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美洛西林、阿洛西林和羧苄西林对拟杆菌科的体外活性,特别针对脆弱拟杆菌(作者译)

[In vitro activity of mezlocillin, azlocillin and carbenicillin against bacteroidaceae with particular reference to bacteroides fragilis (author's transl)].

作者信息

Werner H, Krassemann C, Ungerechts J, Schmitz H J

出版信息

Infection. 1977;5(1):17-21. doi: 10.1007/BF01639104.

Abstract

The in vitro susceptibility of approximately 90 Bacteroidaceae strains to the the new broad-spectrum penicillins mezlocillin and azlocillin was determined by tube dilution tests and compared to susceptibility to carbenicillin. Bacteroides fragilis and Bacteroides thetaiotaomicron predominated among the strains tested. These strains are particularly important as pathogens and are known to produce beta-lactamase. At concentrations of 16 microng/ml or less, mezlocilin inhibited 81% of the Bacteroides cultures, and at 32 microng/ml 96% of the cultures. The amount of Bacteroides strains inhibited by 16 and 32 microng/ml of azlocillin was 67% and 93% respectively. Similar results were obtained with carbenicillin, concentrations of 32, 64 and 256 microng/ml inhibiting 55%, 87% and 94% of the strains respectively. Mezlocillin and azlocillin did not appear to be any more effective than carbenicillin against Sphaerophorus strains. Statistical analysis of the relationship between minimal inhibiting concentration and inhibition zone diameter showed that the susceptibility of Bacteroidaceae to mezlocillin, azlocillin and carbenicillin cannot be determined with sufficient accuracy by a standardized agar diffusion test.

摘要

通过试管稀释试验测定了约90株拟杆菌科菌株对新型广谱青霉素美洛西林和阿洛西林的体外敏感性,并与对羧苄西林的敏感性进行了比较。在所测试的菌株中,脆弱拟杆菌和多形拟杆菌占主导地位。这些菌株作为病原体尤为重要,并且已知会产生β-内酰胺酶。在浓度为16微克/毫升或更低时,美洛西林抑制了81%的拟杆菌培养物,在32微克/毫升时抑制了96%的培养物。16微克/毫升和32微克/毫升的阿洛西林抑制的拟杆菌菌株数量分别为67%和93%。羧苄西林也得到了类似结果,32、64和256微克/毫升的浓度分别抑制了55%、87%和94%的菌株。美洛西林和阿洛西林对球杆菌属菌株的效果似乎并不比羧苄西林更好。对最低抑菌浓度和抑菌圈直径之间关系的统计分析表明,通过标准化琼脂扩散试验无法足够准确地测定拟杆菌科对美洛西林、阿洛西林和羧苄西林的敏感性。

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