Origins of sequence diversity in the malaria vaccine candidate merozoite surface protein-2 (MSP-2) in Amazonian isolates of Plasmodium falciparum

被引:16
|
作者
Hoffmann, Erika H. E.
Malafronte, Rosely S.
Moraes-Avila, Sandra L.
Osakabe, Ana Lucia
Wunderlich, Gerhard
Durham, Alan M.
Ribolla, Paulo Eduardo M.
del Portillo, Hernando A.
Ferreira, Marcelo U.
机构
[1] Univ Sao Paulo, Inst Biomed Sci, Dept Parasitol, BR-05508900 Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Inst Trop Med Sao Paulo, BR-05403000 Sao Paulo, SP, Brazil
[3] Univ Sao Paulo, Inst Math & Stat, Dept Comp Sci, BR-05508900 Sao Paulo, SP, Brazil
[4] State Univ Sao Paulo, Inst Biosci Botucatu, Dept Parasitol, BR-18618000 Botucatu, SP, Brazil
[5] Harvard Univ, Dept Organism & Evolutionary Biol, Cambridge, MA 01238 USA
基金
巴西圣保罗研究基金会;
关键词
malaria; MSP-2; recombination; antigenic diversity; replication slippage; gene conversion;
D O I
10.1016/j.gene.2006.03.011
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The recent evolution of Plasmodium falciparum is at odds with the extensive polymorphism found in most genes coding for antigens. Here, we examined the patterns and putative mechanisms of sequence diversification in the merozoite surface protein-2 (MSP-2), a major malarial repetitive surface antigen. We compared the msp-2 gene sequences from closely related clones derived from sympatric parasite isolates from Brazilian Amazonia and used microsatellite typing to examine, in these same clones, the haplotype background of chromosome 2, where msp-2 is located. We found examples of msp-2 sequence rearrangements putatively created by nonreciprocal recombinational events, such as replication slippage and gene conversion, while maintaining the chromosome haplotype. We conclude that these nonreciprocal recombination events may represent a major source of antigenic diversity in MSP-2 in P falciparum populations with low rates of classical meiotic recombination. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:224 / 230
页数:7
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