Greischar Megan A, Read Andrew F, Bjørnstad Ottar N
Center for Infectious Disease Dynamics, Departments of Entomology and Biology, Pennsylvania State University, University Park, Pennsylvania 16802.
Am Nat. 2014 Feb;183(2):E36-49. doi: 10.1086/674357. Epub 2013 Dec 16.
Malaria parasites exhibit great diversity in the coordination of their asexual life cycle within the host, ranging from asynchronous growth to tightly synchronized cycles of invasion and emergence from red blood cells. Synchronized reproduction should come at a high cost--intensifying competition among offspring--so why would some Plasmodium species engage in such behavior and others not? We use a delayed differential equation model to show that synchronized infections can be favored when (1) there is limited interference among parasites competing for red blood cells, (2) transmission success is an accelerating function of sexual parasite abundance, (3) the target of saturating immunity is short-lived, and (4) coinfections with asynchronous parasites are rare. As a consequence, synchrony may be beneficial or costly, in line with the diverse patterns of synchronization observed in natural and lab infections. By allowing us to characterize diverse temporal dynamics, the model framework provides a basis for making predictions about disease severity and for projecting evolutionary responses to interventions.
疟原虫在宿主体内无性生命周期的协调方面表现出极大的多样性,从不同步生长到红细胞入侵和逸出的紧密同步循环。同步繁殖应该付出高昂的代价——加剧后代之间的竞争——那么为什么有些疟原虫物种会有这种行为而其他物种却没有呢?我们使用一个延迟微分方程模型来表明,当(1)竞争红细胞的寄生虫之间干扰有限,(2)传播成功是有性寄生虫丰度的加速函数,(3)饱和免疫的目标寿命短暂,以及(4)与不同步寄生虫的共感染很少见时,同步感染可能会受到青睐。因此,同步可能是有益的或代价高昂的,这与在自然和实验室感染中观察到的不同同步模式一致。通过使我们能够描述不同的时间动态,该模型框架为预测疾病严重程度和预测对干预措施的进化反应提供了基础。