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Transcriptome responses of intestinal epithelial cells induced by membrane vesicles of Listeria monocytogenes unveil novel insights into the host-pathogen cross talk

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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/pmic.200900338openalex-snapshot

Gram‐positive bacteria produce membrane vesicles: Proteomics‐based characterization of Staphylococcus aureus ‐derived membrane vesicles

inferredcites →https://doi.org/10.1016/b978-0-12-394590-7.00002-6openalex-snapshot

Innate Immune Pathways Triggered by Listeria monocytogenes and Their Role in the Induction of Cell-Mediated Immunity

inferredcites →https://doi.org/10.1016/j.addr.2007.11.004openalex-snapshot

Recognition of viral single-stranded RNA by Toll-like receptors☆

inferredcites →https://doi.org/10.1016/j.ijmm.2014.02.006openalex-snapshot

Membrane vesicles of Clostridium perfringens type A strains induce innate and adaptive immunity

inferredcites →https://doi.org/10.1016/j.ijmm.2019.03.008openalex-snapshot

Comprehensive proteomic analysis and pathogenic role of membrane vesicles of Listeria monocytogenes serotype 4b reveals proteins associated with virulence and their possible interaction with host

inferredcites →https://doi.org/10.1016/j.micinf.2007.05.011openalex-snapshot

The epidemiology of human listeriosis

inferredcites →https://doi.org/10.1016/j.ygeno.2008.07.001openalex-snapshot

Applications of next-generation sequencing technologies in functional genomics

inferredcites →https://doi.org/10.1038/nmeth.2811openalex-snapshot

BoxPlotR: a web tool for generation of box plots

inferredcites →https://doi.org/10.1038/nmeth.3317openalex-snapshot

HISAT: a fast spliced aligner with low memory requirements

inferredcites →https://doi.org/10.1038/nprot.2008.211openalex-snapshot

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

inferredcites →https://doi.org/10.1038/nrg2484openalex-snapshot

RNA-Seq: a revolutionary tool for transcriptomics

inferredcites →https://doi.org/10.1073/pnas.1008843107openalex-snapshot

Bacillus anthracis produces membrane-derived vesicles containing biologically active toxins

inferredcites →https://doi.org/10.1084/jem.20041215openalex-snapshot

Anthrolysin O and Other Gram-positive Cytolysins Are Toll-like Receptor 4 Agonists

inferredcites →https://doi.org/10.1086/315214openalex-snapshot

Pro‐ versus Anti‐inflammatory Cytokine Profile in Patients with Severe Sepsis: A Marker for Prognosis and Future Therapeutic Options

inferredcites →https://doi.org/10.1093/bioinformatics/btn654openalex-snapshot

bioDBnet: the biological database network

inferredcites →https://doi.org/10.1093/bioinformatics/btt656openalex-snapshot

featureCounts: an efficient general purpose program for assigning sequence reads to genomic features

inferredcites →https://doi.org/10.1093/bioinformatics/btu170openalex-snapshot

Trimmomatic: a flexible trimmer for Illumina sequence data

inferredcites →https://doi.org/10.1093/nar/gks1055openalex-snapshot

The ConsensusPathDB interaction database: 2013 update

inferredcites →https://doi.org/10.1093/nar/gkw419openalex-snapshot

Heatmapper: web-enabled heat mapping for all

inferredcites →https://doi.org/10.1111/cmi.12445openalex-snapshot

Modulation of the host innate immune and inflammatory response by translocated bacterial proteins

inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05522.xopenalex-snapshot

Release of outer membrane vesicles by Gram‐negative bacteria is a novel envelope stress response

inferredcites →https://doi.org/10.1111/j.1469-0691.2009.03109.xopenalex-snapshot

Listeriosis: a resurgent foodborne infection

inferredcites →https://doi.org/10.1128/aem.67.6.2692-2698.2001openalex-snapshot

Analysis of the Role of OpuC, an Osmolyte Transport System, in Salt Tolerance and Virulence Potential of Listeria monocytogenes

inferredcites →https://doi.org/10.1128/iai.00532-10openalex-snapshot

Listeria monocytogenesPrsA2 Is Required for Virulence Factor Secretion and Bacterial Viability within the Host Cell Cytosol

inferredcites →https://doi.org/10.1128/iai.01365-15openalex-snapshot

Cytotoxic and Inflammatory Responses Induced by Outer Membrane Vesicle-Associated Biologically Active Proteases from Vibrio cholerae

inferredcites →https://doi.org/10.1128/iai.03012-14openalex-snapshot

Transcriptomic and Proteomic Analyses Reveal Key Innate Immune Signatures in the Host Response to the Gastrointestinal Pathogen Campylobacter concisus

inferredcites →https://doi.org/10.1128/jb.01493-14openalex-snapshot

Streptococcus mutans Extracellular DNA Is Upregulated during Growth in Biofilms, Actively Released via Membrane Vesicles, and Influenced by Components of the Protein Secretion Machinery

inferredcites →https://doi.org/10.1128/mbio.00207-16openalex-snapshot

A Two-Component Regulatory System Impacts Extracellular Membrane-Derived Vesicle Production in Group A Streptococcus

inferredcites →https://doi.org/10.1128/mbio.01188-17openalex-snapshot

Inflammasome Activation by Bacterial Outer Membrane Vesicles Requires Guanylate Binding Proteins

inferredcites →https://doi.org/10.1128/mmbr.00031-09openalex-snapshot

Virulence and Immunomodulatory Roles of Bacterial Outer Membrane Vesicles

inferredcites →https://doi.org/10.1146/annurev.immunol.21.120601.141126openalex-snapshot

