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新型半合成大环内酯类药物罗红霉素对专性厌氧菌的体外活性

[In vitro activity of roxithromycin, new semisynthetic macrolide against obligate anaerobes].

作者信息

Dubreuil L, Devos J, Romond C, Bryskier A

出版信息

Pathol Biol (Paris). 1986 May;34(5):440-4.

PMID:3534717
Abstract

The "in vitro" susceptibility to roxithromycin and three other macrolides of 236 anaerobes isolated from clinical samples in 1984/1985 was determined by an agar-dilution method on Wilkins Chalgren medium. 90% of Gram positive cocci were susceptible to both roxithromycin and josamycin (MIC less than 1 mg/l, whereas 1 mg/l erythromycin and 2 mg/l spiramycin were able to inhibit respectively 46 and 86% of the same tested strains. No resistance to the four macrolides was observed among Eubacterium, propionibacterium and Bifidobacterium. Two C. perfringens strains and one C. difficile strain were resistant to all four macrolides, while 97% of Clostridium sp. strains were inhibited by 4 mg/l erythromycin, josamycin or roxithromycin. Against Gram positive anaerobes, roxithromycin was equal or superior to erythromycin and spiramycin. At a concentration of 4 mg/l, roxithromycin inhibited 82% of B. fragilis strains. Roxithromycin and josamycin were more active against Gram negative bacilli that erythromycin and spiramycin. Macrolides had no effect on Fusobacterium strains. In this study, 4 mg/l roxithromycin inhibited 217 of the 236 anaerobic strains investigated (92%).

摘要

采用琼脂稀释法,在威尔金斯·查尔格伦培养基上测定了1984/1985年从临床样本中分离出的236株厌氧菌对罗红霉素及其他三种大环内酯类药物的“体外”敏感性。90%的革兰氏阳性球菌对罗红霉素和交沙霉素均敏感(最低抑菌浓度小于1毫克/升),而1毫克/升的红霉素和2毫克/升的螺旋霉素分别能抑制46%和86%的相同受试菌株。在真杆菌、丙酸杆菌和双歧杆菌中未观察到对这四种大环内酯类药物的耐药性。两株产气荚膜梭菌菌株和一株艰难梭菌菌株对所有四种大环内酯类药物均耐药,而97%的梭菌属菌株能被4毫克/升的红霉素、交沙霉素或罗红霉素抑制。对于革兰氏阳性厌氧菌,罗红霉素等同于或优于红霉素和螺旋霉素。在浓度为4毫克/升时,罗红霉素能抑制82%的脆弱拟杆菌菌株。罗红霉素和交沙霉素对革兰氏阴性杆菌的活性高于红霉素和螺旋霉素。大环内酯类药物对梭杆菌属菌株无作用。在本研究中,4毫克/升的罗红霉素抑制了所研究的236株厌氧菌中的217株(92%)。

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