Axelsson Carolina, Nilson Bo, Rehnstam-Holm Ann-Sofi
Department of Environmental Science and Biomedical Science, Faculty of Natural Science, Kristianstad University, 288 91 Kristianstad, Sweden.
Department of Clinical Microbiology, Office for Medical Services, Region Skåne, 223 62 Lund, Sweden.
Antibiotics (Basel). 2024 Sep 6;13(9):852. doi: 10.3390/antibiotics13090852.
It is increasingly important to rapidly receive information on the antimicrobial susceptibility of bacteria due to the rise in antimicrobial resistance worldwide. However, traditional phenotypic methods are time-consuming. Thus, the objective of this study was to develop a rapid assay that can detect antibiotic-resistant bacterial isolates phenotypically in less than 2 h. The microplate assay used in this study is based on absorbance measurements of pure bacterial isolates grown in liquid media with and without antibiotics. Absorbance was measured at the beginning of the assay and after 90 min of incubation at 37 °C. Susceptibility was calculated for bacterial isolates that, in the absence of antibiotics, exhibited more than a 50% growth increase by comparing the absorbance value of the culture in the presence of an antibiotic at 90 min with its initial value. Here, we show that it is possible to phenotypically screen the antibiotic susceptibility of Enterobacterales and spp. isolates to three different antibiotics in 90 min. The test demonstrated an accuracy of 98.8%, sensitivity of 97.6%, and specificity of 99.6%. The false susceptibility rates were 0.2% and false resistance rates were 1.0%. This rapid and simple absorbance test has proven suitable for the screening of antibiotic susceptibility for a large number of strains with high accuracy and sensitivity. This method can be performed without specialized and costly materials and/or equipment, which makes it highly suitable for laboratories with limited resources.
由于全球抗菌药物耐药性的增加,快速获得细菌抗菌药物敏感性信息变得越来越重要。然而,传统的表型方法耗时较长。因此,本研究的目的是开发一种快速检测方法,能够在不到2小时的时间内从表型上检测出抗生素耐药性细菌分离株。本研究中使用的微孔板检测方法基于对在含有和不含有抗生素的液体培养基中生长的纯细菌分离株的吸光度测量。在检测开始时以及在37°C孵育90分钟后测量吸光度。通过将在90分钟时存在抗生素的培养物的吸光度值与其初始值进行比较,计算在无抗生素情况下生长增加超过50%的细菌分离株的敏感性。在此,我们表明可以在90分钟内从表型上筛选肠杆菌科细菌和其他菌株对三种不同抗生素的敏感性。该测试的准确率为98.8%,灵敏度为97.6%,特异性为99.6%。假敏感率为0.2%,假耐药率为1.0%。这种快速且简单的吸光度测试已被证明适用于以高精度和高灵敏度筛选大量菌株的抗生素敏感性。该方法无需使用专门且昂贵的材料和/或设备即可进行,这使其非常适合资源有限的实验室。