Plasmodium falciparum variant surface antigen expression patterns during malaria

被引:136
作者
Bull, Peter C.
Berriman, Matthew
Kyes, Sue
Quail, Michael A.
Hall, Neil
Kortok, Moses M.
Marsh, Kevin
Newbold, Chris I.
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Med, Oxford OX3 9DU, England
[2] Wellcome Trust Res Labs, Kenya Med Res Inst Collaborat Programme, Kilifi, Kenya
[3] Wellcome Trust Sanger Inst, Hinxton, England
[4] Inst Genom Res, Rockville, MD USA
基金
英国惠康基金;
关键词
D O I
10.1371/journal.ppat.0010026
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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
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收藏
页码:202 / 213
页数:12
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