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Evaluation of a real-time method of simultaneous amplification and testing in diagnosis of Mycoplasma pneumoniae infection in children with pneumonia

机译:实时同步扩增和检测方法在肺炎患儿肺炎支原体感染诊断中的价值

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摘要

Mycoplasma pneumoniae (M. pneumoniae) infection can cause community acquired pneumonia in children. A real-time method of simultaneous amplification and testing of M. pneumoniae (SAT-MP) was developed to diagnose M. pneumoniae targeting a region of the ribosomal RNA. The SAT-MP assay can accurately identify M. pneumoniae with a detection range from 101 to 107 CFU/ml. In this study, the specimens from 315 children with pneumonia were collected and analyzed by SAT-MP in parallel with real-time PCR method and IgM ELISA assay. The positive rates of these specimens examined by SAT-MP assay, real-time PCR method and IgM ELISA assay were 16.51%, 15.56% and 12.70% respectively. While there was statistical significance (p = 0.04) between SAT-MP assay and IgM ELISA assay, no statistical significance (p = 0.25) was found between SAT-MP assay and real-time PCR method and these two methods had high consistency (kappa value = 0.97). These findings indicate that the newly developed SAT-MP assay is a rapid, sensitive and specific method for identifying M. pneumoniae with potential clinical application in the early diagnosis of M. pneumoniae infection.
机译:肺炎支原体(M. pneumoniae)感染可引起儿童社区获得性肺炎。开发了一种同时扩增和测试肺炎支原体的实时方法(SAT-MP),以诊断靶向核糖体RNA区域的肺炎支原体。 SAT-MP检测可以准确鉴定肺炎支原体,检测范围为10 1 至10 7 CFU / ml。在这项研究中,收集了315例肺炎患儿的标本,并通过SAT-MP结合实时PCR方法和IgM ELISA分析进行了分析。 SAT-MP,实时荧光定量PCR和IgM ELISA检测的阳性率分别为16.51%,15.56%和12.70%。尽管SAT-MP测定法和IgM ELISA测定法之间具有统计学意义(p = 0.04),但SAT-MP测定法和实时PCR方法之间没有统计学意义(p = 0.25),并且这两种方法具有高度一致性(kappa)值= 0.97)。这些发现表明,新开发的SAT-MP测定法是一种快速,灵敏和特异的鉴定肺炎支原体的方法,在肺炎支原体感染的早期诊断中具有潜在的临床应用价值。

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