Fouchier R A, Brouwer M, Broersen S M, Schuitemaker H
Department of Clinical Viro-Immunology, Central Laboratory of The Netherlands Red Cross Blood Transfusion Service, Amsterdam.
J Clin Microbiol. 1995 Apr;33(4):906-11. doi: 10.1128/jcm.33.4.906-911.1995.
Human immunodeficiency virus type 1 (HIV-1) phenotype variability plays an important role in the pathogenesis of AIDS. The presence of syncytium-inducing (SI) HIV-1 isolates in infected individuals is associated with a rapid decline of CD4+ T cells, rapid disease progression, and reduced survival time after AIDS diagnosis. The strong association between the SI capacity of HIV-1 and the presence of positively charged amino acid residues at positions 306 and/or 320 in the third variable domain (V3) of gp120 could here be confirmed in 97% of 402 primary HIV-1 isolates, indicating that the V3 genotype may be useful for prediction of the viral phenotype. The V3 DNA sequences revealed a remarkably limited codon usage for the amino acid residues that are responsible for virus phenotype. On the basis of this limited SI-specific DNA sequence variation, four SI-specific oligonucleotides were designed for selective amplification of V3 from SI but not non-SI HIV-1 isolates. This PCR analysis allowed the prediction of the biological phenotype of HIV-1 isolates on the basis of the V3 genotype and may prove to be useful for monitoring SI capacity of HIV-1 isolates in infected individuals.
1型人类免疫缺陷病毒(HIV-1)的表型变异在艾滋病发病机制中起着重要作用。在受感染个体中,合胞体诱导(SI)HIV-1毒株的存在与CD4+T细胞的快速减少、疾病的快速进展以及艾滋病诊断后的生存时间缩短有关。在402株原发性HIV-1分离株中,97%证实了HIV-1的SI能力与gp120第三可变区(V3)第306位和/或320位带正电荷氨基酸残基的存在之间存在强关联,这表明V3基因型可能有助于预测病毒表型。V3 DNA序列显示,负责病毒表型的氨基酸残基的密码子使用非常有限。基于这种有限的SI特异性DNA序列变异,设计了四种SI特异性寡核苷酸,用于从SI而非非SI HIV-1分离株中选择性扩增V3。这种PCR分析能够根据V3基因型预测HIV-1分离株的生物学表型,可能对监测受感染个体中HIV-1分离株的SI能力有用。