Rinder H, Thomschke A, Rüsch-Gerdes S, Bretzel G, Feldmann K, Rifai M, Löscher T
Department of Infectious Diseases and Tropical Medicine, Klinikum Innenstadt, University of Munich, Germany.
Eur J Clin Microbiol Infect Dis. 1998 Jul;17(7):508-11. doi: 10.1007/BF01691135.
To determine the value of ahpC promoter mutations for the rapid prediction of isoniazid resistance, this genomic region was characterized in 50 isoniazid-resistant and 12 isoniazid-sensitive Mycobacterium tuberculosis isolates. Of the resistant isolates, 12 had ahpC promoter mutations, but only one possessed both an ahpC promoter mutation and a katG codon 315 substitution, although the latter was found in the majority (54%) of the isoniazid-resistant isolates investigated. This investigation presents empirical evidence that the central portion of the ahpC promoter is the most valuable genetic locus to complement katG codon 315 characterizations in order to increase the sensitivity of molecular tests for the prediction of isoniazid resistance.
为了确定ahpC启动子突变对于快速预测异烟肼耐药性的价值,对50株异烟肼耐药和12株异烟肼敏感的结核分枝杆菌分离株的该基因组区域进行了特征分析。在耐药分离株中,12株存在ahpC启动子突变,但只有1株同时具有ahpC启动子突变和katG密码子315替换,尽管在大多数(54%)所研究的异烟肼耐药分离株中发现了后者。本研究提供了经验证据,表明ahpC启动子的中央部分是补充katG密码子315特征分析最有价值的基因位点,以提高分子检测预测异烟肼耐药性的敏感性。