Trypanosoma cruzi surface mucins with exposed variant epitopes

The protozoan parasite Trypanosoma cruzi, the agent of Chagas disease, has a large number of mucin molecules on its surface, whose expression is regulated during the life cycle. These mucins are the main acceptors of sialic acid, a monosaccharide that is required by the parasite to infect and surviv...

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Autores principales: Pollevick, G.D., Di Noia, J.M., Salto, M.L., Lima, C., Leguizamón, M.S., De Lederkremer, R.M., Frasch, A.C.C.
Formato: Artículo publishedVersion
Lenguaje:Inglés
Publicado: 2000
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00219258_v275_n36_p27671_Pollevick
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spelling paperaa:paper_00219258_v275_n36_p27671_Pollevick2023-06-12T16:42:48Z Trypanosoma cruzi surface mucins with exposed variant epitopes J. Biol. Chem. 2000;275(36):27671-27680 Pollevick, G.D. Di Noia, J.M. Salto, M.L. Lima, C. Leguizamón, M.S. De Lederkremer, R.M. Frasch, A.C.C. epitope gene product glycosylphosphatidylinositol monosaccharide mucin sialic acid amino terminal sequence animal cell article cell interaction cell membrane Chagas disease gene expression gene sequence genetic transfection mammal multigene family nonhuman polyacrylamide gel electrophoresis priority journal protein expression tandem repeat Trypanosoma cruzi vertebrate Amino Acid Sequence Animals Antigens, Protozoan Base Sequence Carbohydrate Sequence Chagas Disease Epitopes Glycosylation Glycosylphosphatidylinositols Mice Molecular Sequence Data Mucins Oligosaccharides Recombinant Proteins Transfection Trypanosoma cruzi Variation (Genetics) Animalia Insecta Mammalia Protozoa Trypanosoma Trypanosoma cruzi Vertebrata The protozoan parasite Trypanosoma cruzi, the agent of Chagas disease, has a large number of mucin molecules on its surface, whose expression is regulated during the life cycle. These mucins are the main acceptors of sialic acid, a monosaccharide that is required by the parasite to infect and survive in the mammalian host. A large mucin-like gene family named TcMUC containing about 500 members has been identified previously in T. cruzi. TcMUC can be divided into two subfamilies according to the presence or absence of tandem repeats in the central region of the genes. In this work, T. cruzi parasites were transfected with one tagged member of each subfamily. Only the product from the gene with repeats was highly O-glycosylated in vivo. The O-linked oligosaccharides consisted mainly of β-D-Galp(1→4)-GlcNAc and β-D-Galp(1→4)[β-D-Galp(1→6)]-D-GlcNAc. The same glycosyl moieties were found in endogenous mucins. The mature product was anchored by glycosylphosphatidylinositol to the plasma membrane and exposed to the medium. Sera from infected mice recognized the recombinant product of one repeats-containing gene thus showing that they are expressed during the infection. TcMUC genes encode a hypervariable region at the N terminus. We now show that the hypervariable region is indeed present in the exposed mature N termini of the mucins because sera from infected hosts recognized peptides having sequences from this region. The results are discussed in comparison with the mucins from the insect stages of the parasite (Di Noia, J. M., D'Orso, I., Sanchez, D. O., and Frasch, A. C. C. (2000) J. Biol. Chem. 275, 10218-10227) which do not have variable regions. Fil:Pollevick, G.D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Di Noia, J.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Salto, M.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Leguizamón, M.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:De Lederkremer, R.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2000 info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion application/pdf eng info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00219258_v275_n36_p27671_Pollevick
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
language Inglés
orig_language_str_mv eng
topic epitope
gene product
glycosylphosphatidylinositol
monosaccharide
mucin
sialic acid
amino terminal sequence
animal cell
article
cell interaction
cell membrane
Chagas disease
gene expression
gene sequence
genetic transfection
mammal
multigene family
nonhuman
polyacrylamide gel electrophoresis
priority journal
protein expression
tandem repeat
Trypanosoma cruzi
vertebrate
Amino Acid Sequence
Animals
Antigens, Protozoan
Base Sequence
Carbohydrate Sequence
Chagas Disease
Epitopes
Glycosylation
Glycosylphosphatidylinositols
Mice
Molecular Sequence Data
Mucins
Oligosaccharides
Recombinant Proteins
Transfection
Trypanosoma cruzi
Variation (Genetics)
Animalia
Insecta
Mammalia
Protozoa
Trypanosoma
Trypanosoma cruzi
Vertebrata
spellingShingle epitope
gene product
glycosylphosphatidylinositol
monosaccharide
mucin
sialic acid
amino terminal sequence
animal cell
article
cell interaction
cell membrane
Chagas disease
gene expression
gene sequence
genetic transfection
mammal
multigene family
nonhuman
polyacrylamide gel electrophoresis
priority journal
protein expression
tandem repeat
Trypanosoma cruzi
vertebrate
Amino Acid Sequence
Animals
Antigens, Protozoan
Base Sequence
Carbohydrate Sequence
Chagas Disease
Epitopes
Glycosylation
Glycosylphosphatidylinositols
Mice
Molecular Sequence Data
Mucins
Oligosaccharides
Recombinant Proteins
Transfection
Trypanosoma cruzi
Variation (Genetics)
Animalia
Insecta
Mammalia
Protozoa
Trypanosoma
Trypanosoma cruzi
Vertebrata
Pollevick, G.D.
