Jones R N, Gavan T L, Thornsberry C, Fuchs P C, Gerlach E H, Knapp J S, Murray P, Washington J A
Clinical Microbiology Institute, Tualatin, Oregon 97062.
J Clin Microbiol. 1989 Dec;27(12):2758-66. doi: 10.1128/jcm.27.12.2758-2766.1989.
A six-laboratory study developed a standardized method for determining the susceptibilities of Neisseria gonorrhoeae strains to penicillin, tetracycline, spectinomycin, and ceftriaxone. Three quality control organisms were also selected, and quality assurance guidelines were initially generated for the disk diffusion and agar dilution methods. The medium recommended for gonococcal susceptibility testing was GC agar with a defined "XV-like" supplement. The supplement should be free of cysteine, a component implicated in the inactivation of some newer beta-lactam compounds. Penicillin, tetracycline, spectinomycin, and ceftriaxone were stable in agar plates stored at 3 to 5 degrees C for at least 2 weeks. Numerous GC agar and drug disk lots were used during the trials without significant variation in test results. Several other gonococcal strains were recommended for additional medium quality assurance. The disk quality control zone limits were established for N. gonorrhoeae ATCC 49226 (formerly CDC F-18) and Staphylococcus aureus ATCC 25923. MIC quality control ranges were also developed for N. gonorrhoeae ATCC 49226 and S. aureus ATCC 29213. The interpretive criteria for penicillin were as follows: susceptibility, greater than or equal to 47 mm (diameter of inhibition zone) (less than or equal to 0.06 micrograms/ml [MIC]); resistance, less than or equal to 26 mm (greater than or equal to 2 micrograms/ml). For tetracycline they were as follows: susceptibility, greater than or equal to 38 mm (less than or equal to 0.25 microgram/ml); resistance, less than or equal to 30 mm (greater than or equal to 2 micrograms/ml). For spectinomycin they were as follows: susceptibility, >/= 18 mm (</= 32 micrograms/ml); resistance, </= 14 mm (>/= 128 micrograms/ml). For ceftriaxone susceptibility, the criterion was >/= 35 mm (</= 0.25 micrograms/ml) with no other category. Criteria of </= 19 mm for plasmid-mediated resistances to penicillin and tetracycline were also confirmed. The false-susceptibility errors were </= 1% with these criteria.
一项由六个实验室参与的研究开发出了一种标准化方法,用于测定淋病奈瑟菌菌株对青霉素、四环素、壮观霉素和头孢曲松的敏感性。还挑选了三种质量控制微生物,并初步制定了针对纸片扩散法和琼脂稀释法的质量保证指南。推荐用于淋球菌敏感性试验的培养基是添加特定“XV样”添加剂的GC琼脂。该添加剂应不含半胱氨酸,因为半胱氨酸是一些新型β-内酰胺化合物失活的相关成分。青霉素、四环素、壮观霉素和头孢曲松在3至5摄氏度储存的琼脂平板中至少2周内保持稳定。试验期间使用了大量的GC琼脂和药敏纸片批次,测试结果无显著差异。还推荐使用其他几种淋球菌菌株进行额外的培养基质量保证。为淋病奈瑟菌ATCC 49226(原CDC F-18)和金黄色葡萄球菌ATCC 25923确定了纸片质量控制区界限。也为淋病奈瑟菌ATCC 49226和金黄色葡萄球菌ATCC 29213制定了最低抑菌浓度(MIC)质量控制范围。青霉素的解释标准如下:敏感,大于或等于47毫米(抑菌圈直径)(小于或等于0.06微克/毫升[MIC]);耐药,小于或等于26毫米(大于或等于2微克/毫升)。四环素的标准如下:敏感,大于或等于38毫米(小于或等于0.25微克/毫升);耐药,小于或等于30毫米(大于或等于2微克/毫升)。壮观霉素的标准如下:敏感,≥18毫米(≤32微克/毫升);耐药,≤14毫米(≥128微克/毫升)。头孢曲松的敏感标准为≥35毫米(≤0.25微克/毫升),无其他分类。对于质粒介导的对青霉素和四环素的耐药性,≤19毫米的标准也得到了确认。采用这些标准时,假敏感误差≤1%。