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Rapid Quantitative Detection of Salmonella spp. via Magnetic Beads-based Fluorescent Lateral Flow Immunoassay*

机译:沙门氏菌的快速定量检测。基于磁珠的荧光横向流免疫分析 *

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Polymerase chain reaction (PCR) plays an increasingly important role in microbial detection. However, the existing methods are difficult to be widely applied due to factors such as instruments, reagents, and experimental conditions. In this study, we developed a robust and reliable fluorescent lateral flow immunoassay combined with polymerase chain reaction (PCR-LFIA) based on magnetic beads purification for rapid detection of Salmonella app. The PCR-LFIA assay can avoid false positives caused by primer dimers. The sensitivity of PCR-LFIA method was 6×100 CFU/mL of Salmonella pure culture or 6×102 CFU/mL of artificially spiked chicken faeces. The specificity of PCR-LFIA assay was verified by eighteen Salmonella and non-Salmonella reference strains. Six of the eighty-five (7.1%) samples collected were positive by PCR-LFIA assay and the results were further confirmed by biochemical characteristics. This assay allows quantitative detection of Salmonella with a cutoff value of 175 and can be completed in 80 minutes. In conclusion, the optimized PCR-LFIA method can potentially serve as an effective diagnostic tool for timely response to disease outbreaks.
机译:聚合酶链反应(PCR)在微生物检测中起着越来越重要的作用。但是,由于诸如仪器,试剂和实验条件等因素,现有方法难以广泛应用。在这项研究中,我们开发了一种强大且可靠的荧光侧流免疫测定法,该方法结合了基于磁珠纯化的聚合酶链反应(PCR-LFIA),可快速检测沙门氏菌app。 PCR-LFIA分析可避免引物二聚体引起的假阳性。 PCR-LFIA方法的灵敏度为6×10 0 沙门氏菌纯培养物的CFU / mL或6×10 2 CFU / mL人工加标的鸡粪。通过18株沙门氏菌和非沙门氏菌参考菌株验证了PCR-LFIA检测的特异性。通过PCR-LFIA测定,在八十五(7.1%)个样本中有六个呈阳性,并通过生化特性进一步证实了结果。该测定法可以定量检测沙门氏菌,其截断值为175,可以在80分钟内完成。总之,优化的PCR-LFIA方法可以潜在地用作对疾病暴发及时做出反应的有效诊断工具。

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