Genetic structure of Trypanosoma cruzi in Colombia revealed by a High-throughput Nuclear Multilocus Sequence Typing (nMLST) approach

Background Chagas disease is a systemic pathology caused by Trypanosoma cruzi. This parasite reveals remarkable genetic variability, evinced in six Discrete Typing Units (DTUs) named from T. cruzi I to T. cruzi VI (TcI to TcVI). Recently newly identified genotypes have emerged such as TcBat in Brazi...

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Fecha de publicación:
2013
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/27772
Acceso en línea:
https://doi.org/10.1186/1471-2156-14-96
https://repository.urosario.edu.co/handle/10336/27772
Palabra clave:
Chagas disease
Clonality
Sexuality
Disease ecology
Transmission dynamics
Genotypes
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spelling 1011716118600e837747d-8abc-4279-88b4-6fa1b2b01912fe062efa-2c45-40ad-9076-805a8d1e00ac2020-08-19T14:43:48Z2020-08-19T14:43:48Z2013-09-30Background Chagas disease is a systemic pathology caused by Trypanosoma cruzi. This parasite reveals remarkable genetic variability, evinced in six Discrete Typing Units (DTUs) named from T. cruzi I to T. cruzi VI (TcI to TcVI). Recently newly identified genotypes have emerged such as TcBat in Brazil, Colombia and Panama associated to anthropogenic bats. The genotype with the broadest geographical distribution is TcI, which has recently been associated to severe cardiomyopathies in Argentina and Colombia. Therefore, new studies unraveling the genetic structure and natural history of this DTU must be pursued. Results We conducted a spatial and temporal analysis on 50 biological clones of T. cruzi I (TcI) isolated from humans with different clinical phenotypes, triatomine bugs and mammal reservoirs across three endemic regions for Chagas disease in Colombia. These clones were submitted to a nuclear Multilocus Sequence Typing (nMLST) analysis in order to elucidate its genetic diversity and clustering. After analyzing 13 nuclear housekeeping genes and obtaining a 5821 bp length alignment, we detected two robust genotypes within TcI henceforth named TcIDOM (associated to human infections) and a second cluster associated to peridomestic and sylvatic populations. Additionaly, we detected putative events of recombination and an intriguing lack of linkage disequilibrium. Conclusions These findings reinforce the emergence of an enigmatic domestic T. cruzi genotype (TcIDOM), and demonstrates the high frequency of recombination at nuclear level across natural populations of T. cruzi. Therefore, the need to pursue studies focused on the diferential virulence profiles of TcI strains. The biological and epidemiological implications of these findings are herein discussed.application/pdfhttps://doi.org/10.1186/1471-2156-14-96EISSN: 1471-2156https://repository.urosario.edu.co/handle/10336/27772engBioMed CentralNo. 96BMC GeneticsVol. 14BMC Genetics, EISSN: 1471-2156, Vol.14, No.96 (2013); 11 pp.https://bmcgenet.biomedcentral.com/track/pdf/10.1186/1471-2156-14-96Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2BMC Geneticsinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURChagas diseaseClonalitySexualityDisease ecologyTransmission dynamicsGenotypesGenetic structure of Trypanosoma cruzi in Colombia revealed by a High-throughput Nuclear Multilocus Sequence Typing (nMLST) approachEstructura genética de Trypanosoma cruzi en Colombia revelada por un enfoque de tipificación de secuencia nuclear multilocus de alto rendimiento (nMLST)articleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Ramírez, Juan DavidTapia-Calle, GabrielaGuhl, FelipeORIGINAL1471-2156-14-96.pdfapplication/pdf1359576https://repository.urosario.edu.co/bitstreams/963b3786-f959-4641-a4f8-9cf98acdec6b/download33eb793b3d3a4fac3ffb7cdef10b29a3MD51TEXT1471-2156-14-96.pdf.txt1471-2156-14-96.pdf.txtExtracted texttext/plain49396https://repository.urosario.edu.co/bitstreams/bf521b2f-024a-4f46-b538-cf1736ca6e98/downloade5b912da219e83a1ab6a8bc3241114dcMD52THUMBNAIL1471-2156-14-96.pdf.jpg1471-2156-14-96.pdf.jpgGenerated Thumbnailimage/jpeg4087https://repository.urosario.edu.co/bitstreams/fc2bcc84-6226-4b45-b40e-d12e9b354573/downloadc5a916f1aa1439101b720379008e140dMD5310336/27772oai:repository.urosario.edu.co:10336/277722021-10-05 06:51:00.628https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Genetic structure of Trypanosoma cruzi in Colombia revealed by a High-throughput Nuclear Multilocus Sequence Typing (nMLST) approach
