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      Cryo-EM structure of infectious bronchitis coronavirus spike protein reveals structural and functional evolution of coronavirus spike proteins

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          Abstract

          As cell-invading molecular machinery, coronavirus spike proteins pose an evolutionary conundrum due to their high divergence. In this study, we determined the cryo-EM structure of avian infectious bronchitis coronavirus (IBV) spike protein from the γ-genus. The trimeric IBV spike ectodomain contains three receptor-binding S1 heads and a trimeric membrane-fusion S2 stalk. While IBV S2 is structurally similar to those from the other genera, IBV S1 possesses structural features that are unique to different other genera, thereby bridging these diverse spikes into an evolutionary spectrum. Specifically, among different genera, the two domains of S1, the N-terminal domain (S1-NTD) and C-terminal domain (S1-CTD), diverge from simpler tertiary structures and quaternary packing to more complex ones, leading to different functions of the spikes in receptor usage and membrane fusion. Based on the above structural and functional comparisons, we propose that the evolutionary spectrum of coronavirus spikes follows the order of α-, δ-, γ-, and β-genus. This study has provided insight into the evolutionary relationships among coronavirus spikes and deepened our understanding of their structural and functional diversity.

          Author summary

          Because of their structural and functional diversity, coronavirus spike proteins represent a model system for studying viral evolution. Their evolutionary relationships and history pose major puzzles in virology. A critical missing piece in understanding the evolution of coronavirus spikes is the unavailability of the tertiary structure of γ-coronavirus spikes. Here we determined the first cryo-EM structure of avian infectious bronchitis coronavirus (IBV) spike from the γ-genus. The IBV spike contains structural features that are unique to different other genera; hence it brings the spikes from different coronavirus genera into one evolutionary spectrum, with itself sitting in the middle of this spectrum. The order of the evolutionary spectrum is α-, δ-, γ-, and β-genus. Importantly, through comparisons between IBV spike and other coronavirus spikes, this study illustrates how coronavirus spikes have achieved structural and functional diversity through evolution to guide viral entry into host cells.

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          Most cited references20

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          Structure, Function, and Evolution of Coronavirus Spike Proteins

          Fang Li (2016)
          The coronavirus spike protein is a multifunctional molecular machine that mediates coronavirus entry into host cells. It first binds to a receptor on the host cell surface through its S1 subunit and then fuses viral and host membranes through its S2 subunit. Two domains in S1 from different coronaviruses recognize a variety of host receptors, leading to viral attachment. The spike protein exists in two structurally distinct conformations, prefusion and postfusion. The transition from prefusion to postfusion conformation of the spike protein must be triggered, leading to membrane fusion. This article reviews current knowledge about the structures and functions of coronavirus spike proteins, illustrating how the two S1 domains recognize different receptors and how the spike proteins are regulated to undergo conformational transitions. I further discuss the evolution of these two critical functions of coronavirus spike proteins, receptor recognition and membrane fusion, in the context of the corresponding functions from other viruses and host cells.
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            Mechanisms of Coronavirus Cell Entry Mediated by the Viral Spike Protein

            Coronaviruses are enveloped positive-stranded RNA viruses that replicate in the cytoplasm. To deliver their nucleocapsid into the host cell, they rely on the fusion of their envelope with the host cell membrane. The spike glycoprotein (S) mediates virus entry and is a primary determinant of cell tropism and pathogenesis. It is classified as a class I fusion protein, and is responsible for binding to the receptor on the host cell as well as mediating the fusion of host and viral membranes—A process driven by major conformational changes of the S protein. This review discusses coronavirus entry mechanisms focusing on the different triggers used by coronaviruses to initiate the conformational change of the S protein: receptor binding, low pH exposure and proteolytic activation. We also highlight commonalities between coronavirus S proteins and other class I viral fusion proteins, as well as distinctive features that confer distinct tropism, pathogenicity and host interspecies transmission characteristics to coronaviruses.
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              Ready, Set, Fuse! The Coronavirus Spike Protein and Acquisition of Fusion Competence

