Vanderbilt University Medical Center, Nashville, Tennesee, USA.
Next Gen Diagnostics, LLC, Cambridge, United Kingdom.
J Clin Microbiol. 2023 Mar 23;61(3):e0143122. doi: 10.1128/jcm.01431-22. Epub 2023 Feb 22.
The declining cost of performing bacterial whole-genome sequencing (WGS) coupled with the availability of large libraries of sequence data for well-characterized isolates have enabled the application of machine-learning (ML) methods to the development of nonlinear sequence-based predictive models. We tested the ML-based model developed by Next Gen Diagnostics for prediction of cefepime phenotypic susceptibility results in Escherichia coli. A cohort of 100 isolates of E. coli recovered from urine ( = 77) and blood ( = 23) cultures were used. The cefepime MIC was determined in triplicate by reference broth microdilution and classified as susceptible (MIC of ≤2 μg/mL) or not susceptible (MIC of ≥4 μg/mL) using the 2022 Clinical and Laboratory Standards Institute breakpoints. Five isolates generated both susceptible and not susceptible MIC results, yielding categorical agreement of 95% for the reference method to itself. Categorical agreement of ML to MIC interpretations was 97%, with 2 very major (false, susceptible) and 1 major (false, not susceptible) errors. One very major error occurred for an isolate with (MIC mode, ≥32 μg/mL) and one for an isolate with for which the MIC cefepime mode was 4 μg/mL. One major error was for an isolate with but with a MIC mode of 2 μg/mL. These preliminary data demonstrated performance of ML for a clinically important antimicrobial-species pair at a caliber similar to phenotypic methods, encouraging wider development of sequence-based susceptibility prediction and its validation and use in clinical practice.
细菌全基因组测序(WGS)成本的降低,加上大量经过充分特征描述的分离株序列数据的可用性,使得机器学习(ML)方法能够应用于开发基于序列的非线性预测模型。我们测试了 Next Gen Diagnostics 开发的基于 ML 的模型,用于预测大肠埃希菌中头孢吡肟表型药敏结果。使用了从尿液( = 77)和血液( = 23)培养物中回收的 100 株大肠埃希菌分离株的队列。头孢吡肟 MIC 通过参考肉汤微量稀释法重复测定,并使用 2022 年临床和实验室标准协会的折点分类为敏感(MIC ≤2 μg/mL)或不敏感(MIC ≥4 μg/mL)。有 5 株分离物产生了敏感和不敏感的 MIC 结果,参考方法本身的分类一致性为 95%。ML 与 MIC 解释的分类一致性为 97%,有 2 个非常大(错误,敏感)和 1 个主要(错误,不敏感)错误。一个非常大的错误发生在一个 MIC 模式为 (MIC 模式,≥32 μg/mL)的分离物上,另一个发生在一个 MIC 模式为 4 μg/mL 的分离物上。一个主要错误发生在一个 MIC 模式为 2 μg/mL 的分离物上。这些初步数据表明,对于一种临床重要的抗菌药物-物种对,ML 的性能与表型方法相似,这鼓励了更广泛地开发基于序列的药敏预测及其验证,并将其应用于临床实践。