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论寄生虫菌株的进化共存

On the evolutionary coexistence of parasite strains.

作者信息

Pugliese Andrea

机构信息

Dipartimento di Matematica, Università degli Studi di Trento, Via Sommarive 14, 38050 Povo (TN), Italy.

出版信息

Math Biosci. 2002 May-Jun;177-178:355-75. doi: 10.1016/s0025-5564(02)00083-4.

Abstract

Classical models of parasite competition show that coexistence is impossible if different strains give complete cross-immunity. However, parasite coexistence is possible if some of the model assumptions are changed. For instance, coexistence is impossible if density-dependence operates only in hosts' fertility, but surprisingly becomes possible if hosts' mortality is density-dependent. Parasite strains can also coexist if a host already infected with one strain may become infected by another strain (superinfection). I examine here if these reasons for coexistence carry over to evolutionary timescales: in other words, suppose that potentially a continuum of parasite strains may arise by mutations; will evolution arrive at a halt? in that case, will only one or several strains persist? The paradigm and methods of adaptive dynamics are used in this study. It is found, under reasonably general assumptions, that a unique evolutionarily stable state for virulence, alpha(), exist for both models. However, the pattern of the invasibility plots depends on the shape of the trade-off (between virulence and transmissibility, or superinfection rates) functions, and on the host demography. In many cases, the state alpha() is evolutionarily stable only with respect to small mutations, not to larger ones; hence, evolutionary dynamics will bring virulence to alpha(*) only if mutations are sufficiently small; for larger mutations, evolutionary dynamics are more complex and still mainly unresolved.

摘要

经典的寄生虫竞争模型表明,如果不同菌株产生完全交叉免疫,共存是不可能的。然而,如果改变一些模型假设,寄生虫共存是可能的。例如,如果密度依赖仅作用于宿主的繁殖力,共存是不可能的,但令人惊讶的是,如果宿主的死亡率是密度依赖的,共存就有可能。如果已经感染一种菌株的宿主可能被另一种菌株感染(重复感染),寄生虫菌株也可以共存。我在此研究这些共存的原因是否适用于进化时间尺度:换句话说,假设潜在地可能通过突变产生一系列连续的寄生虫菌株;进化会停止吗?在那种情况下,只有一种或几种菌株会持续存在吗?本研究使用了适应性动力学的范式和方法。发现在合理的一般假设下,两种模型都存在一个唯一的毒力进化稳定状态,α*。然而,入侵性图的模式取决于权衡(毒力与传播性或重复感染率之间)函数的形状以及宿主种群统计学。在许多情况下,状态α仅对小突变是进化稳定的,对大突变则不是;因此,只有当突变足够小时,进化动力学才会将毒力带到α;对于大突变,进化动力学更复杂且仍主要未得到解决。

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