Evidence map›Paper›PMID 36383785›Full record

ArticleMemorias do Instituto Oswaldo Cruz2022

Genetic diversity of Trypanosoma cruzi strains isolated from chronic chagasic patients and non-human hosts in the state of São Paulo, Brazil.

Thiago Kury Moreno de Souza, Elizabeth Visone Nunes Westphalen, Sansão da Rocha Westphalen, Helena Hilomi Taniguchi, Carlos Roberto Elias, Gabriela Motoie, Ricardo Gava, Vera Lucia Pereira-Chioccola, Christina Terra Gallafrio Novaes, Noêmia Barbosa Carvalho and 8 more

Abstract read
In one paragraph

Article in Memorias do Instituto Oswaldo Cruz, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

18 authors.

Thiago Kury Moreno de SouzaInstituto Adolfo Lutz, Centro de Parasitologia e Micologia, São Paulo, SP, Brasil.ORCID http://orcid.org/0000-0002-0986-0117
Elizabeth Visone Nunes WestphalenInstituto Adolfo Lutz, Centro de Parasitologia e Micologia, São Paulo, SP, Brasil.
Sansão da Rocha WestphalenInstituto Adolfo Lutz, Centro de Parasitologia e Micologia, São Paulo, SP, Brasil.
Helena Hilomi TaniguchiInstituto Adolfo Lutz, Centro de Parasitologia e Micologia, São Paulo, SP, Brasil.
Carlos Roberto EliasInstituto Adolfo Lutz, Centro de Parasitologia e Micologia, São Paulo, SP, Brasil.
Gabriela MotoieInstituto Adolfo Lutz, Centro de Parasitologia e Micologia, São Paulo, SP, Brasil.
Ricardo GavaInstituto Adolfo Lutz, Centro de Parasitologia e Micologia, São Paulo, SP, Brasil.
Vera Lucia Pereira-ChioccolaInstituto Adolfo Lutz, Centro de Parasitologia e Micologia, São Paulo, SP, Brasil.
Christina Terra Gallafrio NovaesUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Divisão de Clínica de Moléstias Infecciosas e Parasitárias, São Paulo, SP, Brasil.
Noêmia Barbosa CarvalhoUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Divisão de Clínica de Moléstias Infecciosas e Parasitárias, São Paulo, SP, Brasil.
Edimar Alcides BocchiUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Instituto do Coração, Unidade Clínica de Insuficiência Cardíaca, São Paulo, SP, Brasil.
Fátima das Dores da CruzUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Instituto do Coração, Unidade Clínica de Insuficiência Cardíaca, São Paulo, SP, Brasil.
Mussya Cisotto RochaUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Laboratório de Imunologia (LIM 48), São Paulo, SP, Brasil.
Samuel Katsuyuki ShinjoUniversidade de São Paulo, Faculdade de Medicina, Disciplina de Reumatologia, São Paulo, SP, Brasil.
Maria Aparecida Shikanai-YasudaUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Laboratório de Imunologia (LIM 48), São Paulo, SP, Brasil.
Paola Andrea OrtizUniversidade de São Paulo, Instituto de Ciências Biomédicas, Laboratório de Filogenia, Taxonomia e Diagnóstico de Tripanossomatídeos, São Paulo, SP, Brasil.
Marta Maria Geraldes TeixeiraUniversidade de São Paulo, Instituto de Ciências Biomédicas, Laboratório de Filogenia, Taxonomia e Diagnóstico de Tripanossomatídeos, São Paulo, SP, Brasil.
José Eduardo TolezanoInstituto Adolfo Lutz, Centro de Parasitologia e Micologia, São Paulo, SP, Brasil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrypanosoma cruzi shows an exuberant genetic diversity. Currently, seven phylogenetic lineages, called discrete typing units (DTUs), are recognised: TcI-TcVI and Tcbat. Despite advances in studies on T. cruzi and its populations, there is no consensus regarding its heterogeneity.

objectivesThis study aimed to perform molecular characterisation of T. cruzi strains, isolated in the state of São Paulo, to identify the DTUs involved and evaluate their genetic diversity.

methodsT. cruzi strains were isolated from biological samples of chronic chagasic patients, marsupials and triatomines through culture techniques and subjected to molecular characterisation using the fluorescent fragment length barcoding (FFLB) technique. Subsequently, the results were correlated with complementary information to enable better discrimination between the identified DTUs.

findingsIt was possible to identify TcI in two humans and two triatomines; TcII/VI in 19 humans, two marsupials and one triatomine; and TcIII in one human host, an individual that also presented a result for TcI, which indicated the possibility of a mixed infection. Regarding the strains characterised by the TcII/VI profile, the correlation with complementary information allowed to suggest that, in general, these parasite populations indeed correspond to the TcII genotype. MAIN

conclusionsThe TcII/VI profile, associated with domestic cycles and patients with chronic Chagas disease, was the most prevalent among the identified DTUs. Furthermore, the correlation of the study results with complementary information made it possible to suggest that TcII is the predominant lineage of this work.

Indexed as

Chagas DiseaseMarsupialiaTrypanosoma cruziAnimalsBrazilGenetic VariationGenotypeHumansPhylogeny

Identifiers

PMID36383785
PMCPMC9651066

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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.