首页> 外文期刊>Journal of Medical Virology >Detection of D151G/N mutations in the neuraminidase gene of influenza A (H3N2) viruses by real-time RT-PCR allelic discrimination assay
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Detection of D151G/N mutations in the neuraminidase gene of influenza A (H3N2) viruses by real-time RT-PCR allelic discrimination assay

机译:通过实时RT-PCR等等辨别测定检测流感A(H3N2)病毒的神经氨酸基因D151G / N突变

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摘要

Single nucleotide polymorphisms (SNPs) at D151 position of neuraminidase (NA) gene of influenza A (H3N2) virus has been associated with drug resistance and increased binding affinity. NA-D151G/N-substitutions of influenza A (H3N2) viruses are frequently induced and selected by culturing in Madin-Darby canine kidney (MDCK) cell lines. It is important to consider and exclude D151G/N mutants after isolation of influenza virus in MDCK cell line; since, the substitutions can highly influence the results of experimental research. The study aims to develop an allelic discrimination real-time reverse transcriptase polymerase chain reaction (RT-PCR) for the screening of D151G/N mutants. Thirty-six influenza A (H3N2) virus isolates were included and screened for D151G/N mutants using allelic discrimination assay. Out of the 36 isolates, 11 isolates (30.5%) were detected as heterozygous for D and G/N substitutions. Twenty-one (58.3%) isolates were identified as homozygous wild type and four isolates (11.1%) were undetermined. Isolates with substitutions at D151 position were sequenced by Sanger sequencing method. The present study demonstrates a rapid and convenient method for primary screening of the mutation after culturing of the influenza virus in MDCK cell lines in order to avoid potential misinterpretations of results and improve the quality of experimental research.
机译:单核苷酸多态性(SNP)在甲型(H3N2)病毒的神经氨酸酶(NA)基因的D151位置(Na)基因的位置与耐药性和增强的亲和力增加。通过在Madin-Darby犬肾(MDCK)细胞系中培养,经常诱导和选择流感A(H3N2)病毒的Na-D151G / N-替代。在分离MDCK细胞系中的流感病毒后,重要的是考虑和排除D151G / N突变体;由于,替代可以影响实验研究的结果。该研究旨在开发一种等位基因辨别实时逆转录酶聚合酶链反应(RT-PCR),用于筛选D151G / N突变体。将三十六种流感A(H3N2)病毒分离物使用等位基因辨别测定筛选并筛选D151G / N突变体。在36个分离物中,将11个分离物(30.5%)被检测为D和G / N替代的杂合。将二十一(58.3%)分离物鉴定为纯合野生型,未确定四个分离物(11.1%)。通过Sanger测序法测序D151位置的取代的分离物。本研究表明,在MDCK细胞系中培养流感病毒后突变的初次筛选的快速和方便的方法,以避免结果误解并提高实验研究的质量。

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