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广西猪瘟流行毒株全基因组的克隆与序列分析 被引量:5

Cloning and Sequence Analysis of Genome of Classical Swine Fever Virus GXWZ02 Strain Epidemic in Guangxi
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摘要 参考已发表的猪瘟病毒 (CSFV) Shimen株、HCL V株、Paderborn株的核苷酸序列 ,设计并合成 1 1对引物 ,应用RT- PCR技术 ,成功地分 1 1个片段扩增了 CSFV广西流行毒株 GXWZ0 2的全基因组。将这 1 1个基因片段克隆 ,并测定了其核苷酸序列。应用计算机生物软件 Vector NTI将 1 1个基因片段进行拼接 ,确认 CSFV GXWZ0 2株全基因组序列的长度为 1 2 2 96个核苷酸 (Gen Bank收录号 AY3 6 776 7)。将 GXWZ0 2株与国内外已发表的 Shimen、HCL V、3 9、Brescia、Eystrup、Glentorf、Alfort1 87、Paderborn、CS、AL D、GPE- 、P97、L PC毒株进行全基因组核苷酸序列和推定的氨基酸序列比较 ,核苷酸同源性分别为 85 .4 %、 84 .6 %、88.7%、85 .7%、 85 .7%、 85 .3 %、85 .6 %、 95 .3 %、 85 .7%、85 .7%85 .4 %、83 .4 %、84 .3 % ,推定的氨基酸同源性分别为 92 .6 %、91 .7%、94 .2 %、 93 .1 %、92 .9%、92 .3 %、 93 .0 %、97.7%、92 .6 %、93 .0 %、92 .6 %、90 .5 %、90 .6 %。 GXWZ0 2与 Shimen、HCL V的全基因组序列及推定的氨基酸序列有明显差异 ,表明 GXWZ0 2株在遗传性和抗原性上发生了较明显的变化。系统发育树分析 ,所比较的 1 4株 CSFV被分为2个群 :GXWZ0 2、Paderborn和 3 9这 3个毒株被归为群 . In this study,11 pairs of specific primers were designed and synthesized.Using these primers,Eleven fragments had been successfully amplified from CSFV GXWZ02 strain by RT-PCR.These amplified fragments were cloned and sequenced.Assembly of sequences of the 11 fragments into a contiguous sequence was done using Vector NTI software.There are (12 296) nucleotides in the genome of GXWZ02 strain.Comparison of the genomic nucleotide sequence and the deduced amino acid sequence of GXWZ02 with that of Shimen,HCLV,39,Brescia,Eystrup,Glentorf,Alfort187,Paderborn,CS,ALD,GPE^(-),P97 and LPC,showed that the nucleotide homologies were 85.4%,84.6%,88.7%,85.7%,85.7%,85.3%,85.6%,95.3%,85.7%,85.7%,85.4%,83.4% and 84.3%,respectively,the amino acid sequence homologies were 92.6%,91.7%,94.2%,93.1%,92.9%,92.3%,93.0%,97.7%,92.6%,93.0%,92.6%,90.5% and 90.6%,respectively.The homologies of genomic nucleotide sequence and deduced amino acid sequence of CSFV GXWZ02 with that of Shimen,HCLV were low,indicating that GXWZ02 was genetically different from Shimen and HCLV.Phylogenetic tree analysis based on the genomic nucleotide sequence showed that the 14 CSFV stains belonged to two groups.GXWZ02,Paderborn and 39 were classified into groupⅠ,and the other strains were classified into groupⅡ.The genetic relationship is very close between GXWZ02 and Paderborn.Comparison of the nucleotide sequences and the deduced amino acid sequences of different gene of GXWZ02 with that of Shimen,HCLV,demonstrated that the genetic variation rate of E^(rns),E2,P7,NS2 and NS5A genes was high,while that of NS3,NS4A and NS4B genes was low.
出处 《中国兽医学报》 CAS CSCD 北大核心 2005年第2期125-128,共4页 Chinese Journal of Veterinary Science
基金 广西科技厅科研基金项目(桂科青9912015)
关键词 猪瘟病毒 基因组克隆 序列分析 GXWZ02株 猪瘟 classical swine fever virus genome sequence analysis GXWZ02 strain
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  • 1尹革芬,朱建波,姚俊,高华峰,信爱国,张念祖.猪瘟病毒云南毒株E2基因片段序列测定及分析[J].中国预防兽医学报,2001,23(3):167-169. 被引量:9
  • 2罗廷荣,波丹,黄宪高,梁家权,刘芳,黄伟坚,秦爱珍,温荣辉,陆芹章,余克伦.RT-PCR检测猪瘟病毒初探[J].广西农业生物科学,2001,20(1):17-20. 被引量:24
  • 3吴健敏,蒋冬福,韦志峰,杜坚,吕宗吉,李月红,涂长春.广西猪瘟流行现状的调查分析[J].中国兽医科技,2002,32(2):16-18. 被引量:13
  • 4张永国,刘湘涛,韩雪清,张彦明,薛青红.广西猪瘟流行毒与C-株疫苗毒gp55(E_2)主要抗原区DNA序列差异的比较[J].西北农林科技大学学报(自然科学版),2002,30(1):79-84. 被引量:8
  • 5韩雪清 李红卫 刘湘涛.中国猪瘟兔化弱毒(C-株)兔脾组织毒E2(gp55)基因的序列分析[A]..中国农业科学院第五次青年优秀论文获奖论文集[C].,1999.12..
  • 6赵耘,王在时,王琴,李博,丘惠深.23株猪瘟病毒E2基因主要抗原编码区序列差异分析[J].中国兽医科技,2002,32(3):3-7. 被引量:17
  • 7Konig M, Lengsfeld T, Pauly T,et al. Classical swine fever virus; independent induction of protective immunity by two structural protect [J]. J Virol, 1995,69:6 479-6 486.
  • 8van Rijn A,van Gennip H G P,de Meijer E J,et al. A preliminary map of epitope glycoprotein E2 of hog cholera virus strain Brescia[J]. J Gen Virol, 1993,74 : 2 053-2 060.
  • 9van Rijn P A,Miedema G K W,van Gennip H G P,et al. Antigenic structure of envelope glycoprotein E2 of hog cholera virus[J]. J Virol,1994,68:3 934-3 942.
  • 10Lin M, Lin F, Mallory M,et al, Deletions of structural glycoprotein E2 of classical swine fever virus strain alfort/87 resolve a linear of monoclonal antibody WH303 and the minimal N-terminal domain essential for binding immunoglobulin G antibodies of a pig hyperimmune serum[J]. J Virol, 2000, 74:11 619-11 625.

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