Literature DB >> 27974541

Characterization and Diagnostic Application of Trypanosoma cruzi Trypomastigote Excreted-Secreted Antigens Shed in Extracellular Vesicles Released from Infected Mammalian Cells.

Norma L Bautista-López1,2, Momar Ndao2,3, Fabio Vasquez Camargo2,3, Takeshi Nara4, Takeshi Annoura5, Darryl B Hardie6, Christoph H Borchers6, Armando Jardim7,2.   

Abstract

Chagas disease, caused by Trypanosoma cruzi, although endemic in many parts of Central and South America, is emerging as a global health threat through the potential contamination of blood supplies. Consequently, in the absence of a gold standard assay for the diagnosis of Chagas disease, additional antigens or strategies are needed. A proteomic analysis of the trypomastigote excreted-secreted antigens (TESA) associated with exosomal vesicles shed by T. cruzi identified ∼80 parasite proteins, with the majority being trans-sialidases. Mass spectrometry analysis of immunoprecipitation products performed using Chagas immune sera showed a marked enrichment in a subset of TESA proteins. Of particular relevance for diagnostic applications were the retrotransposon hot spot (RHS) proteins, which are absent in Leishmania spp., parasites that often confound diagnosis of Chagas disease. Interestingly, serological screens using recombinant RHS showed a robust immunoreactivity with sera from patients with clinical stages of Chagas ranging from asymptomatic to advance cardiomyopathy and this immunoreactivity was comparable to that of crude TESA. More importantly, no cross-reactivity with RHS was detected with sera from patients with malaria, leishmaniasis, toxoplasmosis, or African sleeping sickness, making this protein an attractive reagent for diagnosis of Chagas disease.
Copyright © 2017 American Society for Microbiology.

Entities:  

Keywords:  TESA; Trypanosoma cruzi; parasite; proteomics; trypomastigote

Mesh:

Substances:

Year:  2016        PMID: 27974541      PMCID: PMC5328442          DOI: 10.1128/JCM.01649-16

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  76 in total

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2.  Trypanosoma cruzi: shedding of surface antigens as membrane vesicles.

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Journal:  Exp Parasitol       Date:  1991-01       Impact factor: 2.011

3.  Trypanosoma cruzi immune evasion mediated by host cell-derived microvesicles.

Authors:  Igor Cestari; Ephraim Ansa-Addo; Poliana Deolindo; Jameel M Inal; Marcel I Ramirez
Journal:  J Immunol       Date:  2012-01-18       Impact factor: 5.422

4.  Amastigote and epimastigote stage-specific components of Trypanosoma cruzi characterized by using monoclonal antibodies. Purification and molecular characterization of an 83-kilodalton amastigote protein.

Authors:  A A Pan; D McMahon-Pratt
Journal:  J Immunol       Date:  1989-08-01       Impact factor: 5.422

5.  Matrix metalloproteinases 2 and 9 as diagnostic markers in the progression to Chagas cardiomyopathy.

Authors:  Norma Leticia Bautista-López; Carlos A Morillo; Patricio López-Jaramillo; Roberto Quiroz; Carlos Luengas; Sandra Y Silva; Jacques Galipeau; Manoj Mathew Lalu; Richard Schulz
Journal:  Am Heart J       Date:  2013-02-15       Impact factor: 4.749

6.  Chagas disease: a Latin American health problem becoming a world health problem.

Authors:  Gabriel A Schmunis; Zaida E Yadon
Journal:  Acta Trop       Date:  2009-11-20       Impact factor: 3.112

7.  Extracellular Vesicles from Trypanosoma brucei Mediate Virulence Factor Transfer and Cause Host Anemia.

Authors:  Anthony J Szempruch; Steven E Sykes; Rudo Kieft; Lauren Dennison; Allison C Becker; Anzio Gartrell; William J Martin; Ernesto S Nakayasu; Igor C Almeida; Stephen L Hajduk; John M Harrington
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8.  Demonstration of Trypanosoma cruzi antigen in serum from patients with Chagas' disease.

Authors:  F G Araujo; E Chiari; J C Dias
Journal:  Lancet       Date:  1981-01-31       Impact factor: 79.321

9.  SUMOylation of paraflagellar rod protein, PFR1, and its stage-specific localization in Trypanosoma cruzi.

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Journal:  PLoS One       Date:  2012-05-17       Impact factor: 3.240

10.  TcTASV-C, a protein family in Trypanosoma cruzi that is predominantly trypomastigote-stage specific and secreted to the medium.

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Journal:  PLoS One       Date:  2013-07-29       Impact factor: 3.240

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3.  Plasma-Derived Extracellular Vesicles as Potential Biomarkers in Heart Transplant Patient with Chronic Chagas Disease.

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4.  Characterization of Plasmodium vivax Proteins in Plasma-Derived Exosomes From Malaria-Infected Liver-Chimeric Humanized Mice.

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Journal:  Front Microbiol       Date:  2018-06-25       Impact factor: 5.640

Review 5.  Isolation and Functions of Extracellular Vesicles Derived from Parasites: The Promise of a New Era in Immunotherapy, Vaccination, and Diagnosis.

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7.  The protein family TcTASV-C is a novel Trypanosoma cruzi virulence factor secreted in extracellular vesicles by trypomastigotes and highly expressed in bloodstream forms.

Authors:  Lucas D Caeiro; Catalina D Alba-Soto; Mariana Rizzi; María Elisa Solana; Giselle Rodriguez; Agustina M Chidichimo; Matías E Rodriguez; Daniel O Sánchez; Gabriela V Levy; Valeria Tekiel
Journal:  PLoS Negl Trop Dis       Date:  2018-05-04

Review 8.  Perils and Promises of Pathogenic Protozoan Extracellular Vesicles.

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9.  Genomic Organization and Generation of Genetic Variability in the RHS (Retrotransposon Hot Spot) Protein Multigene Family in Trypanosoma cruzi.

Authors:  Werica P Bernardo; Renata T Souza; André G Costa-Martins; Eden R Ferreira; Renato A Mortara; Marta M G Teixeira; José Luis Ramirez; José F Da Silveira
Journal:  Genes (Basel)       Date:  2020-09-17       Impact factor: 4.096

10.  A novel Trypanosoma cruzi secreted antigen as a potential biomarker of Chagas disease.

Authors:  Rana Nagarkatti; David Acosta; Nirmallya Acharyya; Fernanda Fortes de Araujo; Silvana Maria Elói-Santos; Olindo Assis Martins-Filho; Andréa Teixeira-Carvalho; Alain Debrabant
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