Sun Zhao-Hui, Yang Hui-Lan, Wei Min, Wang Shu-Yan, Wang Cong-Rong, Shi Yu-Ling, Ma Wen-Li
Clinical Laboratory, Guangzhou Army General Hospital, Guangzhou 510010, China.
Zhonghua Gan Zang Bing Za Zhi. 2007 Nov;15(11):816-20.
To prepare oligo microarrays for hepatitis virus detection and genotyping.
By analyzing the DNA or cDNA of HBV, HDV and 4 different genotypes of HCV with the BLAST program, a group of specific sequences for the candidate probes was specified. Array Designer 3.0 software was applied to analyze the candidates to select probes with high specificity, identical length and similar melting temperature (Tm). Altogether 16, 8 and 68 oligonucleotide probes were designed for diagnosis of HBV, HDV, and genotyping HCV. Following the synthesizing and purification, oligo probes were deposited on oligonucleotide chips as microarrays for hepatitis virus detection and genotyping. The samples were labeled by RD-PCR method. Hybridization results were analyzed to cross out those probes with low specificity and sensitivity, and those with signal to noise ratios (SNR) less than 4.0.
Two types of gene chips were successfully developed: microarrays for HBV and HDV simultaneous detection and for HCV genotyping.
Using oligo probes to construct gene chips for clinical diagnosis of hepatitis virus is a simple and effective method. It may be widely used in detecting hepatitis viruses and their genotyping in clinical settings.
制备用于肝炎病毒检测和基因分型的寡核苷酸微阵列。
通过使用BLAST程序分析乙肝病毒(HBV)、丁肝病毒(HDV)以及丙肝病毒(HCV)4种不同基因型的DNA或cDNA,确定了一组用于候选探针的特异性序列。应用Array Designer 3.0软件对候选序列进行分析,以选择具有高特异性、相同长度和相似解链温度(Tm)的探针。总共设计了16条、8条和68条寡核苷酸探针用于HBV诊断、HDV诊断以及HCV基因分型。经过合成和纯化后,将寡核苷酸探针点样到寡核苷酸芯片上,制成用于肝炎病毒检测和基因分型的微阵列。样本采用RD-PCR方法进行标记。对杂交结果进行分析,剔除特异性和敏感性低以及信噪比(SNR)小于4.0的探针。
成功研制出两种类型的基因芯片:用于同时检测HBV和HDV以及HCV基因分型的微阵列。
使用寡核苷酸探针构建基因芯片用于肝炎病毒的临床诊断是一种简单有效的方法。它可能广泛应用于临床环境中肝炎病毒的检测及其基因分型。