Institute of Preventive Veterinary Medicine, Zhejiang University, Hangzhou 310058, China.
Zhejiang Provincial Key Laboratory of Preventive Veterinary Medicine, Hangzhou 310058, China.
J Zhejiang Univ Sci B. 2020 Jul;21(7):560-570. doi: 10.1631/jzus.B1900657.
Porcine circovirus 3 (PCV3) has been detected in major pig-producing countries around the world since its first report in the US in 2016. Most current studies have focused on epidemiological investigations and detection methods of PCV3 because of lack of live virus strains for research on its pathogenesis in porcine cells or even in pigs. We constructed a recombinant plasmid pCMV-Cap carrying the PCV3 orf2 gene to investigate the effects of capsid (Cap) protein expression on autophagic response in human embryonic kidney cell line 293T (HEK293T). We demonstrate that PCV3 Cap protein induced complete autophagy shown as formation of autophagosomes and autophagosome-like vesicles as well as LC3-II conversion from LC3-I via inhibiting phosphorylation of the mammalian target of rapamycin (mTOR) in HEK293T cells. The ubiquitin-proteasome pathway is also involved in the autophagy process. These findings provide insight for further exploration of PCV3 pathogenetic mechanisms in porcine cells.
自 2016 年美国首次报道以来,猪圆环病毒 3 型(PCV3)已在世界主要养猪国家被检出。由于缺乏用于研究其在猪细胞甚至猪体内发病机制的活病毒株,目前大多数研究都集中在 PCV3 的流行病学调查和检测方法上。我们构建了携带 PCV3 orf2 基因的重组质粒 pCMV-Cap,以研究衣壳(Cap)蛋白表达对人胚肾细胞系 293T(HEK293T)自噬反应的影响。我们证明 PCV3 Cap 蛋白通过抑制哺乳动物雷帕霉素靶蛋白(mTOR)的磷酸化,诱导完全自噬,表现为自噬体和自噬体样小泡的形成以及 LC3-I 向 LC3-II 的转化。泛素-蛋白酶体途径也参与自噬过程。这些发现为进一步探索 PCV3 在猪细胞中的致病机制提供了思路。