生产用于检测肉毒杆菌神经毒素 A 型和 B 型基因的 PCR 测试模板的阳性对照材料

Hanh Ninh Thi, Hoa Le Vinh, Ba Tran Hong, Quan Pham Van, Long Le Thanh, Loan Pham Thi
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摘要

肉毒杆菌神经毒素(BoNT)由肉毒梭菌和其他一些细菌菌株(如丁酸杆菌和巴拉蒂肉毒杆菌)产生。它被认为是人类已知的最强毒素,可导致肉毒中毒。肉毒杆菌神经毒素可致人死亡,大多数肉毒中毒病例都是由 A 型和 B 型毒素引起的。在这项研究中,研究小组使用了从越南肉毒中毒病例中分离出的肉毒杆菌菌株,经鉴定,这些菌株可产生A型和B型毒素,根据TCVN 11395:2016的参考基因序列,我们成功地从这些菌株中转化了携带BoNT A型和B型特异性基因的质粒。这些质粒被成功用作 PCR 反应的模板 DNA。在 PCR 反应中,用于转化产生 A 型和 B 型肉毒毒素基因的质粒的检测限为 102 个拷贝/微升。该研究完全验证了验证参数,准确率和特异性均为 100%。
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Producing positive control materials for template in PCR testing to detect botulinum neurotoxin types A and B genes
Botulinum neurotoxin (BoNT) is produced by the bacterium Clostridium botulinum and some other bacterial strains such as C. butyricum and C. baratii. It is considered the strongest toxin known to humans and can cause botulism. Botulinum neurotoxin can be fatal in humans and most botulism cases are caused by type A and B toxins. In this study, the research team used C. botulinum strains isolated from botulism poisoning cases in Vietnam, which were identified to produce type A and B toxins, from which we successfully transformed plasmids carrying genes specific for BoNT type A and type B genes based on the reference gene sequence according to TCVN 11395:2016. These plasmids were successfully used as template DNA for PCR reactions. In the PCR reaction, plasmids used to transform genes producing botulinum toxin types A and B have a detection limit of 102 copies/µL. The study has fully verified the validation parameters, with 100% accuracy and specificity.
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