Imwidthaya P, Mieskes K, Rienthong S
Department of Microbiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
J Med Assoc Thai. 2001 Jun;84(6):864-9.
Nine isoniazid (INH)-susceptible and 11 INH-resistant Mycobacterium tuberculosis clinical isolates were analyzed for katG codon 315 mutations by polymerase chain reaction (PCR) assay using primers MYC-32 and MYC-33, followed by restriction fragment length polymorphism. After AciI digestion of PCR products, all 9 INH-susceptible isolates and 5 out of 11 (45%) INH-resistant isolates showed 0.12 kb band, which was previously reported to indicate wild type, whereas, 6 of 11 (55%) INH-resistant isolates lacked this band.
使用引物MYC - 32和MYC - 33通过聚合酶链反应(PCR)分析9株异烟肼(INH)敏感和11株INH耐药结核分枝杆菌临床分离株的katG密码子315突变,随后进行限制性片段长度多态性分析。PCR产物经AciI消化后,所有9株INH敏感分离株和11株INH耐药分离株中的5株(45%)显示出0.12 kb条带,此前报道该条带表明为野生型,而11株INH耐药分离株中的6株(55%)缺乏该条带。