Department of Electrical and Computer Engineering, University of Alberta, Edmonton, Alberta, Canada T6G 2V4.
Analyst. 2013 Oct 7;138(19):5619-26. doi: 10.1039/c3an01100c.
We present a novel phage receptor binding protein-based magnetic separation and pre-enrichment method as an alternative to the immunomagnetic separation methods by replacing antibodies with bacteriophage receptor binding proteins (RBPs). We couple the proposed RBP-based magnetic separation with real time PCR for rapid, sensitive and specific detection of Campylobacter jejuni cells in artificially contaminated skim milk, milk with 2% fat and chicken broth. Recovery rates, assessed by real time PCR, were greater than 80% for the samples spiked with as low as 100 cfu mL(-1) of C. jejuni cells. The specificity of capture was confirmed using Salmonella Typhimurium as a negative control where no bacteria were captured on the RBP-derivatized magnetic beads. The combination of RBP-based magnetic separation and real time PCR improved PCR sensitivity and allowed the detection of C. jejuni cells in milk and chicken broth samples without a time consuming pre-enrichment step through culturing. The total sample preparation and analysis time in the proposed RBP-based enrichment method coupled with real time PCR was less than 3 h.
我们提出了一种新型的噬菌体受体结合蛋白磁分离和预富集方法,作为免疫磁分离方法的替代方法,用噬菌体受体结合蛋白 (RBP) 替代抗体。我们将所提出的基于 RBP 的磁分离与实时 PCR 相结合,用于快速、灵敏和特异性检测人工污染的脱脂奶、2%脂肪奶和鸡汁中的空肠弯曲菌细胞。通过实时 PCR 评估,回收率对于用低至 100 cfu mL(-1) 的空肠弯曲菌细胞污染的样品大于 80%。使用鼠伤寒沙门氏菌作为阴性对照物,通过实时 PCR 确认了捕获的特异性,在 RBP 衍生的磁珠上没有捕获到细菌。基于 RBP 的磁分离和实时 PCR 的结合提高了 PCR 的灵敏度,并允许在不经过培养的耗时预富集步骤的情况下检测牛奶和鸡汁样品中的空肠弯曲菌细胞。与实时 PCR 结合的基于 RBP 的富集方法的总样品制备和分析时间少于 3 小时。