Beijing Key Laboratory for Prevention and Control of Infectious Diseases in Livestock and Poultry, Institute of Animal Husbandry and Veterinary Medicine, Beijing Academy of Agriculture and Forestry Sciences, Beijing, China.
College of Veterinary Medicine, China Agricultural University, Beijing, China.
J Virol. 2019 Feb 5;93(4). doi: 10.1128/JVI.02045-18. Print 2019 Feb 15.
Porcine circovirus type 3 (PCV3) is an emerging porcine circovirus that has been associated with porcine dermatitis and nephropathy syndrome (PDNS)-like clinical signs, reproductive failure, cardiac pathologies, and multisystemic inflammation in piglets and sows. Many aspects of PCV3 infection biology and pathogenesis, however, remain unknown. Here, we used a PCV3 virus stock from the rescue of an infectious PCV3 DNA clone to intranasally inoculate 4- and 8-week-old specific-pathogen-free piglets for evaluation of PCV3 pathogenesis. For 4-week-old piglets, typical clinical signs resembling those of PDNS-like disease were observed when piglets were inoculated with PCV3 alone or PCV3 combined with immunostimulation by keyhole limpet hemocyanin, with a mortality of 40% (2/5) for both types of inoculated piglets during a 28-day observation period postinoculation. Both types of inoculated piglets showed similar progressive increases in viral loads in the sera and had seroconverted to PCV3 capsid antibody after inoculation. Pathological lesions and PCV3-specific antigen were detected in various tissues and organs, including the lung, heart, kidney, lymph nodes, spleen, liver, and small intestine, in both types of inoculated piglets. The levels of proinflammatory cytokines and chemokines, including interleukin 1 beta (IL-1β), IL-6, IL-23α, gamma interferon (IFN-γ), tumor necrosis factor alpha (TNF-α), and chemokine ligand 5 (CCL5), were significantly upregulated in both groups of inoculated piglets. Eight-week-old piglets also exhibited a similar PDNS-like disease but without death after PCV3 inoculation, as evidenced by pathological lesions and PCV3 antigen in various tissues and organs. These results show for the first time successful reproduction of PDNS-like disease by PCV3 infection and further provide significant information regarding the pathogenesis of PCV3 in piglets. Porcine circovirus type 3 (PCV3), an emerging porcine circovirus, is considered the cause of porcine dermatitis and nephropathy syndrome (PDNS)-like clinical signs and other systemic diseases in piglets and sows. To evaluate the pathogenesis of PCV3 infection , we used a PCV3 virus stock from the rescue of an infectious PCV3 DNA clone to intranasally inoculate 4- and 8-week-old specific-pathogen-free piglets and demonstrated successful reproduction of PDNS-like disease in animals that were inoculated with PCV3 alone or PCV3 combined with immunostimulation by keyhole limpet hemocyanin. Both 4- and 8-week-old PCV3-inoculated piglets showed similar increases in viral loads in the sera and had seroconverted to PCV3 capsid antibody. Pathological lesions and PCV3-specific antigen were detected in various tissues and organs, while numerous proinflammatory cytokines and chemokines in the sera were significantly upregulated after PCV3 inoculation. These results will provide significant information regarding the pathogenesis of PCV3 in piglets.
猪圆环病毒 3 型(PCV3)是一种新兴的猪圆环病毒,与猪皮炎肾病综合征(PDNS)样临床症状、繁殖失败、心脏病变和仔猪及母猪的多系统炎症有关。然而,PCV3 感染生物学和发病机制的许多方面仍不清楚。在这里,我们使用从拯救感染性 PCV3 DNA 克隆中获得的 PCV3 病毒株,通过鼻腔接种 4 周和 8 周龄的无特定病原体猪,以评估 PCV3 的发病机制。对于 4 周龄的仔猪,当仔猪单独接种 PCV3 或 PCV3 与血蓝蛋白免疫刺激联合接种时,会观察到类似于 PDNS 样疾病的典型临床症状,在 28 天的接种后观察期内,两种接种类型的仔猪的死亡率均为 40%(2/5)。两种接种类型的仔猪在血清中的病毒载量均呈相似的逐渐增加,并在接种后对 PCV3 衣壳抗体产生血清转化。在两种接种类型的仔猪的各种组织和器官中,包括肺、心、肾、淋巴结、脾、肝和小肠,均检测到病理损伤和 PCV3 特异性抗原。在两组接种仔猪中,促炎细胞因子和趋化因子,包括白细胞介素 1β(IL-1β)、IL-6、IL-23α、γ干扰素(IFN-γ)、肿瘤坏死因子α(TNF-α)和趋化因子配体 5(CCL5)的水平均显著上调。8 周龄的仔猪在接种 PCV3 后也表现出类似的 PDNS 样疾病,但没有死亡,这从各种组织和器官中的病理损伤和 PCV3 抗原可以看出。这些结果首次成功地通过 PCV3 感染复制了 PDNS 样疾病,并进一步提供了有关 PCV3 在仔猪中发病机制的重要信息。猪圆环病毒 3 型(PCV3)是一种新兴的猪圆环病毒,被认为是引起仔猪皮炎肾病综合征(PDNS)样临床症状和其他系统性疾病的原因。为了评估 PCV3 感染的发病机制,我们使用从拯救感染性 PCV3 DNA 克隆中获得的 PCV3 病毒株,通过鼻腔接种 4 周和 8 周龄的无特定病原体猪,并证明了单独接种 PCV3 或 PCV3 与血蓝蛋白免疫刺激联合接种均可成功复制 PDNS 样疾病。单独接种 PCV3 或 PCV3 联合免疫刺激的 4 周和 8 周龄 PCV3 接种仔猪,血清中的病毒载量均呈相似增加,并对 PCV3 衣壳抗体产生血清转化。在各种组织和器官中均检测到病理损伤和 PCV3 特异性抗原,而在接种 PCV3 后,血清中的多种促炎细胞因子和趋化因子明显上调。这些结果将为了解 PCV3 在仔猪中的发病机制提供重要信息。