力地捕获活跃根际微生物群落的分类多样性。有效地利用小样本为样本数量有限的环境中的详细研究开辟了新的可能性。我们还得出结论,本实验中应用的生长系统适合于高度控制的植物实验,重点是根际总RNA的提取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Plant Methods
Plant Methods 生物-植物科学
CiteScore
9.20
自引率
3.90%
发文量
121
审稿时长
2 months
期刊介绍: Plant Methods is an open access, peer-reviewed, online journal for the plant research community that encompasses all aspects of technological innovation in the plant sciences. There is no doubt that we have entered an exciting new era in plant biology. The completion of the Arabidopsis genome sequence, and the rapid progress being made in other plant genomics projects are providing unparalleled opportunities for progress in all areas of plant science. Nevertheless, enormous challenges lie ahead if we are to understand the function of every gene in the genome, and how the individual parts work together to make the whole organism. Achieving these goals will require an unprecedented collaborative effort, combining high-throughput, system-wide technologies with more focused approaches that integrate traditional disciplines such as cell biology, biochemistry and molecular genetics. Technological innovation is probably the most important catalyst for progress in any scientific discipline. Plant Methods’ goal is to stimulate the development and adoption of new and improved techniques and research tools and, where appropriate, to promote consistency of methodologies for better integration of data from different laboratories.
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