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The population and evolutionary dynamics of bacteriophage: Why be temperate revisited
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.201700112openalex-snapshot
Ecological and Evolutionary Benefits of Temperate Phage: What Does or Doesn't Kill You Makes You Stronger
inferredcites →https://doi.org/10.1006/jtbi.1994.1146openalex-snapshot
The Evolution of Virulence in Parasites and Pathogens: Reconciliation Between Two Competing Hypotheses
inferredcites →https://doi.org/10.1007/bf01310012openalex-snapshot
A long lytic cycle in filamentous phage Cf1tv infectingXanthomonas campestris pv.citri
inferredcites →https://doi.org/10.1016/0022-2836(88)90630-4openalex-snapshot
Maltose transport and starch binding in phage-resistant point mutants of maltoporin
inferredcites →https://doi.org/10.1016/0040-5809(84)90026-1openalex-snapshot
The population biology of bacterial viruses: Why be temperate
inferredcites →https://doi.org/10.1016/0042-6822(57)90022-3openalex-snapshot
Mutations in a temperate bacteriophage affecting its ability to lysogenize Escherichia coli
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.tim.2016.02.008openalex-snapshot
Why Be Temperate: Lessons from Bacteriophage λ
inferredcites →https://doi.org/10.1016/s0022-2836(75)80167-7openalex-snapshot
Reversible interaction between coliphage lambda and its receptor protein
inferredcites →https://doi.org/10.1016/s0065-2911(08)60069-7openalex-snapshot
The Adaptive Responses of Escherichia coli to a Feast and Famine Existence
inferredcites →https://doi.org/10.1038/255735a0openalex-snapshot
λ Lysogens of E. coli reproduce more rapidly than non-lysogens
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/ncomms13333openalex-snapshot
Bacterial viruses enable their host to acquire antibiotic resistance genes from neighbouring cells
inferredcites →https://doi.org/10.1038/s41559-017-0424-zopenalex-snapshot
Phage–host population dynamics promotes prophage acquisition in bacteria with innate immunity
inferredcites →https://doi.org/10.1038/srep10523openalex-snapshot
Well-temperate phage: optimal bet-hedging against local environmental collapses
inferredcites →https://doi.org/10.1046/j.1365-2672.2000.01031.xopenalex-snapshot
Virulence factors of Escherichia coli O157 and other Shiga toxin-producing E. coli
inferredcites →https://doi.org/10.1051/vetres:2001126openalex-snapshot
Molecular characterization, spread and evolution of multidrug resistance in Salmonella enterica Typhimurium DT104
inferredcites →https://doi.org/10.1073/pnas.76.3.1122openalex-snapshot
Mutations reducing the activity of c17, a promoter of phage lambda formed by a tandem duplication.
