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

Authors :
George S
Xu Y
Rodger G
Morgan M
Sanderson ND
Hoosdally SJ
Thulborn S
Robinson E
Rathod P
Walker AS
Peto TEA
Crook DW
Dingle KE
Source :
Journal of clinical microbiology [J Clin Microbiol] 2020 Sep 22; Vol. 58 (10). Date of Electronic Publication: 2020 Sep 22 (Print Publication: 2020).
Publication Year :
2020

Abstract

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 <superscript>5</superscript> 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 <superscript>1</superscript> BCG cells/ml, with 31 to 59 M. tuberculosis complex reads. Maximal genome coverage (>97% at 5× depth) occurred at 10 <superscript>4</superscript> BCG cells/ml; >91% coverage (1× depth) occurred at 10 <superscript>3</superscript> 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.<br /> (Copyright © 2020 George et al.)

Details

Language :
English
ISSN :
1098-660X
Volume :
58
Issue :
10
Database :
MEDLINE
Journal :
Journal of clinical microbiology
Publication Type :
Academic Journal
Accession number :
32719032
Full Text :
https://doi.org/10.1128/JCM.00670-20