Institute of Physical Chemistry and Abbe Center of Photonics, Friedrich Schiller University Jena , Helmholtzweg 4, 07743 Jena, Germany.
InfectoGnostics Research Campus Jena , Center for Applied Research, Philosophenweg 7, Jena, 07743, Germany.
Anal Chem. 2016 Feb 2;88(3):1570-7. doi: 10.1021/acs.analchem.5b02829. Epub 2016 Jan 8.
Pyoverdine is a substance which is excreted by fluorescent pseudomonads in order to scavenge iron from their environment. Due to specific receptors of the bacterial cell wall, the iron loaded pyoverdine molecules are recognized and transported into the cell. This process can be exploited for developing efficient isolation and enrichment strategies for members of the Pseudomonas genus, which are capable of colonizing various environments and also include human pathogens like P. aeruginosa and the less virulent P. fluorescens. A significant advantage over antibody based systems is the fact that siderophores like pyoverdine can be considered as "immutable ligands," since the probability for mutations within the siderophore uptake systems of bacteria is very low. While each species of Pseudomonas usually produces structurally unique pyoverdines, which can be utilized only by the producer strain, cross reactivity does occur. In order to achieve a reliable identification of the captured pathogens, further investigations of the isolated cells are necessary. In this proof of concept study, we combine the advantages of an isolation strategy relying on "immutable ligands" with the high specificity and speed of Raman microspectroscopy. In order to isolate the bacterial cells, pyoverdine was immobilized covalently on planar aluminum chip substrates. After capturing, single cell Raman spectra of the isolated species were acquired. Due to the specific spectroscopic fingerprint of each species, the bacteria can be identified. This approach allows a very rapid detection of potential pathogens, since time-consuming culturing steps are unnecessary. We could prove that pyoverdine based isolation of bacteria is fully Raman compatible and further investigated the capability of this approach by isolating and identifying P. aeruginosa and P. fluorescens from tap water samples, which are both opportunistic pathogens and can pose a threat for immunocompromised patients.
绿脓菌素是荧光假单胞菌分泌的一种物质,用于从环境中掠夺铁。由于细菌细胞壁的特定受体,负载铁的绿脓菌素分子被识别并运入细胞。这个过程可以被用来开发有效的分离和富集策略,用于能够定植于各种环境的假单胞菌属成员,其中包括人类病原体如铜绿假单胞菌和毒力较弱的荧光假单胞菌。与基于抗体的系统相比,一个显著的优势是,像绿脓菌素这样的铁载体可以被视为“不可变配体”,因为细菌中铁载体摄取系统发生突变的概率非常低。虽然每种假单胞菌通常产生结构独特的绿脓菌素,只能被产生菌利用,但确实会发生交叉反应。为了可靠地识别捕获的病原体,需要对分离的细胞进行进一步的研究。在这项概念验证研究中,我们将依赖“不可变配体”的分离策略的优势与拉曼微光谱的高特异性和快速性结合起来。为了分离细菌细胞,绿脓菌素通过共价键固定在平面铝芯片基底上。在捕获之后,获取了分离物种的单细胞拉曼光谱。由于每种物种都有特定的光谱指纹,因此可以识别细菌。这种方法可以非常快速地检测潜在的病原体,因为不需要耗时的培养步骤。我们证明了基于绿脓菌素的细菌分离完全兼容拉曼技术,并通过从自来水中分离和鉴定铜绿假单胞菌和荧光假单胞菌进一步研究了这种方法的能力,这两种菌都是机会性病原体,可能对免疫功能低下的患者构成威胁。