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A Host-Produced Quorum-Sensing Autoinducer Controls a Phage Lysis-Lysogeny Decision

https://doi.org/10.1016/j.cell.2018.10.059

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Autodigestion of lexA and phage lambda repressors.

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A satellite phage‐encoded antirepressor induces repressor aggregation and cholera toxin gene transfer

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Toxin-coregulated pilus, but not mannose-sensitive hemagglutinin, is required for colonization by Vibrio cholerae O1 El Tor biotype and O139 strains

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The Antirepressor Needed for Induction of Linear Plasmid-Prophage N15 Belongs to the SOS Regulon

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The Transcriptional Regulator VqmA Increases Expression of the Quorum-Sensing Activator HapR in Vibrio cholerae

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The Linear Plasmid Prophage Vp58.5 of Vibrio parahaemolyticus Is Closely Related to the Integrating Phage VHML and Constitutes a New Incompatibility Group of Telomere Phages

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Replication and Maintenance of Linear Phage-Plasmid N15

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Phage-bacterial interactions in the evolution of toxigenicVibrio cholerae

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Should I stay or should I go: transmission trade-offs in phages and plasmids

inferred← citeshttps://doi.org/10.1016/j.tim.2026.05.019openalex-snapshot

Beyond AMGs: Phage-encoded transcription and sigma factors as understudied virocell reprogramming tools

inferred← citeshttps://doi.org/10.1016/j.vetmic.2026.111028openalex-snapshot

Isolation of lytic phage and its inhibition of multidrug-resistant Salmonella and its biofilm

inferred← citeshttps://doi.org/10.1016/j.virol.2024.110209openalex-snapshot

A game of resistance: War between bacteria and phages and how phage cocktails can be the solution

inferred← citeshttps://doi.org/10.1016/j.virusres.2019.197759openalex-snapshot

Resistance mechanisms adopted by a Salmonella Typhimurium mutant against bacteriophage

inferred← citeshttps://doi.org/10.1016/j.watres.2024.121620openalex-snapshot

Phage phylogeny, molecular signaling, and auxiliary antimicrobial resistance in aerobic and anaerobic membrane bioreactors

inferred← citeshttps://doi.org/10.1016/j.watres.2026.126466openalex-snapshot

Viral suppression constrains environmentally stimulated microbial methylmercury production in wastewater treatment plants

inferred← citeshttps://doi.org/10.1021/acs.accounts.8b00576openalex-snapshot

Going Viral: Emerging Opportunities for Phage-Based Bacterial Control in Water Treatment and Reuse

inferred← citeshttps://doi.org/10.1021/acs.est.2c08443openalex-snapshot

Prophage Induction Causes Geobacter Electroactive Biofilm Decay

inferred← citeshttps://doi.org/10.1021/acs.nanolett.1c01062openalex-snapshot

Deciphering Single-Bacterium Adhesion Behavior Modulated by Extracellular Electron Transfer

inferred← citeshttps://doi.org/10.1021/acscentsci.9b01076openalex-snapshot

Characterization of Autoinducer-3 Structure and Biosynthesis in E. coli

inferred← citeshttps://doi.org/10.1021/acschembio.5c00932openalex-snapshot

Multiple Adenylate-Forming Enzymes Contribute to Biosynthesis of the DPO Quorum-Sensing Autoinducer

inferred← citeshttps://doi.org/10.1021/acssynbio.2c00314openalex-snapshot

Intestinal Engineered Probiotics as Living Therapeutics: Chassis Selection, Colonization Enhancement, Gene Circuit Design, and Biocontainment

inferred← citeshttps://doi.org/10.1021/jacs.1c01275openalex-snapshot

A Metabolite of Pseudomonas Triggers Prophage-Selective Lysogenic to Lytic Conversion in Staphylococcus aureus

inferred← citeshttps://doi.org/10.1038/d41586-019-01880-6openalex-snapshot

The secret social lives of viruses

inferred← citeshttps://doi.org/10.1038/s41396-019-0469-xopenalex-snapshot

Microbe-driven chemical ecology: past, present and future

inferred← citeshttps://doi.org/10.1038/s41396-020-00870-1openalex-snapshot

Host population diversity as a driver of viral infection cycle in wild populations of green sulfur bacteria with long standing virus-host interactions

