Contemporary cryptic sexuality in Trypanosoma cruzi

Juan David Ramírez, Felipe Guhl, Louisa A. Messenger, Michael D. Lewis, Marleny Montilla, Zulma Cucunuba, Michael A. Miles, Martin S. Llewellyn

Resultado de la investigación: Contribución a RevistaArtículo

66 Citas (Scopus)

Resumen

Clonal propagation is considered to be the predominant mode of reproduction among many parasitic protozoa. However, this assumption may overlook unorthodox, infrequent or cryptic sexuality. Trypanosoma cruzi, which causes Chagas disease, is known to undergo non-Mendelian genetic exchange in the laboratory. In the field, evidence of extant genetic exchange is limited. In this study, we undertook intensive sampling of T. cruzi Discrete Typing Unit I in endemic eastern Colombia. Using Fluorescence-activated cell sorting, we generated 269 biological clones from 67 strains. Each clone was genotyped across 24 microsatellite loci. Subsequently, 100 representative clones were typed using 10 mitochondrial sequence targets (3.76 Kbp total). Clonal diversity among humans, reservoir hosts and vectors suggested complex patterns of superinfection and/or coinfection in oral and vector-borne Chagas disease cases. Clonal diversity between mother and foetus in a congenital case demonstrates that domestic TcI genotypes are infective in utero. Importantly, gross incongruence between nuclear and mitochondrial markers is strong evidence for widespread genetic exchange throughout the data set. Furthermore, a confirmed mosaic maxicircle sequence suggests intermolecular recombination between individuals as a further mechanism of genetic reassortment. Finally, robust dating based on mitochondrial DNA indicates that the emergence of a widespread domestic TcI clade that we now name TcIDOM (formerly TcIa/VEN Dom) occurred 23 000 ± 12 000 years ago and was followed by population expansion, broadly corresponding with the earliest human migration into the Americas. © 2012 Blackwell Publishing Ltd.
Idioma originalEnglish (US)
Páginas (desde-hasta)4216-4226
Número de páginas11
PublicaciónMolecular Ecology
DOI
EstadoPublished - sep 1 2012

Huella dactilar

sexuality
Trypanosoma cruzi
Sexuality
Chagas Disease
Clone Cells
Chagas disease
clone
Human Migration
clones
Superinfection
Colombia
Coinfection
Mitochondrial DNA
Microsatellite Repeats
disease reservoirs
Genetic Recombination
Names
Reproduction
Flow Cytometry
Fetus

Citar esto

Ramírez, J. D., Guhl, F., Messenger, L. A., Lewis, M. D., Montilla, M., Cucunuba, Z., ... Llewellyn, M. S. (2012). Contemporary cryptic sexuality in Trypanosoma cruzi. Molecular Ecology, 4216-4226. https://doi.org/10.1111/j.1365-294X.2012.05699.x
Ramírez, Juan David ; Guhl, Felipe ; Messenger, Louisa A. ; Lewis, Michael D. ; Montilla, Marleny ; Cucunuba, Zulma ; Miles, Michael A. ; Llewellyn, Martin S. / Contemporary cryptic sexuality in Trypanosoma cruzi. En: Molecular Ecology. 2012 ; pp. 4216-4226.
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abstract = "Clonal propagation is considered to be the predominant mode of reproduction among many parasitic protozoa. However, this assumption may overlook unorthodox, infrequent or cryptic sexuality. Trypanosoma cruzi, which causes Chagas disease, is known to undergo non-Mendelian genetic exchange in the laboratory. In the field, evidence of extant genetic exchange is limited. In this study, we undertook intensive sampling of T. cruzi Discrete Typing Unit I in endemic eastern Colombia. Using Fluorescence-activated cell sorting, we generated 269 biological clones from 67 strains. Each clone was genotyped across 24 microsatellite loci. Subsequently, 100 representative clones were typed using 10 mitochondrial sequence targets (3.76 Kbp total). Clonal diversity among humans, reservoir hosts and vectors suggested complex patterns of superinfection and/or coinfection in oral and vector-borne Chagas disease cases. Clonal diversity between mother and foetus in a congenital case demonstrates that domestic TcI genotypes are infective in utero. Importantly, gross incongruence between nuclear and mitochondrial markers is strong evidence for widespread genetic exchange throughout the data set. Furthermore, a confirmed mosaic maxicircle sequence suggests intermolecular recombination between individuals as a further mechanism of genetic reassortment. Finally, robust dating based on mitochondrial DNA indicates that the emergence of a widespread domestic TcI clade that we now name TcIDOM (formerly TcIa/VEN Dom) occurred 23 000 ± 12 000 years ago and was followed by population expansion, broadly corresponding with the earliest human migration into the Americas. {\circledC} 2012 Blackwell Publishing Ltd.",
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Ramírez, JD, Guhl, F, Messenger, LA, Lewis, MD, Montilla, M, Cucunuba, Z, Miles, MA & Llewellyn, MS 2012, 'Contemporary cryptic sexuality in Trypanosoma cruzi', Molecular Ecology, pp. 4216-4226. https://doi.org/10.1111/j.1365-294X.2012.05699.x

Contemporary cryptic sexuality in Trypanosoma cruzi. / Ramírez, Juan David; Guhl, Felipe; Messenger, Louisa A.; Lewis, Michael D.; Montilla, Marleny; Cucunuba, Zulma; Miles, Michael A.; Llewellyn, Martin S.

