Protocol optimization for the detection of Trypanosoma cruzi DNA in açai (Euterpe oleraceae) pulp
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Acta Amazonica |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0044-59672021000100079 |
Resumo: | ABSTRACT Chagas disease, caused by the protozoan Trypanosoma cruzi, has often been linked to oral transmission through açai consumption. Molecular methods that allow fast and accurate identification of the pathogen are important for the detection of the presence of the parasite in this food. This study aimed to optimize polymerase chain reaction (PCR)-based detection of T. cruzi DNA in açai pulp. Several dilutions of T. cruzi DTU TcI trypomastigote forms were cultured in liver infusion tryptose (LIT) medium. Trypanosoma cruzi DNA was extracted from the cells and subjected to PCR. Subsequently, culture dilutions were added to açai pulp to evaluate the detection threshold of the optimized PCR assay. We demonstrate that our assay can detect T. cruzi DNA in açai pulp at a concentration of 1.08 × 10-10 ng µL-1. We conclude that our optimized protocol is effective and can be used as an important tool for the detection of T. cruzi contamination in açaí. |
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Acta Amazonica |
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Protocol optimization for the detection of Trypanosoma cruzi DNA in açai (Euterpe oleraceae) pulpdetection methodfoodborne diseasefood pathogenmolecular detectionChagas diseaseABSTRACT Chagas disease, caused by the protozoan Trypanosoma cruzi, has often been linked to oral transmission through açai consumption. Molecular methods that allow fast and accurate identification of the pathogen are important for the detection of the presence of the parasite in this food. This study aimed to optimize polymerase chain reaction (PCR)-based detection of T. cruzi DNA in açai pulp. Several dilutions of T. cruzi DTU TcI trypomastigote forms were cultured in liver infusion tryptose (LIT) medium. Trypanosoma cruzi DNA was extracted from the cells and subjected to PCR. Subsequently, culture dilutions were added to açai pulp to evaluate the detection threshold of the optimized PCR assay. We demonstrate that our assay can detect T. cruzi DNA in açai pulp at a concentration of 1.08 × 10-10 ng µL-1. We conclude that our optimized protocol is effective and can be used as an important tool for the detection of T. cruzi contamination in açaí.Instituto Nacional de Pesquisas da Amazônia2021-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0044-59672021000100079Acta Amazonica v.51 n.1 2021reponame:Acta Amazonicainstname:Instituto Nacional de Pesquisas da Amazônia (INPA)instacron:INPA10.1590/1809-4392201903426info:eu-repo/semantics/openAccessCARDOSO,Gabrielle Virgínia FerreiraOLIVEIRA,Andrey Carlos do Sacramento deSILVA,Andréia Silva daSILVA,Marcos Clécio de LemosLIMA,Joelson SousaROOS,Talita BandeiraMORAES,Carina Martins deeng2021-02-26T00:00:00Zoai:scielo:S0044-59672021000100079Revistahttps://acta.inpa.gov.br/PUBhttps://old.scielo.br/oai/scielo-oai.phpacta@inpa.gov.br||acta@inpa.gov.br1809-43920044-5967opendoar:2021-02-26T00:00Acta Amazonica - Instituto Nacional de Pesquisas da Amazônia (INPA)false |
dc.title.none.fl_str_mv |
Protocol optimization for the detection of Trypanosoma cruzi DNA in açai (Euterpe oleraceae) pulp |
title |
Protocol optimization for the detection of Trypanosoma cruzi DNA in açai (Euterpe oleraceae) pulp |
spellingShingle |
Protocol optimization for the detection of Trypanosoma cruzi DNA in açai (Euterpe oleraceae) pulp CARDOSO,Gabrielle Virgínia Ferreira detection method foodborne disease food pathogen molecular detection Chagas disease |
title_short |
Protocol optimization for the detection of Trypanosoma cruzi DNA in açai (Euterpe oleraceae) pulp |
title_full |
Protocol optimization for the detection of Trypanosoma cruzi DNA in açai (Euterpe oleraceae) pulp |
title_fullStr |
Protocol optimization for the detection of Trypanosoma cruzi DNA in açai (Euterpe oleraceae) pulp |
title_full_unstemmed |
Protocol optimization for the detection of Trypanosoma cruzi DNA in açai (Euterpe oleraceae) pulp |
title_sort |
Protocol optimization for the detection of Trypanosoma cruzi DNA in açai (Euterpe oleraceae) pulp |
author |
CARDOSO,Gabrielle Virgínia Ferreira |
author_facet |
CARDOSO,Gabrielle Virgínia Ferreira OLIVEIRA,Andrey Carlos do Sacramento de SILVA,Andréia Silva da SILVA,Marcos Clécio de Lemos LIMA,Joelson Sousa ROOS,Talita Bandeira MORAES,Carina Martins de |
author_role |
author |
author2 |
OLIVEIRA,Andrey Carlos do Sacramento de SILVA,Andréia Silva da SILVA,Marcos Clécio de Lemos LIMA,Joelson Sousa ROOS,Talita Bandeira MORAES,Carina Martins de |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
CARDOSO,Gabrielle Virgínia Ferreira OLIVEIRA,Andrey Carlos do Sacramento de SILVA,Andréia Silva da SILVA,Marcos Clécio de Lemos LIMA,Joelson Sousa ROOS,Talita Bandeira MORAES,Carina Martins de |
dc.subject.por.fl_str_mv |
detection method foodborne disease food pathogen molecular detection Chagas disease |
topic |
detection method foodborne disease food pathogen molecular detection Chagas disease |
description |
ABSTRACT Chagas disease, caused by the protozoan Trypanosoma cruzi, has often been linked to oral transmission through açai consumption. Molecular methods that allow fast and accurate identification of the pathogen are important for the detection of the presence of the parasite in this food. This study aimed to optimize polymerase chain reaction (PCR)-based detection of T. cruzi DNA in açai pulp. Several dilutions of T. cruzi DTU TcI trypomastigote forms were cultured in liver infusion tryptose (LIT) medium. Trypanosoma cruzi DNA was extracted from the cells and subjected to PCR. Subsequently, culture dilutions were added to açai pulp to evaluate the detection threshold of the optimized PCR assay. We demonstrate that our assay can detect T. cruzi DNA in açai pulp at a concentration of 1.08 × 10-10 ng µL-1. We conclude that our optimized protocol is effective and can be used as an important tool for the detection of T. cruzi contamination in açaí. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-03-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0044-59672021000100079 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0044-59672021000100079 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1809-4392201903426 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Instituto Nacional de Pesquisas da Amazônia |
publisher.none.fl_str_mv |
Instituto Nacional de Pesquisas da Amazônia |
dc.source.none.fl_str_mv |
Acta Amazonica v.51 n.1 2021 reponame:Acta Amazonica instname:Instituto Nacional de Pesquisas da Amazônia (INPA) instacron:INPA |
instname_str |
Instituto Nacional de Pesquisas da Amazônia (INPA) |
instacron_str |
INPA |
institution |
INPA |
reponame_str |
Acta Amazonica |
collection |
Acta Amazonica |
repository.name.fl_str_mv |
Acta Amazonica - Instituto Nacional de Pesquisas da Amazônia (INPA) |
repository.mail.fl_str_mv |
acta@inpa.gov.br||acta@inpa.gov.br |
_version_ |
1752129841292902400 |