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Sendai Virus a Strong Inducer of Anti-Lentiviral State in Ovine Cells

机译:仙台病毒羊细胞中抗慢病毒状态的强诱导剂

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摘要

Small ruminant lentiviruses (SRLVs) are widely spread in the ovine and caprine populations, causing an incurable disease affecting animal health and production. Vaccine development is hindered owing to the high genetic heterogeneity of lentiviruses and the selection of T-cell and antibody escape mutants, requiring antigen delivery optimization. Sendai virus (SeV) is a respiratory paramyxovirus in mice that has been recognized as a potent inducer of innate immune responses in several species, including mouse and human. The aim of this study was to stimulate an innate antiviral response in ovine cells and evaluate the potential inhibitory effect upon small ruminant lentivirus (SRLV) infections. Ovine alveolar macrophages (AMs), blood-derived macrophages (BDMs), and skin fibroblasts (OSFs) were stimulated through infection with SeV encoding green fluorescent protein (GFP). SeV efficiently infected ovine cells, inducing an antiviral state in AM from SRLV naturally-infected animals, as well as in in vitro SRLV-infected BDM and OSF from non-infected animals. Supernatants from SeV-infected AM induced an antiviral state when transferred to fresh cells challenged with SRLV. Similar to SRLV, infectivity of an HIV-1-GFP lentiviral vector was also restricted in ovine cells infected with SeV. In myeloid cells, an M1-like proinflammatory polarization was observed together with an APOBEC3Z1 induction, among other lentiviral restriction factors. Our observations may boost new approximations in ameliorating the SRLV burden by stimulation of the innate immune response using SeV-based vaccine vectors.
机译:小型反刍动物慢病毒(SRLV)广泛分布在绵羊和山羊种群中,导致无法治愈的疾病,影响动物的健康和生产。由于慢病毒的高度遗传异质性以及选择T细胞和抗体逃逸突变体(需要抗原传递最优化)而阻碍了疫苗的开发。仙台病毒(SeV)是小鼠的呼吸副粘病毒,已被公认是小鼠和人类等多种物种中先天免疫应答的有效诱导剂。这项研究的目的是刺激绵羊细胞中固有的抗病毒反应,并评估其对小反刍动物慢病毒(SRLV)感染的潜在抑制作用。通过感染编码绿色荧光蛋白(GFP)的SeV可以刺激绵羊肺泡巨噬细胞(AMs),血液来源的巨噬细胞(BDM)和皮肤成纤维细胞(OSF)。 SeV有效感染了绵羊细胞,从而诱导了SRLV自然感染动物的AM中的抗病毒状态,以及体外SRLV感染未感染动物的BDM和OSF中的抗病毒状态。当被SeV感染的AM的上清液转移到用SRLV攻击的新鲜细胞中时,会诱导出抗病毒状态。与SRLV相似,HIV-1-GFP慢病毒载体的感染性也受到SeV感染的绵羊细胞的限制。在骨髓细胞中,除其他慢病毒限制因子外,还观察到了M1样的促炎性极化以及APOBEC3Z1诱导。我们的观察结果可能会通过使用基于SeV的疫苗载体刺激先天免疫应答而在减轻SRLV负担方面提供新的近似值。

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