inferred← citeshttps://doi.org/10.1038/s41396-020-0641-3openalex-snapshot

High cell densities favor lysogeny: induction of an H20 prophage is repressed by quorum sensing and enhances biofilm formation in Vibrio anguillarum

inferred← citeshttps://doi.org/10.1038/s41396-021-00946-6openalex-snapshot

The effect of Quorum sensing inhibitors on the evolution of CRISPR-based phage immunity in Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1038/s41396-021-01097-4openalex-snapshot

Highly diverse flavobacterial phages isolated from North Sea spring blooms

inferred← citeshttps://doi.org/10.1038/s41396-023-01529-3openalex-snapshot

Coevolution between marine Aeromonas and phages reveals temporal trade-off patterns of phage resistance and host population fitness

inferred← citeshttps://doi.org/10.1038/s41423-020-00532-4openalex-snapshot

Phages and their potential to modulate the microbiome and immunity

inferred← citeshttps://doi.org/10.1038/s41467-020-18078-4openalex-snapshot

Temperate infection in a virus–host system previously known for virulent dynamics

inferred← citeshttps://doi.org/10.1038/s41467-021-26520-4openalex-snapshot

Lateral transduction is inherent to the life cycle of the archetypical Salmonella phage P22

inferred← citeshttps://doi.org/10.1038/s41467-022-33771-2openalex-snapshot

Response of soil viral communities to land use changes

inferred← citeshttps://doi.org/10.1038/s41467-023-37512-xopenalex-snapshot

Mutation-induced infections of phage-plasmids

inferred← citeshttps://doi.org/10.1038/s41467-023-40724-wopenalex-snapshot

Next-generation proteomics for quantitative Jumbophage-bacteria interaction mapping

inferred← citeshttps://doi.org/10.1038/s41467-024-51913-6openalex-snapshot

Using bacterial population dynamics to count phages and their lysogens

inferred← citeshttps://doi.org/10.1038/s41467-025-61946-0openalex-snapshot

Gut Phage Biobank: a collection of bacteriophages targeting human commensal bacteria

inferred← citeshttps://doi.org/10.1038/s41467-026-71398-9openalex-snapshot

Complex temporal dynamics of phage-bacteria populations in an animal-associated marine system

inferred← citeshttps://doi.org/10.1038/s41522-025-00727-5openalex-snapshot

Bacteriophage-driven microbial phenotypic heterogeneity: ecological and biogeochemical importance

inferred← citeshttps://doi.org/10.1038/s41522-025-00886-5openalex-snapshot

DPO production by gut commensals suggests a broader role in bacterial communication and host-microbiome interactions

inferred← citeshttps://doi.org/10.1038/s41564-022-01128-6openalex-snapshot

Widespread stop-codon recoding in bacteriophages may regulate translation of lytic genes

inferred← citeshttps://doi.org/10.1038/s41564-023-01550-4openalex-snapshot

Antagonistic interactions between phage and host factors control arbitrium lysis–lysogeny decision

