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Temperate phages as self-replicating weapons in bacterial competition
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/jtbi.2000.2198openalex-snapshot
Understanding Bacteriophage Therapy as a Density-dependent Kinetic Process
inferredcites →https://doi.org/10.1007/s12275-015-4695-2openalex-snapshot
Microbial ecology in Hydra: Why viruses matter
inferredcites →https://doi.org/10.1016/j.cell.2012.01.035openalex-snapshot
The Impact of the Gut Microbiota on Human Health: An Integrative View
inferredcites →https://doi.org/10.1016/j.cell.2015.01.002openalex-snapshot
Disease-Specific Alterations in the Enteric Virome in Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1016/j.cub.2006.08.089openalex-snapshot
Ecology of Microbial Invasions: Amplification Allows Virus Carriers to Invade More Rapidly When Rare
inferredcites →https://doi.org/10.1016/j.cub.2013.05.038openalex-snapshot
Phage-Mediated Selection on Microbiota of a Long-Lived Host
inferredcites →https://doi.org/10.1016/j.resmic.2008.04.010openalex-snapshot
Phages across the biosphere: contrasts of viruses in soil and aquatic environments
inferredcites →https://doi.org/10.1016/j.tim.2015.12.009openalex-snapshot
The Significance of Mutualistic Phages for Bacterial Ecology and Evolution
inferredcites →https://doi.org/10.1038/ismej.2011.169openalex-snapshot
Evidence of a robust resident bacteriophage population revealed through analysis of the human salivary virome
inferredcites →https://doi.org/10.1038/ismej.2014.239openalex-snapshot
Bacteria–bacteria interactions within the microbiota of the ancestral metazoan Hydra contribute to fungal resistance
inferredcites →https://doi.org/10.1038/ismej.2016.51openalex-snapshot
Temperate phages enhance pathogen fitness in chronic lung infection
inferredcites →https://doi.org/10.1038/nature03891openalex-snapshot
The contribution of species richness and composition to bacterial services
inferredcites →https://doi.org/10.1038/nature08821openalex-snapshot
A human gut microbial gene catalogue established by metagenomic sequencing
inferredcites →https://doi.org/10.1038/nature09199openalex-snapshot
Viruses in the faecal microbiota of monozygotic twins and their mothers
inferredcites →https://doi.org/10.1038/nature11550openalex-snapshot
Diversity, stability and resilience of the human gut microbiota
inferredcites →https://doi.org/10.1038/nature12506openalex-snapshot
Richness of human gut microbiome correlates with metabolic markers
inferredcites →https://doi.org/10.1038/nrmicro.2017.30openalex-snapshot
Ménage à trois in the human gut: interactions between host, bacteria and phages
inferredcites →https://doi.org/10.1038/nrmicro1750openalex-snapshot
Marine viruses — major players in the global ecosystem
inferredcites →https://doi.org/10.1046/j.1462-2920.2003.00539.xopenalex-snapshot
Are viruses driving microbial diversification and diversity?
inferredcites →https://doi.org/10.1067/mcp.2000.109520openalex-snapshot
Phage therapy: The peculiar kinetics of self-replicating pharmaceuticals
inferredcites →https://doi.org/10.1073/pnas.1706879114openalex-snapshot
Host modification of a bacterial quorum-sensing signal induces a phenotypic switch in bacterial symbionts
inferredcites →https://doi.org/10.1098/rsif.2015.0121openalex-snapshot
Which games are growing bacterial populations playing?
