Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients

Romer, Guadalupe - Bracco, Leonel A. - Ricci, Alejandro D. - Balouz, Virginia - Berná, Luisa - Villar Arismendi, Carlos - Ramsey, Janine M. - Nolan, Melissa S. - Torrico, Faustino - Kesper, Norival - Altcheh, Jaime - Robello Porto, Carlos - Buscaglia, Carlos A. - Agüero, Fernán

Resumen:

Trypanosoma cruzi, the agent of Chagas disease, displays a highly structured population, with multiple strains that can be grouped into 6–7 evolutionary lineages showing variable eco-epidemiological traits and likely also distinct disease-associated features. Previous works have shown that antibody responses to ‘isoforms’ of the polymorphic parasite antigen TSSA enable robust and sensitive identification of the infecting strain with near lineage-level resolution. To optimize the serotyping performance of this molecule, we herein used a combination of immunosignaturing approaches based on peptide microarrays and serum samples from Chagas disease patients to establish a deep linear B-cell epitope profiling of TSSA. Methods/Principle findings: Our assays revealed variations in the seroprevalence of TSSA isoforms among Chagas disease populations from different settings, hence strongly supporting the differential distribution of parasite lineages in domestic cycles across the Americas. Alanine scanning mutagenesis and the use of peptides of different lengths allowed us to identify key residues involved in antibody pairing and the presence of three discrete B-cell linear epitopes in TSSAII, the isoform with highest seroprevalence in human infections. Comprehensive screening of parasite genomic repositories led to the discovery of 9 novel T. cruzi TSSA variants and one TSSA sequence from the phylogenetically related bat parasite T. cruzi marinkellei. Further residue permutation analyses enabled the identification of diagnostically relevant or non-relevant substitutions among TSSA natural polymorphisms. Interestingly, T. cruzi marinkellei TSSA displayed specific serorecognition by one chronic Chagas disease patient from Colombia, which warrant further investigations on the diagnostic impact of such atypical TSSA. Conclusions/Significance: Overall, our findings shed new light into TSSA evolution, epitope landscape and modes of recognition by Chagas disease patients; and have practical implications for the design and/or evaluation of T. cruzi serotyping strategies.


Detalles Bibliográficos
2023
Trypanosoma cruzi
Chagas disease
Parasitic diseases
Genomics
Inglés
Universidad de la República
COLIBRI
https://hdl.handle.net/20.500.12008/42843
Acceso abierto
Licencia Creative Commons Atribución (CC - By 4.0)
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author Romer, Guadalupe
author2 Bracco, Leonel A.
Ricci, Alejandro D.
Balouz, Virginia
Berná, Luisa
Villar Arismendi, Carlos
Ramsey, Janine M.
Nolan, Melissa S.
Torrico, Faustino
Kesper, Norival
Altcheh, Jaime
Robello Porto, Carlos
Buscaglia, Carlos A.
Agüero, Fernán
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author_facet Romer, Guadalupe
Bracco, Leonel A.
Ricci, Alejandro D.
Balouz, Virginia
Berná, Luisa
Villar Arismendi, Carlos
Ramsey, Janine M.
Nolan, Melissa S.
Torrico, Faustino
Kesper, Norival
Altcheh, Jaime
Robello Porto, Carlos
Buscaglia, Carlos A.
Agüero, Fernán
author_role author
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collection COLIBRI
dc.contributor.filiacion.none.fl_str_mv Romer Guadalupe
Bracco Leonel A.
Ricci Alejandro D.
Balouz Virginia
Berná Luisa, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.
Villar Arismendi Carlos
Ramsey Janine M.
Nolan Melissa S.
Torrico Faustino
Kesper Norival
Altcheh Jaime
Robello Porto Carlos, Instituto Pasteur (Montevideo).
Buscaglia Carlos A.
Agüero Fernán
dc.creator.none.fl_str_mv Romer, Guadalupe
Bracco, Leonel A.
Ricci, Alejandro D.
Balouz, Virginia
Berná, Luisa
Villar Arismendi, Carlos
Ramsey, Janine M.
Nolan, Melissa S.
Torrico, Faustino
Kesper, Norival
Altcheh, Jaime
Robello Porto, Carlos
Buscaglia, Carlos A.
