Paximadi Eleni, Karakasiliotis Ioannis, Bolanaki Eugenia, Krikelis Aris, Markoulatos Panayotis
Department of Biochemistry and Biotechnology, School of Health Sciences, University of Thessaly, Ploutonos 26 & Aiolou, 41221 Larissa, Greece.
Virus Genes. 2007 Dec;35(3):541-8. doi: 10.1007/s11262-007-0146-4. Epub 2007 Aug 7.
A retrospective analysis of five Sabin intertypic recombinant strains, isolated from human feacal specimens during the time period 1978-1985 in Greece, was performed by RT-PCR, Restriction Fragment Length Polymorphism (R.F.L.P.) and sequencing. Of the studied strains, three (EPA, EPB, EPC) were found to be bi-recombinant Sabin3/Sabin2/Sabin3 (S3/S2/S3), one strain was characterized as a probable S3/S2- CAV18 or CAV21-S2/S1 multi-recombinant (EDP11) and one was identified as a tripartite one S3/S2/S1 (EDP12). Samples EPA, EPB and EPC presented a common recombination junction in the 2C genomic region. Moreover, strains EPA and EPB shared also the second recombination site in the 3D genomic region, whereas the second recombination of EPC was also determined in 3D but in a different nucleotide position. Strains EDP11 and EDP12 presented both identical recombination motifs and recombination sites. The first was detected in the 2C genomic region and the second in the 3D region. Strain EDP11 presented an interesting feature since a sequence of 120 nucleotides seems to have derived from a member of human enteroviruses species C (CAV18 or CAV21). This finding is of great importance, considering that this strain (EDP11) was isolated from an area and time period, where no Coxsackie A virus or poliovirus epidemics occurred. Our study underlines the role of specific positions and motifs of the poliovirus genomic sequences involved in recombination events and prompts that Coxsackie A viruses belonging to human enterovirus species C (genetically closely related to PV) are considered as the possible counterparts of the recombination.
对1978年至1985年期间在希腊从人类粪便标本中分离出的5株Sabin型间重组毒株进行了回顾性分析,采用逆转录聚合酶链反应(RT-PCR)、限制性片段长度多态性分析(R.F.L.P.)和测序技术。在所研究的毒株中,3株(EPA、EPB、EPC)被发现是双重组的Sabin3/Sabin2/Sabin3(S3/S2/S3),1株被鉴定为可能的S3/S2 - CAV18或CAV21 - S2/S1多重组毒株(EDP11),1株被确定为三方重组的S3/S2/S1(EDP12)。样本EPA、EPB和EPC在2C基因组区域呈现出一个共同的重组连接点。此外,毒株EPA和EPB在3D基因组区域也共享第二个重组位点,而EPC的第二个重组位点也在3D区域被确定,但在不同的核苷酸位置。毒株EDP11和EDP12呈现出相同的重组基序和重组位点。第一个在2C基因组区域被检测到,第二个在3D区域。毒株EDP11呈现出一个有趣的特征,因为一段120个核苷酸的序列似乎源自人类肠道病毒C型的一个成员(CAV18或CAV21)。考虑到该毒株(EDP11)是在一个没有柯萨奇A病毒或脊髓灰质炎病毒流行的地区和时间段分离出来的,这一发现具有重要意义。我们的研究强调了脊髓灰质炎病毒基因组序列中参与重组事件的特定位置和基序的作用,并提示属于人类肠道病毒C型(与脊髓灰质炎病毒在基因上密切相关)的柯萨奇A病毒被认为是重组的可能对应物。