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...
- Autores:
- Tipo de recurso:
- 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
- Rights
- License
- Abierto (Texto Completo)
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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 |
dc.date.created.spa.fl_str_mv |
2013-09-30 |
dc.date.accessioned.none.fl_str_mv |
2020-08-19T14:43:48Z |
dc.date.available.none.fl_str_mv |
2020-08-19T14:43:48Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1186/1471-2156-14-96 |
dc.identifier.issn.none.fl_str_mv |
EISSN: 1471-2156 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/27772 |
url |
https://doi.org/10.1186/1471-2156-14-96 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. |
dc.relation.uri.spa.fl_str_mv |
https://bmcgenet.biomedcentral.com/track/pdf/10.1186/1471-2156-14-96 |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
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Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
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Universidad del Rosario |
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