Cargando…

DNA Thermo-Protection Facilitates Whole-Genome Sequencing of Mycobacteria Direct from Clinical Samples

Mycobacterium tuberculosis is the leading cause of death from bacterial infection. Improved rapid diagnosis and antimicrobial resistance determination, such as by whole-genome sequencing, are required. Our aim was to develop a simple, low-cost method of preparing DNA for sequencing direct from M. tu...

Descripción completa

Detalles Bibliográficos
Autores principales: George, Sophie, Xu, Yifei, Rodger, Gillian, Morgan, Marcus, Sanderson, Nicholas D., Hoosdally, Sarah J., Thulborn, Samantha, Robinson, Esther, Rathod, Priti, Walker, A. Sarah, Peto, Timothy E. A., Crook, Derrick W., Dingle, Kate E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7512152/
https://www.ncbi.nlm.nih.gov/pubmed/32719032
http://dx.doi.org/10.1128/JCM.00670-20
_version_ 1783586096853024768
author George, Sophie
Xu, Yifei
Rodger, Gillian
Morgan, Marcus
Sanderson, Nicholas D.
Hoosdally, Sarah J.
Thulborn, Samantha
Robinson, Esther
Rathod, Priti
Walker, A. Sarah
Peto, Timothy E. A.
Crook, Derrick W.
Dingle, Kate E.
author_facet George, Sophie
Xu, Yifei
Rodger, Gillian
Morgan, Marcus
Sanderson, Nicholas D.
Hoosdally, Sarah J.
Thulborn, Samantha
Robinson, Esther
Rathod, Priti
Walker, A. Sarah
Peto, Timothy E. A.
Crook, Derrick W.
Dingle, Kate E.
author_sort George, Sophie
collection PubMed
description Mycobacterium tuberculosis is the leading cause of death from bacterial infection. Improved rapid diagnosis and antimicrobial resistance determination, such as by whole-genome sequencing, are required. Our aim was to develop a simple, low-cost method of preparing DNA for sequencing direct from M. tuberculosis-positive clinical samples (without culture). Simultaneous sputum liquefaction, bacteria heat inactivation (99°C/30 min), and enrichment for mycobacteria DNA were achieved using an equal volume of thermo-protection buffer (4 M KCl, 0.05 M HEPES buffer, pH 7.5, 0.1% dithiothreitol [DTT]). The buffer emulated intracellular conditions found in hyperthermophiles, thus protecting DNA from rapid thermodegradation, which renders it a poor template for sequencing. Initial validation experiments employed mycobacteria DNA, either extracted or intracellular. Next, mock clinical samples (infection-negative human sputum spiked with 0 to 10(5) Mycobacterium bovis BCG cells/ml) underwent liquefaction in thermo-protection buffer and heat inactivation. DNA was extracted and sequenced. Human DNA degraded faster than mycobacteria DNA, resulting in target enrichment. Four replicate experiments achieved M. tuberculosis detection at 10(1) BCG cells/ml, with 31 to 59 M. tuberculosis complex reads. Maximal genome coverage (>97% at 5× depth) occurred at 10(4) BCG cells/ml; >91% coverage (1× depth) occurred at 10(3) BCG cells/ml. Final validation employed M. tuberculosis-positive clinical samples (n = 20), revealing that initial sample volumes of ≥1 ml typically yielded higher mean depths of M. tuberculosis genome coverage, with an overall range of 0.55 to 81.02. A mean depth of 3 gave >96% 1-fold tuberculosis (TB) genome coverage (in 15/20 clinical samples). A mean depth of 15 achieved >99% 5-fold genome coverage (in 9/20 clinical samples). In summary, direct-from-sample sequencing of M. tuberculosis genomes was facilitated by a low-cost thermo-protection buffer.
format Online
Article
Text
id pubmed-7512152
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-75121522020-10-02 DNA Thermo-Protection Facilitates Whole-Genome Sequencing of Mycobacteria Direct from Clinical Samples George, Sophie Xu, Yifei Rodger, Gillian Morgan, Marcus Sanderson, Nicholas D. Hoosdally, Sarah J. Thulborn, Samantha Robinson, Esther Rathod, Priti Walker, A. Sarah Peto, Timothy E. A. Crook, Derrick W. Dingle, Kate E. J Clin Microbiol Mycobacteriology and Aerobic Actinomycetes Mycobacterium tuberculosis is the leading cause of death from bacterial infection. Improved rapid diagnosis and antimicrobial resistance determination, such as by whole-genome sequencing, are required. Our aim was to develop a simple, low-cost method of preparing