A 16S rRNA gene sequencing and analysis protocol for the Illumina MiniSeq platform

被引:111
作者
Pichler, Monica [1 ]
Coskun, Oemer K. [1 ]
Ortega-Arbulu, Ana-Sofia [1 ]
Conci, Nicola [1 ]
Woerheide, Gert [1 ,2 ,3 ]
Vargas, Sergio [1 ]
Orsi, William D. [1 ,2 ]
机构
[1] Ludwig Maximilians Univ Munchen, Dept Earth & Environm Sci Paleontol & Geobiol, Munich, Germany
[2] Ludwig Maximilians Univ Munchen, GeoBio Ctr LMU, Munich, Germany
[3] SNSB Bayer Staatssammlung Palaontol & Geol, Munich, Germany
关键词
16S rRNA gene; high-throughput sequencing; Illumina; microbial diversity; DIVERSITY; SEARCH;
D O I
10.1002/mbo3.611
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
High-throughput sequencing of the 16S rRNA gene on the Illumina platform is commonly used to assess microbial diversity in environmental samples. The MiniSeq, Illumina's latest benchtop sequencer, enables more cost-efficient DNA sequencing relative to larger Illumina sequencing platforms (e.g., MiSeq). Here we used a modified custom primer sequencing approach to test the fidelity of the MiniSeq for high-throughput sequencing of the V4 hypervariable region of 16S rRNA genes from complex communities in environmental samples. To this end, we designed additional sequencing primers that enabled application of a dual-index barcoding method on the MiniSeq. A mock community was sequenced alongside the environmental samples in four different sequencing runs as a quality control benchmark. We were able to recapture a realistic richness of the mock community in all sequencing runs, and identify meaningful differences in alpha and beta diversity in the environmental samples. Furthermore, rarefaction analysis indicated diversity in many environmental samples was close to saturation. These results show that the MiniSeq can produce similar quantities of high-quality V4 reads compared to the MiSeq, yet is a cost-effective option for any laboratory interested in performing high-throughput 16S rRNA gene sequencing.
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页数:9
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