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从泰国东北部分离出的耐多药结核分枝杆菌中检测到的新突变。

Novel mutations detected from drug resistant Mycobacterium tuberculosis isolated from North East of Thailand.

作者信息

Thwe Ei Phoo, Namwat Wises, Pinlaor Porntip, Rueangsak Kulrattana, Sangka Arunnee

机构信息

Medical Technology Program, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.

Centre for Research and Development of Medical Diagnostic Laboratories (CMDL), Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.

出版信息

World J Microbiol Biotechnol. 2021 Oct 13;37(11):194. doi: 10.1007/s11274-021-03163-7.

Abstract

The emergence of drug-resistant tuberculosis is a major global public health threat. Thailand is one of the top 14 countries with high tuberculosis and multi-drug resistant tuberculosis rates. Immediate detection of drug-resistant tuberculosis is necessary to reduce mortality and morbidity by effectively providing treatment to ameliorate the formation of resistant strains. Limited data exist of mutation profiles in Northeastern Thailand. Here, 65 drug-resistant Mycobacterium tuberculosis isolates were used to detect mutations by polymerase chain reaction (PCR) and DNA sequencing. In the katG gene, mutations were occurred in 47 (79.7%) among 59 isoniazid resistant samples. For rpoB gene, 31 (96.9%) were observed as mutations in 32 rifampicin resistant isolates. Of 47 katG mutation samples, 45 (95.7%) had mutations in katG315 codon and 2 (4.3%) showed novel mutations at katG365 with amino acid substitution of CCG-CGG (Pro-Arg). Moreover, out of 31 rpoB mutation isolates, the codon positions rpoB516, rpoB526, rpoB531 and rpoB533 were 3 (9.7%), 8 (25.8%), 11 (35.5%) and 1 (3.2%), respectively. Seven isolates of double point mutation were found [rpoB516, 526; 1 (3.2%) and rpoB516, 531; 6 (19.4%)]. In addition, 1 (3.2%) sample had triple point mutation at codon positions rpoB516, 526 and 531. Common and novel mutation codons of the rpoB and katG genes were generated. Although DNA sequencing showed high accuracy, conventional PCR could be applied as an initial marker for screening drug-resistant Mycobacterium tuberculosis isolates in limit resources region. Mutations reported here should be considered when developing new molecular diagnostic methods for implementation in Northeastern Thailand.

摘要

耐多药结核病的出现是全球主要的公共卫生威胁。泰国是结核病和耐多药结核病发病率最高的14个国家之一。为了通过有效治疗以减少死亡率和发病率,从而改善耐药菌株的形成,必须立即检测出耐多药结核病。泰国东北部地区关于突变谱的数据有限。在此,利用65株耐多药结核分枝杆菌分离株,通过聚合酶链反应(PCR)和DNA测序来检测突变。在katG基因中,59株异烟肼耐药样本中有47株(79.7%)发生了突变。对于rpoB基因,在32株利福平耐药分离株中观察到31株(96.9%)发生了突变。在47株katG突变样本中,45株(95.7%)在katG315密码子处发生突变,2株(4.3%)在katG365处出现新突变,氨基酸由CCG替换为CGG(脯氨酸-精氨酸)。此外,在31株rpoB突变分离株中,rpoB516、rpoB526、rpoB531和rpoB533密码子位置的突变率分别为3株(9.7%)、8株(25.8%)、11株(35.5%)和1株(3.2%)。发现7株双点突变分离株[rpoB516、526;1株(3.2%)和rpoB516、531;6株(19.4%)]。此外,1株(3.2%)样本在rpoB516、526和531密码子位置发生了三点突变。生成了rpoB和katG基因常见和新的突变密码子。虽然DNA测序显示出高准确性,但在资源有限的地区,传统PCR可作为筛选耐多药结核分枝杆菌分离株的初始标记。在为泰国东北部地区开发新的分子诊断方法时,应考虑此处报告的突变情况。

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