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不同培养基和血液对扩散法抗生素敏感性试验结果的影响。

Influence of different media and bloods on results of diffusion antibiotic susceptibility tests.

作者信息

Brenner V C, Sherris J C

出版信息

Antimicrob Agents Chemother. 1972 Feb;1(2):116-22. doi: 10.1128/AAC.1.2.116.

Abstract

As part of an International Collaborative Study, the influence of medium and certain medium components on the results of disc susceptibility testing with nine antibiotics was examined and statistically evaluated. Four basic media, Trypticase Soy Agar, Grove and Randall's formula # 9 agar, and Mueller-Hinton agar with and without 1 mg of l-tryptophan per 100 ml, were used with six bacterial strains. Significant differences in zone diameters occurred with most antibiotics. The largest consistent differences were seen with tetracycline, and appeared to result from varying degrees of chelation of the antibiotic with free cations in the media. Reproducibility studies on different batches of Mueller-Hinton agar from two manufacturers showed some statistically significant differences, which were small except with tetracycline. Reproducibility between the products of a single manufacturer was excellent. The results of experiments to determine the effect of the addition of 5% blood of different species to agar medium showed that medium containing citrated or defibrinated horse, rabbit, sheep, or human blood yielded closely similar zone diameters, except that tetracycline zones were larger with citrated blood. A single type of medium should be selected for routine susceptibility tests whenever possible, and reproducibility of performance of the products of different manufacturers should be sought.

摘要

作为一项国际合作研究的一部分,研究并统计评估了培养基及某些培养基成分对9种抗生素进行椎间盘药敏试验结果的影响。使用了4种基础培养基,即胰蛋白胨大豆琼脂、格罗夫和兰德尔配方9号琼脂,以及每100毫升含和不含1毫克L-色氨酸的Mueller-Hinton琼脂,对6种细菌菌株进行试验。大多数抗生素的抑菌圈直径存在显著差异。四环素的差异最为一致且明显,这似乎是由于抗生素与培养基中游离阳离子不同程度的螯合所致。对来自两家制造商的不同批次Mueller-Hinton琼脂的再现性研究显示,除四环素外,其他差异在统计学上虽有显著意义,但差异较小。同一制造商产品之间的再现性极佳。在琼脂培养基中添加5%不同种类血液的试验结果表明,含有枸橼酸化或去纤维蛋白的马、兔、羊或人血的培养基产生的抑菌圈直径非常相似,只是枸橼酸化血液的四环素抑菌圈更大。应尽可能选择单一类型的培养基进行常规药敏试验,并应寻求不同制造商产品性能的再现性。

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