Department of Viroscience, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
Viruses. 2022 Jan 17;14(1):165. doi: 10.3390/v14010165.
Highly pathogenic avian influenza viruses (HPAIVs) cause fatal systemic infections in chickens, which are associated with endotheliotropism. HPAIV infections in wild birds are generally milder and not endotheliotropic. Here, we aimed to elucidate the species-specific endotheliotropism of HPAIVs using primary chicken and duck aortic endothelial cells (chAEC and dAEC respectively). Viral replication kinetics and host responses were assessed in chAEC and dAEC upon inoculation with HPAIV H5N1 and compared to embryonic fibroblasts. Although dAEC were susceptible to HPAIV upon inoculation at high multiplicity of infection, HPAIV replicated to lower levels in dAEC than chAEC during multi-cycle replication. The susceptibility of duck embryonic endothelial cells to HPAIV was confirmed in embryos. Innate immune responses upon HPAIV inoculation differed between chAEC, dAEC, and embryonic fibroblasts. Expression of the pro-inflammatory cytokine increased in chicken cells but decreased in dAEC. Contrastingly, the induction of antiviral responses was stronger in dAEC than in chAEC, and chicken and duck fibroblasts. Taken together, these data demonstrate that although duck endothelial cells are permissive to HPAIV infection, they display markedly different innate immune responses than chAEC and embryonic fibroblasts. These differences may contribute to the species-dependent differences in endotheliotropism and consequently HPAIV pathogenesis.
高致病性禽流感病毒(HPAIVs)可引起鸡的致命全身感染,与内皮嗜性有关。野生鸟类的 HPAIV 感染通常较轻,不具有内皮嗜性。在这里,我们旨在使用原代鸡和鸭主动脉内皮细胞(分别为 chAEC 和 dAEC)阐明 HPAIV 的种特异性内皮嗜性。在接种 HPAIV H5N1 后,评估 chAEC 和 dAEC 中的病毒复制动力学和宿主反应,并与胚胎成纤维细胞进行比较。尽管在高感染复数下接种时 dAEC 易感染 HPAIV,但在多轮复制过程中,HPAIV 在 dAEC 中的复制水平低于 chAEC。在胚胎中证实了鸭胚胎内皮细胞对 HPAIV 的易感性。接种 HPAIV 后,chAEC、dAEC 和胚胎成纤维细胞之间的先天免疫反应不同。鸡细胞中促炎细胞因子 的表达增加,但 dAEC 中则减少。相反,dAEC 中的抗病毒反应诱导强于 chAEC,也强于鸡和鸭成纤维细胞。总之,这些数据表明,尽管鸭内皮细胞允许 HPAIV 感染,但它们与 chAEC 和胚胎成纤维细胞表现出明显不同的先天免疫反应。这些差异可能导致内皮嗜性和 HPAIV 发病机制的种间差异。