抗生素诱导的形态变化增强了噬菌体的捕食:结构化环境中斑块形成的数学模型

Julian Bulssico, Swapnesh Panigrahi, Nicolas Ginet, Mireille Ansaldi
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摘要

噬菌体在固体培养基中感染的一个独特表现是出现裂解斑块,与细菌草坪的环状变薄相对应。在斑块形成过程中,噬菌体从单个感染点开始进行连续的循环复制,并在固定细菌宿主的基质中呈放射状扩散。影响菌斑大小的因素有很多,如繁殖基质的成分和网状结构、噬菌体的特性,以及与细菌宿主生理有关的参数。由于抗生素和噬菌体的联合用药是一种常见的治疗方法,我们的研究重点是抗生素对噬菌体捕食的影响,这可能对噬菌体的治疗应用至关重要。亚致死浓度会极大地影响细菌的生理机能,使噬菌体更快地传播,从而更好地消灭细菌。以前的实验工作主要关注噬菌体的特性。然而,由于斑块的形成受宿主生长动态的影响很大,因此需要一个综合了宿主生长和噬菌体感染参数的全面模型。我们认为,斑块的扩大与宿主的形态变化有关,而宿主的形态变化会影响流行病的传播速度和噬菌体在基质中的扩散。为了支持这一假设,我们对两种不同噬菌体和细菌在各种抗生素存在下的半固体培养基中的生长参数进行了描述。通过综合这些数据,我们建立了一个数学模型来解释这些观察结果,并解释了当宿主形态受到影响时斑块体积增大的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antibiotic-Induced Morphological Changes Enhance Phage Predation: A Mathematical Model of Plaque Formation in Structured Environments
A distinctive manifestation of phage infection in solid media is the appearance of lysis plaques, corresponding to the circular thinning of a bacterial lawn. During plaque formation, successive cycles of phage replication take place from a single point of infection and spread radially in a matrix of immobilized bacterial hosts. Many factors affect plaque size, such as the composition and the reticulation of the propagation matrix, the characteristics of the phage, but also parameters related to the physiology of the bacterial host. As the combined administration of antibiotics and phages is a common practice in compassionate treatments, our research focuses on the effects of antibiotics on phage predation, which may be of crucial importance for phage therapeutic applications. Sublethal concentrations can drastically affect bacterial physiology, allowing phages to spread more rapidly and resulting in better bacterial eradication. Previous experimental work has focused on the phage characteristics. However, as plaque formation is strongly influenced by host growth dynamics, a comprehensive model integrating both the host growth and phage infection parameters is required. We suggest that plaque enlargement is linked to morphological changes of the host that have an impact on the rate of epidemic propagation and on phage diffusion into the matrix. To support this hypothesis, we characterized the growth parameters of two different phages and bacteria in semi-solid media in the presence of various antibiotics. By combining these data, we have produced a mathematical model that accounts for these observations and explains the increase in plaque size when the host morphology is affected.
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