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SURFIN is a polymorphic antigen expressed on Plasmodium falciparum merozoites and infected erythrocytes
The surfaces of the infected erythrocyte (IE) and the merozoite, two developmental stages of malaria parasites, expose antigenic determinants to the host immune system. We report on surface-associated interspersed genes (surf genes), which encode a novel polymorphic protein family, SURFINs, present...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213267/ https://www.ncbi.nlm.nih.gov/pubmed/15939796 http://dx.doi.org/10.1084/jem.20041392 |
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author | Winter, Gerhard Kawai, Satoru Haeggström, Malin Kaneko, Osamu von Euler, Anne Kawazu, Shin-ichiro Palm, Daniel Fernandez, Victor Wahlgren, Mats |
author_facet | Winter, Gerhard Kawai, Satoru Haeggström, Malin Kaneko, Osamu von Euler, Anne Kawazu, Shin-ichiro Palm, Daniel Fernandez, Victor Wahlgren, Mats |
author_sort | Winter, Gerhard |
collection | PubMed |
description | The surfaces of the infected erythrocyte (IE) and the merozoite, two developmental stages of malaria parasites, expose antigenic determinants to the host immune system. We report on surface-associated interspersed genes (surf genes), which encode a novel polymorphic protein family, SURFINs, present on both IEs and merozoites. A SURFIN expressed in 3D7 parasites, SURFIN(4.2), was identified by mass spectrometric analysis of peptides cleaved off the surface of live IEs with trypsin. SURFINs are encoded by a family of 10 surf genes, including three predicted pseudogenes, located within or close to the subtelomeres of five of the chromosomes. SURFINs show structural and sequence similarities with exported surface-exposed proteins (PvSTP1, PkSICAvar, PvVIR, Pf332, and PfEMP1) of several Plasmodium species. SURFIN(4.2) of a parasite other than 3D7 (FCR3S1.2) showed polymorphisms in the extracellular domain, suggesting sequence variability between genotypes. SURFIN(4.2) not only was found cotransported with PfEMP1 and RIFIN to the IE surface, but also accumulated in the parasitophorous vacuole. In released merozoites, SURFIN(4.2) was present in an amorphous cap at the parasite apex, where it may be involved in the invasion of erythrocytes. By exposing shared polymorphic antigens on IEs and merozoites, the parasite may coordinate the antigenic composition of these attachment surfaces during growth in the bloodstream. |
format | Text |
id | pubmed-2213267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22132672008-03-11 SURFIN is a polymorphic antigen expressed on Plasmodium falciparum merozoites and infected erythrocytes Winter, Gerhard Kawai, Satoru Haeggström, Malin Kaneko, Osamu von Euler, Anne Kawazu, Shin-ichiro Palm, Daniel Fernandez, Victor Wahlgren, Mats J Exp Med Article The surfaces of the infected erythrocyte (IE) and the merozoite, two developmental stages of malaria parasites, expose antigenic determinants to the host immune system. We report on surface-associated interspersed genes (surf genes), which encode a novel polymorphic protein family, SURFINs, present on both IEs and merozoites. A SURFIN expressed in 3D7 parasites, SURFIN(4.2), was identified by mass spectrometric analysis of peptides cleaved off the surface of live IEs with trypsin. SURFINs are encoded by a family of 10 surf genes, including three predicted pseudogenes, located within or close to the subtelomeres of five of the chromosomes. SURFINs show structural and sequence similarities with exported surface-exposed proteins (PvSTP1, PkSICAvar, PvVIR, Pf332, and PfEMP1) of several Plasmodium species. SURFIN(4.2) of a parasite other than 3D7 (FCR3S1.2) showed polymorphisms in the extracellular domain, suggesting sequence variability between genotypes. SURFIN(4.2) not only was found cotransported with PfEMP1 and RIFIN to the IE surface, but also accumulated in the parasitophorous vacuole. In released merozoites, SURFIN(4.2) was present in an amorphous cap at the parasite apex, where it may be involved in the invasion of erythrocytes. By exposing shared polymorphic antigens on IEs and merozoites, the parasite may coordinate the antigenic composition of these attachment surfaces during growth in the bloodstream. The Rockefeller University Press 2005-06-06 /pmc/articles/PMC2213267/ /pubmed/15939796 http://dx.doi.org/10.1084/jem.20041392 Text en Copyright © 2005, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Winter, Gerhard Kawai, Satoru Haeggström, Malin Kaneko, Osamu von Euler, Anne Kawazu, Shin-ichiro Palm, Daniel Fernandez, Victor Wahlgren, Mats SURFIN is a polymorphic antigen expressed on Plasmodium falciparum merozoites and infected erythrocytes |
title | SURFIN is a polymorphic antigen expressed on Plasmodium falciparum merozoites and infected erythrocytes |
title_full | SURFIN is a polymorphic antigen expressed on Plasmodium falciparum merozoites and infected erythrocytes |
title_fullStr | SURFIN is a polymorphic antigen expressed on Plasmodium falciparum merozoites and infected erythrocytes |
title_full_unstemmed | SURFIN is a polymorphic antigen expressed on Plasmodium falciparum merozoites and infected erythrocytes |
title_short | SURFIN is a polymorphic antigen expressed on Plasmodium falciparum merozoites and infected erythrocytes |
title_sort | surfin is a polymorphic antigen expressed on plasmodium falciparum merozoites and infected erythrocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213267/ https://www.ncbi.nlm.nih.gov/pubmed/15939796 http://dx.doi.org/10.1084/jem.20041392 |
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