Benfield Camilla T O, Smith Sarah E, Wright Edward, Wash Rachael S, Ferrara Francesca, Temperton Nigel J, Kellam Paul
Department of Pathology and Pathogen Biology, The Royal Veterinary College, Hatfield, UK.
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK.
J Gen Virol. 2015 May;96(Pt 5):991-1005. doi: 10.1099/vir.0.000058. Epub 2015 Jan 22.
IFN-induced transmembrane protein 3 (IFITM3) is a restriction factor that blocks cytosolic entry of numerous viruses that utilize acidic endosomal entry pathways. In humans and mice, IFITM3 limits influenza-induced morbidity and mortality. Although many IFITM3-sensitive viruses are zoonotic, whether IFITMs function as antiviral restriction factors in mammalian species other than humans and mice is unknown. Here, IFITM3 orthologues in the microbat (Myotis myotis) and pig (Sus scrofa domesticus) were identified using rapid amplification of cDNA ends. Amino acid residues known to be important for IFITM3 function were conserved in the pig and microbat orthologues. Ectopically expressed pig and microbat IFITM3 co-localized with transferrin (early endosomes) and CD63 (late endosomes/multivesicular bodies). Pig and microbat IFITM3 restricted cell entry mediated by multiple influenza haemagglutinin subtypes and lyssavirus glycoproteins. Expression of pig or microbat IFITM3 in A549 cells reduced influenza virus yields and nucleoprotein expression. Conversely, small interfering RNA knockdown of IFITM3 in pig NPTr cells and primary microbat cells enhanced virus replication, demonstrating that these genes are functional in their species of origin at endogenous levels. In summary, we showed that IFITMs function as potent broad-spectrum antiviral effectors in two mammals - pigs and bats - identified as major reservoirs for emerging viruses.
干扰素诱导跨膜蛋白3(IFITM3)是一种限制因子,可阻止许多利用酸性内体进入途径的病毒进入细胞质。在人类和小鼠中,IFITM3可限制流感引起的发病率和死亡率。尽管许多对IFITM3敏感的病毒是人畜共患病原体,但IFITM在人类和小鼠以外的其他哺乳动物物种中是否作为抗病毒限制因子尚不清楚。在这里,利用cDNA末端快速扩增技术鉴定了小鼠(Myotis myotis)和猪(Sus scrofa domesticus)中的IFITM3直系同源物。已知对IFITM3功能重要的氨基酸残基在猪和小鼠的直系同源物中是保守的。异位表达的猪和小鼠IFITM3与转铁蛋白(早期内体)和CD63(晚期内体/多囊泡体)共定位。猪和小鼠IFITM3可限制多种流感血凝素亚型和狂犬病病毒糖蛋白介导的细胞进入。在A549细胞中表达猪或小鼠IFITM3可降低流感病毒产量和核蛋白表达。相反,在猪NPTr细胞和原代小鼠细胞中用小干扰RNA敲低IFITM3可增强病毒复制,表明这些基因在内源水平上在其起源物种中具有功能。总之,我们表明IFITM在被确定为新兴病毒主要宿主的两种哺乳动物——猪和蝙蝠中作为强大的广谱抗病毒效应物发挥作用。