麻风分枝杆菌和结核分枝杆菌获得新喹诺酮类药物耐药性的分子机制及耐药杆菌的快速鉴别方法

Q4 Medicine Japanese Journal of Leprosy Pub Date : 2011-02-01 DOI:10.5025/hansen.80.17
Hyun Kim, Haruka Suzuki, Masanori Matsuoka, Takashi Matsuba, Kazumasa Yokoyama, Chie Nakajima, Yasuhiko Suzuki
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引用次数: 2

摘要

新喹诺酮类药物中包括的药物用于治疗单一病变的麻风病。这些药物也被认为是治疗多重耐药结核分枝杆菌的有效药物。最近新喹诺酮耐药麻风分枝杆菌和结核分枝杆菌的出现迫使迫切阐明新喹诺酮耐药菌株的出现模式。本文综述了新型喹诺酮类药物及其在麻风分枝杆菌和结核分枝杆菌中获得耐药的作用方式和机制。并介绍了耐药杆菌的快速鉴别方法。
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[Molecular mechanism of the acquisition of new-quinolone resistance in Mycobacterium leprae and M. tuberculosis and rapid differentiation methods for resistant bacilli].

Drugs included in new-quinolone are used for the treatment of leprosy with single lesion. These drugs are also known to be effective drugs for the treatment of multi-drug resistant M. tuberculosis. Recent emergence of new-quinolone resistant M. leprae and M. tuberculosis enforced the urgent elucidation of the mode of emergence of new-quinolone resistant strains. In this review, new-quinolone drugs, their mode of action and mechanism of acquisition of resistance by M. leprae and M. tuberculosis were explained. And rapid differentiation methods for resistant bacilli were also introduced.

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来源期刊
Japanese Journal of Leprosy
Japanese Journal of Leprosy Medicine-Dermatology
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