Evidence map›Paper›PMID 41091829›Full record

ArticlePLoS neglected tropical diseases2025

Genetic diversity of Trypanosoma cruzi in individuals with chronic Chagas disease in the Northern Minas Gerais and Vale do Jequitinhonha regions, Minas Gerais, Brazil.

Emanuelle de Moura Santos Xavier, Paula Finamore Araujo, Jenifer Raiane Silva Pedras, Thainara da Silva Gonçalves, Núbia Nunes de Souza, Ariela Mota Ferreira, Léa Campos de Oliveira-da Silva, Ester Cerdeira Sabino, Maria do Carmo Pereira Nunes, Antonio Luiz Pinho Ribeiro and 2 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Long-Term Parasitological Clearance and Cardiac Progression inTropical medicine and infectious disease · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Emanuelle de Moura Santos XavierHealth Science Programme, State University of Montes Claros, Montes Claros, Brazil.
Paula Finamore AraujoMolecular Virology and Parasitology Laboratory, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Jenifer Raiane Silva PedrasHealth Science Programme, State University of Montes Claros, Montes Claros, Brazil.
Thainara da Silva GonçalvesHealth Science Programme, State University of Montes Claros, Montes Claros, Brazil.
Núbia Nunes de SouzaHealth Science Programme, State University of Montes Claros, Montes Claros, Brazil.
Ariela Mota FerreiraHealth Science Programme, State University of Montes Claros, Montes Claros, Brazil.
Léa Campos de Oliveira-da SilvaLaboratorio de Genetica de Microorganismos Aplicado a Medicina (LIM46), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
Ester Cerdeira SabinoLaboratorio de Genetica de Microorganismos Aplicado a Medicina (LIM46), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
Maria do Carmo Pereira NunesFederal University of Minas Gerais, School of Medicine, Department of Internal Medicine, Minas Gerais, Brazil.
Antonio Luiz Pinho RibeiroFederal University of Minas Gerais, School of Medicine, Department of Internal Medicine, Minas Gerais, Brazil.
Otacilio C MoreiraMolecular Virology and Parasitology Laboratory, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.ORCID 0000-0002-5340-8697
Thallyta Maria VieiraHealth Science Programme, State University of Montes Claros, Montes Claros, Brazil.

Funding

Sao Paulo-Minas Gerais Tropical Medicine Research Center for Chagas Disease Biomarker DiscoveryU19AI098461 · NIAID · FUNDACAO FACULDADE DE MEDICINA · PI RIBEIRO, ANTONIO LUIZ PINHO · 2017 to 2021
$2.1M
"Sao Paulo-Minas Gerais Center for Chagas Disease Treatment (SaMiTrop)"U01AI168383 · NIAID · FUNDACAO FACULDADE DE MEDICINA · PI Ester Cerdeira Sabino · 2022 to 2026
$1.9M
Sao Paulo- MInas Gerais Neglected Tropical Disease Research Center for BiomarkerP50AI098461 · NIAID · FUNDACAO FACULDADE DE MEDICINA · PI SABINO, ESTER CERDEIRA · 2012 to 2016
$1.5M
NIAID NIH HHS P50 AI098461NIAID NIH HHS U01 AI168383NIAID NIH HHS U19 AI098461
6 · The paper itself

Abstract

Chagas disease, caused by the hemoflagellate parasite Trypanosoma cruzi, is a major public health problem in Latin America due to its high prevalence and significant morbidity and mortality. The T. cruzi is classified into seven distinct genetic groups (TcI-TcVI) and TcBat, know as Discrete Typing Units (DTUs). Understanding DTU diversity is essential for improving diagnostic and therapeutic strategies and strengthening epidemiological surveillance. This study aimed to investigate the genetic diversity of T. cruzi in individuals with chronic Chagas disease from endemic municipalities in Northern Minas Gerais and the Jequitinhonha Valley, Brazil. It also evaluated associations between DTUs and age, parasitic load, antibody levels, and cardiac disease severity in participants from the SaMi-Trop cohort. Molecular typing was performed using conventional multilocus PCR directly from peripheral blood samples of individuals with the chronic cardiac form. Of the 80 patients included in the study, T. cruzi genotyping was performed in 37 samples (46.25%). Among the samples in which a single DTU was identified, TcI and TcVI presented equal frequencies (n = 5, 13.51% each). TcII was identified in four samples (n = 4, 10.81%), while TcV was identified in three samples (n = 3, 8.10%). Furthermore, three individuals presented mixed infections: TcV + TcVI, TcI + TcV + TcII/TcVI, and TcV + TcII. The highest frequency was observed for TcII/TcVI (n = 17, 45.94%), a classification that does not represent mixed infection. For statistical analysis, TcII/TcVI samples were classified as TcII. No significant differences were found between the DTUs and age or parasitic load. However, a wide variation in the average parasitic load was observed among individuals, ranging from 0.06 to 667 parasite equivalents/mL. An increase in anti-T. cruzi antibody titers was also observed. The findings of this study demonstrate the genetic diversity of the parasite in individuals with chronic cardiac Chagas disease and its distribution in a highly endemic region.

Indexed as

Chagas DiseaseGenetic VariationTrypanosoma cruziAdolescentAdultAgedAntibodies, ProtozoanBrazilChronic DiseaseFemaleGenotypeHumansMaleMiddle AgedParasite LoadYoung AdultAntibodies, Protozoan

Identifiers

PMID41091829
PMCPMC12548877

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.