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Characterization of a Highly Evolved Vaccine-Derived Poliovirus Type 3 Isolated from Sewage in Estonia

机译:从爱沙尼亚的污水中分离出的高度进化的疫苗衍生脊髓灰质炎病毒3型的表征。

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摘要

Two types of vaccine-derived polioviruses have been recently designated to emphasize the different origins of the evolved viruses: circulating vaccine-derived polioviruses (cVDPV) associated with outbreaks of paralytic disease and strains isolated from chronically infected immunodeficient individuals (iVDPV). We describe here a type 3 VDPV (PV3/EST/02/E252; later E252) isolated from sewage collected in Tallinn, Estonia, in October 2002. Due to aberrant properties in subtyping, the virus was subjected to detailed characterization. Partial genomic sequencing suggested that the closest relative was the oral vaccine strain PV3/Sabin, but the two virus strains shared only 86.7% of the 900 nucleotides (nt) coding for the capsid protein VP1. Phylogenetic analysis of the nearly complete genome [nt 19 to poly(A)] revealed multiple nucleotide substitutions throughout the genome and a possible Sabin 3/Sabin 1-recombination junction site in the 2C coding region. A calculation based on the estimated mutation frequency of the P1 region of polioviruses suggested that the E252 virus might have replicated in one or more individuals for approximately 10 years. No persons chronically excreting poliovirus are known in Estonia. Amino acid substitutions were seen in all known antigenic sites, which was consistent with the observed aberrant antigenic properties of the virus demonstrated by both monoclonal antibodies and human sera from vaccinated children. In spite of the apparent transmission potential, no evidence was obtained for circulation of the virus in the Estonian population.
机译:最近已指定了两种类型的疫苗衍生脊髓灰质炎病毒来强调进化病毒的不同来源:与麻痹性疾病爆发相关的循环疫苗衍生脊髓灰质炎病毒(cVDPV)和从慢性感染的免疫缺陷个体(iVDPV)分离的菌株。我们在这里描述了2002年10月从爱沙尼亚塔林收集的污水中分离出的3型VDPV(PV3 / EST / 02 / E252;后来的E252)。由于亚型的异常特性,对病毒进行了详细的表征。部分基因组测序表明,最接近的亲戚是口服疫苗株PV3 / Sabin,但两个病毒株仅共享编码衣壳蛋白VP1的900个核苷酸(nt)中的86.7%。对近乎完整的基因组[聚(A)的第19核苷酸]的系统进化分析显示,整个基因组中存在多个核苷酸取代,并且在2C编码区域可能存在Sabin 3 / Sabin 1-重组连接位点。根据估计的脊髓灰质炎病毒P1区突变频率进行的计算表明,E252病毒可能已经在一个或多个个体中复制了大约10年。在爱沙尼亚,没有人知道慢性分泌脊髓灰质炎病毒。在所有已知的抗原位点均发现了氨基酸置换,这与从接种疫苗的儿童获得的单克隆抗体和人血清所证明的病毒异常抗原特性一致。尽管有明显的传播潜力,但仍未获得有关爱沙尼亚人群中病毒传播的证据。

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