Kim Deok-Song, Kang Mun-Il, Son Kyu-Yeol, Bak Geon-Yong, Park Jun-Gyu, Hosmillo Myra, Seo Ja-Young, Kim Ji-Yun, Alfajaro Mia Madel, Soliman Mahmoud, Baek Yeong-Bin, Cho Eun-Hyo, Lee Ju-Hwan, Kwon Joseph, Choi Jong-Soon, Goodfellow Ian, Cho Kyoung-Oh
Laboratory of Veterinary Pathology, College of Veterinary Medicine, Chonnam National University, Gwangju, Republic of Korea.
Division of Virology, Department of Pathology, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.
J Gen Virol. 2016 Oct;97(10):2566-2574. doi: 10.1099/jgv.0.000571. Epub 2016 Aug 2.
Sapelovirus A (SV-A), formerly known as porcine sapelovirus as a member of a new genus Sapelovirus, is known to cause enteritis, pneumonia, polioencephalomyelitis and reproductive disorders in pigs. We have recently identified α2,3-linked sialic acid on GD1a ganglioside as a functional SV-A receptor rich in the cells of pigs and chickens. However, the role of GD1a in viral pathogenesis remains elusive. Here, we demonstrated that a Korean SV-A strain could induce diarrhoea and intestinal pathology in piglets but not in chicks. Moreover, this Korean SV-A strain had mild extra-intestinal tropisms appearing as mild, non-suppurative myelitis, encephalitis and pneumonia in piglets, but not in chicks. By real-time reverse transcription (RT) PCR, higher viral RNA levels were detected in faecal samples than in sera or extra-intestinal organs from virus-inoculated piglets. Immunohistochemistry confirmed that high viral antigens were detected in the epithelial cells of intestines from virus-inoculated piglets but not from chicks. This Korean SV-A strain could bind the cultured cell lines originated from various species, but replication occurred only in cells of porcine origin. These data indicated that this Korean SV-A strain could replicate and induce pathology in piglets but not in chicks, suggesting that additional porcine-specific factors are required for virus entry and replication. In addition, this Korean SV-A strain is enteropathogenic, but could spread to the bloodstream from the gut and disseminate to extra-intestinal organs and tissues. These results will contribute to our understanding of SV-A pathogenesis so that efficient anti-sapelovirus drugs and vaccines could be developed in the future.
A 型萨佩洛病毒(SV-A),以前称为猪萨佩洛病毒,是新属萨佩洛病毒的成员,已知可导致猪的肠炎、肺炎、脑脊髓灰质炎和生殖障碍。我们最近在 GD1a 神经节苷脂上鉴定出α2,3 连接的唾液酸是猪和鸡细胞中富含的功能性 SV-A 受体。然而,GD1a 在病毒发病机制中的作用仍然难以捉摸。在这里,我们证明一株韩国 SV-A 毒株可在仔猪中诱导腹泻和肠道病变,但在雏鸡中不会。此外,该韩国 SV-A 毒株具有轻度的肠外嗜性,在仔猪中表现为轻度、非化脓性脊髓炎、脑炎和肺炎,但在雏鸡中没有。通过实时逆转录(RT)PCR,在粪便样本中检测到的病毒 RNA 水平高于接种病毒的仔猪的血清或肠外器官。免疫组织化学证实,在接种病毒的仔猪肠道上皮细胞中检测到高病毒抗原,但在雏鸡中未检测到。该韩国 SV-A 毒株可与源自各种物种的培养细胞系结合,但仅在猪源细胞中复制。这些数据表明,该韩国 SV-A 毒株可在仔猪中复制并诱导病变,但在雏鸡中不会,这表明病毒进入和复制需要额外的猪特异性因子。此外,该韩国 SV-A 毒株具有肠道致病性,但可从肠道扩散到血液中,并传播到肠外器官和组织。这些结果将有助于我们理解 SV-A 的发病机制,以便未来能够开发出有效的抗萨佩洛病毒药物和疫苗。