Agüero, Fernán
dc.date.accessioned.none.fl_str_mv 2024-03-01T14:31:57Z
dc.date.available.none.fl_str_mv 2024-03-01T14:31:57Z
dc.date.issued.none.fl_str_mv 2023
dc.description.abstract.none.fl_txt_mv Trypanosoma cruzi, the agent of Chagas disease, displays a highly structured population, with multiple strains that can be grouped into 6–7 evolutionary lineages showing variable eco-epidemiological traits and likely also distinct disease-associated features. Previous works have shown that antibody responses to ‘isoforms’ of the polymorphic parasite antigen TSSA enable robust and sensitive identification of the infecting strain with near lineage-level resolution. To optimize the serotyping performance of this molecule, we herein used a combination of immunosignaturing approaches based on peptide microarrays and serum samples from Chagas disease patients to establish a deep linear B-cell epitope profiling of TSSA. Methods/Principle findings: Our assays revealed variations in the seroprevalence of TSSA isoforms among Chagas disease populations from different settings, hence strongly supporting the differential distribution of parasite lineages in domestic cycles across the Americas. Alanine scanning mutagenesis and the use of peptides of different lengths allowed us to identify key residues involved in antibody pairing and the presence of three discrete B-cell linear epitopes in TSSAII, the isoform with highest seroprevalence in human infections. Comprehensive screening of parasite genomic repositories led to the discovery of 9 novel T. cruzi TSSA variants and one TSSA sequence from the phylogenetically related bat parasite T. cruzi marinkellei. Further residue permutation analyses enabled the identification of diagnostically relevant or non-relevant substitutions among TSSA natural polymorphisms. Interestingly, T. cruzi marinkellei TSSA displayed specific serorecognition by one chronic Chagas disease patient from Colombia, which warrant further investigations on the diagnostic impact of such atypical TSSA. Conclusions/Significance: Overall, our findings shed new light into TSSA evolution, epitope landscape and modes of recognition by Chagas disease patients; and have practical implications for the design and/or evaluation of T. cruzi serotyping strategies.
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dc.identifier.citation.es.fl_str_mv Romer, G, Bracco, L, Ricci, A [y otros autores]. "Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients". Plos Neglected Tropical Diseases. [en línea] 2023, 17(8): e0011542. 22 h. DOI: 10.1371/journal.pntd.0011542.
dc.identifier.doi.none.fl_str_mv 10.1371/journal.pntd.0011542
dc.identifier.issn.none.fl_str_mv 1935-2735
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12008/42843
dc.language.iso.none.fl_str_mv en
eng
dc.publisher.es.fl_str_mv PLOS
dc.relation.ispartof.es.fl_str_mv Plos Neglected Tropical Diseases, 2023, 17(8): e0011542.
dc.rights.license.none.fl_str_mv Licencia Creative Commons Atribución (CC - By 4.0)
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv reponame:COLIBRI
instname:Universidad de la República
instacron:Universidad de la República
dc.subject.es.fl_str_mv Trypanosoma cruzi
Chagas disease
Parasitic diseases
Genomics
dc.title.none.fl_str_mv Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients
dc.type.es.fl_str_mv Artículo
dc.type.none.fl_str_mv info:eu-repo/semantics/article
dc.type.version.none.fl_str_mv info:eu-repo/semantics/publishedVersion
description Trypanosoma cruzi, the agent of Chagas disease, displays a highly structured population, with multiple strains that can be grouped into 6–7 evolutionary lineages showing variable eco-epidemiological traits and likely also distinct disease-associated features. Previous works have shown that antibody responses to ‘isoforms’ of the polymorphic parasite antigen TSSA enable robust and sensitive identification of the infecting strain with near lineage-level resolution. To optimize the serotyping performance of this molecule, we herein used a combination of immunosignaturing approaches based on peptide microarrays and serum samples from Chagas disease patients to establish a deep linear B-cell epitope profiling of TSSA. Methods/Principle findings: Our assays revealed variations in the seroprevalence of TSSA isoforms among Chagas disease populations from different settings, hence strongly supporting the differential distribution of parasite lineages in domestic cycles across the Americas. Alanine scanning mutagenesis and the use of peptides of different lengths allowed us to identify key residues involved in antibody pairing and the presence of three discrete B-cell linear epitopes in TSSAII, the isoform with highest seroprevalence in human infections. Comprehensive screening of parasite genomic repositories led to the discovery of 9 novel T. cruzi TSSA variants and one TSSA sequence from the phylogenetically related bat parasite T. cruzi marinkellei. Further residue permutation analyses enabled the identification of diagnostically relevant or non-relevant substitutions among TSSA natural polymorphisms. Interestingly, T. cruzi marinkellei TSSA displayed specific serorecognition by one chronic Chagas disease patient from Colombia, which warrant further investigations on the diagnostic impact of such atypical TSSA. Conclusions/Significance: Overall, our findings shed new light into TSSA evolution, epitope landscape and modes of recognition by Chagas disease patients; and have practical implications for the design and/or evaluation of T. cruzi serotyping strategies.
eu_rights_str_mv openAccess
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identifier_str_mv Romer, G, Bracco, L, Ricci, A [y otros autores]. "Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients". Plos Neglected Tropical Diseases. [en línea] 2023, 17(8): e0011542. 22 h. DOI: 10.1371/journal.pntd.0011542.
