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Generation and Segregation of Hantaviral RNA Genomic Diploid; Implications of Reassortant Generation Mechanism  

Park Sun-Whan (Department of Microbiology, College of Medicine,Korea University)
Chung Dong-Hoon (Southern Research Institute 2000)
Ahn Byung-Yoon (School of Life Sciences and Biotechnology, Korea University)
Lee Pyung-Woo (Department of Microbiology, College of Medicine, Korea University)
Publication Information
Journal of Microbiology and Biotechnology / v.16, no.7, 2006 , pp. 1017-1025 More about this Journal
Abstract
Hantaviruses possess three RNA segments of negative sense. Co-infection of closely related hantaviruses may result in generation of a progeny virus with genomic polyploidy, containing a partial or complete set of genome originated from more than one parental virus. To characterize the formation of viral genomic polyploidy, cultured Vero-E6 cells were co-infected with two closely related hantaviruses, Hantaan and Maaji, and the progeny viruses examined. The genotype of plaque-purified viruses was analyzed by a virus-specific RT-PCR. Seventy percent (67/96) of the progeny virus was categorized as Hantaan and 3.3% (2/96) was classified as Maaji, whereas 20% (21/96) was considered polyploidy as they contained both types of the S RNA segment. Most of the polyploidy progeny viruses were unstable and gave rise to either one of the parental viruses or a reassortant after several rounds of plaque purification. No recombination between the heterologous pair of S RNA was observed for those polyploid viruses during three consecutive plaque-to-plaque passages. These data suggest that the viral polyploidy formation constitutes a primary mechanism underlying the generation of a newly emerged hantavirus.
Keywords
Hantavirus; diploid; genetic; reassortment; Hantaan virus; Maaji virus;
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1 Lee, P. W., D. H. Chung, and Y. C. Kim. 1992. Maaji virus: I. Identification and antigenic characterization of a new hantavirus isolated from Apodemus mice (Apodemus agrarius coreae) in Korea. J. Kor. Soc. Virol. 22: 187-196
2 Lee, P. W., C. J. Gibbs Jr., D. C. Gajdusek, and R. Yanagihara. 1985. Serotypic classification of hantaviruses by indirect immunofluorescent antibody and plaque reduction neutralization tests. J. Clin. Microbiol. 22: 940-944
3 Pringle, C. R., J. F. Lees, W. Clark, and R. M. Elliott. 1984. Genome subunit reassortment among Bunyaviruses analysed by dot hybridization using molecularly cloned complementary DNA probes. Virology 135: 244-256   DOI   ScienceOn
4 Urquidi, V. and D. H. Bishop. 1992. Non-random reassortment between the tripartite RNA genomes of La Crosse and snowshoe hare viruses. J. Gen. Virol. 73: 2255-2265   DOI   ScienceOn
5 Xiao, S. Y, J. W. Leduc, Y K. Chu, and C. S. Schmaljohn. 1994. Phylogenetic analyses of virus isolates in the genus Hantavirus, family Bunyaviridae. Virology 198: 205-217   DOI   ScienceOn
6 Lee, P. W., H. L. Amyx, D. C. Gajdusek, R. T. Yanagihara, D. Goldgaber, and C. J. Gibbs Jr. 1982. New hemorrhagic fever with renal syndrome-related virus in rodents in the United States. Lancet 2: 1405
7 Li, D., A. L. Schmaljohn, K. Anderson, and C. S. Schmaljohn. 1995. Complete nucleotide sequences of the M and S segments of two hantavirus isolates from California: Evidence for reassortment in nature among viruses related to hantavirus pulmonary syndrome. Virology 206: 973-983   DOI   ScienceOn
8 Bishop, D. H. 1985. The genetic basis for describing viruses as species. Intervirology 24: 79-93   DOI
9 Antic, D., C. Y. Kang, K. Spik, C. Schmaljohn, O. Vapalahti, and A. Vaheri. 1992. Comparison of the deduced gene products of the L, M and S genome segments of hantaviruses. Virus Res. 24: 35-46   DOI   ScienceOn
