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Spectroscopic Method for Fast and Accurate Group A Streptococcus Bacteria Detection

机译:快速准确地检测A组链球菌细菌的光谱方法

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Rapid and accurate detection of pathogens is paramount to human health. Spectroscopic techniques have been shown to be viable methods for detecting various pathogens. Enhanced methods of Raman spectroscopy can discriminate unique bacterial signatures; however, many of these require precise conditions and do not have in vivo replicability. Common biological detection methods such as rapid antigen detection tests have high specificity but do not have high sensitivity. Here we developed a new method of bacteria detection that is both highly specific and highly sensitive by combining the specificity of antibody staining and the sensitivity of spectroscopic characterization. Bacteria samples, treated with a fluorescent antibody complex specific to Streptococcus pyogenes, were volumetrically normalized according to their Raman bacterial signal intensity and characterized for fluorescence, eliciting a positive result for samples containing Streptococcus pyogenes and a negative result for those without. The normalized fluorescence intensity of the Streptococcus pyogenes gave a signal that is up to 16.4 times higher than that of other bacteria samples for bacteria stained in solution and up to 12.7 times higher in solid state. This method can be very easily replicated for other bacteria species using suitable antibody dye complexes. In addition, this method shows viability for in vivo detection as it requires minute amounts of bacteria, low laser excitation power, and short integration times in order to achieve high signal.
机译:快速,准确地检测病原体对人类健康至为重要。光谱技术已被证明是检测各种病原体的可行方法。拉曼光谱法的增强方法可以区分独特的细菌特征。但是,其中许多要求精确的条件,并且不具有体内复制性。常用的生物检测方法(例如快速抗原检测测试)具有高特异性,但灵敏度不高。在这里,我们通过结合抗体染色的特异性和光谱表征的敏感性,开发了一种新的细菌检测方法,该方法既具有高度特异性又具有高度敏感性。根据化脓性链球菌特异的荧光抗体复合物处理的细菌样品,根据其拉曼细菌信号强度进行体积归一化,并对其荧光进行表征,从而对含有化脓性链球菌的样品得出阳性结果,对不含化脓性链球菌的样品得出阴性结果。化脓性链球菌的归一化荧光强度给出的信号比溶液中染色的细菌的其他细菌样品的信号强度高多达16.4倍,而固态的信号强度的信号强度高达12.7倍。使用合适的抗体染料复合物,该方法可以很容易地复制到其他细菌种类。另外,该方法显示了体内检测的可行性,因为它需要微量的细菌,低的激光激发功率和较短的积分时间才能获得高信号。

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