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

Bibliographic Details
Main Author: Kangussu-Marcolino, Monica Mendes
Publication Date: 2013
Other Authors: Paiva, Rita Marcia Cardoso de, Araujo, Patricia Rosa, Mendonca-Neto, Rondon Pessoa de, Lemos, Laiane, Bartholomeu, Daniella Castanheira, Mortara, Renato Arruda [UNIFESP], Da Rocha, Wanderson Duarte, Teixeira, Santuza Maria Ribeiro
Format: Article
Language: eng
Source: Repositório Institucional da UNIFESP
Download full: http://dx.doi.org/10.1186/1471-2180-13-10
http://repositorio.unifesp.br/handle/11600/35883
Summary: Background: Amastins 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.Results: Based 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 delta-amastin genes are organized in two or more clusters with alternating copies of tuzin genes, the two copies of beta-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 delta-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, beta-amastin transcripts are more abundant in epimastigotes, the stage found in the insect vector.Conclusions: Here 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 delta-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 delta-amastin expression is down regulated in a strain presenting low infection capacity.
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spelling Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruziTrypanosoma cruziAmastigoteAmastinmRNABackground: Amastins 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.Results: Based 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 delta-amastin genes are organized in two or more clusters with alternating copies of tuzin genes, the two copies of beta-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 delta-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, beta-amastin transcripts are more abundant in epimastigotes, the stage found in the insect vector.Conclusions: Here 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 delta-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 delta-amastin expression is down regulated in a strain presenting low infection capacity.Univ Fed Parana, Dept Bioquim & Biol Mol, Ctr Curitiba, BR-80060000 Curitiba, PR, BrazilDept Bioquim & Imunol, BR-31270901 Pampulha Belo Horizonte, MG, BrazilUniv Fed Minas Gerais, Dept Parasitol, BR-31270901 Pampulha Belo Horizonte, MG, BrazilUniversidade Federal de São Paulo, Dept Microbiol Imunol & Parasitol, Escola Paulista Med, BR-04021001 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol Imunol & Parasitol, Escola Paulista Med, BR-04021001 São Paulo, BrazilWeb of ScienceConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)Instituto Nacional de Ciencia e Tecnologia de Vacinas (INCTV, Brazil)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)PPSUS/MSBiomed Central LtdUniv Fed ParanaDept Bioquim & ImunolUniversidade Federal de Minas Gerais (UFMG)Universidade Federal de São Paulo (UNIFESP)Kangussu-Marcolino, Monica MendesPaiva, Rita Marcia Cardoso deAraujo, Patricia RosaMendonca-Neto, Rondon Pessoa deLemos, LaianeBartholomeu, Daniella CastanheiraMortara, Renato Arruda [UNIFESP]Da Rocha, Wanderson DuarteTeixeira, Santuza Maria Ribeiro2016-01-24T14:31:08Z2016-01-24T14:31:08Z2013-01-17info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion11application/pdfhttp://dx.doi.org/10.1186/1471-2180-13-10Bmc Microbiology. London: Biomed Central Ltd, v. 13, 11 p., 2013.10.1186/1471-2180-13-10WOS000315712500001.pdf1471-2180http://repositorio.unifesp.br/handle/11600/35883WOS:000315712500001engBmc Microbiologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-08T17:54:26Zoai:repositorio.unifesp.br/:11600/35883Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-08T17:54:26Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruzi
title Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruzi
spellingShingle Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruzi
Kangussu-Marcolino, Monica Mendes
Trypanosoma cruzi
Amastigote
Amastin
mRNA
title_short Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruzi
title_full Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruzi
title_fullStr Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruzi
title_full_unstemmed Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruzi
title_sort Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruzi
author Kangussu-Marcolino, Monica Mendes
author_facet Kangussu-Marcolino, Monica Mendes
Paiva, Rita Marcia Cardoso de
Araujo, Patricia Rosa
Mendonca-Neto, Rondon Pessoa de
Lemos, Laiane
Bartholomeu, Daniella Castanheira
Mortara, Renato Arruda [UNIFESP]
Da Rocha, Wanderson Duarte
Teixeira, Santuza Maria Ribeiro
author_role author
author2 Paiva, Rita Marcia Cardoso de
Araujo, Patricia Rosa
Mendonca-Neto, Rondon Pessoa de
Lemos, Laiane
Bartholomeu, Daniella Castanheira
Mortara, Renato Arruda [UNIFESP]
Da Rocha, Wanderson Duarte
Teixeira, Santuza Maria Ribeiro
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Univ Fed Parana
Dept Bioquim & Imunol
Universidade Federal de Minas Gerais (UFMG)
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Kangussu-Marcolino, Monica Mendes
Paiva, Rita Marcia Cardoso de
Araujo, Patricia Rosa
Mendonca-Neto, Rondon Pessoa de
Lemos, Laiane
Bartholomeu, Daniella Castanheira
Mortara, Renato Arruda [UNIFESP]
Da Rocha, Wanderson Duarte
Teixeira, Santuza Maria Ribeiro
dc.subject.por.fl_str_mv Trypanosoma cruzi
Amastigote
Amastin
mRNA
topic Trypanosoma cruzi
Amastigote
Amastin
mRNA
description Background: Amastins 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.Results: Based 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 delta-amastin genes are organized in two or more clusters with alternating copies of tuzin genes, the two copies of beta-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 delta-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, beta-amastin transcripts are more abundant in epimastigotes, the stage found in the insect vector.Conclusions: Here 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 delta-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 delta-amastin expression is down regulated in a strain presenting low infection capacity.
publishDate 2013
dc.date.none.fl_str_mv 2013-01-17
2016-01-24T14:31:08Z
2016-01-24T14:31:08Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/1471-2180-13-10
Bmc Microbiology. London: Biomed Central Ltd, v. 13, 11 p., 2013.
10.1186/1471-2180-13-10
WOS000315712500001.pdf
1471-2180
http://repositorio.unifesp.br/handle/11600/35883
WOS:000315712500001
url http://dx.doi.org/10.1186/1471-2180-13-10
http://repositorio.unifesp.br/handle/11600/35883
identifier_str_mv Bmc Microbiology. London: Biomed Central Ltd, v. 13, 11 p., 2013.
10.1186/1471-2180-13-10
WOS000315712500001.pdf
1471-2180
WOS:000315712500001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Bmc Microbiology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 11
application/pdf
dc.publisher.none.fl_str_mv Biomed Central Ltd
publisher.none.fl_str_mv Biomed Central Ltd
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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