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使用单组荧光共振能量转移探针通过熔解曲线分析确定丙型肝炎病毒基因型

Hepatitis C genotype determination by melting curve analysis with a single set of fluorescence resonance energy transfer probes.

作者信息

Bullock Grant C, Bruns David E, Haverstick Doris M

机构信息

Department of Pathology, University of Virginia, Charlottesville, VA 22908, USA.

出版信息

Clin Chem. 2002 Dec;48(12):2147-54.

Abstract

BACKGROUND

The genotype of hepatitis C virus (HCV) is a predictor of antiviral therapeutic response. We describe an approach for HCV genotype determination by real-time PCR and melting curve analysis.

METHODS

After automated nucleic acid extraction, we used reverse transcription-PCR in a block cycler to amplify nucleotides 6-329 of the 5'-untranslated region of HCV. The product was further amplified by single-tube real-time seminested PCR in a LightCycler instrument (Roche). The final product was analyzed by melting curves with the use of fluorescence resonance energy transfer (FRET) probes. The FRET sensor probe was directed at nucleotides 151-170 of type 1 HCV and was designed to distinguish types 1a/b, 2a/c, 2b, 3a, and 4, with melting temperatures (T(m)s) predicted to differ by 1 degrees C. Genotypes were compared in a blinded fashion with those of the INNO-LiPA(TM) test (Bayer Diagnostics) on 111 serum samples.

RESULTS

In preliminary experiments, the Mg(2+) concentration was found to be critical in allowing clear separation of melting points, with the best separation at a Mg(2+) concentration of 2 mmol/L. The results for 111 samples clustered at expected T(m)s for genotypes 1a/b (n = 78), 2a/c (n = 2), 2b (n = 11), 3a (n = 14), and 4 (n = 2). Of the 111 samples, results for 110 were concordant with the comparison method at the level of type 1, 2, 3, or 4. Subtyping results were discordant for two samples, both of type 2. For 108 samples concordant with INNO-LiPA at the genotype and subtype levels, the mean T(m)s were 64.1, 59.5, 54.2, 52.6, and 50.1 degrees C for types 1a/b, 2a/c, 4, 2b, and 3a, respectively, with SDs of 0.2, 0.3, 0.3, 0.2, and 0.3 degrees C. All 78 samples identified as type 1 were concordant with results of the comparison method.

CONCLUSIONS

Melting analysis with a single pair of FRET probes can rapidly provide information about HCV genotypes and identifies type 1 samples with high specificity.

摘要

背景

丙型肝炎病毒(HCV)基因型是抗病毒治疗反应的一个预测指标。我们描述了一种通过实时聚合酶链反应(PCR)和熔解曲线分析来确定HCV基因型的方法。

方法

在自动核酸提取后,我们在块式循环仪中使用逆转录PCR扩增HCV 5'非翻译区的核苷酸6 - 329。产物在LightCycler仪器(罗氏公司)中通过单管实时半巢式PCR进一步扩增。最终产物使用荧光共振能量转移(FRET)探针通过熔解曲线进行分析。FRET传感器探针针对1型HCV的核苷酸151 - 170,设计用于区分1a/b、2a/c、2b、3a和4型,预测熔解温度(Tm)相差1℃。对111份血清样本的基因型与INNO - LiPA(商标)检测(拜耳诊断公司)的结果进行盲法比较。

结果

在初步实验中,发现Mg(2+)浓度对于清晰分离熔解点至关重要,在Mg(2+)浓度为2 mmol/L时分离效果最佳。111份样本的结果聚集在1a/b型(n = 78)、2a/c型(n = 2)、2b型(n = 11)、3a型(n = 14)和4型(n = 2)的预期Tm处。在111份样本中,110份样本在1、2、3或4型水平上与比较方法的结果一致。两个2型样本的亚型分型结果不一致。对于108份在基因型和亚型水平上与INNO - LiPA一致的样本,1a/b型、2a/c型、4型、2b型和3a型的平均Tm分别为64.1、59.5、54.2、52.6和50.1℃,标准差分别为0.2、0.3、0.3、0.2和0.3℃。所有78份被鉴定为1型的样本与比较方法的结果一致。

结论

使用一对FRET探针进行熔解分析可快速提供有关HCV基因型的信息,并能高度特异性地鉴定1型样本。

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