首页> 美国卫生研究院文献>Theranostics >Development of a Loop Mediated Isothermal Amplification (LAMP) - Surface Enhanced Raman spectroscopy (SERS) Assay for the Detection of Salmonella Enterica Serotype Enteritidis
【2h】

Development of a Loop Mediated Isothermal Amplification (LAMP) - Surface Enhanced Raman spectroscopy (SERS) Assay for the Detection of Salmonella Enterica Serotype Enteritidis

机译:回路介导的等温扩增(LAMP)-表面增强拉曼光谱(SERS)检测沙门氏菌肠型血清肠炎沙门氏菌的检测方法的开发

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

As a major foodborne pathogen, Salmonella enterica serotype Enteritidis is increasingly rising as a global health concern. Here, we developed an integrated assay that combines loop mediated isothermal amplification (LAMP) and surface enhanced Raman spectroscopy (SERS) for DNA detection of S. Enteritidis using specifically designed Raman active Au-nanoprobes. The target DNA was amplified by LAMP and then labeled with Au-nanoprobes comprised of gold nanoparticle-modified with specific cy5/DNA probes to allow the detection by SERS. The sensitivity of the developed LAMP-SERS detection assay (66 CFU/mL) was ~100-fold higher than the conventional polymerase chain reaction (PCR) method. Significantly, this technique allowed highly specific detection of the target DNA of S. Enteritidis and could differentiate it from the DNA of closely related bacterial species or non-specific contamination, making it more accurate and reliable than the standard LAMP technique. The applicability of detection of S. Enteritidis in milk samples using LAMP-SERS assay was validated as well. In sum, the developed LAMP-SERS assay is highly specific and sensitive, and has the potential to be applied for rapid detection of different foodborne pathogens and other microbial contaminants.
机译:作为一种主要的食源性病原体,肠炎沙门氏菌血清型肠炎沙门氏菌日益引起全球关注。在这里,我们开发了一种结合了环介导的等温扩增(LAMP)和表面增强拉曼光谱(SERS)的整合测定,用于使用专门设计的拉曼活性金纳米探针对肠炎沙门氏菌进行DNA检测。用LAMP扩增靶DNA,然后用金纳米颗粒标记金纳米探针,该金纳米颗粒用特定的cy5 / DNA探针修饰,可以通过SERS检测。所开发的LAMP-SERS检测方法(66 CFU / mL)的灵敏度比常规聚合酶链反应(PCR)方法高约100倍。重要的是,该技术可以高度特异性地检测肠炎沙门氏菌的目标DNA,并且可以将其与密切相关的细菌或非特异性污染的DNA区别开来,从而使其比标准LAMP技术更为准确和可靠。还验证了使用LAMP-SERS测定法检测牛奶样品中肠炎链球菌的适用性。总而言之,已开发的LAMP-SERS测定具有高度特异性和敏感性,并有潜力用于快速检测各种食源性病原体和其他微生物污染物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号