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[鸟分枝杆菌和胞内分枝杆菌在杜博斯琼脂培养基上对新型大环内酯类、新型喹诺酮类及抗结核药物的体外敏感性]

[In vitro susceptibilities of Mycobacterium avium and Mycobacterium intracellulare to new macrolides, new quinolones, and antituberculous drugs on Dubos agar medium].

作者信息

Ogawa K, Miwa T, Sasamoto M, Sasaki T, Tsuda M, Honda K, Furui H, Torii K, Takagi K

机构信息

Department of Internal Medicine, Higashi Nagoya National Hospital, Japan.

出版信息

Kekkaku. 1992 Nov;67(11):735-8.

PMID:1487866
Abstract

Mycobacterium avium and M. intracellulare were isolated from the sputum of patients infected with atypical mycobacteria using 1% Ogawa medium and identified by the DNA probe test. Then the MICs of various kinds of drugs against these mycobacterial species were determined on Dubos agar medium, and the drug susceptibilities were also determined on 1% Ogawa medium in parallel. The drugs tested were new macrolides, such as clarithromycin (CAM) and roxithromycin (RXM), new quinolones, such as ofloxacin (OFLX) and ciprofloxacin (CPFX), and antituberculous drugs, such as isoniazid (INH), rifampicin (PFP), streptomycin (SM), and ethambutol (EB). The MICs of the drugs tested, especially those of CAM, OFLX, and RFP, when determined on Dubos agar medium, were generally lower against M. intracellulare than against M. avium. The susceptibilities of the mycobacterial isolates tested to RFP and SM determined on Dubos agar medium were markedly different from those determined on 1% Ogawa medium. Such discrepancies may be accounted for by absorption of these drugs to the egg medium and instability of RFP in the egg medium. Overall, our results indicate that the new macrolides and new quinolones are effective against atypical mycobacteria.

摘要

使用1%小川培养基从非典型分枝杆菌感染患者的痰液中分离出鸟分枝杆菌和胞内分枝杆菌,并通过DNA探针试验进行鉴定。然后在杜博斯琼脂培养基上测定各种药物对这些分枝杆菌的最低抑菌浓度(MIC),同时也在1%小川培养基上平行测定药物敏感性。所测试的药物包括新型大环内酯类,如克拉霉素(CAM)和罗红霉素(RXM),新型喹诺酮类,如氧氟沙星(OFLX)和环丙沙星(CPFX),以及抗结核药物,如异烟肼(INH)、利福平(PFP)、链霉素(SM)和乙胺丁醇(EB)。在杜博斯琼脂培养基上测定时,所测试药物的MIC,尤其是CAM、OFLX和RFP的MIC,对胞内分枝杆菌通常比对鸟分枝杆菌低。在杜博斯琼脂培养基上测定的分枝杆菌分离株对RFP和SM的敏感性与在1%小川培养基上测定的结果明显不同。这些差异可能是由于这些药物在鸡蛋培养基中的吸附以及RFP在鸡蛋培养基中的不稳定性所致。总体而言,我们的结果表明新型大环内酯类和新型喹诺酮类对非典型分枝杆菌有效。

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