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      Intracellular Transport of Vaccinia Virus in HeLa Cells Requires WASH-VPEF/FAM21-Retromer Complexes and Recycling Molecules Rab11 and Rab22.

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          Abstract

          Vaccinia virus, the prototype of the Orthopoxvirus genus in the family Poxviridae, infects a wide range of cell lines and animals. Vaccinia mature virus particles of the WR strain reportedly enter HeLa cells through fluid-phase endocytosis. However, the intracellular trafficking process of the vaccinia mature virus between cellular uptake and membrane fusion remains unknown. We used live imaging of single virus particles with a combination of various cellular vesicle markers, to track fluorescent vaccinia mature virus particle movement in cells. Furthermore, we performed functional interference assays to perturb distinct vesicle trafficking processes in order to delineate the specific route undertaken by vaccinia mature virus prior to membrane fusion and virus core uncoating in cells. Our results showed that vaccinia virus traffics to early endosomes, where recycling endosome markers Rab11 and Rab22 are recruited to participate in subsequent virus trafficking prior to virus core uncoating in the cytoplasm. Furthermore, we identified WASH-VPEF/FAM21-retromer complexes that mediate endosome fission and sorting of virus-containing vesicles prior to virus core uncoating in the cytoplasm.

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          Author and article information

          Journal
          J. Virol.
          Journal of virology
          1098-5514
          0022-538X
          Aug 2015
          : 89
          : 16
          Affiliations
          [1 ] Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan, Republic of China.
          [2 ] Department and Institute of Pharmacology, National Yang-Ming University, Taipei, Taiwan, Republic of China Institute of Biophotonics, National Yang-Ming University, Taipei, Taiwan, Republic of China.
          [3 ] Imaging Core, Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan, Republic of China.
          [4 ] Institute of Genome Sciences, National Yang-Ming University, Taipei, Taiwan, Republic of China.
          [5 ] Department and Institute of Pharmacology, National Yang-Ming University, Taipei, Taiwan, Republic of China Institute of Biophotonics, National Yang-Ming University, Taipei, Taiwan, Republic of China Biophotonics and Molecular Imaging Research Center, National Yang-Ming University, Taipei, Taiwan, Republic of China VYM Genome Research Center, National Yang-Ming University, Taipei, Taiwan, Republic of China Infection and Immunity Research Center, National Yang-Ming University, Taipei, Taiwan, Republic of China mbwen@ccvax.sinica.edu.tw yhping@ym.edu.tw.
          [6 ] Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan, Republic of China Institute of Genome Sciences, National Yang-Ming University, Taipei, Taiwan, Republic of China mbwen@ccvax.sinica.edu.tw yhping@ym.edu.tw.
          Article
          JVI.00209-15
          10.1128/JVI.00209-15
          4524218
          26041286
          95f47c91-97dc-4a77-932a-bdbb68fd71cc
          Copyright © 2015, American Society for Microbiology. All Rights Reserved.
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