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Encapsidated Host Factors in Alphavirus Particles Influence Midgut Infection of Aedes aegypti

Transmission of mosquito-borne viruses requires the efficient infection of both a permissive vertebrate host and a competent mosquito vector. The infectivity of Sindbis virus (SINV), the type species of the Alphavirus genus, is influenced by both the original and new host cell. We have shown that in...

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Autores principales: Mackenzie-Liu, David, Sokoloski, Kevin J., Purdy, Sarah, Hardy, Richard W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977256/
https://www.ncbi.nlm.nih.gov/pubmed/29772674
http://dx.doi.org/10.3390/v10050263
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author Mackenzie-Liu, David
Sokoloski, Kevin J.
Purdy, Sarah
Hardy, Richard W.
author_facet Mackenzie-Liu, David
Sokoloski, Kevin J.
Purdy, Sarah
Hardy, Richard W.
author_sort Mackenzie-Liu, David
collection PubMed
description Transmission of mosquito-borne viruses requires the efficient infection of both a permissive vertebrate host and a competent mosquito vector. The infectivity of Sindbis virus (SINV), the type species of the Alphavirus genus, is influenced by both the original and new host cell. We have shown that infection of vertebrate cells by SINV, chikungunya virus (CHIKV), and Ross River virus (RRV) produces two subpopulations of virus particles separable based on density. In contrast, a single population of viral particles is produced by mosquito cells. Previous studies demonstrated that the denser vertebrate-derived particles and the mosquito-derived particles contain components of the small subunit of the host cell ribosome, whereas the less dense vertebrate-derived particles do not. Infection of mice with RRV showed that both particle subpopulations are produced in an infected vertebrate, but in a tissue specific manner with serum containing only the less dense version of the virus particles. Previous infectivity studies using SINV particles have shown that the denser particles (SINV(Heavy)) and mosquito derived particles SINV(C6/36) are significantly more infectious in vertebrate cells than the less dense vertebrate derived particles (SINV(Light)). The current study shows that SINV(Light) particles, initiate the infection of the mosquito midgut more efficiently than SINV(Heavy) particles and that this enhanced infectivity is associated with an exacerbated immune response to SINV(Light) infection in midgut tissues. The enhanced infection of SINV(Light) is specific to the midgut as intrathoracically injected virus do not exhibit the same fitness advantage. Together, our data indicate a biologically significant role for the SINV(Light) subpopulation in the efficient transmission from infected vertebrates to the mosquito vector.
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spelling pubmed-59772562018-06-01 Encapsidated Host Factors in Alphavirus Particles Influence Midgut Infection of Aedes aegypti Mackenzie-Liu, David Sokoloski, Kevin J. Purdy, Sarah Hardy, Richard W. Viruses Article Transmission of mosquito-borne viruses requires the efficient infection of both a permissive vertebrate host and a competent mosquito vector. The infectivity of Sindbis virus (SINV), the type species of the Alphavirus genus, is influenced by both the original and new host cell. We have shown that infection of vertebrate cells by SINV, chikungunya virus (CHIKV), and Ross River virus (RRV) produces two subpopulations of virus particles separable based on density. In contrast, a single population of viral particles is produced by mosquito cells. Previous studies demonstrated that the denser vertebrate-derived particles and the mosquito-derived particles contain components of the small subunit of the host cell ribosome, whereas the less dense vertebrate-derived particles do not. Infection of mice with RRV showed that both particle subpopulations are produced in an infected vertebrate, but in a tissue specific manner with serum containing only the less dense version of the virus particles. Previous infectivity studies using SINV particles have shown that the denser particles (SINV(Heavy)) and mosquito derived particles SINV(C6/36) are significantly more infectious in vertebrate cells than the less dense vertebrate derived particles (SINV(Light)). The current study shows that SINV(Light) particles, initiate the infection of the mosquito midgut more efficiently than SINV(Heavy) particles and that this enhanced infectivity is associated with an exacerbated immune response to SINV(Light) infection in midgut tissues. The enhanced infection of SINV(Light) is specific to the midgut as intrathoracically injected virus do not exhibit the same fitness advantage. Together, our data indicate a biologically significant role for the SINV(Light) subpopulation in the efficient transmission from infected vertebrates to the mosquito vector. MDPI 2018-05-16 /pmc/articles/PMC5977256/ /pubmed/29772674 http://dx.doi.org/10.3390/v10050263 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mackenzie-Liu, David
Sokoloski, Kevin J.
Purdy, Sarah
Hardy, Richard W.
Encapsidated Host Factors in Alphavirus Particles Influence Midgut Infection of Aedes aegypti
title Encapsidated Host Factors in Alphavirus Particles Influence Midgut Infection of Aedes aegypti
title_full Encapsidated Host Factors in Alphavirus Particles Influence Midgut Infection of Aedes aegypti
title_fullStr Encapsidated Host Factors in Alphavirus Particles Influence Midgut Infection of Aedes aegypti
title_full_unstemmed Encapsidated Host Factors in Alphavirus Particles Influence Midgut Infection of Aedes aegypti
title_short Encapsidated Host Factors in Alphavirus Particles Influence Midgut Infection of Aedes aegypti
title_sort encapsidated host factors in alphavirus particles influence midgut infection of aedes aegypti
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977256/
https://www.ncbi.nlm.nih.gov/pubmed/29772674
http://dx.doi.org/10.3390/v10050263
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