Bull James J, Vegge Christina Skovgaard, Schmerer Matthew, Chaudhry Waqas Nasir, Levin Bruce R
The Institute for Cellular and Molecular Biology, The University of Texas, Austin, Texas, United States of America; Center for Computational Biology and Bioinformatics, The University of Texas, Austin, Texas, United States of America; Department of Integrative Biology, The University of Texas, Austin, Texas, United States of America.
Department of Veterinary Disease Biology, University of Copenhagen, Frederiksberg, Denmark.
PLoS One. 2014 Apr 17;9(4):e94690. doi: 10.1371/journal.pone.0094690. eCollection 2014.
The canonical view of phage - bacterial interactions in dense, liquid cultures is that the phage will eliminate most of the sensitive cells; genetic resistance will then ascend to restore high bacterial densities. Yet there are various mechanisms by which bacteria may remain sensitive to phages but still attain high densities in their presence - because bacteria enter a transient state of reduced adsorption. Importantly, these mechanisms may be cryptic and inapparent prior to the addition of phage yet result in a rapid rebound of bacterial density after phage are introduced. We describe mathematical models of these processes and suggest how different types of this 'phenotypic' resistance may be elucidated. We offer preliminary in vitro studies of a previously characterized E. coli model system and Campylobacter jejuni illustrating apparent phenotypic resistance. As phenotypic resistance may be specific to the receptors used by phages, awareness of its mechanisms may identify ways of improving the choice of phages for therapy. Phenotypic resistance can also explain several enigmas in the ecology of phage-bacterial dynamics. Phenotypic resistance does not preclude the evolution of genetic resistance and may often be an intermediate step to genetic resistance.
在密集的液体培养物中,噬菌体与细菌相互作用的传统观点是,噬菌体将消除大多数敏感细胞;然后遗传抗性会上升以恢复高细菌密度。然而,细菌可能通过多种机制在噬菌体存在的情况下仍保持敏感但仍能达到高密度——因为细菌进入了吸附减少的短暂状态。重要的是,这些机制在添加噬菌体之前可能是隐蔽且不明显的,但在引入噬菌体后会导致细菌密度迅速反弹。我们描述了这些过程的数学模型,并提出了如何阐明不同类型的这种“表型”抗性。我们提供了对先前表征的大肠杆菌模型系统和空肠弯曲菌的初步体外研究,说明了明显的表型抗性。由于表型抗性可能特定于噬菌体使用的受体,了解其机制可能会找到改善噬菌体治疗选择的方法。表型抗性还可以解释噬菌体 - 细菌动力学生态学中的几个谜团。表型抗性并不排除遗传抗性的进化,并且通常可能是遗传抗性的中间步骤。