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

**Authors:** Weiye Zuo, Congxue Shao, He Qin, Hongwei Gao, Xuemei Sun, Pengyan Wang, Jingjing Ren

PMC · DOI: 10.3389/fvets.2025.1684537 · Frontiers in Veterinary Science · 2025-11-03

## TL;DR

This paper introduces a fast, visual test for detecting two types of Salmonella in poultry feces, offering a practical tool for on-site food safety monitoring.

## Contribution

A dual-target RAA-LFD assay for rapid, sensitive, and specific detection of S. pullorum and S. typhimurium in fecal samples.

## Key findings

- The assay achieved detection within 20 minutes at 37°C with high specificity and no cross-reactivity.
- Detection limits in pure cultures were as low as 5.91 × 10¹ CFU/mL for S. typhimurium and 2.37 × 10² CFU/mL for S. pullorum.
- Clinical validation showed 96.88–100% agreement with traditional methods like biochemical identification and multiplex PCR.

## Abstract

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 × 101 CFU/mL (S. typhimurium) and 2.37 × 102 CFU/mL (S. pullorum) in pure cultures. In contrast, genomic DNA detection achieved identical limits of 5.70 × 101 fg/μL (S. typhimurium) and 4.53 × 101 fg/μL (S. pullorum). In artificially contaminated samples, the detection limits reached 3.92 × 102 CFU/mL for S. pullorum and 6.26 × 101 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.

## Linked entities

- **Genes:** ipaJ (IpaJ, invasion plasmid antigen) [NCBI Gene 3170828], STM4497 (putative cytoplasmic protein) [NCBI Gene 1256023]

## Full-text entities

- **Diseases:** salmonellosis (MESH:D012480)
- **Species:** Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Salmonella enterica subsp. enterica serovar Pullorum (no rank) [taxon 605]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12621324/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12621324/full.md

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Source: https://tomesphere.com/paper/PMC12621324