Pyrosequencing for rapid detection of Mycobacterium tuberculosis second-line drugs and ethambutol resistance

被引:16
作者
Lacoma, Alicia [1 ,3 ]
Molina-Moya, Barbara [1 ,3 ]
Prat, Cristina [1 ,3 ]
Pimkina, Edita [4 ]
Diaz, Jessica [1 ,3 ]
Dudnyk, Andriy [5 ]
Garcia-Sierra, Nerea [1 ]
Haba, Lucia [1 ]
Maldonado, Jose [6 ]
Samper, Sofia [3 ,7 ]
Ruiz-Manzano, Juan [2 ,3 ]
Ausina, Vicente [1 ,3 ]
Dominguez, Jose [1 ,3 ]
机构
[1] Univ Autonoma Barcelona, Inst Invest Germans Trias & Pujol, Hosp Univ Germans Trias & Pujol, Microbiol Serv, Badalona 08916, Spain
[2] Univ Autonoma Barcelona, Inst Invest Germans Trias & Pujol, Hosp Univ Germans Trias & Pujol, Serv Pneumol, Badalona 08916, Spain
[3] Inst Salud Carlos III, CIBER Enfermedades Resp CIBERES, Madrid, Spain
[4] Vilnius Univ Hosp Santariskiu Klin, Infect Dis & TB Hosp, Vilnius, Lithuania
[5] Vinnitsa Natl Pirogov Mem Med Univ, Dept TB Clin Immunol & Allergol, Vinnitsa, Ukraine
[6] Serv Clin, Barcelona, Spain
[7] Hosp Univ Miguel Servet, Inst Aragones Ciencias Salud, Zaragoza, Spain
关键词
Tuberculosis; Molecular diagnostic testing; Extensively drug-resistant tuberculosis; Fluoroquinolones; Injectable drugs; Ethambutol; MOLECULAR-DETECTION; ISONIAZID RESISTANCE; KANAMYCIN RESISTANCE; GENETIC MUTATIONS; CROSS-RESISTANCE; GENOTYPE MTBDRSL; GYRASE MUTATIONS; EMBB CODON-306; MULTIPLEX PCR; GYRB GENES;
D O I
10.1016/j.diagmicrobio.2015.07.004
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The aim of this work was to study the diagnostic accuracy of pyrosequencing to detect resistance to fluoroquinolones, kanamycin, amikacin, capreomycin, and ethambutol (EMB) in Mycobacterium tuberculosis clinical strains. One hundred four clinical isolates previously characterized by BACTEC 460TB/MGIT 960 were included. Specific mutations were targeted in gyrA, rrs, eis promoter, and embB. When there was a discordant result between BACTEC and pyrosequencing, Genotype MTBDRsl (Ham Lifescience, Nehren, Germany) was performed. Sensitivity and specificity of pyrosequencing were 70.6% and 100%, respectively, for fluoroquinolones; 93.3% and 81.7%, respectively, for kanamycin; 94.1% and 95.9%, respectively, for amikacin; 90.0% and 100%, respectively, for capreomycin; and 64.8% and 87.8%, respectively, for EMB. This study shows that pyrosequencing may be a useful tool for making early decisions regarding second-line drugs and EMB resistance. However, for a correct management of patients with suspected extensively drug-resistant tuberculosis, susceptibility results obtained by molecular methods should be confirmed by a phenotypic method. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:263 / 269
页数:7
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