期刊文献+

一株自然基因重排鸡传染性法氏囊病病毒的分离鉴定及其分子特征分析 被引量:1

Isolation of Infectious Bursal Disease Virus and Characterization of its Genome
原文传递
导出
摘要 研究通过鸡胚绒毛尿囊膜(CAM)接种SPF鸡胚的方法从可疑鸡群的法氏囊样品中分离获得了1株鸡传染性法氏囊病病毒(infectious bursal disease,IBDV),命名为YY1213。基于IBDV基因组A节段的VP2基因高变区(vVP2)和B节段的VP1-b区的序列测定和分析表明,分离株YY1213在vVP2上的关键氨基酸特征与vvIBDV类似,并与vvIBDV参考株具有较高的同源性,但在VP1-b上的特征性氨基酸位点则既有弱毒株的特征,又具有vvIBDV的特征,与中国内地分离株重组毒株HLJ-0504的同源性较高,氨基酸同源性达到了99.6%;此外,在遗传进化分析上,基于vVP2,YY1213与vvIBDV高度同源,而基于VP1-b,则介于vvIBDV和弱毒株之间,形成独特分支。结果表明,分离株YY1213的vVP2和VP1-b具有不同的来源,属于基因重排病毒。 An infectious bursal disease virus(IBDV isolate YY1213) was isolated from the IBD suspected chicken flock by chicken embryo inoculation of the Fabricus' bursa suspension via chorio-allantoic membrane(CAM). The sequence analysis of VP2 hypervariable region(vVP2) from IBDV genome segment A indicated that, the isolate was classified to be potent virulent IBDV(vvIBDV) according to critical amino acid sequences and showed the highest similarity to reference strains of vvIBDV. But when the sequence analysis of VP1-b fragment from IBDV genome segment B was done, the isolate showed mixed characteristic amino acid sites, some of these sites were similar to vvIBDV, others were similar to attenuated IBDVs, and showed 99.6% homology to a Chinese reassortant strain HLJ-0504. Furthermore, in the phylogenetic analysis, YY1213 was grouped with vvIBDV reference strains based on vVP2, however it was showed an independent cluster between vvIBDV and classical strains when based on VP1-b. These results suggested that genomic fragments A-vVP2 and B-VP1-b of the isolate YY1213 were of different origins, and YY1213 seems to be a reassortment virus.
出处 《基因组学与应用生物学》 CAS CSCD 北大核心 2014年第2期282-287,共6页 Genomics and Applied Biology
基金 广西自然科学基金项目(2012GXNSFAA053060) 广西高校科学技术研究项目(2013YB069) 广西民族大学2013年研究生教育创新计划项目(gxun-chx201300) 广西科技攻关项目(2007A04024)共同资助
关键词 传染性法氏囊病病毒 基因重排 分子特征 RT-PCR Infectious bursal disease virus Segment reassortant Molecular character RT-PCR
  • 相关文献

参考文献13

  • 1Dhillon A.S., Kibenge F.S., and Russol R.G., 1988, Biochemistry and immunology of infectious bursal disease virus, J. Gen. Virol., 69(Pt8): 17:;7-1775.
  • 2高立,祁小乐,高玉龙,高宏雷,秦立廷,邓小芸,宇文延青,王笑梅.传染性法氏囊病病毒超强毒株HLJ-0504全基因组克隆及其新特征分析[J].中国预防兽医学报,2010,32(5):401-404. 被引量:11
  • 3He C.Q., Ma L.Y., Wang D., Li G.R., and Ding N.Z., 2009, Homologous reeorabination is apparent in infectious bursal disease virus, Virology, 384(1): 51-58.
  • 4何秀苗,官丁明,韦平,禤金彩,屈祖平,秦爱建.广西地区传染性囊病病毒超强毒株的分离鉴定及其VP2基因高变区的序列分析[J].中国兽医杂志,2009,45(9):7-9. 被引量:8
  • 5He X.M., Wei P., Yang X.Y., Guan D., Wang G., and Qin A., 2012, Molecular epidemiology of infectious bursal disease viruses isolated frc:m southern China during the years of 2000-2010, Virus. Gene., 45(2): 246-255.
  • 6Jackwood J., Sommer-Wagner S.E., Crossley B.M., Stoute S.T., Woolcock P.R., and Charlton B.R., 2011, Identification and pathogenicity of a natural reassortant between a very viru- lent serotype 1 inti:ctious bursal disease virus (IBDV) and a serotype 2 IBDV, Virology, 420(3): 98-105.
  • 7Kasanga C.J., Yamaguchi T., Munang'andu H.M., Ohya K., and Fukushi H., 2013, Genomic sequence of an infectious bursal disease virus isolale from Zambia: Classical attenuated seg- ment B reassortment in nature with existing very virulent segment A, Arch. Virol., 158(1): 685-689.
  • 8Le Nou:n C., Rivallan G., Toquin D., and Eterradossi N., 2005, Significance of the genetic relationships deduced from par- tial nucleotide seqaencing of infectious bursal disease virus genome segments A or B, Arch.Virol., 150(2): 313-325.
  • 9Le Nouen C., Rivallan 13., Toquin D., Darlu P., Morin Y., Beven V., de Boisseson C., Cazaban C., Comte S., Gardin Y., and Eterradossi N., 2006, Very virulent infectious bursal disease virus: Reduced pathogenicity in a rare natural segment-B- reassorted isolate, .r. Gen. Virol., 87(1): 209-216.
  • 10萨姆布鲁克J.,拉塞尔D.W.,主编,黄培堂,王嘉玺,朱厚础.主译,2002,分子克隆实验指南,第三版,科学出版社,中国,北京,PP.123-124.

二级参考文献41

共引文献29

同被引文献14

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部