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Nat Commun ; 14(1): 1803, 2023 03 31.
Article in English | MEDLINE | ID: mdl-37002219

ABSTRACT

Detection of microbial cell-free DNA (cfDNA) circulating in the bloodstream has emerged as a promising new approach for diagnosing infection. Microbial diagnostics based on cfDNA require assays that can detect rare and highly fragmented pathogen nucleic acids. We now report WATSON (Whole-genome Assay using Tiled Surveillance Of Nucleic acids), a method to detect low amounts of pathogen cfDNA that couples pooled amplification of genomic targets tiled across the genome with pooled CRISPR/Cas13-based detection of these targets. We demonstrate that this strategy of tiling improves cfDNA detection compared to amplification and detection of a single targeted locus. WATSON can detect cfDNA from Mycobacterium tuberculosis in plasma of patients with active pulmonary tuberculosis, a disease that urgently needs accurate, minimally-invasive, field-deployable diagnostics. We thus demonstrate the potential for translating WATSON to a lateral flow platform. WATSON demonstrates the ability to capitalize on the strengths of targeting microbial cfDNA to address the need for point-of-care diagnostic tests for infectious diseases.


Subject(s)
Mycobacterium tuberculosis , Cell-Free System , DNA, Bacterial/analysis , DNA, Bacterial/genetics , Mycobacterium tuberculosis/genetics , Genome, Bacterial , CRISPR-Cas Systems , Humans , Tuberculosis/diagnosis , Tuberculosis/microbiology
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