《中国畜牧兽医》 ›› 2017, Vol. 44 ›› Issue (12): 3585-3591.doi: 10.16431/j.cnki.1671-7236.2017.12.027

• 预防兽医 • 上一篇    下一篇

传染性法氏囊病病毒C4毒株VP2基因的原核表达及生物信息学分析

王洁琼, 赵玉杰, 周云飞, 黄宗梅, 陈盼盼, 周薇帆, 刘琳, 李新生   

  1. 河南农业大学牧医工程学院, 郑州 450002
  • 收稿日期:2017-05-18 出版日期:2017-12-20 发布日期:2017-12-20
  • 通讯作者: 李新生 E-mail:harmony69@163.com
  • 作者简介:王洁琼(1993-),女,河南郑州人,硕士,研究方向:畜禽疫病分子病原学及免疫学,E-mail:994925992@qq.com
  • 基金资助:

    国家十三五科技专项(2017YFD0500701)

Prokaryotic Expression and Bioinformatics Analysis of VP2 Gene of Infectious Bursal Disease Virus C4 Strain

WANG Jie-qiong, ZHAO Yu-jie, ZHOU Yun-fei, HUANG Zong-mei, CHEN Pan-pan, ZHOU Wei-fan, LIU Lin, LI Xin-sheng   

  1. College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou 450002, China
  • Received:2017-05-18 Online:2017-12-20 Published:2017-12-20

摘要:

试验旨在研究一株传染性法氏囊病病毒(IBDV)河南分离株的毒力特征及其与VP2氨基酸序列特征的关系。通过提取IBDV C4株RNA,利用RT-PCR扩增其VP2基因,与其他不同毒力IBDV毒株进行核苷酸及推导的氨基酸序列比对分析,同时使用pET-32a(+)原核表达载体表达VP2基因,用SDS-PAGE和Western blotting检测重组VP2蛋白的表达。结果显示,扩增的IBDV C4株的VP2基因序列在进化关系上属于超强毒力IBDV(vvIBDV)分类,与选取的vvIBDV毒株代表毒株核苷酸序列同源性在98.1%~98.7%之间,其七肽区为S-W-S-A-S-G-S(第326-332位氨基酸)符合超强毒株特征,且222(A)、256(I)、294(I)和299(S)位氨基酸与超强毒力毒株的4个特征性氨基酸一致;但IBDV C4毒株的VP2蛋白氨基酸序列与超强毒力毒株代表毒株UK661相比,201(D/G)、281(G/R)、313(V/A)位氨基酸不同,其中281位氨基酸的改变处于279-290的小亲水区内,与病毒抗原性有关;构建的pET-32a(+)-VP2原核表达载体在大肠杆菌BL21感受态细胞上表达出分子质量约67 ku的重组VP2蛋白,为进一步比较201(G)、281(R)、313(A)位氨基酸差异导致的抗原特性改变提供了研究基础。本试验结果表明,IBDV C4株VP2基因与vvIBDV毒株VP2基因的主要特性一致,但也有3处氨基酸与代表毒株UK661存在差异,这些改变可能与中国IBDV毒株毒力的进化有关。

关键词: 传染性法氏囊病病毒(IBDV); VP2; 分子特征; 原核表达

Abstract:

This study was aimed to investigate the relationship between the virulence characteristics of infectious bursal disease virus(IBDV) C4 strain and its VP2 amino acid sequence. The RNA of IBDV C4 strain was extracted,and its VP2 gene was amplified by RT-PCR.VP2 nucleotide sequences and deduced amino acids of different virulent IBDV strains were compared. At the same time, prokaryotic expression vector pET-32a(+) was used to express the VP2 gene. The expression of recombinant VP2 protein was detected by SDS-PAGE and Western blotting. The results showed that the VP2 gene of IBDV C4 strain belonged to the very virulent infectious bursal disease virus (vvIBDV) in evolutionary relationship, the VP2 nucleotides homology between IBDV C4 strain and other vvIBDV strains were 98.1% to 98.7%, and there were no mutations in S-W-S-A-S-G-S (326-332 amino acids) and 222(A), 256(I), 294(I) and 299(S). The VP2 amino acid sequence of IBDV C4 strain was consistent with the characteristics of other vvIBDV strains. However, there were three differences amino acids sites at 201(D/G), 281(G/R) and 313(V/A) between the amino acids of the C4 strain and the very virulent strain UK661. And the change of 281(R) was in the small hydrophilic region of 279 to 290, which was related to the antigenicity of the virus; The recombinant VP2 protein molecular weight expressed in Escherichia coli BL21 was about 67 ku. This study provided a basis for further research on antigenic changes resulting from amino acid variation of 201(G), 281 (R) and 313(A). These results indicated that the VP2 gene of the IBDV C4 strain was consistent with the major characteristics of the vvIBDV strain VP2 gene. The difference of three amino acid sites in the vvIBDV strain C4 might be related to the evolution of virulence of IBDV strain in China.

Key words: infectious bursal disease virus (IBDV); VP2; molecular characterization; prokaryotic expression

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