Nebraska Center for Virology, University of Nebraska, Lincoln, NE 68583-0900, USA.
Virology. 2010 May 10;400(2):164-74. doi: 10.1016/j.virol.2009.12.019. Epub 2010 Jan 25.
Understanding the properties of viruses capable of establishing infection during perinatal transmission of HIV-1 is critical for designing effective means of limiting transmission. We previously demonstrated that the newly transmitted viruses (in infant) were more fit in growth, as imparted by their envelope glycoproteins, than those in their corresponding mothers. Here, we further characterized the viral envelope glycoproteins from six mother-infant transmission pairs and determined whether any specific envelope functions correlate with HIV-1 subtype C perinatal transmission. We found that most newly transmitted viruses were less susceptible to neutralization by their maternal plasma compared to contemporaneous maternal viruses. However, the newly transmitted variants were sensitive to neutralization by pooled heterologous plasma but in general were resistant to IgG1 b12. Neither Env processing nor incorporation efficiency was predictive of viral transmissibility. These findings provide further insight into the characteristics of perinatally transmissible HIV-1 and may have implications for intervention approaches.
了解能够在 HIV-1 围产期传播期间建立感染的病毒特性对于设计有效限制传播的方法至关重要。我们之前证明,新传播的病毒(在婴儿中)在生长方面比其相应的母亲中的病毒更具适应性,这是由它们的包膜糖蛋白赋予的。在这里,我们进一步表征了来自六对母婴传播对的病毒包膜糖蛋白,并确定了任何特定的包膜功能是否与 HIV-1 亚型 C 围产期传播相关。我们发现,与同期的母体病毒相比,大多数新传播的病毒对母体血浆的中和作用的敏感性较低。然而,新传播的变体对混合异源血浆的中和作用敏感,但通常对 IgG1 b12 具有抗性。Env 加工和掺入效率都不能预测病毒的传染性。这些发现进一步深入了解了可围产期传播的 HIV-1 的特征,可能对干预方法具有重要意义。