Correlative multi-scale cryo-imaging unveils SARS-CoV-2 assembly and egress

Author:

Mendonça LuizaORCID,Howe AndrewORCID,Gilchrist James B.ORCID,Sheng YuewenORCID,Sun DapengORCID,Knight Michael L.ORCID,Zanetti-Domingues Laura C.ORCID,Bateman BenjiORCID,Krebs Anna-SophiaORCID,Chen LongORCID,Radecke JulikaORCID,Li Vivian D.ORCID,Ni TaoORCID,Kounatidis Ilias,Koronfel Mohamed A.ORCID,Szynkiewicz Marta,Harkiolaki MariaORCID,Martin-Fernandez Marisa L.ORCID,James WilliamORCID,Zhang PeijunORCID

Abstract

AbstractSince the outbreak of the SARS-CoV-2 pandemic, there have been intense structural studies on purified viral components and inactivated viruses. However, structural and ultrastructural evidence on how the SARS-CoV-2 infection progresses in the native cellular context is scarce, and there is a lack of comprehensive knowledge on the SARS-CoV-2 replicative cycle. To correlate cytopathic events induced by SARS-CoV-2 with virus replication processes in frozen-hydrated cells, we established a unique multi-modal, multi-scale cryo-correlative platform to image SARS-CoV-2 infection in Vero cells. This platform combines serial cryoFIB/SEM volume imaging and soft X-ray cryo-tomography with cell lamellae-based cryo-electron tomography (cryoET) and subtomogram averaging. Here we report critical SARS-CoV-2 structural events – e.g. viral RNA transport portals, virus assembly intermediates, virus egress pathway, and native virus spike structures, in the context of whole-cell volumes revealing drastic cytppathic changes. This integrated approach allows a holistic view of SARS-CoV-2 infection, from the whole cell to individual molecules.

Funder

Wellcome Trust

RCUK | Biotechnology and Biological Sciences Research Council

U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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