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Specific targeting of intestinal Prevotella copri by a Listeria monocytogenes bacteriocin

https://doi.org/10.1101/680801
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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/art.39783openalex-snapshot
Dysbiosis Contributes to Arthritis Development via Activation of Autoreactive T Cells in the Intestine
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Preservation of Mucus in Histological Sections, Immunostaining of Mucins in Fixed Tissue, and Localization of Bacteria with FISH
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Bacteroides and Prevotella
inferredcites →https://doi.org/10.1016/j.cell.2005.05.007openalex-snapshot
An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System
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Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria
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NLRP6 Inflammasome Regulates Colonic Microbial Ecology and Risk for Colitis
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Sphingolipids from a Symbiotic Microbe Regulate Homeostasis of Host Intestinal Natural Killer T Cells
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A Dietary Fiber-Deprived Gut Microbiota Degrades the Colonic Mucus Barrier and Enhances Pathogen Susceptibility
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Gut Microbiota-Produced Succinate Promotes C. difficile Infection after Antibiotic Treatment or Motility Disturbance
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The Gut Commensal Bacteroides thetaiotaomicron Exacerbates Enteric Infection through Modification of the Metabolic Landscape
inferredcites →https://doi.org/10.1016/j.chom.2016.11.010openalex-snapshot
Prevotella as a Hub for Vaginal Microbiota under the Influence of Host Genetics and Their Association with Obesity
inferredcites →https://doi.org/10.1016/j.chom.2017.05.004openalex-snapshot
Shigella sonnei Encodes a Functional T6SS Used for Interbacterial Competition and Niche Occupancy
inferredcites →https://doi.org/10.1016/j.immuni.2009.08.020openalex-snapshot
The Key Role of Segmented Filamentous Bacteria in the Coordinated Maturation of Gut Helper T Cell Responses
inferredcites →https://doi.org/10.1016/j.resmic.2008.11.002openalex-snapshot
Bacillus subtilis isolated from the human gastrointestinal tract
inferredcites →https://doi.org/10.1016/s0378-1097(00)00324-4openalex-snapshot
Prevotella enzymes involved in mucin oligosaccharide degradation and evidence for a small operon of genes expressed during growth on mucin
inferredcites →https://doi.org/10.1017/s0007114519000680openalex-snapshot
Gut Prevotella as a possible biomarker of diet and its eubiotic versus dysbiotic roles: a comprehensive literature review
inferredcites →https://doi.org/10.1021/pr1003642openalex-snapshot
Comprehensive Appraisal of the Extracellular Proteins from a Monoderm Bacterium: Theoretical and Empirical Exoproteomes ofListeria monocytogenesEGD-e by Secretomics
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Butyrate-producingClostridiumcluster XIVa species specifically colonize mucins in anin vitrogut model
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Gut dendritic cell activation links an altered colonic microbiome to mucosal and systemic T-cell activation in untreated HIV-1 infection
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A microbial symbiosis factor prevents intestinal inflammatory disease
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Enterotypes of the human gut microbiome
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The evolution of cooperation within the gut microbiota
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Human gut microbes impact host serum metabolome and insulin sensitivity
inferredcites →https://doi.org/10.1038/nature18849openalex-snapshot
Interactions between the microbiota and pathogenic bacteria in the gut
inferredcites →https://doi.org/10.1038/ng.3501openalex-snapshot
Uncovering Listeria monocytogenes hypervirulence by harnessing its biodiversity
inferredcites →https://doi.org/10.1038/nmicrobiol.2016.215openalex-snapshot
Genome-guided design of a defined mouse microbiota that confers colonization resistance against Salmonella enterica serovar Typhimurium
inferredcites →https://doi.org/10.1038/nrgastro.2016.4openalex-snapshot
Prevotella in the gut: choose carefully
inferredcites →https://doi.org/10.1038/nri3535openalex-snapshot
