| 钟华敏 谢永强 邓秋连 黄莲芬 钟玉葵.一种检测马尔尼菲青霉菌实时荧光定量PCR 方法
的建立和应用[J].现代生物医学进展英文版,2014,14(7):1247-1249. |
| 一种检测马尔尼菲青霉菌实时荧光定量PCR 方法
的建立和应用 |
| Development and Application of a Quantitative Real-Time PCR Assayfor Detection of PenicilliumMarneffei |
| |
| DOI： |
| 中文关键词: 马尔尼菲青霉菌 实时荧光定量PCR 荧光染料 |
| 英文关键词: Penicilliummarneffei Real-Time PCR Fluorescent dye |
| 基金项目:广州市医药卫生科技项目（201102A213023） |
|
| Hits: 973 |
| Download times: 1277 |
| 中文摘要: |
| 目的：建立一种检测马尔尼菲青霉菌的实时荧光定量PCR的方法。方法：针对马尔尼菲青霉菌5.8S rRNA 设计特异性PCR
引物,采用核酸荧光染料SYBR GreenⅠ进行实时荧光定量PCR检测，探讨该方法的灵敏度和特异性,并进行临床样品检测验证。
结果：该方法的特异性较好,与该菌属内的其他细菌间无交叉反应；灵敏度可检测出10 个细胞/mL全血，在检测范围内线性良好，
相关系数R2=0.981。临床样品检测和传统的培养方法结果完全相符。结论：该方法特异性好，灵敏度高，操作简单，检测时间短；临
床样品检测具有很好的准确性，从本研究的结果显示实时荧光定量PCR 方法在检测马尔尼菲青霉菌中的应用可以大大缩短临床
的诊断时间，提高临床诊断的准确度和效率。 |
| 英文摘要: |
| Objective:To develop a quantitative Real-Time PCR assay for detection of penicillium marneffei.Methods:A pair of
PCR primers of penicillium marneffei 5.8S rRNA was designed, and Real-Time PCR assay with SYBR GreenⅠ fluorescent dye was
performed. Specificity and sensitivity of the assay were verified. The accuracy of the assay was verified, and clinic samples were detected
with the PCR assay. Results:The PCR assay was specific to penicillium marneffei, and it had not cross-react with other strains of this
Genus. Its detection sensitivity reached 10 cells per ml of blood. It had good linearity in the detection range, and R2 is 0.981. The results
of detecting clinic samples were consistent with that of traditional culture method.Conclusion:The quantitative Real-Time PCR assay
has good specificity and sensitivity. The method is easy manipulation and quick. The good accuracy of the assay was shown in detecting
clinic samples. The clinic application of the quantitative Real-Time PCR can accelerate the diagnosis of penicilliosis mamefei, and improve
the diagnostic accuracy and efficiency. |
|
View Full Text
View/Add Comment Download reader |
| Close |
