Kagoshima Research Station, National Institute of Animal Health (NIAH), National Agriculture and Food Research Organization (NARO), 2702 Chuzan, Kagoshima, Kagoshima, 891-0105, Japan.
Division of Infectious Animal Disease Research, NIAH, NARO, 3-1-5 Kannondai, Tsukuba, Ibaraki, 305-0856, Japan.
Arch Virol. 2024 Jun 3;169(6):133. doi: 10.1007/s00705-024-06058-8.
Akabane virus (AKAV), Aino virus, Peaton virus, Sathuperi virus, and Shamonda virus are arthropod-borne viruses belonging to the order Elliovirales, family Peribunyaviridae, genus Orthobunyavirus. These viruses cause or may cause congenital malformations in ruminants, including hydranencephaly, poliomyelitis, and arthrogryposis, although their pathogenicity may vary among field cases. AKAV may cause relatively severe congenital lesions such as hydranencephaly in calves. Furthermore, strains of AKAV genogroups I and II exhibit different disease courses. Genogroup I strains predominantly cause postnatal viral encephalomyelitis, while genogroup II strains are primarily detected in cases of congenital malformation. However, the biological properties of AKAV and other orthobunyaviruses are insufficiently investigated in hosts in the field and in vitro. Here, we used an immortalized bovine brain cell line (FBBC-1) to investigate viral replication efficiency, cytopathogenicity, and host innate immune responses. AKAV genogroup II and Shamonda virus replicated to higher titers in FBBC-1 cells compared with the other viruses, and only AKAV caused cytopathic effects. These results may be associated with the severe congenital lesions in the brain caused by AKAV genogroup II. AKAV genogroup II strains replicated to higher titers in FBBC-1 cells than AKAV genogroup I strains, suggesting that genogroup II strains replicated more efficiently in fetal brain cells, accounting for the detection of the latter strains mainly in fetal infection cases. Therefore, FBBC-1 cells may serve as a valuable tool for investigating the virulence and tropism of the orthobunyaviruses for bovine neonatal brain tissues in vitro.
阿卡斑病毒(AKAV)、Aino 病毒、Peaton 病毒、Sathuperi 病毒和 Shamonda 病毒是属于呼肠孤病毒目、布尼亚病毒科、正呼肠孤病毒属的虫媒病毒。这些病毒可引起或可能引起反刍动物的先天性畸形,包括无脑畸形、脊髓灰质炎和多发性关节弯曲症,尽管它们的致病性在田间病例中可能有所不同。AKAV 可引起相对严重的先天性病变,如犊牛的无脑畸形。此外,AKAV 基因Ⅰ组和Ⅱ组的毒株表现出不同的疾病过程。基因Ⅰ组毒株主要引起产后病毒性脑脊髓炎,而基因Ⅱ组毒株主要在先天性畸形病例中检测到。然而,AKAV 和其他正呼肠孤病毒在田间和体外宿主中的生物学特性研究还不够充分。在这里,我们使用永生化牛脑细胞系(FBBC-1)来研究病毒复制效率、细胞病变作用和宿主先天免疫反应。与其他病毒相比,AKAV 基因Ⅱ组和 Shamonda 病毒在 FBBC-1 细胞中的复制滴度更高,并且只有 AKAV 引起细胞病变效应。这些结果可能与 AKAV 基因Ⅱ组引起的大脑严重先天性病变有关。与 AKAV 基因Ⅰ组相比,AKAV 基因Ⅱ组毒株在 FBBC-1 细胞中的复制滴度更高,这表明基因Ⅱ组毒株在胎牛脑细胞中复制效率更高,这也是后者毒株主要在胎牛感染病例中检测到的原因。因此,FBBC-1 细胞可能是体外研究正呼肠孤病毒对牛新生脑组织毒力和嗜性的一种有价值的工具。