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...
Autores principales: | , , , , , , , , , , , , |
---|---|
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 |