PCR -杂交-荧光法定量检测临床材料中乙型肝炎病毒DNA试剂盒的研制

O. N. Zhigaleva, S. G. Mardanly, T. Yu. Gashenko, I. I. Ermolaev
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引用次数: 0

摘要

的相关性。乙型肝炎病毒(HBV)是影响全世界人群的最常见病毒感染之一,可导致慢性肝炎、肝硬化和肝细胞癌。目前,世界上3%的人口感染了乙型肝炎病毒,并有发展为危及生命的肝脏疾病的危险。免疫和分子生物学方法检测HBV目前用于实验室诊断。聚合酶链反应(PCR)是目前检测和定量HBV最灵敏的方法。HBV DNA定量被广泛用于监测HBV感染的抗病毒治疗。的目标。目的:研制一种用于HBV DNA定量的实时PCR试剂盒。材料和方法。该研究共使用了200份HBV阳性和阴性的血浆和血清样本。将开发的试剂盒的性能与俄罗斯其他商业注册的HBV诊断试剂盒的使用进行了比较。此外,利用GeneBank系统分析所有现有病毒基因型的核苷酸序列,选择引物。结果和讨论。对200份临床血清和血浆标本的实时荧光定量PCR检测结果进行对比分析,试剂盒的诊断敏感性为100%,特异性为100%。这些引物是针对POL基因区域开发的。该试剂盒能够检测所有类型的病毒基因型。结论。开发的试剂盒可以检测乙型肝炎病毒,并在70分钟内确定其数量。除了大量的基因型和亚基因型外,该病毒的特点是基因组发生突变变化,这使其诊断复杂化,并因此影响了正在进行的药物治疗。开发过程中考虑了引物和探针选择的保守区域,获得的测序结果适用于所有HBV基因型。该试剂盒旨在监测HBV感染患者,并允许分析不同的HBV病毒载量。
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Development of a Reagent Kit for the Quantitative Determination of Hepatitis B Virus (HBV) DNA in Clinical Material by PCR with Hybridization-Fluorescence Detection
Relevance. Hepatitis B virus (HBV) is one of the most common viral infections affecting people worldwide and can lead to chronic hepatitis, cirrhosis and hepatocellular carcinoma. Currently 3% of the world's population are infected with hepatitis B virus and are at risk of developing life-threatening liver disease. Immunological and molecular biological methods of detection of HBV are currently used in laboratory diagnostics. The polymerase chain reaction (PCR) is currently the most sensitive method for the detection and quantification of HBV. HBV DNA quantification is widely used to monitor the antiviral treatment of HBV infection. Aim. To develop a real-time PCR kit for the quantification of HBV DNA. Materials and methods. A total of 200 plasma and serum samples positive and negative for HBV were used in the development. The performance of the developed kit was compared with the use of other commercially registered HBV diagnostic kits in Russia. Additionally, the nucleotide sequences of all existing virus genotypes analysed for the selection of primers using GeneBank system. Results and discussion. Comparison analysis of the results of quantitative determination by real-time PCR in 200 clinical serum and blood plasma samples showed that the diagnostic sensitivity of the developed kit was 100% and specificity 100%. The primers developed specific to the POL gene region. The kit is capable of detecting all types of virus genotypes. Conclusions. The developed reagent kit allows detection of hepatitis B virus and determination of its quantity within 70 minutes. In addition to a large number of genotypes and subgenotypes, the virus is characterized by mutational changes in the genome, which complicates its diagnosis and, as a consequence, the ongoing therapy with drugs. Conservative regions for primer and probe selection taken into account in the development, and the sequencing results obtained are applicable to all HBV genotypes. The reagent kit is designed to monitor HBV infected patients and will allow the analysis of different HBV viral loads.
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来源期刊
Epidemiologiya i Vaktsinoprofilaktika
Epidemiologiya i Vaktsinoprofilaktika Medicine-Infectious Diseases
CiteScore
1.10
自引率
0.00%
发文量
58
审稿时长
8 weeks
期刊最新文献
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