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Nutritional stress compromises mosquito fitness and antiviral immunity, while enhancing dengue virus infection susceptibility
Diet-induced nutritional stress can influence pathogen transmission potential in mosquitoes by impacting life history traits, infection susceptibility, and immunity. To investigate these effects, we manipulate mosquito diets at larval and adult stages, creating two nutritional levels (low and normal...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628303/ https://www.ncbi.nlm.nih.gov/pubmed/37932414 http://dx.doi.org/10.1038/s42003-023-05516-4 |
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author | Yan, Jiayue Kim, Chang-Hyun Chesser, Leta Ramirez, Jose L. Stone, Chris M. |
author_facet | Yan, Jiayue Kim, Chang-Hyun Chesser, Leta Ramirez, Jose L. Stone, Chris M. |
author_sort | Yan, Jiayue |
collection | PubMed |
description | Diet-induced nutritional stress can influence pathogen transmission potential in mosquitoes by impacting life history traits, infection susceptibility, and immunity. To investigate these effects, we manipulate mosquito diets at larval and adult stages, creating two nutritional levels (low and normal), and expose adults to dengue virus (DENV). We observe that egg number is reduced by nutritional stress at both stages and viral exposure separately and jointly, while the likelihood of laying eggs is exclusively influenced by adult nutritional stress. Adult nutritional stress alone shortens survival, while any pairwise combination between both-stage stress and viral exposure have a synergistic effect. Additionally, adult nutritional stress increases susceptibility to DENV infection, while larval nutritional stress likely has a similar effect operating via smaller body size. Furthermore, adult nutritional stress negatively impacts viral titers in infected mosquitoes; however, some survive and show increased titers over time. The immune response to DENV infection is overall suppressed by larval and adult nutritional stress, with specific genes related to Toll, JAK-STAT, and Imd immune signaling pathways, and antimicrobial peptides being downregulated. Our findings underscore the importance of nutritional stress in shaping mosquito traits, infection outcomes, and immune responses, all of which impact the vectorial capacity for DENV transmission. |
format | Online Article Text |
id | pubmed-10628303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106283032023-11-08 Nutritional stress compromises mosquito fitness and antiviral immunity, while enhancing dengue virus infection susceptibility Yan, Jiayue Kim, Chang-Hyun Chesser, Leta Ramirez, Jose L. Stone, Chris M. Commun Biol Article Diet-induced nutritional stress can influence pathogen transmission potential in mosquitoes by impacting life history traits, infection susceptibility, and immunity. To investigate these effects, we manipulate mosquito diets at larval and adult stages, creating two nutritional levels (low and normal), and expose adults to dengue virus (DENV). We observe that egg number is reduced by nutritional stress at both stages and viral exposure separately and jointly, while the likelihood of laying eggs is exclusively influenced by adult nutritional stress. Adult nutritional stress alone shortens survival, while any pairwise combination between both-stage stress and viral exposure have a synergistic effect. Additionally, adult nutritional stress increases susceptibility to DENV infection, while larval nutritional stress likely has a similar effect operating via smaller body size. Furthermore, adult nutritional stress negatively impacts viral titers in infected mosquitoes; however, some survive and show increased titers over time. The immune response to DENV infection is overall suppressed by larval and adult nutritional stress, with specific genes related to Toll, JAK-STAT, and Imd immune signaling pathways, and antimicrobial peptides being downregulated. Our findings underscore the importance of nutritional stress in shaping mosquito traits, infection outcomes, and immune responses, all of which impact the vectorial capacity for DENV transmission. Nature Publishing Group UK 2023-11-06 /pmc/articles/PMC10628303/ /pubmed/37932414 http://dx.doi.org/10.1038/s42003-023-05516-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yan, Jiayue Kim, Chang-Hyun Chesser, Leta Ramirez, Jose L. Stone, Chris M. Nutritional stress compromises mosquito fitness and antiviral immunity, while enhancing dengue virus infection susceptibility |
title | Nutritional stress compromises mosquito fitness and antiviral immunity, while enhancing dengue virus infection susceptibility |
title_full | Nutritional stress compromises mosquito fitness and antiviral immunity, while enhancing dengue virus infection susceptibility |
title_fullStr | Nutritional stress compromises mosquito fitness and antiviral immunity, while enhancing dengue virus infection susceptibility |
title_full_unstemmed | Nutritional stress compromises mosquito fitness and antiviral immunity, while enhancing dengue virus infection susceptibility |
title_short | Nutritional stress compromises mosquito fitness and antiviral immunity, while enhancing dengue virus infection susceptibility |
title_sort | nutritional stress compromises mosquito fitness and antiviral immunity, while enhancing dengue virus infection susceptibility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628303/ https://www.ncbi.nlm.nih.gov/pubmed/37932414 http://dx.doi.org/10.1038/s42003-023-05516-4 |
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