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Non-competitive resource exploitation within mosquito shapes within-host malaria infectivity and virulence
Malaria is a fatal human parasitic disease transmitted by a mosquito vector. Although the evolution of within-host malaria virulence has been the focus of many theoretical and empirical studies, the vector’s contribution to this process is not well understood. Here, we explore how within-vector reso...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110728/ https://www.ncbi.nlm.nih.gov/pubmed/30150763 http://dx.doi.org/10.1038/s41467-018-05893-z |
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author | Costa, G. Gildenhard, M. Eldering, M. Lindquist, R. L. Hauser, A. E. Sauerwein, R. Goosmann, C. Brinkmann, V. Carrillo-Bustamante, P. Levashina, E. A. |
author_facet | Costa, G. Gildenhard, M. Eldering, M. Lindquist, R. L. Hauser, A. E. Sauerwein, R. Goosmann, C. Brinkmann, V. Carrillo-Bustamante, P. Levashina, E. A. |
author_sort | Costa, G. |
collection | PubMed |
description | Malaria is a fatal human parasitic disease transmitted by a mosquito vector. Although the evolution of within-host malaria virulence has been the focus of many theoretical and empirical studies, the vector’s contribution to this process is not well understood. Here, we explore how within-vector resource exploitation would impact the evolution of within-host Plasmodium virulence. By combining within-vector dynamics and malaria epidemiology, we develop a mathematical model, which predicts that non-competitive parasitic resource exploitation within-vector restricts within-host parasite virulence. To validate our model, we experimentally manipulate mosquito lipid trafficking and gauge within-vector parasite development and within-host infectivity and virulence. We find that mosquito-derived lipids determine within-host parasite virulence by shaping development (quantity) and metabolic activity (quality) of transmissible sporozoites. Our findings uncover the potential impact of within-vector environment and vector control strategies on the evolution of malaria virulence. |
format | Online Article Text |
id | pubmed-6110728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61107282018-08-29 Non-competitive resource exploitation within mosquito shapes within-host malaria infectivity and virulence Costa, G. Gildenhard, M. Eldering, M. Lindquist, R. L. Hauser, A. E. Sauerwein, R. Goosmann, C. Brinkmann, V. Carrillo-Bustamante, P. Levashina, E. A. Nat Commun Article Malaria is a fatal human parasitic disease transmitted by a mosquito vector. Although the evolution of within-host malaria virulence has been the focus of many theoretical and empirical studies, the vector’s contribution to this process is not well understood. Here, we explore how within-vector resource exploitation would impact the evolution of within-host Plasmodium virulence. By combining within-vector dynamics and malaria epidemiology, we develop a mathematical model, which predicts that non-competitive parasitic resource exploitation within-vector restricts within-host parasite virulence. To validate our model, we experimentally manipulate mosquito lipid trafficking and gauge within-vector parasite development and within-host infectivity and virulence. We find that mosquito-derived lipids determine within-host parasite virulence by shaping development (quantity) and metabolic activity (quality) of transmissible sporozoites. Our findings uncover the potential impact of within-vector environment and vector control strategies on the evolution of malaria virulence. Nature Publishing Group UK 2018-08-27 /pmc/articles/PMC6110728/ /pubmed/30150763 http://dx.doi.org/10.1038/s41467-018-05893-z Text en © The Author(s) 2018 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 Costa, G. Gildenhard, M. Eldering, M. Lindquist, R. L. Hauser, A. E. Sauerwein, R. Goosmann, C. Brinkmann, V. Carrillo-Bustamante, P. Levashina, E. A. Non-competitive resource exploitation within mosquito shapes within-host malaria infectivity and virulence |
title | Non-competitive resource exploitation within mosquito shapes within-host malaria infectivity and virulence |
title_full | Non-competitive resource exploitation within mosquito shapes within-host malaria infectivity and virulence |
title_fullStr | Non-competitive resource exploitation within mosquito shapes within-host malaria infectivity and virulence |
title_full_unstemmed | Non-competitive resource exploitation within mosquito shapes within-host malaria infectivity and virulence |
title_short | Non-competitive resource exploitation within mosquito shapes within-host malaria infectivity and virulence |
title_sort | non-competitive resource exploitation within mosquito shapes within-host malaria infectivity and virulence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110728/ https://www.ncbi.nlm.nih.gov/pubmed/30150763 http://dx.doi.org/10.1038/s41467-018-05893-z |
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