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Genetic Characterization and Pathogenicity of a Novel Recombined Porcine Reproductive and Respiratory Syndrome Virus 2 among Nadc30-Like, Jxa1-Like, and Mlv-Like Strains

机译:新型重组猪繁殖与呼吸综合征病毒2在Nadc30-like,Jxa1-Like和Mlv-Like株之间的遗传特征和致病性

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Recombination among porcine reproductive and respiratory syndrome viruses (PRRSVs), coupled with point mutations, insertions, and deletions occurring in the genome, is considered to contribute to the emergence of new variants. Here, we report the complete genome sequences of a PRRSV field strain, designated SCN17, isolated from a RespPRRS MLV-vaccinated piglet in China in 2017. Sequence alignment revealed that SCN17 had discontinuous 131-amino acid (111 + 1 + 19-aa) deletion in the NSP2-coding region identical to that of NADC30 when compared to VR-2332. Notably, the strain, SCN17, contained an additional 1-aa deletion in NSP2, a 1-aa deletion in ORF5, and a unique 3-nt deletion in the 3′-UTR. Phylogenetic analysis showed that SCN17 clustered into NADC30-like lineage based on ORF5 genotyping, whereas it belonged to an inter-lineage between the NADC30-like and VR-2332-like lineages as established based on the full-length genome. Importantly, the SCN17 was identified as a novel virus recombined between a NADC30-like (moderately pathogenic), a JXA1-like (highly pathogenic), and an attenuated vaccine strain, RespPRRS MLV (parental strain VR-2332). Furthermore, we tested its pathogenicity in piglets. SCN17 infection caused a persistent fever, moderate interstitial pneumonia, and increased the viremia and antibody levels in the inoculated piglets. Of note, all SCN17-infected piglets survived throughout the study. The new virus was showed to be a moderately virulent isolate and have lower pathogenicity than HP-PRRSV strain, SCwhn09CD. Our results provide evidence for the continuing evolution of PRRSV field strain by genetic recombination and mutation leading to outbreaks in the vaccinated pig populations in China.
机译:猪生殖和呼吸综合症病毒(PRRSV)之间的重组与基因组中发生的点突变,插入和缺失相结合,被认为有助于新变体的出现。在这里,我们报告了2017年从中国RespPRRS MLV疫苗接种的小猪中分离出的PRRSV野毒株SCN17的完整基因组序列。序列比对显示SCN17具有不连续的131个氨基酸(111 + 1 + 19-aa)与VR-2332相比,NSP2编码区域中的缺失与NADC30相同。值得注意的是,菌株SCN17在NSP2中包含一个额外的1-aa缺失,在ORF5中包含一个1-aa缺失,在3'-UTR中包含一个独特的3-nt缺失。系统发育分析表明,基于ORF5基因分型,SCN17聚类为NADC30样谱系,而它属于基于全长基因组建立的NADC30样谱系和VR-2332样谱系之间的谱系。重要的是,SCN17被鉴定为在NADC30样(中等致病性),JXA1样(高致病性)和减毒疫苗株RespPRRS MLV(亲本株VR-2332)之间重组的新型病毒。此外,我们测试了它在仔猪中的致病性。 SCN17感染导致持续发烧,中度间质性肺炎,并增加了已接种仔猪的病毒血症和抗体水平。值得注意的是,所有SCN17感染的仔猪在整个研究中均存活。与HP-PRRSV株SCwhn09CD相比,该新病毒显示为中等毒性分离株,病原性较低。我们的结果为通过基因重组和突变导致中国疫苗接种猪群暴发的PRRSV田间毒株的持续进化提供了证据。

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