Genetic variation in Tula hantaviruses: Sequence analysis of the S and M segments of strains from Central Europe

被引:77
作者
Plyusnin, A
Cheng, Y
Vapalahti, O
Pejcoch, M
Unar, J
Jelinkova, Z
Lehvaslaiho, H
Lundkvist, A
Vaheri, A
机构
[1] REG HYGIEN INST S MORAVIA, BRNO, CZECH REPUBLIC
[2] CTR COMP SCI, SF-02101 ESPOO, FINLAND
[3] INST INFECT DIS CONTROL, S-10521 STOCKHOLM, SWEDEN
基金
英国医学研究理事会;
关键词
evolution; genetic variation; hantavirus; Tula virus;
D O I
10.1016/0168-1702(95)00086-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hantavirus carried by the European common vole Microtus arvalis from Moravia (Czech Republic) was analyzed by RT-PCR-sequencing and by reactivity with a panel of monoclonal antibodies (MAbs). Sequencing of the full-length S segment and the proximal part of the M segment showed that the virus belonged to genotype Tula (TUL) we discovered earlier in Microtus arvalis from Central Russia. This finding supported the concept of host dependence of hantaviruses. Phylogenetic analyses suggested a similar evolutionary history for S and M genes of TUL strains; thus far there is no evidence for reassortment in TUL. Geographic clustering of TUL genetic variants was observed and different levels of the genetic variability were revealed resembling those estimated for another hantavirus, Puumala (PUU). Comparison of the deduced N protein sequence from Russia and from Moravia showed that genetic drift in TUL occurred not only by accumulation of point mutations but also by the deletion of a nucleotide triplet. It encoded Ser(252) which was located within a highly variable hydrophilic part of the N protein carrying B-cell epitopes and presumably forming a loop. Analysis of naturally expressed TUL N-antigen derived from lung tissue of infected voles with MAbs indicated antigenic heterogeneity among TUL strains.
引用
收藏
页码:237 / 250
页数:14
相关论文
共 48 条
[1]  
Antic, Kang, Spik, Schmaljohn, Vapalahti, Vaheri, Comparison of the deduced gene products of the L, M and S genome segments of hantaviruses, Virus Res., 24, pp. 35-46, (1992)
[2]  
Arikawa, LaPenotiere, Iacono-Connors, Wang, Schmaljohn, Coding properties of the S and the M genome segments of SR-11 virus: Comparison to other caussative agents of hemorrhagic fever with renal syndrome, Virology, 176, pp. 114-125, (1990)
[3]  
Avsic-Zupanc, Xiao, Stojanovic, Gligic, van der Groen, LeDuc, Characterization of Dobrava virus: A hantavirus from Slovenia, Yugoslavia, J. Med. Virol., 38, pp. 132-137, (1992)
[4]  
Brummer-Korvenkontio, Vaheri, Hovi, von Bonsdorff, Vuorimes, Manni, Penttinen, Oker-Blom, Lahdevirta, Nephropatia epidemica: detection antigen in bank voles and serological diagnosis of human infection, J. Infect. Dis., 141, pp. 131-134, (1980)
[5]  
Carey, Reuben, Paniker, Shope, Myers, Thottapalayam virus: A presumptive arbovirus isolated from a shrew in India, Indian J. Med. Res., 59, pp. 1758-1760, (1971)
[6]  
Centers for Disease Control and Prevention (CDC), Newly identified hantavirus, Florida, Morbid. Mortal. Weekly Rep., 43, (1994)
[7]  
Centers for Disease Control and Prevention (CDC), Newly identified hantavirus, Florida, Morbid. Mortal. Weekly Rep., 43, (1994)
[8]  
De Soete, A least squares algorithm for fitting additive trees to proximity data, Psychometrika, 48, pp. 621-626, (1983)
[9]  
Dzagurova, Tkachenko, Slonova, Ivanov, Ivanidze, Markeshin, Dekonenko, Niklasson, Lundkvist, Antigenic relationship of hantavirus strains identified by monoclonal antibodies, Arch Virol, (1995)
[10]  
Elliott, Schmaljohn, Collet, Bunyaviridae genome structure and gene expression, Curr. Topics Microbiol. Immunol., 169, pp. 91-141, (1991)