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人类免疫缺陷病毒的Pol基因准种:来自未接受药物治疗患者的病毒中与耐药性相关的突变

Pol gene quasispecies of human immunodeficiency virus: mutations associated with drug resistance in virus from patients undergoing no drug therapy.

作者信息

Nájera I, Holguín A, Quiñones-Mateu M E, Muñoz-Fernández M A, Nájera R, López-Galíndez C, Domingo E

机构信息

Centro de Biología Molecular Severo Ochoa (Consejo Superior de Investigaciones Científicas-UAM, Universidad Autónoma de Madrid, Spain.

出版信息

J Virol. 1995 Jan;69(1):23-31. doi: 10.1128/JVI.69.1.23-31.1995.

Abstract

The nucleotide sequences of two pol gene regions (codons 41 to 108 and 181 to 219 of reverse transcriptase) of 60 human immunodeficiency virus type 1 genomes obtained directly from primary lymphocytes from infected individuals are reported. In addition, the mutant spectra of several quasispecies have been sampled by repetitive sequencing of molecular clones representing the same pol genomic regions. Average mutation frequencies ranged from 1.6 x 10(-2) to 3.4 x 10(-2) substitutions per nucleotide for independent samples (relative to their consensus nucleotide sequence) and from 3.6 x 10(-3) to 1.1 x 10(-2) substitutions per nucleotide for individual quasispecies distributions. Several mutations leading to amino acid substitutions related to loss of sensitivity to reverse transcriptase inhibitors have been identified in samples from patients not subjected to antiretroviral therapy. Mutation frequencies in the codons previously identified as involved in resistance to reverse transcriptase inhibitors were very similar to the average mutation frequencies in the pol region analyzed. Thus, the finding of mutations related to drug resistance (even in the absence of positive selection by the corresponding drugs) is the expected consequence of the statistical distribution of mutations along the pol gene. The presence of such critical amino acid replacements in human immunodeficiency virus type 1 populations underscores the importance of viral quasispecies as reservoirs of phenotypic virus variants and has a number of implications for AIDS control.

摘要

报道了直接从感染个体的原代淋巴细胞中获得的60个1型人类免疫缺陷病毒基因组的两个pol基因区域(逆转录酶的第41至108密码子和第181至219密码子)的核苷酸序列。此外,通过对代表相同pol基因组区域的分子克隆进行重复测序,对几个准种的突变谱进行了采样。独立样本的平均突变频率为每核苷酸1.6×10⁻²至3.4×10⁻²个替换(相对于其共有核苷酸序列),个体准种分布的平均突变频率为每核苷酸3.6×10⁻³至1.1×10⁻²个替换。在未接受抗逆转录病毒治疗的患者样本中,已鉴定出几种导致与对逆转录酶抑制剂敏感性丧失相关的氨基酸替换的突变。先前确定与逆转录酶抑制剂耐药性有关的密码子中的突变频率与所分析的pol区域中的平均突变频率非常相似。因此,发现与耐药性相关的突变(即使在没有相应药物的阳性选择的情况下)是pol基因沿线突变统计分布的预期结果。1型人类免疫缺陷病毒群体中此类关键氨基酸替换的存在强调了病毒准种作为表型病毒变体库的重要性,并对艾滋病控制有许多影响。

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本文引用的文献

1
Rates of spontaneous mutation among RNA viruses.RNA病毒的自发突变率。
Proc Natl Acad Sci U S A. 1993 May 1;90(9):4171-5. doi: 10.1073/pnas.90.9.4171.

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