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人类免疫缺陷病毒1型F亚型基因组中p6 gag蛋白的序列变异性及gag/pol的共同进化

Sequence variability in p6 gag protein and gag/pol coevolution in human immunodeficiency type 1 subtype F genomes.

作者信息

Rossi Andres H, Rocco Carlos A, Mangano Andrea, Sen Luisa, Aulicino Paula C

机构信息

Laboratorio de Biología Celular y Retrovirus, Hospital de Pediatría Juan P. Garran, CONICET, Buenos Aires, Argentina.

出版信息

AIDS Res Hum Retroviruses. 2013 Jul;29(7):1056-60. doi: 10.1089/aid.2012.0311. Epub 2013 Mar 26.

Abstract

Polymorphisms occurring at the p6gag protein of HIV-1 have been previously found to have an impact on viral fitness and antiretroviral (ARV) resistance, mainly on subtype B genomes. We compared p6gag variability in a large group of 165 subtype F gag-pol sequences, with 36 subtype B sequences from the same study source, and identified sites of gag-pol coevolution under ARV selection pressure. Subtype-specific differences in the frequency of point mutations, insertions, and deletions previously associated with ARV resistance were found. Also, in our dataset of subtype F genomes a strong association between mutation P5L in the p1/p6 cleavage region of gag and the nelfinavir (NFV) resistance mutation N88D(PR) was found with no impact on the preference for any of the NFV resistance pathways.

摘要

先前已发现,HIV-1的p6gag蛋白上出现的多态性会影响病毒适应性和抗逆转录病毒(ARV)耐药性,主要影响B亚型基因组。我们比较了来自同一研究来源的165个F亚型gag-pol序列的大样本组与36个B亚型序列的p6gag变异性,并确定了在ARV选择压力下gag-pol共同进化的位点。发现了先前与ARV耐药性相关的点突变、插入和缺失频率的亚型特异性差异。此外,在我们的F亚型基因组数据集中,发现gag的p1/p6切割区域中的P5L突变与奈非那韦(NFV)耐药性突变N88D(PR)之间存在强关联,且对任何NFV耐药途径的偏好均无影响。

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