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Genome-wide tiled detection of circulating Mycobacterium tuberculosis cell-free DNA using Cas13.
Thakku, Sri Gowtham; Lirette, Jackson; Murugesan, Kanagavel; Chen, Julie; Theron, Grant; Banaei, Niaz; Blainey, Paul C; Gomez, James; Wong, Sharon Y; Hung, Deborah T.
Afiliação
  • Thakku SG; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Lirette J; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Murugesan K; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Chen J; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Theron G; DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research and SAMRC Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
  • Banaei N; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Blainey PC; Department of Medicine, Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA, USA.
  • Gomez J; Clinical Microbiology Laboratory, Stanford Health Care, Palo Alto, CA, USA.
  • Wong SY; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Hung DT; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Nat Commun ; 14(1): 1803, 2023 03 31.
Article em En | MEDLINE | ID: mdl-37002219
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mycobacterium tuberculosis Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mycobacterium tuberculosis Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article