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DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing

Identification of bacteria causing tissue infections can be comprehensive and, in the cases of non- or slow-growing bacteria, near impossible with conventional methods. Performing shotgun metagenomic sequencing on bacterial DNA extracted directly from the infected tissue may improve time to diagnosi...

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Autores principales: Helmersen, Karin, Aamot, Hege Vangstein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031281/
https://www.ncbi.nlm.nih.gov/pubmed/32076089
http://dx.doi.org/10.1038/s41598-020-59957-6
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author Helmersen, Karin
Aamot, Hege Vangstein
author_facet Helmersen, Karin
Aamot, Hege Vangstein
author_sort Helmersen, Karin
collection PubMed
description Identification of bacteria causing tissue infections can be comprehensive and, in the cases of non- or slow-growing bacteria, near impossible with conventional methods. Performing shotgun metagenomic sequencing on bacterial DNA extracted directly from the infected tissue may improve time to diagnosis and targeted treatment considerably. However, infected tissue consists mainly of human DNA (hDNA) which hampers bacterial identification. In this proof of concept study, we present a modified version of the Ultra-Deep Microbiome Prep kit for DNA extraction procedure, removing additional human DNA. Tissue biopsies from 3 patients with orthopedic implant-related infections containing varying degrees of Staphylococcus aureus were included. Subsequent DNA shotgun metagenomic sequencing using Oxford Nanopore Technologies’ (ONT) MinION platform and ONTs EPI2ME WIMP and ARMA bioinformatic workflows for microbe and antibiotic resistance genes identification, respectively. The modified DNA extraction protocol led to an additional ~10-fold reduction of human DNA while preserving S. aureus DNA. Including the DNA sequencing and bioinformatics analyses, the presented protocol has the potential of identifying the infection-causing pathogen in infected tissue within 7 hours after biopsy. However, due to low number of S. aureus reads, positive identification of antibiotic resistance genes was not possible.
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spelling pubmed-70312812020-02-27 DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing Helmersen, Karin Aamot, Hege Vangstein Sci Rep Article Identification of bacteria causing tissue infections can be comprehensive and, in the cases of non- or slow-growing bacteria, near impossible with conventional methods. Performing shotgun metagenomic sequencing on bacterial DNA extracted directly from the infected tissue may improve time to diagnosis and targeted treatment considerably. However, infected tissue consists mainly of human DNA (hDNA) which hampers bacterial identification. In this proof of concept study, we present a modified version of the Ultra-Deep Microbiome Prep kit for DNA extraction procedure, removing additional human DNA. Tissue biopsies from 3 patients with orthopedic implant-related infections containing varying degrees of Staphylococcus aureus were included. Subsequent DNA shotgun metagenomic sequencing using Oxford Nanopore Technologies’ (ONT) MinION platform and ONTs EPI2ME WIMP and ARMA bioinformatic workflows for microbe and antibiotic resistance genes identification, respectively. The modified DNA extraction protocol led to an additional ~10-fold reduction of human DNA while preserving S. aureus DNA. Including the DNA sequencing and bioinformatics analyses, the presented protocol has the potential of identifying the infection-causing pathogen in infected tissue within 7 hours after biopsy. However, due to low number of S. aureus reads, positive identification of antibiotic resistance genes was not possible. Nature Publishing Group UK 2020-02-19 /pmc/articles/PMC7031281/ /pubmed/32076089 http://dx.doi.org/10.1038/s41598-020-59957-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Helmersen, Karin
Aamot, Hege Vangstein
DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing
title DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing
title_full DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing
title_fullStr DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing
title_full_unstemmed DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing
title_short DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing
title_sort dna extraction of microbial dna directly from infected tissue: an optimized protocol for use in nanopore sequencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031281/
https://www.ncbi.nlm.nih.gov/pubmed/32076089
http://dx.doi.org/10.1038/s41598-020-59957-6
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