利用重组生物发光铜绿假单胞菌定量评价细菌粘附性。

Lu Wang, Xinhua Qiao, Lei Gao, Chang Chen, Yi Wan
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引用次数: 1

摘要

生物发光技术在医学检测领域有着广泛的应用。生物发光流通量报告系统为实时监测细菌生长和表达提供了一个无创平台。本研究旨在利用含有lux报告因子的重组生物发光铜绿假单胞菌,建立检测包括医疗器械在内的材料表面细菌粘附的方法。通过监测重组菌株PAO1-lux的生长和生物发光特性,确定体外细菌粘附检测的最佳试验条件为:初始接种密度为105 ~ 106 CFU/mL, M9培养基pH为6.2,粘附时间为6 h,超声清洗收集粘附菌。比较了传统的CFU计数法和生物发光法,并通过测试细菌在各种材料表面的粘附情况,验证了新方法的适用性。经过验证的生物发光菌株可以作为细菌检测工具的有力候选者,用于细菌粘附性评估等应用,以及传统微生物检测程序的补充和替代。此外,该方法还具有研究细菌粘附在无生命物体和活组织表面的潜力。随着该方法的发展和广泛的适用性,有望成为细菌粘附检测和抗粘附材料筛选的标准方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A quantitative method to assess bacterial adhesion using recombinant bioluminescent <i>Pseudomonas aeruginosa</i>.

A quantitative method to assess bacterial adhesion using recombinant bioluminescent <i>Pseudomonas aeruginosa</i>.

A quantitative method to assess bacterial adhesion using recombinant bioluminescent <i>Pseudomonas aeruginosa</i>.

A quantitative method to assess bacterial adhesion using recombinant bioluminescent Pseudomonas aeruginosa.

Bioluminescence technology has been widely used in the field of medical detection. The bioluminescent lux reporter system provides a non-invasive platform to monitor bacterial growth and expression in real time. This study aimed to establish a method for detecting bacterial adhesion on the surface of materials, including medical devices, by using recombinant bioluminescent Pseudomonas aeruginosa containing a lux reporter. By monitoring the growth and bioluminescent properties of the recombinant PAO1-lux strain, the optimal test conditions for bacterial adhesion detection in vitro were determined to be as follows: an initial inoculation density of 105 to 106 CFU/mL, M9 medium at a pH 6.2, an adhesion time of 6 h, and the collection of adherent bacteria by ultrasonic cleaning. The traditional CFU counting method and the bioluminescence method were compared, and the applicability of the new method was verified by testing the adhesion of bacteria on the surface of various materials. The validated bioluminescent strains could serve as strong candidates to be used as bacterial detection tools in applications such as bacterial adhesion evaluation as well as supplements and alternatives to traditional microbiological testing procedures. In addition, this method has the potential to enable the study of bacterial adhesion on the surface of inanimate objects and living tissues. With the development of this method and its wide applicability, it is expected to become a standard method for the detection of bacterial adhesion and the screening of anti-adhesion materials.

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CiteScore
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