              Coronavirus-cell entry programs involve virus-cell membrane fusions mediated by viral spike (S) proteins. Coronavirus S proteins acquire membrane fusion competence by receptor interactions, proteolysis, and acidification in endosomes. This review describes our current understanding of the S proteins, their interactions with and their responses to these entry triggers. We focus on receptors and proteases in prompting entry and highlight the type II transmembrane serine proteases (TTSPs) known to activate several virus fusion proteins. These and other proteases are essential cofactors permitting coronavirus infection, conceivably being in proximity to cell-surface receptors and thus poised to split entering spike proteins into the fragments that refold to mediate membrane fusion. The review concludes by noting how understanding of coronavirus entry informs antiviral therapies.
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: ValidationRole: Writing – review & editing
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: ValidationRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: ValidationRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: ValidationRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: ValidationRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: ValidationRole: Writing – review & editing
                Role: ConceptualizationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: ValidationRole: Writing – review & editing
                Role: ConceptualizationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: Project administrationRole: ResourcesRole: SupervisionRole: ValidationRole: Writing – original draft
                Role: Editor
                Journal
                PLoS Pathog
                PLoS Pathog
                plos
                plospath
                PLoS Pathogens
                Public Library of Science (San Francisco, CA USA )
                1553-7366
                1553-7374
                23 April 2018
                April 2018
                : 14
                : 4
                : e1007009
                Affiliations
                [1 ] Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota, Saint Paul, MN, United States of America
                [2 ] Department of Diagnostic and Biological Sciences, School of Dentistry, University of Minnesota, Minneapolis, MN, United States of America
                [3 ] Characterization Facility, College of Science and Engineering, University of Minnesota, Minneapolis, MN, United States of America
                Loyola University Chicago Stritch School of Medicine, UNITED STATES
                Author notes

                The authors have declared that no competing interests exist.

                Author information
                http://orcid.org/0000-0001-9061-3828
                http://orcid.org/0000-0002-1958-366X
                Article
                PPATHOGENS-D-18-00180
                10.1371/journal.ppat.1007009
                5933801
                29684066
                fe6021fa-a38f-4960-8a75-b2e654e480dc
                © 2018 Shang et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 30 January 2018
                : 3 April 2018
                Page count
                Figures: 5, Tables: 0, Pages: 19
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/100000060, National Institute of Allergy and Infectious Diseases;
                Award ID: R01AI089728
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/100000060, National Institute of Allergy and Infectious Diseases;
                Award ID: R01AI110700
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/100008961, College of Science and Engineering, University of Minnesota;
                Award Recipient :
                This work was supported by National Institute of Allergy and Infectious Diseases grants R01AI089728 and R01AI110700 (to FL) and University of Minnesota funding (to WZ). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Microbiology
                Microbial Evolution
                Viral Evolution
                Biology and Life Sciences
                Evolutionary Biology
                Organismal Evolution
                Microbial Evolution
                Viral Evolution
                Biology and Life Sciences
                Microbiology
                Virology
                Viral Evolution
                Biology and Life Sciences
                Evolutionary Biology
                Evolutionary Immunology
                Biology and Life Sciences
                Microbiology
                Virology
                Viral Structure
                Research and Analysis Methods
                Microscopy
                Electron Microscopy
                Electron Cryo-Microscopy
                Biology and Life Sciences
                Molecular Biology
                Macromolecular Structure Analysis
                Protein Structure
                Protein Structure Determination
                Biology and Life Sciences
                Biochemistry
                Proteins
                Protein Structure
                Protein Structure Determination
                Biology and Life Sciences
                Molecular Biology
                Macromolecular Structure Analysis
                Protein Structure
                Biology and Life Sciences
                Biochemistry
                Proteins
                Protein Structure
                Biology and Life Sciences
                Evolutionary Biology
                Molecular Evolution
                Research and Analysis Methods
                Spectrum Analysis Techniques
                Spectrophotometry
                Cytophotometry
                Flow Cytometry
                Custom metadata
                vor-update-to-uncorrected-proof
                2018-05-03
                The cryo-EM map has been deposited in the Electron Microscopy Data Bank (EMD) under accession code EMD-7631. The atomic model has been deposited in the Protein Data Bank (PDB) under accession code 6CV0.

                Infectious disease & Microbiology
                Infectious disease & Microbiology

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