非洲猪瘟病毒
多路复用
荧光计
病毒学
生物
非洲猪瘟
爆发
病毒
拉伤
计算生物学
人畜共患病
疾病控制
高致病性
工作流程
溶解
疾病监测
协议(科学)
多重聚合酶链反应
作者
Wenyan Li,Yunpeng Yang,Wenyi Xu,Yongchong Zhu,Yue Li,Lihui Cao,Shuyao Lyu,Jingqun Liu,Yan Xie,Xueping Li,Xianghua Hu,Lizhen Huang
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2026-01-28
卷期号:11 (2): 1201-1213
标识
DOI:10.1021/acssensors.5c03287
摘要
African swine fever virus (ASFV) causes devastating outbreaks in swine populations worldwide. The co-existence of wild-type and emerging gene-deleted variants (e.g., ASFV-ΔI177L) necessitates rapid on-site diagnostic tools for strain identification, which is critical for timely disease control and tailored farm management. Here, we developed a field-deployable, extraction-free one-pot assay (CORDSv2) that combines multiplex RPA and CRISPR/Cas12a to target conserved ASFV sequences and specific fluorescent markers (eGFP/mCherry) of gene-deleted variants. The assay achieved ultrasensitive detection (LOD: 6 copies/μL) and demonstrated 97.9% accuracy with 96 field samples. To streamline field operations, we integrated an extraction-free protocol (for serum/saliva) with freeze-dried reagent microspheres, enabling stable storage and direct use with minimal manual handling. When paired with a portable fluorometer (hippoCORDS), the system completes the entire sample-to-answer workflow within 1 h with a single step: addition of lysate to the microspheres. This robust, portable system addresses the urgent need for simple, on-site ASFV variant surveillance and is adaptable for other high-threat pathogens.
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