Cargando…
MinION™ Nanopore Sequencing of Skin Microbiome 16S and 16S-23S rRNA Gene Amplicons
Human skin microbiome dysbiosis can have clinical consequences. Characterizing taxonomic composition of bacterial communities associated with skin disorders is important for dermatological advancement in both diagnosis and novel treatments. This study aims to analyze and improve the accuracy of taxo...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766866/ https://www.ncbi.nlm.nih.gov/pubmed/35071053 http://dx.doi.org/10.3389/fcimb.2021.806476 |
_version_ | 1784634619764670464 |
---|---|
author | Rozas, Miquel Brillet, François Callewaert, Chris Paetzold, Bernhard |
author_facet | Rozas, Miquel Brillet, François Callewaert, Chris Paetzold, Bernhard |
author_sort | Rozas, Miquel |
collection | PubMed |
description | Human skin microbiome dysbiosis can have clinical consequences. Characterizing taxonomic composition of bacterial communities associated with skin disorders is important for dermatological advancement in both diagnosis and novel treatments. This study aims to analyze and improve the accuracy of taxonomic classification of skin bacteria with MinION™ nanopore sequencing using a defined skin mock community and a skin microbiome sample. We compared the Oxford Nanopore Technologies recommended procedures and concluded that their protocols highly bias the relative abundance of certain skin microbiome genera, most notably a large overrepresentation of Staphylococcus and underrepresentation of Cutibacterium and Corynebacterium. We demonstrated that changes in the amplification protocols improved the accuracy of the taxonomic classification for these three main skin bacterial genera. This study shows that MinION™ nanopore could be an efficient technology for full-length 16S rRNA sequencing; however, the analytical advantage is strongly influenced by the methodologies. The suggested alternatives in the sample processing improved characterization of a complex skin microbiome community using MinION™ nanopore sequencing. |
format | Online Article Text |
id | pubmed-8766866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87668662022-01-20 MinION™ Nanopore Sequencing of Skin Microbiome 16S and 16S-23S rRNA Gene Amplicons Rozas, Miquel Brillet, François Callewaert, Chris Paetzold, Bernhard Front Cell Infect Microbiol Cellular and Infection Microbiology Human skin microbiome dysbiosis can have clinical consequences. Characterizing taxonomic composition of bacterial communities associated with skin disorders is important for dermatological advancement in both diagnosis and novel treatments. This study aims to analyze and improve the accuracy of taxonomic classification of skin bacteria with MinION™ nanopore sequencing using a defined skin mock community and a skin microbiome sample. We compared the Oxford Nanopore Technologies recommended procedures and concluded that their protocols highly bias the relative abundance of certain skin microbiome genera, most notably a large overrepresentation of Staphylococcus and underrepresentation of Cutibacterium and Corynebacterium. We demonstrated that changes in the amplification protocols improved the accuracy of the taxonomic classification for these three main skin bacterial genera. This study shows that MinION™ nanopore could be an efficient technology for full-length 16S rRNA sequencing; however, the analytical advantage is strongly influenced by the methodologies. The suggested alternatives in the sample processing improved characterization of a complex skin microbiome community using MinION™ nanopore sequencing. Frontiers Media S.A. 2022-01-05 /pmc/articles/PMC8766866/ /pubmed/35071053 http://dx.doi.org/10.3389/fcimb.2021.806476 Text en Copyright © 2022 Rozas, Brillet, Callewaert and Paetzold https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Rozas, Miquel Brillet, François Callewaert, Chris Paetzold, Bernhard MinION™ Nanopore Sequencing of Skin Microbiome 16S and 16S-23S rRNA Gene Amplicons |
title | MinION™ Nanopore Sequencing of Skin Microbiome 16S and 16S-23S rRNA Gene Amplicons |
title_full | MinION™ Nanopore Sequencing of Skin Microbiome 16S and 16S-23S rRNA Gene Amplicons |
title_fullStr | MinION™ Nanopore Sequencing of Skin Microbiome 16S and 16S-23S rRNA Gene Amplicons |
title_full_unstemmed | MinION™ Nanopore Sequencing of Skin Microbiome 16S and 16S-23S rRNA Gene Amplicons |
title_short | MinION™ Nanopore Sequencing of Skin Microbiome 16S and 16S-23S rRNA Gene Amplicons |
title_sort | minion™ nanopore sequencing of skin microbiome 16s and 16s-23s rrna gene amplicons |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766866/ https://www.ncbi.nlm.nih.gov/pubmed/35071053 http://dx.doi.org/10.3389/fcimb.2021.806476 |
work_keys_str_mv | AT rozasmiquel minionnanoporesequencingofskinmicrobiome16sand16s23srrnageneamplicons AT brilletfrancois minionnanoporesequencingofskinmicrobiome16sand16s23srrnageneamplicons AT callewaertchris minionnanoporesequencingofskinmicrobiome16sand16s23srrnageneamplicons AT paetzoldbernhard minionnanoporesequencingofskinmicrobiome16sand16s23srrnageneamplicons |