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Fitness consequences of altered feeding behavior in immune-challenged mosquitoes

BACKGROUND: Malaria-infected mosquitoes have been reported to be more likely to take a blood meal when parasites are infectious than when non-infectious. This change in feeding behavior increases the likelihood of malaria transmission, and has been considered an example of parasite manipulation of h...

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Autores principales: Ohm, Johanna R., Teeple, Janet, Nelson, William A., Thomas, Matthew B., Read, Andrew F., Cator, Lauren J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772315/
https://www.ncbi.nlm.nih.gov/pubmed/26927687
http://dx.doi.org/10.1186/s13071-016-1392-x
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author Ohm, Johanna R.
Teeple, Janet
Nelson, William A.
Thomas, Matthew B.
Read, Andrew F.
Cator, Lauren J.
author_facet Ohm, Johanna R.
Teeple, Janet
Nelson, William A.
Thomas, Matthew B.
Read, Andrew F.
Cator, Lauren J.
author_sort Ohm, Johanna R.
collection PubMed
description BACKGROUND: Malaria-infected mosquitoes have been reported to be more likely to take a blood meal when parasites are infectious than when non-infectious. This change in feeding behavior increases the likelihood of malaria transmission, and has been considered an example of parasite manipulation of host behavior. However, immune challenge with heat-killed Escherichia coli induces the same behavior, suggesting that altered feeding behavior may be driven by adaptive responses of hosts to cope with an immune response, rather than by parasite-specific factors. Here we tested the alternative hypothesis that down-regulated feeding behavior prior to infectiousness is a mosquito adaptation that increases fitness during infection. METHODS: We measured the impact of immune challenge and blood feeding on the fitness of individual mosquitoes. After an initial blood meal, Anopheles stephensi Liston mosquitoes were experimentally challenged with heat-killed E. coli at a dose known to mimic the same temporal changes in mosquito feeding behavior as active malaria infection. We then tracked daily egg production and survivorship of females maintained on blood-feeding regimes that either mimicked down-regulated feeding behaviors observed during early malaria infection, or were fed on a four-day feeding cycle typically associated with uninfected mosquitoes. RESULTS: Restricting access to blood meals enhanced mosquito survival but lowered lifetime reproduction. Immune-challenge did not impact either fitness component. Combining fecundity and survival to estimate the population-scale intrinsic rate of increase (r), we found that, contrary to the mosquito adaptation hypothesis, mosquito fitness decreased if blood feeding was delayed following an immune challenge. CONCLUSIONS: Our data provide no support for the idea that malaria-induced suppression of blood feeding is an adaptation by mosquitoes to reduce the impact of immune challenge. Alternatively, the behavioral alterations may be neither host nor parasite adaptations, but rather a consequence of constraints imposed on feeding by activation of the mosquito immune response, i.e. non-adaptive illness-induced anorexia. Future work incorporating field conditions and different immune challenges could further clarify the effect of altered feeding on mosquito and parasite fitness. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1392-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-47723152016-03-02 Fitness consequences of altered feeding behavior in immune-challenged mosquitoes Ohm, Johanna R. Teeple, Janet Nelson, William A. Thomas, Matthew B. Read, Andrew F. Cator, Lauren J. Parasit Vectors Research BACKGROUND: Malaria-infected mosquitoes have been reported to be more likely to take a blood meal when parasites are infectious than when non-infectious. This change in feeding behavior increases the likelihood of malaria transmission, and has been considered an example of parasite manipulation of host behavior. However, immune challenge with heat-killed Escherichia coli induces the same behavior, suggesting that altered feeding behavior may be driven by adaptive responses of hosts to cope with an immune response, rather than by parasite-specific factors. Here we tested the alternative hypothesis that down-regulated feeding behavior prior to infectiousness is a mosquito adaptation that increases fitness during infection. METHODS: We measured the impact of immune challenge and blood feeding on the fitness of individual mosquitoes. After an initial blood meal, Anopheles stephensi Liston mosquitoes were experimentally challenged with heat-killed E. coli at a dose known to mimic the same temporal changes in mosquito feeding behavior as active malaria infection. We then tracked daily egg production and survivorship of females maintained on blood-feeding regimes that either mimicked down-regulated feeding behaviors observed during early malaria infection, or were fed on a four-day feeding cycle typically associated with uninfected mosquitoes. RESULTS: Restricting access to blood meals enhanced mosquito survival but lowered lifetime reproduction. Immune-challenge did not impact either fitness component. Combining fecundity and survival to estimate the population-scale intrinsic rate of increase (r), we found that, contrary to the mosquito adaptation hypothesis, mosquito fitness decreased if blood feeding was delayed following an immune challenge. CONCLUSIONS: Our data provide no support for the idea that malaria-induced suppression of blood feeding is an adaptation by mosquitoes to reduce the impact of immune challenge. Alternatively, the behavioral alterations may be neither host nor parasite adaptations, but rather a consequence of constraints imposed on feeding by activation of the mosquito immune response, i.e. non-adaptive illness-induced anorexia. Future work incorporating field conditions and different immune challenges could further clarify the effect of altered feeding on mosquito and parasite fitness. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1392-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-29 /pmc/articles/PMC4772315/ /pubmed/26927687 http://dx.doi.org/10.1186/s13071-016-1392-x Text en © Ohm et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ohm, Johanna R.
Teeple, Janet
Nelson, William A.
Thomas, Matthew B.
Read, Andrew F.
Cator, Lauren J.
Fitness consequences of altered feeding behavior in immune-challenged mosquitoes
title Fitness consequences of altered feeding behavior in immune-challenged mosquitoes
title_full Fitness consequences of altered feeding behavior in immune-challenged mosquitoes
title_fullStr Fitness consequences of altered feeding behavior in immune-challenged mosquitoes
title_full_unstemmed Fitness consequences of altered feeding behavior in immune-challenged mosquitoes
title_short Fitness consequences of altered feeding behavior in immune-challenged mosquitoes
title_sort fitness consequences of altered feeding behavior in immune-challenged mosquitoes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772315/
https://www.ncbi.nlm.nih.gov/pubmed/26927687
http://dx.doi.org/10.1186/s13071-016-1392-x
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