Mulders M N, van Loon A M, van der Avoort H G, Reimerink J H, Ras A, Bestebroer T M, Drebot M A, Kew O M, Koopmans M P
Laboratory of Virology, World Health Organization Collaborating Centre for Reference and Research on Poliomyelitis, National Institute of Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
J Clin Microbiol. 1995 Dec;33(12):3252-6. doi: 10.1128/jcm.33.12.3252-3256.1995.
An outbreak of poliomyelitis due to wild poliovirus type 3 (PV3) occurred in an unvaccinated community in The Netherlands between September 1992 and February 1993. The outbreak involved 71 patients. The aim of this study was to characterize the virus at the molecular level and to analyze the molecular evolution of the epidemic virus. Molecular analysis was carried out by sequencing the VP1/2A junction region (150 nucleotides) of 50 PV3 strains isolated in association with this outbreak and the entire VP1 gene of 14 strains. In addition, the sequence of the VP1/2A junction region of strains from geographical regions endemic for PV3 (Egypt, India, and Central Asia) was analyzed and compared with the nucleotide sequence of the epidemic strain from The Netherlands. The earliest isolate was obtained from river water sampled 3 weeks before diagnosis of the first poliomyelitis patient and was found by VP1/2A sequence analysis to be genetically identical to the strain isolated from the first patient. Sequence divergence among the strains from the epidemic in The Netherlands was less than 2%. The closest genetic similarity (97.3%) was found with an Indian isolate (New Delhi, December 1991), indicating the likely source of the virus. A more than 99% sequence similarity was found in the VP1/2A region. Finally, the sequence information was used to design primers for the specific and highly sensitive molecular detection of PV3 strains during the epidemic.
1992年9月至1993年2月期间,荷兰一个未接种疫苗的社区爆发了由3型野生脊髓灰质炎病毒(PV3)引起的脊髓灰质炎疫情。此次疫情涉及71名患者。本研究的目的是在分子水平上对病毒进行特征分析,并分析流行病毒的分子进化。通过对与此次疫情相关的50株PV3病毒株的VP1/2A连接区(150个核苷酸)进行测序以及对14株病毒的整个VP1基因进行测序,开展了分子分析。此外,还对来自PV3流行地区(埃及、印度和中亚)的病毒株的VP1/2A连接区序列进行了分析,并与来自荷兰的流行病毒株的核苷酸序列进行了比较。最早的分离株是在首例脊髓灰质炎患者确诊前3周采集的河水中获得的,通过VP1/2A序列分析发现其与从首例患者分离出的病毒株在基因上完全相同。荷兰疫情中的病毒株之间的序列差异小于2%。与一株印度分离株(新德里,1991年12月)的遗传相似性最高(97.3%),这表明了该病毒的可能来源。在VP1/2A区域发现了超过99%的序列相似性。最后,利用这些序列信息设计了引物,用于在疫情期间对PV3病毒株进行特异性和高灵敏度的分子检测。