Frank Steven A
Department of Ecology and Evolutionary Biology, University of California, Irvine, California, 92717.
Evolution. 1993 Dec;47(6):1721-1732. doi: 10.1111/j.1558-5646.1993.tb01264.x.
Hosts and parasites often have extensive genetic diversity for resistance and virulence (host range). Qualitative diversity occurs when the success of attack is an all-or-nothing response that varies according to the genotypes of the host and parasite. Quantitative diversity occurs when the success of attack is a graded response that depends on additive genetic variation in the host and parasite. Community diversity occurs when parasites vary in the success with which they can attack different host species, leading to a mixture of specialists and generalists. I developed a series of models that classify components of host-parasite interactions according to whether they cause stabilizing or disruptive selection for resistance and virulence. Stabilizing selection reduces diversity by favoring a single optimal phenotype. Disruptive selection creates diversity by favoring a mixture of widely separated phenotypes. The evolution of maximal resistance and virulence are opposed by one of three forces: metabolic costs, frequency dependence, or negative genetic correlations among beneficial traits. The models predict that qualitatively inherited resistance and virulence traits typically cause greater diversity than quantitatively inherited traits. However, each natural system is composed of many stabilizing factors that reduce diversity and disruptive factors that promote diversity. I advocate a style of modeling in which families of related assumptions are compared by their equilibrium properties, and general conclusions from equilibrium properties are tested by complete dynamical analysis. The comparison among models highlights the need for empirical studies that compare levels of diversity among related host-parasite systems.
宿主和寄生虫在抗性和毒力(宿主范围)方面往往具有广泛的遗传多样性。当攻击的成功与否是一种全或无的反应,且这种反应因宿主和寄生虫的基因型而异时,就会出现定性多样性。当攻击的成功是一种分级反应,且取决于宿主和寄生虫的加性遗传变异时,就会出现定量多样性。当寄生虫在攻击不同宿主物种的成功程度上存在差异,从而导致专性寄生虫和兼性寄生虫混合存在时,就会出现群落多样性。我开发了一系列模型,根据宿主 - 寄生虫相互作用的组成部分对抗性和毒力是导致稳定选择还是分裂选择进行分类。稳定选择通过青睐单一的最优表型来减少多样性。分裂选择通过青睐广泛分离的表型的混合来创造多样性。最大抗性和毒力的进化受到三种力量之一的对抗:代谢成本、频率依赖性或有益性状之间的负遗传相关性。这些模型预测,定性遗传的抗性和毒力性状通常比定量遗传的性状导致更大的多样性。然而,每个自然系统都由许多减少多样性的稳定因素和促进多样性的分裂因素组成。我提倡一种建模方式,即通过相关假设族的平衡属性进行比较,并通过完整的动力学分析来检验从平衡属性得出的一般结论。模型之间的比较突出了进行实证研究的必要性,这些研究要比较相关宿主 - 寄生虫系统之间的多样性水平。