inferredcites →https://doi.org/10.1086/283134openalex-snapshot
Resource-Limited Growth, Competition, and Predation: A Model and Experimental Studies with Bacteria and Bacteriophage
inferredcites →https://doi.org/10.1086/285929openalex-snapshot
Host-Parasite Coexistence: The Role of Spatial Refuges in Stabilizing Bacteria-Phage Interactions
inferredcites →https://doi.org/10.1093/genetics/71.2.207openalex-snapshot
ON SOME GENETIC ASPECTS OF PHAGE Λ RESISTANCE IN E. COLI K12
inferredcites →https://doi.org/10.1093/genetics/87.2.209openalex-snapshot
THE POPULATION BIOLOGY OF BACTERIAL PLASMIDS: A PRIORI CONDITIONS FOR THE EXISTENCE OF CONJUGATIONALLY TRANSMITTED FACTORS
inferredcites →https://doi.org/10.1093/ve/vez006openalex-snapshot
Viral invasion fitness across a continuum from lysis to latency†
inferredcites →https://doi.org/10.1098/rspb.1997.0178openalex-snapshot
Adaptation to the fitness costs of antibiotic resistance inEscherichia coli
inferredcites →https://doi.org/10.1098/rspb.2006.3512openalex-snapshot
Bacteriophage-mediated competition in Bordetella bacteria
inferredcites →https://doi.org/10.1103/physreve.74.066105openalex-snapshot
Network models of phage-bacteria coevolution
inferredcites →https://doi.org/10.1111/j.1558-5646.1961.tb03139.xopenalex-snapshot
CONDITIONS FOR THE EXISTENCE OF BACTERIOPHAGE
inferredcites →https://doi.org/10.1111/jeb.12291openalex-snapshot
The evolution of resistance against good and bad infections
inferredcites →https://doi.org/10.1126/science.172.3982.480openalex-snapshot
Bacteriophage and the Toxigenicity of Clostridium botulinum Type C
inferredcites →https://doi.org/10.1128/aem.02363-15openalex-snapshot
Abundance of Antibiotic Resistance Genes in Bacteriophage following Soil Fertilization with Dairy Manure or Municipal Biosolids, and Evidence for Potential Transduction
inferredcites →https://doi.org/10.1128/jb.00965-15openalex-snapshot
Population Dynamics of Phage and Bacteria in Spatially Structured Habitats Using Phage λ and Escherichia coli
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/jb.69.1.9-15.1955openalex-snapshot
EVIDENCE FOR THE ACTIVE ROLE OF BACTERIOPHAGE IN THE CONVERSION OF NONTOXIGENIC CORYNEBACTERIUM DIPHTHERIAE TO TOXIN PRODUCTION
inferredcites →https://doi.org/10.1128/jvi.7.5.559-568.1971openalex-snapshot
Virulent Mutants of Bacteriophage P22 I. Isolation and Genetic Analysis
inferredcites →https://doi.org/10.1128/msystems.00191-18openalex-snapshot
Temperate Bacteriophages from Chronic Pseudomonas aeruginosa Lung Infections Show Disease-Specific Changes in Host Range and Modulate Antimicrobial Susceptibility
inferredcites →https://doi.org/10.1146/annurev.mi.03.100149.002103openalex-snapshot
THE GROWTH OF BACTERIAL CULTURES
inferredcites →https://doi.org/10.1179/joc.2001.13.3.331openalex-snapshot
Bacteriophages Transducing Antibiotic Resistance from a Cluster of Lysogenic Strains ofPseudomonas aeruginosaIsolated from Patients
inferredcites →https://doi.org/10.1186/1743-422x-4-121openalex-snapshot
Evolution of temperate pathogens: the bacteriophage/bacteria paradigm
inferredcites →https://doi.org/10.1371/journal.pbio.2005971openalex-snapshot
Leaky resistance and the conditions for the existence of lytic bacteriophage
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.0102507openalex-snapshot
Population Dynamics of a Salmonella Lytic Phage and Its Host: Implications of the Host Bacterial Growth Rate in Modelling
inferredcites →https://doi.org/10.1371/journal.pone.0126915openalex-snapshot
Malthusian Parameters as Estimators of the Fitness of Microbes: A Cautionary Tale about the Low Side of High Throughput
inferredcites →https://doi.org/10.2307/1935611openalex-snapshot
A Complex Community in a Simple Habitat: An Experimental Study with Bacteria and Phage
inferredcites →https://doi.org/10.2307/2406076openalex-snapshot
Conditions for the Existence of Bacteriophage
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/2020.04.08.028340openalex-snapshot
Phage and bacteria diversification through a prophage acquisition ratchet
inferred← citeshttps://doi.org/10.1111/1462-2920.15640openalex-snapshot
The landscape of lysogeny across microbial community density, diversity and energetics
inferred← citeshttps://doi.org/10.1128/msystems.00353-20openalex-snapshot
Quantification of Lysogeny Caused by Phage Coinfections in Microbial Communities from Biophysical Principles
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