Insight into multidrug-resistant Beijing genotype Mycobacterium tuberculosis isolates in Myanmar
Myanmar is a World Health Organization high tuberculosis (TB) burden country with a high multidrug-resistant (MDR)-TB burden. Of significance, a high prevalence of the Beijing genotype of Mycobacterium tuberculosis (MTB) among MDR-MTB has been reported previously. A detailed genetic characterization...
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Veröffentlicht in: | International journal of infectious diseases 2018-11, Vol.76, p.109-119 |
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Sprache: | eng |
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Zusammenfassung: | Myanmar is a World Health Organization high tuberculosis (TB) burden country with a high multidrug-resistant (MDR)-TB burden. Of significance, a high prevalence of the Beijing genotype of Mycobacterium tuberculosis (MTB) among MDR-MTB has been reported previously. A detailed genetic characterization of TB clinical isolates was performed in order to explore whether there is an association between the prevalence of the Beijing MTB genotype and MDR-TB in Myanmar.
A total of 265 MDR-MTB clinical isolates collected in 2010 and 2012 were subjected to spoligotyping, mycobacterial interspersed repetitive unit–variable number tandem repeat (MIRU-VNTR) analysis, single nucleotide polymorphism (SNP) typing, and drug resistance-associated gene sequencing, including rpoC to detect potential compensatory evolution.
Of the total MDR-MTB isolates, 79.2% (210/265) were of the Beijing genotype, the majority of which were the ‘modern’ subtype. Beijing genotype isolates were differentiated by 15-locus MIRU-VNTR and a high clustering rate (53.0%) was observed in the modern subtype. These MIRU-VNTR patterns were similar to Beijing genotype clones spreading across Russia and Central Asia. A high prevalence of katG Ser315Thr, and genetic evidence of extensive drug resistance (XDR) and pre-XDR and compensatory mutations in rpoC were observed among clustered isolates.
MDR-MTB strains of the Beijing genotype might be spreading in Myanmar and present a major challenge to TB control in this country. |
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ISSN: | 1201-9712 1878-3511 |
DOI: | 10.1016/j.ijid.2018.06.009 |