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Experimental evaluation of the relationship between lethal or non-lethal virulence and transmission success in malaria parasite infections

BACKGROUND: Evolutionary theory suggests that the selection pressure on parasites to maximize their transmission determines their optimal host exploitation strategies and thus their virulence. Establishing the adaptive basis to parasite life history traits has important consequences for predicting p...

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Autores principales: Paul, REL, Lafond, T, Müller-Graf, CDM, Nithiuthai, S, Brey, PT, Koella, JC
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC520815/
https://www.ncbi.nlm.nih.gov/pubmed/15355551
http://dx.doi.org/10.1186/1471-2148-4-30
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author Paul, REL
Lafond, T
Müller-Graf, CDM
Nithiuthai, S
Brey, PT
Koella, JC
author_facet Paul, REL
Lafond, T
Müller-Graf, CDM
Nithiuthai, S
Brey, PT
Koella, JC
author_sort Paul, REL
collection PubMed
description BACKGROUND: Evolutionary theory suggests that the selection pressure on parasites to maximize their transmission determines their optimal host exploitation strategies and thus their virulence. Establishing the adaptive basis to parasite life history traits has important consequences for predicting parasite responses to public health interventions. In this study we examine the extent to which malaria parasites conform to the predicted adaptive trade-off between transmission and virulence, as defined by mortality. The majority of natural infections, however, result in sub-lethal virulent effects (e.g. anaemia) and are often composed of many strains. Both sub-lethal effects and pathogen population structure have been theoretically shown to have important consequences for virulence evolution. Thus, we additionally examine the relationship between anaemia and transmission in single and mixed clone infections. RESULTS: Whereas there was a trade-off between transmission success and virulence as defined by host mortality, contradictory clone-specific patterns occurred when defining virulence by anaemia. A negative relationship between anaemia and transmission success was found for one of the parasite clones, whereas there was no relationship for the other. Notably the two parasite clones also differed in a transmission phenotype (gametocyte sex ratio) that has previously been shown to respond adaptively to a changing blood environment. In addition, as predicted by evolutionary theory, mixed infections resulted in increased anaemia. The increased anaemia was, however, not correlated with any discernable parasite trait (e.g. parasite density) or with increased transmission. CONCLUSIONS: We found some evidence supporting the hypothesis that there is an adaptive basis correlating virulence (as defined by host mortality) and transmission success in malaria parasites. This confirms the validity of applying evolutionary virulence theory to biomedical research and adds support to the prediction that partially effective vaccines may select for increasingly virulent malaria parasite strains. By contrast, there was no consistent correlation between transmission and sub-lethal anaemia, a more common outcome of malaria infection. However, overall, the data are not inconsistent with the recent proposal that sub-lethal effects may impose an upper limit on virulence. Moreover, clone specific differences in transmission phenotypes linked to anaemia do suggest that there is considerable adaptive potential relating anaemia and transmission that may lead to uncertain consequences following intervention strategies.
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spelling pubmed-5208152004-10-01 Experimental evaluation of the relationship between lethal or non-lethal virulence and transmission success in malaria parasite infections Paul, REL Lafond, T Müller-Graf, CDM Nithiuthai, S Brey, PT Koella, JC BMC Evol Biol Research Article BACKGROUND: Evolutionary theory suggests that the selection pressure on parasites to maximize their transmission determines their optimal host exploitation strategies and thus their virulence. Establishing the adaptive basis to parasite life history traits has important consequences for predicting parasite responses to public health interventions. In this study we examine the extent to which malaria parasites conform to the predicted adaptive trade-off between transmission and virulence, as defined by mortality. The majority of natural infections, however, result in sub-lethal virulent effects (e.g. anaemia) and are often composed of many strains. Both sub-lethal effects and pathogen population structure have been theoretically shown to have important consequences for virulence evolution. Thus, we additionally examine the relationship between anaemia and transmission in single and mixed clone infections. RESULTS: Whereas there was a trade-off between transmission success and virulence as defined by host mortality, contradictory clone-specific patterns occurred when defining virulence by anaemia. A negative relationship between anaemia and transmission success was found for one of the parasite clones, whereas there was no relationship for the other. Notably the two parasite clones also differed in a transmission phenotype (gametocyte sex ratio) that has previously been shown to respond adaptively to a changing blood environment. In addition, as predicted by evolutionary theory, mixed infections resulted in increased anaemia. The increased anaemia was, however, not correlated with any discernable parasite trait (e.g. parasite density) or with increased transmission. CONCLUSIONS: We found some evidence supporting the hypothesis that there is an adaptive basis correlating virulence (as defined by host mortality) and transmission success in malaria parasites. This confirms the validity of applying evolutionary virulence theory to biomedical research and adds support to the prediction that partially effective vaccines may select for increasingly virulent malaria parasite strains. By contrast, there was no consistent correlation between transmission and sub-lethal anaemia, a more common outcome of malaria infection. However, overall, the data are not inconsistent with the recent proposal that sub-lethal effects may impose an upper limit on virulence. Moreover, clone specific differences in transmission phenotypes linked to anaemia do suggest that there is considerable adaptive potential relating anaemia and transmission that may lead to uncertain consequences following intervention strategies. BioMed Central 2004-09-08 /pmc/articles/PMC520815/ /pubmed/15355551 http://dx.doi.org/10.1186/1471-2148-4-30 Text en Copyright © 2004 Paul et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Paul, REL
Lafond, T
Müller-Graf, CDM
Nithiuthai, S
Brey, PT
Koella, JC
Experimental evaluation of the relationship between lethal or non-lethal virulence and transmission success in malaria parasite infections
title Experimental evaluation of the relationship between lethal or non-lethal virulence and transmission success in malaria parasite infections
title_full Experimental evaluation of the relationship between lethal or non-lethal virulence and transmission success in malaria parasite infections
title_fullStr Experimental evaluation of the relationship between lethal or non-lethal virulence and transmission success in malaria parasite infections
title_full_unstemmed Experimental evaluation of the relationship between lethal or non-lethal virulence and transmission success in malaria parasite infections
title_short Experimental evaluation of the relationship between lethal or non-lethal virulence and transmission success in malaria parasite infections
title_sort experimental evaluation of the relationship between lethal or non-lethal virulence and transmission success in malaria parasite infections
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC520815/
https://www.ncbi.nlm.nih.gov/pubmed/15355551
http://dx.doi.org/10.1186/1471-2148-4-30
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