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Midgut barriers prevent the replication and dissemination of the yellow fever vaccine in Aedes aegypti

BACKGROUND: To be transmitted to vertebrate hosts via the saliva of their vectors, arthropod-borne viruses have to cross several barriers in the mosquito body, including the midgut infection and escape barriers. Yellow fever virus (YFV) belongs to the genus Flavivirus, which includes human viruses t...

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Autores principales: Danet, Lucie, Beauclair, Guillaume, Berthet, Michèle, Moratorio, Gonzalo, Gracias, Ségolène, Tangy, Frédéric, Choumet, Valérie, Jouvenet, Nolwenn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709925/
https://www.ncbi.nlm.nih.gov/pubmed/31412040
http://dx.doi.org/10.1371/journal.pntd.0007299
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author Danet, Lucie
Beauclair, Guillaume
Berthet, Michèle
Moratorio, Gonzalo
Gracias, Ségolène
Tangy, Frédéric
Choumet, Valérie
Jouvenet, Nolwenn
author_facet Danet, Lucie
Beauclair, Guillaume
Berthet, Michèle
Moratorio, Gonzalo
Gracias, Ségolène
Tangy, Frédéric
Choumet, Valérie
Jouvenet, Nolwenn
author_sort Danet, Lucie
collection PubMed
description BACKGROUND: To be transmitted to vertebrate hosts via the saliva of their vectors, arthropod-borne viruses have to cross several barriers in the mosquito body, including the midgut infection and escape barriers. Yellow fever virus (YFV) belongs to the genus Flavivirus, which includes human viruses transmitted by Aedes mosquitoes, such as dengue and Zika viruses. The live-attenuated YFV-17D vaccine has been used safely and efficiently on a large scale since the end of World War II. Early studies have shown, using viral titration from salivary glands of infected mosquitoes, that YFV-17D can infect Aedes aegypti midgut, but does not disseminate to other tissues. METHODOLOGY/PRINCIPAL FINDINGS: Here, we re-visited this issue using a panel of techniques, such as RT-qPCR, Western blot, immunofluorescence and titration assays. We showed that YFV-17D replication was not efficient in Aedes aegypti midgut, as compared to the clinical isolate YFV-Dakar. Viruses that replicated in the midgut failed to disseminate to secondary organs. When injected into the thorax of mosquitoes, viruses succeeded in replicating into midgut-associated tissues, suggesting that, during natural infection, the block for YFV-17D replication occurs at the basal membrane of the midgut. CONCLUSIONS/SIGNIFICANCE: The two barriers associated with Ae. aegypti midgut prevent YFV-17D replication. Our study contributes to our basic understanding of vector–pathogen interactions and may also aid in the development of non-transmissible live virus vaccines.
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spelling pubmed-67099252019-09-10 Midgut barriers prevent the replication and dissemination of the yellow fever vaccine in Aedes aegypti Danet, Lucie Beauclair, Guillaume Berthet, Michèle Moratorio, Gonzalo Gracias, Ségolène Tangy, Frédéric Choumet, Valérie Jouvenet, Nolwenn PLoS Negl Trop Dis Research Article BACKGROUND: To be transmitted to vertebrate hosts via the saliva of their vectors, arthropod-borne viruses have to cross several barriers in the mosquito body, including the midgut infection and escape barriers. Yellow fever virus (YFV) belongs to the genus Flavivirus, which includes human viruses transmitted by Aedes mosquitoes, such as dengue and Zika viruses. The live-attenuated YFV-17D vaccine has been used safely and efficiently on a large scale since the end of World War II. Early studies have shown, using viral titration from salivary glands of infected mosquitoes, that YFV-17D can infect Aedes aegypti midgut, but does not disseminate to other tissues. METHODOLOGY/PRINCIPAL FINDINGS: Here, we re-visited this issue using a panel of techniques, such as RT-qPCR, Western blot, immunofluorescence and titration assays. We showed that YFV-17D replication was not efficient in Aedes aegypti midgut, as compared to the clinical isolate YFV-Dakar. Viruses that replicated in the midgut failed to disseminate to secondary organs. When injected into the thorax of mosquitoes, viruses succeeded in replicating into midgut-associated tissues, suggesting that, during natural infection, the block for YFV-17D replication occurs at the basal membrane of the midgut. CONCLUSIONS/SIGNIFICANCE: The two barriers associated with Ae. aegypti midgut prevent YFV-17D replication. Our study contributes to our basic understanding of vector–pathogen interactions and may also aid in the development of non-transmissible live virus vaccines. Public Library of Science 2019-08-14 /pmc/articles/PMC6709925/ /pubmed/31412040 http://dx.doi.org/10.1371/journal.pntd.0007299 Text en © 2019 Danet et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Danet, Lucie
Beauclair, Guillaume
Berthet, Michèle
Moratorio, Gonzalo
Gracias, Ségolène
Tangy, Frédéric
Choumet, Valérie
Jouvenet, Nolwenn
Midgut barriers prevent the replication and dissemination of the yellow fever vaccine in Aedes aegypti
title Midgut barriers prevent the replication and dissemination of the yellow fever vaccine in Aedes aegypti
title_full Midgut barriers prevent the replication and dissemination of the yellow fever vaccine in Aedes aegypti
title_fullStr Midgut barriers prevent the replication and dissemination of the yellow fever vaccine in Aedes aegypti
title_full_unstemmed Midgut barriers prevent the replication and dissemination of the yellow fever vaccine in Aedes aegypti
title_short Midgut barriers prevent the replication and dissemination of the yellow fever vaccine in Aedes aegypti
title_sort midgut barriers prevent the replication and dissemination of the yellow fever vaccine in aedes aegypti
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709925/
https://www.ncbi.nlm.nih.gov/pubmed/31412040
http://dx.doi.org/10.1371/journal.pntd.0007299
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