Leymarie Olivier, Embury-Hyatt Carissa, Chevalier Christophe, Jouneau Luc, Moroldo Marco, Da Costa Bruno, Berhane Yohannes, Delmas Bernard, Weingartl Hana M, Le Goffic Ronan
Unité de Virologie et Immunologie Moléculaires, Unité de Recherche UR892, Institut National de la Recherche Agronomique, Jouy-en-Josas, France.
National Centre for Foreign Animal Disease, Canadian Food Inspection Agency, Winnipeg, Manitoba, Canada.
PLoS One. 2014 Jun 24;9(6):e100679. doi: 10.1371/journal.pone.0100679. eCollection 2014.
Highly pathogenic avian influenza virus (HPAIV) is a permanent threat due to its capacity to cross species barriers and generate severe infections and high mortality in humans. Recent findings have highlighted the potential role of PB1-F2, a small accessory influenza protein, in the pathogenesis process mediated by HPAIV in mammals. In this study, using a recombinant H5N1 HPAIV (wt) and its PB1-F2-deleted mutant (ΔF2), we studied the effects of PB1-F2 in a chicken model. Unexpectedly, when using low inoculation dose we observed that the wt-infected chickens had a higher survival rate than the ΔF2-infected chickens, a feature that contrasts with what is usually observed in mammals. High inoculation dose had similar mortality rate for both viruses, and comparison of the bio-distribution of the two viruses indicated that the expression of PB1-F2 allows a better spreading of the virus within chicken embryos. Transcriptomic profiles of lungs and blood cells were characterized at two days post-infection in chickens inoculated with the wild type (wt) or the ΔF2 mutant viruses. In lungs, the expression of PB1-F2 during the infection induced pathways related to calcium signaling and repressed a large panel of immunological functions. In blood cells, PB1-F2 was associated with a gene signature specific for mitochondrial dysfunction and down-modulated leucocytes activation. Finally we compared the effect of PB1-F2 in lungs of chickens and mice. We identified that gene signature associated to tissue damages is a PB1-F2 feature shared by the two species; by contrast, the early inhibition of immune response mediated by PB1-F2 observed in chickens is not seen in mice. In summary, our data suggest that PB1-F2 expression deeply affect the immune response in chickens in a way that may attenuate pathogenicity at low infection dose, a feature differing from what was previously observed in mammal species.
高致病性禽流感病毒(HPAIV)因其能够跨越物种屏障并在人类中引发严重感染和高死亡率而构成持续威胁。最近的研究结果突出了PB1-F2(一种小型辅助流感蛋白)在HPAIV介导的哺乳动物发病过程中的潜在作用。在本研究中,我们使用重组H5N1 HPAIV(野生型)及其缺失PB1-F2的突变体(ΔF2),在鸡模型中研究了PB1-F2的作用。出乎意料的是,当使用低接种剂量时,我们观察到野生型感染的鸡比ΔF2感染的鸡具有更高的存活率,这一特征与在哺乳动物中通常观察到的情况形成对比。高接种剂量下两种病毒的死亡率相似,两种病毒的生物分布比较表明,PB1-F2的表达使病毒在鸡胚内的传播更好。对接种野生型(wt)或ΔF2突变病毒的鸡在感染后两天对肺和血细胞的转录组谱进行了表征。在肺中,感染期间PB1-F2的表达诱导了与钙信号相关的途径,并抑制了大量免疫功能。在血细胞中,PB1-F2与线粒体功能障碍特有的基因特征相关,并下调白细胞激活。最后,我们比较了PB1-F2在鸡和小鼠肺中的作用。我们发现与组织损伤相关的基因特征是这两个物种共有的PB1-F2特征;相比之下,在鸡中观察到的由PB1-F2介导的免疫反应早期抑制在小鼠中未见到。总之,我们的数据表明,PB1-F2的表达以一种可能在低感染剂量下减弱致病性的方式深刻影响鸡的免疫反应,这一特征与先前在哺乳动物物种中观察到的不同。