inferredcites →https://doi.org/10.1098/rspb.2006.3512openalex-snapshot
Bacteriophage-mediated competition in Bordetella bacteria
inferredcites →https://doi.org/10.1101/gr.122705.111openalex-snapshot
The human gut virome: Inter-individual variation and dynamic response to diet
inferredcites →https://doi.org/10.1101/gr.138297.112openalex-snapshot
CRISPR targeting reveals a reservoir of common phages associated with the human gut microbiome
inferredcites →https://doi.org/10.1111/1462-2920.12923openalex-snapshot
Phage–bacteria interaction network in human oral microbiome
inferredcites →https://doi.org/10.1126/science.aad2602openalex-snapshot
The ecology of the microbiome: Networks, competition, and stability
inferredcites →https://doi.org/10.1128/aem.00950-09openalex-snapshot
Acyl-Homoserine Lactones Can Induce Virus Production in Lysogenic Bacteria: an Alternative Paradigm for Prophage Induction
inferredcites →https://doi.org/10.1128/aem.49.1.19-23.1985openalex-snapshot
Minimum bacterial density for bacteriophage replication: implications for significance of bacteriophages in natural ecosystems
inferredcites →https://doi.org/10.1128/aem.69.1.285-289.2003openalex-snapshot
Elevated Abundance of Bacteriophage Infecting Bacteria in Soil
inferredcites →https://doi.org/10.1128/jb.02230-14openalex-snapshot
Impact of Spontaneous Prophage Induction on the Fitness of Bacterial Populations and Host-Microbe Interactions
inferredcites →https://doi.org/10.1128/jb.185.21.6467-6471.2003openalex-snapshot
Prophage Contribution to Bacterial Population Dynamics
inferredcites →https://doi.org/10.1128/jvi.00865-10openalex-snapshot
Inhibition of Superinfection and the Evolution of Viral Latency
inferredcites →https://doi.org/10.1128/mbio.01790-16openalex-snapshot
Probiotic Diversity Enhances Rhizosphere Microbiome Function and Plant Disease Suppression
inferredcites →https://doi.org/10.1128/mmbr.00034-09openalex-snapshot
Trade-Offs between Competition and Defense Specialists among Unicellular Planktonic Organisms: the “Killing the Winner” Hypothesis Revisited
inferredcites →https://doi.org/10.1146/annurev-ecolsys-120213-091917openalex-snapshot
Biodiversity and Ecosystem Functioning
inferredcites →https://doi.org/10.1186/1472-6785-6-19openalex-snapshot
The impact of phages on interspecific competition in experimental populations of bacteria.
inferredcites →https://doi.org/10.1186/gb-2013-14-7-127openalex-snapshot
Microbiota's 'little helpers': bacteriophages and antibiotic-associated responses in the gut microbiome
inferredcites →https://doi.org/10.1371/journal.pgen.1005861openalex-snapshot
Carriage of λ Latent Virus Is Costly for Its Bacterial Host due to Frequent Reactivation in Monoxenic Mouse Intestine
inferredcites →https://doi.org/10.1371/journal.pone.0059043openalex-snapshot
Temperate Bacterial Viruses as Double-Edged Swords in Bacterial Warfare
inferredcites →https://doi.org/10.1371/journal.pone.0109952openalex-snapshot
Species-Specific Viromes in the Ancestral Holobiont Hydra
inferredcites →https://doi.org/10.1890/0012-9658(2002)083[1537:ecoblt]2.0.co;2openalex-snapshot
ECOSYSTEM CONSEQUENCES OF BIODIVERSITY LOSS: THE EVOLUTION OF A PARADIGM
inferredcites →https://doi.org/10.3354/ame018217openalex-snapshot
Lysogeny and prophage induction in coastal and offshore bacterial communities
inferredcites →https://doi.org/10.3389/fmicb.2015.00320openalex-snapshot
What difference does it make if viruses are strain-, rather than species-specific?
inferredcites →https://doi.org/10.4319/lo.2000.45.6.1320openalex-snapshot
Elements of a theory for the mechanisms controlling abundance, diversity, and biogeochemical role of lytic bacterial viruses in aquatic systems
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1038/s41598-019-39773-3openalex-snapshot
Environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation
inferred← citeshttps://doi.org/10.1101/2020.03.13.990044openalex-snapshot
FITNESS BENEFITS TO BACTERIA OF CARRYING PROPHAGES AND PROPHAGE-ENCODED ANTIBIOTIC-RESISTANCE GENES PEAK IN DIFFERENT ENVIRONMENTS
inferred← citeshttps://doi.org/10.1101/2025.03.28.645916openalex-snapshot
A higher-order equivalence of Lotka-Volterra and replicator dynamics reveals tight connections between ecology and evolution
inferred← citeshttps://doi.org/10.1111/ele.14464openalex-snapshot
Lysogeny destabilizes computationally simulated microbiomes
inferred← citeshttps://doi.org/10.1186/s12915-022-01347-7openalex-snapshot
To kill or to be killed: pangenome analysis of Escherichia coli strains reveals a tailocin specific for pandemic ST131
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