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Plasticity in transmission strategies of the malaria parasite, Plasmodium chabaudi: environmental and genetic effects
Parasites may alter their behaviour to cope with changes in the within-host environment. In particular, investment in transmission may alter in response to the availability of parasite resources or host immune responses. However, experimental and theoretical studies have drawn conflicting conclusion...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586624/ https://www.ncbi.nlm.nih.gov/pubmed/23467678 http://dx.doi.org/10.1111/eva.12005 |
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author | Cameron, Angus Reece, Sarah E Drew, Damien R Haydon, Daniel T Yates, Andrew J |
author_facet | Cameron, Angus Reece, Sarah E Drew, Damien R Haydon, Daniel T Yates, Andrew J |
author_sort | Cameron, Angus |
collection | PubMed |
description | Parasites may alter their behaviour to cope with changes in the within-host environment. In particular, investment in transmission may alter in response to the availability of parasite resources or host immune responses. However, experimental and theoretical studies have drawn conflicting conclusions regarding parasites' optimal (adaptive) responses to deterioration in habitat quality. We analyse data from acute infections with six genotypes of the rodent malaria species Plasmodium chabaudi to quantify how investment in transmission (gametocytes) is influenced by the within-host environment. Using a minimum of modelling assumptions, we find that proportional investment in gametocytogenesis increases sharply with host anaemia and also increases at low parasite densities. Further, stronger dependence of investment on parasite density is associated with greater virulence of the parasite genotype. Our study provides a robust quantitative framework for studying parasites' responses to the host environment and whether these responses are adaptive, which is crucial for predicting the short-term and evolutionary impact of transmission-blocking treatments for parasitic diseases. |
format | Online Article Text |
id | pubmed-3586624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35866242013-03-05 Plasticity in transmission strategies of the malaria parasite, Plasmodium chabaudi: environmental and genetic effects Cameron, Angus Reece, Sarah E Drew, Damien R Haydon, Daniel T Yates, Andrew J Evol Appl Original Articles Parasites may alter their behaviour to cope with changes in the within-host environment. In particular, investment in transmission may alter in response to the availability of parasite resources or host immune responses. However, experimental and theoretical studies have drawn conflicting conclusions regarding parasites' optimal (adaptive) responses to deterioration in habitat quality. We analyse data from acute infections with six genotypes of the rodent malaria species Plasmodium chabaudi to quantify how investment in transmission (gametocytes) is influenced by the within-host environment. Using a minimum of modelling assumptions, we find that proportional investment in gametocytogenesis increases sharply with host anaemia and also increases at low parasite densities. Further, stronger dependence of investment on parasite density is associated with greater virulence of the parasite genotype. Our study provides a robust quantitative framework for studying parasites' responses to the host environment and whether these responses are adaptive, which is crucial for predicting the short-term and evolutionary impact of transmission-blocking treatments for parasitic diseases. Blackwell Publishing Ltd 2013-02 2012-10-10 /pmc/articles/PMC3586624/ /pubmed/23467678 http://dx.doi.org/10.1111/eva.12005 Text en Journal compilation © 2013 Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Cameron, Angus Reece, Sarah E Drew, Damien R Haydon, Daniel T Yates, Andrew J Plasticity in transmission strategies of the malaria parasite, Plasmodium chabaudi: environmental and genetic effects |
title | Plasticity in transmission strategies of the malaria parasite, Plasmodium chabaudi: environmental and genetic effects |
title_full | Plasticity in transmission strategies of the malaria parasite, Plasmodium chabaudi: environmental and genetic effects |
title_fullStr | Plasticity in transmission strategies of the malaria parasite, Plasmodium chabaudi: environmental and genetic effects |
title_full_unstemmed | Plasticity in transmission strategies of the malaria parasite, Plasmodium chabaudi: environmental and genetic effects |
title_short | Plasticity in transmission strategies of the malaria parasite, Plasmodium chabaudi: environmental and genetic effects |
title_sort | plasticity in transmission strategies of the malaria parasite, plasmodium chabaudi: environmental and genetic effects |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586624/ https://www.ncbi.nlm.nih.gov/pubmed/23467678 http://dx.doi.org/10.1111/eva.12005 |
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