Computational Biology Laboratory, CHU de Québec - Université Laval Research Center, Québec City, Quebec, Canada; Proteomics Platform, CHU de Québec - Université Laval Research Center, Québec City, Quebec, Canada.
Centre de Recherche en Infectiologie de l'Université Laval, Axe Maladies Infectieuses et Immunitaires, Centre de Recherche du CHU de Québec-Université Laval, Québec City, Quebec, Canada.
Mol Cell Proteomics. 2024 Nov;23(11):100832. doi: 10.1016/j.mcpro.2024.100832. Epub 2024 Aug 22.
Urinary tract infections (UTIs) are a worldwide health problem. Fast and accurate detection of bacterial infection is essential to provide appropriate antibiotherapy to patients and to avoid the emergence of drug-resistant pathogens. While the gold standard requires 24 h to 48 h of bacteria culture prior to MALDI-TOF species identification, we propose a culture-free workflow, enabling bacterial identification and quantification in less than 4 h using 1 ml of urine. After rapid and automatable sample preparation, a signature of 82 bacterial peptides, defined by machine learning, was monitored in LC-MS, to distinguish the 15 species causing 84% of the UTIs. The combination of the sensitivity of the SRM mode on a triple quadrupole TSQ Altis instrument and the robustness of capillary flow enabled us to analyze up to 75 samples per day, with 99.2% accuracy on bacterial inoculations of healthy urines. We have also shown our method can be used to quantify the spread of the infection, from 8 × 10 to 3 × 10 CFU/ml. Finally, the workflow was validated on 45 inoculated urines and on 84 UTI-positive urine from patients, with respectively 93.3% and 87.1% of agreement with the culture-MALDI procedure at a level above 1 × 10 CFU/ml corresponding to an infection requiring antibiotherapy.
尿路感染(UTIs)是一个全球性的健康问题。快速准确地检测细菌感染对于为患者提供适当的抗生素治疗以及避免耐药病原体的出现至关重要。虽然金标准需要在 MALDI-TOF 物种鉴定前进行 24 小时到 48 小时的细菌培养,但我们提出了一种无培养物的工作流程,能够在不到 4 小时的时间内使用 1 毫升尿液进行细菌鉴定和定量。在快速自动的样品制备后,通过机器学习监测到 82 种细菌肽的特征,可区分引起 84%UTI 的 15 种细菌。三重四极杆 TSQ Altis 仪器上 SRM 模式的灵敏度与毛细管流量的稳健性相结合,使我们能够每天分析多达 75 个样本,对健康尿液的细菌接种的准确率达到 99.2%。我们还表明,我们的方法可用于量化感染的传播,从 8×10 到 3×10 CFU/ml。最后,该工作流程在 45 份接种尿液和 84 份来自患者的 UTI 阳性尿液中进行了验证,与培养-MALDI 程序的一致性分别为 93.3%和 87.1%,在 1×10 CFU/ml 以上的水平上需要进行抗生素治疗。