State Key Laboratory of Biocontrol, Guangzhou Higher Education Mega Center, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Guangdong YIHAO Food Co., Ltd., Guangzhou, China.
Front Immunol. 2019 Aug 8;10:1846. doi: 10.3389/fimmu.2019.01846. eCollection 2019.
Porcine reproductive and respiratory syndrome virus (PRRSV) 1 and 2 differ in their recognition of CD163. Substitution of porcine CD163 SRCR5 domain with a human CD163-like SRCR8 confers resistance to PRRSV 1 but not PRRSV 2. The deletion of CD163 SRCR5 has been shown to confer resistance to PRRSV 1 and both PRRSV 1 and 2 . However, the anti-PRRSV 2 activity of modifying the CD163 SRCR5 domain has not yet been reported. Here, we describe the highly efficient generation of two pig breeds (Liang Guang Small Spotted and Large White pigs) lacking a short region of CD163 SRCR5, including the ligand-binding pocket. We generated a large number of gene-edited Large White pigs of the F0 generation for use in viral challenge studies. The results of this study show that these pigs are completely resistant to infection by species 2 PRRSV, JXA1, and MY strains. There were no clinical symptoms, pathological abnormalities, viremia, or anti-PRRSV antibodies in the CD163 SRCR5-edited pigs compared to wild-type controls after viral challenge. Porcine alveolar macrophages (PAMs) isolated from CD163 SRCR5-edited Large White pigs also displayed resistance to PRRSV . In addition, CD163 SRCR5-edited PAMs still exhibited a cytokine response to PRRSV infection, and no significant difference was observed in cytokine expression compared to wild-type PAMs. Taken together, these data suggest that CD163 SRCR5-edited pigs are resistant to PRRSV 2, providing a basis for the establishment of PRRSV-resistant pig lines for commercial application and further investigation of the essential region of SRCR5 involved in virus infection.
猪繁殖与呼吸综合征病毒(PRRSV)1 和 2 在识别 CD163 方面存在差异。用猪 CD163 的 SRCR5 结构域替换人 CD163 样的 SRCR8 赋予了对 PRRSV 1 的抗性,但对 PRRSV 2 没有抗性。已经证明,CD163 SRCR5 的缺失赋予了对 PRRSV 1 和 PRRSV 1 和 2 的抗性。然而,修饰 CD163 SRCR5 结构域对 PRRSV 2 的抗病毒活性尚未得到报道。在这里,我们描述了两种猪品种(梁光小斑点和大白猪)缺乏 CD163 SRCR5 的短区域,包括配体结合口袋的高效产生。我们产生了大量的 F0 代基因编辑大白猪,用于病毒挑战研究。这项研究的结果表明,这些猪对 2 型 PRRSV、JXA1 和 MY 株完全抵抗感染。与野生型对照相比,在病毒挑战后,CD163 SRCR5 编辑猪没有临床症状、病理异常、病毒血症或抗 PRRSV 抗体。从 CD163 SRCR5 编辑的大白猪分离的肺泡巨噬细胞(PAMs)也对 PRRSV 表现出抗性。此外,CD163 SRCR5 编辑的 PAMs 对 PRRSV 感染仍表现出细胞因子反应,与野生型 PAMs 相比,细胞因子表达没有显著差异。总之,这些数据表明,CD163 SRCR5 编辑的猪对 PRRSV 2 具有抗性,为建立用于商业应用的 PRRSV 抗性猪系提供了基础,并进一步研究了参与病毒感染的 SRCR5 的必需区域。