# The detection of Edwardsiella tarda by aptamer-based qPCR

**Authors:** Yue Bai, Xuefei Li, Wei Yan, Lingmin Zhao, Lixing Huang, Qingpi Yan, Jiaen Wang, Qibiao Weng, Jiang Zheng

PMC · DOI: 10.3389/fvets.2025.1635525 · Frontiers in Veterinary Science · 2025-07-23

## TL;DR

This study introduces a new method using aptamers and qPCR to detect and quantify the fish pathogen Edwardsiella tarda with high accuracy and sensitivity.

## Contribution

A novel aptamer-based qPCR method is developed for specific and quantitative detection of Edwardsiella tarda.

## Key findings

- The method showed significantly lower Ct values for E. tarda compared to non-target bacteria (p < 0.01).
- The detection range was linear from 1 to 109 CFU/mL with a minimum detection limit of 1 CFU/mL.
- The method successfully detected E. tarda in spiked water and tissue samples, demonstrating practical applicability.

## Abstract

The Edwardsiella tarda bacterium can infect a wide variety of fish species and is a common pathogen in aquaculture. Rapid and accurate detection of the pathogen is the premise and basis for its disease prevention and control. In this study, an aptamer with high affinity and specificity was used to bind E. tarda. The aptamers that bound to the pathogen were then separated and used as the templates for SYBR Green I real-time quantitative polymerase chain reaction (qPCR) amplification. The Ct values obtained by qPCR can be used to quantitatively analyze the concentration of E. tarda, thereby establishing an aptamer-qPCR method for the quantitative detection of the pathogen with good specificity. Results showed that the Ct value of E. tarda was significantly lower than that of non-target bacteria (Pseudomonas plecoglossicida, Pseudomonas aeruginosa, Escherichia coli, Vibrio anguillarum, Vibrio alginolyticus, Vibrio harveyi and Aeromonas hydrophila) (p < 0.01). It had a good quantitative detection effect and showed good linearity in the range of 1–109 CFU/mL. This method also had high sensitivity and stability, with minimum detection limit reaching 1 CFU/mL. This method was used to detect E. tarda in spiked water and tissue samples, proving its applicability for the detection of E. tarda in aquatic products, foods, and in the aquatic environment.

## Linked entities

- **Species:** Edwardsiella tarda (taxon 636), Pseudomonas plecoglossicida (taxon 70775), Pseudomonas aeruginosa (taxon 287), Escherichia coli (taxon 562), Vibrio anguillarum (taxon 55601), Vibrio alginolyticus (taxon 663), Vibrio harveyi (taxon 669), Aeromonas hydrophila (taxon 644)

## Full-text entities

- **Chemicals:** SYBR Green I (MESH:C098022), water (MESH:D014867)
- **Species:** Edwardsiella tarda (species) [taxon 636], Escherichia coli (E. coli, species) [taxon 562], Aeromonas hydrophila (species) [taxon 644], Vibrio harveyi (species) [taxon 669], Pseudomonas plecoglossicida (species) [taxon 70775], Pseudomonas aeruginosa (species) [taxon 287], Vibrio anguillarum (species) [taxon 55601], Vibrio alginolyticus (species) [taxon 663]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12327390/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12327390/full.md

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Source: https://tomesphere.com/paper/PMC12327390