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Molecular epidemiology of PRRSV from China’s Guangxi Province between 2007 and 2009
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  • 作者:Hong-Yun Zhang (2)
    Jing-Jing Liang (1) (2)
    Xian-Ming Meng (2)
    Hui Li (2)
    Jian Yang (2)
    Li-Juan Su (2)
    Hong-Pu Zhang (2)
    Lin-Juan Xie (2)
    Xiao-Xia He (2)
    Yan-Sheng Li (2)
    Shan Yin (2)
    Xiao-Quan Li (2)
    Xiao-ning Li (1) (2)
    Ting Rong Luo (1) (2)
  • 关键词:Porcine reproductive and respiratory syndrome virus (PRRSV) ; ORF5 ; Nsp2 ; Molecular epidemiology
  • 刊名:Virus Genes
  • 出版年:2013
  • 出版时间:February 2013
  • 年:2013
  • 卷:46
  • 期:1
  • 页码:71-80
  • 全文大小:999KB
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  • 作者单位:Hong-Yun Zhang (2)
    Jing-Jing Liang (1) (2)
    Xian-Ming Meng (2)
    Hui Li (2)
    Jian Yang (2)
    Li-Juan Su (2)
    Hong-Pu Zhang (2)
    Lin-Juan Xie (2)
    Xiao-Xia He (2)
    Yan-Sheng Li (2)
    Shan Yin (2)
    Xiao-Quan Li (2)
    Xiao-ning Li (1) (2)
    Ting Rong Luo (1) (2)

    2. College of Animal Sciences and Veterinary Medicine, Guangxi University, 100 Daxue Road, Nanning, 530004, Guangxi, China
    1. State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi University, 100 Daxue Road, Nanning, 530004, Guangxi, China
  • ISSN:1572-994X
文摘
Porcine reproductive and respiratory syndrome (PRRS) is considered to be one of the most important infectious diseases affecting livestock. This study used gene sequence analysis of ORF5 and Nsp2 to determine the molecular epidemiology of PRRSV in different parts of the Guangxi province of China. These genes were selected due to their extensive variation within the genome. Out of 189 samples from animals suspected to have PRRS, 145 were PRRSV RNA positive. ORF5 and Nsp2 gene sequence analysis of 31 of these samples showed that all of the Guangxi isolates were of type 2. A phylogenetic tree analysis based on ORF5 showed that the Guangxi isolates were divided into two groups. Most of these were closely related to highly pathogenic strains, showing a 30 amino acid deletion at positions 481 and 533-61 of Nsp2, but an additional unique isolate (GXNN06) possessed a further four amino acid deletion at positions 485-88 of Nsp2.

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