Validation of the TadpoleTMCampylobacter jejuni Real-Time PCR Identification Kit

Author:

Jiang Yuan1,Shen Jinling2,Xue Feng3,Zhao Lina2,Yang Jielin2,Shao Jingdong4,Zhu Changqing5,Su Jing6,Chen Yi7,Brodsky Michael8,Salfinger Yvonne9

Affiliation:

1. Shanghai Customs, 13 Zhongshan East 1st Rd, Shanghai 200001, China

2. Shanghai Entry-Exit Inspection and Quarantine Bureau, Technical Center of Animal Plant and Food Inspection and Quarantine, 1208 Minsheng Rd, Shanghai 200135, China

3. Nanjing Agricultural University, College of Veterinary Medicine, 1 Weigang Rd, Nanjing 210095, China

4. Technology Center of Zhangjiagang Entry-Exit Inspection and Quarantine Bureau, 59 Renmin Middle Rd, Zhangjiagang 215600, China

5. Nanjing Xiaozhuang University, 41 Beiwei Rd, Nanjing 210017, China

6. Suzhou Tadpole Biotechnology Co., Ltd, 218 Xinghu St, Suzhou 215000, China

7. U.S. Food and Drug Administration, Center for Food Safety and Nutrition, 5001 Campus Dr, College Park, MD 20740

8. Brodsky Consultants, 73 Donnamora Crescent, Thornhill, ON L3T 4K6, Canada

9. Consultant, Association of Public Health Laboratories, 1488 Madison St, Denver, CO 80206

Abstract

Abstract Background: The gene-based real-time PCR method for identification of Campylobacter jejuni is more simple, rapid and accurate than the traditional biochemical method. Objective: A performance validation of the TadpoleTMCampylobacter jejuni Real-Time PCR Identification Kit was performed. Method: The assay uses TaqMan Real-time PCR technology to amplify target genes from isolated colonies. Bacterial deoxyribonucleic acid (DNA) from inclusivity and exclusivity organisms cultured on Columbia Blood Agar, Campy-Cefex agar and modified Charcoal Cefoperazone Deoxycholate was extracted and analyzed on three instruments: Applied Biosystems (ABI) 7500 Fast, ABI StepOne Plus and Bio-Rad CFX96. Results: When 57 distinct strains of C. jejuni were tested for inclusivity, all 57 strains produced positive results on the three instruments. In exclusivity testing, all 35 strains of related organisms, including 7 non-target Campylobacter strains and other common species, produced negative results on the three instruments. The Independent Laboratory validation consisting of an inclusivity and exclusivity evaluation for 10 C. jejuni isolates and 10 nontarget Campylobacter isolates also showed 100% expected results on the three instruments. In addition, in robustness testing, small, deliberate changes to the assay parameters, including cell suspension turbidity, heat lysis time, and DNA template volume in the PCR reaction, did not affect the kit performance. Finally, the combined lot-to-lot and stability study on both the ABI 7500 Fast and the ABI StepOne Plus showed that the 11 C. jejuni strains and 5 nontarget Campylobacter strains can be correctly identified by the three independently manufactured, lots and it supported a shelf life of 9 months when stored at –20°C. Conclusions: The Tadpole method offers a rapid, accurate, and robust alternative for C. jejuni identification. Highlights: Rapid and accurate method to identify C. jejuni, which has a good robustness and high stability. It is flexible and offers the advantages of reduced labor and time saving.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology,Agronomy and Crop Science,Environmental Chemistry,Food Science,Analytical Chemistry

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