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Chimeric symbionts expressing a Wolbachia protein stimulate mosquito immunity and inhibit filarial parasite development

Wolbachia can reduce the capability of mosquitoes to transmit infectious diseases to humans and is currently exploited in campaigns for the control of arboviruses, like dengue and Zika. Under the assumption that Wolbachia-mediated activation of insect immunity plays a role in the reduction of mosqui...

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Autores principales: Epis, Sara, Varotto-Boccazzi, Ilaria, Crotti, Elena, Damiani, Claudia, Giovati, Laura, Mandrioli, Mauro, Biggiogera, Marco, Gabrieli, Paolo, Genchi, Marco, Polonelli, Luciano, Daffonchio, Daniele, Favia, Guido, Bandi, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060271/
https://www.ncbi.nlm.nih.gov/pubmed/32144396
http://dx.doi.org/10.1038/s42003-020-0835-2
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author Epis, Sara
Varotto-Boccazzi, Ilaria
Crotti, Elena
Damiani, Claudia
Giovati, Laura
Mandrioli, Mauro
Biggiogera, Marco
Gabrieli, Paolo
Genchi, Marco
Polonelli, Luciano
Daffonchio, Daniele
Favia, Guido
Bandi, Claudio
author_facet Epis, Sara
Varotto-Boccazzi, Ilaria
Crotti, Elena
Damiani, Claudia
Giovati, Laura
Mandrioli, Mauro
Biggiogera, Marco
Gabrieli, Paolo
Genchi, Marco
Polonelli, Luciano
Daffonchio, Daniele
Favia, Guido
Bandi, Claudio
author_sort Epis, Sara
collection PubMed
description Wolbachia can reduce the capability of mosquitoes to transmit infectious diseases to humans and is currently exploited in campaigns for the control of arboviruses, like dengue and Zika. Under the assumption that Wolbachia-mediated activation of insect immunity plays a role in the reduction of mosquito vectorial capacity, we focused our attention on the Wolbachia surface protein (WSP), a potential inductor of innate immunity. We hypothesized that the heterologous expression of this protein in gut- and tissue-associated symbionts may reduce parasite transmission. We thus engineered the mosquito bacterial symbiont Asaia to express WSP (Asaia(WSP)). Asaia(WSP) induced activation of the host immune response in Aedes aegypti and Anopheles stephensi mosquitoes, and inhibited the development of the heartworm parasite Dirofilaria immitis in Ae. aegypti. These results consolidate previous evidence on the immune-stimulating property of WSP and make Asaia(WSP) worth of further investigations as a potential tool for the control of mosquito-borne diseases.
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spelling pubmed-70602712020-03-19 Chimeric symbionts expressing a Wolbachia protein stimulate mosquito immunity and inhibit filarial parasite development Epis, Sara Varotto-Boccazzi, Ilaria Crotti, Elena Damiani, Claudia Giovati, Laura Mandrioli, Mauro Biggiogera, Marco Gabrieli, Paolo Genchi, Marco Polonelli, Luciano Daffonchio, Daniele Favia, Guido Bandi, Claudio Commun Biol Article Wolbachia can reduce the capability of mosquitoes to transmit infectious diseases to humans and is currently exploited in campaigns for the control of arboviruses, like dengue and Zika. Under the assumption that Wolbachia-mediated activation of insect immunity plays a role in the reduction of mosquito vectorial capacity, we focused our attention on the Wolbachia surface protein (WSP), a potential inductor of innate immunity. We hypothesized that the heterologous expression of this protein in gut- and tissue-associated symbionts may reduce parasite transmission. We thus engineered the mosquito bacterial symbiont Asaia to express WSP (Asaia(WSP)). Asaia(WSP) induced activation of the host immune response in Aedes aegypti and Anopheles stephensi mosquitoes, and inhibited the development of the heartworm parasite Dirofilaria immitis in Ae. aegypti. These results consolidate previous evidence on the immune-stimulating property of WSP and make Asaia(WSP) worth of further investigations as a potential tool for the control of mosquito-borne diseases. Nature Publishing Group UK 2020-03-06 /pmc/articles/PMC7060271/ /pubmed/32144396 http://dx.doi.org/10.1038/s42003-020-0835-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Epis, Sara
Varotto-Boccazzi, Ilaria
Crotti, Elena
Damiani, Claudia
Giovati, Laura
Mandrioli, Mauro
Biggiogera, Marco
Gabrieli, Paolo
Genchi, Marco
Polonelli, Luciano
Daffonchio, Daniele
Favia, Guido
Bandi, Claudio
Chimeric symbionts expressing a Wolbachia protein stimulate mosquito immunity and inhibit filarial parasite development
title Chimeric symbionts expressing a Wolbachia protein stimulate mosquito immunity and inhibit filarial parasite development
title_full Chimeric symbionts expressing a Wolbachia protein stimulate mosquito immunity and inhibit filarial parasite development
title_fullStr Chimeric symbionts expressing a Wolbachia protein stimulate mosquito immunity and inhibit filarial parasite development
title_full_unstemmed Chimeric symbionts expressing a Wolbachia protein stimulate mosquito immunity and inhibit filarial parasite development
title_short Chimeric symbionts expressing a Wolbachia protein stimulate mosquito immunity and inhibit filarial parasite development
title_sort chimeric symbionts expressing a wolbachia protein stimulate mosquito immunity and inhibit filarial parasite development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060271/
https://www.ncbi.nlm.nih.gov/pubmed/32144396
http://dx.doi.org/10.1038/s42003-020-0835-2
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