Zhou Niu, Xing Gang, Zhou Jianwei, Jin Yulan, Liang Cuiqin, Gu Jinyan, Hu Boli, Liao Min, Wang Qin, Zhou Jiyong
Key Laboratory of Animal Virology of Ministry of Agriculture, Zhejiang University, Hangzhou, PR China.
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, PR China.
PLoS One. 2015 Oct 2;10(10):e0139457. doi: 10.1371/journal.pone.0139457. eCollection 2015.
Increasing clinical lines of evidence have shown the coinfection/superinfection of porcine circovirus type 2 (PCV2) and classical swine fever virus (CSFV). Here, we investigated whether PCV2 and CSFV could infect the same cell productively by constructing an in vitro coinfection model. Our results indicated that PCV2-free PK15 cells but not ST cells were more sensitive to PCV2, and the PK15 cell line could stably harbor replicating CSFV (PK15-CSFV cells) with a high infection rate. Confocal and super-resolution microscopic analysis showed that PCV2 and CSFV colocalized in the same PK15-CSFV cell, and the CSFV E2 protein translocated from the cytoplasm to the nucleus in PK15-CSFV cells infected with PCV2. Moreover, PCV2-CSFV dual-positive cells increased gradually in PK15-CSFV cells in a PCV2 dose-dependent manner. In PK15-CSFV cells, PCV2 replicated well, and the production of PCV2 progeny was not influenced by CSFV infection. However, CSFV reproduction decreased in a PCV2 dose-dependent manner. In addition, cellular apoptosis was not strengthened in PK15-CSFV cells infected with PCV2 in comparison with PCV2-infected PK15 cells. Moreover, using this coinfection model we further demonstrated PCV2-induced apoptosis might contribute to the impairment of CSFV HCLV strain replication in coinfected cells. Taken together, our results demonstrate for the first time the coinfection/superinfection of PCV2 and CSFV within the same cell, providing an in vitro model to facilitate further investigation of the underlying mechanism of CSFV and PCV2 coinfection.
越来越多的临床证据表明存在猪圆环病毒2型(PCV2)和经典猪瘟病毒(CSFV)的混合感染/重叠感染。在此,我们通过构建体外混合感染模型,研究了PCV2和CSFV是否能在同一细胞中有效感染。我们的结果表明,无PCV2的PK15细胞而非ST细胞对PCV2更敏感,并且PK15细胞系能够以高感染率稳定容纳复制型CSFV(PK15-CSFV细胞)。共聚焦和超分辨率显微镜分析显示,PCV2和CSFV在同一PK15-CSFV细胞中共定位,并且在感染PCV2的PK15-CSFV细胞中,CSFV E2蛋白从细胞质转移到细胞核。此外,在PK15-CSFV细胞中,PCV2-CSFV双阳性细胞以PCV2剂量依赖性方式逐渐增加。在PK15-CSFV细胞中,PCV2复制良好,并且PCV2子代的产生不受CSFV感染的影响。然而,CSFV的增殖以PCV2剂量依赖性方式降低。此外,与感染PCV2的PK15细胞相比,感染PCV2的PK15-CSFV细胞中的细胞凋亡并未增强。此外,使用该混合感染模型我们进一步证明,PCV2诱导的凋亡可能导致混合感染细胞中CSFV HCLV株复制受损。综上所述,我们的结果首次证明了PCV2和CSFV在同一细胞内的混合感染/重叠感染,提供了一个体外模型,便于进一步研究CSFV和PCV2混合感染的潜在机制。