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黑蜂王台病毒中国BQCV-JL1株5'UTR的序列分析

Analysis of the sequence of the 5'UTR region of the Chinese black queen cell virus-JL1
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摘要 蜜蜂黑蜂王台病毒(Black queen cell virus,BQCV)是引起蜜蜂蜜蜂黑蜂王台病的病原体,主要侵染蜜蜂蜂王幼虫。BQCV基因组为单正链RNA,包括5'端的ORF 1和3'端的ORF 2两个开放阅读框。分别编码非结构蛋白和结构蛋白。本实验室首次成功分离鉴定得到中国首株BQCV毒株,命名为中国BQCV-JL1株。该株全长为8 358 nt。【目的】本文主要研究该株核苷酸序列位置为1~1 124 nt的片段,该段序列的1~545 nt为该毒株的5'UTR区域。【方法】通过Blast及DNAStar等软件对核苷酸及氨基酸序列进行分析。【结果】5'UTR区域的同源性为94%~99%,为高度保守序列。【结论】经Mega5软件作多重序列对比分析得知,该中国BQCV-JL1株的5'UTR区域与其他毒株差异性很大,经分析推断原因为碱基的缺失与碱基置换。 Black queen cell virus (BQCV) is a pathogen that mainly infects the queen bee larvae. The BQCV genome has a single positive-stranded RNA and two open reading frames (ORF); ORF 1 at the 5 ' end and ORF 2 at the 3' end, encoding non-structural, and structural, proteins respectively. Our laboratory has successfully isolated and identified the first BQCV strain in China, named Chinese BQCV-JL1 strain, which consists of 8 358 nucleotides. |Objeetivesi To characterize BQCV nucleotide sequences between 1 nt and 1 124 nt, and specifically the fragment containing the 5'UTR region (1-545 nt). [Metbodsl Nucleotide and amino acid sequences were analyzed using Blast and DNAStar software. [Results] The 5'UTR region is highly conserved with homology between 94% and 99%. [Conclusion] Mega5 software for multiple sequence alignment analysis shows that the Chinese BQCV-JL1 strain is very different from other BQCV strains. We infer that this is because of base deletion and base replacement.
出处 《应用昆虫学报》 CAS CSCD 北大核心 2015年第2期308-314,共7页 Chinese Journal of Applied Entomology
基金 国家自然科学基金项目(31001065) 国家质检总局科技计划项目(2013IK033)
关键词 BQCV 5'UTR RT-PCR 序列分析 进化树分析 BQCV, 5'UTR, RT-PCR, sequence analysis, phylogenetic tree
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参考文献8

  • 1Bailey L,Woods RD.1977.Two more small RNA viruses fromhoney bees and further observations on sacbrood and acutebee-paralysis viruses.J.Gen.Virol.,37:175-182.
  • 2Baker AC,Schroeder DC.2008.Occurrence and genetic analysis ofpicorna-like viruses infecting worker bees of Apis mellifera L.populations in Devon,South West England.J.Invert.Path.,98(2):239-242.
  • 3Berényi O,Bakonyi T,Derakhshifar I,K-glberger H,Nowotny N.2006.Occurrence of six honeybee viruses in diseased Austrianapiaries.Appl.Environ.Microbiol.,72(4):2414-2420.
  • 4Kajobe R,Marris G,Budge G,Laurenson L,Cordoni G,Jones B,Wilkins S,Cuthbertson AG,Brown MA.2010.First moleculardetection of a viral pathogen in Ugandan honey bees.J.Invertebr.Pathol.,104(2):153-156.
  • 5Leat N,Ball B,Govan V,Davison S.2000.Analysis of the completegenome sequence of black queen-cell virus,a picorna-like virusof honey bees.J.Gen.Virol.,81(8):2111-2119.
  • 6Mayo MA.2002.Virus taxonomy-Houston.Arch.Virol.,147(5):1071-1076.
  • 7Tamura K,Peterson D,Peterson N,Stecher G,Nei M,Kumar S.2011.MEGA5:molecular evolutionary genetics analysis usingmaximum likelihood,evolutionary distance,and maximumparsimony methods.Mol.Biol.Evol.,28(10):2731-2739.
  • 8Tentcheva D,Gauthier L,Zappulla N,Dainat B,Cousserans F,ColinME,Bergoin M.2004.Prevalence and seasonal variations of sixbee viruses in Apis mellifera L.and Varroa destructormitepopulations in France.Appl.Environ.Microbiol.,70(12):7185-7191.

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