Department of Clinical Microbiology and Immunology, Sackler School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.
Department of Energy, Joint Genome Institute, Walnut Creek, California 94598, USA.
Nat Microbiol. 2016 Apr 18;1(6):16047. doi: 10.1038/nmicrobiol.2016.47.
The emergence of mutations following growth-limiting conditions underlies bacterial drug resistance, viral escape from the immune system and fundamental evolution-driven events. Intriguingly, whether mutations are induced by growth limitation conditions or are randomly generated during growth and then selected by growth limitation conditions remains an open question(1). Here, we show that bacteriophage T7 undergoes apparent stress-induced mutagenesis when selected for improved recognition of its host's receptor. In our unique experimental set-up, the growth limitation condition is physically and temporally separated from mutagenesis: growth limitation occurs while phage DNA is outside the host, and spontaneous mutations occur during phage DNA replication inside the host. We show that the selected beneficial mutations are not pre-existing and that the initial slow phage growth is enabled by the phage particle's low-efficiency DNA injection into the host. Thus, the phage particle allows phage populations to initially extend their host range without mutagenesis by virtue of residual recognition of the host receptor. Mutations appear during non-selective intracellular replication, and the frequency of mutant phages increases by natural selection acting on free phages, which are not capable of mutagenesis.
在生长受限条件下出现的突变是细菌耐药性、病毒逃避免疫系统以及基本的进化驱动事件的基础。有趣的是,突变是由生长限制条件诱导的,还是在生长过程中随机产生的,然后被生长限制条件选择,这仍然是一个悬而未决的问题(1)。在这里,我们表明噬菌体 T7 在选择提高对其宿主受体的识别能力时,会经历明显的应激诱导突变。在我们独特的实验设置中,生长限制条件在物理上和时间上与突变分离:噬菌体 DNA 在宿主外时发生生长限制,而自发突变发生在噬菌体 DNA 复制过程中宿主内。我们表明,选择的有益突变不是预先存在的,并且初始缓慢的噬菌体生长是由噬菌体颗粒低效率的 DNA 注入宿主来实现的。因此,噬菌体颗粒允许噬菌体种群通过对宿主受体的残余识别,在不进行突变的情况下,最初扩展其宿主范围。突变出现在非选择性的细胞内复制过程中,并且通过作用于不能进行突变的游离噬菌体的自然选择,突变噬菌体的频率增加。