4.6 Article

Rab8b Regulates Transport of West Nile Virus Particles from Recycling Endosomes

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 291, Issue 12, Pages 6559-6568

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M115.712760

Keywords

flavivirus; infection; Rab; transport; vesicles

Funding

  1. JSPS [15K19069]
  2. Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT)
  3. Ministry of Health, Labour, and Welfare of Japan
  4. Japan Initiative for Global Research Network on Infectious Diseases (J-GRID)
  5. Grant from MEXT for Joint Research Program of the Research Center for Zoonosis Control, Hokkaido University
  6. Grants-in-Aid for Scientific Research [26860307, 15K19069] Funding Source: KAKEN

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West Nile virus (WNV) particles assemble at and bud into the endoplasmic reticulum (ER) and are secreted from infected cells through the secretory pathway. However, the host factor related to these steps is not fully understood. Rab proteins, belonging to the Ras superfamily, play essential roles in regulating many aspects of vesicular trafficking. In this study, we sought to determine which Rab proteins are involved in intracellular trafficking of nascent WNV particles. RNAi analysis revealed that Rab8b plays a role in WNV particle release. We found that Rab8 and WNV antigen were colocalized in WNV-infected human neuroblastoma cells, and that WNV infection enhanced Rab8 expression in the cells. In addition, the amount of WNV particles in the supernatant of Rab8b-deficient cells was significantly decreased compared with that of wild-type cells. We also demonstrated that WNV particles accumulated in the recycling endosomes in WNV-infected cells. In summary, these results suggest that Rab8b is involved in trafficking of WNV particles from recycling endosomes to the plasma membrane.

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