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Gold nanoparticle-based immunodetection of Staphylococcus aureus leukotoxin M/F'-PV in subclinical samples of bovine mastitis

机译:基于金纳米颗粒的金黄色葡萄球菌白细胞毒素M / F'-PV在牛乳腺炎亚临床样品中的免疫检测

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摘要

In the present study, an immunosensor was designed to assess bovine mastitis at the earliest by quantifying leukotoxin M/F'-PV (LukM/F'-PV), a potent neutrophil targeting and beta-barrel pore-forming toxin secreted by bovine strains of S. aureus. Polyclonal antibodies to the recombinant LukF (rLukF) component of LukM/F'-PV was raised and purified by affinity chromatography. Further, anti-rLukF antibody was used to design a classical ELISA detection system in which we obtained 1000 ng ml~(-1) LOD. Considering the drawbacks of the classical detection system, antibodies were functionalized to gold nanoparticles of a large surface plasmon band providing an opportunity to design immunoassays based on nanosurface energy transfer (NSET) from dye to gold nanoparticles (GNPs). In an experimental set up, rLukF was incubated with functionalized GNPs, fluorescein isothiocyanate (FITC)-labeled secondary antibodies were added, and fluorescence quenching was monitored as a function of toxin concentration. With this method, leukotoxin was detected in the 100-0.1 ng ml~(-1) range, with a LOD of 0.1 ng ml~(-1) and R~2 = 0.9908. In addition, the above proposed assay was performed to detect toxins in spiked and field samples with 89-95% recovery. Thus, the proposed method overcomes the major drawbacks of ELISA systems and can provide a window for sensitive detection of toxin before onset of mastitis.
机译:在本研究中,设计了一种免疫传感器,旨在通过量化白细胞毒素M / F'-PV(LukM / F'-PV)来最早评估牛乳腺炎,白细胞毒素M / F'-PV(一种有效的中性粒细胞靶向性和牛株分泌的β-桶形成孔毒素)金黄色葡萄球菌。产生针对LukM / F'-PV的重组LukF(rLukF)组件的多克隆抗体,并通过亲和色谱法纯化。此外,使用抗rLukF抗体设计了一种经典的ELISA检测系统,在该系统中我们获得了1000 ng ml〜(-1)LOD。考虑到经典检测系统的弊端,将抗体功能化至大表面等离激元带的金纳米颗粒,这为基于染料到金纳米颗粒(GNP)的纳米表面能量转移(NSET)设计免疫测定提供了机会。在实验设置中,将rLukF与功能化的GNP孵育,加入异硫氰酸荧光素(FITC)标记的二抗,并根据毒素浓度监测荧光猝灭。用这种方法检测到的白细胞毒素在100-0.1 ng ml〜(-1)范围内,LOD为0.1 ng ml〜(-1),R〜2 = 0.9908。另外,进行上述提议的测定以检测加标样品和现场样品中的毒素,回收率为89-95%。因此,所提出的方法克服了ELISA系统的主要缺点,并且可以为乳腺炎发作之前毒素的敏感检测提供一个窗口。

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