Clinic for Gastroenterology, Hepatology and Infectiology, Heinrich-Heine-University, Building 23.12.U1.87, Moorenstr. 5, 40225 Düsseldorf, Germany.
J Virol. 2010 Jul;84(14):7312-24. doi: 10.1128/JVI.00209-10. Epub 2010 May 5.
To get more insight into the role of APOBEC3 (A3) cytidine deaminases in the species-specific restriction of feline immunodeficiency virus (FIV) of the domestic cat, we tested the A3 proteins present in big cats (puma, lion, tiger, and lynx). These A3 proteins were analyzed for expression and sensitivity to the Vif protein of FIV. While A3Z3s and A3Z2-Z3s inhibited Deltavif FIV, felid A3Z2s did not show any antiviral activity against Deltavif FIV or wild-type (wt) FIV. All felid A3Z3s and A3Z2-Z3s were sensitive to Vif of the domestic cat FIV. Vif also induced depletion of felid A3Z2s. Tiger A3s showed a moderate degree of resistance against the Vif-mediated counter defense. These findings may imply that the A3 restriction system does not play a major role to prevent domestic cat FIV transmission to other Felidae. In contrast to the sensitive felid A3s, many nonfelid A3s actively restricted wt FIV replication. To test whether Vif(FIV) can protect also the distantly related human immunodeficiency virus type 1 (HIV-1), a chimeric HIV-1.Vif(FIV) was constructed. This HIV-1.Vif(FIV) was replication competent in nonpermissive feline cells expressing human CD4/CCR5 that did not support the replication of wt HIV-1. We conclude that the replication of HIV-1 in some feline cells is inhibited only by feline A3 restriction factors and the absence of the appropriate receptor or coreceptor.
为了更深入地了解 APOBEC3(A3)胞嘧啶脱氨酶在猫科动物免疫缺陷病毒(FIV)种间限制中的作用,我们检测了大型猫科动物(美洲狮、狮子、老虎和猞猁)中存在的 A3 蛋白。分析了这些 A3 蛋白的表达情况,并检测了它们对 FIV 的 Vif 蛋白的敏感性。虽然 A3Z3s 和 A3Z2-Z3s 抑制了 Deltavif FIV,但猫科动物的 A3Z2s 对 Deltavif FIV 或野生型(wt)FIV 没有任何抗病毒活性。所有猫科动物的 A3Z3s 和 A3Z2-Z3s 对家猫 FIV 的 Vif 均敏感。Vif 还诱导了猫科动物 A3Z2s 的耗竭。老虎 A3s 对 Vif 介导的反防御表现出中等程度的抗性。这些发现可能意味着 A3 限制系统在阻止家猫 FIV 传播到其他猫科动物中不起主要作用。与敏感的猫科 A3s 相反,许多非猫科 A3s 积极限制了 wt FIV 的复制。为了测试 Vif(FIV)是否也能保护与 HIV-1 关系较远的人类免疫缺陷病毒 1(HIV-1),构建了一种嵌合 HIV-1.Vif(FIV)。这种 HIV-1.Vif(FIV)在表达人 CD4/CCR5 的非允许猫科细胞中具有复制能力,而不会支持 wt HIV-1 的复制。我们得出结论,只有猫科 A3 限制因子和适当的受体或共受体的缺失,才会抑制某些猫科细胞中 HIV-1 的复制。