...
首页> 外文期刊>Virus Genes >Sequence analysis of the variable VP2 gene of infectious bursal disease viruses passaged in Vero cells.
【24h】

Sequence analysis of the variable VP2 gene of infectious bursal disease viruses passaged in Vero cells.

机译:在Vero细胞中传代的传染性法氏囊病病毒VP2可变基因的序列分析。

获取原文
获取原文并翻译 | 示例

摘要

Korean field infectious bursal disease viruses (IBDVs) were isolated from IBDV suspected commercial chickens. A previous study revealed that these IBDV field isolates were virulent or very virulent IBDVs. The isolates were passaged three times in the chorioallantoic membrane of specific-pathogen-free embryonated chicken eggs and four times in Vero cells. After passage, viral RNAs were isolated and purified to determine the genetic changes. The hypervariable regions of the VP2 gene were amplified by reverse transcriptase-polymerase chain reaction (RT-PCR). To confirm the genetic changes, PCR products were cloned, sequenced and compared to the sequences of the parental IBDVs and published IBDV strains. By sequencing analysis, the passaged IBDVs had amino acid changes at positions 253 (Q --> H), 279 (D or N --> N) and 284 (A --> T) which were commonly found in the attenuated IBDV strains. Two serines in the serine-rich heptapeptide (residue 326-332) were substituted into other amino acids which were similar to the IBDV vaccine strains.
机译:从可疑IBDV商业鸡中分离出大韩民国传染性法氏囊病病毒(IBDV)。先前的研究表明,这些IBDV野外分离株是有毒的或非常有毒的IBDV。分离株在无特定病原体的胚鸡蛋的绒毛尿囊膜中传代3次,在Vero细胞中传代4次。传代后,分离并纯化病毒RNA,以确定遗传变化。 VP2基因的高变区通过逆转录聚合酶链反应(RT-PCR)进行扩增。为了证实遗传变化,将PCR产物克隆,测序并与亲本IBDV和已发表的IBDV菌株的序列进行比较。通过测序分析,传代的IBDVs在减毒的IBDV菌株中通常在253位(Q-> H),279位(D或N-> N)和284位(A-> T)具有氨基酸变化。 。富含丝氨酸的七肽中的两个丝氨酸(残基326-332)被替换为与IBDV疫苗株相似的其他氨基酸。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号