DNA Thermo-Protection Facilitates Whole-Genome Sequencing of Mycobacteria Direct from Clinical Samples.
Sophie GeorgeYifei XuGillian RodgerMarcus MorganNicholas D SandersonSarah J HoosdallySamantha ThulbornEsther RobinsonPriti RathodA Sarah WalkerTimothy E A PetoDerrick W CrookKate E DinglePublished in: Journal of clinical microbiology (2020)
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 105 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 101 BCG cells/ml, with 31 to 59 M. tuberculosis complex reads. Maximal genome coverage (>97% at 5× depth) occurred at 104 BCG cells/ml; >91% coverage (1× depth) occurred at 103 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.
Keyphrases
- mycobacterium tuberculosis
- circulating tumor
- pulmonary tuberculosis
- cell free
- induced apoptosis
- single molecule
- cell cycle arrest
- endothelial cells
- hiv aids
- antimicrobial resistance
- emergency department
- optical coherence tomography
- genome wide
- healthcare
- affordable care act
- cystic fibrosis
- oxidative stress
- reactive oxygen species
- body composition
- heat stress
- circulating tumor cells
- cell proliferation
- high resolution
- heavy metals
- mass spectrometry
- health insurance
- induced pluripotent stem cells
- human immunodeficiency virus