Rapid and specific detection of Streptococcus suis serotype 2 using a RPA–PfAgo system coupled with fluorescence and lateral flow dipstick

作者：Kexin Wang, Xujie Zhao, Jinɡjinɡ Li, Mingzhu Zhou, Bingze Jiao, Yilin Bai, Zhanwei Teng, Meinan Chang, Yueyu Bai, Jianhe HU, Ke Ding, Xiaojing XIA · 发表于：Frontiers in Veterinary Science · 年份：2026 · DOI：10.3389/fvets.2025.1748435 · 被引用次数：2 · 研究领域：Streptococcal Infections and Treatments、Fungal Infections and Studies、Oral microbiology and periodontitis research

Objective To develop and validate dual detection platforms integrating recombinase polymerase amplification (RPA) with Pyrococcus furiosus Argonaute (PfAgo) for the rapid and specific identification of Streptococcus suis serotype 2. Methods The conserved cps2J gene was selected as the molecular target. Key RPA parameters and PfAgo reaction conditions were systematically optimized, including temperature, reaction time, MnCl 2 concentration, gDNA design and probe concentration. Specificity and sensitivity were evaluated using plasmid dilutions and multiple S. suis serotypes together with other common swine pathogens. A total of 41 clinical samples were also tested and compared with the national standard PCR assay (GB/T 19915.3–2005). Results Two assay formats were established: real-time fluorescence system (RPA-PfAgo-RTF) and lateral flow dipstick system (RPA-PfAgo-LFD). The RPA-PfAgo-RTF assay achieved a detection limit of 10 0 copies/μL, while the RPA-PfAgo-LFD assay detected 10 2 copies/μL. Both formats showed high specificity without cross-reactivity. Among 41 field samples, six were SS2-positive, and results showed 100% agreement with the reference PCR method. Total detection time for either assay was < 1 h. Conclusion Both assay formats provide rapid, sensitive, and accurate tools for SS2 detection suitable for laboratory use and on-farm point-of-care testing.