inferred← citeshttps://doi.org/10.1038/s41579-021-00530-xopenalex-snapshot

Revisiting the rules of life for viruses of microorganisms

inferred← citeshttps://doi.org/10.1038/s41579-026-01318-7openalex-snapshot

Revisiting the life cycle of temperate phages

inferred← citeshttps://doi.org/10.1038/s41586-019-1894-8openalex-snapshot

The arms race between bacteria and their phage foes

inferred← citeshttps://doi.org/10.1038/s41586-022-04444-3openalex-snapshot

The bacterial toxin colibactin triggers prophage induction

inferred← citeshttps://doi.org/10.1038/s41586-023-06376-yopenalex-snapshot

Small protein modules dictate prophage fates during polylysogeny

inferred← citeshttps://doi.org/10.1038/s41586-024-07396-yopenalex-snapshot

Ligand cross-feeding resolves bacterial vitamin B12 auxotrophies

inferred← citeshttps://doi.org/10.1038/s41586-025-09260-zopenalex-snapshot

Prophages block cell surface receptors to preserve their viral progeny

inferred← citeshttps://doi.org/10.1038/s41586-025-09614-7openalex-snapshot

Isolation, engineering and ecology of temperate phages from the human gut

inferred← citeshttps://doi.org/10.1038/s41598-022-07763-7openalex-snapshot

Genetic analysis of the cold-sensitive growth phenotype of Burkholderia pseudomallei/thailandensis bacteriophage AMP1

inferred← citeshttps://doi.org/10.1038/s41598-023-42505-3openalex-snapshot

Bacteriophages with depolymerase activity in the control of antibiotic resistant Klebsiella pneumoniae biofilms

inferred← citeshttps://doi.org/10.1038/s41598-024-68747-3openalex-snapshot

Serratia marcescens ATCC 274 increases production of the red pigment prodigiosin in response to Chi phage infection

inferred← citeshttps://doi.org/10.1038/s41598-024-70056-8openalex-snapshot

Nanomechanical resilience and thermal stability of RSJ2 phage

inferred← citeshttps://doi.org/10.1038/s42003-024-07038-zopenalex-snapshot

Growth stage-related capsular polysaccharide translocon Wza in Vibrio splendidus modifies phage vB_VspM_VS2 susceptibility

inferred← citeshttps://doi.org/10.1038/s42003-025-07608-9openalex-snapshot

A review of quorum-sensing and its role in mediating interkingdom interactions in the ocean

inferred← citeshttps://doi.org/10.1038/s43705-023-00299-5openalex-snapshot

Slow growing bacteria survive bacteriophage in isolation

inferred← citeshttps://doi.org/10.1039/d2ew00755jopenalex-snapshot

Emerging investigator series: the role of phage lifestyle in wastewater microbial community structures and functions: insights into diverse microbial environments

inferred← citeshttps://doi.org/10.1039/d4tb01685hopenalex-snapshot

Bioinspired peptide/polyamino acid assemblies as quorum sensing inhibitors for the treatment of bacterial infections

inferred← citeshttps://doi.org/10.1039/d5np00014aopenalex-snapshot

Natural products influence bacteriophage infectivity

inferred← citeshttps://doi.org/10.1042/ebc20240014openalex-snapshot

Characteristics of phage-plasmids and their impact on microbial communities

inferred← citeshttps://doi.org/10.1051/medsci/2020215openalex-snapshot

Un bactériophage exploite le système de communication de son hôte bactérien pour entrer en cycle lytique

inferred← citeshttps://doi.org/10.1071/ma19009openalex-snapshot

Future prospects of structural studies to advance our understanding of phage biology

inferred← citeshttps://doi.org/10.1071/mav40n1openalex-snapshot

Volume 40 Number 1

inferred← citeshttps://doi.org/10.1073/pnas.2104163118openalex-snapshot

Bacteriophage self-counting in the presence of viral replication

inferred← citeshttps://doi.org/10.1073/pnas.2117748119openalex-snapshot

Historical contingencies and phage induction diversify bacterioplankton communities at the microscale

inferred← citeshttps://doi.org/10.1073/pnas.2417058122openalex-snapshot

Spatial propagation of temperate phages within and among biofilms

inferred← citeshttps://doi.org/10.1073/pnas.2526952123openalex-snapshot

Social cues drive the evolution of plastic pathogen virulence in spatially and temporally variable environments

inferred← citeshttps://doi.org/10.1074/jbc.ra118.006082openalex-snapshot

Crystal structure of the Vibrio cholerae VqmA–ligand–DNA complex provides insight into ligand-binding mechanisms relevant for drug design

inferred← citeshttps://doi.org/10.1074/jbc.ra119.012104openalex-snapshot

Mechanism underlying autoinducer recognition in the Vibrio cholerae DPO-VqmA quorum-sensing pathway

