Comparison of parasite loads in serum and blood samples from patients in acute and chronic phases of Chagas disease

Molecular methods have been developed for the detection and quantification of Trypanosoma cruzi DNA in blood samples from patients with Chagas disease. However, aspects of sample processing necessary for quantitative real-time PCR (qPCR), such as the addition of guanidine hydrochloride to whole bloo...

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Autores:
Tipo de recurso:
Fecha de publicación:
2018
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/22759
Acceso en línea:
https://doi.org/10.1017/S0031182018000598
https://repository.urosario.edu.co/handle/10336/22759
Palabra clave:
Enalapril maleate
Guanidine
Satellite dna
Acute disease
Adult
Article
Blood sampling
Chagas disease
Chronic disease
Comparative study
Female
Human
Limit of quantitation
Major clinical study
Male
Molecular diagnosis
Parasite load
Parasitemia
Polymerase chain reaction
Priority journal
Quantitative analysis
Real time polymerase chain reaction
Simulation
Dna
Qpcr
Satellite dna
Trypanosoma cruzi
Rights
License
Abierto (Texto Completo)
Description
Summary:Molecular methods have been developed for the detection and quantification of Trypanosoma cruzi DNA in blood samples from patients with Chagas disease. However, aspects of sample processing necessary for quantitative real-time PCR (qPCR), such as the addition of guanidine hydrochloride to whole blood samples, may limit timely access to molecular diagnosis. We analysed 169 samples from serum and guanidine-EDTA blood (GEB) obtained from patients in acute and chronic phases of Chagas disease. We applied qPCR targeted to the satellite DNA region. Finally, we compared the parasite loads and cycle of threshold values of the qPCR. The results confirmed the usefulness of serum samples for the detection and quantification of parasite DNA in patients with Chagas disease, especially in the acute phase. However, the parasite loads detected in serum samples from patients in the chronic phase were lower than those detected in GEB samples. The epidemiological implications of the findings are herein discussed. © Cambridge University Press 2018.