Church Jessica D, Huang Wei, Mwatha Anthony, Toma Jonathan, Stawiski Eric, Donnell Deborah, Guay Laura A, Mmiro Francis, Musoke Philippa, Jackson J Brooks, Parkin Neil, Eshleman Susan H
Johns Hopkins University, Baltimore, Maryland, USA.
J Infect Dis. 2008 May 15;197(10):1382-8. doi: 10.1086/587492.
Human immunodeficiency virus type 1 (HIV-1) may utilize the CXCR4 coreceptor (X4 virus), the CCR5 coreceptor (R5 virus), or both (dual/mixed [DM] virus). We analyzed HIV-1 coreceptor tropism in Ugandan infants enrolled in the HIVNET (HIV Network for Prevention Trials) 012 trial.
Plasma or serum was analyzed using a commercial coreceptor tropism assay. HIV env subtype was determined by phylogenetic methods.
Tropism results were obtained for 57 samples from infants collected 6-14 weeks after birth. Fifty-two infants had only R5 virus, and 5 had either X4 or DM virus. The mothers of those 5 infants also had X4 or DM virus. In infants, subtype D infection was associated with high-level infectivity in CCR5-bearing cells and also with the detection of X4 or DM strains. High-level infectivity in CCR5-bearing cells was associated with decreased infant survival, but infection with X4 or DM virus was not. HIV clones from infants with DM viral populations showed different patterns of coreceptor use. V3 loop sequence-based algorithms predicted the tropism of some, but not all, env clones.
Complex patterns of HIV tropism were found in HIV-infected newborn infants. Subtype D infection was associated with X4 virus and with high-level replication in CCR5-bearing cells. High-level replication of R5 virus was associated with decreased infant survival.
1型人类免疫缺陷病毒(HIV-1)可利用CXCR4共受体(X4病毒)、CCR5共受体(R5病毒)或两者(双嗜性/混合性[DM]病毒)。我们分析了参与HIVNET(预防试验HIV网络)012试验的乌干达婴儿的HIV-1共受体嗜性。
使用商业共受体嗜性检测法分析血浆或血清。通过系统发育方法确定HIV env亚型。
对出生后6 - 14周收集的婴儿的57份样本进行了嗜性结果分析。52名婴儿仅感染R5病毒,5名婴儿感染X4或DM病毒。这5名婴儿的母亲也感染了X4或DM病毒。在婴儿中,D亚型感染与CCR5阳性细胞中的高感染性相关,也与X4或DM毒株的检测相关。CCR5阳性细胞中的高感染性与婴儿存活率降低相关,但感染X4或DM病毒则不然。来自具有DM病毒群体的婴儿的HIV克隆显示出不同的共受体使用模式。基于V3环序列的算法预测了部分但并非所有env克隆的嗜性。
在感染HIV的新生儿中发现了复杂的HIV嗜性模式。D亚型感染与X4病毒以及CCR5阳性细胞中的高复制水平相关。R5病毒的高复制水平与婴儿存活率降低相关。