inferred← citeshttps://doi.org/10.1080/10408398.2023.2214818openalex-snapshot

A critical review of novel antibiotic resistance prevention approaches with a focus on postbiotics

inferred← citeshttps://doi.org/10.1080/19420889.2023.2196145openalex-snapshot

Cellular and Natural Viral Engineering in Cognition-Based Evolution

inferred← citeshttps://doi.org/10.1080/19490976.2021.1937015openalex-snapshot

The Interface of Vibrio cholerae and the Gut Microbiome

inferred← citeshttps://doi.org/10.1080/19490976.2023.2298254openalex-snapshot

Isolation and characterization of a novel lytic Parabacteroides distasonis bacteriophage φPDS1 from the human gut

inferred← citeshttps://doi.org/10.1080/19490976.2025.2481178openalex-snapshot

Effects of bacteriophages on gut microbiome functionality

inferred← citeshttps://doi.org/10.1080/20002297.2024.2344272openalex-snapshot

A review and new perspective on oral bacteriophages: manifestations in the ecology of oral diseases

inferred← citeshttps://doi.org/10.1080/21505594.2020.1845039openalex-snapshot

Pathogenicity and virulence regulation of Vibrio cholerae at the interface of host-gut microbiome interactions

inferred← citeshttps://doi.org/10.1080/21505594.2021.2022276openalex-snapshot

A temperate Siphoviridae bacteriophage isolate from Siberian tiger enhances the virulence of methicillin-resistant Staphylococcus aureus through distinct mechanisms

inferred← citeshttps://doi.org/10.1093/evolut/qpag061openalex-snapshot

Responsive lysogeny under nonproductive phage binding

inferred← citeshttps://doi.org/10.1093/femsec/fiz053openalex-snapshot

Gene mobility in microbiomes of the mycosphere and mycorrhizosphere –role of plasmids and bacteriophages

inferred← citeshttps://doi.org/10.1093/femsml/uqac026openalex-snapshot

The New Microbiology: an international lecture course on the island of Spetses

inferred← citeshttps://doi.org/10.1093/femsml/uqad030openalex-snapshot

Small regulatory RNAs in Vibrio cholerae

inferred← citeshttps://doi.org/10.1093/femsre/fuaa017openalex-snapshot

Current challenges and future opportunities of phage therapy

inferred← citeshttps://doi.org/10.1093/femsre/fuaa041openalex-snapshot

Bacteriophages as drivers of bacterial virulence and their potential for biotechnological exploitation

inferred← citeshttps://doi.org/10.1093/femsre/fuab048openalex-snapshot

Mechanisms and clinical importance of bacteriophage resistance

inferred← citeshttps://doi.org/10.1093/femsre/fuac024openalex-snapshot

Trans-kingdom interactions in mixed biofilm communities

inferred← citeshttps://doi.org/10.1093/femsre/fuad029openalex-snapshot

Microbiota and fungal-bacterial interactions in the cystic fibrosis lung

inferred← citeshttps://doi.org/10.1093/femsre/fuaf061openalex-snapshot

Phage cocktails: state-of-the-art technologies and strategies for effective design

inferred← citeshttps://doi.org/10.1093/femsre/fuaf067openalex-snapshot

Spatial structure: shaping the ecology and evolution of microbial communities

inferred← citeshttps://doi.org/10.1093/jacamr/dlae017openalex-snapshot

Improving phage therapy by evasion of phage resistance mechanisms

inferred← citeshttps://doi.org/10.1093/molbev/msad062openalex-snapshot

Large-Scale Identification of Known and Novel RRNPP Quorum-Sensing Systems by RRNPP_Detector Captures Novel Features of Bacterial, Plasmidic, and Viral Coevolution

inferred← citeshttps://doi.org/10.1093/nar/gkaf652openalex-snapshot

The extended mobility of plasmids

inferred← citeshttps://doi.org/10.1093/nar/gkag901openalex-snapshot

The molecular basis of ADP-ribose pyrophosphorylation by a phage PRPS-like enzyme in NAD+ reconstitution

showing the first 200 of 365

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