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

نویسندگان

چکیده

Early diagnostics of resistance to fluoroquinolones facilitates early start adequate therapy and increases the chance a favorable outcome tuberculosis. Application genetic methods permits obtain within 1–2 days results Mycobacterium tuberculosis detection anti-tuberculosis drugs, unlike classical requiring up 1−2 month. The aim study is develop method for M. identification point mutations in codons 90, 91, 94 gyrA gene associated with fluoroquinolones. There were 88 cultures mycobacteria studied: (n = 81), H37Rv, chelonae 1), gordonae fortuitum other three isolates non-tuberculosis isolated from patients Republican Scientific Practical Center Pulmonology Phthisiatry. types studied by standard GenoTypeMTBDRsl (HAIN, Germany), Sanger sequencing, developed real-time PCR method. Based on analysis 78 tuberculosis, dominant found be Asp94Gly Ala90Val, which identified 21 27 correspondingly: they accounted 64 % all mutations. also harbored p.ASP94ALA p.ASP94TYR/HIS 6 (8.0 %) 9 (12.0 isolates, respectively. One strain mutation at triplet one had double (p.ALA90VAL p.ASP94GLY). demonstrated high frequency coincidence phenotypic determination ofloxacin testing sequencing. accomplished identify discriminate p.ALA90VAL, p.SER91PRO, p.ASP94ALA, p.ASP94TYR/HIS, p.ASP94GLY, p.ASP94ASN providing

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ژورنال

عنوان ژورنال: Vescì Nacyânal?naj akadèmìì navuk Belarusì

سال: 2023

ISSN: ['1814-6023', '2524-2350']

DOI: https://doi.org/10.29235/1814-6023-2023-20-2-158-167