Broussard S R, Staprans S I, White R, Whitehead E M, Feinberg M B, Allan J S
Department of Virology and Immunology, Southwest Foundation for Biomedical Research, San Antonio, Texas 78227, USA.
J Virol. 2001 Mar;75(5):2262-75. doi: 10.1128/JVI.75.5.2262-2275.2001.
African green monkeys can maintain long-term persistent infection with simian immunodeficiency viruses (SIVagm) without developing AIDS and thus provide an important model for understanding mechanisms of natural host resistance to disease. This study assessed the levels and anatomic distribution of SIVagm in healthy, naturally infected monkeys. Quantitative competitive reverse transcriptase PCR assays developed to measure SIVagm from two African green monkey subspecies demonstrated high levels of SIV RNA in plasma (>6 x 10(6) RNA copies/ml) in sabaeus and vervet monkeys. Infectious virus was readily recovered from plasma and peripheral blood mononuclear cells and shown to be highly cytopathic in human cell lines and macrophages. SIVagm DNA levels were highest in the gastrointestinal tract, suggesting that the gut is a major site for SIVagm replication in vivo. Appreciable levels of virus were also found within the brain parenchyma and the cerebrospinal fluid (CSF), with lower levels detected in peripheral blood cells and lymph nodes. Virus isolates from the CSF and brain parenchyma readily infected macrophages in culture, whereas lymph node isolates were more restricted to growth in human T-cell lines. Comparison of env V2-C4 sequences showed extensive amino acid diversity between SIVagm recovered from the central nervous system and that recovered from lymphoid tissues. Homology between brain and CSF viruses, macrophage tropism, and active replication suggest compartmentalization in the central nervous system without associated neuropathology in naturally infected monkeys. These studies provide evidence that the nonpathogenic nature of SIVagm in the natural host can be attributed neither to more effective host control over viral replication nor to differences in the tissue and cell tropism from those for human immunodeficiency virus type 1-infected humans or SIV-infected macaques.
非洲绿猴能够长期持续感染猿猴免疫缺陷病毒(SIVagm)而不发展为艾滋病,因此为理解自然宿主抗病机制提供了重要模型。本研究评估了健康、自然感染的猴子体内SIVagm的水平及解剖分布。为测量来自两个非洲绿猴亚种的SIVagm而开发的定量竞争性逆转录酶PCR检测显示,在黑绿猴和绿猴的血浆中SIV RNA水平很高(>6×10⁶ RNA拷贝/毫升)。传染性病毒很容易从血浆和外周血单核细胞中分离出来,并在人类细胞系和巨噬细胞中显示出高度细胞病变性。SIVagm DNA水平在胃肠道中最高,这表明肠道是SIVagm在体内复制的主要部位。在脑实质和脑脊液(CSF)中也发现了相当水平的病毒,在外周血细胞和淋巴结中检测到的水平较低。从脑脊液和脑实质分离出的病毒在培养中很容易感染巨噬细胞,而从淋巴结分离出的病毒在人类T细胞系中的生长更受限制。env V2 - C4序列的比较显示,从中枢神经系统分离出的SIVagm与从淋巴组织分离出的SIVagm之间存在广泛的氨基酸多样性。脑和脑脊液病毒之间的同源性、巨噬细胞嗜性和活跃复制表明,在自然感染的猴子中,中枢神经系统存在区室化现象,但无相关神经病理学改变。这些研究提供了证据,表明SIVagm在自然宿主中的非致病性既不能归因于宿主对病毒复制的更有效控制,也不能归因于其组织和细胞嗜性与感染人类免疫缺陷病毒1型的人类或感染SIV的猕猴的组织和细胞嗜性存在差异。