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Dengue virus dominates lipid metabolism modulations in Wolbachia-coinfected Aedes aegypti
Competition between viruses and Wolbachia for host lipids is a proposed mechanism of Wolbachia-mediated virus blocking in insects. Yet, the metabolomic interaction between virus and symbiont within the mosquito has not been clearly defined. We compare the lipid profiles of Aedes aegypti mosquitoes b...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501868/ https://www.ncbi.nlm.nih.gov/pubmed/32948809 http://dx.doi.org/10.1038/s42003-020-01254-z |
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author | Koh, Cassandra Islam, M. Nurul Ye, Yixin H. Chotiwan, Nunya Graham, Barbara Belisle, John T. Kouremenos, Konstantinos A. Dayalan, Saravanan Tull, Dedreia L. Klatt, Stephan Perera, Rushika McGraw, Elizabeth A. |
author_facet | Koh, Cassandra Islam, M. Nurul Ye, Yixin H. Chotiwan, Nunya Graham, Barbara Belisle, John T. Kouremenos, Konstantinos A. Dayalan, Saravanan Tull, Dedreia L. Klatt, Stephan Perera, Rushika McGraw, Elizabeth A. |
author_sort | Koh, Cassandra |
collection | PubMed |
description | Competition between viruses and Wolbachia for host lipids is a proposed mechanism of Wolbachia-mediated virus blocking in insects. Yet, the metabolomic interaction between virus and symbiont within the mosquito has not been clearly defined. We compare the lipid profiles of Aedes aegypti mosquitoes bearing mono- or dual-infections of the Wolbachia wMel strain and dengue virus serotype 3 (DENV3). We found metabolic signatures of infection-induced intracellular events but little evidence to support direct competition between Wolbachia and virus for host lipids. Lipid profiles of dual-infected mosquitoes resemble those of DENV3 mono-infected mosquitoes, suggesting virus-driven modulation dominates over that of Wolbachia. Interestingly, knockdown of key metabolic enzymes suggests cardiolipins are host factors for DENV3 and Wolbachia replication. These findings define the Wolbachia-DENV3 metabolic interaction as indirectly antagonistic, rather than directly competitive, and reveal new research avenues with respect to mosquito × virus interactions at the molecular level. |
format | Online Article Text |
id | pubmed-7501868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75018682020-10-05 Dengue virus dominates lipid metabolism modulations in Wolbachia-coinfected Aedes aegypti Koh, Cassandra Islam, M. Nurul Ye, Yixin H. Chotiwan, Nunya Graham, Barbara Belisle, John T. Kouremenos, Konstantinos A. Dayalan, Saravanan Tull, Dedreia L. Klatt, Stephan Perera, Rushika McGraw, Elizabeth A. Commun Biol Article Competition between viruses and Wolbachia for host lipids is a proposed mechanism of Wolbachia-mediated virus blocking in insects. Yet, the metabolomic interaction between virus and symbiont within the mosquito has not been clearly defined. We compare the lipid profiles of Aedes aegypti mosquitoes bearing mono- or dual-infections of the Wolbachia wMel strain and dengue virus serotype 3 (DENV3). We found metabolic signatures of infection-induced intracellular events but little evidence to support direct competition between Wolbachia and virus for host lipids. Lipid profiles of dual-infected mosquitoes resemble those of DENV3 mono-infected mosquitoes, suggesting virus-driven modulation dominates over that of Wolbachia. Interestingly, knockdown of key metabolic enzymes suggests cardiolipins are host factors for DENV3 and Wolbachia replication. These findings define the Wolbachia-DENV3 metabolic interaction as indirectly antagonistic, rather than directly competitive, and reveal new research avenues with respect to mosquito × virus interactions at the molecular level. Nature Publishing Group UK 2020-09-18 /pmc/articles/PMC7501868/ /pubmed/32948809 http://dx.doi.org/10.1038/s42003-020-01254-z 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 Koh, Cassandra Islam, M. Nurul Ye, Yixin H. Chotiwan, Nunya Graham, Barbara Belisle, John T. Kouremenos, Konstantinos A. Dayalan, Saravanan Tull, Dedreia L. Klatt, Stephan Perera, Rushika McGraw, Elizabeth A. Dengue virus dominates lipid metabolism modulations in Wolbachia-coinfected Aedes aegypti |
title | Dengue virus dominates lipid metabolism modulations in Wolbachia-coinfected Aedes aegypti |
title_full | Dengue virus dominates lipid metabolism modulations in Wolbachia-coinfected Aedes aegypti |
title_fullStr | Dengue virus dominates lipid metabolism modulations in Wolbachia-coinfected Aedes aegypti |
title_full_unstemmed | Dengue virus dominates lipid metabolism modulations in Wolbachia-coinfected Aedes aegypti |
title_short | Dengue virus dominates lipid metabolism modulations in Wolbachia-coinfected Aedes aegypti |
title_sort | dengue virus dominates lipid metabolism modulations in wolbachia-coinfected aedes aegypti |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501868/ https://www.ncbi.nlm.nih.gov/pubmed/32948809 http://dx.doi.org/10.1038/s42003-020-01254-z |
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