Amplification‐Free, Sequencing‐Free, Detection of Viral RNAs with Variant Specification by Discrete Nanocounting

Author:

Wang Zixun12,Zhao Xi13,Chan Wan‐Mui4,Ji Xianglin1,Huang Linfeng5,Xie Xi6,Li Wei7,Zhang Wenjun8910,To Kelvin Kai‐Wang4111213,Shi Peng13910ORCID

Affiliation:

1. Department of Biomedical Engineering City University of Hong Kong Kowloon Hong Kong SAR 999077 China

2. CAS Key Laboratory of Nano‐Bio Interface Suzhou Institute of Nano‐Tech and Nano‐Bionics Chinese Academy of Sciences Suzhou 215123 China

3. Hong Kong Centre for Cerebro‐Cardiovascular Health Engineering Hong Kong Science Park Hong Kong SAR 999077 China

4. State Key Laboratory for Emerging Infectious Diseases Carol Yu Centre for Infection Department of Microbiology School of Clinical Medicine Li Ka Shing Faculty of Medicine The University of Hong Kong Pokfulam Hong Kong SAR 999077 China

5. Division of Natural and Applied Sciences Duke Kunshan University Kunshan 215316 China

6. State Key Laboratory of Optoelectronic Materials and Technologies Guangdong Province Key Laboratory of Display Material and Technology School of Electronics and Information Technology Sun Yat‐Sen University Guangzhou 510006 China

7. School of Pharmaceutical Sciences Wuhan University Wuhan 430071 China

8. Department of Materials Science and Engineering City University of Hong Kong Kowloon Hong Kong SAR 999077 China

9. Center of Super‐Diamond and Advanced Films (COSDAF) City University of Hong Kong Kowloon Hong Kong SAR 999077 China

10. Shenzhen Research Institute City University of Hong Kong Shenzhen 518000 China

11. Centre for Virology Vaccinology and Therapeutics Hong Kong Science and Technology Park Hong Kong SAR 999077 China

12. Department of Microbiology Queen Mary Hospital Pokfulam Hong Kong SAR 999077 China

13. Department of Infectious Disease and Microbiology The University of Hong Kong‐Shenzhen Hospital Shenzhen 518000 China

Abstract

AbstractThis study describes an amplification‐free, sequencing‐free platform (NanoPick‐array) for fast analysis of viral RNAs. The platform combines selective short‐cut of viral RNAs, cherry‐picking isolation of target genes, and micro‐arrayed discrete nanoimaging to enable the detection of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) at a concentration of 60 copies µL−1, a detection limit that is hardly achieved by Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)‐based methods without amplification, regardless of electrochemical or colorimetric approaches. Notably, the NanoPick‐array provides specific virus variant information with differentiation to single‐nucleotide genetic mutation. The avoidance of the amplification procedure gives direct quantification of viral copy number and reduces false positive results caused by amplicon contamination; the sequencing‐free viral variant specification significantly reduces the turn‐over time for the acquisition of a complete diagnostic viral picture within just 2 h. In a demonstration using clinical samples with a wide range of viral loads of cycle threshold (Ct) value ranging from 18 to 36, the technique achieves an overall accuracy of 89.7% viral detection and 100% accuracy for identifying all Delta variants. The viral detection accuracy is further tested to be 100% for the clinical samples with Ct values around or less than 28.

Funder

National Natural Science Foundation of China

City University of Hong Kong

Publisher

Wiley

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