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Development and physiological effects of an artificial diet for Wolbachia-infected Aedes aegypti

The endosymbiotic bacterium Wolbachia spreads rapidly through populations of Aedes aegypti mosquitoes, and strongly inhibits infection with key human pathogens including the dengue and Zika viruses. Mosquito control programs aimed at limiting transmission of these viruses are ongoing in multiple cou...

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Autores principales: Dutra, Heverton Leandro Carneiro, Rodrigues, Silvia Lomeu, Mansur, Simone Brutman, de Oliveira, Sofia Pimenta, Caragata, Eric Pearce, Moreira, Luciano Andrade
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691197/
https://www.ncbi.nlm.nih.gov/pubmed/29146940
http://dx.doi.org/10.1038/s41598-017-16045-6
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author Dutra, Heverton Leandro Carneiro
Rodrigues, Silvia Lomeu
Mansur, Simone Brutman
de Oliveira, Sofia Pimenta
Caragata, Eric Pearce
Moreira, Luciano Andrade
author_facet Dutra, Heverton Leandro Carneiro
Rodrigues, Silvia Lomeu
Mansur, Simone Brutman
de Oliveira, Sofia Pimenta
Caragata, Eric Pearce
Moreira, Luciano Andrade
author_sort Dutra, Heverton Leandro Carneiro
collection PubMed
description The endosymbiotic bacterium Wolbachia spreads rapidly through populations of Aedes aegypti mosquitoes, and strongly inhibits infection with key human pathogens including the dengue and Zika viruses. Mosquito control programs aimed at limiting transmission of these viruses are ongoing in multiple countries, yet there is a dearth of mass rearing infrastructure specific to Wolbachia-infected mosquitoes. One example is the lack of a blood meal substitute, which accounts for the Wolbachia-specific physiological changes in infected mosquitoes, that allows the bacterium to spread, and block viral infections. To that end, we have developed a blood meal substitute specifically for mosquitoes infected with the wMel Wolbachia strain. This diet, ADM, contains milk protein, and infant formula, dissolved in a mixture of bovine red blood cells and Aedes physiological saline, with ATP as a phagostimulant. Feeding with ADM leads to high levels of viable egg production, but also does not affect key Wolbachia parameters including, bacterial density, cytoplasmic incompatibility, or resistance to infection with Zika virus. ADM represents an effective substitute for human blood, which could potentially be used for the mass rearing of wMel-infected A. aegypti, and could easily be optimized in the future to improve performance.
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spelling pubmed-56911972017-11-24 Development and physiological effects of an artificial diet for Wolbachia-infected Aedes aegypti Dutra, Heverton Leandro Carneiro Rodrigues, Silvia Lomeu Mansur, Simone Brutman de Oliveira, Sofia Pimenta Caragata, Eric Pearce Moreira, Luciano Andrade Sci Rep Article The endosymbiotic bacterium Wolbachia spreads rapidly through populations of Aedes aegypti mosquitoes, and strongly inhibits infection with key human pathogens including the dengue and Zika viruses. Mosquito control programs aimed at limiting transmission of these viruses are ongoing in multiple countries, yet there is a dearth of mass rearing infrastructure specific to Wolbachia-infected mosquitoes. One example is the lack of a blood meal substitute, which accounts for the Wolbachia-specific physiological changes in infected mosquitoes, that allows the bacterium to spread, and block viral infections. To that end, we have developed a blood meal substitute specifically for mosquitoes infected with the wMel Wolbachia strain. This diet, ADM, contains milk protein, and infant formula, dissolved in a mixture of bovine red blood cells and Aedes physiological saline, with ATP as a phagostimulant. Feeding with ADM leads to high levels of viable egg production, but also does not affect key Wolbachia parameters including, bacterial density, cytoplasmic incompatibility, or resistance to infection with Zika virus. ADM represents an effective substitute for human blood, which could potentially be used for the mass rearing of wMel-infected A. aegypti, and could easily be optimized in the future to improve performance. Nature Publishing Group UK 2017-11-16 /pmc/articles/PMC5691197/ /pubmed/29146940 http://dx.doi.org/10.1038/s41598-017-16045-6 Text en © The Author(s) 2017 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
Dutra, Heverton Leandro Carneiro
Rodrigues, Silvia Lomeu
Mansur, Simone Brutman
de Oliveira, Sofia Pimenta
Caragata, Eric Pearce
Moreira, Luciano Andrade
Development and physiological effects of an artificial diet for Wolbachia-infected Aedes aegypti
title Development and physiological effects of an artificial diet for Wolbachia-infected Aedes aegypti
title_full Development and physiological effects of an artificial diet for Wolbachia-infected Aedes aegypti
title_fullStr Development and physiological effects of an artificial diet for Wolbachia-infected Aedes aegypti
title_full_unstemmed Development and physiological effects of an artificial diet for Wolbachia-infected Aedes aegypti
title_short Development and physiological effects of an artificial diet for Wolbachia-infected Aedes aegypti
title_sort development and physiological effects of an artificial diet for wolbachia-infected aedes aegypti
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691197/
https://www.ncbi.nlm.nih.gov/pubmed/29146940
http://dx.doi.org/10.1038/s41598-017-16045-6
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