Objective To explore the application of the combination of real-time fluorescence quantitative polymerase chain reaction (qPCR) and droplet digital polymerase chain reaction (ddPCR) in the quantitative detection of meat adulteration. Methods This study employed qPCR and ddPCR technologies to develop a detection system with specific primers and probes for beef, lamb and pork samples, aiming to assess meat adulteration in the Beijing market. Results The experimental results revealed that the sample “Chang 5” contained adulteration of lamb and pork at a ratio of 17:10. qPCR demonstrated high sensitivity and specificity in qualitative detection, while ddPCR enabled absolute quantification of adulteration proportions. The combination of these 2 methods significantly improved detection accuracy. Conclusion The established qPCR-ddPCR combined method exhibits high sensitivity and specificity, making it suitable for rapid and precise detection of meat adulteration. This approach provides reliable technical support for food safety regulation.
| 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 |