用机器学习辅助拉曼光谱预测结核病耐药性。

ArXiv Pub Date : 2024-04-09
Babatunde Ogunlade, Loza F Tadesse, Hongquan Li, Nhat Vu, Niaz Banaei, Amy K Barczak, Amr A E Saleh, Manu Prakash, Jennifer A Dionne
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摘要

结核病是世界上最致命的传染病,每年有150万人死亡,50万人感染。快速结核病诊断和抗生素敏感性检测(AST)对于改善患者治疗和减少新耐药性的上升至关重要。在这里,我们开发了一种快速、无标记的方法来鉴定结核分枝杆菌(Mtb)菌株和抗生素耐药性突变体。我们从对四种主要抗结核药物之一(异烟肼、利福平、莫西沙星和阿米卡星)具有耐药性的同基因分枝杆菌菌株中收集了20000多个单细胞拉曼光谱,并在这些光谱上训练了一个机器学习模型。在干燥的结核病样本上,我们实现了>98%的抗生素耐药性分类准确率,而不需要抗生素共孵育;在干燥的患者痰中,我们实现了约79%的平均分类准确率。我们还开发了一种低成本的便携式拉曼显微镜,适用于结核病流行地区的现场部署。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Rapid, antibiotic incubation-free determination of tuberculosis drug resistance using machine learning and Raman spectroscopy.

Tuberculosis (TB) is the world's deadliest infectious disease, with over 1.5 million deaths annually and 10 million new cases reported each year1. The causative organism, Mycobacterium tuberculosis (Mtb) can take nearly 40 days to culture2,3, a required step to determine the pathogen's antibiotic susceptibility. Both rapid identification of Mtb and rapid antibiotic susceptibility testing (AST) are essential for effective patient treatment and combating antimicrobial resistance. Here, we demonstrate a rapid, culture-free, and antibiotic incubation-free drug susceptibility test for TB using Raman spectroscopy and machine learning. We collect few-to-single-cell Raman spectra from over 25,000 cells of the MtB complex strain Bacillus Calmette-Guérin (BCG) resistant to one of the four mainstay anti-TB drugs, isoniazid, rifampicin, moxifloxacin and amikacin, as well as a pan-susceptible wildtype strain. By training a neural network on this data, we classify the antibiotic resistance profile of each strain, both on dried samples and in patient sputum samples. On dried samples, we achieve >98% resistant versus susceptible classification accuracy across all 5 BCG strains. In patient sputum samples, we achieve ~79% average classification accuracy. We develop a feature recognition algorithm in order to verify that our machine learning model is using biologically relevant spectral features to assess the resistance profiles of our mycobacterial strains. Finally, we demonstrate how this approach can be deployed in resource-limited settings by developing a low-cost, portable Raman microscope that costs <$5000. We show how this instrument and our machine learning model enables combined microscopy and spectroscopy for accurate few-to-single-cell drug susceptibility testing of BCG.

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