Cargando…

Sex and Death: The Effects of Innate Immune Factors on the Sexual Reproduction of Malaria Parasites

Malaria parasites must undergo a round of sexual reproduction in the blood meal of a mosquito vector to be transmitted between hosts. Developing a transmission-blocking intervention to prevent parasites from mating is a major goal of biomedicine, but its effectiveness could be compromised if parasit...

Descripción completa

Detalles Bibliográficos
Autores principales: Ramiro, Ricardo S., Alpedrinha, João, Carter, Lucy, Gardner, Andy, Reece, Sarah E.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048364/
https://www.ncbi.nlm.nih.gov/pubmed/21408620
http://dx.doi.org/10.1371/journal.ppat.1001309
_version_ 1782199145928327168
author Ramiro, Ricardo S.
Alpedrinha, João
Carter, Lucy
Gardner, Andy
Reece, Sarah E.
author_facet Ramiro, Ricardo S.
Alpedrinha, João
Carter, Lucy
Gardner, Andy
Reece, Sarah E.
author_sort Ramiro, Ricardo S.
collection PubMed
description Malaria parasites must undergo a round of sexual reproduction in the blood meal of a mosquito vector to be transmitted between hosts. Developing a transmission-blocking intervention to prevent parasites from mating is a major goal of biomedicine, but its effectiveness could be compromised if parasites can compensate by simply adjusting their sex allocation strategies. Recently, the application of evolutionary theory for sex allocation has been supported by experiments demonstrating that malaria parasites adjust their sex ratios in response to infection genetic diversity, precisely as predicted. Theory also predicts that parasites should adjust sex allocation in response to host immunity. Whilst data are supportive, the assumptions underlying this prediction – that host immune responses have differential effects on the mating ability of males and females – have not yet been tested. Here, we combine experimental work with theoretical models in order to investigate whether the development and fertility of male and female parasites is affected by innate immune factors and develop new theory to predict how parasites' sex allocation strategies should evolve in response to the observed effects. Specifically, we demonstrate that reactive nitrogen species impair gametogenesis of males only, but reduce the fertility of both male and female gametes. In contrast, tumour necrosis factor-α does not influence gametogenesis in either sex but impairs zygote development. Therefore, our experiments demonstrate that immune factors have complex effects on each sex, ranging from reducing the ability of gametocytes to develop into gametes, to affecting the viability of offspring. We incorporate these results into theory to predict how the evolutionary trajectories of parasite sex ratio strategies are shaped by sex differences in gamete production, fertility and offspring development. We show that medical interventions targeting offspring development are more likely to be ‘evolution-proof’ than interventions directed at killing males or females. Given the drive to develop medical interventions that interfere with parasite mating, our data and theoretical models have important implications.
format Text
id pubmed-3048364
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-30483642011-03-15 Sex and Death: The Effects of Innate Immune Factors on the Sexual Reproduction of Malaria Parasites Ramiro, Ricardo S. Alpedrinha, João Carter, Lucy Gardner, Andy Reece, Sarah E. PLoS Pathog Research Article Malaria parasites must undergo a round of sexual reproduction in the blood meal of a mosquito vector to be transmitted between hosts. Developing a transmission-blocking intervention to prevent parasites from mating is a major goal of biomedicine, but its effectiveness could be compromised if parasites can compensate by simply adjusting their sex allocation strategies. Recently, the application of evolutionary theory for sex allocation has been supported by experiments demonstrating that malaria parasites adjust their sex ratios in response to infection genetic diversity, precisely as predicted. Theory also predicts that parasites should adjust sex allocation in response to host immunity. Whilst data are supportive, the assumptions underlying this prediction – that host immune responses have differential effects on the mating ability of males and females – have not yet been tested. Here, we combine experimental work with theoretical models in order to investigate whether the development and fertility of male and female parasites is affected by innate immune factors and develop new theory to predict how parasites' sex allocation strategies should evolve in response to the observed effects. Specifically, we demonstrate that reactive nitrogen species impair gametogenesis of males only, but reduce the fertility of both male and female gametes. In contrast, tumour necrosis factor-α does not influence gametogenesis in either sex but impairs zygote development. Therefore, our experiments demonstrate that immune factors have complex effects on each sex, ranging from reducing the ability of gametocytes to develop into gametes, to affecting the viability of offspring. We incorporate these results into theory to predict how the evolutionary trajectories of parasite sex ratio strategies are shaped by sex differences in gamete production, fertility and offspring development. We show that medical interventions targeting offspring development are more likely to be ‘evolution-proof’ than interventions directed at killing males or females. Given the drive to develop medical interventions that interfere with parasite mating, our data and theoretical models have important implications. Public Library of Science 2011-03-03 /pmc/articles/PMC3048364/ /pubmed/21408620 http://dx.doi.org/10.1371/journal.ppat.1001309 Text en Ramiro et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ramiro, Ricardo S.
Alpedrinha, João
Carter, Lucy
Gardner, Andy
Reece, Sarah E.
Sex and Death: The Effects of Innate Immune Factors on the Sexual Reproduction of Malaria Parasites
title Sex and Death: The Effects of Innate Immune Factors on the Sexual Reproduction of Malaria Parasites
title_full Sex and Death: The Effects of Innate Immune Factors on the Sexual Reproduction of Malaria Parasites
title_fullStr Sex and Death: The Effects of Innate Immune Factors on the Sexual Reproduction of Malaria Parasites
title_full_unstemmed Sex and Death: The Effects of Innate Immune Factors on the Sexual Reproduction of Malaria Parasites
title_short Sex and Death: The Effects of Innate Immune Factors on the Sexual Reproduction of Malaria Parasites
title_sort sex and death: the effects of innate immune factors on the sexual reproduction of malaria parasites
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048364/
https://www.ncbi.nlm.nih.gov/pubmed/21408620
http://dx.doi.org/10.1371/journal.ppat.1001309
work_keys_str_mv AT ramiroricardos sexanddeaththeeffectsofinnateimmunefactorsonthesexualreproductionofmalariaparasites
AT alpedrinhajoao sexanddeaththeeffectsofinnateimmunefactorsonthesexualreproductionofmalariaparasites
AT carterlucy sexanddeaththeeffectsofinnateimmunefactorsonthesexualreproductionofmalariaparasites
AT gardnerandy sexanddeaththeeffectsofinnateimmunefactorsonthesexualreproductionofmalariaparasites
AT reecesarahe sexanddeaththeeffectsofinnateimmunefactorsonthesexualreproductionofmalariaparasites