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A 16S rRNA gene sequencing and analysis protocol for the Illumina MiniSeq platform
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.,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291791/ https://www.ncbi.nlm.nih.gov/pubmed/29575567 http://dx.doi.org/10.1002/mbo3.611 |
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author | Pichler, Monica Coskun, Ömer K. Ortega‐Arbulú, Ana‐Sofia Conci, Nicola Wörheide, Gert Vargas, Sergio Orsi, William D. |
author_facet | Pichler, Monica Coskun, Ömer K. Ortega‐Arbulú, Ana‐Sofia Conci, Nicola Wörheide, Gert Vargas, Sergio Orsi, William D. |
author_sort | Pichler, Monica |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6291791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62917912018-12-18 A 16S rRNA gene sequencing and analysis protocol for the Illumina MiniSeq platform Pichler, Monica Coskun, Ömer K. Ortega‐Arbulú, Ana‐Sofia Conci, Nicola Wörheide, Gert Vargas, Sergio Orsi, William D. Microbiologyopen Original Articles 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. John Wiley and Sons Inc. 2018-03-25 /pmc/articles/PMC6291791/ /pubmed/29575567 http://dx.doi.org/10.1002/mbo3.611 Text en © 2018 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Pichler, Monica Coskun, Ömer K. Ortega‐Arbulú, Ana‐Sofia Conci, Nicola Wörheide, Gert Vargas, Sergio Orsi, William D. A 16S rRNA gene sequencing and analysis protocol for the Illumina MiniSeq platform |
title | A 16S rRNA gene sequencing and analysis protocol for the Illumina MiniSeq platform |
title_full | A 16S rRNA gene sequencing and analysis protocol for the Illumina MiniSeq platform |
title_fullStr | A 16S rRNA gene sequencing and analysis protocol for the Illumina MiniSeq platform |
title_full_unstemmed | A 16S rRNA gene sequencing and analysis protocol for the Illumina MiniSeq platform |
title_short | A 16S rRNA gene sequencing and analysis protocol for the Illumina MiniSeq platform |
title_sort | 16s rrna gene sequencing and analysis protocol for the illumina miniseq platform |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291791/ https://www.ncbi.nlm.nih.gov/pubmed/29575567 http://dx.doi.org/10.1002/mbo3.611 |
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