Zhang Zhendong, Li Duo, He Sun, Du Jiubin, Li Yubo, Liu Qiangde, Wang Pengjiang, Wang Wenqiang, Wen Wei, Zhu Zhenbang, Tang Xudong, Li Xiangdong
Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, College of Veterinary Medicine, Yangzhou University, Yangzhou, China.
School of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang, China.
Front Vet Sci. 2025 Apr 2;12:1531861. doi: 10.3389/fvets.2025.1531861. eCollection 2025.
In order to better understand the pathogenicity of the current porcine A group rotavirus (PoRVA) field strains, AHBZ2304 (G9P[23]) and AHBZ2303 (G11P[7]) isolated from diarrhea suckling piglets were selected for pathogenicity analysis in the present study. Experimental inoculation of colostrum-deprived 2-day-old piglets revealed that both isolates caused severe clinical sings, high level of virus shedding and significant damage to the small intestinal villi. Additionally, both gross and microscopic lung lesions were identified at 72 h post infection (HPI) compared to control. Alterations in the microbiota and the overexpression of inflammatory cytokines may serve as critical mechanisms driving the bowel disease associated with PoRVA infection. Our results are of great significance for understanding the pathogenicity of PoRVA emerged in recent years, highlighting the potential for porcine rotavirus to become epidemic and complex, and necessitating heightened attention of the often-overlooked disease in the field.
为了更好地了解当前猪 A 组轮状病毒(PoRVA)野毒株的致病性,本研究选取了从腹泻仔猪中分离出的 AHBZ2304(G9P[23])和 AHBZ2303(G11P[7])进行致病性分析。对初乳剥夺的 2 日龄仔猪进行实验接种发现,这两种分离株均引起严重的临床症状、高水平的病毒排出以及对小肠绒毛的显著损伤。此外,与对照组相比,在感染后 72 小时(HPI)均发现了肉眼可见和显微镜下的肺部病变。微生物群的改变和炎性细胞因子的过度表达可能是驱动与 PoRVA 感染相关肠道疾病的关键机制。我们的结果对于理解近年来出现的 PoRVA 的致病性具有重要意义,凸显了猪轮状病毒流行和复杂化的可能性,并且有必要提高对该领域中常被忽视疾病的关注度。