Schweighardt Becky, Roy Ann-Marie, Meiklejohn Duncan A, Grace Edward J, Moretto Walter J, Heymann Jonas J, Nixon Douglas F
Gladstone Institute of Virology and Immunology, University of California, San Francisco, California 94141-9100, USA.
J Virol. 2004 Sep;78(17):9164-73. doi: 10.1128/JVI.78.17.9164-9173.2004.
In this report, we present evidence that R5 human immunodeficiency virus type 1 (HIV-1) replicates more efficiently in primary CD4+ T cells than X4 HIV-1. By comparing CD3/CD28-costimulated CD4+ T-cell cultures infected by several X4 and R5 HIV-1 strains, we determined that R5-infected CD4+ T cells produce more virus over time than X4-infected CD4+ T cells. In the first comparison, we found that more cells were infected by the X4-tropic strain LAI than by the R5-tropic strain JR-CSF and yet that higher levels of viral production were detected in the R5-infected cultures. The differential viral production was partially due to the severe cytopathic effects of the X4 virus. We also compared cultures infected with the isogenic HIV-1 strains NL4-3 (X4) and 49.5 (R5). We found that fewer cells were infected by the R5 strain, and yet similar levels of viral production were detected in both infected cultures. Cell death played less of a role in the differential viral production of these strains, as the cell viability remained comparable in both X4- and R5-infected cultures over time. The final comparison involved the primary R5-tropic isolate KP1 and the primary dual-tropic isolate KP2. Although both strains infected similar numbers of cells and induced comparable levels of cytopathicity, viral production was considerably higher in the R5-infected culture. In summary, these data demonstrate that R5 HIV-1 has an increased capacity to replicate in costimulated CD4+ T cells compared to X4 HIV-1.
在本报告中,我们提供证据表明,R5型人类免疫缺陷病毒1型(HIV-1)在原代CD4+ T细胞中的复制效率高于X4型HIV-1。通过比较由几种X4和R5型HIV-1毒株感染的经CD3/CD28共刺激的CD4+ T细胞培养物,我们确定随着时间推移,被R5感染的CD4+ T细胞比被X4感染的CD4+ T细胞产生更多病毒。在首次比较中,我们发现X4嗜性毒株LAI感染的细胞比R5嗜性毒株JR-CSF感染的细胞更多,但在R5感染的培养物中检测到更高水平的病毒产生。病毒产生的差异部分归因于X4病毒的严重细胞病变效应。我们还比较了由同基因HIV-1毒株NL4-3(X4)和49.5(R5)感染的培养物。我们发现R5毒株感染的细胞较少,但在两种感染的培养物中检测到相似水平的病毒产生。细胞死亡在这些毒株的病毒产生差异中所起的作用较小,因为随着时间推移,在X4和R5感染的培养物中细胞活力保持相当。最后一次比较涉及原代R5嗜性分离株KP1和原代双嗜性分离株KP2。尽管两种毒株感染的细胞数量相似且诱导的细胞病变水平相当,但在R5感染的培养物中病毒产生显著更高。总之,这些数据表明,与X4型HIV-1相比,R5型HIV-1在共刺激的CD4+ T细胞中的复制能力增强。