首页> 外文期刊>Veterinary World >Molecular characterization of field infectious bursal disease virus isolates from Nigeria
【24h】

Molecular characterization of field infectious bursal disease virus isolates from Nigeria

机译:来自尼日利亚的现场传染性法氏囊病病毒分离株的分子表征

获取原文
获取外文期刊封面目录资料

摘要

Aim: To characterize field isolates of infectious bursal disease virus (IBDV) from outbreaks in nine states in Nigeria through reverse transcription polymerase chain reaction (RT-PCR) and sequence analysis of portions of the VP2 and VP1 genes and to determine the presence or absence of reassortant viruses. Materials and Methods: A total of 377 bursa samples were collected from 201 suspected IBD outbreaks during 2009 to 2014 from nine states in Nigeria. Samples were subjected to RT-PCR using VP2 and VP1 gene specific primers, and the resulting PCR products were sequenced. Results: A total of 143 samples were positive for IBDV by RT-PCR. These assays amplified a 743 bp fragment from nt 701 to 1444 in the IBDV VP2 hypervariable region (hvVP2) of segment A and a 722 bp fragment from nt 168 to 889 in the VP1 gene of segment B. RT-PCR products were sequenced, aligned and compared with reference IBDV sequences obtained from GenBank. All but one hvVP2 sequence showed similarity to very virulent IBDV (vvIBDV) reference strains, yet only 3 of the VP1 67 VP1 sequences showed similarity to the VP1 gene of vvIBDV. Phylogenetic analysis revealed a new lineage of Nigerian reassortant IBDV strains. Conclusion: Phylogenetic analysis of partial sequences of genome segment A and B of IBDV in Nigeria confirmed the existence of vvIBDV in Nigeria. In addition, we noted the existence of reassortant IBDV strains with novel triplet amino acid motifs at positions 145, 146 and 147 in the reassorted Nigerian IBDV.
机译:目的:通过逆转录聚合酶链反应(RT-PCR)以及VP2和VP1基因部分的序列分析来鉴定尼日利亚九个州爆发的传染性法氏囊病病毒(IBDV)的野外分离株,并确定其存在与否重配病毒。材料和方法:2009年至2014年期间,从尼日利亚9个州的201例可疑IBD暴发中收集了377个滑囊样本。使用VP2和VP1基因特异性引物对样品进行RT-PCR,并对得到的PCR产物进行测序。结果:RT-PCR共检测到143份IBDV阳性。这些测定扩增了片段A的IBDV VP2高变区(hvVP2)中从nt 701到1444的743 bp片段和片段B的VP1基因从nt 168到889的722 bp片段。RT-PCR产物进行了测序,比对并与从GenBank获得的参考IBDV序列进行比较。除一个hvVP2序列外,其他所有序列均显示与极强力IBDV(vvIBDV)参考菌株的相似性,但只有3个VP1 67 VP1序列与vvIBDV的VP1基因相似。系统发育分析揭示了尼日利亚重配的IBDV毒株的新谱系。结论:对尼日利亚IBDV基因组片段A和B的部分序列进行的系统进化分析证实了尼日利亚存在vvIBDV。此外,我们注意到在重新分类的尼日利亚IBDV中位置145、146和147处具有新的三联体氨基酸基序的重新分类的IBDV菌株的存在。

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