Sakhaee Fatemeh, Ghazanfari Morteza, Ebrahimzadeh Nayereh, Vaziri Farzam, Jamnani Fatemeh Rahimi, Davari Mehdi, Gharibzadeh Safoora, Mandjin Fatemeh Hemati, Fateh Abolfazl, Siadat Seyed Davar
Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran.
Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran; Microbiology Research Center (MRC), Pasteur Institute of Iran, Tehran, Iran.
Biologicals. 2017 Sep;49:33-38. doi: 10.1016/j.biologicals.2017.07.003. Epub 2017 Jul 15.
This study aimed to evaluate the frequency of resistance to first- and second-line drugs using phenotypic and genotypic methods and its correlation with resistance-linked mutations in Mycobacterium tuberculosis (M. tb) isolated in Iran. Three different methods, including the indirect proportion method(PM), direct and indirect nitrate reductase assay(NRA), and direct sequencing were used to assess drug resistance. In this study, sensitivity, specificity, agreement, costs, and turnaround time of these methods were compared in 395 smear positive isolates. Compared to the PM, the NRA and the direct sequencing methods demonstrated higher specificity, sensitivity, and agreement for detection of all anti-tuberculosis drugs. The NRA had a short turnaround time and was more cost-effective than the other methods. Mutations in codon 531 in rpoB, 315 in katG, 18 in rpsL, and 306 in embB were associated with high-level resistance to the first-line drugs, and mutations in codon 94 in gyrA, and A1401G in rrs were correlated with resistance to the second-line drugs. We found that the NRA is a highly sensitive, specific, inexpensive, and rapid test with strong potential to be a useful and interesting alternative tool, particularly in low-income countries. In addition, these molecular data will be helpful for developing new molecular methods for detecting first- and second-line drug-resistant M. tb.
本研究旨在采用表型和基因型方法评估伊朗分离出的结核分枝杆菌(M. tb)对一线和二线药物的耐药频率及其与耐药相关突变的相关性。使用了三种不同方法,包括间接比例法(PM)、直接和间接硝酸还原酶测定法(NRA)以及直接测序法来评估耐药性。在本研究中,对395株涂片阳性分离株比较了这些方法的敏感性、特异性、一致性、成本和周转时间。与PM相比,NRA和直接测序法在检测所有抗结核药物时表现出更高的特异性、敏感性和一致性。NRA周转时间短,且比其他方法更具成本效益。rpoB基因第531位密码子、katG基因第315位密码子、rpsL基因第18位密码子和embB基因第306位密码子的突变与对一线药物的高水平耐药相关,gyrA基因第94位密码子和rrs基因A1401G突变与对二线药物的耐药相关。我们发现NRA是一种高度敏感、特异、廉价且快速的检测方法,极有可能成为一种有用且有趣的替代工具,尤其是在低收入国家。此外,这些分子数据将有助于开发检测一线和二线耐药结核分枝杆菌的新分子方法。