Dillon J A, Tostowaryk W, Pauzé M
Antimicrobials and Molecular Biology Division, Laboratory Centre for Disease Control, Ottawa, Ontario, Canada.
Antimicrob Agents Chemother. 1987 Nov;31(11):1744-9. doi: 10.1128/AAC.31.11.1744.
The effects of two methods of inoculum preparation (the opacity standard method and a template method) and three different types of media on the penicillin, tetracycline, spectinomycin, and erythromycin MICs for 191 non-penicillinase-producing, 49 penicillinase-producing, and 5 tetracycline-resistant isolates of Neisseria gonorrhoeae were evaluated. Three World Health Organization reference strains (III, V, and VII) were similarly evaluated. Inoculum preparation method did not significantly alter the MIC (i.e., within a twofold dilution) of either susceptible or chromosomally resistant non-penicillinase-producing isolates; MICs achieved by the template method were slightly higher, but these differences were not significant. However, with penicillinase-producing and tetracycline-resistant isolates, the template method, which delivered 10(4) CFU, produced unequivocal MICs (denoting clinical resistance) which were significantly higher than MICs observed with the opacity standard method (inoculum, 10(3) CFU). With penicillin-, spectinomycin-, and erythromycin-containing medium, addition of hemoglobin to the medium produced lower, though not significantly different, MICs with all isolates as compared with MICs on medium without hemoglobin. Media supplemented with hemoglobin produced higher tetracycline MICs with all isolates, which were significantly different (greater than twofold) from MICs on the same hemoglobin-free media. Changes in auxotype did not alter overall observations concerning the effects of different media and inocula on MICs.
评估了两种接种物制备方法(浊度标准法和模板法)以及三种不同类型的培养基对191株非产青霉素酶、49株产青霉素酶和5株四环素耐药淋病奈瑟菌的青霉素、四环素、壮观霉素和红霉素最低抑菌浓度(MIC)的影响。对三种世界卫生组织参考菌株(III、V和VII)也进行了类似评估。接种物制备方法对敏感或染色体耐药的非产青霉素酶分离株的MIC(即两倍稀释范围内)没有显著影响;模板法获得的MIC略高,但这些差异不显著。然而,对于产青霉素酶和四环素耐药分离株,提供10⁴CFU的模板法产生的明确MIC(表示临床耐药)显著高于浊度标准法(接种物为10³CFU)观察到的MIC。在含青霉素、壮观霉素和红霉素的培养基中,与不含血红蛋白的培养基相比,向培养基中添加血红蛋白会使所有分离株的MIC降低,尽管差异不显著。添加血红蛋白的培养基会使所有分离株的四环素MIC升高,与相同的不含血红蛋白的培养基上的MIC有显著差异(大于两倍)。菌型的变化并未改变关于不同培养基和接种物对MIC影响的总体观察结果。