Attoui Houssam, Sailleau Corinne, Mohd Jaafar Fauziah, Belhouchet Mourad, Biagini Philippe, Cantaloube Jean François, de Micco Philippe, Mertens Peter, Zientara Stephan
Department of Arbovirology, Institute for Animal Health, Pirbright, Woking, Surrey GU24 0NF, UK.
Agence Française de Sécurité Sanitaire des Aliments, 22 rue Pierre Curie, 94703 Maisons-Alfort Cedex 07, France.
J Gen Virol. 2007 Nov;88(Pt 11):3078-3088. doi: 10.1099/vir.0.83076-0.
The complete nucleotide sequence of Middelburg virus (MIDV) was determined for strain MIDV-857 from Zimbabwe. The isolation of this virus in 1993 from a horse that died showing severe clinical signs represents the first indication that MIDV can cause severe disease in equids. Full-length cDNA copies of the viral genome were successfully synthesized by an innovative RT-PCR amplification approach using an 'anchor primer' combined with the SMART methodology described previously for the synthesis of full-length cDNA copies from genome segments of dsRNA viruses. The MIDV-857 genome is 11,674 nt, excluding the 5'-terminal cap structure and poly(A) tail (which varies in length from approximately 180 to approximately 220 residues). The organization of the genome is like that of other alphaviruses, including a read-through stop codon between the nsP3 and nsP4 genes. However, phylogenetic analyses of the structural protein amino acid sequences suggested that the MIDV E1 gene was generated by recombination with a Semliki Forest virus-like virus. This hypothesis was supported by bootscanning analysis using a recombination-detection program. The 3' untranslated region of MIDV-857 also contains a 112 nt duplication. This study reports the first full-length sequence of MIDV, which was obtained from a single RT-PCR product.
已确定来自津巴布韦的米德尔堡病毒(MIDV)毒株MIDV - 857的完整核苷酸序列。1993年从一匹出现严重临床症状后死亡的马身上分离出这种病毒,这是MIDV可在马科动物中引起严重疾病的首个迹象。通过一种创新的RT - PCR扩增方法,使用“锚定引物”并结合先前描述的用于从双链RNA病毒基因组片段合成全长cDNA拷贝的SMART方法,成功合成了病毒基因组的全长cDNA拷贝。MIDV - 857基因组为11,674个核苷酸,不包括5'末端帽结构和聚(A)尾(其长度在约180至约220个残基之间变化)。该基因组的组织方式与其他甲病毒相似,包括在nsP3和nsP4基因之间有一个通读终止密码子。然而,对结构蛋白氨基酸序列的系统发育分析表明,MIDV的E1基因是通过与一种塞姆利基森林病毒样病毒重组产生的。使用重组检测程序进行的引导扫描分析支持了这一假设。MIDV - 857的3'非翻译区还包含一个112个核苷酸的重复序列。本研究报告了从单个RT - PCR产物获得的MIDV的首个全长序列。