Phosphorothioate Modification-Regulated One-Pot CRISPR Assay for Arbovirus Detection
The ongoing arthropod-borne Chikungunya virus (CHIKV) highlights the requirements of rapid and accurate diagnostic methods to enhance the epidemic control. CRISPR diagnostic (CRISPR-Dx) technology holds promise, but the development of a highly efficient one-pot diagnostic system usually requires fine-tuning of the balance between isothermal amplification and Cas cleavage procedures. Here, we describe a simple method (psHOLMES) to create one-pot, two-step CRISPR-Dx systems, using photocleavable partially phosphorothioate-modified DNA (ppPS-DNA) to regulate Cas12a activity. Cas12a activity is first inactivated via binding of ppPS-DNA during the target sequence amplification procedure, which is then reactivated by ultraviolet (UV)-mediated photolysis of ppPS-DNA after amplification, triggering Cas12a trans-cleavage reactions. psHOLMES demonstrates attomolar sensitivity for CHIKV RNA detection and zero cross-reactivity against other related arboviruses. When applied to clinical samples, psHOLMES achieved 100% (50/50) accuracy and could detect CHIKV within 30 min. As traditional efforts for fine-tuning Cas cis-cleavage activity can be omitted, psHOLMES thus enables rapid development of one-pot CRISPR-Dx systems for clinical applications.
Authors
- Jin Wang (ORCID: https://orcid.org/0009-0000-4659-6688)
- Hongzhong Zhou
- Dayong Xu (ORCID: https://orcid.org/0000-0002-6980-4344)
- Li Zhu
- Jianan He
- Songkuan Zhuang
- Ran Zhang
- Yong Xu
- Jie Li
- Zhoubin Fang
- Dayong Gu
Institutions
- Huaibei Normal University (CN)
- Guangdong Medical College (CN)
- Shenzhen University (CN)
- Southern University of Science and Technology (CN)
- Shenzhen Inno Translational Medicine Institute (CN)
- Shenzhen International Travel Health Care Center (CN)
- Shenzhen Second People's Hospital (CN)
- Shenzhen Third People’s Hospital (CN)
- Graduate School USA (US)
Publication Details
- Journal
- ACS Infectious Diseases
- Published
- 2026-03-23
- DOI
- https://doi.org/10.1021/acsinfecdis.6c00013
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 0.00