Evidence map›Paper›PMID 23327097›Full record

ArticleBMC microbiology2013

Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruzi.

Monica Mendes Kangussu-Marcolino, Rita Márcia Cardoso de Paiva, Patrícia Rosa Araújo, Rondon Pessoa de Mendonça-Neto, Laiane Lemos, Daniella Castanheira Bartholomeu, Renato A Mortara, Wanderson Duarte daRocha, Santuza Maria Ribeiro Teixeira

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2013. 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
1.8field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

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  7. All Roads Lead to Cytosol:Frontiers in cellular and infection microbiology · 2021
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  13. A Brief View of the Surface Membrane Proteins fromJournal of parasitology research · 2017
    Review
  14. Article
  15. Article
  16. Review
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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

9 authors at 3 institutions in 1 country.

Monica Mendes Kangussu-MarcolinoDepartamento de Bioquímica e Biologia Molecular, Universidade Federal do Paraná, Rua Quinze de Novembro, 1299, 80060-000, Centro Curitiba, PR, Brazil.
Rita Márcia Cardoso de Paiva
Patrícia Rosa Araújo
Rondon Pessoa de Mendonça-Neto
Laiane Lemos
Daniella Castanheira Bartholomeu
Renato A Mortara
Wanderson Duarte daRocha
Santuza Maria Ribeiro Teixeira
Universidade Federal de Minas Gerais · BRUniversidade Federal do Paraná · BRUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmastins are surface glycoproteins (approximately 180 residues long) initially described in Trypanosoma cruzi as particularly abundant during the amastigote stage of this protozoan parasite. Subsequently, they have been found to be encoded by large gene families also present in the genomes of several species of Leishmania and in other Trypanosomatids. Although most amastin genes are organized in clusters associated with tuzin genes and are up-regulated in the intracellular stage of T. cruzi and Leishmania spp, distinct genomic organizations and mRNA expression patterns have also been reported.

resultsBased on the analysis of the complete genome sequences of two T. cruzi strains, we identified a total of 14 copies of amastin genes in T. cruzi and showed that they belong to two of the four previously described amastin subfamilies. Whereas δ-amastin genes are organized in two or more clusters with alternating copies of tuzin genes, the two copies of β-amastins are linked together in a distinct chromosome. Most T. cruzi amastins have similar surface localization as determined by confocal microscopy and western blot analyses. Transcript levels for δ-amastins were found to be up-regulated in amastigotes from several T. cruzi strains, except in the G strain, which is known to have low infection capacity. In contrast, in all strains analysed, β-amastin transcripts are more abundant in epimastigotes, the stage found in the insect vector.

conclusionsHere we showed that not only the number and diversity of T. cruzi amastin genes is larger than what has been predicted, but also their mode of expression during the parasite life cycle is more complex. Although most T. cruzi amastins have a similar surface localization, only δ-amastin genes have their expression up-regulated in amastigotes. The results showing that a sub-group of this family is up-regulated in epimastigotes, suggest that, in addition of their role in intracellular amastigotes, T. cruzi amastins may also serve important functions during the insect stage of the parasite life cycle. Most importantly, evidence for their role as virulence factors was also unveiled from the data showing that δ-amastin expression is down regulated in a strain presenting low infection capacity.

Indexed as

Gene Expression RegulationGene OrderAnimalsBlotting, WesternGene Expression ProfilingGenetic VariationMembrane GlycoproteinsMicroscopy, ConfocalProtozoan ProteinsRNA, MessengerTrypanosoma cruziamastin protein, Trypanosoma cruziMembrane GlycoproteinsProtozoan ProteinsRNA, Messenger

Identifiers

PMID23327097
PMCPMC3598723
OpenAlexW2036910636

What OpenQuestion holds

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LicenceCC BY
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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.