Evidence map›Paper›PMID 22848457›Full record

Trial reportPloS one2012

Trypanosoma cruzi IV causing outbreaks of acute Chagas disease and infections by different haplotypes in the Western Brazilian Amazonia.

Wuelton Marcelo Monteiro, Laylah Kelre Costa Magalhães, Amanda Regina Nichi de Sá, Mônica Lúcia Gomes, Max Jean de Ornelas Toledo, Lara Borges, Isa Pires, Jorge Augusto de Oliveira Guerra, Henrique Silveira, Maria das Graças Vale Barbosa

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% of its field
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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Overview of Chagas disease in Amazonas: an integrated approach.Revista da Sociedade Brasileira de Medicina Tropical · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Observational
  9. Article
  10. Article
  11. Article
  12. New insights intoFrontiers in immunology · 2024
    Review
  13. Fifteen Years after the Definition ofLife (Basel, Switzerland) · 2023
    Review
  14. Article
  15. Review
  16. Article
  17. Molecular characterization ofJournal of parasitic diseases : official organ of the Indian Society for Parasitology · 2022
    Article
  18. Article
  19. Article
  20. 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

10 authors at 3 institutions in 3 countries.

Wuelton Marcelo MonteiroTropical Medicine Foundation Dr. Heitor Vieira Dourado, Manaus, Amazonas, Brazil.
Laylah Kelre Costa Magalhães
Amanda Regina Nichi de Sá
Mônica Lúcia Gomes
Max Jean de Ornelas Toledo
Lara Borges
Isa Pires
Jorge Augusto de Oliveira Guerra
Henrique Silveira
Maria das Graças Vale Barbosa
Fundação de Medicina Tropical · BRUniversidade Estadual de Maringá · BRInstituto de Medicina Tropical · PY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChagas disease is an emergent tropical disease in the Brazilian Amazon Region, with an increasing number of cases in recent decades. In this region, the sylvatic cycle of Trypanosoma cruzi transmission, which constitutes a reservoir of parasites that might be associated with specific molecular, epidemiological and clinical traits, has been little explored. The objective of this work is to genetically characterize stocks of T. cruzi from human cases, triatomines and reservoir mammals in the State of Amazonas, in the Western Brazilian Amazon. METHODOLOGY/PRINCIPAL

findingsWe analyzed 96 T. cruzi samples from four municipalities in distant locations of the State of Amazonas. Molecular characterization of isolated parasites from cultures in LIT medium or directly from vectors or whole human blood was performed by PCR of the non-transcribed spacer of the mini-exon and of the 24 S alfa ribosomal RNA gene, RFLP and sequencing of the mitochondrial cytochrome c oxidase subunit II (COII) gene, and by sequencing of the glucose-phosphate isomerase gene. The T. cruzi parasites from two outbreaks of acute disease were all typed as TcIV. One of the outbreaks was triggered by several haplotypes of the same DTU. TcIV also occurred in isolated cases and in Rhodnius robustus. Incongruence between mitochondrial and nuclear phylogenies is likely to be indicative of historical genetic exchange events resulting in mitochondrial introgression between TcIII and TcIV DTUs from Western Brazilian Amazon. TcI predominated among triatomines and was the unique DTU infecting marsupials. CONCLUSION/SIGNIFICANCE: DTU TcIV, rarely associated with human Chagas disease in other areas of the Amazon basin, is the major strain responsible for the human infections in the Western Brazilian Amazon, occurring in outbreaks as single or mixed infections by different haplotypes.

Indexed as

Disease OutbreaksHaplotypesAcute DiseaseAnimalsBrazilChagas DiseaseDNA, MitochondrialDNA, ProtozoanElectron Transport Complex IVFemaleGenes, ProtozoanGenes, rRNAHumansMaleMarsupialiaProtozoan Proteinscytochrome C oxidase subunit IIDNA, MitochondrialDNA, ProtozoanElectron Transport Complex IVProtozoan Proteins

Identifiers

PMID22848457
PMCPMC3405119
OpenAlexW1973707561

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.