Identification of Trypanosoma cruzi Discrete Typing Units (DTUs) through the implementation of a High-Resolution Melting (HRM) genotyping assay

Background Chagas disease, caused by Trypanosoma cruzi, is a geographically widespread anthropozoonosis that is considered a major public health problem in Latin America. Because this parasite presents high genetic variability, a nomenclature has been adopted to classify the parasite into six discre...

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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:10336/27838
Acceso en línea:
https://doi.org/10.1186/1756-3305-6-112
https://repository.urosario.edu.co/handle/10336/27838
Palabra clave:
Chagas disease
Trypanosoma cruzi
DTU
High-resolution melting
Genotyping
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spelling 0c1650cd-2f12-4898-8b7b-fc7baa067a14fe062efa-2c45-40ad-9076-805a8d1e00ac10117161186002020-08-19T14:44:10Z2020-08-19T14:44:10Z2013-04-20Background Chagas disease, caused by Trypanosoma cruzi, is a geographically widespread anthropozoonosis that is considered a major public health problem in Latin America. Because this parasite presents high genetic variability, a nomenclature has been adopted to classify the parasite into six discrete typing units (DTUs): TcI, TcII, TcIII, TcIV, TcV, and TcVI, which present different eco-epidemiological, clinical, and geographic associations. Currently, the available genotyping methods present a series of drawbacks that implies the need for developing new methods for characterizing T. cruzi DTU’s. The aim of this work was to genotype reference populations from T. cruzi by means of a High-Resolution Melting (HRM) genotyping assay. To genotype the DTUs of 38 strains and 14 reference clones of T. cruzi from diverse sources, real-time PCR (qPCR) was coupled to high-resolution melting (HRM) based on the amplification of two molecular markers—the divergent domain of the 24 s? rRNA gene and the intergenic region of the mini-exon gene. Findings Amplification of the mini-exon gene allowed the genotyping of three distinct groups: TcI, TcII- TcIV- TcV, and TcIII-TcVI, while amplification of the 24s? gene generated non-overlapping melting temperature ranges for each DTU that were used to identify the groups in the six existing DTUs of Trypanosoma cruzi. Conclusions The proposed genotyping assay allowed discrimination of the six genetic groups by obtaining specific melting curves for each DTU. The application of this technique is proposed because of its specificity, sensitivity, high performance, and low cost compared with other previously described characterization methods.application/pdfhttps://doi.org/10.1186/1756-3305-6-112EISSN: 1756-3305https://repository.urosario.edu.co/handle/10336/27838engBioMed CentralNo. 112Parasites and VectorsVol. 6Parasites and Vectors, EISSN: 1756-3305, Vol.6, No.112 (2013); 6 pp.https://parasitesandvectors.biomedcentral.com/track/pdf/10.1186/1756-3305-6-112Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Parasites and Vectorsinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURChagas diseaseTrypanosoma cruziDTUHigh-resolution meltingGenotypingIdentification of Trypanosoma cruzi Discrete Typing Units (DTUs) through the implementation of a High-Resolution Melting (HRM) genotyping assayIdentificación de unidades de tipificación discreta (DTU) de Trypanosoma cruzi mediante la implementación de un ensayo de genotipado de fusión de alta resolución (HRM)articleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Higuera, Sonia LGuhl, FelipeRamírez, Juan DavidORIGINAL1756-3305-6-112.pdfapplication/pdf625304https://repository.urosario.edu.co/bitstreams/6a521fc6-8f42-4dcd-a8ec-c3fed2d03003/downloadaf73035de014164c1c7f8d6416125cbaMD51TEXT1756-3305-6-112.pdf.txt1756-3305-6-112.pdf.txtExtracted texttext/plain24390https://repository.urosario.edu.co/bitstreams/6a0dbd9b-9b1f-4a9b-a830-a8dadd8229e6/downloade7b1f7fd39df05cfb14cbe8885ca1a91MD52THUMBNAIL1756-3305-6-112.pdf.jpg1756-3305-6-112.pdf.jpgGenerated Thumbnailimage/jpeg4724https://repository.urosario.edu.co/bitstreams/edb300c8-9fe1-47b6-adaa-eec5ce251807/download0795651d4cec3881b75def94e81761bcMD5310336/27838oai:repository.urosario.edu.co:10336/278382021-10-05 06:52:37.643https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Identification of Trypanosoma cruzi Discrete Typing Units (DTUs) through the implementation of a High-Resolution Melting (HRM) genotyping assay
