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Wolbachia-Conferred Antiviral Protection Is Determined by Developmental Temperature

Wolbachia is a maternally transmitted bacterium that is widespread in arthropods and filarial nematodes and confers strong antiviral protection in Drosophila melanogaster and other arthropods. Wolbachia-transinfected Aedes aegypti mosquitoes are currently being deployed to fight transmission of deng...

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Autores principales: Chrostek, Ewa, Martins, Nelson, Marialva, Marta S., Teixeira, Luís
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546536/
https://www.ncbi.nlm.nih.gov/pubmed/34488458
http://dx.doi.org/10.1128/mBio.02923-20
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author Chrostek, Ewa
Martins, Nelson
Marialva, Marta S.
Teixeira, Luís
author_facet Chrostek, Ewa
Martins, Nelson
Marialva, Marta S.
Teixeira, Luís
author_sort Chrostek, Ewa
collection PubMed
description Wolbachia is a maternally transmitted bacterium that is widespread in arthropods and filarial nematodes and confers strong antiviral protection in Drosophila melanogaster and other arthropods. Wolbachia-transinfected Aedes aegypti mosquitoes are currently being deployed to fight transmission of dengue and Zika viruses. However, the mechanism of antiviral protection and the factors influencing are still not fully understood. Here, we show that temperature modulates Wolbachia-conferred protection in Drosophila melanogaster. Temperature after infection directly impacts Drosophila C virus (DCV) replication and modulates Wolbachia protection. At higher temperatures, viruses proliferate more and are more lethal, while Wolbachia confers lower protection. Strikingly, host developmental temperature is a determinant of Wolbachia-conferred antiviral protection. While there is strong protection when flies develop from egg to adult at 25°C, the protection is highly reduced or abolished when flies develop at 18°C. However, Wolbachia-induced changes during development are not sufficient to limit virus-induced mortality, as Wolbachia is still required to be present in adults at the time of infection. This developmental effect is general, since it was present in different host genotypes, Wolbachia variants, and upon infection with different viruses. Overall, we show that Wolbachia-conferred antiviral protection is temperature dependent, being present or absent depending on the environmental conditions. This interaction likely impacts Wolbachia-host interactions in nature and, as a result, frequencies of host and symbionts in different climates. Dependence of Wolbachia-mediated pathogen blocking on developmental temperature could be used to dissect the mechanistic bases of protection and influence the deployment of Wolbachia to prevent transmission of arboviruses.
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spelling pubmed-85465362021-11-04 Wolbachia-Conferred Antiviral Protection Is Determined by Developmental Temperature Chrostek, Ewa Martins, Nelson Marialva, Marta S. Teixeira, Luís mBio Research Article Wolbachia is a maternally transmitted bacterium that is widespread in arthropods and filarial nematodes and confers strong antiviral protection in Drosophila melanogaster and other arthropods. Wolbachia-transinfected Aedes aegypti mosquitoes are currently being deployed to fight transmission of dengue and Zika viruses. However, the mechanism of antiviral protection and the factors influencing are still not fully understood. Here, we show that temperature modulates Wolbachia-conferred protection in Drosophila melanogaster. Temperature after infection directly impacts Drosophila C virus (DCV) replication and modulates Wolbachia protection. At higher temperatures, viruses proliferate more and are more lethal, while Wolbachia confers lower protection. Strikingly, host developmental temperature is a determinant of Wolbachia-conferred antiviral protection. While there is strong protection when flies develop from egg to adult at 25°C, the protection is highly reduced or abolished when flies develop at 18°C. However, Wolbachia-induced changes during development are not sufficient to limit virus-induced mortality, as Wolbachia is still required to be present in adults at the time of infection. This developmental effect is general, since it was present in different host genotypes, Wolbachia variants, and upon infection with different viruses. Overall, we show that Wolbachia-conferred antiviral protection is temperature dependent, being present or absent depending on the environmental conditions. This interaction likely impacts Wolbachia-host interactions in nature and, as a result, frequencies of host and symbionts in different climates. Dependence of Wolbachia-mediated pathogen blocking on developmental temperature could be used to dissect the mechanistic bases of protection and influence the deployment of Wolbachia to prevent transmission of arboviruses. American Society for Microbiology 2021-09-07 /pmc/articles/PMC8546536/ /pubmed/34488458 http://dx.doi.org/10.1128/mBio.02923-20 Text en Copyright © 2021 Chrostek 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
Chrostek, Ewa
Martins, Nelson
Marialva, Marta S.
Teixeira, Luís
Wolbachia-Conferred Antiviral Protection Is Determined by Developmental Temperature
title Wolbachia-Conferred Antiviral Protection Is Determined by Developmental Temperature
title_full Wolbachia-Conferred Antiviral Protection Is Determined by Developmental Temperature
title_fullStr Wolbachia-Conferred Antiviral Protection Is Determined by Developmental Temperature
title_full_unstemmed Wolbachia-Conferred Antiviral Protection Is Determined by Developmental Temperature
title_short Wolbachia-Conferred Antiviral Protection Is Determined by Developmental Temperature
title_sort wolbachia-conferred antiviral protection is determined by developmental temperature
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546536/
https://www.ncbi.nlm.nih.gov/pubmed/34488458
http://dx.doi.org/10.1128/mBio.02923-20
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