PCR with hydrolysis probes for detection of fluoroquinolone resistance mutations in Mycobacterium tuberculosis

V. V. Slizen, L. K. Surkova, G. L. Gurevich
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Abstract

Early diagnostics of resistance to fluoroquinolones facilitates early start of adequate therapy and increases the chance of a favorable outcome of the tuberculosis. Application of genetic methods permits to obtain within 1–2 days the results of Mycobacterium tuberculosis resistance detection to anti-tuberculosis drugs, unlike the classical methods requiring up to 1−2 month. The aim of the study is to develop a method for the M. tuberculosis identification and detection of point mutations in codons 90, 91, 94 of the gyrA gene associated with the resistance to fluoroquinolones. There were 88 cultures of mycobacteria studied: M. tuberculosis (n = 81), M. tuberculosis H37Rv, M. chelonae (n = 1), M. gordonae (n = 1), M. fortuitum (n = 1), and other three isolates of non-tuberculosis mycobacteria isolated from patients in the Republican Scientific and Practical Center for Pulmonology and Phthisiatry. The types of mutations in the gyrA gene were studied by the standard GenoTypeMTBDRsl method (HAIN, Germany), Sanger sequencing, and by the developed real-time PCR method. Based on the analysis of mutations in the gyrA gene in 78 isolates of M. tuberculosis, the dominant mutations were found to be mutations Asp94Gly and Ala90Val, which were identified in 21 and 27 isolates correspondingly: they accounted for 64 % of all mutations. M. tuberculosis also harbored mutations p.ASP94ALA and p.ASP94TYR/HIS in 6 (8.0 %) and 9 (12.0 %) isolates, respectively. One strain harbored a mutation at triplet 88 and one strain had a double mutation (p.ALA90VAL and p.ASP94GLY). The developed real-time PCR method demonstrated a high frequency of coincidence of results with the phenotypic determination of resistance to ofloxacin and the results testing by the standard GenoTypeMTBDRsl method and sequencing. The developed method is accomplished to identify M. tuberculosis, and discriminate mutations p.ALA90VAL, p.SER91PRO, p.ASP94ALA, p.ASP94TYR/HIS, p.ASP94GLY, p.ASP94ASN providing diagnostics of resistance to fluoroquinolones.
水解探针PCR检测结核分枝杆菌氟喹诺酮类耐药突变
对氟喹诺酮类药物耐药性的早期诊断有助于及早开始适当的治疗,并增加结核病获得有利结果的机会。应用遗传方法可以在1 - 2天内获得结核分枝杆菌对抗结核药物耐药性检测的结果,而传统方法需要长达1 - 2个月。本研究旨在建立结核分枝杆菌对氟喹诺酮类药物耐药相关gyrA基因90、91、94密码子点突变的鉴定和检测方法。共培养结核分枝杆菌88株:结核分枝杆菌(81株)、结核分枝杆菌H37Rv、chelonae分枝杆菌(1株)、gordonae分枝杆菌(1株)、fortuitum分枝杆菌(1株)和其他3株从共和肺病科学与实用中心患者身上分离的非结核分枝杆菌。采用标准gentypemtbdrsl方法(HAIN, Germany)、Sanger测序和开发的实时PCR方法研究gyrA基因的突变类型。通过对78株结核分枝杆菌gyrA基因突变的分析,发现优势突变为Asp94Gly和Ala90Val突变,分别在21株和27株结核分枝杆菌中发现,占全部突变的64%。结核分枝杆菌还分别在6株(8.0%)和9株(12.0%)分离株中携带p.a asp94ala和p.a asp94tyr /HIS突变。其中一株在三联体88处发生突变,另一株发生双突变(p.a ala90val和p.a asp94gly)。所建立的实时PCR方法与氧氟沙星耐药表型测定和标准gentypemtbdrsl方法及测序检测结果吻合度高。所开发的方法用于鉴定结核分枝杆菌,并区分p.a ala90val、p.SER91PRO、p.p asp94ala、p.p asp94tyr /HIS、p.p asp94gly、p.p asp94asn突变,提供对氟喹诺酮类药物耐药的诊断。
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