Ka Lok Hong, Eamonn Maher, Ryan M Williams, Letha J Sooter
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引用次数: 6
摘要
毒素B是艰难梭菌(Clostridium difficile)的主要毒力因子之一,艰难梭菌是导致急性护理环境中大量腹泻病例的细菌。由于艰难梭菌性腹泻的流行,快速和正确的诊断在疾病管理中至关重要。在本研究中,我们采用了严格的体外筛选方法来鉴定毒素B特异性的单链DNA分子识别元件(MRE)。在12轮筛选结束时,鉴定出一个毒素B高亲和力(K d = 47.3 nM)的MRE。所选择的MRE对阴性靶点:牛血清白蛋白、金黄色葡萄球菌α毒素、铜绿假单胞菌外毒素A和霍乱弧菌霍乱毒素具有低交叉结合活性。利用所选择的ssDNA MRE作为抗原捕获元件,建立了一种改进的夹心ELISA法,对人粪便制剂中50 nM的毒素B进行了灵敏检测。
In Vitro Selection of a Single-Stranded DNA Molecular Recognition Element against Clostridium difficile Toxin B and Sensitive Detection in Human Fecal Matter.
Toxin B is one of the major virulence factors of Clostridium difficile, a bacterium that is responsible for a significant number of diarrhea cases in acute care settings. Due to the prevalence of C. difficile induced diarrhea, rapid and correct diagnosis is crucial in the disease management. In this study, we have employed a stringent in vitro selection method to identify single-stranded DNA molecular recognition elements (MRE) specific for toxin B. At the end of the 12-round selection, one MRE with high affinity (K d = 47.3 nM) for toxin B was identified. The selected MRE demonstrated low cross binding activities on negative targets: bovine serum albumin, Staphylococcus aureus alpha toxin, Pseudomonas aeruginosa exotoxin A, and cholera toxin of Vibrio cholera. A modified sandwich ELISA assay was developed utilizing the selected ssDNA MRE as the antigen capturing element and achieved a sensitive detection of 50 nM of toxin B in human fecal preparations.