Foerster Sunniva, Desilvestro Valentino, Hathaway Lucy J, Althaus Christian L, Unemo Magnus
Institute for Infectious Diseases, University of Bern, Bern, Switzerland.
Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.
J Antimicrob Chemother. 2017 Jul 1;72(7):1961-1968. doi: 10.1093/jac/dkx113.
Rapid, cost-effective and objective methods for antimicrobial susceptibility testing of Neisseria gonorrhoeae would greatly enhance surveillance of antimicrobial resistance. Etest, disc diffusion and agar dilution methods are subjective, mostly laborious for large-scale testing and take ∼24 h. We aimed to develop a rapid broth microdilution assay using resazurin (blue), which is converted into resorufin (pink fluorescence) in the presence of viable bacteria.
The resazurin-based broth microdilution assay was established using 132 N. gonorrhoeae strains and the antimicrobials ceftriaxone, cefixime, azithromycin, spectinomycin, ciprofloxacin, tetracycline and penicillin. A regression model was used to estimate the MICs. Assay results were obtained in ∼7.5 h.
The EC 50 of the dose-response curves correlated well with Etest MIC values (Pearson's r = 0.93). Minor errors resulting from misclassifications of intermediate strains were found for 9% of the samples. Major errors (susceptible strains misclassified as resistant) occurred for ceftriaxone (4.6%), cefixime (3.3%), azithromycin (0.6%) and tetracycline (0.2%). Only one very major error was found (a ceftriaxone-resistant strain misclassified as susceptible). Overall the sensitivity of the assay was 97.1% (95% CI 95.2-98.4) and the specificity 78.5% (95% CI 74.5-82.9).
A rapid, objective, high-throughput, quantitative and cost-effective broth microdilution assay was established for gonococci. For use in routine diagnostics without confirmatory testing, the specificity might remain suboptimal for ceftriaxone and cefixime. However, the assay is an effective low-cost method to evaluate novel antimicrobials and for high-throughput screening, and expands the currently available methodologies for surveillance of antimicrobial resistance in gonococci.
用于淋病奈瑟菌抗菌药物敏感性检测的快速、经济高效且客观的方法将极大地加强对抗菌药物耐药性的监测。Etest法、纸片扩散法和琼脂稀释法主观性较强,大规模检测大多费力,且耗时约24小时。我们旨在开发一种使用刃天青(蓝色)的快速肉汤微量稀释测定法,刃天青在有活菌存在时会转化为试卤灵(粉红色荧光)。
使用132株淋病奈瑟菌菌株以及头孢曲松、头孢克肟、阿奇霉素、大观霉素、环丙沙星、四环素和青霉素等抗菌药物建立基于刃天青的肉汤微量稀释测定法。采用回归模型估算最低抑菌浓度(MIC)。在约7.5小时内获得测定结果。
剂量反应曲线的半数有效浓度(EC50)与Etest法的MIC值相关性良好(皮尔逊相关系数r = 0.93)。9%的样本存在因中间型菌株误分类导致的轻微误差。头孢曲松(4.6%)、头孢克肟(3.3%)、阿奇霉素(0.6%)和四环素(0.2%)出现主要误差(敏感菌株误分类为耐药)。仅发现一处非常重大的误差(一株对头孢曲松耐药的菌株误分类为敏感)。总体而言,该测定法的敏感性为97.1%(95%置信区间95.2 - 98.4),特异性为78.5%(95%置信区间74.5 - 82.9)。
为淋球菌建立了一种快速、客观、高通量、定量且经济高效的肉汤微量稀释测定法。对于无需确证检测的常规诊断应用,头孢曲松和头孢克肟的特异性可能仍不理想。然而,该测定法是评估新型抗菌药物和进行高通量筛选的有效低成本方法,扩展了目前可用的淋球菌抗菌药物耐药性监测方法。