Distinct genomic organization, mRNA expression and cellular localization of members of two amastin sub-families present in Trypanosoma cruzi
Main Author: | |
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Publication Date: | 2013 |
Other Authors: | , , , , , , , |
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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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 |
_version_ |
1841453723052670976 |