Emergence and evolution of highly pathogenic porcine epidemic diarrhea virus by natural recombination of a low pathogenic vaccine isolate and a highly pathogenic strain in the spike gene
文献类型:期刊论文
作者 | Wang, Huinan2; Zhang, Libo2; Shang, Yuanbin2; Tan, Rongrong3; Ji, Mingxiang2; Yue, Xinliang2; Wang, Nannan2; Liu, Jun1; Wang, Chunhua2; Li, Yonggang4 |
刊名 | VIRUS EVOLUTION |
出版日期 | 2020-07-01 |
卷号 | 6期号:2页码:10 |
关键词 | porcine epidemic diarrhea virus evolution recombination pathogenicity spike gene |
DOI | 10.1093/ve/veaa049 |
通讯作者 | Li, Yonggang(lygjo@hotmail.com) ; Zhou, Tiezhong(ztz1818@126.com) |
英文摘要 | Outbreaks of a new variant of porcine epidemic diarrhea virus (PEDV) at the end of 2010 have raised interest in the mutation and recombination of PEDV. A PEDV strain (CN/Liaoning25/2018) isolated from a clinical outbreak of piglet diarrhea contained a 49-bp deletion in the ORF3 gene. This deletion is considered a genetic characteristic of low pathogenic attenuated vaccine strains. However, CN/Liaoning25/2018 was highly pathogenic. Complete genome sequencing, identity analysis, phylogenetic tree construction, and recombination analysis showed that this virus was a recombinant strain containing the Spike (S) gene from the highly pathogenic CN/GDZQ/2014 strain and the remaining genomic regions from the low pathogenic vaccine isolate SQ2014. Histopathology and immunohistochemistry results confirmed that this strain was highly pathogenic and indicated that intestinal epithelial cell vacuolation was positively correlated with the intensity and density of PEDV antigens. A new natural recombination model for PEDV was identified. Our results suggest that new highly pathogenic recombinant strains in the field may be generated by recombination between low pathogenic attenuated live PEDV vaccines and pathogenic circulating PEDV strains. Our findings also highlight that the 49-bp deletion of the ORF3 gene in low pathogenic attenuated vaccine strains will no longer be a reliable standard to differentiate the classical vaccine attenuated from the field strains. |
WOS关键词 | PCR ASSAY ; CORONAVIRUS ; DELTACORONAVIRUS ; DIVERSITY ; DIAGNOSIS ; AMERICAN ; GENOTYPE ; RECEPTOR ; OHIO |
资助项目 | Liaoning Provincial Natural Science Foundation of China[2019-ZD-0804] ; Liaoning Provincial Natural Science Foundation of China[2019-ZD-0817] ; Liaoning Provincial Natural Science Foundation of China[2019-ZD-0836] ; Liaoning Provincial Natural Science Foundation of China[2019-ZD-0613] ; Liaoning Provincial Natural Science Foundation of China[2015020779] ; Jinzhou Medical University Undergraduate Training Programs for Innovation and Entrepreneurship[201827] |
WOS研究方向 | Virology |
语种 | 英语 |
出版者 | OXFORD UNIV PRESS |
WOS记录号 | WOS:000610104700012 |
源URL | [http://119.78.100.183/handle/2S10ELR8/295936] |
专题 | 中国科学院上海药物研究所 |
通讯作者 | Li, Yonggang; Zhou, Tiezhong |
作者单位 | 1.Beijing Institude Feed Conrrol, Beijing 100107, Peoples R China 2.Jinzhou Med Univ, Coll Anim Husb & Vet Med, Dept Basic Vet Med, Jinzhou 121000, Peoples R China 3.Chinese Acad Sci, Ctr Drug Safety Evaluat & Res, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China 4.Jinzhou Med Univ, Sch Basic Med Sci, Dept Pathogen Biol, Jinzhou 121000, Peoples R China |
推荐引用方式 GB/T 7714 | Wang, Huinan,Zhang, Libo,Shang, Yuanbin,et al. Emergence and evolution of highly pathogenic porcine epidemic diarrhea virus by natural recombination of a low pathogenic vaccine isolate and a highly pathogenic strain in the spike gene[J]. VIRUS EVOLUTION,2020,6(2):10. |
APA | Wang, Huinan.,Zhang, Libo.,Shang, Yuanbin.,Tan, Rongrong.,Ji, Mingxiang.,...&Zhou, Tiezhong.(2020).Emergence and evolution of highly pathogenic porcine epidemic diarrhea virus by natural recombination of a low pathogenic vaccine isolate and a highly pathogenic strain in the spike gene.VIRUS EVOLUTION,6(2),10. |
MLA | Wang, Huinan,et al."Emergence and evolution of highly pathogenic porcine epidemic diarrhea virus by natural recombination of a low pathogenic vaccine isolate and a highly pathogenic strain in the spike gene".VIRUS EVOLUTION 6.2(2020):10. |
入库方式: OAI收割
来源:上海药物研究所
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