Suppr超能文献

实时荧光共振能量转移 PCR 对马来丝虫和班氏丝虫的差异检测及其在班氏丝虫感染犬诊断中的评价。

Differential detection of Brugia malayi and Brugia pahangi by real-time fluorescence resonance energy transfer PCR and its evaluation for diagnosis of B. pahangi-infected dogs.

机构信息

Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand.

出版信息

Parasitol Res. 2010 Feb;106(3):621-5. doi: 10.1007/s00436-009-1706-4.

Abstract

A real-time fluorescence resonance energy transfer PCR combined with melting curve analysis was developed for differentiating Brugia malayi and Brugia pahangi DNA in host blood using one set of primers and fluorophore-labeled hybridization probes specific for HhaI repetitive DNA. The differentiation of both species was based on their melting temperatures (Tm). The mean Tm +/- SD of B. malayi and B. pahangi were 56.18+/-0.21 and 52.49+/-0.07, respectively. The method was used for the molecular detection of B. pahangi in infected dog blood samples. The diagnostic sensitivity, specificity, accuracy,and positive and negative predictive values of this method were 100%. The detected mean difference of the Tm might allow the simple discrimination of two related species. This method is fast, sensitive, allows for a high throughput, can be performed on very small volumes, and has potential for diagnosis of B. pahangi-infected dogs in endemic areas as well as for large epidemiological investigations.

摘要

建立了一种实时荧光共振能量转移 PCR 结合熔解曲线分析方法,使用一组针对 HhaI 重复 DNA 的引物和荧光标记杂交探针,可区分宿主血液中的马来丝虫和班氏丝虫 DNA。两种物种的区分基于其熔点 (Tm)。B. malayi 和 B. pahangi 的平均 Tm ± SD 分别为 56.18±0.21 和 52.49±0.07。该方法用于检测感染犬血液样本中的 B. pahangi。该方法的诊断灵敏度、特异性、准确性以及阳性和阴性预测值均为 100%。检测到的 Tm 平均差异可能允许简单地区分两种相关物种。该方法快速、敏感、高通量、可在非常小的体积上进行,并且有可能用于诊断流行地区感染 B. pahangi 的犬,以及进行大规模的流行病学调查。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验