Cargando…

Imaging analysis reveals budding of filamentous human metapneumovirus virions and direct transfer of inclusion bodies through intercellular extensions

Human metapneumovirus (HMPV) can spread between cells through budding of virus particles or direct cell-to-cell spread. A network of budding filaments and intercellular extensions forms in HMPV-infected cells; however, the involvement of these structures in direct cell-to-cell spread of infection re...

Descripción completa

Detalles Bibliográficos
Autores principales: El Najjar, Farah, Castillo, Santiago Restrepo, Moncman, Carole L., Wu, Cheng-Yu, Isla, Eduardo, Velez Ortega, A. Catalina, Frolenkov, Gregory I., Cifuentes-Munoz, Nicolas, Dutch, Rebecca Ellis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653870/
https://www.ncbi.nlm.nih.gov/pubmed/37681946
http://dx.doi.org/10.1128/mbio.01589-23
_version_ 1785136506263830528
author El Najjar, Farah
Castillo, Santiago Restrepo
Moncman, Carole L.
Wu, Cheng-Yu
Isla, Eduardo
Velez Ortega, A. Catalina
Frolenkov, Gregory I.
Cifuentes-Munoz, Nicolas
Dutch, Rebecca Ellis
author_facet El Najjar, Farah
Castillo, Santiago Restrepo
Moncman, Carole L.
Wu, Cheng-Yu
Isla, Eduardo
Velez Ortega, A. Catalina
Frolenkov, Gregory I.
Cifuentes-Munoz, Nicolas
Dutch, Rebecca Ellis
author_sort El Najjar, Farah
collection PubMed
description Human metapneumovirus (HMPV) can spread between cells through budding of virus particles or direct cell-to-cell spread. A network of budding filaments and intercellular extensions forms in HMPV-infected cells; however, the involvement of these structures in direct cell-to-cell spread of infection remains to be investigated. Utilizing advanced imaging techniques, we show that budding filaments contain the viral RNA genome, and not the antigenome, and become enriched with HMPV F protein as infection progresses. Multiple filaments containing the F protein on their surface were seen emanating from one cell to contact a neighboring cell, strongly suggesting that these are budding filamentous HMPV virions. In addition, changes in the morphology and properties of intercellular extensions following HMPV infection were detected. We show that intercellular extensions allow the transfer of a cytosolic dye only in HMPV-infected cells. In addition, using live imaging, we provide novel evidence of the direct passage of inclusion bodies from cell-to-cell across intercellular extensions. These results provide novel insights into the direct cell-to-cell spread of HMPV and suggest that this mode of transmission can occur through different mechanisms. IMPORTANCE: Human metapneumovirus is an important respiratory pathogen that causes significant morbidity and mortality, particularly in the very young, the elderly, and the immunosuppressed. However, the molecular details of how this virus spreads to new target cells are unclear. This work provides important new information on the formation of filamentous structures that are consistent with virus particles and adds critical new insight into the structure of extensions between cells that form during infection. In addition, it demonstrates for the first time the movement of viral replication centers through these intercellular extensions, representing a new mode of direct cell-to-cell spread that may be applicable to other viral systems.
format Online
Article
Text
id pubmed-10653870
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-106538702023-09-08 Imaging analysis reveals budding of filamentous human metapneumovirus virions and direct transfer of inclusion bodies through intercellular extensions El Najjar, Farah Castillo, Santiago Restrepo Moncman, Carole L. Wu, Cheng-Yu Isla, Eduardo Velez Ortega, A. Catalina Frolenkov, Gregory I. Cifuentes-Munoz, Nicolas Dutch, Rebecca Ellis mBio Research Article Human metapneumovirus (HMPV) can spread between cells through budding of virus particles or direct cell-to-cell spread. A network of budding filaments and intercellular extensions forms in HMPV-infected cells; however, the involvement of these structures in direct cell-to-cell spread of infection remains to be investigated. Utilizing advanced imaging techniques, we show that budding filaments contain the viral RNA genome, and not the antigenome, and become enriched with HMPV F protein as infection progresses. Multiple filaments containing the F protein on their surface were seen emanating from one cell to contact a