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A new colorimetric peptide nucleic acid-based assay for the specific detection of bacteria

机译:一种基于比色肽核酸的新方法,用于细菌的特异性检测

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摘要

Aim: Developments on synthetic molecules, such as peptide nucleic acid (PNA), make FISH procedures more robust for microbial identification. Fluorochromes use might hinder a broader implementation of PNA-FISH, but colorimetric applications are inexistent so far. Methods: A biotin-labeled eubacteria probe was used to develop a colorimetric PNA-in situ hybridization (ISH) assay. An enzymatic-conjugate, targeting biotin, was introduced. The procedure was optimized and evaluated regarding sensitivity, specificity and detection limit. Results: Results have shown strong ISH signals. The method was specific, but permeabilization problems were observed for Gram-positive bacteria. Detection limit was 5 × 107 CFU/ml, limiting current applications to pre-enriched samples. Conclusion: The PNA-ISH procedure described here is a simple alternative to other detection methods, and is also the base for the development of other PNA colorimetric systems.
机译:目的:诸如肽核酸(PNA)之类的合成分子的发展,使得FISH程序对于微生物鉴定更加可靠。荧光染料的使用可能会阻碍PNA-FISH的更广泛实施,但到目前为止,色度应用尚不存在。方法:使用生物素标记的真细菌探针进行比色PNA原位杂交(ISH)分析。介绍了靶向生物素的酶结合物。对程序进行了优化,并评估了灵敏度,特异性和检测限。结果:结果显示出强烈的ISH信号。该方法是特定的,但是对于革兰氏阳性细菌观察到通透性问题。检出限为5×107 CFU / ml,限制了当前对预富集样品的应用。结论:此处描述的PNA-ISH程序是其他检测方法的简单替代方法,也是开发其他PNA比色系统的基础。

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