Apical Transport of Influenza A Virus Ribonucleoprotein Requires Rab11-positive Recycling Endosome

被引:96
作者
Momose, Fumitaka [1 ]
Sekimoto, Tetsuya [1 ]
Ohkura, Takashi [1 ]
Jo, Shuichi [2 ]
Kawaguchi, Atsushi [1 ,2 ]
Nagata, Kyosuke [2 ]
Morikawa, Yuko [1 ]
机构
[1] Kitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
[2] Univ Tsukuba, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki, Japan
来源
PLOS ONE | 2011年 / 6卷 / 06期
关键词
RESPIRATORY SYNCYTIAL VIRUS; MICROTUBULE-MEDIATED TRANSPORT; NUCLEAR IMPORT; MEMBRANE TRAFFICKING; STRUCTURAL BASIS; MATRIX PROTEIN; RNA SEGMENTS; RAB GTPASES; POLYMERASE; INFECTION;
D O I
10.1371/journal.pone.0021123
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Influenza A virus RNA genome exists as eight-segmented ribonucleoprotein complexes containing viral RNA polymerase and nucleoprotein (vRNPs). Packaging of vRNPs and virus budding take place at the apical plasma membrane (APM). However, little is known about the molecular mechanisms of apical transport of newly synthesized vRNP. Transfection of fluorescent-labeled antibody and subsequent live cell imaging revealed that punctate vRNP signals moved along microtubules rapidly but intermittently in both directions, suggestive of vesicle trafficking. Using a series of Rab family protein, we demonstrated that progeny vRNP localized to recycling endosome (RE) in an active/GTP-bound Rab11-dependent manner. The vRNP interacted with Rab11 through viral RNA polymerase. The localization of vRNP to RE and subsequent accumulation to the APM were impaired by overexpression of Rab binding domains (RBD) of Rab11 family interacting proteins (Rab11-FIPs). Similarly, no APM accumulation was observed by overexpression of class II Rab11-FIP mutants lacking RBD. These results suggest that the progeny vRNP makes use of Rab11-dependent RE machinery for APM trafficking.
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页数:15
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