BRIEF RESEARCH REPORT article

Front. Vet. Sci.

Sec. Veterinary Infectious Diseases

Volume 12 - 2025 | doi: 10.3389/fvets.2025.1635525

The detection of Edwardsiella tarda by aptamer-based qPCR

Provisionally accepted
Yue  BaiYue Bai1Xuefei  LiXuefei Li1Wei  YanWei Yan1Lingmin  ZhaoLingmin Zhao1Lixing  HuangLixing Huang1Qingpi  YanQingpi Yan1Qibiao  WengQibiao Weng2Jiaen  WangJiaen Wang2Jiang  ZhengJiang Zheng1*
  • 1Fisheries College, Jimei University, Xiamen, China
  • 2Changle Juquan Food Co. Ltd., Fuzhou, China

The final, formatted version of the article will be published soon.

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 1-10 9 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.

Keywords: Edwardsiella tarda, aptamer, SYBR Green I real-time quantitative PCR, Minimum detection limit, Aptamer-qPCR

Received: 26 May 2025; Accepted: 10 Jul 2025.

Copyright: © 2025 Bai, Li, Yan, Zhao, Huang, Yan, Weng, Wang and Zheng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Jiang Zheng, Fisheries College, Jimei University, Xiamen, China

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