Immunity promotes virulence evolution in a malaria model.

Evolutionary models predict that host immunity will shape the evolution of parasite virulence. While some assumptions of these models have been tested, the actual evolutionary outcome of immune selection on virulence has not. Using the mouse malaria model, Plasmodium chabaudi, we experimentally test...

Full description

Bibliographic Details
Main Authors: Margaret J Mackinnon, Andrew F Read
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2004-09-01
Series:PLoS Biology
Online Access:http://europepmc.org/articles/PMC434153?pdf=render
id doaj-f700949a023f4f47be457fd8b07aa412
record_format Article
spelling doaj-f700949a023f4f47be457fd8b07aa4122021-07-02T04:28:51ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852004-09-0129E23010.1371/journal.pbio.0020230Immunity promotes virulence evolution in a malaria model.Margaret J MackinnonAndrew F ReadEvolutionary models predict that host immunity will shape the evolution of parasite virulence. While some assumptions of these models have been tested, the actual evolutionary outcome of immune selection on virulence has not. Using the mouse malaria model, Plasmodium chabaudi, we experimentally tested whether immune pressure promotes the evolution of more virulent pathogens by evolving parasite lines in immunized and nonimmunized ("naïve") mice using serial passage. We found that parasite lines evolved in immunized mice became more virulent to both naïve and immune mice than lines evolved in naïve mice. When these evolved lines were transmitted through mosquitoes, there was a general reduction in virulence across all lines. However, the immune-selected lines remained more virulent to naïve mice than the naïve-selected lines, though not to immunized mice. Thus, immune selection accelerated the rate of virulence evolution, rendering parasites more dangerous to naïve hosts. These results argue for further consideration of the evolutionary consequences for pathogen virulence of vaccination.http://europepmc.org/articles/PMC434153?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Margaret J Mackinnon
Andrew F Read
spellingShingle Margaret J Mackinnon
Andrew F Read
Immunity promotes virulence evolution in a malaria model.
PLoS Biology
author_facet Margaret J Mackinnon
Andrew F Read
author_sort Margaret J Mackinnon
title Immunity promotes virulence evolution in a malaria model.
title_short Immunity promotes virulence evolution in a malaria model.
title_full Immunity promotes virulence evolution in a malaria model.
title_fullStr Immunity promotes virulence evolution in a malaria model.
title_full_unstemmed Immunity promotes virulence evolution in a malaria model.
title_sort immunity promotes virulence evolution in a malaria model.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2004-09-01
description Evolutionary models predict that host immunity will shape the evolution of parasite virulence. While some assumptions of these models have been tested, the actual evolutionary outcome of immune selection on virulence has not. Using the mouse malaria model, Plasmodium chabaudi, we experimentally tested whether immune pressure promotes the evolution of more virulent pathogens by evolving parasite lines in immunized and nonimmunized ("naïve") mice using serial passage. We found that parasite lines evolved in immunized mice became more virulent to both naïve and immune mice than lines evolved in naïve mice. When these evolved lines were transmitted through mosquitoes, there was a general reduction in virulence across all lines. However, the immune-selected lines remained more virulent to naïve mice than the naïve-selected lines, though not to immunized mice. Thus, immune selection accelerated the rate of virulence evolution, rendering parasites more dangerous to naïve hosts. These results argue for further consideration of the evolutionary consequences for pathogen virulence of vaccination.
url http://europepmc.org/articles/PMC434153?pdf=render
work_keys_str_mv AT margaretjmackinnon immunitypromotesvirulenceevolutioninamalariamodel
AT andrewfread immunitypromotesvirulenceevolutioninamalariamodel
_version_ 1721340198688653312