Rescue of Ebola virus from cDNA using heterologous support proteins

被引:29
|
作者
Theriault, S
Groseth, A
Neumann, G
Kawaoka, Y
Feldmann, H [1 ]
机构
[1] Hlth Canada, Natl Microbiol Lab, Natl Lab Zoonot Dis & Special Pathogens, Special Pathogens Program, Ottawa, ON, Canada
[2] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB R3E 3R2, Canada
[3] Univ Wisconsin, Dept Pathobiol Sci, Madison, WI 53706 USA
[4] Univ Tokyo, Inst Med Sci, Tokyo, Japan
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
filoviruses; Zaire ebolavirus; infectious clone; ribonucleoprotein complex; protein-protein interaction; protein-RNA interaction;
D O I
10.1016/j.virusres.2004.06.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Using the infectious clone for Zaire ebolavirus, the functional specificity of viral proteins of the ribonucleoprotein complex in transcription/replication was investigated by substituting them with heterologous proteins derived from closely (Reston ebolavirus) and distantly related filoviruses (Marburgvirus). The data clearly demonstrated that transcription/replication are neither strictly species-specific nor genus-specific. Protein interactions between the nucleoprotein NP and the virion protein VP35 and the polymerase L and VP35 seemed to be the most critical steps. In contrast to previous data, viral proteins were able to target heterologous filovirus RNA. Together these results indicated that protein-protein interactions are more critical than protein-RNA interactions. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 50
页数:8
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