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Dual role of the Anopheles coluzzii Venus Kinase Receptor in both larval growth and immunity
Vector-borne diseases and especially malaria are responsible for more than half million deaths annually. The increase of insecticide resistance in wild populations of Anopheles malaria vectors emphasises the need for novel vector control strategies as well as for identifying novel vector targets. Ve...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401105/ https://www.ncbi.nlm.nih.gov/pubmed/30837655 http://dx.doi.org/10.1038/s41598-019-40407-x |
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author | Gouignard, Nadège Cherrier, Floriane Brito-Fravallo, Emma Pain, Adrien Zmarlak, Natalia Marta Cailliau, Katia Genève, Corinne Vernick, Kenneth D. Dissous, Colette Mitri, Christian |
author_facet | Gouignard, Nadège Cherrier, Floriane Brito-Fravallo, Emma Pain, Adrien Zmarlak, Natalia Marta Cailliau, Katia Genève, Corinne Vernick, Kenneth D. Dissous, Colette Mitri, Christian |
author_sort | Gouignard, Nadège |
collection | PubMed |
description | Vector-borne diseases and especially malaria are responsible for more than half million deaths annually. The increase of insecticide resistance in wild populations of Anopheles malaria vectors emphasises the need for novel vector control strategies as well as for identifying novel vector targets. Venus kinase receptors (VKRs) constitute a Receptor Tyrosine Kinase (RTK) family only found in invertebrates. In this study we functionally characterized Anopheles VKR in the Gambiae complex member, Anopheles coluzzii. Results showed that Anopheles VKR can be activated by L-amino acids, with L-arginine as the most potent agonist. VKR was not required for the fecundity of A. coluzzii, in contrast to reports from other insects, but VKR function is required in both Anopheles males and females for development of larval progeny. Anopheles VKR function is also required for protection against infection by Plasmodium parasites, thus identifying a novel linkage between reproduction and immunity in Anopheles. The insect specificity of VKRs as well as the essential function for reproduction and immunity suggest that Anopheles VKR could be a potentially druggable target for novel vector control strategies. |
format | Online Article Text |
id | pubmed-6401105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64011052019-03-07 Dual role of the Anopheles coluzzii Venus Kinase Receptor in both larval growth and immunity Gouignard, Nadège Cherrier, Floriane Brito-Fravallo, Emma Pain, Adrien Zmarlak, Natalia Marta Cailliau, Katia Genève, Corinne Vernick, Kenneth D. Dissous, Colette Mitri, Christian Sci Rep Article Vector-borne diseases and especially malaria are responsible for more than half million deaths annually. The increase of insecticide resistance in wild populations of Anopheles malaria vectors emphasises the need for novel vector control strategies as well as for identifying novel vector targets. Venus kinase receptors (VKRs) constitute a Receptor Tyrosine Kinase (RTK) family only found in invertebrates. In this study we functionally characterized Anopheles VKR in the Gambiae complex member, Anopheles coluzzii. Results showed that Anopheles VKR can be activated by L-amino acids, with L-arginine as the most potent agonist. VKR was not required for the fecundity of A. coluzzii, in contrast to reports from other insects, but VKR function is required in both Anopheles males and females for development of larval progeny. Anopheles VKR function is also required for protection against infection by Plasmodium parasites, thus identifying a novel linkage between reproduction and immunity in Anopheles. The insect specificity of VKRs as well as the essential function for reproduction and immunity suggest that Anopheles VKR could be a potentially druggable target for novel vector control strategies. Nature Publishing Group UK 2019-03-05 /pmc/articles/PMC6401105/ /pubmed/30837655 http://dx.doi.org/10.1038/s41598-019-40407-x Text en © The Author(s) 2019 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 Gouignard, Nadège Cherrier, Floriane Brito-Fravallo, Emma Pain, Adrien Zmarlak, Natalia Marta Cailliau, Katia Genève, Corinne Vernick, Kenneth D. Dissous, Colette Mitri, Christian Dual role of the Anopheles coluzzii Venus Kinase Receptor in both larval growth and immunity |
title | Dual role of the Anopheles coluzzii Venus Kinase Receptor in both larval growth and immunity |
title_full | Dual role of the Anopheles coluzzii Venus Kinase Receptor in both larval growth and immunity |
title_fullStr | Dual role of the Anopheles coluzzii Venus Kinase Receptor in both larval growth and immunity |
title_full_unstemmed | Dual role of the Anopheles coluzzii Venus Kinase Receptor in both larval growth and immunity |
title_short | Dual role of the Anopheles coluzzii Venus Kinase Receptor in both larval growth and immunity |
title_sort | dual role of the anopheles coluzzii venus kinase receptor in both larval growth and immunity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401105/ https://www.ncbi.nlm.nih.gov/pubmed/30837655 http://dx.doi.org/10.1038/s41598-019-40407-x |
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