10 Lee, P. W., D. H. Chung, Y. C. Kim, and C. Y. Kang. 1992. Maaji virus: II. Molecular characterization of a new hantavirus isolated from Apodemus mice (Apodemus agrarius coreae) in Korea. J. Kor. Soc. Virol. 22: 197-205
11 Kruger, D. H., R. Ulrich, and A. A. Lundkvist. 2001. Hantavirus infections and their prevention. Microbes Infect. 3: 1129-1144   DOI   ScienceOn
12 Klimas, R. A., W. H. Thompson, C. H. Calisher, G. G. Clark, P. R. Grimstad, and D. H. Bishop. 1981. Genotypic varieties of La Crosse virus isolated from different geographic regions of the continental United States and evidence for a naturally occurring intertypic recombinant La Crosse virus. Am. J. Epidemiol. 114: 112-131   DOI
13 Murphy, B. R. and R. G. Webster. 1996. Orthomyxoviruses, pp. 1091-1152. In B. N. Fields, D. M. Knipe, R. M. Chanock, M. S. Hirsch, J. L. Melnick, T. P. Monath, and B. Roizman (eds.), Fields Virology, 2nd Ed. Vol. 1. LippincottRaven Publishers, Philadelphia
14 Elliott, L. H., M. P. Kiley, and J. B. McCormick. 1984. Hantaan virus: Identification of virion proteins. J. Med. Virol. 65: 1285-1293
15 Rodriguez, L. L., J. H. Owens, C. J. Peters, and S. T. Nichol. 1998. Genetic reassortment among viruses causing hantavirus pulmonary syndrome. Virology 242: 99-106   DOI   ScienceOn
16 Gouvea, V. and M. Brantly. 1995. Is rotavirus a population of reassortants? Trends Microbiol. 3: 159-162   DOI   ScienceOn
17 Spiropoulou, C. F., S. Morzunov, H. Feldmann, A. Sanchez, C. J. Peters, and S. T. Nichol. 1994. Genome structure and variability of a virus causing hantavirus pulmonary syndrome. Virology 200: 715-723   DOI   ScienceOn
18 Beaty, B. J., M. Borucki, J. Farfan, and D. White. 1996. Factors in the Emergence of Arbovirus Diseases, Emerging Diseases, pp. 23-35. Elsevier, Paris
19 Henderson, W. W., M. C. Monroe, S. C. St. Jeor, W. P. Thayer, J. E. Rowe, C. J. Peters, and S. T. Nichol. 1995. Naturally occurring Sin Nombre virus genetic reassortants. Virology 214: 602-610   DOI   ScienceOn
20 Endres, M. J., A. Valsamakis, F. Gonzalez-Scarano, and N. Nathanson. 1990. Neuroattenuated bunyavirus variant: Derivation, characterization, and revertant clones. J. Virol. 64: 1927-1933
21 Beaty, B. J., D. R. Sundin, L. J. Chandler, and D. H. Bishop. 1985. Evolution of bunyaviruses by genome reassortment in dually infected mosquitoes (Aedes triseriatus). Science 230: 548-550   DOI
22 Peng, G., S. Hongo, H. Kimura, Y. Muraki, K. Sugawara, F. Kitame, Y. Numazaki, H. Suzuki, and K. Nakamura. 1996. Frequent occurrence of genetic reassortment between influenza C virus strains in nature. J. Gen. Virol. 77: 1489-1492   DOI   ScienceOn
23 Plyusnin, A., O. Vapalahti, and A. Vaheri. 1996. Hantaviruses: Genome structure, expression and evolution. J. Gen. Virol. 77: 2677-2687   DOI   ScienceOn
24 Plyusnin, A., S. K. Kukkonen, A. Plyusnina, O. Vapalahti, and A. Vaheri. 2002. Transfection-mediated generation of functionally competent Tula hantavirus with recombinant S RNA segment. EMBO J. 21: 1497-1503   DOI   ScienceOn
25 Griot, C., A. Pekosz, D. Lukac, S. S. Scherer, K. Stillmock, D. Schmeidler, M. J. Endres, F. Gonzalez-Scarano, and N. Nathanson. 1993. Polygenic control of neuroinvasiveness in California serogroup bunyaviruses. J. Virol. 67: 3861-3867
26 Bishop, D. H. and B. J. Beaty, 1988. Molecular and biochemical studies of the evolution, infection and transmission of insect bunyaviruses. Philos. Trans. R. Soc. Lond. B Biol. Sci. 321: 463-483   DOI   ScienceOn
27 Schmaljohn, C. and B. Hjelle. 1997. Hantaviruses: A global disease problem. Emerg. Infect. Dis. 3: 95-104   DOI   ScienceOn
28 Turell, M. J. and P. V. Perkins. 1990. Transmission of Rift Valley fever virus by the sand fly, Phlebotomus duboscqi (Diptera: Psychodidae). Am. J. Trop. Med. Hyg. 42: 185188