Cargando…
16S rRNA nanopore sequencing for the diagnosis of ocular infection: a feasibility study
OBJECTIVE: We conducted a feasibility study to verify the effectiveness of 16S ribosomal RNA (rRNA) gene analysis using the nanopore sequencer MinION for identifying causative bacteria in several types of ocular infections. METHODS AND ANALYSIS: Four cases of corneal ulcers, one case of endophthalmi...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131114/ https://www.ncbi.nlm.nih.gov/pubmed/36161861 http://dx.doi.org/10.1136/bmjophth-2021-000910 |
_version_ | 1784713116989259776 |
---|---|
author | Omi, Masatoshi Matsuo, Yoshiyuki Araki-Sasaki, Kaoru Oba, Shimpei Yamada, Haruhiko Hirota, Kiichi Takahashi, Kanji |
author_facet | Omi, Masatoshi Matsuo, Yoshiyuki Araki-Sasaki, Kaoru Oba, Shimpei Yamada, Haruhiko Hirota, Kiichi Takahashi, Kanji |
author_sort | Omi, Masatoshi |
collection | PubMed |
description | OBJECTIVE: We conducted a feasibility study to verify the effectiveness of 16S ribosomal RNA (rRNA) gene analysis using the nanopore sequencer MinION for identifying causative bacteria in several types of ocular infections. METHODS AND ANALYSIS: Four cases of corneal ulcers, one case of endophthalmitis and one case of a conjunctival abscess were included in this study. DNA was extracted from corneal scraping, vitreous samples and secretions from the conjunctival abscess. We conducted 16S rRNA gene amplicon sequencing using MinION and metagenomic DNA analysis. The efficacy of bacterial identification was verified by comparing the conventional culture method with smear observations. RESULTS: 16S rRNA gene sequencing analysis with MinION identified the causative organisms promptly with high accuracy in approximately 4 hours, from ophthalmic specimens. The results of the conventional culture method and 16S rRNA gene sequencing were consistent in all cases. In four of the six cases, a greater variety of organisms was found in the 16S rRNA gene analysis than in bacterial culture. CONCLUSION: Using our workflow, 16S rRNA gene analysis using MinION enabled rapid and accurate identification possible in various kinds of bacterial ocular infections. |
format | Online Article Text |
id | pubmed-9131114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-91311142022-06-09 16S rRNA nanopore sequencing for the diagnosis of ocular infection: a feasibility study Omi, Masatoshi Matsuo, Yoshiyuki Araki-Sasaki, Kaoru Oba, Shimpei Yamada, Haruhiko Hirota, Kiichi Takahashi, Kanji BMJ Open Ophthalmol Genetics OBJECTIVE: We conducted a feasibility study to verify the effectiveness of 16S ribosomal RNA (rRNA) gene analysis using the nanopore sequencer MinION for identifying causative bacteria in several types of ocular infections. METHODS AND ANALYSIS: Four cases of corneal ulcers, one case of endophthalmitis and one case of a conjunctival abscess were included in this study. DNA was extracted from corneal scraping, vitreous samples and secretions from the conjunctival abscess. We conducted 16S rRNA gene amplicon sequencing using MinION and metagenomic DNA analysis. The efficacy of bacterial identification was verified by comparing the conventional culture method with smear observations. RESULTS: 16S rRNA gene sequencing analysis with MinION identified the causative organisms promptly with high accuracy in approximately 4 hours, from ophthalmic specimens. The results of the conventional culture method and 16S rRNA gene sequencing were consistent in all cases. In four of the six cases, a greater variety of organisms was found in the 16S rRNA gene analysis than in bacterial culture. CONCLUSION: Using our workflow, 16S rRNA gene analysis using MinION enabled rapid and accurate identification possible in various kinds of bacterial ocular infections. BMJ Publishing Group 2022-05-23 /pmc/articles/PMC9131114/ /pubmed/36161861 http://dx.doi.org/10.1136/bmjophth-2021-000910 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Genetics Omi, Masatoshi Matsuo, Yoshiyuki Araki-Sasaki, Kaoru Oba, Shimpei Yamada, Haruhiko Hirota, Kiichi Takahashi, Kanji 16S rRNA nanopore sequencing for the diagnosis of ocular infection: a feasibility study |
title | 16S rRNA nanopore sequencing for the diagnosis of ocular infection: a feasibility study |
title_full | 16S rRNA nanopore sequencing for the diagnosis of ocular infection: a feasibility study |
title_fullStr | 16S rRNA nanopore sequencing for the diagnosis of ocular infection: a feasibility study |
title_full_unstemmed | 16S rRNA nanopore sequencing for the diagnosis of ocular infection: a feasibility study |
title_short | 16S rRNA nanopore sequencing for the diagnosis of ocular infection: a feasibility study |
title_sort | 16s rrna nanopore sequencing for the diagnosis of ocular infection: a feasibility study |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131114/ https://www.ncbi.nlm.nih.gov/pubmed/36161861 http://dx.doi.org/10.1136/bmjophth-2021-000910 |
work_keys_str_mv | AT omimasatoshi 16srrnananoporesequencingforthediagnosisofocularinfectionafeasibilitystudy AT matsuoyoshiyuki 16srrnananoporesequencingforthediagnosisofocularinfectionafeasibilitystudy AT arakisasakikaoru 16srrnananoporesequencingforthediagnosisofocularinfectionafeasibilitystudy AT obashimpei 16srrnananoporesequencingforthediagnosisofocularinfectionafeasibilitystudy AT yamadaharuhiko 16srrnananoporesequencingforthediagnosisofocularinfectionafeasibilitystudy AT hirotakiichi 16srrnananoporesequencingforthediagnosisofocularinfectionafeasibilitystudy AT takahashikanji 16srrnananoporesequencingforthediagnosisofocularinfectionafeasibilitystudy |