Dang Que, Chen Jianbo, Unutmaz Derya, Coffin John M, Pathak Vinay K, Powell Douglas, KewalRamani Vineet N, Maldarelli Frank, Hu Wei-Shau
HIV Drug Resistance Program and Data Management Services, National Cancer Institute-Frederick, National Institutes of Health, MD 21702, USA.
Proc Natl Acad Sci U S A. 2004 Jan 13;101(2):632-7. doi: 10.1073/pnas.0307636100. Epub 2004 Jan 5.
Cells infected with two related retroviruses can generate heterozygous virions, which are the precursors of recombinant proviruses. Although many studies have focused on the frequencies and mechanisms of retroviral recombination, little is known about the dynamics of double infection. To examine this issue, viruses generated from two HIV-1 vectors containing different markers were mixed together, and were used to infect target cells. The numbers of cells expressing none, one, or both markers were measured and were used to calculate whether double infection occurred at frequencies expected from random infection events. We found that double infection occurred significantly more frequently than predicted from random distribution; increased rates of double infection were observed in both a T cell line and primary activated CD4(+) T cells. In addition to direct virus infection, we also examined the nature of cell-mediated HIV-1 double infection. Increased double infection was observed in all experiments regardless of whether a cell line or primary human dendritic cells were used for capture and transmission of HIV-1. Therefore, our results indicate that HIV-1 double infection occurs more frequently than it would at random in both direct and cell-mediated HIV-1 infections. To our knowledge, this is the first direct evidence of nonrandom double infection in HIV-1. Frequent double HIV-1 infections in infected individuals would allow the generation of recombinant viruses that could then affect their pathogenesis and evolution.
感染了两种相关逆转录病毒的细胞可产生杂合病毒粒子,它们是重组前病毒的前体。尽管许多研究聚焦于逆转录病毒重组的频率和机制,但对于双重感染的动态变化却知之甚少。为研究此问题,将由两种含有不同标记的HIV-1载体产生的病毒混合在一起,并用于感染靶细胞。对不表达标记、表达一种标记或表达两种标记的细胞数量进行测定,并用于计算双重感染是否以随机感染事件预期的频率发生。我们发现双重感染发生的频率显著高于随机分布的预测;在T细胞系和原代活化CD4(+) T细胞中均观察到双重感染率增加。除了直接病毒感染外,我们还研究了细胞介导的HIV-1双重感染的性质。无论使用细胞系还是原代人树突状细胞来捕获和传播HIV-1,在所有实验中均观察到双重感染增加。因此,我们的结果表明,在直接和细胞介导的HIV-1感染中,HIV-1双重感染发生的频率均高于随机发生的频率。据我们所知,这是HIV-1中非随机双重感染的首个直接证据。感染个体中频繁的HIV-1双重感染会促使重组病毒的产生,进而可能影响其发病机制和进化。