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一套全面的真菌特异性 18S rRNA 基因序列引物工具包,适用于各种研究问题和测序平台。

A comprehensive fungi-specific 18S rRNA gene sequence primer toolkit suited for diverse research issues and sequencing platforms.

机构信息

Molecular Ecology, Institute of Ecology, FB02, University of Bremen, Leobener Str. 2, 28359, Bremen, Germany.

Department of Soil Ecology, Helmholtz Centre for Environmental Research GmbH - UFZ, Halle-Saale, Germany.

出版信息

BMC Microbiol. 2018 Nov 20;18(1):190. doi: 10.1186/s12866-018-1331-4.

Abstract

BACKGROUND

Several fungi-specific primers target the 18S rRNA gene sequence, one of the prominent markers for fungal classification. The design of most primers goes back to the last decades. Since then, the number of sequences in public databases increased leading to the discovery of new fungal groups and changes in fungal taxonomy. However, no reevaluation of primers was carried out and relevant information on most primers is missing. With this study, we aimed to develop an 18S rRNA gene sequence primer toolkit allowing an easy selection of the best primer pair appropriate for different sequencing platforms, research aims (biodiversity assessment versus isolate classification) and target groups.

RESULTS

We performed an intensive literature research, reshuffled existing primers into new pairs, designed new Illumina-primers, and annealing blocking oligonucleotides. A final number of 439 primer pairs were subjected to in silico PCRs. Best primer pairs were selected and experimentally tested. The most promising primer pair with a small amplicon size, nu-SSU-1333-5'/nu-SSU-1647-3' (FF390/FR-1), was successful in describing fungal communities by Illumina sequencing. Results were confirmed by a simultaneous metagenomics and eukaryote-specific primer approach. Co-amplification occurred in all sample types but was effectively reduced by blocking oligonucleotides.

CONCLUSIONS

The compiled data revealed the presence of an enormous diversity of fungal 18S rRNA gene primer pairs in terms of fungal coverage, phylum spectrum and co-amplification. Therefore, the primer pair has to be carefully selected to fulfill the requirements of the individual research projects. The presented primer toolkit offers comprehensive lists of 164 primers, 439 primer combinations, 4 blocking oligonucleotides, and top primer pairs holding all relevant information including primer's characteristics and performance to facilitate primer pair selection.

摘要

背景

几种真菌特异性引物靶向 18S rRNA 基因序列,这是真菌分类的主要标志之一。大多数引物的设计可以追溯到上个世纪。从那时起,公共数据库中的序列数量增加,导致新的真菌群体的发现和真菌分类学的变化。然而,没有对引物进行重新评估,并且大多数引物的相关信息都缺失了。本研究旨在开发一个 18S rRNA 基因序列引物工具包,以便于为不同的测序平台、研究目的(生物多样性评估与分离物分类)和目标群体选择最佳的引物对。

结果

我们进行了广泛的文献研究,将现有的引物重新组合成新的引物对,设计了新的 Illumina 引物和退火阻断寡核苷酸。最终有 439 对引物进行了计算机 PCR 检测。选择了最佳的引物对,并进行了实验测试。具有较小扩增子大小的最有前途的引物对,nu-SSU-1333-5'/nu-SSU-1647-3'(FF390/FR-1),通过 Illumina 测序成功地描述了真菌群落。通过同时进行宏基因组学和真核生物特异性引物方法得到了证实。在所有样本类型中都发生了共扩增,但通过阻断寡核苷酸有效地减少了共扩增。

结论

编译的数据显示,在真菌覆盖范围、门谱和共扩增方面,真菌 18S rRNA 基因引物对存在着巨大的多样性。因此,引物对的选择必须仔细,以满足各个研究项目的要求。所提出的引物工具包提供了综合的 164 对引物、439 对引物组合、4 个阻断寡核苷酸和顶级引物对的列表,这些引物对包含了所有相关信息,包括引物的特征和性能,以方便引物对的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/6247509/dbe90a9b72c0/12866_2018_1331_Fig1_HTML.jpg

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