4.8 Article

Architecture of the chikungunya virus replication organelle

Journal

ELIFE
Volume 11, Issue -, Pages -

Publisher

eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.83042

Keywords

Alphavirus; virus replication; cryo-electron tomography; membrane dynamics; simulations; Viruses

Categories

Funding

  1. Human Frontier Science Program [CDA00047/2017-C]
  2. Vetenskapsradet [2018-05851, 2021-01145]
  3. Kempestiftelserna [JCK-1723.2]
  4. Max Planck Institute for the Physics of Complex Systems
  5. Swedish Research Council [2021-01145, 2018-05851] Funding Source: Swedish Research Council

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Alphaviruses, including chikungunya virus (CHIKV), are mosquito-borne viruses that cause serious disease in humans and other mammals. CHIKV has been rapidly spreading in the last 20 years without an approved treatment. Researchers used cryo-electron tomography to image CHIKV spherules, specialized organelles for viral RNA replication, on the plasma membrane of infected cells. They discovered that the viral protein nsP1 serves as a base for a larger protein complex assembly at the neck of the membrane bud. The tomograms also revealed that full-sized spherules contain a single copy of the viral genome in double-stranded form. Additionally, a mathematical model was presented to explain the membrane remodeling of the spherule, which showed good agreement with experimental data.
Alphaviruses are mosquito-borne viruses that cause serious disease in humans and other mammals. Along with its mosquito vector, the Alphavirus chikungunya virus (CHIKV) has spread explosively in the last 20 years, and there is no approved treatment for chikungunya fever. On the plasma membrane of the infected cell, CHIKV generates dedicated organelles for viral RNA replication, so-called spherules. Whereas structures exist for several viral proteins that make up the spherule, the architecture of the full organelle is unknown. Here, we use cryo-electron tomography to image CHIKV spherules in their cellular context. This reveals that the viral protein nsP1 serves as a base for the assembly of a larger protein complex at the neck of the membrane bud. Biochemical assays show that the viral helicase-protease nsP2, while having no membrane affinity on its own, is recruited to membranes by nsP1. The tomograms further reveal that full-sized spherules contain a single copy of the viral genome in double-stranded form. Finally, we present a mathematical model that explains the membrane remodeling of the spherule in terms of the pressure exerted on the membrane by the polymerizing RNA, which provides a good agreement with the experimental data. The energy released by RNA polymerization is found to be sufficient to remodel the membrane to the characteristic spherule shape.

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