Institute for Modeling Collaboration and Innovation, University of Idaho, Moscow, Idaho, USA.
Department of Biological Sciences, University of Idaho, Moscow, Idaho, USA.
Appl Environ Microbiol. 2024 Nov 20;90(11):e0088424. doi: 10.1128/aem.00884-24. Epub 2024 Oct 30.
Various directed evolution methods exist that seek to procure bacteriophages with expanded host ranges, typically targeting phage-resistant or non-permissive bacterial hosts. The general premise of these methods involves propagating phage(s) on multiple bacterial hosts, pooling the lysate, and repeating this process until phage(s) can form plaques on the target host(s). In theory, this produces a lysate containing input phages and their evolved phage progeny. However, in practice, this lysate can also include prophages originating from bacterial hosts. Here, we describe our experience implementing one directed evolution method, the Appelmans protocol, to study phage evolution in the phage-host system, where we observed rapid host-range expansion of the phage cocktail. Further experimentation and sequencing revealed that the observed host-range expansion was due to a prophage originating from a lysogenic host that was only included in the first three rounds of the experiment. This prophage could infect five of eight bacterial hosts initially used, allowing it to persist and proliferate until the termination of the experiment. This prophage was represented in half of the sequenced phage samples isolated from the Appelmans experiment, but despite being subjected to directed evolution conditions, it does not appear to have evolved. This work highlights the impact of prophages in directed evolution experiments and the importance of genetically verifying output phages, particularly for those attempting to procure phages intended for phage therapy applications. This study also notes the usefulness of intraspecies antagonism assays between bacterial host strains to establish a baseline for inhibitory activity and determine the presence of prophage.IMPORTANCEDirected evolution is a common strategy for evolving phages to expand the host range, often targeting pathogenic strains of bacteria. In this study, we investigated phage host-range expansion using directed evolution in the system. We show that prophages are active players in directed evolution and can contribute to observation of host-range expansion. Since prophages are prevalent in bacterial hosts, particularly pathogenic strains of bacteria, and all directed evolution approaches involve iteratively propagating phage on one or more bacterial hosts, the presence of prophage in phage preparations is a factor that needs to be considered in experimental design and interpretation of results. These results highlight the importance of screening for prophages either genetically or through intraspecies antagonism assays during selection of bacterial strains and will contribute to improving the experimental design of future directed evolution studies.
存在各种定向进化方法,旨在获得宿主范围扩大的噬菌体,通常针对具有抗噬菌体或非允许性的细菌宿主。这些方法的一般前提是在多个细菌宿主上繁殖噬菌体,混合裂解物,并重复此过程,直到噬菌体能够在目标宿主上形成噬菌斑。理论上,这会产生含有输入噬菌体及其进化的噬菌体后代的裂解物。然而,实际上,这种裂解物也可能包含来自细菌宿主的原噬菌体。在这里,我们描述了实施一种定向进化方法(即 Appelmans 方案)的经验,以研究噬菌体在噬菌体-宿主系统中的进化,我们观察到噬菌体鸡尾酒的宿主范围迅速扩大。进一步的实验和测序表明,观察到的宿主范围扩大是由于来自溶原宿主的原噬菌体引起的,该原噬菌体仅包含在实验的前三轮中。该原噬菌体可以感染最初使用的八个细菌宿主中的五个,使其能够持续增殖,直到实验结束。该原噬菌体在从 Appelmans 实验中分离的一半测序噬菌体样本中都有出现,但尽管受到定向进化条件的影响,它似乎并没有进化。这项工作强调了原噬菌体在定向进化实验中的影响,以及对输出噬菌体进行遗传验证的重要性,特别是对于那些试图获得用于噬菌体治疗应用的噬菌体的人。本研究还指出了在细菌宿主菌株之间进行种内拮抗测定的有用性,以建立抑制活性的基线,并确定原噬菌体的存在。
重要性
定向进化是一种常用的策略,用于扩大噬菌体的宿主范围,通常针对细菌的致病性菌株。在本研究中,我们使用 系统研究了噬菌体的宿主范围扩展。我们表明,原噬菌体是定向进化中的活跃参与者,并可以促进宿主范围扩展的观察。由于原噬菌体在细菌宿主中很普遍,特别是在细菌的致病性菌株中,并且所有定向进化方法都涉及在一个或多个细菌宿主上迭代地繁殖噬菌体,因此噬菌体制剂中原噬菌体的存在是在实验设计和结果解释中需要考虑的一个因素。这些结果强调了在选择细菌菌株时进行遗传筛选或通过种内拮抗测定筛选原噬菌体的重要性,并将有助于改进未来定向进化研究的实验设计。