dc.title.TranslatedTitle.spa.fl_str_mv Estructura genética de Trypanosoma cruzi en Colombia revelada por un enfoque de tipificación de secuencia nuclear multilocus de alto rendimiento (nMLST)
title Genetic structure of Trypanosoma cruzi in Colombia revealed by a High-throughput Nuclear Multilocus Sequence Typing (nMLST) approach
spellingShingle Genetic structure of Trypanosoma cruzi in Colombia revealed by a High-throughput Nuclear Multilocus Sequence Typing (nMLST) approach
Chagas disease
Clonality
Sexuality
Disease ecology
Transmission dynamics
Genotypes
title_short Genetic structure of Trypanosoma cruzi in Colombia revealed by a High-throughput Nuclear Multilocus Sequence Typing (nMLST) approach
title_full Genetic structure of Trypanosoma cruzi in Colombia revealed by a High-throughput Nuclear Multilocus Sequence Typing (nMLST) approach
title_fullStr Genetic structure of Trypanosoma cruzi in Colombia revealed by a High-throughput Nuclear Multilocus Sequence Typing (nMLST) approach
title_full_unstemmed Genetic structure of Trypanosoma cruzi in Colombia revealed by a High-throughput Nuclear Multilocus Sequence Typing (nMLST) approach
title_sort Genetic structure of Trypanosoma cruzi in Colombia revealed by a High-throughput Nuclear Multilocus Sequence Typing (nMLST) approach
dc.subject.keyword.spa.fl_str_mv Chagas disease
Clonality
Sexuality
Disease ecology
Transmission dynamics
Genotypes
topic Chagas disease
Clonality
Sexuality
Disease ecology
Transmission dynamics
Genotypes
description Background Chagas disease is a systemic pathology caused by Trypanosoma cruzi. This parasite reveals remarkable genetic variability, evinced in six Discrete Typing Units (DTUs) named from T. cruzi I to T. cruzi VI (TcI to TcVI). Recently newly identified genotypes have emerged such as TcBat in Brazil, Colombia and Panama associated to anthropogenic bats. The genotype with the broadest geographical distribution is TcI, which has recently been associated to severe cardiomyopathies in Argentina and Colombia. Therefore, new studies unraveling the genetic structure and natural history of this DTU must be pursued. Results We conducted a spatial and temporal analysis on 50 biological clones of T. cruzi I (TcI) isolated from humans with different clinical phenotypes, triatomine bugs and mammal reservoirs across three endemic regions for Chagas disease in Colombia. These clones were submitted to a nuclear Multilocus Sequence Typing (nMLST) analysis in order to elucidate its genetic diversity and clustering. After analyzing 13 nuclear housekeeping genes and obtaining a 5821 bp length alignment, we detected two robust genotypes within TcI henceforth named TcIDOM (associated to human infections) and a second cluster associated to peridomestic and sylvatic populations. Additionaly, we detected putative events of recombination and an intriguing lack of linkage disequilibrium. Conclusions These findings reinforce the emergence of an enigmatic domestic T. cruzi genotype (TcIDOM), and demonstrates the high frequency of recombination at nuclear level across natural populations of T. cruzi. Therefore, the need to pursue studies focused on the diferential virulence profiles of TcI strains. The biological and epidemiological implications of these findings are herein discussed.
publishDate 2013
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dc.date.accessioned.none.fl_str_mv 2020-08-19T14:43:48Z
dc.date.available.none.fl_str_mv 2020-08-19T14:43:48Z
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dc.type.spa.spa.fl_str_mv Artículo
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https://repository.urosario.edu.co/handle/10336/27772
identifier_str_mv EISSN: 1471-2156
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationIssue.none.fl_str_mv No. 96
dc.relation.citationTitle.none.fl_str_mv BMC Genetics
dc.relation.citationVolume.none.fl_str_mv Vol. 14
dc.relation.ispartof.spa.fl_str_mv BMC Genetics, EISSN: 1471-2156, Vol.14, No.96 (2013); 11 pp.
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dc.source.spa.fl_str_mv BMC Genetics
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