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首页> 外文期刊>Analytical and bioanalytical chemistry >Carbon nanoparticles in lateral flow methods to detect genes encoding virulence factors of Shiga toxin-producing Escherichia coli
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Carbon nanoparticles in lateral flow methods to detect genes encoding virulence factors of Shiga toxin-producing Escherichia coli

机译:侧流法中的碳纳米颗粒检测编码志贺毒素生产大肠杆菌致病因子的基因

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摘要

The use of carbon nanoparticles is shown for the detection and identification of different Shiga toxin-producing Escherichia coli virulence factors (vt1, vt2, eae and ehxA) and a 16S control (specific for E. coli) based on the use of lateral flow strips (nucleic acid lateral flow immunoassay, NALFIA). Prior to the detection with NALFIA, a rapid amplification method with tagged primers was applied. In the evaluation of the optimised NALFIA strips, no cross-reactivity was found for any of the antibodies used. The limit of detection was higher than for quantitative PCR (q-PCR), in most cases between 10~4 and 10~5 colony forming units/mL or 0.1-0.9 ng/μL DNA. NALFIA strips were applied to 48 isolates from cattle faeces, and results were compared to those achieved by q-PCR. E. coli virulence factors identified by NALFIA were in very good agreement with those observed in q-PCR, showing in most cases sensitivity and specificity values of 1.0 and an almost perfect agreement between both methods (kappa coefficient larger than 0.9). The results demonstrate that the screening method developed is reliable, cost-effective and user-friendly, and that the procedure is fast as the total time required is <1 h, which includes amplification.
机译:显示了使用碳纳米颗粒检测和鉴定产生志贺毒素的不同大肠杆菌毒力因子(vt1,vt2,eae和ehxA)和基于侧向流动条的16S对照(特异于大肠杆菌)。 (核酸侧流免疫测定,NALFIA)。在用NALFIA检测之前,应用了带有标记引物的快速扩增方法。在优化的NALFIA条的评估中,未发现所用任何抗体的交叉反应性。检测极限高于定量PCR(q-PCR),在大多数情况下,菌落形成单位为10〜4至10〜5个/ mL或0.1-0.9 ng /μLDNA。将NALFIA条应用于牛粪的48个分离株,并将结果与​​q-PCR所得结果进行比较。通过NALFIA鉴定的大肠杆菌毒力因子与q-PCR观察到的毒力因子非常吻合,在大多数情况下,灵敏度和特异性值为1.0,两种方法之间的吻合度几乎完美(kappa系数大于0.9)。结果表明,开发的筛选方法可靠,具有成本效益且用户友好,并且由于所需的总时间<1 h(包括扩增),因此该过程非常快捷。

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