Evidence map›Paper›PMID 23056658›Full record

ArticlePLoS neglected tropical diseases2012

Differential infectivity by the oral route of Trypanosoma cruzi lineages derived from Y strain.

Cristian Cortez, Rafael M Martins, Renan M Alves, Richard C Silva, Luciana C Bilches, Silene Macedo, Vanessa D Atayde, Silvia Y Kawashita, Marcelo R S Briones, Nobuko Yoshida

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Optimization of anBiology methods & protocols · 2026
    Article
  2. Oral Route Infection byPathogens (Basel, Switzerland) · 2026
    Review
  3. Review
  4. Biological features of TcM: A newCurrent research in microbial sciences · 2022
    Article
  5. Review
  6. All Roads Lead to Cytosol:Frontiers in cellular and infection microbiology · 2021
    Review
  7. Early Immune Response Elicited by DifferentFrontiers in cellular and infection microbiology · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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.

Cristian CortezDepartamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de São Paulo, São Paulo, Brazil.
Rafael M Martins
Renan M Alves
Richard C Silva
Luciana C Bilches
Silene Macedo
Vanessa D Atayde
Silvia Y Kawashita
Marcelo R S Briones
Nobuko Yoshida

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiversity of T. cruzi strains is a central problem in Chagas disease research because of its correlation with the wide range of clinical manifestations and the biogeographical parasite distribution. The role played by parasite microdiversity in Chagas disease epidemiology is still debatable. Also awaits clarification whether such diversity is associated with the outcome of oral T. cruzi infection, responsible for frequent outbreaks of acute Chagas disease. METHODS AND

findingsWe addressed the impact of microdiversity in oral T. cruzi infection, by comparative analysis of two strains, Y30 and Y82, both derived from Y strain, a widely used experimental model. Network genealogies of four nuclear genes (SSU rDNA, actin, DHFR-TS, EF1α) revealed that Y30 is closely related to Discrete Typing Unit TcII while Y82 is more closely related to TcVI, a group containing hybrid strains. Nevertheless, excepting one A-G transition at position 1463, Y30 and Y82 SSU rDNAs were identical. Y82 strain, expressing the surface molecule gp82, infected mice orally more efficiently than Y30, which expresses a related gp30 molecule. Both molecules are involved in lysosome exocytosis-dependent host cell invasion, but exhibit differential gastric mucin-binding capacity, a property critical for parasite migration toward the gastric mucosal epithelium. Upon oral infection of mice, the number of Y30 and Y82 parasites in gastric epithelial cells differed widely.

conclusionsWe conclude that metacyclic forms of gp82-expressing Y82 strain, closely related to TcVI, are better adapted than Y30 strain (TcII) to traverse the stomach mucous layer and establish oral route infection. The efficiency to infect target cell is the same because gp82 and gp30 strains have similar invasion-promoting properties. Unknown is whether differences in Y30 and Y82 are natural parasite adaptations or a product of lab-induced evolution by differential selection along the 60 years elapsed since the Y strain isolation.

Indexed as

Genetic VariationAnimalsChagas DiseaseDisease Models, AnimalDNA, ProtozoanFemaleMiceMice, Inbred BALB CMolecular Sequence DataProtozoan ProteinsSequence Analysis, DNATrypanosoma cruziVirulenceDNA, ProtozoanProtozoan Proteins

Identifiers

PMID23056658
PMCPMC3464286

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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.