En: Molecular Ecology, 01.09.2012, p. 4216-4226.

Resultado de la investigación: Contribución a RevistaArtículo

TY - JOUR

T1 - Contemporary cryptic sexuality in Trypanosoma cruzi

AU - Ramírez, Juan David

AU - Guhl, Felipe

AU - Messenger, Louisa A.

AU - Lewis, Michael D.

AU - Montilla, Marleny

AU - Cucunuba, Zulma

AU - Miles, Michael A.

AU - Llewellyn, Martin S.

PY - 2012/9/1

Y1 - 2012/9/1

N2 - Clonal propagation is considered to be the predominant mode of reproduction among many parasitic protozoa. However, this assumption may overlook unorthodox, infrequent or cryptic sexuality. Trypanosoma cruzi, which causes Chagas disease, is known to undergo non-Mendelian genetic exchange in the laboratory. In the field, evidence of extant genetic exchange is limited. In this study, we undertook intensive sampling of T. cruzi Discrete Typing Unit I in endemic eastern Colombia. Using Fluorescence-activated cell sorting, we generated 269 biological clones from 67 strains. Each clone was genotyped across 24 microsatellite loci. Subsequently, 100 representative clones were typed using 10 mitochondrial sequence targets (3.76 Kbp total). Clonal diversity among humans, reservoir hosts and vectors suggested complex patterns of superinfection and/or coinfection in oral and vector-borne Chagas disease cases. Clonal diversity between mother and foetus in a congenital case demonstrates that domestic TcI genotypes are infective in utero. Importantly, gross incongruence between nuclear and mitochondrial markers is strong evidence for widespread genetic exchange throughout the data set. Furthermore, a confirmed mosaic maxicircle sequence suggests intermolecular recombination between individuals as a further mechanism of genetic reassortment. Finally, robust dating based on mitochondrial DNA indicates that the emergence of a widespread domestic TcI clade that we now name TcIDOM (formerly TcIa/VEN Dom) occurred 23 000 ± 12 000 years ago and was followed by population expansion, broadly corresponding with the earliest human migration into the Americas. © 2012 Blackwell Publishing Ltd.

AB - Clonal propagation is considered to be the predominant mode of reproduction among many parasitic protozoa. However, this assumption may overlook unorthodox, infrequent or cryptic sexuality. Trypanosoma cruzi, which causes Chagas disease, is known to undergo non-Mendelian genetic exchange in the laboratory. In the field, evidence of extant genetic exchange is limited. In this study, we undertook intensive sampling of T. cruzi Discrete Typing Unit I in endemic eastern Colombia. Using Fluorescence-activated cell sorting, we generated 269 biological clones from 67 strains. Each clone was genotyped across 24 microsatellite loci. Subsequently, 100 representative clones were typed using 10 mitochondrial sequence targets (3.76 Kbp total). Clonal diversity among humans, reservoir hosts and vectors suggested complex patterns of superinfection and/or coinfection in oral and vector-borne Chagas disease cases. Clonal diversity between mother and foetus in a congenital case demonstrates that domestic TcI genotypes are infective in utero. Importantly, gross incongruence between nuclear and mitochondrial markers is strong evidence for widespread genetic exchange throughout the data set. Furthermore, a confirmed mosaic maxicircle sequence suggests intermolecular recombination between individuals as a further mechanism of genetic reassortment. Finally, robust dating based on mitochondrial DNA indicates that the emergence of a widespread domestic TcI clade that we now name TcIDOM (formerly TcIa/VEN Dom) occurred 23 000 ± 12 000 years ago and was followed by population expansion, broadly corresponding with the earliest human migration into the Americas. © 2012 Blackwell Publishing Ltd.

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DO - 10.1111/j.1365-294X.2012.05699.x

M3 - Article

SP - 4216

EP - 4226

JO - Molecular Ecology

JF - Molecular Ecology

SN - 0962-1083

ER -

Ramírez JD, Guhl F, Messenger LA, Lewis MD, Montilla M, Cucunuba Z y otros. Contemporary cryptic sexuality in Trypanosoma cruzi. Molecular Ecology. 2012 sep 1;4216-4226. https://doi.org/10.1111/j.1365-294X.2012.05699.x