The Ecology and Evolution of Animal Medication: Genetically Fixed Response versus Phenotypic Plasticity

被引:8
|
作者
Choisy, Marc [1 ,2 ,3 ]
de Roode, Jacobus C. [4 ]
机构
[1] Univ Montpellier I, MIVEGEC, Inst Rech Dev, CNRS 5290, Montpellier, France
[2] Univ Montpellier 2, MIVEGEC, Inst Rech Dev, CNRS 5290, Montpellier, France
[3] Univ Oxford, Clin Res Unit, Natl Hosp Trop Dis, Hanoi, Vietnam
[4] Emory Univ, Dept Biol, Atlanta, GA 30322 USA
基金
美国国家科学基金会;
关键词
self-medication; phenotypic plasticity; zoopharmacognosy; ecological immunology; behavioral immunity; disease ecology; SELF-MEDICATION; PROTOZOAN PARASITE; BUTTERFLY-PARASITE; MAHALE MOUNTAINS; PROTEIN COSTS; PLEXIPPUS L; MONARCH; PATHOGEN; RESISTANCE; VIRULENCE;
D O I
10.1086/676928
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Animal medication against parasites can occur either as a genetically fixed (constitutive) or phenotypically plastic (induced) behavior. Taking the tritrophic interaction between the monarch butterfly Danaus plexippus, its protozoan parasite Ophryocystis elektroscirrha, and its food plant Asclepias spp. as a test case, we develop a game-theory model to identify the epidemiological (parasite prevalence and virulence) and environmental (plant toxicity and abundance) conditions that predict the evolution of genetically fixed versus phenotypically plastic forms of medication. Our model shows that the relative benefits (the antiparasitic properties of medicinal food) and costs (side effects of medicine, the costs of searching for medicine, and the costs of plasticity itself) crucially determine whether medication is genetically fixed or phenotypically plastic. Our model suggests that animals evolve phenotypic plasticity when parasite risk (a combination of virulence and prevalence and thus a measure of the strength of parasite-mediated selection) is relatively low to moderately high and genetically fixed medication when parasite risk becomes very high. The latter occurs because at high parasite risk, the costs of plasticity are outweighed by the benefits of medication. Our model provides a simple and general framework to study the conditions that drive the evolution of alternative forms of animal medication.
引用
收藏
页码:S31 / S46
页数:16
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