Evidence map›Paper›PMID 28972996›Full record

ArticlePloS one2017

Secretome analysis of Trypanosoma cruzi by proteomics studies.

Jean-Yves Brossas, Julián Ernesto Nicolás Gulin, Margarita Maria Catalina Bisio, Manuel Chapelle, Carine Marinach-Patrice, Mallaury Bordessoules, George Palazon Ruiz, Jeremy Vion, Luc Paris, Jaime Altcheh and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

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  10. The ElusivePathogens (Basel, Switzerland) · 2023
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  12. Molecular Recognition of SurfaceInternational journal of molecular sciences · 2022
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  13. Miltefosine and Benznidazole Combination Improve Anti-Frontiers in cellular and infection microbiology · 2022
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  14. Released Parasite-Derived Kinases as Novel Targets for Antiparasitic Therapies.Frontiers in cellular and infection microbiology · 2022
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  18. All Roads Lead to Cytosol:Frontiers in cellular and infection microbiology · 2021
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  19. Optimization and biological validation of anBiology methods & protocols · 2021
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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

11 authors at 4 institutions in 2 countries.

Jean-Yves BrossasCentre d'Immunologie et des Maladies Infectieuses, INSERM U1135, Paris, France.ORCID http://orcid.org/0000-0003-1190-7698
Julián Ernesto Nicolás GulinServicio de Parasitología y Enfermedad de Chagas, Hospital de Niños "Dr. Ricardo Gutiérrez", Buenos Aires, Argentina.
Margarita Maria Catalina BisioServicio de Parasitología y Enfermedad de Chagas, Hospital de Niños "Dr. Ricardo Gutiérrez", Buenos Aires, Argentina.
Manuel ChapelleBruker Daltonics, Champs-sur Marne, France.
Carine Marinach-PatriceCentre d'Immunologie et des Maladies Infectieuses, INSERM U1135, Paris, France.
Mallaury BordessoulesCentre d'Immunologie et des Maladies Infectieuses, INSERM U1135, Paris, France.
George Palazon RuizCentre d'Immunologie et des Maladies Infectieuses, INSERM U1135, Paris, France.
Jeremy VionCentre d'Immunologie et des Maladies Infectieuses, INSERM U1135, Paris, France.
Luc ParisSorbonne Universités, UPMC Univ Paris 06, Paris, France.
Jaime AltchehServicio de Parasitología y Enfermedad de Chagas, Hospital de Niños "Dr. Ricardo Gutiérrez", Buenos Aires, Argentina.
Dominique MazierCentre d'Immunologie et des Maladies Infectieuses, INSERM U1135, Paris, France.
Inserm · FRConsejo Nacional de Investigaciones Científicas y Técnicas · ARBruker (France) · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChagas disease is a debilitating often fatal disease resulting from infection by the protozoan parasite Trypanosoma cruzi. Chagas disease is endemic in 21 countries of the Americas, and it is an emerging disease in other countries as a result of migration. Given the chronic nature of the infection where intracellular parasites persist for years, the diagnosis of T. cruzi by direct detection is difficult, whereas serologic tests though sensitive may yield false-positive results. The development of new rapid test based on the identification of soluble parasitic antigens in serum would be a real innovation in the diagnosis of Chagas disease.

methodsTo identify new soluble biomarkers that may improve diagnostic tests, we investigated the proteins secreted by T. cruzi using mass spectrometric analyses of conditioned culture media devoid of serum collected during the emergence of trypomastigotes from infected Vero cells. In addition, we compared the secretomes of two T. cruzi strains from DTU Tc VI (VD and CL Brener).

resultsAnalysis of the secretome collected during the emergence of trypomastigotes from Vero cells led to the identification of 591 T. cruzi proteins. Three hundred sixty three proteins are common to both strains and most belong to different multigenic super families (i.e. TcS, GP63, MASP, and DGF1). Ultimately we have established a list of 94 secreted proteins, common to both DTU Tc VI strains that do not belong to members of multigene families.

conclusionsThis study provides the first comparative analysis of the secretomes from two distinct T. cruzi strains of DTU TcVI. This led us to identify a subset of common secreted proteins that could potentially serve as serum markers for T. cruzi infection. Their potential could now be evaluated, with specific antibodies using sera collected from patients and residents from endemic regions.

Indexed as

ProteomicsAnimalsChlorocebus aethiopsChromatography, LiquidElectrophoresis, Polyacrylamide GelProtozoan ProteinsTandem Mass SpectrometryTrypanosoma cruziVero CellsProtozoan Proteins

Identifiers

PMID28972996
PMCPMC5626432
OpenAlexW2760884089

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.