Zhang Huawei, Chen Pin, Hao Genxi, Liu Wenqiang, Chen Huanchun, Qian Ping, Li Xiangmin
State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
Laboratory of Animal Virology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China.
Pathogens. 2020 Jan 2;9(1):39. doi: 10.3390/pathogens9010039.
Senecavirus A (SVA), an emerging infectious disease, is associated with the porcine idiopathic vesicular disease. Here, the pathogenesis of different strains of SVA was investigated in growing-finishing pigs. We aimed to evaluate the replication characteristics, virus particle morphology, clinical signs, and vesicular lesions in comparison with two different strains of SVA. The animals were infected with SVA HB-CH-2016 or CH/AH-02/2017 by intranasal routes (3 mL, 10TCID/mL) and monitored daily for 14 days post-inoculation (dpi) for clinical signs and vesicular lesions. Viremia or viral shedding was detected in the blood, fecal swab, and nasal swab samples. Results showed no distinct differences in plaque size, replication ability, and characteristic virions between SVA HB-CH-2016 and CH/AH-02/2017 strains. Animal experimental results showed that both SVA CH/AH-02/2017 and SVA HB-CH-2016 could infect pigs. However, an obvious difference in the pathogenicity and dynamics of infection was observed between SVA HB-CH-2016 and CH/AH-02/2017 strains. The pathogenesis of SVA CH/AH-02/2017 was similar to that of published results of USA strains, whereas the SVA HB-CH-2016 strain had low pathogenicity to pigs. Clinical signs and vesicular lesions were observed in SVA CH/AH-02/2017-infected pigs. Additionally, the different branches of SVA should be capable of inducing broad cross-reactive neutralizing antibodies, which play an important role in clearing the SVA virus. This study of animal models for SVA infection will be beneficial to develop vaccines and antivirals.
A组赛内卡病毒(SVA)是一种新发传染病,与猪特发性水疱病有关。在此,我们对生长育肥猪中不同毒株的SVA发病机制进行了研究。我们旨在与两种不同的SVA毒株比较,评估其复制特性、病毒颗粒形态、临床症状和水疱病变。通过鼻内途径(3 mL,10TCID/mL)用SVA HB-CH-2016或CH/AH-02/2017感染动物,并在接种后14天(dpi)每天监测临床症状和水疱病变。在血液、粪便拭子和鼻拭子样本中检测病毒血症或病毒脱落情况。结果显示,SVA HB-CH-2016和CH/AH-02/2017毒株在蚀斑大小、复制能力和特征性病毒粒子方面没有明显差异。动物实验结果表明,SVA CH/AH-02/2017和SVA HB-CH-2016均可感染猪。然而,在SVA HB-CH-2016和CH/AH-02/2017毒株之间观察到致病性和感染动态存在明显差异。SVA CH/AH-02/2017的发病机制与美国毒株已发表的结果相似,而SVA HB-CH-2016毒株对猪的致病性较低。在感染SVA CH/AH-02/2017的猪中观察到临床症状和水疱病变。此外,SVA的不同分支应能够诱导广泛的交叉反应性中和抗体,这在清除SVA病毒中起重要作用。这项对SVA感染动物模型的研究将有助于开发疫苗和抗病毒药物。