Deep serological profiling of the Trypanosoma cruzi TSSA antigen reveals different epitopes and modes of recognition by Chagas disease patients
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.
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. |
dc.format.extent.es.fl_str_mv | 22 h. |
dc.format.mimetype.es.fl_str_mv | application/pdf |
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 |
format | article |
id | COLIBRI_41ebb809bfefab615418ac1112afe681 |
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. 1935-2735 10.1371/journal.pntd.0011542 |
instacron_str | Universidad de la República |
institution | Universidad de la República |
instname_str | Universidad de la República |
language | eng |
language_invalid_str_mv | en |
network_acronym_str | COLIBRI |
network_name_str | COLIBRI |
oai_identifier_str | oai:colibri.udelar.edu.uy:20.500.12008/42843 |
publishDate | 2023 |
reponame_str | COLIBRI |
repository.mail.fl_str_mv | mabel.seroubian@seciu.edu.uy |
repository.name.fl_str_mv | COLIBRI - Universidad de la República |
repository_id_str | 4771 |
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 |