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The Development of a One-Step RT-qPCR for the Detection and Quantification of Viable Forms of Trypanosoma cruzi in Açai Samples from Areas at Risk of Chagas Disease through Oral Transmission.
Faier-Pereira, Amanda; Finamore-Araujo, Paula; Brito, Carlos Ramon do Nascimento; Peres, Eldrinei Gomes; de Lima Yamaguchi, Klenicy Kazumy; de Castro, Daniele Pereira; Moreira, Otacilio C.
Afiliação
  • Faier-Pereira A; Laboratory of Molecular Virology and Parasitology, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro 21040-360, Brazil.
  • Finamore-Araujo P; Laboratory of Molecular Virology and Parasitology, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro 21040-360, Brazil.
  • Brito CRDN; Departament of Clinical e Toxicological Analysis, Federal University of Rio Grande do Norte, Natal 59078-970, Brazil.
  • Peres EG; Departament of Chemistry, Federal University of Amazonas, Manaus 69067-005, Brazil.
  • de Lima Yamaguchi KK; Institute of Health and Biotecnology, Federal University of Amazonas, Coari 69460-000, Brazil.
  • de Castro DP; Laboratory of Biochemistry and Physiology of Insects, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro 21040-360, Brazil.
  • Moreira OC; Laboratory of Molecular Virology and Parasitology, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro 21040-360, Brazil.
Int J Mol Sci ; 25(10)2024 May 18.
Article em En | MEDLINE | ID: mdl-38791565
ABSTRACT
Currently, approximately 70% of new cases of Chagas disease (CD) in Brazil are attributed to oral transmission, particularly through foods such as açaí, bacaba, and sugarcane juice, primarily in the northern and northeastern regions of the country. This underscores the imperative need to control the spread of the disease. The methods utilized to conduct quality control for food associated with outbreaks and to assess the potential for the oral transmission of CD through consuming açaí primarily rely on isolating the parasite or inoculating food into experimental animals, restricting the analyses to major research centers. While there are existing studies in the literature on the detection and quantification of T. cruzi DNA in açaí, the evaluation of parasites' viability using molecular methods in this type of sample and differentiating between live and dead parasites in açaí pulp remain challenging. Consequently, we developed a molecular methodology based on RT-qPCR for detecting and quantifying viable T. cruzi in açaí pulp samples. This protocol enables the stabilization and preservation of nucleic acids in açaí, along with incorporating an exogenous internal amplification control. The standardization of the RNA extraction method involved a simple and reproducible approach, coupled with a one-step RT-qPCR assay. The assay underwent validation with various T. cruzi DTUs and demonstrated sensitivity in detecting up to 0.1 viable parasite equivalents/mL in açaí samples. Furthermore, we investigated the effectiveness of a bleaching method in eliminating viable parasites in açaí samples contaminated with T. cruzi by comparing the detection of DNA versus RNA. Finally, we validated this methodology using açaí pulp samples positive for T. cruzi DNA, which were collected in a municipality with a history of oral CD outbreaks (Coari-AM). This validation involved comparing the detection and quantification of total versus viable T. cruzi. Collectively, our findings demonstrate the feasibility of this methodology in detecting viable forms of T. cruzi in açaí pulp samples, emerging as a crucial tool for monitoring oral outbreaks of Chagas disease resulting from açaí consumption.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trypanosoma cruzi / Doença de Chagas Limite: Animals / Humans País como assunto: America do sul / Brasil Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trypanosoma cruzi / Doença de Chagas Limite: Animals / Humans País como assunto: America do sul / Brasil Idioma: En Ano de publicação: 2024 Tipo de documento: Article