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KMID : 0383820050590030250
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Tuberculosis and Respiratory Diseases
2005 Volume.59 No. 3 p.250 ~ p.256
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Cross Resistance of Fluoroquinolone Drugs on gyrA Gene Mutation in Mycobacterium tuberculosis
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Park Young-Kil
Park Chan-Hong
Koh Won-Jung
Kwon O-Jung
Kim Bum-Joon
Kook Yoon-Hoh
Cho Sang-Nae
Chang Chul-Hoon
Bai Gill-Han
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Abstract
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b>Background : Fluoroquinolone drugs are an important anti-tuberculous agent for the treatment of multi-drug resistant tuberculosis. However, many drugs belonging to the fluoroquinolones have different cross resistance to each other.
Methods : Sixty-three ofloxacin (OFX) resistant and 10 pan-susceptible M. tuberculosis isolates were selected, and compared for their cross resistance using a proportion method on Lowenstein-Jensen media, containing ofloxacin (OFX), ciprofloxacin (CIP), levofloxacin (LVX), moxifloxacin (MXF), gatifloxacin (GAT) and sparfloxacin (SPX), at concentrations ranging from 0.5 to 3킽/ml. DNA extracted from the isolates was directly sequenced after amplifying from the gyrA and gyrB genes.
Results : The 63 OFX resistant M. tuberculosis isolates showed complete cross resistance to CIP, but only 90.5, 44.4,36.5 and 46.0% to LVX, MXF, GAT, and to SPX, respectively. Fifty-one of the isolates (81.0%) had point mutations in codons 88, 90, 91 and 94 in gyrA, which are known to be correlated with OFX resistance. The Gly88Ala, Ala90Valand Asp94Ala mutations in gyrA showed a tendency to be susceptible to MXF, GAT and SPX. Only 4 isolates had mutations in the gyrB gene, which did not affect the OFX resistance.
Conclusion : About 60% of the OFX resistant M. tuberculosis isolates were susceptible to GAT, SPX and MXF. These fluoroquinolones may be useful in the treatment of TB patients showing OFX resistance.
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KEYWORD
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Mycobacterium tuberculosis, Fluoroquinolones, Cross resistance, gyrA, Genotypes
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