Abstract
The global predominance of three clonal Toxoplasma gondii lineages suggests that they are endowed with an exceptional trait responsible for their current parasitism of nearly all warm-blooded vertebrates. Genetic polymorphism analyses indicate that these clonal lineages emerged within the last 10,000 years after a single genetic cross. Comparison with ancient strains (approximately 1 million years) suggests that the success of the clonal lineages resulted from the concurrent acquisition of direct oral infectivity. This key adaptation circumvented sexual recombination, simultaneously promoting transmission through successive hosts, hence leading to clonal expansion. Thus, changes in complex life cycles can occur rapidly and can profoundly influence pathogenicity.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Cats
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DNA, Ribosomal / genetics
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DNA, Ribosomal Spacer / genetics
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Food Parasitology
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Genes, Protozoan*
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Introns
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Life Cycle Stages
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Mice
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Molecular Sequence Data
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Mouth
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Mutation
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Phylogeny
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Polymorphism, Genetic
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Polymorphism, Single Nucleotide
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Recombination, Genetic
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Reproduction
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Selection, Genetic*
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Toxoplasma / genetics*
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Toxoplasma / pathogenicity
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Toxoplasma / physiology*
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Toxoplasmosis / parasitology*
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Toxoplasmosis / transmission
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Toxoplasmosis, Animal / parasitology*
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Toxoplasmosis, Animal / transmission
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Virulence
Substances
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DNA, Ribosomal
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DNA, Ribosomal Spacer
Associated data
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GENBANK/AY143096
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GENBANK/AY143097
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GENBANK/AY143098
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