dc.title.TranslatedTitle.spa.fl_str_mv Identificación de unidades de tipificación discreta (DTU) de Trypanosoma cruzi mediante la implementación de un ensayo de genotipado de fusión de alta resolución (HRM)
title Identification of Trypanosoma cruzi Discrete Typing Units (DTUs) through the implementation of a High-Resolution Melting (HRM) genotyping assay
spellingShingle Identification of Trypanosoma cruzi Discrete Typing Units (DTUs) through the implementation of a High-Resolution Melting (HRM) genotyping assay
Chagas disease
Trypanosoma cruzi
DTU
High-resolution melting
Genotyping
title_short Identification of Trypanosoma cruzi Discrete Typing Units (DTUs) through the implementation of a High-Resolution Melting (HRM) genotyping assay
title_full Identification of Trypanosoma cruzi Discrete Typing Units (DTUs) through the implementation of a High-Resolution Melting (HRM) genotyping assay
title_fullStr Identification of Trypanosoma cruzi Discrete Typing Units (DTUs) through the implementation of a High-Resolution Melting (HRM) genotyping assay
title_full_unstemmed Identification of Trypanosoma cruzi Discrete Typing Units (DTUs) through the implementation of a High-Resolution Melting (HRM) genotyping assay
title_sort Identification of Trypanosoma cruzi Discrete Typing Units (DTUs) through the implementation of a High-Resolution Melting (HRM) genotyping assay
dc.subject.keyword.spa.fl_str_mv Chagas disease
Trypanosoma cruzi
DTU
High-resolution melting
Genotyping
topic Chagas disease
Trypanosoma cruzi
DTU
High-resolution melting
Genotyping
description Background Chagas disease, caused by Trypanosoma cruzi, is a geographically widespread anthropozoonosis that is considered a major public health problem in Latin America. Because this parasite presents high genetic variability, a nomenclature has been adopted to classify the parasite into six discrete typing units (DTUs): TcI, TcII, TcIII, TcIV, TcV, and TcVI, which present different eco-epidemiological, clinical, and geographic associations. Currently, the available genotyping methods present a series of drawbacks that implies the need for developing new methods for characterizing T. cruzi DTU’s. The aim of this work was to genotype reference populations from T. cruzi by means of a High-Resolution Melting (HRM) genotyping assay. To genotype the DTUs of 38 strains and 14 reference clones of T. cruzi from diverse sources, real-time PCR (qPCR) was coupled to high-resolution melting (HRM) based on the amplification of two molecular markers—the divergent domain of the 24 s? rRNA gene and the intergenic region of the mini-exon gene. Findings Amplification of the mini-exon gene allowed the genotyping of three distinct groups: TcI, TcII- TcIV- TcV, and TcIII-TcVI, while amplification of the 24s? gene generated non-overlapping melting temperature ranges for each DTU that were used to identify the groups in the six existing DTUs of Trypanosoma cruzi. Conclusions The proposed genotyping assay allowed discrimination of the six genetic groups by obtaining specific melting curves for each DTU. The application of this technique is proposed because of its specificity, sensitivity, high performance, and low cost compared with other previously described characterization methods.
publishDate 2013
dc.date.created.spa.fl_str_mv 2013-04-20
dc.date.accessioned.none.fl_str_mv 2020-08-19T14:44:10Z
dc.date.available.none.fl_str_mv 2020-08-19T14:44:10Z
dc.type.eng.fl_str_mv article
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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/10.1186/1756-3305-6-112
dc.identifier.issn.none.fl_str_mv EISSN: 1756-3305
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/27838
url https://doi.org/10.1186/1756-3305-6-112
https://repository.urosario.edu.co/handle/10336/27838
identifier_str_mv EISSN: 1756-3305
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationIssue.none.fl_str_mv No. 112
dc.relation.citationTitle.none.fl_str_mv Parasites and Vectors
dc.relation.citationVolume.none.fl_str_mv Vol. 6
dc.relation.ispartof.spa.fl_str_mv Parasites and Vectors, EISSN: 1756-3305, Vol.6, No.112 (2013); 6 pp.
dc.relation.uri.spa.fl_str_mv https://parasitesandvectors.biomedcentral.com/track/pdf/10.1186/1756-3305-6-112
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rights_invalid_str_mv Abierto (Texto Completo)
http://purl.org/coar/access_right/c_abf2
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dc.publisher.spa.fl_str_mv BioMed Central
dc.source.spa.fl_str_mv Parasites and Vectors
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