DNA for sequencing direct from M. tuberculosis-positive clinical samples (without culture). Simultaneous sputum liquefaction, bacteria heat inactivation (99°C/30 min), and enrichment for mycobacteria DNA were achieved using an equal volume of thermo-protection buffer (4 M KCl, 0.05 M HEPES buffer, pH 7.5, 0.1% dithiothreitol [DTT]). The buffer emulated intracellular conditions found in hyperthermophiles, thus protecting DNA from rapid thermodegradation, which renders it a poor template for sequencing. Initial validation experiments employed mycobacteria DNA, either extracted or intracellular. Next, mock clinical samples (infection-negative human sputum spiked with 0 to 10(5) Mycobacterium bovis BCG cells/ml) underwent liquefaction in thermo-protection buffer and heat inactivation. DNA was extracted and sequenced. Human DNA degraded faster than mycobacteria DNA, resulting in target enrichment. Four replicate experiments achieved M. tuberculosis detection at 10(1) BCG cells/ml, with 31 to 59 M. tuberculosis complex reads. Maximal genome coverage (>97% at 5× depth) occurred at 10(4) BCG cells/ml; >91% coverage (1× depth) occurred at 10(3) BCG cells/ml. Final validation employed M. tuberculosis-positive clinical samples (n = 20), revealing that initial sample volumes of ≥1 ml typically yielded higher mean depths of M. tuberculosis genome coverage, with an overall range of 0.55 to 81.02. A mean depth of 3 gave >96% 1-fold tuberculosis (TB) genome coverage (in 15/20 clinical samples). A mean depth of 15 achieved >99% 5-fold genome coverage (in 9/20 clinical samples). In summary, direct-from-sample sequencing of M. tuberculosis genomes was facilitated by a low-cost thermo-protection buffer. American Society for Microbiology 2020-09-22 /pmc/articles/PMC7512152/ /pubmed/32719032 http://dx.doi.org/10.1128/JCM.00670-20 Text en Copyright © 2020 George et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Mycobacteriology and Aerobic Actinomycetes
George, Sophie
Xu, Yifei
Rodger, Gillian
Morgan, Marcus
Sanderson, Nicholas D.
Hoosdally, Sarah J.
Thulborn, Samantha
Robinson, Esther
Rathod, Priti
Walker, A. Sarah
Peto, Timothy E. A.
Crook, Derrick W.
Dingle, Kate E.
DNA Thermo-Protection Facilitates Whole-Genome Sequencing of Mycobacteria Direct from Clinical Samples
title DNA Thermo-Protection Facilitates Whole-Genome Sequencing of Mycobacteria Direct from Clinical Samples
title_full DNA Thermo-Protection Facilitates Whole-Genome Sequencing of Mycobacteria Direct from Clinical Samples
title_fullStr DNA Thermo-Protection Facilitates Whole-Genome Sequencing of Mycobacteria Direct from Clinical Samples
title_full_unstemmed DNA Thermo-Protection Facilitates Whole-Genome Sequencing of Mycobacteria Direct from Clinical Samples
title_short DNA Thermo-Protection Facilitates Whole-Genome Sequencing of Mycobacteria Direct from Clinical Samples
title_sort dna thermo-protection facilitates whole-genome sequencing of mycobacteria direct from clinical samples
topic Mycobacteriology and Aerobic Actinomycetes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7512152/
https://www.ncbi.nlm.nih.gov/pubmed/32719032
http://dx.doi.org/10.1128/JCM.00670-20
work_keys_str_mv AT georgesophie dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT xuyifei dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT rodgergillian dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT morganmarcus dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT sandersonnicholasd dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT hoosdallysarahj dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT thulbornsamantha dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT robinsonesther dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT rathodpriti dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT walkerasarah dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT petotimothyea dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT crookderrickw dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples
AT dinglekatee dnathermoprotectionfacilitateswholegenomesequencingofmycobacteriadirectfromclinicalsamples