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精英控制者中1型人类免疫缺陷病毒的基因特征:不存在明显的基因缺陷或常见氨基酸变化。

Genetic characterization of human immunodeficiency virus type 1 in elite controllers: lack of gross genetic defects or common amino acid changes.

作者信息

Miura Toshiyuki, Brockman Mark A, Brumme Chanson J, Brumme Zabrina L, Carlson Jonathan M, Pereyra Florencia, Trocha Alicja, Addo Marylyn M, Block Brian L, Rothchild Alissa C, Baker Brett M, Flynn Theresa, Schneidewind Arne, Li Bin, Wang Yaoyu E, Heckerman David, Allen Todd M, Walker Bruce D

机构信息

Partners AIDS Research Center, Massachusetts General Hospital, Charlestown, Massachusetts 02129, USA.

出版信息

J Virol. 2008 Sep;82(17):8422-30. doi: 10.1128/JVI.00535-08. Epub 2008 Jun 18.

Abstract

Despite reports of viral genetic defects in persons who control human immunodeficiency virus type 1 (HIV-1) in the absence of antiviral therapy, the extent to which such defects contribute to the long-term containment of viremia is not known. Most previous studies examining for such defects have involved small numbers of subjects, primarily focused on subjects expressing HLA-B57, or have examined single viral genes, and they have focused on cellular proviral DNA rather than plasma viral RNA sequences. Here, we attempted viral sequencing from 95 HIV-1 elite controllers (EC) who maintained plasma viral loads of <50 RNA copies/ml in the absence of therapy, the majority of whom did not express HLA-B57. HIV-1 gene fragments were obtained from 94% (89/95) of the EC, and plasma viral sequences were obtained from 78% (61/78), the latter indicating the presence of replicating virus in the majority of EC. Of 63 persons for whom nef was sequenced, only three cases of nef deletions were identified, and gross genetic defects were rarely observed in other HIV-1 coding genes. In a codon-by-codon comparison between EC and persons with progressive infection, correcting for HLA bias and coevolving secondary mutations, a significant difference was observed at only three codons in Gag, all three of which represented the historic population consensus amino acid at the time of infection. These results indicate that the spontaneous control of HIV replication is not attributable to shared viral genetic defects or shared viral polymorphisms.

摘要

尽管有报道称,在未接受抗病毒治疗的情况下能够控制1型人类免疫缺陷病毒(HIV-1)的人群存在病毒基因缺陷,但尚不清楚此类缺陷在多大程度上有助于长期抑制病毒血症。以往大多数检测此类缺陷的研究涉及的受试者数量较少,主要集中在表达HLA-B57的受试者,或者检测单个病毒基因,并且这些研究关注的是细胞前病毒DNA而非血浆病毒RNA序列。在此,我们尝试对95名HIV-1精英控制者(EC)进行病毒测序,这些人在未接受治疗的情况下血浆病毒载量维持在<50 RNA拷贝/毫升,其中大多数人不表达HLA-B57。从94%(89/95)的EC中获得了HIV-1基因片段,从78%(61/78)的EC中获得了血浆病毒序列,后者表明大多数EC中存在正在复制的病毒。在63名对nef进行测序的人中,仅鉴定出3例nef缺失,在其他HIV-1编码基因中很少观察到明显的基因缺陷。在对EC与进行性感染患者进行逐个密码子比较时,校正HLA偏差和共同进化的二级突变后,仅在Gag的三个密码子处观察到显著差异,所有这三个密码子均代表感染时的历史人群共有氨基酸。这些结果表明,HIV复制的自发控制并非归因于共同的病毒基因缺陷或共同的病毒多态性。

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