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香豆霉素A1的体外活性。

In vitro activity of coumermycin A1.

作者信息

Fedorko J, Katz S, Allnoch H

出版信息

Appl Microbiol. 1969 Nov;18(5):869-73. doi: 10.1128/am.18.5.869-873.1969.

Abstract

The in vitro activity of coumermycin A(1) was compared with that of novobiocin, ampicillin, and minocycline. Coumermycin was found to be the most active antibiotic of the four against Staphylococcus aureus. It was about 50 times more active than novobiocin or minocycline against the strains tested. Coumermycin also showed good activity against group A streptococci and pneumococci, moderate activity against Escherichia coli, indole-positive Proteus species, and Pseudomonas aeruginosa, and poor activity against Klebsiella-Enterobacter and enterococci. Against P. mirabilis, however, coumermycin activity was almost equal to that of ampicillin. The new antibiotic was further found to be greatly reduced in activity in the presence of plasma, but its minimal inhibitory concentration was not greatly affected by inoculum size. Coumermycin was found to be bacteriostatic in its action, and resistance to it developed slowly. Also, cross-resistance was present with novobiocin but absent with ampicillin or minocycline.

摘要

将香豆霉素A(1)的体外活性与新生霉素、氨苄青霉素和米诺环素进行了比较。发现香豆霉素是这四种抗生素中对金黄色葡萄球菌活性最强的。它对所测试菌株的活性比新生霉素或米诺环素高约50倍。香豆霉素对A组链球菌和肺炎球菌也显示出良好的活性,对大肠杆菌、吲哚阳性变形杆菌属和铜绿假单胞菌有中等活性,对克雷伯菌属-肠杆菌属和肠球菌活性较差。然而,对于奇异变形杆菌,香豆霉素的活性几乎与氨苄青霉素相当。进一步发现,在有血浆存在的情况下,这种新抗生素的活性大大降低,但其最低抑菌浓度受接种量大小的影响不大。发现香豆霉素具有抑菌作用,对其产生耐药性的速度较慢。此外,对香豆霉素存在与新生霉素的交叉耐药性,但与氨苄青霉素或米诺环素不存在交叉耐药性。

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