Rapid and ultrasensitive detection of mpox virus using CRISPR/Cas12b-empowered graphene field-effect transistors

Author:

Wang Li1,Xu Chang2ORCID,Zhang Shaohui34ORCID,Chen Shang1ORCID,Wang Hao3ORCID,Duan Zhaojun5,Al-Hartomy Omar A.6ORCID,Wageh Swelm6ORCID,Wen Xiaosha1ORCID,Liu Yi4ORCID,Lin Yi1ORCID,Pu Huijie1ORCID,Xie Zhongjian2,Liu Quan1ORCID,Zhang Han4ORCID,Luo Dixian1ORCID

Affiliation:

1. Department of Laboratory Medicine, Huazhong University of Science and Technology Union Shenzhen Hospital (Nanshan Hospital) 1 , Shenzhen 518052, People's Republic of China

2. Institute of Pediatrics, Shenzhen Children's Hospital 2 , Shenzhen 518038, People's Republic of China

3. Guangdong Provincial Key Laboratory of Micro/Nano Optomechatronic Engineering, College of Mechatronics and Control Engineering, Shenzhen University 3 , Shenzhen 518060, People's Republic of China

4. Shenzhen Engineering Laboratory of Phosphorene and Optoelectronics, International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education, Institute of Microscale Optoelectronics, Shenzhen University 4 , Shenzhen 518060, People's Republic of China

5. National Institute for Viral Disease Control and Prevention, China Center for Disease Control and Prevention 5 , Beijing 102206, People's Republic of China

6. Department of Physics, Faculty of Science, King Abdulaziz University 6 , Jeddah 21589, Saudi Arabia

Abstract

Mpox is an infectious viral disease, and, as of January 12, 2023, about 84 560 distinct cases have been detected, involving about 110 countries since May 2022. Most clustered regularly interspaced short palindromic repeat (CRISPR)-based detection methods require long assay time because of the pre-amplification to target nucleic acids. Herein, we designed a new prototypal mpox biosensor that allows amplification-free nucleic acid detection by combining CRISPR/Cas12b system and ultrasensitive graphene field-effect transistor (gFET). The CRISPR/Cas12b–gFET enabled the detection of the mpox virus (MPXV) DNA targets at a sensitivity of ∼1 aM within about 20 min. We designed several sgRNAs to recognize the target genes of MPXV and then Cas12b protein cleaved the target genes to form a double-strand break. The specificity of sgRNAs of MPXV designed was verified among other homologous Orthopoxviruses, and the sgRNA could distinguish between recent 2022 MPXV and West African MPXV with the mutation site, showing its potential application in MPXV detection. Thus, the demonstrated CRISPR–gFET detection technology could serve as a sensitive and rapid diagnostic tool for MPXV and other DNA viruses in the future.

Funder

Shenzhen Science and Technology Innovation Program

Research Center for Advanced Materials Science, King Khalid University

Science and Technology Foundation of Chenzhou

Shenzhen Nanshan District Science and Technology Plan Project

Research and Start-up Fund for Discipline leaders of Huazhong University of Science and Technology Union Shenzhen Hospital

Daan Gene Horizontal Project

the Key Program of the Natural Science Foundation of Fujian Province

Publisher

AIP Publishing

Subject

General Physics and Astronomy

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