Author
Listed:
- Monty Liong
(Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School)
- Anh N. Hoang
(BioMEMS Resource Center, Surgical Services, Massachusetts General Hospital, Harvard Medical School)
- Jaehoon Chung
(Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School)
- Nil Gural
(BioMEMS Resource Center, Surgical Services, Massachusetts General Hospital, Harvard Medical School)
- Christopher B. Ford
(Harvard School of Public Health, Boston, Massachusetts 02115, USA)
- Changwook Min
(Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School)
- Rupal R. Shah
(Harvard School of Public Health, Boston, Massachusetts 02115, USA)
- Rushdy Ahmad
(Broad Institute of Harvard and MIT, Cambridge, Massachusetts 02142, USA)
- Marta Fernandez-Suarez
(BioMEMS Resource Center, Surgical Services, Massachusetts General Hospital, Harvard Medical School
Harvard School of Public Health, Boston, Massachusetts 02115, USA
Present address: Daktari Diagnostics, 85 Bolton Street, Cambridge, Massachusetts 02139, USA)
- Sarah M. Fortune
(Harvard School of Public Health, Boston, Massachusetts 02115, USA)
- Mehmet Toner
(BioMEMS Resource Center, Surgical Services, Massachusetts General Hospital, Harvard Medical School)
- Hakho Lee
(Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School)
- Ralph Weissleder
(Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School
Harvard Medical School)
Abstract
The task of rapidly identifying patients infected with Mycobacterium tuberculosis in resource-constrained environments remains a challenge. A sensitive and robust platform that does not require bacterial isolation or culture is critical in making informed diagnostic and therapeutic decisions. Here we introduce a platform for the detection of nucleic acids based on a magnetic barcoding strategy. PCR-amplified mycobacterial genes are sequence-specifically captured on microspheres, labelled by magnetic nanoprobes and detected by nuclear magnetic resonance. All components are integrated into a single, small fluidic cartridge for streamlined on-chip operation. We use this platform to detect M. tuberculosis and identify drug-resistance strains from mechanically processed sputum samples within 2.5 h. The specificity of the assay is confirmed by detecting a panel of clinically relevant non-M. tuberculosis bacteria, and the clinical utility is demonstrated by the measurements in M. tuberculosis-positive patient specimens. Combined with portable systems, the magnetic barcode assay holds promise to become a sensitive, high-throughput and low-cost platform for point-of-care diagnostics.
Suggested Citation
Monty Liong & Anh N. Hoang & Jaehoon Chung & Nil Gural & Christopher B. Ford & Changwook Min & Rupal R. Shah & Rushdy Ahmad & Marta Fernandez-Suarez & Sarah M. Fortune & Mehmet Toner & Hakho Lee & Ral, 2013.
"Magnetic barcode assay for genetic detection of pathogens,"
Nature Communications, Nature, vol. 4(1), pages 1-9, June.
Handle:
RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2745
DOI: 10.1038/ncomms2745
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