基于吸收率的高效肠杆菌抗生素敏感性快速检测方法

Carolina Axelsson, Bo Nilson, Ann-Sofi Rehnstam-Holm
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引用次数: 0

摘要

由于全球范围内抗菌药耐药性的增加,快速获得细菌的抗菌药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,可在 2 小时内从表型上检测出耐药细菌分离物。本研究中使用的微孔板检测方法是基于对先前在含抗生素和不含抗生素的液体培养基中生长的纯细菌分离物的吸光度测量。吸光度在检测开始时和 37 °C 培养 90 分钟后测量。通过比较培养物在有抗生素存在的情况下 90 分钟后的吸光度值与初始值,计算出细菌分离物在无抗生素存在的情况下生长增加 50%以上的敏感性。在此,我们证明了可以在 90 分钟内对肠杆菌属和醋杆菌属分离物对三种不同抗生素的敏感性进行表型筛选。该测试的准确率为 98.8%,灵敏度为 97.6%,特异性为 99.6%。错误药敏率为 0.2%,错误耐药率为 1.0%。事实证明,这种快速、简单的吸光度测试适用于大量菌株的抗生素敏感性筛查,准确性和敏感性都很高。该方法无需昂贵的专业材料和/或设备,因此非常适合资源有限的实验室使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficient Absorbance-Based Assay for Rapid Antibiotic Susceptibility Testing of Enterobacterales
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 previously 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 Acinetobacter 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.
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