Besnier Caroline, Takeuchi Yasuhiro, Towers Greg
Wohl Virion Centre, Department of Immunology and Molecular Pathology, University College London, 46 Cleveland Street, London W1T 4JF, United Kingdom.
Proc Natl Acad Sci U S A. 2002 Sep 3;99(18):11920-5. doi: 10.1073/pnas.172384599. Epub 2002 Aug 1.
Retroviruses are able to cross species barriers and have done so many times throughout evolution. Perhaps as a consequence, dominant mechanisms have arisen to block infection by murine retroviruses in mice (restriction factor Fv1) and humans (restriction factor Ref1), as well as in other mammals. Here we describe a block to HIV and simian immunodeficiency virus in monkeys. Like previously described restrictions the block is saturable and gives rise to multiple-hit infection kinetics. Furthermore, like restriction of murine leukemia virus in humans, the block is before reverse transcription. Intriguingly, African green monkey cells are able to block both HIV and simian immunodeficiency virus, and each virus is able to saturate and abrogate the restriction of the other, suggesting that a common factor is responsible.
逆转录病毒能够跨越物种屏障,并且在整个进化过程中多次如此。或许正因如此,在小鼠(限制因子Fv1)、人类(限制因子Ref1)以及其他哺乳动物中,已经出现了阻止鼠类逆转录病毒感染的主要机制。在此,我们描述了猴子体内对HIV和猴免疫缺陷病毒的一种阻断作用。与先前描述的限制作用一样,这种阻断作用是可饱和的,并产生多次击中感染动力学。此外,与人类对鼠白血病病毒的限制作用一样,这种阻断作用发生在逆转录之前。有趣的是,非洲绿猴细胞能够同时阻断HIV和猴免疫缺陷病毒,并且每种病毒都能够饱和并消除另一种病毒的限制作用,这表明存在一个共同的因素在起作用。