Development of a dual-target RAA-LFD assay for point-of-care and visual detection of Salmonella pullorum and Salmonella typhimurium in fecal samples

作者：Weiye Zuo, Congxue Shao, Qin He, Hongwei Gao, Xuemei Sun, Pengyan Wang, Jingjing Ren · 发表于：Frontiers in Veterinary Science · 年份：2025 · DOI：10.3389/fvets.2025.1684537 · 被引用次数：1 · 研究领域：Biosensors and Analytical Detection、Salmonella and Campylobacter epidemiology、Vibrio bacteria research studies

To address the need for rapid detection of Salmonella pullorum ( S. pullorum) and Salmonella typhimurium ( S. typhimurium) in the poultry industry, we developed a dual-target point-of-care system integrating recombinase-aided amplification (RAA) with lateral flow dipsticks (LFD) for visual pathogen identification (RAA-LFD). Using primers and probes specifically targeting the ipaj gene of S. pullorum and the STM4497 gene of S. typhimurium, the optimized assay achieved detection at 37 °C within 20 min. The dual RAA-LFD assay showed exceptional specificity with no cross-reactivity toward non-target pathogens. Detection sensitivities reached 5.91 × 10 1 CFU/mL ( S. typhimurium) and 2.37 × 10 2 CFU/mL ( S. pullorum) in pure cultures. In contrast, genomic DNA detection achieved identical limits of 5.70 × 10 1 fg/μL ( S. typhimurium) and 4.53 × 10 1 fg/μL ( S. pullorum). In artificially contaminated samples, the detection limits reached 3.92 × 10 2 CFU/mL for S. pullorum and 6.26 × 10 1 CFU/mL for S. typhimurium. Clinical validation demonstrated 96.88–100% coincidence with biochemical identification and multiplex PCR results. This study confirms the precision and high sensitivity of the dual RAA-LFD assay as a detection methodology. Furthermore, by eliminating reliance on complex traditional techniques, this technology provides an efficient grassroots-level field screening tool with significant potential for preventing avian salmonellosis and enhancing food safety monitoring.