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Molecular analysis of kanamycin ressitance of mycobacterium tuberculosis

机译:结核分枝杆菌卡那霉素抗性的分子分析

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Tuberculosis has reemerged as a significant public health problem. Furthermore, multiple-drug resistant (MDR) M. tuberculosis strains have become an additional handicap in the control of tuberculosis. Recently, to rapid diagnosis of MdR M. tuberculosis, considerable work has been done on the characterization of genes involved in drug resistance in mycobacteria. Kanamycin (KM) is an aminoglycoside antibiotic that was discovered by Umezawa et al. in 1957, and has been used as a second-line antibiotic for the treatment of tuberculosis. Although its usefulness had declined because of its toxicity, it has been revived because of MDR M.tuberculosis. Therefore, we have examined a molecular mechanism of kanamycin resistance of M.tuberculosis.
机译:结核病再次成为一个重大的公共卫生问题。此外,耐多药(MDR)的结核分枝杆菌菌株已成为控制结核病的另一个障碍。最近,为了快速诊断MdR结核分枝杆菌,在分枝杆菌中与耐药性有关的基因的表征方面已进行了大量工作。卡那霉素(KM)是一种由Umezawa等人发现的氨基糖苷类抗生素。 1957年,它已被用作治疗肺结核的二线抗生素。尽管由于毒性而使其有用性下降,但由于耐多药结核分枝杆菌而使它复活。因此,我们研究了结核分枝杆菌卡那霉素抗性的分子机制。

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