The fitness of drug-resistant malaria parasites in a rodent model: Multiplicity of infection

S. Huijben, D. G. Sim, W. A. Nelson, A. F. Read

Research output: Contribution to journalArticle

25 Scopus citations

Abstract

Malaria infections normally consist of more than one clonally replicating lineage. Within-host interactions between sensitive and resistant parasites can have profound effects on the evolution of drug resistance. Here, using the Plasmodium chabaudi mouse malaria model, we ask whether the costs and benefits of resistance are affected by the number of co-infecting strains competing with a resistant clone. We found strong competitive suppression of resistant parasites in untreated infections and marked competitive release following treatment. The magnitude of competitive suppression depended on competitor identity. However, there was no overall effect of the diversity of susceptible parasites on the extent of competitive suppression or release. If these findings generalize, then transmission intensity will impact on resistance evolution because of its effect on the frequency of mixed infections, not because of its effect on the distribution of clones per host. This would greatly simplify the computational problems of adequately capturing within-host ecology in models of drug resistance evolution in malaria.

Original languageEnglish (US)
Pages (from-to)2410-2422
Number of pages13
JournalJournal of Evolutionary Biology
Volume24
Issue number11
DOIs
StatePublished - Nov 1 2011

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Keywords

  • Competition
  • Competitive release
  • Complexity of infection
  • Drug resistance
  • Malaria
  • Multiplicity of infection
  • Plasmodium chabaudi
  • Selection coefficient
  • Within-host dynamics

ASJC Scopus subject areas

  • Ecology, Evolution, Behavior and Systematics

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