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Determinations of the sensitivity of Neisseria gonorrhoeae to penicillin performed on solid media of different composition

机译:在不同组成的固体培养基上测定淋病奈瑟菌对青霉素的敏感性

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摘要

The increasing frequency of strains of Neisseria gonorrhoeae with reduced sensitivity to penicillin is making it more and more important to determine the sensitivity of individual strains before and after treatment with this antibiotic. It was recently demonstrated that the concentrations of penicillin inhibitory to Neisseria gonorrhoea depend upon the medium employed. This important observation made it desirable to have available for interlaboratory comparisons a non-commercial reproducible medium which would support the growth of the vast majority of the gonococcal strains in circulation. Using a plate dilution procedure, various modifications of the HYL medium described elsewhere were compared with the routine medium for carrying out sensitivity determinations. Both stock and fresh strains of Neisseria gonorrhoeae were used in the experiments. The 50% inhibitory concentrations observed on the two media did not differ to any great extent, being only about 40% higher on the routine medium than on the HYL medium. The difference between the HYL medium and the routine medium was somewhat greater for the less sensitive strains than for the more sensitive strains. The variations in the difference from strain to strain were larger for the more sensitive fresh strains than for the less sensitive strains and the stock strains. This observation limits the value of a correction method employing, for example, three reference strains as a means of ensuring comparability between the results of different laboratories.
机译:淋病奈瑟氏球菌菌株对青霉素敏感性降低的频率不断增加,因此确定使用该抗生素治疗前后各个菌株的敏感性变得越来越重要。最近证实,对淋病奈瑟氏菌的青霉素抑制浓度取决于所用的培养基。这一重要发现使得人们需要一种非商业可复制的培养基用于实验室间的比较,该培养基将支持循环中绝大多数淋球菌菌株的生长。使用平板稀释程序,将其他地方描述的HYL培养基的各种改良方法与常规培养基进行比较,以确定灵敏度。实验中使用了淋病奈瑟氏菌的原种和新鲜菌株。在两种培养基上观察到的50%抑制浓度没有太大差异,在常规培养基上仅比在HYL培养基上高约40%。对于敏感性较低的菌株,HYL培养基与常规培养基之间的差异要比敏感性较高的菌株更大。敏感性较高的新鲜菌株比敏感性较低的菌株和原种菌株之间的差异差异更大。这种观察限制了采用例如三个参考菌株作为确保不同实验室结果之间可比性的手段的校正方法的价值。

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