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高致病性猪繁殖与呼吸综合征病毒变异株主要囊膜糖蛋白GP5的遗传变异分析 被引量:14

Genetic diversity of glycoprotein 5 of highly pathogenic porcine reproductive and respiratory syndrome virus isolates in China
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摘要 为了探究高致病性猪蓝耳病病毒(HP-PRRSV)的遗传变异特征,本研究对GenBank中235株HP-PRRSV GP5序列的遗传进化、主要氨基酸基序、抗原性以及N-糖基化位点数量和位置的变异进行了分析。结果表明HP-PRRSV之间的同源性较高,与其他参考毒株相比,这些病毒处于一个相对独立的分支中,而且与经典疫苗株的亲缘关系较远。这有助于解释经典疫苗株对于HP-PRRSV为何起不到理想的免疫保护效果。在病毒的中和表位序列中存在着规律的点突变,同时抗原性比较显示HP-PRRSV与经典毒株之间存在着一定的差异。绝大多数的HP-PRRSV的N-糖基化位点在数量上多一个,而且位置要向羧基端平移2个氨基酸,从而使得中和表位两侧直接与糖链相连,可能会造成中和表位被糖侧链所遮掩,本研究由此推测减弱中和抗体对HP-PRRSV的有效识别,促进病毒逃避机体体液免疫。 A highly pathogenic porcine reproductive and respiratory syndrome (HP-PRRSV) was emerged in China since the summer of 2006. In order to investigate the genetic diversity of HP-PRRSV, we analyzed 235 GP5 sequences of HP-PRRSVs deposited in GenBank and compared with those of homologous amino acid neutralizing among themselves, but genetically distinct classical from the strains. The results showed that the HP-PRRSVs were highly vaccine strains which were derivated from classical mutation occurred in the prime neutralizing epitope and an additional N-glyscan chain was found close epitope. It was proposed that this N-glyscan chain could contribute to the viral immunological escape PRRSVs. An to the prime from humoral immunity.
出处 《中国预防兽医学报》 CAS CSCD 北大核心 2008年第11期851-856,共6页 Chinese Journal of Preventive Veterinary Medicine
基金 国家基础研究973基金资助项目(2005CB523200) 国家科技支撑计划(2007BAD86B05/03)
关键词 高致病性猪繁殖与呼吸综合征 GP5 序列分析 遗传变异 糖基化 highly pathogenic porcine reproductive and respiratory syndrome GP5 sequence analysis genetic diversity N-glyscan
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参考文献17

  • 1Tian K, Yu X, Zhao T, et al. Emergence of fatal PRRSV variants: unparalleled outbreaks of atypical PRRS in China and molecular dissection of the unique hallmark [J]. PLoS ONE, 2007, 6(13): 526.
  • 2Li Y, Wang X, Bo K, et al. Emergence of a highly pathogenic porcine reproductive and respiratory syndrome virus in the Mid- Eastern region of China [J]. Vet J, 2007, 174(3): 577-584.
  • 3Tong G Z, Zhou Y J, Hao X F, et al. Emergence of the high pathogenic porcine reproductive and respiratory syndrome in China [J]. Emerging Infectious Diseases, 2007, 13(9): 1434-1436.
  • 4Zhou Y J, Hao X F, Tian Z J, et al. Highly virulent porcine reproductive and respiratory syndrome virus emerged in China [J]. Transbound Emerg Dis, 2008, 55(3-4): 152-164.
  • 5An T Q, Zhou Y J, Eiu G Q, et al. Genetic diversity and phylogenetic analysis of glycoprotein 5 of PRRSV isolates in China's Mainland from 1996 to 2006: coexistence of two NA- subgenotypes with polar diversity [J]. Vet Microbiol, 2007, 123: 43-52.
  • 6Indik S, Schmoll F, Sipos W, et al. Genetic variability of PRRS virus in Austria: consequences for molecular diagnostics and viral quantification [J]. Vet Microbiol, 2005, 107: 171-178.
  • 7Cha S H, Choi E J, Park J H, et al. Molecular characterization of recent Korean porcine reproductive and respiratory syndrome (PRRS) viruses and comparison to other Asian PRRS viruses [J]. Vet Microbiol, 2006, 117: 248-257.
  • 8Mateu E, Diaz I, Darwich L, et al. Evolution of ORF5 of Spanish porcine reproductive and respiratory syndrome virus strains from 1991 to 2005 [J]. Virus Res, 2006, 115: 198-206.
  • 9Thompson J D, Gibson T J, Plewniak F, et al. The ClustalX windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools [J]. Nucleic Acids Research, 1997, 25: 4876-4882.
  • 10Kumar S, Tamura K, Nei M. MEGA3: Integrated software for molecular evolutionary genetics analysis and sequence alignment [J]. Briefings in Bioinformatics, 2000, 5: 150-163.

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