Population structuring of multi-copy, antigen-encoding genes in Plasmodium falciparum

被引:23
作者
Artzy-Randrup, Yael [1 ,2 ]
Rorick, Mary M. [1 ,2 ]
Day, Karen [3 ]
Chen, Donald [3 ,4 ]
Dobson, Andrew P. [5 ,6 ]
Pascual, Mercedes [1 ,2 ,6 ]
机构
[1] Howard Hughes Med Inst, Dept Ecol & Evolutionary Biol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Ann Arbor, MI 48109 USA
[3] NYU, Sch Med, Dept Microbiol, Div Med Parasitol, New York, NY 10016 USA
[4] NYU, Sch Med, Dept Med, Div Infect Dis, New York, NY USA
[5] Princeton Univ, Dept Ecol & Evolutionary Biol, Princeton, NJ 08544 USA
[6] Santa Fe Inst, Santa Fe, NM 87501 USA
基金
美国国家卫生研究院; 英国惠康基金;
关键词
ERYTHROCYTE SURFACE-ANTIGENS; CROSS-SPECIES REGULATION; TRANSMISSION DYNAMICS; PARASITIC PROTOZOA; ACQUIRED-IMMUNITY; STRAIN STRUCTURE; CLONAL THEORY; MALARIA; RECOMBINATION; DIVERSITY;
D O I
10.7554/eLife.00093
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The coexistence of multiple independently circulating strains in pathogen populations that undergo sexual recombination is a central question of epidemiology with profound implications for control. An agent-based model is developed that extends earlier 'strain theory' by addressing the var gene family of Plasmodium falciparum. The model explicitly considers the extensive diversity of multicopy genes that undergo antigenic variation via sequential, mutually exclusive expression. It tracks the dynamics of all unique var repertoires in a population of hosts, and shows that even under high levels of sexual recombination, strain competition mediated through cross-immunity structures the parasite population into a subset of coexisting dominant repertoires of var genes whose degree of antigenic overlap depends on transmission intensity. Empirical comparison of patterns of genetic variation at antigenic and neutral sites supports this role for immune selection in structuring parasite diversity.
引用
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页数:17
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