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1型人类免疫缺陷病毒糖蛋白120 V2结构域延长与向合胞体诱导表型转化之间的时间关系。

Temporal relationship between elongation of the HIV type 1 glycoprotein 120 V2 domain and the conversion toward a syncytium-inducing phenotype.

作者信息

Fouchier R A, Broersen S M, Brouwer M, Tersmette M, Van't Wout A B, Groenink M, Schuitemaker H

机构信息

Department of Clinical Viro-Immunology, University of Amsterdam, Netherlands.

出版信息

AIDS Res Hum Retroviruses. 1995 Dec;11(12):1473-8. doi: 10.1089/aid.1995.11.1473.

DOI:10.1089/aid.1995.11.1473
PMID:8679291
Abstract

The second and third variable domains (V2 and V3) of the human immunodeficiency virus type 1 (HIV-1) gp120 envelope molecule have been shown to be determinants of syncytium-inducing (SI) capacity. Previously we have reported evidence that increased length of the V2 domain and duplication or relocation of potential N-linked glycosylation sites in V2 might be used as prognostic markers for evolution toward an SI phenotype. Here, we used a PCR assay that discriminates a 6-nucleotide difference in the length of the V2 domain, with a sensitivity of 1 elongated V2 domain when present in a background of 125 to 625 short V2 domains. Analysis of DNA isolated directly from PBMCs from 11 HIV-1-infected individuals prior to SI phenotype conversion revealed, however, that the usefulness of this PCR for V2 length polymorphism as predictive marker for SI phenotype evolution is limited. The strong association as observed in our previous study between elongation of the V2 domain and an SI phenotype prompted us to expand our first analysis. An extremely significant correlation was observed between V2 length and virus phenotype for samples obtained at about the moment of SI conversion, but not for samples obtained 3 to 35 months after SI phenotype conversion, suggesting that changes in V2 may be only transiently required to allow SI phenotype evolution. This possibly only transient nature of V2 elongation may explain the discrepancy between results by our group and others.

摘要

人类免疫缺陷病毒1型(HIV-1)gp120包膜分子的第二个和第三个可变区(V2和V3)已被证明是合胞体诱导(SI)能力的决定因素。此前我们曾报道,有证据表明V2区长度增加以及V2区潜在N-糖基化位点的重复或重新定位可能被用作向SI表型进化的预后标志物。在此,我们使用了一种PCR检测方法,该方法可区分V2区长度上6个核苷酸的差异,当在125至625个短V2区的背景中存在1个延长的V2区时,其灵敏度为1。然而,对11名HIV-1感染个体在SI表型转换前直接从外周血单核细胞(PBMC)中分离的DNA进行分析发现,这种用于检测V2长度多态性的PCR作为SI表型进化预测标志物的实用性有限。我们之前的研究中观察到的V2区延长与SI表型之间的强关联促使我们扩大首次分析。在大约SI转换时刻获得的样本中,观察到V2长度与病毒表型之间存在极其显著的相关性,但在SI表型转换后3至35个月获得的样本中未观察到这种相关性,这表明V2的变化可能仅在允许SI表型进化时短暂需要。V2延长可能仅具有这种短暂性质,这或许可以解释我们小组与其他研究结果之间的差异。

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