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Detection of Urogenital Mycoplasmas using Culture and PCR: a Descriptive Pilot Study

机译:使用培养和PCR检测泌尿生殖道支原体:描述性试验研究

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Mycoplasmas, as human urogenital tract pathogens, are associated with infections, reproductive failures and adverse pregnancy outcomes. Several methods have been used to detect genitourinary Mycoplasmas, each having their own limitations, advantages and disadvantages. In the present study, we used microbial culture and PCR to detect Mycoplasmas in urogenital specimens with the aim of comparing detection rate, sensitivity and specificity of the two methods. In this study, 30 urogenital samples including 17 vaginal swabs, 7 male urine and 6 female urine samples were collected from patients referring to hospitals regardless of their disease and studied for Mycoplasmas by culture (using two media: PPLO broth and PPLO agar) and PCR. Of the total 30 specimens, Mycoplasmas were detected in 14 PPLO broth medium, 11 PPLO agar medium and 11 PCR sample reactions. Accordingly, the sensitivity and specificity of the PCR method was determined 100 and 95% respectively while culture was found to have a sensitivity of 77% and specificity of 66%. We found PCR based on 16S rRNA sequences to be highly sensitive and specific offering a rapid, easy and cost benefit method for detection of Mycoplasmas in comparison to microbial culture method.
机译:支原体作为人类泌尿生殖道病原体,与感染,生殖功能衰竭和不良妊娠结局有关。已经使用了几种方法来检测生殖泌尿道支原体,每种方法都有其自身的局限性,优点和缺点。在本研究中,我们使用微生物培养和PCR检测泌尿生殖道标本中的支原体,旨在比较两种方法的检测率,敏感性和特异性。在这项研究中,从无论病情如何均转诊给医院的患者中收集了30例泌尿生殖道标本,包括17个阴道拭子,7个男性尿液和6个女性尿液样本,并通过培养(使用两种培养基:PPLO肉汤和PPLO琼脂)和PCR研究了支原体。在总共30个样本中,在14种PPLO肉汤培养基,11种PPLO琼脂培养基和11种PCR样品反应中检测到支原体。因此,测定PCR方法的灵敏度和特异性分别为100%和95%,而发现培养物具有77%的灵敏度和66%的特异性。我们发现基于16S rRNA序列的PCR具有高度的敏感性和特异性,与微生物培养法相比,提供了一种快速,简便且成本效益高的支原体检测方法。

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