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Human and Extracellular DNA Depletion for Metagenomic Analysis of Complex Clinical Infection Samples Yields Optimized Viable Microbiome Profiles
Metagenomic sequencing is a promising approach for identifying and characterizing organisms and their functional characteristics in complex, polymicrobial infections, such as airway infections in people with cystic fibrosis. These analyses are often hampered, however, by overwhelming quantities of h...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435281/ https://www.ncbi.nlm.nih.gov/pubmed/30784601 http://dx.doi.org/10.1016/j.celrep.2019.01.091 |
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author | Nelson, Maria T. Pope, Christopher E. Marsh, Robyn L. Wolter, Daniel J. Weiss, Eli J. Hager, Kyle R. Vo, Anh T. Brittnacher, Mitchell J. Radey, Matthew C. Hayden, Hillary S. Eng, Alexander Miller, Samuel I. Borenstein, Elhanan Hoffman, Lucas R. |
author_facet | Nelson, Maria T. Pope, Christopher E. Marsh, Robyn L. Wolter, Daniel J. Weiss, Eli J. Hager, Kyle R. Vo, Anh T. Brittnacher, Mitchell J. Radey, Matthew C. Hayden, Hillary S. Eng, Alexander Miller, Samuel I. Borenstein, Elhanan Hoffman, Lucas R. |
author_sort | Nelson, Maria T. |
collection | PubMed |
description | Metagenomic sequencing is a promising approach for identifying and characterizing organisms and their functional characteristics in complex, polymicrobial infections, such as airway infections in people with cystic fibrosis. These analyses are often hampered, however, by overwhelming quantities of human DNA, yielding only a small proportion of microbial reads for analysis. In addition, many abundant microbes in respiratory samples can produce large quantities of extracellular bacterial DNA originating either from biofilms or dead cells. We describe a method for simultaneously depleting DNA from intact human cells and extracellular DNA (human and bacterial) in sputum, using selective lysis of eukaryotic cells and endonuclease digestion. We show that this method increases microbial sequencing depth and, consequently, both the number of taxa detected and coverage of individual genes such as those involved in antibiotic resistance. This finding underscores the substantial impact of DNA from sources other than live bacteria in micro-biological analyses of complex, chronic infection specimens. |
format | Online Article Text |
id | pubmed-6435281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-64352812019-03-26 Human and Extracellular DNA Depletion for Metagenomic Analysis of Complex Clinical Infection Samples Yields Optimized Viable Microbiome Profiles Nelson, Maria T. Pope, Christopher E. Marsh, Robyn L. Wolter, Daniel J. Weiss, Eli J. Hager, Kyle R. Vo, Anh T. Brittnacher, Mitchell J. Radey, Matthew C. Hayden, Hillary S. Eng, Alexander Miller, Samuel I. Borenstein, Elhanan Hoffman, Lucas R. Cell Rep Article Metagenomic sequencing is a promising approach for identifying and characterizing organisms and their functional characteristics in complex, polymicrobial infections, such as airway infections in people with cystic fibrosis. These analyses are often hampered, however, by overwhelming quantities of human DNA, yielding only a small proportion of microbial reads for analysis. In addition, many abundant microbes in respiratory samples can produce large quantities of extracellular bacterial DNA originating either from biofilms or dead cells. We describe a method for simultaneously depleting DNA from intact human cells and extracellular DNA (human and bacterial) in sputum, using selective lysis of eukaryotic cells and endonuclease digestion. We show that this method increases microbial sequencing depth and, consequently, both the number of taxa detected and coverage of individual genes such as those involved in antibiotic resistance. This finding underscores the substantial impact of DNA from sources other than live bacteria in micro-biological analyses of complex, chronic infection specimens. 2019-02-19 /pmc/articles/PMC6435281/ /pubmed/30784601 http://dx.doi.org/10.1016/j.celrep.2019.01.091 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Nelson, Maria T. Pope, Christopher E. Marsh, Robyn L. Wolter, Daniel J. Weiss, Eli J. Hager, Kyle R. Vo, Anh T. Brittnacher, Mitchell J. Radey, Matthew C. Hayden, Hillary S. Eng, Alexander Miller, Samuel I. Borenstein, Elhanan Hoffman, Lucas R. Human and Extracellular DNA Depletion for Metagenomic Analysis of Complex Clinical Infection Samples Yields Optimized Viable Microbiome Profiles |
title | Human and Extracellular DNA Depletion for Metagenomic Analysis of Complex Clinical Infection Samples Yields Optimized Viable Microbiome Profiles |
title_full | Human and Extracellular DNA Depletion for Metagenomic Analysis of Complex Clinical Infection Samples Yields Optimized Viable Microbiome Profiles |
title_fullStr | Human and Extracellular DNA Depletion for Metagenomic Analysis of Complex Clinical Infection Samples Yields Optimized Viable Microbiome Profiles |
title_full_unstemmed | Human and Extracellular DNA Depletion for Metagenomic Analysis of Complex Clinical Infection Samples Yields Optimized Viable Microbiome Profiles |
title_short | Human and Extracellular DNA Depletion for Metagenomic Analysis of Complex Clinical Infection Samples Yields Optimized Viable Microbiome Profiles |
title_sort | human and extracellular dna depletion for metagenomic analysis of complex clinical infection samples yields optimized viable microbiome profiles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435281/ https://www.ncbi.nlm.nih.gov/pubmed/30784601 http://dx.doi.org/10.1016/j.celrep.2019.01.091 |
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