Multiplexed detection of bacterial nucleic acids using Cas13 in droplet microarrays

Author:

Thakku Sri Gowtham12,Ackerman Cheri M1,Myhrvold Cameron1,Bhattacharyya Roby P13ORCID,Livny Jonathan1,Ma Peijun1,Gomez Giselle Isabella1,Sabeti Pardis C145,Blainey Paul C167ORCID,Hung Deborah T189

Affiliation:

1. Broad Institute of MIT and Harvard , Cambridge, MA 02142 , USA

2. Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology , Cambridge, MA 02142 , USA

3. Infectious Diseases Division, Department of Medicine, Massachusetts General Hospital , Boston, MA 02114 , USA

4. Department of Immunology and Infectious Disease, Harvard T.H. Chan School of Public Health , Boston, MA 02115 , USA

5. Howard Hughes Medical Institute , Chevy Chase, MD 20815 , USA

6. Department of Biological Engineering, Massachusetts Institute of Technology , Cambridge, MA 02139 , USA

7. Koch Institute for Integrative Cancer Research at MIT , Cambridge, MA 02139 , USA

8. Department of Genetics, Harvard Medical School , Boston, MA 02115 , USA

9. Department of Molecular Biology and Center for Computational and Integrative Biology, Massachusetts General Hospital , Boston, MA 02114 , USA

Abstract

Abstract Rapid and accurate diagnosis of infections is fundamental to individual patient care and public health management. Nucleic acid detection methods are critical to this effort, but are limited either in the breadth of pathogens targeted or by the expertise and infrastructure required. We present here a high-throughput system that enables rapid identification of bacterial pathogens, bCARMEN, which utilizes: (1) modular CRISPR-Cas13-based nucleic acid detection with enhanced sensitivity and specificity; and (2) a droplet microfluidic system that enables thousands of simultaneous, spatially multiplexed detection reactions at nanoliter volumes; and (3) a novel preamplification strategy that further enhances sensitivity and specificity. We demonstrate bCARMEN is capable of detecting and discriminating 52 clinically relevant bacterial species and several key antibiotic resistance genes. We further develop a simple proof of principle workflow using stabilized reagents and cell phone camera optical readout, opening up the possibility of a rapid point-of-care multiplexed bacterial pathogen identification and antibiotic susceptibility testing.

Funder

NIH

Broad Institute Tuberculosis

Pershing Square Foundation

MIT IMES Broshy Fellowship

Publisher

Oxford University Press (OUP)

Reference35 articles.

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