Vapalahti O, Kallio-Kokko H, Salonen E M, Brummer-Korvenkontio M, Vaheri A
Department of Virology, University of Helsinki, Finland.
J Gen Virol. 1992 Apr;73 ( Pt 4):829-38. doi: 10.1099/0022-1317-73-4-829.
The prototype Puumala virus (PV) Sotkamo strain small (S) and medium (M) RNA genome segments were amplified by the polymerase chain reaction (PCR), cloned and sequenced. The S segment is 1830 nucleotides long with an open reading frame coding for 433 amino acids. The identity to the PV Hällnäs strain was 83% at the nucleotide and 96% at the amino acid level. The M segment in the Sotkamo strain is 3616 nucleotides long and contains one open reading frame of 1148 amino acids with 83% nucleotide and 94% amino acid identity to the Hällnäs strain. Most amino acid changes were conservative and the five predicted glycosylation sites are identical. The amino acid identity to the prototype hantavirus, Hantaan virus, was 62 and 54% for S and M segments, respectively. The coding region of the S segment was further amplified by PCR, ligated to pEX vectors and expressed in Escherichia coli as a beta-galactosidase fusion protein and was seen to be specifically detected by nephropathia epidemica sera in immunoblotting.
通过聚合酶链反应(PCR)扩增原型普马拉病毒(PV)索特卡莫毒株的小(S)和中(M)RNA基因组片段,进行克隆和测序。S片段长1830个核苷酸,有一个编码433个氨基酸的开放阅读框。与PV哈尔纳斯毒株在核苷酸水平的同一性为83%,在氨基酸水平为96%。索特卡莫毒株的M片段长3616个核苷酸,包含一个1148个氨基酸的开放阅读框,与哈尔纳斯毒株在核苷酸水平的同一性为83%,在氨基酸水平为94%。大多数氨基酸变化是保守的,五个预测的糖基化位点相同。与原型汉坦病毒汉滩病毒相比,S和M片段的氨基酸同一性分别为62%和54%。通过PCR进一步扩增S片段的编码区,连接到pEX载体上,并在大肠杆菌中作为β-半乳糖苷酶融合蛋白表达,在免疫印迹中可被流行性肾病血清特异性检测到。