插膜法直接检测脂磷胆酸

Jessica Z. Kubicek-Sutherland, Astrid C. Hengartner, H. Mukundan
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引用次数: 4

摘要

细菌病原体的错误诊断导致抗生素的滥用,这是抗生素耐药性演变的主要因素。快速识别病原体的能力可以促进更有效的治疗策略,减少不必要的抗生素使用。目前对细菌感染的诊断通常需要细胞生长,因此不能及时提供治疗方案。在这里,我们描述了一种快速测定(<45分钟)的发展,可以直接在人血清中鉴定革兰氏阳性细菌,而无需任何生长或分离。我们开发了一种基于荧光的免疫测定方法,专门针对革兰氏阳性细菌生物标志物脂磷胆酸(LTA)。LTA是一种两亲分子,同时具有疏水性和亲水性。我们的方法,称为膜插入,利用分子的两亲性生物化学,允许它被动地将自己插入脂质双分子层,从而捕获它,以便随后用荧光标记的α -LTA抗体进行探测。使用该方法,我们已经成功地在加标的人血清中直接检测到低于10µg/ml的LTA。我们打算将这种快速检测方法与目前正在开发的其他方法结合起来,成为一种即时检测细菌病原体的诊断工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Membrane Insertion for Direct Detection of Lipoteichoic Acid
The incorrect diagnosis of bacterial pathogens results in the misuse of antibiotics, a major contributor to the evolution of antibiotic resistance. The ability to rapidly identify a pathogen could facilitate more effective treatment strategies, reducing the unnecessary use of antibiotics. Current diagnostics of bacterial infections often require cell growth, and are therefore less capable of informing timely treatment options. Here, we describe the development of a rapid assay (<45 min) to identify Gram-positive bacteria directly in human serum without any growth or isolation required. We have developed a fluorescence-based immunoassay specifically targeting the Gram-positive bacterial biomarker lipoteichoic acid (LTA). LTA is an amphiphilic molecule with both hydrophobic and hydrophilic portions. Our approach, termed membrane insertion, exploits the amphiphilic biochemistry of the molecule by allowing it to passively insert itself into a lipid bilayer, thereby trapping it for subsequent probing with a fluorescently labeled α -LTA antibody. Using this assay, we have successfully detected less than 10 µ g/ml of LTA directly in spiked human serum. We intend to combine this rapid assay with others currently in development into a diagnostic tool for point-of-care detection of bacterial pathogens.
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