Activity of Toscana and Rift Valley fever virus transcription complexes on heterologous templates

被引:25
作者
Accardi, L
Prehaud, C
Di Bonito, P
Mochi, S
Bouloy, M
Giorgi, C
机构
[1] Ist Super Sanita, Virol Lab, I-00161 Rome, Italy
[2] Inst Pasteur, Unite Arbovirus & Virus Fievres Haemorragiques, Grp Bunyavirides, F-75724 Paris, France
关键词
D O I
10.1099/0022-1317-82-4-781
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A transcription system for Toscana virus (TOSV) (a member of the family Bunyaviridae, genus Phlebovirus) was constructed. For in vivo expression, the TOSV transcription system uses the viral N and L proteins and an S-like RNA genome containing the chloramphenicol acetyltransferase reporter gene in the antisense orientation Ranked by the viral genomic 5'- and 3'-terminal S sequences. It was found that the N and L proteins represent the minimal protein requirement for an active transcription complex. To investigate the possibility of reassortment between TOSV and Rift Valley fever virus (RVFV), the activity of their polymerase complexes was tested on their heterologous S-like RNA genomes and this showed that both virus complexes were active. Moreover, hybrid transcriptase complexes with protein components originating from the two viruses were tested on both virus templates and only the combination RVFV L + TOSV N on RVFV S-like RNA was found to be active in this assay. These results suggest that virus reassortants might be generated whenever the two viruses infect the same host.
引用
收藏
页码:781 / 785
页数:5
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