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The mosquito Aedes aegypti requires a gut microbiota for normal fecundity, longevity and vector competence
Mosquitoes shift from detritus-feeding larvae to blood-feeding adults that can vector pathogens to humans and other vertebrates. The sugar and blood meals adults consume are rich in carbohydrates and protein but are deficient in other nutrients including B vitamins. Facultatively hematophagous insec...
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/PMC10643675/ https://www.ncbi.nlm.nih.gov/pubmed/37957247 http://dx.doi.org/10.1038/s42003-023-05545-z |
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author | Harrison, Ruby E. Yang, Xiushuai Eum, Jai Hoon Martinson, Vincent G. Dou, Xiaoyi Valzania, Luca Wang, Yin Boyd, Bret M. Brown, Mark R. Strand, Michael R. |
author_facet | Harrison, Ruby E. Yang, Xiushuai Eum, Jai Hoon Martinson, Vincent G. Dou, Xiaoyi Valzania, Luca Wang, Yin Boyd, Bret M. Brown, Mark R. Strand, Michael R. |
author_sort | Harrison, Ruby E. |
collection | PubMed |
description | Mosquitoes shift from detritus-feeding larvae to blood-feeding adults that can vector pathogens to humans and other vertebrates. The sugar and blood meals adults consume are rich in carbohydrates and protein but are deficient in other nutrients including B vitamins. Facultatively hematophagous insects like mosquitoes have been hypothesized to avoid B vitamin deficiencies by carryover of resources from the larval stage. However, prior experimental studies have also used adults with a gut microbiota that could provision B vitamins. Here, we used Aedes aegypti, which is the primary vector of dengue virus (DENV), to ask if carryover effects enable normal function in adults with no microbiota. We show that adults with no gut microbiota produce fewer eggs, live longer with lower metabolic rates, and exhibit reduced DENV vector competence but are rescued by provisioning B vitamins or recolonizing the gut with B vitamin autotrophs. We conclude carryover effects do not enable normal function. |
format | Online Article Text |
id | pubmed-10643675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106436752023-11-13 The mosquito Aedes aegypti requires a gut microbiota for normal fecundity, longevity and vector competence Harrison, Ruby E. Yang, Xiushuai Eum, Jai Hoon Martinson, Vincent G. Dou, Xiaoyi Valzania, Luca Wang, Yin Boyd, Bret M. Brown, Mark R. Strand, Michael R. Commun Biol Article Mosquitoes shift from detritus-feeding larvae to blood-feeding adults that can vector pathogens to humans and other vertebrates. The sugar and blood meals adults consume are rich in carbohydrates and protein but are deficient in other nutrients including B vitamins. Facultatively hematophagous insects like mosquitoes have been hypothesized to avoid B vitamin deficiencies by carryover of resources from the larval stage. However, prior experimental studies have also used adults with a gut microbiota that could provision B vitamins. Here, we used Aedes aegypti, which is the primary vector of dengue virus (DENV), to ask if carryover effects enable normal function in adults with no microbiota. We show that adults with no gut microbiota produce fewer eggs, live longer with lower metabolic rates, and exhibit reduced DENV vector competence but are rescued by provisioning B vitamins or recolonizing the gut with B vitamin autotrophs. We conclude carryover effects do not enable normal function. Nature Publishing Group UK 2023-11-13 /pmc/articles/PMC10643675/ /pubmed/37957247 http://dx.doi.org/10.1038/s42003-023-05545-z 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 Harrison, Ruby E. Yang, Xiushuai Eum, Jai Hoon Martinson, Vincent G. Dou, Xiaoyi Valzania, Luca Wang, Yin Boyd, Bret M. Brown, Mark R. Strand, Michael R. The mosquito Aedes aegypti requires a gut microbiota for normal fecundity, longevity and vector competence |
title | The mosquito Aedes aegypti requires a gut microbiota for normal fecundity, longevity and vector competence |
title_full | The mosquito Aedes aegypti requires a gut microbiota for normal fecundity, longevity and vector competence |
title_fullStr | The mosquito Aedes aegypti requires a gut microbiota for normal fecundity, longevity and vector competence |
title_full_unstemmed | The mosquito Aedes aegypti requires a gut microbiota for normal fecundity, longevity and vector competence |
title_short | The mosquito Aedes aegypti requires a gut microbiota for normal fecundity, longevity and vector competence |
title_sort | mosquito aedes aegypti requires a gut microbiota for normal fecundity, longevity and vector competence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643675/ https://www.ncbi.nlm.nih.gov/pubmed/37957247 http://dx.doi.org/10.1038/s42003-023-05545-z |
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