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使用扩增子测序方法对田间样本中的假单胞菌属物种进行鉴定和区分。

Identification and Differentiation of Pseudomonas Species in Field Samples Using an Amplicon Sequencing Methodology.

作者信息

Lauritsen Jonas Greve, Hansen Morten Lindqvist, Bech Pernille Kjersgaard, Jelsbak Lars, Gram Lone, Strube Mikael Lenz

机构信息

Department of Biotechnology and Biomedicine, Technical University of Denmarkgrid.5170.3, Kongens Lyngby, Denmark.

出版信息

mSystems. 2021 Aug 31;6(4):e0070421. doi: 10.1128/mSystems.00704-21. Epub 2021 Aug 3.

Abstract

Species of the genus Pseudomonas are used for several biotechnological purposes, including plant biocontrol and bioremediation. To exploit the Pseudomonas genus in environmental, agricultural, or industrial settings, the organisms must be profiled at the species level as their bioactivity potential differs markedly between species. Standard 16S rRNA gene amplicon profiling does not allow for accurate species differentiation. Thus, the purpose of this study was to develop an amplicon-based high-resolution method targeting a 760-nucleotide (nt) region of the gene enabling taxonomic differentiation of Pseudomonas species in soil samples. The method was benchmarked on a 16-member Pseudomonas species mock community. All 16 species were correctly and semiquantitatively identified using gene amplicons, whereas 16S rRNA V3-V4 amplicon sequencing only correctly identified one species. We analyzed the Pseudomonas profiles in 13 soil samples in northern Zealand, Denmark, where samples were collected from grassland (3 samples) and agriculture soil (10 samples). Pseudomonas species represented up to 0.7% of the 16S rRNA gene abundance, of which each sampling site contained a unique Pseudomonas composition. Thirty culturable Pseudomonas strains were isolated from each grassland site and 10 from each agriculture site and identified by Sanger sequencing of the gene. In all cases, the amplicon approach identified more species than were found by cultivation, including hard-to-culture nonfluorescent pseudomonads, as well as more than were found by 16S rRNA V3-V4 amplicon sequencing. Thus, profiling can be used for species profiling of Pseudomonas, and large-scale prospecting of bioactive Pseudomonas may be guided by initial screening using this method. A high-throughput sequencing-based method for profiling of Pseudomonas species in soil microbiomes was developed and identified more species than 16S rRNA gene sequencing or cultivation. Pseudomonas species are used as biocontrol organisms and plant growth-promoting agents, and the method will allow tracing of specific species of Pseudomonas as well as enable screening of environmental samples for further isolation and exploitation.

摘要

假单胞菌属的物种被用于多种生物技术目的,包括植物生物防治和生物修复。为了在环境、农业或工业环境中利用假单胞菌属,必须在物种水平上对这些微生物进行分析,因为它们的生物活性潜力在不同物种之间存在显著差异。标准的16S rRNA基因扩增子分析无法实现准确的物种区分。因此,本研究的目的是开发一种基于扩增子的高分辨率方法,该方法针对基因的一个760个核苷酸(nt)的区域,能够对土壤样品中的假单胞菌属物种进行分类区分。该方法在一个由16个假单胞菌属物种组成的模拟群落上进行了基准测试。使用基因扩增子能够正确且半定量地鉴定出所有16个物种,而16S rRNA V3-V4扩增子测序仅正确鉴定出一个物种。我们分析了丹麦西兰岛北部13个土壤样品中的假单胞菌谱,这些样品采自草地(3个样品)和农业土壤(10个样品)。假单胞菌属物种在16S rRNA基因丰度中占比高达0.7%,每个采样点都有独特的假单胞菌组成。从每个草地采样点分离出30株可培养的假单胞菌菌株,从每个农业采样点分离出10株,并通过对基因进行Sanger测序来鉴定。在所有情况下,基因扩增子方法鉴定出的物种比通过培养发现的更多,包括难以培养的非荧光假单胞菌,也比通过16S rRNA V3-V4扩增子测序发现的更多。因此,基因分析可用于假单胞菌属的物种分析,并且可以通过使用该方法进行初步筛选来指导对具有生物活性的假单胞菌的大规模勘探。开发了一种基于高通量测序的方法来分析土壤微生物群落中的假单胞菌属物种,该方法鉴定出的物种比16S rRNA基因测序或培养法更多。假单胞菌属物种被用作生物防治生物和植物生长促进剂,该方法将能够追踪特定的假单胞菌物种,并能够对环境样品进行筛选,以便进一步分离和利用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb0/8407407/8dcb49992792/msystems.00704-21-f001.jpg

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