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repository.mail.fl_str_mv mabel.seroubian@seciu.edu.uy
repository.name.fl_str_mv COLIBRI - Universidad de la República
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rights_invalid_str_mv Licencia Creative Commons Atribución (CC - By 4.0)
spelling Romer GuadalupeBracco Leonel A.Ricci Alejandro D.Balouz VirginiaBerná Luisa, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.Villar Arismendi CarlosRamsey Janine M.Nolan Melissa S.Torrico FaustinoKesper NorivalAltcheh JaimeRobello Porto Carlos, Instituto Pasteur (Montevideo).Buscaglia Carlos A.Agüero Fernán2024-03-01T14:31:57Z2024-03-01T14:31:57Z2023Romer, G, Bracco, L, Ricci, A [y otros autores]. "Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients". Plos Neglected Tropical Diseases. [en línea] 2023, 17(8): e0011542. 22 h. DOI: 10.1371/journal.pntd.0011542.1935-2735https://hdl.handle.net/20.500.12008/4284310.1371/journal.pntd.0011542Trypanosoma cruzi, the agent of Chagas disease, displays a highly structured population, with multiple strains that can be grouped into 6–7 evolutionary lineages showing variable eco-epidemiological traits and likely also distinct disease-associated features. Previous works have shown that antibody responses to ‘isoforms’ of the polymorphic parasite antigen TSSA enable robust and sensitive identification of the infecting strain with near lineage-level resolution. To optimize the serotyping performance of this molecule, we herein used a combination of immunosignaturing approaches based on peptide microarrays and serum samples from Chagas disease patients to establish a deep linear B-cell epitope profiling of TSSA. Methods/Principle findings: Our assays revealed variations in the seroprevalence of TSSA isoforms among Chagas disease populations from different settings, hence strongly supporting the differential distribution of parasite lineages in domestic cycles across the Americas. Alanine scanning mutagenesis and the use of peptides of different lengths allowed us to identify key residues involved in antibody pairing and the presence of three discrete B-cell linear epitopes in TSSAII, the isoform with highest seroprevalence in human infections. Comprehensive screening of parasite genomic repositories led to the discovery of 9 novel T. cruzi TSSA variants and one TSSA sequence from the phylogenetically related bat parasite T. cruzi marinkellei. Further residue permutation analyses enabled the identification of diagnostically relevant or non-relevant substitutions among TSSA natural polymorphisms. Interestingly, T. cruzi marinkellei TSSA displayed specific serorecognition by one chronic Chagas disease patient from Colombia, which warrant further investigations on the diagnostic impact of such atypical TSSA. Conclusions/Significance: Overall, our findings shed new light into TSSA evolution, epitope landscape and modes of recognition by Chagas disease patients; and have practical implications for the design and/or evaluation of T. cruzi serotyping strategies.Submitted by Pintos Natalia (nataliapintosmvd@gmail.com) on 2024-02-29T15:56:44Z No. of bitstreams: 2 license_rdf: 24251 bytes, checksum: 71ed42ef0a0b648670f707320be37b90 (MD5) 10.1371journal.pntd.0011542.pdf: 3903970 bytes, checksum: 9f1171310d80a379c879cf8028fa1299 (MD5)Approved for entry into archive by Faget Cecilia (lfaget@fcien.edu.uy) on 2024-03-01T13:44:35Z (GMT) No. of bitstreams: 2 license_rdf: 24251 bytes, checksum: 71ed42ef0a0b648670f707320be37b90 (MD5) 10.1371journal.pntd.0011542.pdf: 3903970 bytes, checksum: 9f1171310d80a379c879cf8028fa1299 (MD5)Made available in DSpace by Luna Fabiana (fabiana.luna@seciu.edu.uy) on 2024-03-01T14:31:57Z (GMT). No. of bitstreams: 2 license_rdf: 24251 bytes, checksum: 71ed42ef0a0b648670f707320be37b90 (MD5) 10.1371journal.pntd.0011542.pdf: 3903970 bytes, checksum: 9f1171310d80a379c879cf8028fa1299 (MD5) Previous issue date: 202322 h.application/pdfenengPLOSPlos Neglected Tropical Diseases, 2023, 17(8): e0011542.Las obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)info:eu-repo/semantics/openAccessLicencia Creative Commons Atribución (CC - By 4.0)Trypanosoma cruziChagas diseaseParasitic diseasesGenomicsDeep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patientsArtículoinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionreponame:COLIBRIinstname:Universidad de la Repúblicainstacron:Universidad de la RepúblicaRomer, GuadalupeBracco, Leonel A.Ricci, Alejandro D.Balouz, VirginiaBerná, LuisaVillar Arismendi, CarlosRamsey, Janine M.Nolan, Melissa S.Torrico, FaustinoKesper, NorivalAltcheh, JaimeRobello Porto, CarlosBuscaglia, Carlos A.Agüero, FernánLICENSElicense.txtlicense.txttext/plain; charset=utf-84267http://localhost:8080/xmlui/bitstream/20.500.12008/42843/5/license.txt6429389a7df7277b72b7924fdc7d47a9MD55CC-LICENSElicense_urllicense_urltext/plain; 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- Universidad de la Repúblicafalse
spellingShingle Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients
Romer, Guadalupe
Trypanosoma cruzi
Chagas disease
Parasitic diseases
Genomics
status_str publishedVersion
title Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients
title_full Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients
title_fullStr Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients
title_full_unstemmed Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients
title_short Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients
title_sort Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients
topic Trypanosoma cruzi
Chagas disease
Parasitic diseases
Genomics
url https://hdl.handle.net/20.500.12008/42843