A rapid high-throughput sequencing-based approach for the identification of unknown bacterial pathogens in whole blood.
Ofir IsraeliEfi MakdasiInbar Cohen-GihonAnat ZviShirley LazarOhad ShifmanHaim LevyDavid GurOrly LaskarAdi Beth-DinPublished in: Future science OA (2020)
High-throughput DNA sequencing (HTS) of pathogens in whole blood samples is hampered by the high host/pathogen nucleic acids ratio. We describe a novel and rapid bacterial enrichment procedure whose implementation is exemplified in simulated bacteremic human blood samples. The procedure involves depletion of the host DNA, rapid HTS and bioinformatic analyses. Following this procedure, Y. pestis, F. tularensis and B. anthracis spiked-in samples displayed an improved host/pathogen DNA ratio of 2.5-5.9 orders of magnitude, in samples with bacteria spiked-in at 103-105 CFU/ml. The procedure described in this study enables rapid and detailed metagenomic profiling of pathogens within 8-9 h, circumventing the challenges imposed by the high background present in the bacteremic blood and by the unknown nature of the sample.
Keyphrases
- circulating tumor
- minimally invasive
- high throughput
- loop mediated isothermal amplification
- cell free
- single cell
- gram negative
- single molecule
- high throughput sequencing
- antimicrobial resistance
- healthcare
- endothelial cells
- primary care
- nucleic acid
- induced pluripotent stem cells
- wastewater treatment
- sensitive detection