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Detection of Helicobacter pylori in dental plaque using a DNA biosensor for noninvasive diagnosis

机译:使用DNA生物传感器检测牙菌斑中的幽门螺杆菌用于非侵入性诊断

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摘要

Noninvasive diagnosis of Helicobacter pylori ( H. pylori ) infection is very attractive. This study investigated the single strand DNA (ssDNA) acquisition method from H. pylori in dental plaque, and the integration of our previously developed 43-mer H. pylori DNA biosensor with the obtained target ssDNA (tDNA). Dental plaque samples were collected from 34 patients/volunteers, whose gastric H. pylori infection statuses were tested with the ~(13) C urea breath test (UBT). The samples were treated with colony polymerase chain reaction (PCR) to obtain double strand DNA (dsDNA) of 104 basepairs (bp) long. A blocker ssDNA was designed and used in thermal treatment of the dsDNA to release the 104-mer tDNA, which contains the 43-mer DNA sequence in the middle. PCR primers were designed, and the tDNA releasing and detection conditions with the biosensor were optimized. The limit of detection with the biosensor was 12 fM dsDNA. The dental plaque detection results correlated quite well with the UBT results, with a sensitivity of 100%, and specificity of 97%. These results indicate that the residence of H. pylori in dental plaque is highly associated with gastric H. pylori infection, and detection of dental plaque samples with our DNA biosensor is promisingly applicable in noninvasive diagnosis of H. pylori infection.
机译:幽门螺杆菌(H. pylori)感染的非侵入性诊断非常有吸引力。这项研究调查了在牙菌斑中从幽门螺杆菌中获取单链DNA(ssDNA)的方法,以及我们先前开发的43-mer幽门螺杆菌DNA生物传感器与获得的目标ssDNA(tDNA)的整合。从34位患者/志愿者中收集了牙菌斑样品,并通过〜(13)C尿素呼气试验(UBT)对他们的胃幽门螺杆菌感染状况进行了检测。用菌落聚合酶链反应(PCR)处理样品,以获得104个碱基对(bp)长的双链DNA(dsDNA)。设计了封闭剂ssDNA,并将其用于dsDNA的热处理中,以释放104-mer tDNA,其中间包含43-mer DNA序列。设计了PCR引物,并优化了生物传感器的tDNA释放和检测条件。用生物传感器检测的极限是12 fM dsDNA。牙菌斑检测结果与UBT结果非常相关,灵敏度为100%,特异性为97%。这些结果表明幽门螺杆菌在牙菌斑中的驻留与胃幽门螺杆菌感染高度相关,用我们的DNA生物传感器检测牙菌斑样品有望用于无创性诊断幽门螺杆菌感染。

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