Chen Xiao-Fan, Li Tian-Run, Yang Hong, Shao Yong, Zhang Jie, Zhang Wei, Yu Bo, Wei Zhun, Wu Bo, Yu Lin
Biomedical Research Institute, Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center, Shenzhen, Guangdong, China.
Department of Dermatology, Shenzhen Hospital Peking University, Shenzhen, Guangdong, China.
J Clin Lab Anal. 2016 Jul;30(4):319-25. doi: 10.1002/jcla.21858. Epub 2015 May 13.
Human cytomegalovirus (CMV) is an opportunistic pathogen that can be treated with ganciclovir. Mutations in the UL97 gene of CMV render the virus ganciclovir resistance. These include H520Q and C603W mutations, against which we developed a novel genotyping assay for their identification.
PCR reactions were performed to amplify fragments of the UL97 gene containing H520Q or C603W mutations. High resolution melting analysis (HRMA) coupled with unlabeled DNA probes was employed to identify the shift in melting temperature of the probe-template complex, which reflexes the presence of point mutations.
Melting point analysis performed on the dimeric DNA of PCR products of UL97 gene could not identify mutations in the gene. When coupled to unlabeled probes, point mutations in UL97 can be identified by analyzing the melting curve of probe-template complex. When WT and mutant UL97 DNAs were mixed together to mimic heterogeneous viral population in clinical samples, the genotyping assay is sensitive enough to detect H520Q and C603W mutants that constitute 10% of total DNA input.
Probe-based HRMA is effective in detecting H520Q and C603W mutations in the UL97 gene of CMV.
人巨细胞病毒(CMV)是一种机会性病原体,可用更昔洛韦治疗。CMV的UL97基因突变会使病毒产生更昔洛韦抗性。这些突变包括H520Q和C603W突变,我们针对这些突变开发了一种新型基因分型检测方法来进行鉴定。
进行PCR反应以扩增包含H520Q或C603W突变的UL97基因片段。采用高分辨率熔解分析(HRMA)结合未标记的DNA探针来鉴定探针 - 模板复合物熔解温度的变化,这反映了点突变的存在。
对UL97基因PCR产物的二聚体DNA进行熔点分析无法鉴定该基因中的突变。当与未标记的探针结合时,通过分析探针 - 模板复合物的熔解曲线可以鉴定UL97中的点突变。当将野生型和突变型UL97 DNA混合在一起以模拟临床样本中的异质病毒群体时,该基因分型检测方法足够灵敏,能够检测到占总DNA输入量10%的H520Q和C603W突变体。
基于探针的HRMA可有效检测CMV的UL97基因中的H520Q和C603W突变。