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首页> 外文期刊>Journal of Pure & Applied Microbiology >Comparison of PCR and Culture for Detection of Legionella pneumophila in Bronchoalveolar Fluid Samples
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Comparison of PCR and Culture for Detection of Legionella pneumophila in Bronchoalveolar Fluid Samples

机译:PCR和培养物检测支气管肺泡液样品中嗜肺军团菌的比较

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摘要

Atypical pneumonia due to Legionella pneumophila is termed Legionnaires' disease. Clinical manifestations are often undistinguishable from other causes of pneumonia. Laboratory test such as culture, serological test and molecular detection facilitateddiagnosis. The aim of the present study was use of polymerase chain reaction with primers that amplify a 654bp pair segment of the coding region of the 16S rRNA gene of L. pneumophila in bronchoalveolar lavage fluid (BALF) specimens and evaluated results with Culture. A total of fifty archived specimens from patients were evaluated. 8% cases are positive for the PCR. 4% of specimens were culture positive for legionella. 4% positive cases in PCR method had a negative result in culture. After sequencing,specificity and sensitivity for PCR in this study was 100%. Detection of legionella DNA in samples is valuable method for rapid diagnosis. Legionella, PCR, culture, Bronchoalveolar lavage.
机译:由于嗜肺军团杆菌引起的非典型性肺炎被称为军团病。临床表现通常与肺炎的其他原因没有区别。培养,血清学检测和分子检测等实验室检查有助于诊断。本研究的目的是使用聚合酶链反应与在支气管肺泡灌洗液(BALF)标本中扩增肺炎链球菌16S rRNA基因编码区的654bp对片段的引物,并通过培养评估结果。总共评估了来自患者的五十份存档标本。 PCR阳性率为8%。 4%的标本为军团菌培养阳性。 PCR方法中有4%的阳性病例在培养中有阴性结果。测序后,本研究中PCR的特异性和敏感性为100%。检测样品中的军团菌DNA是快速诊断的宝贵方法。军团菌,PCR,培养,支气管肺泡灌洗。

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