Characterization of a cell-adapted completely attenuated genotype GIIa porcine epidemic diarrhea virus strain

IF 2.4 3区 医学 Q3 VIROLOGY Virology Pub Date : 2025-03-01 Epub Date: 2025-01-10 DOI:10.1016/j.virol.2025.110407
Ruiming Yu , Liping Zhang , Dongsheng Wang , Jun Yang , Peng Zhou , Yuhan Wen , Mingxia Li , Yingjie Bai , Zhongwang Zhang , Yousheng Peng , Yanzhen Lu , Dan Li , Jian He , Yonglu Wang , Huichen Guo , Li Pan , Xinsheng Liu
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Abstract

Porcine epidemic diarrhea virus (PEDV) has caused significant harm to the global pig industry since its discovery. In this study, a highly pathogenic strain of GIIa PEDV CH/HBXT/2018, isolated previously, was continuously passaged in Vero cells up to passage (P)240, resulting in a completely attenuated virus. The proliferation characteristics of different passages of the strain in Vero cells, pathogenicity in newborn piglets, and mutations in S gene sequence indicated that as the passage number increased, the replication efficiency of PEDV in Vero cells gradually improved, with a more pronounced cytopathic effect. However, its pathogenicity in piglets decreased progressively, evident as reduced viral loads in the feces and intestinal tissues, less-severe clinical symptoms, less-severe histopathological damage, and lower antigen expression in intestinal tissues. At P240, the strain was completely attenuated. A sequence analysis revealed 17 amino acid mutations in the structural spike protein, which may have contributed to the biological changes observed at P240. Furthermore, compared with P10, the strain's dependence on trypsin had decreased significantly at P200. A differential transcriptomic analysis revealed 1712 differentially expressed genes (DEGs) between the P10 and P200 infection groups, of which 458 were upregulated and 1254 downregulated. These DEGs were primarily involved in signaling pathways such as cytokine–cytokine receptor interaction, inflammatory response, and MHC protein complex. Our findings provide valuable insights into the mechanisms of PEDV attenuation and should facilitate the development of live vaccines.
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猪流行性腹泻病毒GIIa基因型全减毒株的细胞适应性鉴定。
猪流行性腹泻病毒(PEDV)自发现以来,对全球养猪业造成了重大危害。在本研究中,将先前分离的GIIa PEDV CH/HBXT/2018高致病性毒株在Vero细胞中连续传代至传代(P)240,得到完全减毒的病毒。该菌株不同传代在Vero细胞中的增殖特性、在新生仔猪中的致病性以及S基因序列的突变表明,随着传代次数的增加,PEDV在Vero细胞中的复制效率逐渐提高,细胞病变作用更加明显。然而,其在仔猪中的致病性逐渐降低,表现为粪便和肠组织中的病毒载量降低,临床症状不那么严重,组织病理学损伤不那么严重,肠组织中抗原表达降低。在P240时,菌株完全衰减。序列分析显示,结构刺突蛋白中有17个氨基酸突变,这可能导致了P240处观察到的生物学变化。此外,与P10相比,菌株对胰蛋白酶的依赖性在P200时显著降低。差异转录组学分析显示,P10和P200感染组之间有1712个差异表达基因(DEGs),其中458个表达上调,1254个表达下调。这些deg主要参与信号通路,如细胞因子-细胞因子受体相互作用、炎症反应和MHC蛋白复合物。我们的发现为PEDV的衰减机制提供了有价值的见解,并应促进活疫苗的开发。
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来源期刊
Virology
Virology 医学-病毒学
CiteScore
6.00
自引率
0.00%
发文量
157
审稿时长
50 days
期刊介绍: Launched in 1955, Virology is a broad and inclusive journal that welcomes submissions on all aspects of virology including plant, animal, microbial and human viruses. The journal publishes basic research as well as pre-clinical and clinical studies of vaccines, anti-viral drugs and their development, anti-viral therapies, and computational studies of virus infections. Any submission that is of broad interest to the community of virologists/vaccinologists and reporting scientifically accurate and valuable research will be considered for publication, including negative findings and multidisciplinary work.Virology is open to reviews, research manuscripts, short communication, registered reports as well as follow-up manuscripts.
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