Department of Biology, San Diego State University, 5500 Campanile Drive, San Diego, California 92182, USA.
Department of Mathematics and Statistics, San Diego State University, 5500 Campanile Drive, San Diego, California 92182, USA.
Nat Microbiol. 2017 Apr 28;2:17064. doi: 10.1038/nmicrobiol.2017.64.
Temperate bacterial viruses (phages) may enter a symbiosis with their host cell, forming a unit called a lysogen. Infection and viral replication are disassociated in lysogens until an induction event such as DNA damage occurs, triggering viral-mediated lysis. The lysogen-lytic viral reproduction switch is central to viral ecology, with diverse ecosystem impacts. It has been argued that lysogeny is favoured in phages at low host densities. This paradigm is based on the fraction of chemically inducible cells (FCIC) lysogeny proxy determined using DNA-damaging mitomycin C inductions. Contrary to the established paradigm, a survey of 39 inductions publications found FCIC to be highly variable and pervasively insensitive to bacterial host density at global, within-environment and within-study levels. Attempts to determine the source(s) of variability highlighted the inherent complications in using the FCIC proxy in mixed communities, including dissociation between rates of lysogeny and FCIC values. Ultimately, FCIC studies do not provide robust measures of lysogeny or consistent evidence of either positive or negative host density dependence to the lytic-lysogenic switch. Other metrics are therefore needed to understand the drivers of the lytic-lysogenic decision in viral communities and to test models of the host density-dependent viral lytic-lysogenic switch.
温和噬菌体(噬菌体)可能与宿主细胞形成共生关系,形成一个称为溶源体的单位。在溶源体中,感染和病毒复制是分离的,直到发生诱导事件,如 DNA 损伤,触发病毒介导的裂解。溶源体-裂解病毒繁殖开关是病毒生态学的核心,对生态系统有多种影响。有人认为,在宿主密度较低的噬菌体中,溶源体更占优势。这一范式是基于使用 DNA 损伤性丝裂霉素 C 诱导物确定的化学诱导细胞(FCIC)溶源体代理的分数。与既定范式相反,对 39 次诱导研究的调查发现,FCIC 在全球、环境内和研究内水平上高度可变且普遍对细菌宿主密度不敏感。试图确定变异性的来源突出了在混合群落中使用 FCIC 代理的内在复杂性,包括溶源体形成率和 FCIC 值之间的分离。最终,FCIC 研究不能提供溶源体的可靠测量值,也不能提供裂解-溶源体开关的宿主密度依赖性的一致证据。因此,需要其他指标来了解病毒群落中裂解-溶源体决策的驱动因素,并测试宿主密度依赖的病毒裂解-溶源体开关的模型。