Sellon D C, Walker K M, Russell K E, Perry S T, Fuller F J
Department of Food Animal and Equine Medicine, North Carolina State University College of Veterinary Medicine, Raleigh 27606, USA.
Vet Microbiol. 1996 Oct;52(3-4):209-21. doi: 10.1016/s0378-1135(96)00071-5.
Equine infectious anemia virus (EIAV) is a lentivirus that replicates predominantly in mature tissue macrophages. Viral expression is strongly influenced by the state of differentiation of the host cell. While blood monocytes can be infected, viral transcription is limited until the cell differentiates into a mature macrophage. Activation of mature macrophages infected with EIAV might also alter viral expression, presumably through binding of cellular transcription factors to viral nucleic acid sequences within the long terminal repeat (LTR). Using DNA amplification techniques, we compared LTR sequences of U.S. field strains of EIAV to sequences of a laboratory adapted strain of the virus. All field strain sequences were more closely related to Wyoming strain than to the Malmquist laboratory adapted strain or a previously sequenced infectious molecular clone of EIAV. Primary equine monocyte-derived macrophage cultures were infected with virulent and avirulent strains of EIAV and the effects of macrophage stimulation on EIAV expression were determined. Stimulation of macrophages with phorbol ester activated the cells to secrete tumor necrosis factor alpha (TNF alpha). This activation signal also resulted in a significant downregulation of viral expression as determined by supernatant reverse transcriptase activity. This effect occurred independent of the virulence of the virus strain used or the nucleic acid sequence of the viral LTR. This may represent an adaptive response of EIAV to evade the host immune response and establish a persistent infection.
马传染性贫血病毒(EIAV)是一种慢病毒,主要在成熟的组织巨噬细胞中复制。病毒表达受到宿主细胞分化状态的强烈影响。虽然血液单核细胞可以被感染,但在细胞分化为成熟巨噬细胞之前,病毒转录受到限制。感染EIAV的成熟巨噬细胞的激活也可能改变病毒表达,推测是通过细胞转录因子与长末端重复序列(LTR)内的病毒核酸序列结合。使用DNA扩增技术,我们将美国EIAV野外毒株的LTR序列与该病毒的实验室适应株的序列进行了比较。所有野外毒株序列与怀俄明毒株的关系比与马尔姆奎斯特实验室适应株或先前测序的EIAV感染性分子克隆的关系更为密切。用EIAV的强毒株和无毒株感染原代马单核细胞衍生的巨噬细胞培养物,并确定巨噬细胞刺激对EIAV表达的影响。用佛波酯刺激巨噬细胞可激活细胞分泌肿瘤坏死因子α(TNFα)。如通过上清液逆转录酶活性所确定的,这种激活信号也导致病毒表达显著下调。这种效应的发生与所用病毒株的毒力或病毒LTR的核酸序列无关。这可能代表EIAV为逃避宿主免疫反应并建立持续感染的一种适应性反应。