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首页> 外文期刊>Journal of Clinical Microbiology >Microarray-Based Identification of Bacteria in Clinical Samples by Solid-Phase PCR Amplification of 23S Ribosomal DNA Sequences
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Microarray-Based Identification of Bacteria in Clinical Samples by Solid-Phase PCR Amplification of 23S Ribosomal DNA Sequences

机译:固相PCR扩增23S核糖体DNA序列的基于微阵列的临床样品细菌鉴定

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The rapid identification of the bacteria in clinical samples is important for patient management and antimicrobial therapy. We describe a DNA microarray-based PCR approach for the quick detection and identification of bacteria from cervical swab specimens from mares. This on-chip PCR method combines the amplification of a variable region of bacterial 23S ribosomal DNA and the simultaneous sequence-specific detection on a solid phase. The solid phase contains bacterial species-specific primers covalently bound to a glass support. During the solid-phase amplification reaction the polymerase elongates perfectly matched primers and incorporates biotin-labeled nucleotides. The reaction products are visualized by streptavidin-cyanine 5 staining, followed by fluorescence scanning. This procedure successfully identified from pure cultures 22 bacteria that are common causes of abortion and sterility in mares. Using the on-chip PCR method, we also tested 21 cervical swab specimens from mares for the presence of pathogenic bacteria and compared the results with those of conventional bacteriological culture methods. Our method correctly identified the bacteria in 12 cervical swab samples, 8 of which contained more than one bacterial species. Due to the higher sensitivity of the on-chip PCR, this method identified bacteria in five cervical swab samples which were not detected by the conventional identification procedure. Our results show that this method will have great potential to be incorporated into the routine microbiology laboratory.
机译:快速鉴定临床样品中的细菌对于患者管理和抗菌治疗很重要。我们描述了一种基于DNA微阵列的PCR方法,用于快速检测和鉴定母马宫颈拭子标本中的细菌。这种片上PCR方法结合了细菌23S核糖体DNA可变区的扩增和固相上同时的序列特异性检测。固相包含共价结合至玻璃载体的细菌物种特异性引物。在固相扩增反应过程中,聚合酶会延长完美匹配的引物,并掺入生物素标记的核苷酸。通过链霉亲和素-花青5染色,然后进行荧光扫描,使反应产物可视化。该程序成功地从纯培养物中鉴定出了22种细菌,它们是母马流产和不育的常见原因。使用芯片上PCR方法,我们还测试了21头母马的宫颈拭子标本中是否存在病原细菌,并将结果与​​常规细菌培养方法进行了比较。我们的方法正确鉴定了12个宫颈拭子样本中的细菌,其中8个样本包含一种以上细菌。由于片上PCR的较高灵敏度,因此该方法可以鉴定出五个宫颈拭子样品中的细菌,而这些细菌是常规鉴定程序无法检测到的。我们的结果表明,该方法将有很大的潜力被纳入常规微生物学实验室。

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