| Literature DB >> 28452987 |
Ben Knowles1, Barbara Bailey2, Lance Boling1, Mya Breitbart3, Ana Cobián-Güemes1, Javier Del Campo4, Rob Edwards5,6,7, Ben Felts2, Juris Grasis1, Andreas F Haas1, Parag Katira8, Linda Wegley Kelly1, Antoni Luque2,5,7, Jim Nulton2, Lauren Paul1, Gregory Peters1, Nate Robinett1, Stuart Sandin9, Anca Segall1,7, Cynthia Silveira1, Merry Youle10, Forest Rohwer1,7.
Abstract
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.Entities:
Mesh:
Year: 2017 PMID: 28452987 DOI: 10.1038/nmicrobiol.2017.64
Source DB: PubMed Journal: Nat Microbiol ISSN: 2058-5276 Impact factor: 17.745