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首页> 外文期刊>Virus Genes >Comparative nucleotide sequence analyses of the entire genomes of B95a cell-isolated and vero cell-isolated measles viruses from the same patient.
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Comparative nucleotide sequence analyses of the entire genomes of B95a cell-isolated and vero cell-isolated measles viruses from the same patient.

机译:对来自同一患者的B95a细胞分离的和麻疹细胞分离的麻疹病毒的整个基因组进行比较核苷酸序列分析。

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摘要

Experimental infection of monkeys with the IC-B strain of measles virus (MV), which was isolated in marmoset B lymphoblastoid B95a cells from an acute measles patient, caused clinical signs typical for measles, while infection by the IC-V strain isolated in African green monkey kidney Vero cells from the same patient did not cause any clinical signs in infected monkeys. The IC-B strain replicated only in B95a cells, whereas the IC-V strain replicated in both B95a and Vero cells (3,6). To clarify which gene or mutation(s) was responsible for the difference in these phenotypes, the nucleotide sequences of the entire genomes of the IC-B and IC-V strains were determined. Comparative nucleotide sequence analyses revealed only two nucleotide differences, one in the P/V/C gene and the other in the M gene, predicting amino acid differences in the P, V and M proteins and a 19 amino acid deletion in the C protein of the IC-V strain. The truncation in the C protein was confirmed for the IC-V strain by immunoprecipitation using the C protein specific antiserum. No nucleotide difference was found in the envelope H gene. These results indicated that nucleotide difference(s) in the P/V/C or/and M gene, and not H gene, was responsible for the different cell tropism and pathogenicity of MV in this case.
机译:从急性麻疹患者的mar猴B淋巴母细胞B95a细胞中分离出的麻疹病毒IC-B株对猴子进行实验性感染,引起了典型的麻疹临床症状,而非洲人分离出的IC-V株感染了麻疹病毒。绿猴肾脏来自同一患者的Vero细胞未在感染的猴中引起任何临床体征。 IC-B株仅在B95a细胞中复制,而IC-V株在B95a和Vero细胞中均复制(3,6)。为了弄清楚哪个基因或突变是造成这些表型差异的原因,确定了IC-B和IC-V菌株整个基因组的核苷酸序列。比较核苷酸序列分析显示只有两个核苷酸差异,一个在P / V / C基因中,另一个在M基因中,预测了P,V和M蛋白的氨基酸差异和C蛋白的19个氨基酸缺失。 IC-V应变。通过使用C蛋白特异性抗血清的免疫沉淀法确认了IC-V株C蛋白的截短。在包膜H基因中未发现核苷酸差异。这些结果表明,在这种情况下,P / V / C或/和M基因而不是H基因的核苷酸差异是造成MV的不同细胞嗜性和致病性的原因。

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