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Rapid detection of tetracycline resistance gene TetA in freshwater products by cross priming amplification technology
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Yi-Dong LAI1, *, Jun XIONG1, Tian-Tian ZHANG1, Yang YUE2, Zhen-Bo XU2, *
Journal of Food Safety & Quality | 2026, 17(8) : 136 - 142
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Journal of Food Safety & Quality | 2026, 17(8): 136-142
• Special Topic: Detection and Control of Foodborne Pathogenic Bacteria •
Rapid detection of tetracycline resistance gene TetA in freshwater products by cross priming amplification technology
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Yi-Dong LAI1, *, Jun XIONG1, Tian-Tian ZHANG1, Yang YUE2, Zhen-Bo XU2, *
Affiliations
  • 1.Dongguan Quality Supervision and Testing Center, Dongguan 523808, China
  • 2.College of Food Science and Engineering, South China University of Technology, Guangzhou 510641, China
doi: 10.19812/j.cnki.jfsq11-5956/ts.20251118003
Outline
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Objective

To establish a novel method for rapid on-site detection of the tetracycline resistance gene TetA by cross priming amplification (CPA) technology.

Methods

A total of 5 specific primers targeting conserved regions of the TetA gene were designed. Amplification was performed under isothermal conditions (optimized at 51–60 ℃), with the entire detection process completed within 45–60 minutes using only basic heating equipment such as a water bath or metal bath. To validate its performance, the method was systematically evaluated for sensitivity, specificity and interference resistance.

Results

The limit of detection for purified TetA gene templates was as low as 30.0  fg/μL, indicating high sensitivity. Furthermore, no nonspecific amplification was observed in comparative tests against other tetracycline resistance genes (e.g., tetB, tetM) and common clinical pathogenic genes, confirming excellent selectivity. Additionally, simulated sample testing yielded stable and reliable results.

Conclusion

A simple, rapid, low-cost and instrument-free CPA-based method for TetA gene detection is successfully developed. With its high sensitivity and specificity, this method can effectively meet the needs for rapid on-site screening of tetracycline resistance genes in primary healthcare institutions and farming environments. It provides a robust technical tool for real-time monitoring and controlling the spread of antibiotic resistance genes, demonstrating significant practical application value.

tetracycline resistance gene  /  TetA  /  cross priming amplification  /  rapid detection  /  antibiotic resistance
赖毅东, 熊珺, 张甜甜, 岳洋, 徐振波. 交叉引物扩增技术快速检测淡水产品中四环素耐药基因TetA. 食品安全质量检测学报, 2026 , 17 (8) : 136 -142 . DOI: 10.19812/j.cnki.jfsq11-5956/ts.20251118003
Yi-Dong LAI, Jun XIONG, Tian-Tian ZHANG, Yang YUE, Zhen-Bo XU. Rapid detection of tetracycline resistance gene TetA in freshwater products by cross priming amplification technology[J]. Journal of Food Safety & Quality, 2026 , 17 (8) : 136 -142 . DOI: 10.19812/j.cnki.jfsq11-5956/ts.20251118003
Year 2026 volume 17 Issue 8
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1
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doi: 10.19812/j.cnki.jfsq11-5956/ts.20251118003
  • Receive Date:2025-11-18
  • Online Date:2026-11-05
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  • Received:2025-11-18
Funding
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    1.Dongguan Quality Supervision and Testing Center, Dongguan 523808, China
    2.College of Food Science and Engineering, South China University of Technology, Guangzhou 510641, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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