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米诺环素及其他抗生素对不动杆菌属(赫雷拉菌-米马菌)的体外和体内活性

In vitro and in vivo activities of minocycline and other antibiotics against Acinetobacter (Herellea-Mima).

作者信息

Kuck N A

出版信息

Antimicrob Agents Chemother. 1976 Mar;9(3):493-7. doi: 10.1128/AAC.9.3.493.

Abstract

Minocycline was the most active of six antibiotics tested against 65 clinical isolates of Acinetobacter calcoaceticus (syn.: Herellea, Mima) received from six medical centers. In the Bauer-Kirby disk susceptibility test, all isolates were rated susceptible to minocycline, gentamicin, and polymyxin; 25% were resistant to tetracycline. In agar dilution tests, minocycline was two to four times more potent than gentamicin or polymyxin and eight times more potent than tetracycline. Ampicillin and cephalexin were relatively ineffective. Against lethal infections produced by five strains of A. calcoaceticus in mice, minocycline was, in general, more active than gentamicin or polymyxin on a dosage basis and significantly more active on a blood-level basis. Minocycline was significantly more potent than tetracycline on both dosage and blood-level bases against tetracycline-sensitive and -resistant strains. In the last decade there has been an increase in the reported incidence of acinetobacters in a variety of infections. The cultures are susceptible to few antibiotics. Our data show that minocycline could offer an effective alternative to the more toxic drugs for the treatment of these infections. Susceptibility should be determined with minocycline disks.

摘要

对从六个医学中心获得的65株醋酸钙不动杆菌(同义词:赫雷勒菌属、米马菌属)临床分离株进行测试的六种抗生素中,米诺环素活性最强。在鲍尔-柯蒂斯纸片扩散药敏试验中,所有分离株对米诺环素、庆大霉素和多粘菌素均评定为敏感;25%对四环素耐药。在琼脂稀释试验中,米诺环素的效力比庆大霉素或多粘菌素强两到四倍,比四环素强八倍。氨苄西林和头孢氨苄相对无效。在小鼠中针对五株醋酸钙不动杆菌产生的致死性感染,一般来说,按剂量计算米诺环素比庆大霉素或多粘菌素活性更强,按血药浓度计算活性则显著更强。在剂量和血药浓度方面,米诺环素对四环素敏感和耐药菌株的效力均显著高于四环素。在过去十年中,报告的各种感染中不动杆菌的发病率有所增加。这些培养物对少数抗生素敏感。我们的数据表明,米诺环素可为治疗这些感染提供一种有效的替代药物,以取代毒性更强的药物。应使用米诺环素纸片测定敏感性。

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