病毒学
病毒
甲型流感病毒
生物
血凝素(流感)
逆转录聚合酶链式反应
计算生物学
H5N1亚型流感病毒
大流行
检出限
聚合酶链反应
正粘病毒科
逆转录酶
实时聚合酶链反应
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
大流行性流感
新型病毒
诊断试验
塔克曼
分子诊断学
一致性
2019年冠状病毒病(COVID-19)
H1N1流感
作者
Changhai Tian,Lulu Feng,Xu Zhou,Kailun Huang,Feifei Wang,Ru Luo,Fei Meng,He Yang,Chuanling Qiao,X. J. Wang,Jianzhong Shi,Yan Chen
出处
期刊:Viruses
[Multidisciplinary Digital Publishing Institute]
日期:2025-12-28
卷期号:18 (1): 47-47
被引量:1
摘要
The widespread circulation of Eurasian avian-like H1N1 (EA H1N1) swine influenza virus poses significant zoonotic and pandemic risks worldwide. However, current diagnostic methods are difficult to deploy in the field, as they generally require specialized laboratory infrastructure and trained personnel. Here, we present a novel dual-signal detection platform that combines reverse transcription recombinase polymerase amplification (RT-RPA) with CRISPR/Cas12a technology for rapid, on-site EA H1N1 detection. We established an integrated one-tube assay by designing and optimizing RT-RPA primers targeting a conserved region of the hemagglutinin (HA) gene, together with engineered CRISPR/Cas12a guide RNAs exhibiting high specificity. The platform incorporates two complementary readout modes: real-time fluorescence monitoring and visual colorimetric detection using a smartphone. The assay shows excellent analytical specificity, with no cross-reactivity observed against other swine influenza virus subtypes or common swine pathogens, (including CSFV, PRRSV, PEDV, PCV, TGEV, and RV). The detection limit is 2 copies/μL, and the entire procedure can be completed within 30 mins using simple portable equipment. When evaluated on 86 clinical samples, the assay demonstrated 94.18% concordance with RT-qPCR. Compared with conventional diagnostic methods, this RT-RPA-CRISPR/Cas12a assay offers greater convenience and cost-effectiveness. Its strong potential for field-based rapid testing underscores promising application prospects in swine influenza surveillance and control programs.
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