Nanoplasmonic Rapid Antimicrobial‐Resistance Point‐of‐Care Identification Device: RAPIDx

Author:

Lee Jong‐Hwan12ORCID,Song Jihwan3,Hong SoonGweon14,Kim Yun3,Song Minsun14,Cho Byungrae1,Wu Tiffany5,Riley Lee W.5,Landegren Ulf6,Lee Luke P.1478ORCID

Affiliation:

1. Department of Bioengineering University of California Berkeley Berkeley CA 94720 USA

2. Center for Convergent Research of Emerging Virus Infection Korea Research Institute of Chemical Technology Daejeon 34114 South Korea

3. Department of Mechanical Engineering Hanbat National University Daejeon 34158 South Korea

4. Department of Medicine, Brigham and Women's Hospital Harvard Medical School Boston MA 02115 USA

5. Division of Infectious Disease and Vaccinology, School of Public Health University of California Berkeley CA 94720 USA

6. Departments of Immunology Genetics and Pathology Uppsala University Uppsala SE‐751 08 Sweden

7. Department of Electrical Engineering and Computer Science University of California Berkeley Berkeley CA 94720 USA

8. Department of Biophysics, Institute of Quantum Biophysics Sungkyunkwan University Suwon 16419 South Korea

Abstract

AbstractThe emergence of antibiotic resistance has become a global health crisis, and everyone must arm themselves with wisdom to effectively combat the “silent tsunami” of infections that are no longer treatable with antibiotics. However, the overuse or inappropriate use of unnecessary antibiotics is still routine for administering them due to the unavailability of rapid, precise, and point‐of‐care assays. Here, a rapid antimicrobial‐resistance point‐of‐care identification device (RAPIDx) is reported for the accurate and simultaneous identification of bacterial species (genotype) and target enzyme activity (phenotype). First, a contamination‐free active target enzyme is extracted via the photothermal lysis of preconcentrated bacteria cells on a nanoplasmonic functional layer on‐chip. Second, the rapid, precise identification of pathogens is achieved by the photonic rolling circle amplification of DNA on a chip. Third, the simultaneous identification of bacterial species (genotype) and target enzyme activity (phenotype) is demonstrated within a sample‐to‐answer 45 min operation via the RAPIDx. It is believed that the RAPIDx will be a valuable method for solving the bottleneck of employing on‐chip nanotechnology for antibiotic‐resistant bioassay and other infectious diseases.

Funder

Air Force Office of Scientific Research

National Institutes of Health

Publisher

Wiley

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