neighboring cell, strongly suggesting that these are budding filamentous HMPV virions. In addition, changes in the morphology and properties of intercellular extensions following HMPV infection were detected. We show that intercellular extensions allow the transfer of a cytosolic dye only in HMPV-infected cells. In addition, using live imaging, we provide novel evidence of the direct passage of inclusion bodies from cell-to-cell across intercellular extensions. These results provide novel insights into the direct cell-to-cell spread of HMPV and suggest that this mode of transmission can occur through different mechanisms. IMPORTANCE: Human metapneumovirus is an important respiratory pathogen that causes significant morbidity and mortality, particularly in the very young, the elderly, and the immunosuppressed. However, the molecular details of how this virus spreads to new target cells are unclear. This work provides important new information on the formation of filamentous structures that are consistent with virus particles and adds critical new insight into the structure of extensions between cells that form during infection. In addition, it demonstrates for the first time the movement of viral replication centers through these intercellular extensions, representing a new mode of direct cell-to-cell spread that may be applicable to other viral systems. American Society for Microbiology 2023-09-08 /pmc/articles/PMC10653870/ /pubmed/37681946 http://dx.doi.org/10.1128/mbio.01589-23 Text en Copyright © 2023 El Najjar et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
El Najjar, Farah
Castillo, Santiago Restrepo
Moncman, Carole L.
Wu, Cheng-Yu
Isla, Eduardo
Velez Ortega, A. Catalina
Frolenkov, Gregory I.
Cifuentes-Munoz, Nicolas
Dutch, Rebecca Ellis
Imaging analysis reveals budding of filamentous human metapneumovirus virions and direct transfer of inclusion bodies through intercellular extensions
title Imaging analysis reveals budding of filamentous human metapneumovirus virions and direct transfer of inclusion bodies through intercellular extensions
title_full Imaging analysis reveals budding of filamentous human metapneumovirus virions and direct transfer of inclusion bodies through intercellular extensions
title_fullStr Imaging analysis reveals budding of filamentous human metapneumovirus virions and direct transfer of inclusion bodies through intercellular extensions
title_full_unstemmed Imaging analysis reveals budding of filamentous human metapneumovirus virions and direct transfer of inclusion bodies through intercellular extensions
title_short Imaging analysis reveals budding of filamentous human metapneumovirus virions and direct transfer of inclusion bodies through intercellular extensions
title_sort imaging analysis reveals budding of filamentous human metapneumovirus virions and direct transfer of inclusion bodies through intercellular extensions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653870/
https://www.ncbi.nlm.nih.gov/pubmed/37681946
http://dx.doi.org/10.1128/mbio.01589-23
work_keys_str_mv AT elnajjarfarah imaginganalysisrevealsbuddingoffilamentoushumanmetapneumovirusvirionsanddirecttransferofinclusionbodiesthroughintercellularextensions
AT castillosantiagorestrepo imaginganalysisrevealsbuddingoffilamentoushumanmetapneumovirusvirionsanddirecttransferofinclusionbodiesthroughintercellularextensions
AT moncmancarolel imaginganalysisrevealsbuddingoffilamentoushumanmetapneumovirusvirionsanddirecttransferofinclusionbodiesthroughintercellularextensions
AT wuchengyu imaginganalysisrevealsbuddingoffilamentoushumanmetapneumovirusvirionsanddirecttransferofinclusionbodiesthroughintercellularextensions
AT islaeduardo imaginganalysisrevealsbuddingoffilamentoushumanmetapneumovirusvirionsanddirecttransferofinclusionbodiesthroughintercellularextensions
AT velezortegaacatalina imaginganalysisrevealsbuddingoffilamentoushumanmetapneumovirusvirionsanddirecttransferofinclusionbodiesthroughintercellularextensions
AT frolenkovgregoryi imaginganalysisrevealsbuddingoffilamentoushumanmetapneumovirusvirionsanddirecttransferofinclusionbodiesthroughintercellularextensions
AT cifuentesmunoznicolas imaginganalysisrevealsbuddingoffilamentoushumanmetapneumovirusvirionsanddirecttransferofinclusionbodiesthroughintercellularextensions
AT dutchrebeccaellis imaginganalysisrevealsbuddingoffilamentoushumanmetapneumovirusvirionsanddirecttransferofinclusionbodiesthroughintercellularextensions