Toll-Like Receptors

inferredcites →https://doi.org/10.1146/annurev.micro.091208.073413openalex-snapshot

Biological Functions and Biogenesis of Secreted Bacterial Outer Membrane Vesicles

inferredcites →https://doi.org/10.1186/gb-2002-4-1-r2openalex-snapshot

A gene-expression program reflecting the innate immune response of cultured intestinal epithelial cells to infection by Listeria monocytogenes

inferredcites →https://doi.org/10.1186/s12575-017-0052-7openalex-snapshot

LncRNAs and immunity: watchdogs for host pathogen interactions

inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

inferredcites →https://doi.org/10.1371/journal.pone.0027958openalex-snapshot

Staphylococcus aureus Produces Membrane-Derived Vesicles That Induce Host Cell Death

inferredcites →https://doi.org/10.1371/journal.pone.0041645openalex-snapshot

Deep Sequencing-Based Transcriptome Analysis of Chicken Spleen in Response to Avian Pathogenic Escherichia coli (APEC) Infection

inferredcites →https://doi.org/10.1371/journal.pone.0054661openalex-snapshot

Staphylococcus aureus α-Toxin-Dependent Induction of Host Cell Death by Membrane-Derived Vesicles

inferredcites →https://doi.org/10.1371/journal.pone.0073196openalex-snapshot

Transcription Factor σB Plays an Important Role in the Production of Extracellular Membrane-Derived Vesicles in Listeria monocytogenes

inferredcites →https://doi.org/10.1371/journal.pone.0106731openalex-snapshot

Outer Membrane Vesicles Mediate Transport of Biologically Active Vibrio cholerae Cytolysin (VCC) from V. cholerae Strains

inferredcites →https://doi.org/10.1371/journal.pone.0130528openalex-snapshot

Isolation, Characterization and Biological Properties of Membrane Vesicles Produced by the Swine Pathogen Streptococcus suis

inferredcites →https://doi.org/10.1371/journal.ppat.1000382openalex-snapshot

Long-Distance Delivery of Bacterial Virulence Factors by Pseudomonas aeruginosa Outer Membrane Vesicles

inferredcites →https://doi.org/10.1371/journal.ppat.1004470openalex-snapshot

Listeria monocytogenes Dampens the DNA Damage Response

inferredcites →https://doi.org/10.1371/journal.ppat.1005262openalex-snapshot

RNA-seq Brings New Insights to the Intra-Macrophage Transcriptome of Salmonella Typhimurium

inferredcites →https://doi.org/10.1371/journal.ppat.1005592openalex-snapshot

Legionella pneumophila-Derived Outer Membrane Vesicles Promote Bacterial Replication in Macrophages

inferredcites →https://doi.org/10.1371/journal.ppat.1005816openalex-snapshot

Membrane Vesicles of Group B Streptococcus Disrupt Feto-Maternal Barrier Leading to Preterm Birth

inferredcites →https://doi.org/10.1371/journal.ppat.1006159openalex-snapshot

Host cell interactions of outer membrane vesicle-associated virulence factors of enterohemorrhagic Escherichia coli O157: Intracellular delivery, trafficking and mechanisms of cell injury

inferredcites →https://doi.org/10.1371/journal.ppat.1006734openalex-snapshot

Listeria monocytogenes switches from dissemination to persistence by adopting a vacuolar lifestyle in epithelial cells

inferredcites →https://doi.org/10.3389/fcimb.2016.00107openalex-snapshot

Hijacking Host Cell Highways: Manipulation of the Host Actin Cytoskeleton by Obligate Intracellular Bacterial Pathogens

inferredcites →https://doi.org/10.3389/fcimb.2017.00154openalex-snapshot

A Novel Role of Listeria monocytogenes Membrane Vesicles in Inhibition of Autophagy and Cell Death

inferredcites →https://doi.org/10.3389/fmicb.2016.01404openalex-snapshot

Evaluation of Staphylococcus aureus Lipoproteins: Role in Nutritional Acquisition and Pathogenicity

inferredcites →https://doi.org/10.3389/fmicb.2017.00474openalex-snapshot

Non-coding RNAs in Host–Pathogen Interactions: Subversion of Mammalian Cell Functions by Protozoan Parasites

inferredcites →https://doi.org/10.4049/jimmunol.1203245openalex-snapshot

Identification of TLR10 as a Key Mediator of the Inflammatory Response to Listeria monocytogenes in Intestinal Epithelial Cells and Macrophages

inferredcites →https://doi.org/10.4049/jimmunol.1402894openalex-snapshot

Bacterial Membrane Vesicles Mediate the Release of Mycobacterium tuberculosis Lipoglycans and Lipoproteins from Infected Macrophages

inferredcites →https://doi.org/10.4049/jimmunol.1403173openalex-snapshot

TLR8 Senses Bacterial RNA in Human Monocytes and Plays a Nonredundant Role for Recognition of Streptococcus pyogenes

inferredcites →https://doi.org/10.4049/jimmunol.181.3.2028openalex-snapshot

Lipoproteins of Listeria monocytogenes Are Critical for Virulence and TLR2-Mediated Immune Activation

inferredcites →https://doi.org/10.4161/viru.2.5.17703openalex-snapshot

The arsenal of virulence factors deployed byListeria monocytogenesto promote its cell infection cycle

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s00203-025-04562-2openalex-snapshot

Microbial membrane vesicles and the intestinal epithelium: a crosstalk in health and disease

inferred← citeshttps://doi.org/10.1101/2020.06.21.164061openalex-snapshot

TMT-Based Quantitative Proteomic Analysis of Intestinal Organoids Infected by Listeria monocytogenes with Different Virulence

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