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Plasmodium falciparum Variant Surface Antigen Expression Patterns during Malaria
The variant surface antigens expressed on Plasmodium falciparum–infected erythrocytes are potentially important targets of immunity to malaria and are encoded, at least in part, by a family of var genes, about 60 of which are present within every parasite genome. Here we use semi-conserved regions w...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1287908/ https://www.ncbi.nlm.nih.gov/pubmed/16304608 http://dx.doi.org/10.1371/journal.ppat.0010026 |
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author | Bull, Peter C Berriman, Matthew Kyes, Sue Quail, Michael A Hall, Neil Kortok, Moses M Marsh, Kevin Newbold, Chris I |
author_facet | Bull, Peter C Berriman, Matthew Kyes, Sue Quail, Michael A Hall, Neil Kortok, Moses M Marsh, Kevin Newbold, Chris I |
author_sort | Bull, Peter C |
collection | PubMed |
description | The variant surface antigens expressed on Plasmodium falciparum–infected erythrocytes are potentially important targets of immunity to malaria and are encoded, at least in part, by a family of var genes, about 60 of which are present within every parasite genome. Here we use semi-conserved regions within short var gene sequence “tags” to make direct comparisons of var gene expression in 12 clinical parasite isolates from Kenyan children. A total of 1,746 var clones were sequenced from genomic and cDNA and assigned to one of six sequence groups using specific sequence features. The results show the following. (1) The relative numbers of genomic clones falling in each of the sequence groups was similar between parasite isolates and corresponded well with the numbers of genes found in the genome of a single, fully sequenced parasite isolate. In contrast, the relative numbers of cDNA clones falling in each group varied considerably between isolates. (2) Expression of sequences belonging to a relatively conserved group was negatively associated with the repertoire of variant surface antigen antibodies carried by the infected child at the time of disease, whereas expression of sequences belonging to another group was associated with the parasite “rosetting” phenotype, a well established virulence determinant. Our results suggest that information on the state of the host–parasite relationship in vivo can be provided by measurements of the differential expression of different var groups, and need only be defined by short stretches of sequence data. |
format | Text |
id | pubmed-1287908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-12879082005-12-01 Plasmodium falciparum Variant Surface Antigen Expression Patterns during Malaria Bull, Peter C Berriman, Matthew Kyes, Sue Quail, Michael A Hall, Neil Kortok, Moses M Marsh, Kevin Newbold, Chris I PLoS Pathog Research Article The variant surface antigens expressed on Plasmodium falciparum–infected erythrocytes are potentially important targets of immunity to malaria and are encoded, at least in part, by a family of var genes, about 60 of which are present within every parasite genome. Here we use semi-conserved regions within short var gene sequence “tags” to make direct comparisons of var gene expression in 12 clinical parasite isolates from Kenyan children. A total of 1,746 var clones were sequenced from genomic and cDNA and assigned to one of six sequence groups using specific sequence features. The results show the following. (1) The relative numbers of genomic clones falling in each of the sequence groups was similar between parasite isolates and corresponded well with the numbers of genes found in the genome of a single, fully sequenced parasite isolate. In contrast, the relative numbers of cDNA clones falling in each group varied considerably between isolates. (2) Expression of sequences belonging to a relatively conserved group was negatively associated with the repertoire of variant surface antigen antibodies carried by the infected child at the time of disease, whereas expression of sequences belonging to another group was associated with the parasite “rosetting” phenotype, a well established virulence determinant. Our results suggest that information on the state of the host–parasite relationship in vivo can be provided by measurements of the differential expression of different var groups, and need only be defined by short stretches of sequence data. Public Library of Science 2005-11 2005-11-18 /pmc/articles/PMC1287908/ /pubmed/16304608 http://dx.doi.org/10.1371/journal.ppat.0010026 Text en Copyright: © 2005 Bull et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bull, Peter C Berriman, Matthew Kyes, Sue Quail, Michael A Hall, Neil Kortok, Moses M Marsh, Kevin Newbold, Chris I Plasmodium falciparum Variant Surface Antigen Expression Patterns during Malaria |
title |
Plasmodium falciparum Variant Surface Antigen Expression Patterns during Malaria |
title_full |
Plasmodium falciparum Variant Surface Antigen Expression Patterns during Malaria |
title_fullStr |
Plasmodium falciparum Variant Surface Antigen Expression Patterns during Malaria |
title_full_unstemmed |
Plasmodium falciparum Variant Surface Antigen Expression Patterns during Malaria |
title_short |
Plasmodium falciparum Variant Surface Antigen Expression Patterns during Malaria |
title_sort | plasmodium falciparum variant surface antigen expression patterns during malaria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1287908/ https://www.ncbi.nlm.nih.gov/pubmed/16304608 http://dx.doi.org/10.1371/journal.ppat.0010026 |
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