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巴西儿童中1型人类免疫缺陷病毒(HIV-1)nef基因的宿主内和宿主间变异性

Intrahost and interhost variability of the HIV type 1 nef gene in Brazilian children.

作者信息

Cavalieri Elizabeth, Florido Camila, Leal Elcio, Machado Daisy Maria, Camargo Michelle, Diaz Ricardo S, Janini Luiz Mario

机构信息

Federal University of São Paulo, São Paulo, Brazil.

出版信息

AIDS Res Hum Retroviruses. 2009 Nov;25(11):1129-40. doi: 10.1089/aid.2009.0061.

Abstract

Many aspects of HIV-1 pathogenesis are affected by Nef protein activity, and efforts have been made to study variation in the nef gene and how that variation relates to disease outcome. We studied the genetic diversity of the nef gene in distinct clones obtained from the same patient (intrahost) and in sequences obtained from different hosts (interhost). The set of sequences analyzed was obtained from HIV-1-infected Brazilian children and contained 112 clones from 25 children (intrahost samples), as well as 55 sequences from epidemiologically unlinked children (interhost samples). We found extensive site polymorphisms and amino acid length variations, mainly in the amino terminal region of the nef gene, between the myristoylation motif (MGxxxS) and the MHC-1 downregulation motif (Rxx). Analysis of the sequences deposited in the Los Alamos HIV sequences database ( www.hiv.lanl.gov ) indicated that the most frequent motif at the MHC-1 downregulation site in the subtype B strain is R(86%)A(64%)E(82%) (n = 1040) and R(78%)T(74%)E(56%) in the subtype C strain (n = 549). Conversely, the Brazilian subtype B isolates presented the motif R(81%)T(62%)E(67%) at this site (n = 64). A detailed analysis of selective pressures identified a concentration of codons under strong positive selection in the amino terminal region of the nef gene. We also determined that different sites are under positive selection in the subtype B and subtype C viruses. The amino acid composition in the MHC-1 downregulation motif of the nef gene in our sequences may indicate a distinct adaptive pattern of HIV-1 subtype B to the Brazilian host population.

摘要

HIV-1发病机制的许多方面都受到Nef蛋白活性的影响,人们已努力研究nef基因的变异以及该变异与疾病转归的关系。我们研究了从同一患者体内获得的不同克隆(宿主内)以及从不同宿主获得的序列(宿主间)中nef基因的遗传多样性。所分析的序列集来自感染HIV-1的巴西儿童,包括来自25名儿童的112个克隆(宿主内样本),以及来自无流行病学关联儿童的55个序列(宿主间样本)。我们发现,在豆蔻酰化基序(MGxxxS)和MHC-1下调基序(Rxx)之间的nef基因氨基末端区域存在广泛的位点多态性和氨基酸长度变异。对洛斯阿拉莫斯HIV序列数据库(www.hiv.lanl.gov)中存储的序列分析表明,B亚型毒株中MHC-1下调位点最常见的基序是R(86%)A(64%)E(%)(n = 1040),C亚型毒株中是R(78%)T(74%)E(56%)(n = 549)。相反,巴西B亚型分离株在该位点的基序为R(81%)T(62%)E(67%)(n = 64)。对选择压力的详细分析确定了nef基因氨基末端区域有一组密码子处于强正选择之下。我们还确定,B亚型和C亚型病毒中不同的位点处于正选择之下。我们序列中nef基因MHC-1下调基序的氨基酸组成可能表明HIV-1 B亚型对巴西宿主人群有独特的适应性模式。

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