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The structure of an infectious immature flavivirus redefines viral architecture and maturation

Flaviviruses are the cause of severe human diseases transmitted by mosquitoes and ticks. These viruses use a potent fusion machinery to enter target cells that needs to be restrained during viral assembly and egress. A molecular chaperone, premembrane (prM) maintains the virus particles in an immatu...

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Autores principales: Newton, Natalee D., Hardy, Joshua M., Modhiran, Naphak, Hugo, Leon E., Amarilla, Alberto A., Bibby, Summa, Venugopal, Hariprasad, Harrison, Jessica J., Traves, Renee J., Hall, Roy A., Hobson-Peters, Jody, Coulibaly, Fasséli, Watterson, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121421/
https://www.ncbi.nlm.nih.gov/pubmed/33990320
http://dx.doi.org/10.1126/sciadv.abe4507
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author Newton, Natalee D.
Hardy, Joshua M.
Modhiran, Naphak
Hugo, Leon E.
Amarilla, Alberto A.
Bibby, Summa
Venugopal, Hariprasad
Harrison, Jessica J.
Traves, Renee J.
Hall, Roy A.
Hobson-Peters, Jody
Coulibaly, Fasséli
Watterson, Daniel
author_facet Newton, Natalee D.
Hardy, Joshua M.
Modhiran, Naphak
Hugo, Leon E.
Amarilla, Alberto A.
Bibby, Summa
Venugopal, Hariprasad
Harrison, Jessica J.
Traves, Renee J.
Hall, Roy A.
Hobson-Peters, Jody
Coulibaly, Fasséli
Watterson, Daniel
author_sort Newton, Natalee D.
collection PubMed
description Flaviviruses are the cause of severe human diseases transmitted by mosquitoes and ticks. These viruses use a potent fusion machinery to enter target cells that needs to be restrained during viral assembly and egress. A molecular chaperone, premembrane (prM) maintains the virus particles in an immature, fusion-incompetent state until they exit the cell. Taking advantage of an insect virus that produces particles that are both immature and infectious, we determined the structure of the first immature flavivirus with a complete spike by cryo–electron microscopy. Unexpectedly, the prM chaperone forms a supporting pillar that maintains the immature spike in an asymmetric and upright state, primed for large rearrangements upon acidification. The collapse of the spike along a path defined by the prM chaperone is required, and its inhibition by a multivalent immunoglobulin M blocks infection. The revised architecture and collapse model are likely to be conserved across flaviviruses.
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spelling pubmed-81214212021-05-19 The structure of an infectious immature flavivirus redefines viral architecture and maturation Newton, Natalee D. Hardy, Joshua M. Modhiran, Naphak Hugo, Leon E. Amarilla, Alberto A. Bibby, Summa Venugopal, Hariprasad Harrison, Jessica J. Traves, Renee J. Hall, Roy A. Hobson-Peters, Jody Coulibaly, Fasséli Watterson, Daniel Sci Adv Research Articles Flaviviruses are the cause of severe human diseases transmitted by mosquitoes and ticks. These viruses use a potent fusion machinery to enter target cells that needs to be restrained during viral assembly and egress. A molecular chaperone, premembrane (prM) maintains the virus particles in an immature, fusion-incompetent state until they exit the cell. Taking advantage of an insect virus that produces particles that are both immature and infectious, we determined the structure of the first immature flavivirus with a complete spike by cryo–electron microscopy. Unexpectedly, the prM chaperone forms a supporting pillar that maintains the immature spike in an asymmetric and upright state, primed for large rearrangements upon acidification. The collapse of the spike along a path defined by the prM chaperone is required, and its inhibition by a multivalent immunoglobulin M blocks infection. The revised architecture and collapse model are likely to be conserved across flaviviruses. American Association for the Advancement of Science 2021-05-14 /pmc/articles/PMC8121421/ /pubmed/33990320 http://dx.doi.org/10.1126/sciadv.abe4507 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Newton, Natalee D.
Hardy, Joshua M.
Modhiran, Naphak
Hugo, Leon E.
Amarilla, Alberto A.
Bibby, Summa
Venugopal, Hariprasad
Harrison, Jessica J.
Traves, Renee J.
Hall, Roy A.
Hobson-Peters, Jody
Coulibaly, Fasséli
Watterson, Daniel
The structure of an infectious immature flavivirus redefines viral architecture and maturation
title The structure of an infectious immature flavivirus redefines viral architecture and maturation
title_full The structure of an infectious immature flavivirus redefines viral architecture and maturation
title_fullStr The structure of an infectious immature flavivirus redefines viral architecture and maturation
title_full_unstemmed The structure of an infectious immature flavivirus redefines viral architecture and maturation
title_short The structure of an infectious immature flavivirus redefines viral architecture and maturation
title_sort structure of an infectious immature flavivirus redefines viral architecture and maturation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121421/
https://www.ncbi.nlm.nih.gov/pubmed/33990320
http://dx.doi.org/10.1126/sciadv.abe4507
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