Yüksel Sezin, Schwenkbier Lydia, Pollok Sibyll, Weber Karina, Cialla-May Dana, Popp Jürgen
Leibniz Institute of Photonic Technology Jena (IPHT), Albert-Einstein-Straße 9, 07745 Jena, Germany.
Analyst. 2015 Nov 7;140(21):7254-62. doi: 10.1039/c5an01156f.
In this study, we report on a novel approach for the label-free and species-specific detection of the plant pathogen Phytophthora ramorum from real samples using surface enhanced Raman scattering (SERS). In this context, we consider the entire analysis chain including sample preparation, DNA isolation, amplification and hybridization on SERS substrate-immobilized adenine-free capture probes. Thus, the SERS-based detection of target DNA is verified by the strong spectral feature of adenine which indicates the presence of hybridized target DNA. This property was realized by replacing adenine moieties in the species-specific capture probes with 2-aminopurine. In the case of the matching capture and target sequence, the characteristic adenine peak serves as an indicator for specific DNA hybridization. Altogether, this is the first assay demonstrating the detection of a plant pathogen from an infected plant material by label-free SERS employing DNA hybridization on planar SERS substrates consisting of silver nanoparticles.
在本研究中,我们报告了一种利用表面增强拉曼散射(SERS)从实际样本中对植物病原体致病疫霉进行无标记且物种特异性检测的新方法。在此背景下,我们考虑了整个分析流程,包括样品制备、DNA分离、扩增以及在固定于SERS底物上的无腺嘌呤捕获探针上进行杂交。因此,基于SERS的目标DNA检测通过腺嘌呤的强光谱特征得以验证,该特征表明存在杂交的目标DNA。此特性是通过用2-氨基嘌呤取代物种特异性捕获探针中的腺嘌呤部分来实现的。在匹配的捕获序列和目标序列的情况下,特征性的腺嘌呤峰可作为特定DNA杂交的指示物。总之,这是首个通过在由银纳米颗粒组成的平面SERS底物上进行DNA杂交,利用无标记SERS从受感染植物材料中检测植物病原体的检测方法。