Hierarchy among viral RNA (vRNA) segments in their role in vRNA incorporation into influenza A virions

被引:149
作者
Muramoto, Y
Takada, A
Fujii, K
Noda, T
Iwatsuki-Horimoto, K
Watanabe, S
Horimoto, T
Kida, H
Kawaoka, Y
机构
[1] Univ Tokyo, Inst Med Sci, Dept Immunol & Microbiol, Div Virol,Minato Ku, Tokyo 1088639, Japan
[2] Univ Tokyo, Inst Med Sci, Int Res Ctr Infect Dis, Tokyo 1088639, Japan
[3] Hokkaido Univ, Grad Sch Vet Med, Dept Dis Control, Microbiol Lab, Sapporo, Hokkaido 0600818, Japan
[4] Univ Wisconsin, Sch Vet Med, Dept Pathobiol Sci, Madison, WI 53706 USA
关键词
D O I
10.1128/JVI.80.5.2318-2325.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genome of influenza A viruses comprises eight negative-strand RNA segments. Although all eight segments must be present in cells for efficient viral replication, the mechanism(s) by which these viral RNA (vRNA) segments are incorporated into virions is not fully understood. We recently found that sequences at both ends of the coding regions of the HA, NA, and NS vRNA segments of A/WSN/33 play important roles in the incorporation of these vRNAs into virions. In order to similarly identify the regions of the PB2, PB1, and PA vRNAs of this strain that are critical for their incorporation, we generated a series of mutant vRNAs that possessed the green fluorescent protein gene flanked by portions of the coding and noncoding regions of the respective segments. For all three polymerase segments, deletions at the ends of their coding regions decreased their virion incorporation efficiencies. More importantly, these regions not only affected the incorporation of the segment in which they reside, but were also important for the incorporation of other segments. This effect was most prominent with the PB2 vRNA. These findings suggest a hierarchy among vRNA segments for virion incorporation and may imply intersegment association of vRNAs during virus assembly.
引用
收藏
页码:2318 / 2325
页数:8
相关论文
共 34 条
[1]   The generation of recombinant influenza A viruses expressing a PB2 fusion protein requires the conservation of a packaging signal overlapping the coding and noncoding regions at the 5′ end of the PB2 segment [J].
Afonso, EDS ;
Escriou, N ;
Leclercq, I ;
van der Werf, S ;
Naffakh, N .
VIROLOGY, 2005, 341 (01) :34-46
[2]  
Berkowitz R, 1996, CURR TOP MICROBIOL, V214, P177
[3]   Alternative base pairs attenuate influenza A virus when introduced into the duplex region of the conserved viral RNA promoter of either the NS or the PA gene [J].
Catchpole, AP ;
Mingay, LJ ;
Fodor, E ;
Brownlee, GG .
JOURNAL OF GENERAL VIROLOGY, 2003, 84 :507-515
[4]   A novel influenza A virus mitochondrial protein that induces cell death [J].
Chen, WS ;
Calvo, PA ;
Malide, D ;
Gibbs, J ;
Schubert, U ;
Bacik, I ;
Basta, S ;
O'Neill, R ;
Schickli, J ;
Palese, P ;
Henklein, P ;
Bennink, JR ;
Yewdell, JW .
NATURE MEDICINE, 2001, 7 (12) :1306-1312
[5]  
COFFIN JM, 1984, RNA TUMOR VIRUSES 1, P261
[6]   3'-TERMINAL AND 5'-TERMINAL SEQUENCES OF INFLUENZA-A, INFLUENZA-B AND INFLUENZA-C VIRUS-RNA SEGMENTS ARE HIGHLY CONSERVED AND SHOW PARTIAL INVERTED COMPLEMENTARITY [J].
DESSELBERGER, U ;
RACANIELLO, VR ;
ZAZRA, JJ ;
PALESE, P .
GENE, 1980, 8 (03) :315-328
[7]   Approximately 150 nucleotides from the 5′ end of an influenza A segment 1 defective virion RNA are needed for genome stability during passage of defective virus in infected cells [J].
Duhaut, S ;
Dimmock, NJ .
VIROLOGY, 2000, 275 (02) :278-285
[8]   Heterologous protection of mice from a lethal human H1N1 influenza A virus infection by H3N8 equine defective interfering virus: Comparison of defective RNA sequences isolated from the DI inoculum and mouse lung [J].
Duhaut, SD ;
Dimmock, NJ .
VIROLOGY, 1998, 248 (02) :241-253
[9]   Interaction of influenza virus polymerase with viral RNA in the 'corkscrew' conformation [J].
Flick, R ;
Hobom, G .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :2565-2572
[10]   IDENTIFICATION AND CHARACTERIZATION OF A CORONAVIRUS PACKAGING SIGNAL [J].
FOSMIRE, JA ;
HWANG, K ;
MAKINO, S .
JOURNAL OF VIROLOGY, 1992, 66 (06) :3522-3530