Cargando…

Spatially Segregated Transmission of Co-Occluded Baculoviruses Limits Virus–Virus Interactions Mediated by Cellular Coinfection during Primary Infection

The occlusion bodies (OBs) of certain alphabaculoviruses are polyhedrin-rich structures that mediate the collective transmission of tens of viral particles to the same insect host. In addition, in multiple nucleopolyhedroviruses, occlusion-derived virions (ODVs) form nucleocapsid aggregates that are...

Descripción completa

Detalles Bibliográficos
Autores principales: Pazmiño-Ibarra, Verónica, Herrero, Salvador, Sanjuan, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413315/
https://www.ncbi.nlm.nih.gov/pubmed/36016318
http://dx.doi.org/10.3390/v14081697
_version_ 1784775712255770624
author Pazmiño-Ibarra, Verónica
Herrero, Salvador
Sanjuan, Rafael
author_facet Pazmiño-Ibarra, Verónica
Herrero, Salvador
Sanjuan, Rafael
author_sort Pazmiño-Ibarra, Verónica
collection PubMed
description The occlusion bodies (OBs) of certain alphabaculoviruses are polyhedrin-rich structures that mediate the collective transmission of tens of viral particles to the same insect host. In addition, in multiple nucleopolyhedroviruses, occlusion-derived virions (ODVs) form nucleocapsid aggregates that are delivered to the same host cell. It has been suggested that, by favoring coinfection, this transmission mode promotes evolutionarily stable interactions between different baculovirus variants. To quantify the joint transmission of different variants, we obtained OBs from cells coinfected with two viral constructs, each encoding a different fluorescent reporter, and used them for inoculating Spodoptera exigua larvae. The microscopy analysis of midguts revealed that the two reporter genes were typically segregated into different infection foci, suggesting that ODVs show limited ability to promote the co-transmission of different virus variants to the same host cell. However, a polyhedrin-deficient mutant underwent inter-host transmission by exploiting the OBs of a fully functional virus and re-acquired the lost gene through recombination, demonstrating cellular coinfection. Our results suggest that viral spatial segregation during transmission and primary infection limits interactions between different baculovirus variants, but that these interactions still occur within the cells of infected insects later in infection.
format Online
Article
Text
id pubmed-9413315
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-94133152022-08-27 Spatially Segregated Transmission of Co-Occluded Baculoviruses Limits Virus–Virus Interactions Mediated by Cellular Coinfection during Primary Infection Pazmiño-Ibarra, Verónica Herrero, Salvador Sanjuan, Rafael Viruses Article The occlusion bodies (OBs) of certain alphabaculoviruses are polyhedrin-rich structures that mediate the collective transmission of tens of viral particles to the same insect host. In addition, in multiple nucleopolyhedroviruses, occlusion-derived virions (ODVs) form nucleocapsid aggregates that are delivered to the same host cell. It has been suggested that, by favoring coinfection, this transmission mode promotes evolutionarily stable interactions between different baculovirus variants. To quantify the joint transmission of different variants, we obtained OBs from cells coinfected with two viral constructs, each encoding a different fluorescent reporter, and used them for inoculating Spodoptera exigua larvae. The microscopy analysis of midguts revealed that the two reporter genes were typically segregated into different infection foci, suggesting that ODVs show limited ability to promote the co-transmission of different virus variants to the same host cell. However, a polyhedrin-deficient mutant underwent inter-host transmission by exploiting the OBs of a fully functional virus and re-acquired the lost gene through recombination, demonstrating cellular coinfection. Our results suggest that viral spatial segregation during transmission and primary infection limits interactions between different baculovirus variants, but that these interactions still occur within the cells of infected insects later in infection. MDPI 2022-07-31 /pmc/articles/PMC9413315/ /pubmed/36016318 http://dx.doi.org/10.3390/v14081697 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pazmiño-Ibarra, Verónica
Herrero, Salvador
Sanjuan, Rafael
Spatially Segregated Transmission of Co-Occluded Baculoviruses Limits Virus–Virus Interactions Mediated by Cellular Coinfection during Primary Infection
title Spatially Segregated Transmission of Co-Occluded Baculoviruses Limits Virus–Virus Interactions Mediated by Cellular Coinfection during Primary Infection
title_full Spatially Segregated Transmission of Co-Occluded Baculoviruses Limits Virus–Virus Interactions Mediated by Cellular Coinfection during Primary Infection
title_fullStr Spatially Segregated Transmission of Co-Occluded Baculoviruses Limits Virus–Virus Interactions Mediated by Cellular Coinfection during Primary Infection
title_full_unstemmed Spatially Segregated Transmission of Co-Occluded Baculoviruses Limits Virus–Virus Interactions Mediated by Cellular Coinfection during Primary Infection
title_short Spatially Segregated Transmission of Co-Occluded Baculoviruses Limits Virus–Virus Interactions Mediated by Cellular Coinfection during Primary Infection
title_sort spatially segregated transmission of co-occluded baculoviruses limits virus–virus interactions mediated by cellular coinfection during primary infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413315/
https://www.ncbi.nlm.nih.gov/pubmed/36016318
http://dx.doi.org/10.3390/v14081697
work_keys_str_mv AT pazminoibarraveronica spatiallysegregatedtransmissionofcooccludedbaculoviruseslimitsvirusvirusinteractionsmediatedbycellularcoinfectionduringprimaryinfection
AT herrerosalvador spatiallysegregatedtransmissionofcooccludedbaculoviruseslimitsvirusvirusinteractionsmediatedbycellularcoinfectionduringprimaryinfection
AT sanjuanrafael spatiallysegregatedtransmissionofcooccludedbaculoviruseslimitsvirusvirusinteractionsmediatedbycellularcoinfectionduringprimaryinfection