Di Noia, J.M.
Salto, M.L.
Lima, C.
Leguizamón, M.S.
De Lederkremer, R.M.
Frasch, A.C.C.
Trypanosoma cruzi surface mucins with exposed variant epitopes
topic_facet epitope
gene product
glycosylphosphatidylinositol
monosaccharide
mucin
sialic acid
amino terminal sequence
animal cell
article
cell interaction
cell membrane
Chagas disease
gene expression
gene sequence
genetic transfection
mammal
multigene family
nonhuman
polyacrylamide gel electrophoresis
priority journal
protein expression
tandem repeat
Trypanosoma cruzi
vertebrate
Amino Acid Sequence
Animals
Antigens, Protozoan
Base Sequence
Carbohydrate Sequence
Chagas Disease
Epitopes
Glycosylation
Glycosylphosphatidylinositols
Mice
Molecular Sequence Data
Mucins
Oligosaccharides
Recombinant Proteins
Transfection
Trypanosoma cruzi
Variation (Genetics)
Animalia
Insecta
Mammalia
Protozoa
Trypanosoma
Trypanosoma cruzi
Vertebrata
description The protozoan parasite Trypanosoma cruzi, the agent of Chagas disease, has a large number of mucin molecules on its surface, whose expression is regulated during the life cycle. These mucins are the main acceptors of sialic acid, a monosaccharide that is required by the parasite to infect and survive in the mammalian host. A large mucin-like gene family named TcMUC containing about 500 members has been identified previously in T. cruzi. TcMUC can be divided into two subfamilies according to the presence or absence of tandem repeats in the central region of the genes. In this work, T. cruzi parasites were transfected with one tagged member of each subfamily. Only the product from the gene with repeats was highly O-glycosylated in vivo. The O-linked oligosaccharides consisted mainly of β-D-Galp(1→4)-GlcNAc and β-D-Galp(1→4)[β-D-Galp(1→6)]-D-GlcNAc. The same glycosyl moieties were found in endogenous mucins. The mature product was anchored by glycosylphosphatidylinositol to the plasma membrane and exposed to the medium. Sera from infected mice recognized the recombinant product of one repeats-containing gene thus showing that they are expressed during the infection. TcMUC genes encode a hypervariable region at the N terminus. We now show that the hypervariable region is indeed present in the exposed mature N termini of the mucins because sera from infected hosts recognized peptides having sequences from this region. The results are discussed in comparison with the mucins from the insect stages of the parasite (Di Noia, J. M., D'Orso, I., Sanchez, D. O., and Frasch, A. C. C. (2000) J. Biol. Chem. 275, 10218-10227) which do not have variable regions.
format Artículo
Artículo
publishedVersion
author Pollevick, G.D.
Di Noia, J.M.
Salto, M.L.
Lima, C.
Leguizamón, M.S.
De Lederkremer, R.M.
Frasch, A.C.C.
author_facet Pollevick, G.D.
Di Noia, J.M.
Salto, M.L.
Lima, C.
Leguizamón, M.S.
De Lederkremer, R.M.
Frasch, A.C.C.
author_sort Pollevick, G.D.
title Trypanosoma cruzi surface mucins with exposed variant epitopes
title_short Trypanosoma cruzi surface mucins with exposed variant epitopes
title_full Trypanosoma cruzi surface mucins with exposed variant epitopes
title_fullStr Trypanosoma cruzi surface mucins with exposed variant epitopes
title_full_unstemmed Trypanosoma cruzi surface mucins with exposed variant epitopes
title_sort trypanosoma cruzi surface mucins with exposed variant epitopes
publishDate 2000
url http://hdl.handle.net/20.500.12110/paper_00219258_v275_n36_p27671_Pollevick
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AT leguizamonms trypanosomacruzisurfacemucinswithexposedvariantepitopes
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