Occurrence of disputed rpoB mutations among Mycobacterium tuberculosis isolates phenotypically susceptible to rifampicin in a country with a low incidence of multidrug-resistant tuberculosis
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作者:
Al-Mutairi, Noura M.
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Kuwait Univ, Hlth Sci Ctr, Fac Med, Dept Microbiol, POB 24923, Safat 13109, KuwaitKuwait Univ, Hlth Sci Ctr, Fac Med, Dept Microbiol, POB 24923, Safat 13109, Kuwait
Al-Mutairi, Noura M.
[1
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Ahmad, Suhail
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Kuwait Univ, Hlth Sci Ctr, Fac Med, Dept Microbiol, POB 24923, Safat 13109, KuwaitKuwait Univ, Hlth Sci Ctr, Fac Med, Dept Microbiol, POB 24923, Safat 13109, Kuwait
Ahmad, Suhail
[1
]
Mokaddas, Eiman
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机构:
Kuwait Univ, Hlth Sci Ctr, Fac Med, Dept Microbiol, POB 24923, Safat 13109, Kuwait
Kuwait Natl TB Control Lab, Shuwaikh, KuwaitKuwait Univ, Hlth Sci Ctr, Fac Med, Dept Microbiol, POB 24923, Safat 13109, Kuwait
Mokaddas, Eiman
[1
,2
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Eldeen, Hanaa S.
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Kuwait Natl TB Control Lab, Shuwaikh, KuwaitKuwait Univ, Hlth Sci Ctr, Fac Med, Dept Microbiol, POB 24923, Safat 13109, Kuwait
Eldeen, Hanaa S.
[2
]
Joseph, Susan
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Kuwait Natl TB Control Lab, Shuwaikh, KuwaitKuwait Univ, Hlth Sci Ctr, Fac Med, Dept Microbiol, POB 24923, Safat 13109, Kuwait
Joseph, Susan
[2
]
机构:
[1] Kuwait Univ, Hlth Sci Ctr, Fac Med, Dept Microbiol, POB 24923, Safat 13109, Kuwait
BackgroundAccurate drug susceptibility testing (DST) of Mycobacterium tuberculosis in clinical specimens and culture isolates to first-line drugs is crucial for diagnosis and management of multidrug-resistant tuberculosis (MDR-TB). Resistance of M. tuberculosis to rifampicin is mainly due to mutations in hot-spot region of rpoB gene (HSR-rpoB). The prevalence of disputed (generally missed by rapid phenotypic DST methods) rpoB mutations, which mainly include L511P, D516Y, H526N, H526L, H526S, and L533P in HSR-rpoB and I572F in cluster II region of rpoB gene, is largely unknown. This study determined the occurrence of all disputed mutations in HSR-rpoB and at rpoB codon 572 in M. tuberculosis strains phenotypically susceptible to rifampicin in Kuwait.MethodsA total of 242M. tuberculosis isolates phenotypically susceptible to rifampicin were used. The DST against first-line drugs was performed by Mycobacteria growth indicator tube (MGIT) 960 system. Mutations in HSR-rpoB (and katG codon 315 and inhA-regulatory region for isoniazid resistance) were detected by GenoType MDBDRplus assay. The I572F mutation in cluster II region of rpoB was detected by developing a multiplex allele-specific (MAS)-PCR assay. Results were confirmed by PCR-sequencing of respective loci. Molecular detection of resistance for ethambutol and pyrazinamide and fingerprinting by spoligotyping were also performed for isolates with an rpoB mutation.ResultsAmong 242 rifampicin-susceptible isolates, 0 of 130 pansusceptible/monodrug-resistant isolates but 4 of 112 polydrug-resistant isolates contained a disputed rpoB mutation. All 4 isolates were also resistant to isoniazid and molecular screening identified additional resistance to pyrazinamide and ethambutol in one isolate each. In final analysis, 2 of 4 isolates were resistant to all 4 first-line drugs. Spoligotyping showed that the isolates belonged to different M. tuberculosis lineages.ConclusionsFour of 242 (1.7%) rifampicin-susceptible M. tuberculosis isolates contained a disputed rpoB mutation including 2 isolates resistant to all four first-line drugs. The occurrence of a disputed rpoB mutation in polydrug-resistant M. tuberculosis isolates resistant at least to isoniazid (MDR-TB) suggests that polydrug-resistant strains should be checked for genotypic rifampicin resistance for optimal patient management since the failure/relapse rates are nearly same in isolates with a canonical or disputed rpoB mutation.
机构:
Lab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
Univ Tecn Lisboa, Inst Super Tecn, Inst Biotechnol & Bioengn, P-1049001 Lisbon, PortugalLab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
Figueiredo, Ricardo
Ramos, Daniela F.
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Univ Fed Rio Grande, Lab Micobacterias & Biol Mol, Area Acad Saude, Rio Grande Rgs, BrazilLab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
Ramos, Daniela F.
Moiteiro, Cristina
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Lab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
Univ Lisbon, Fac Ciencias, Ctr Quim & Bioquim, P-1749016 Lisbon, PortugalLab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
Moiteiro, Cristina
Medeiros, Maria Augusta
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Lab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, PortugalLab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
Medeiros, Maria Augusta
Marcelo Curto, Maria Joao
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Lab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, PortugalLab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
Marcelo Curto, Maria Joao
de Menezes, Jose Cardoso
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Univ Tecn Lisboa, Inst Super Tecn, Inst Biotechnol & Bioengn, P-1049001 Lisbon, PortugalLab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
de Menezes, Jose Cardoso
Hernandez Pando, Rogelio
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Univ Lisbon, Fac Ciencias, Ctr Quim & Bioquim, P-1749016 Lisbon, Portugal
Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Tlalpan 14000, MexicoLab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
Hernandez Pando, Rogelio
Silva, Pedro E. A.
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Univ Fed Rio Grande, Lab Micobacterias & Biol Mol, Area Acad Saude, Rio Grande Rgs, BrazilLab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
Silva, Pedro E. A.
Costa, Maria do Ceu
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Lab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal
Univ Madeira, Ctr Quim Madeira, P-9000390 Funchal, PortugalLab Nacl Energia & Geol, P-2720866 Alfragide, Amadora, Portugal