Affiliations 

  • 1 Department of Biology, College of Science, Shantou University, Shantou, Guangdong, 515063, China; Xiamen Flygene Medical Technology Co., Ltd., Biomedical Industrial Park, Xiamen, Fujian, 361000, China
  • 2 Department of Biology, College of Science, Shantou University, Shantou, Guangdong, 515063, China
  • 3 Pusat Kanser Tun Abdullah Ahmad Badawi (PKTAAB), Universiti Sains Malaysia, Bertam, Kepala Batas, Penang, 13200, Malaysia
  • 4 Academy of Sciences Malaysia (ASM), Level 20, West Wing, MATRADE Tower, Jalan Sultan Haji Ahmad Shah, Off Jalan Tuanku Abdul Halim, Kuala Lumpur, 50480, Malaysia. Electronic address: tangth.amdi@gmail.com
  • 5 Department of Biology, College of Science, Shantou University, Shantou, Guangdong, 515063, China; Guangdong Provincial Key Laboratory of Marine Biotechnology, Shantou University, Shantou, Guangdong, 515063, China; Shantou Key Laboratory of Marine Microbial Resources and Interactions with Environment, Shantou University, Shantou, Guangdong, 515063, China. Electronic address: zhuhaibao@stu.edu.cn
  • 6 Pusat Kanser Tun Abdullah Ahmad Badawi (PKTAAB), Universiti Sains Malaysia, Bertam, Kepala Batas, Penang, 13200, Malaysia; School of Biotechnology, MILA University, No 1, MIU Boulevard, Putra Nilai, Nilai, Negeri Sembilan, 71800, Malaysia. Electronic address: citartan@usm.my
Talanta, 2027 Mar 01;313(Pt A):130767.
PMID: 42892010 DOI: 10.1016/j.talanta.2026.130767

Abstract

Aptamers and the CRISPR/Cas system have become the cornerstones of target detections due to their numerous advantages. Aptamers enable direct recognition of non-nucleic acid targets, such as pathogens and antigens, while CRISPR/Cas system drives signal amplification and rapid detection. The combined aptamer-CRISPR/Cas system can overcome the limitations of traditional target detection by realizing field-deployable, highly sensitive, specific, versatile, and rapid assays. Given the increasing number of different aptamer-CRISPR/Cas systems developed recently, particularly for infectious diseases, we provide a comprehensive overview of these platforms designed for detecting significant viruses such as SARS-CoV-2, Monkeypox virus, Hepatitis B virus and bacteria that include Mycobacterium tuberculosis, Staphylococcus aureus and Salmonella. Current challenges that impede the deployment of aptamer-CRISPR/Cas for point-of-care pathogen detection were also mapped, including primary barriers such as clinical matrix effect and stability. Several strategies to mitigate these issues were also set forth, predominantly the integration of artificial intelligence and machine learning to accelerate the transition of aptamer-CRISPR/Cas system to the clinical translation and commercialization phase, paving the way towards widespread implementation in global health.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.