Data from: Ecological host fitting of Trypanosoma cruzi TcI in Bolivia: mosaic population structure, hybridization and a role for humans in Andean parasite dispersal
An improved understanding of how a parasite species exploits its genetic repertoire to colonize novel hosts and environmental niches is crucial to establish the epidemiological risk associated with emergent pathogenic genotypes. Trypanosoma cruzi, a genetically heterogeneous, multi-host zoonosis, pr...
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Zusammenfassung: | An improved understanding of how a parasite species exploits its genetic
repertoire to colonize novel hosts and environmental niches is crucial to
establish the epidemiological risk associated with emergent pathogenic
genotypes. Trypanosoma cruzi, a genetically heterogeneous, multi-host
zoonosis, provides an ideal system to examine the sylvatic diversification
of parasitic protozoa. In Bolivia, T. cruzi I, the oldest and most
widespread genetic lineage, is pervasive across a range of ecological
clines. High-resolution nuclear (26 loci) and mitochondrial (10 loci)
genotyping of 199 contemporaneous sylvatic TcI clones was undertaken to
provide insights into the biogeographical basis of T. cruzi evolution.
Three distinct sylvatic parasite transmission cycles were identified: one
highland population among terrestrial rodent and triatomine species,
composed of genetically homogenous strains (Ar = 2.95; PA/L = 0.61; DAS =
0.151), and two highly diverse, parasite assemblages circulating among
predominantly arboreal mammals and vectors in the lowlands (Ar = 3.40 and
3.93; PA/L = 1.12 and 0.60; DAS = 0.425 and 0.311, respectively). Very
limited gene flow between neighbouring terrestrial highland and arboreal
lowland areas (distance ~220 km; FST = 0.42 and 0.35) but strong
connectivity between ecologically similar but geographically disparate
terrestrial highland ecotopes (distance >465 km; FST = 0.016–0.084)
strongly supports ecological host fitting as the predominant mechanism of
parasite diversification. Dissimilar heterozygosity estimates (excess in
highlands, deficit in lowlands) and mitochondrial introgression among
lowland strains may indicate fundamental differences in mating strategies
between populations. Finally, accelerated parasite dissemination between
densely populated, highland areas, compared to uninhabited lowland foci,
likely reflects passive, long-range anthroponotic dispersal. The impact of
humans on the risk of epizootic Chagas disease transmission in Bolivia is
discussed. |
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DOI: | 10.5061/dryad.b8465 |