Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand.
Parasitol Res. 2010 Feb;106(3):621-5. doi: 10.1007/s00436-009-1706-4.
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.
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。