ESCRT machinery components are required for Orthobunyavirus particle production in Golgi compartments

PLoS Pathog. 2018 May 3;14(5):e1007047. doi: 10.1371/journal.ppat.1007047. eCollection 2018 May.

Abstract

Peribunyaviridae is a large family of RNA viruses with several members that cause mild to severe diseases in humans and livestock. Despite their importance in public heath very little is known about the host cell factors hijacked by these viruses to support assembly and cell egress. Here we show that assembly of Oropouche virus, a member of the genus Orthobunyavirus that causes a frequent arboviral infection in South America countries, involves budding of virus particles toward the lumen of Golgi cisternae. As viral replication progresses, these Golgi subcompartments become enlarged and physically separated from Golgi stacks, forming Oropouche viral factory (Vfs) units. At the ultrastructural level, these virally modified Golgi cisternae acquire an MVB appearance, and while they lack typical early and late endosome markers, they become enriched in endosomal complex required for transport (ESCRT) proteins that are involved in MVB biogenesis. Further microscopy and viral replication analysis showed that functional ESCRT machinery is required for efficient Vf morphogenesis and production of infectious OROV particles. Taken together, our results indicate that OROV attracts ESCRT machinery components to Golgi cisternae to mediate membrane remodeling events required for viral assembly and budding at these compartments. This represents an unprecedented mechanism of how viruses hijack host cell components for coordinated morphogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Culture Techniques
  • Endosomal Sorting Complexes Required for Transport / metabolism*
  • Endosomal Sorting Complexes Required for Transport / physiology
  • Endosomes / metabolism
  • Golgi Apparatus / metabolism
  • Golgi Apparatus / virology
  • HeLa Cells
  • Humans
  • Orthobunyavirus / growth & development
  • Orthobunyavirus / metabolism*
  • Orthobunyavirus / pathogenicity
  • Orthobunyavirus / physiology*
  • Virion / metabolism
  • Virus Assembly / physiology
  • Virus Release / physiology
  • Virus Replication / physiology

Substances

  • Endosomal Sorting Complexes Required for Transport

Grants and funding

This work was supported by the by the Fundação de Amparo à Pesquisa do Estado de São Paulo (São Paulo Research Foundation; FAPESP) grants (2014/25812-0 and 2014/02438-6) and Fundação de Apoio ao Ensino, Pesquisa e Assistência do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo (FAEPA) grants to LLPdS. The work was also supported by FAPESP EMU 2009/54014-7 to the Multiuser Laboratory of Multiphoton Microscopy. The DeltaVision OMX SR system (GE Healthcare Life Sciences, Issaquah, WA, USA) was financed by a joint grant of the German research foundation (DFG, INST 2388/59-1) and the University Hospital Tübingen to MS. NSB, EZMdS, MCP and MEdSJ thank FAPESP for doctoral fellowships. LRM was supported by a masters fellowship from CNPq (Brazilian Ministry of Science and Technology). MVSD was supported by a post-doctoral (PNPD) fellowship from CAPES (Brazilian Ministry of Education). EA and LLPdS are recipients of a long-standing investigator scholarship from CNPq. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.