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wMel Wolbachia alters female post-mating behaviors and physiology in the dengue vector mosquito Aedes aegypti
Globally invasive Aedes aegypti disseminate numerous arboviruses that impact human health. One promising method to control Ae. aegypti populations is transinfection with Wolbachia pipientis, which naturally infects ~40–52% of insects but not Ae. aegypti. Transinfection of Ae. aegypti with the wMel W...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442437/ https://www.ncbi.nlm.nih.gov/pubmed/37604924 http://dx.doi.org/10.1038/s42003-023-05180-8 |
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author | Osorio, Jessica Villa-Arias, Sara Camargo, Carolina Ramírez-Sánchez, Luis Felipe Barrientos, Luisa María Bedoya, Carolina Rúa-Uribe, Guillermo Dorus, Steve Alfonso-Parra, Catalina Avila, Frank W. |
author_facet | Osorio, Jessica Villa-Arias, Sara Camargo, Carolina Ramírez-Sánchez, Luis Felipe Barrientos, Luisa María Bedoya, Carolina Rúa-Uribe, Guillermo Dorus, Steve Alfonso-Parra, Catalina Avila, Frank W. |
author_sort | Osorio, Jessica |
collection | PubMed |
description | Globally invasive Aedes aegypti disseminate numerous arboviruses that impact human health. One promising method to control Ae. aegypti populations is transinfection with Wolbachia pipientis, which naturally infects ~40–52% of insects but not Ae. aegypti. Transinfection of Ae. aegypti with the wMel Wolbachia strain induces cytoplasmic incompatibility (CI), allows infected individuals to invade native populations, and inhibits transmission of medically relevant arboviruses by females. Female insects undergo post-mating physiological and behavioral changes—referred to as the female post-mating response (PMR)—required for optimal fertility. PMRs are typically elicited by male seminal fluid proteins (SFPs) transferred with sperm during mating but can be modified by other factors, including microbiome composition. Wolbachia has modest effects on Ae. aegypti fertility, but its influence on other PMRs is unknown. Here, we show that Wolbachia influences female fecundity, fertility, and re-mating incidence and significantly extends the longevity of virgin females. Using proteomic methods to examine the seminal proteome of infected males, we found that Wolbachia moderately affects SFP composition. However, we identified 125 paternally transferred Wolbachia proteins, but the CI factor proteins (Cifs) were not among them. Our findings indicate that Wolbachia infection of Ae. aegypti alters female PMRs, potentially influencing control programs that utilize Wolbachia-infected individuals. |
format | Online Article Text |
id | pubmed-10442437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104424372023-08-23 wMel Wolbachia alters female post-mating behaviors and physiology in the dengue vector mosquito Aedes aegypti Osorio, Jessica Villa-Arias, Sara Camargo, Carolina Ramírez-Sánchez, Luis Felipe Barrientos, Luisa María Bedoya, Carolina Rúa-Uribe, Guillermo Dorus, Steve Alfonso-Parra, Catalina Avila, Frank W. Commun Biol Article Globally invasive Aedes aegypti disseminate numerous arboviruses that impact human health. One promising method to control Ae. aegypti populations is transinfection with Wolbachia pipientis, which naturally infects ~40–52% of insects but not Ae. aegypti. Transinfection of Ae. aegypti with the wMel Wolbachia strain induces cytoplasmic incompatibility (CI), allows infected individuals to invade native populations, and inhibits transmission of medically relevant arboviruses by females. Female insects undergo post-mating physiological and behavioral changes—referred to as the female post-mating response (PMR)—required for optimal fertility. PMRs are typically elicited by male seminal fluid proteins (SFPs) transferred with sperm during mating but can be modified by other factors, including microbiome composition. Wolbachia has modest effects on Ae. aegypti fertility, but its influence on other PMRs is unknown. Here, we show that Wolbachia influences female fecundity, fertility, and re-mating incidence and significantly extends the longevity of virgin females. Using proteomic methods to examine the seminal proteome of infected males, we found that Wolbachia moderately affects SFP composition. However, we identified 125 paternally transferred Wolbachia proteins, but the CI factor proteins (Cifs) were not among them. Our findings indicate that Wolbachia infection of Ae. aegypti alters female PMRs, potentially influencing control programs that utilize Wolbachia-infected individuals. Nature Publishing Group UK 2023-08-21 /pmc/articles/PMC10442437/ /pubmed/37604924 http://dx.doi.org/10.1038/s42003-023-05180-8 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Osorio, Jessica Villa-Arias, Sara Camargo, Carolina Ramírez-Sánchez, Luis Felipe Barrientos, Luisa María Bedoya, Carolina Rúa-Uribe, Guillermo Dorus, Steve Alfonso-Parra, Catalina Avila, Frank W. wMel Wolbachia alters female post-mating behaviors and physiology in the dengue vector mosquito Aedes aegypti |
title | wMel Wolbachia alters female post-mating behaviors and physiology in the dengue vector mosquito Aedes aegypti |
title_full | wMel Wolbachia alters female post-mating behaviors and physiology in the dengue vector mosquito Aedes aegypti |
title_fullStr | wMel Wolbachia alters female post-mating behaviors and physiology in the dengue vector mosquito Aedes aegypti |
title_full_unstemmed | wMel Wolbachia alters female post-mating behaviors and physiology in the dengue vector mosquito Aedes aegypti |
title_short | wMel Wolbachia alters female post-mating behaviors and physiology in the dengue vector mosquito Aedes aegypti |
title_sort | wmel wolbachia alters female post-mating behaviors and physiology in the dengue vector mosquito aedes aegypti |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442437/ https://www.ncbi.nlm.nih.gov/pubmed/37604924 http://dx.doi.org/10.1038/s42003-023-05180-8 |
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