Selective incorporation of vRNP into influenza A virions determined by its specific interaction with M1 protein

被引:18
作者
Chaimayo, Chutikarn [1 ,2 ]
Hayashi, Tsuyoshi [1 ]
Underwood, Andrew [1 ]
Hodges, Erin [1 ,3 ]
Takimoto, Toru [1 ]
机构
[1] Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Rochester, NY 14642 USA
[2] Mahidol Univ, Fac Med, Dept Microbiol, Siriraj Hosp, Bangkok 10700, Thailand
[3] Ctr Dis Control & Prevent, Influenza Div, Natl Ctr Immunizat & Resp Dis, Atlanta, GA USA
基金
美国国家卫生研究院;
关键词
Influenza; VRNP; CRNP; Nuclear export; CRM1; M1; Trafficking; Assembly; NUCLEAR EXPORT SIGNAL; VIRUS MATRIX PROTEIN; RIBONUCLEOPROTEIN COMPLEXES; CYTOPLASMIC TRANSPORT; MEMBRANE ASSOCIATION; RNA; BINDING; IDENTIFICATION; NUCLEOPROTEIN; GLYCOPROTEINS;
D O I
10.1016/j.virol.2017.02.008
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Influenza A viruses contain eight single-stranded, negative-sense RNA segments as viral genomes in the form of viral ribonucleoproteins (vRNPs). During genome replication in the nucleus, positive-sense complementary RNPs (cRNPs) are produced as replicative intermediates, which are not incorporated into progeny virions. To analyze the mechanism of selective vRNP incorporation into progeny virions, we quantified vRNPs and cRNPs in the nuclear and cytosolic fractions of infected cells, using a strand-specific qRT-PCR. Unexpectedly, we found that cRNPs were also exported to the cytoplasm. This export was chromosome region maintenance 1 (CRMI)-independent unlike that of vRNPs. Although both vRNPs and cRNPs were present in the cytosol, viral matrix (M1) protein, a key regulator for viral assembly, preferentially bound vRNPs over cRNPs. These results indicate that influenza A viruses selectively uptake cytosolic vRNPs through a specific interaction with Ml during viral assembly.
引用
收藏
页码:23 / 32
页数:10
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