Department of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI, USA.
Department of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI, USA; Graduate Program in Cellular and Molecular Biology, University of Wisconsin-Madison, Madison, WI, USA.
Cell Rep. 2018 Sep 4;24(10):2581-2588.e4. doi: 10.1016/j.celrep.2018.08.012.
Adaptation of viruses to their hosts can result in specialization and a restricted host range. Species-specific polymorphisms in the influenza virus polymerase restrict its host range during transmission from birds to mammals. ANP32A was recently identified as a cellular co-factor affecting polymerase adaption and activity. Avian influenza polymerases require ANP32A containing an insertion resulting from an exon duplication uniquely encoded in birds. Here we find that natural splice variants surrounding this exon create avian ANP32A proteins with distinct effects on polymerase activity. We demonstrate species-independent direct interactions between all ANP32A variants and the PB2 polymerase subunit. This interaction is enhanced in the presence of viral genomic RNA. In contrast, only avian ANP32A restored ribonucleoprotein complex assembly for a restricted polymerase by enhancing RNA synthesis. Our data suggest that ANP32A splicing variation among birds differentially affects viral replication, polymerase adaption, and the potential of avian hosts to be reservoirs.
病毒对其宿主的适应会导致特化和宿主范围受限。流感病毒聚合酶中的物种特异性多态性限制了其在从鸟类传播到哺乳动物的过程中的宿主范围。ANP32A 最近被确定为一种影响聚合酶适应和活性的细胞辅助因子。禽源流感聚合酶需要包含一个插入物的 ANP32A,该插入物是由鸟类独有的外显子重复产生的。在这里,我们发现该外显子周围的天然剪接变体可产生具有不同聚合酶活性的禽源 ANP32A 蛋白。我们证明了所有 ANP32A 变体与 PB2 聚合酶亚基之间存在物种独立的直接相互作用。这种相互作用在存在病毒基因组 RNA 时会增强。相比之下,只有禽源 ANP32A 通过增强 RNA 合成来恢复受限聚合酶的核糖核蛋白复合物组装。我们的数据表明,鸟类中 ANP32A 的剪接变异会不同程度地影响病毒复制、聚合酶适应以及禽源宿主成为病毒库的潜力。