Bouslama Lamjed, Gharbi Jawhar, Aouni Mahjoub
Laboratoire des Maladies Dominantes Transmissibles, MDT-01, Faculté de Pharmacie de Monastir, Avenue Avicenne, BP 5000 Monastir, Tunisia.
Virus Genes. 2006 Oct;33(2):205-12. doi: 10.1007/s11262-005-0057-1.
The enteroviruses (EV), RNA viruses belonging to the Picornaviridae family, have a high genetic variability due to the absence of the efficient proofreading and post replicative repair activities associated with the RNA polymerase. In the present work, we studied the genetic and the antigenic variability of ECHO virus types 11 (E11) and 30 (E30), which are the most isolated echoviruses serotypes in clinical and environmental samples. We established on the 3' end of the VP1 gene, consensus sequences of E11 and E30 by alignment of 67 E11 and 247 E30 published sequences in GenBank. Our results of sequences comparison showed that the majority of the mutational sites are situated on the third nucleotide of the codon. These mutations were without consequence on the antigenic sequences of the VP1 protein. Thus, E11 and E30 have a high genetic variability (1/3 of the nucleotides are variable), but a relative antigenic conservation. The analysis of the intertypic antigenic variability between E11 and E30 was obtained by the alignment of the corresponding amino acids sequences relative to the N-terminal part of the VP1 protein. Two discriminating parts were highlighted, probably representing antigenic sites for neutralisation antibodies.
肠道病毒(EV)属于小核糖核酸病毒科的RNA病毒,由于缺乏与RNA聚合酶相关的高效校对和复制后修复活性,具有很高的遗传变异性。在本研究中,我们研究了11型(E11)和30型(E30)埃可病毒的遗传和抗原变异性,这两种病毒是临床和环境样本中分离出的最常见的埃可病毒血清型。我们通过比对GenBank中67条E11序列和247条E30序列,在VP1基因的3'端建立了E11和E30的共有序列。我们的序列比较结果表明,大多数突变位点位于密码子的第三个核苷酸上。这些突变对VP1蛋白的抗原序列没有影响。因此,E11和E30具有很高的遗传变异性(三分之一的核苷酸是可变的),但相对抗原保守。通过比对VP1蛋白N端部分的相应氨基酸序列,分析了E11和E30之间的型间抗原变异性。突出显示了两个有区别的部分,可能代表中和抗体的抗原位点。