Microbiota-mediated colonization resistance against intestinal pathogens
inferredcites →https://doi.org/10.1038/s41598-018-35877-4openalex-snapshot
High Abundance of genus Prevotella in the gut of perinatally HIV-infected children is associated with IP-10 levels despite therapy
inferredcites →https://doi.org/10.1073/pnas.0803124105openalex-snapshot
The inner of the two Muc2 mucin-dependent mucus layers in colon is devoid of bacteria
inferredcites →https://doi.org/10.1073/pnas.0909122107openalex-snapshot
Inducible Foxp3 + regulatory T-cell development by a commensal bacterium of the intestinal microbiota
inferredcites →https://doi.org/10.1073/pnas.1212809109openalex-snapshot
Impact of lactobacilli on orally acquired listeriosis
inferredcites →https://doi.org/10.1073/pnas.1523899113openalex-snapshot
Bacteriocin from epidemic Listeria strains alters the host intestinal microbiota to favor infection
inferredcites →https://doi.org/10.1073/pnas.1608858113openalex-snapshot
Salmonella Typhimurium utilizes a T6SS-mediated antibacterial weapon to establish in the host gut
inferredcites →https://doi.org/10.1080/19490976.2018.1564431openalex-snapshot
The intestinal microbiota predisposes to traveler’s diarrhea and to the carriage of multidrug-resistant Enterobacteriaceae after traveling to tropical regions
inferredcites →https://doi.org/10.1084/jem.20170495openalex-snapshot
Commensal microbes provide first line defense against Listeria monocytogenes infection
inferredcites →https://doi.org/10.1093/femsec/fiv054openalex-snapshot
Interindividual differences in response to treatment with butyrate-producing Butyricicoccus pullicaecorum 25–3T studied in an in vitro gut model
inferredcites →https://doi.org/10.1097/coh.0000000000000427openalex-snapshot
Role of the lung microbiome in HIV pathogenesis
inferredcites →https://doi.org/10.1098/rstb.2015.0504openalex-snapshot
When pathogenic bacteria meet the intestinal microbiota
inferredcites →https://doi.org/10.1099/00221287-142-9-2393openalex-snapshot
Lactococcin 972: a homodimeric lactococcal bacteriocin whose primary target is not the plasma membrane
inferredcites →https://doi.org/10.1111/imm.12760openalex-snapshot
The immune response to Prevotella bacteria in chronic inflammatory disease
inferredcites →https://doi.org/10.1111/j.1365-2672.1993.tb03402.xopenalex-snapshot
Inhibition of enterobacteria and Listeria growth by lactic, acetic and formic acids
inferredcites →https://doi.org/10.1111/j.1751-7915.2011.00308.xopenalex-snapshot
Incorporating a mucosal environment in a dynamic gut model results in a more representative colonization by lactobacilli
inferredcites →https://doi.org/10.1126/science.1063447openalex-snapshot
Comparative Genomics of Listeria Species
inferredcites →https://doi.org/10.1128/jb.00045-12openalex-snapshot
Fatty Acids Regulate Stress Resistance and Virulence Factor Production for Listeria monocytogenes
inferredcites →https://doi.org/10.1128/jcm.30.3.663-666.1992openalex-snapshot
Sialidases (neuraminidases) in bacterial vaginosis and bacterial vaginosis-associated microflora
inferredcites →https://doi.org/10.1128/mbio.00707-13openalex-snapshot
The Intestinal Microbiota Interferes with the microRNA Response upon Oral Listeria Infection
inferredcites →https://doi.org/10.1136/annrheumdis-2018-214514openalex-snapshot
Prevotella copri in individuals at risk for rheumatoid arthritis
inferredcites →https://doi.org/10.1136/gutjnl-2014-307649openalex-snapshot
Identification of an anti-inflammatory protein from Faecalibacterium prausnitzii , a commensal bacterium deficient in Crohn’s disease
inferredcites →https://doi.org/10.1136/gutjnl-2016-313099openalex-snapshot
Dietary emulsifiers directly alter human microbiota composition and gene expression ex vivo potentiating intestinal inflammation
inferredcites →https://doi.org/10.1186/gb-2013-14-1-r4openalex-snapshot
Inflammation-associated enterotypes, host genotype, cage and inter-individual effects drive gut microbiota variation in common laboratory mice
inferredcites →https://doi.org/10.1186/s12864-015-1350-6openalex-snapshot
Divergences in gene repertoire among the reference Prevotella genomes derived from distinct body sites of human
inferredcites →https://doi.org/10.1242/dmm.017400openalex-snapshot
How informative is the mouse for human gut microbiota research?
inferredcites →https://doi.org/10.1371/journal.pone.0044328openalex-snapshot
Fecal Lipocalin 2, a Sensitive and Broadly Dynamic Non-Invasive Biomarker for Intestinal Inflammation
inferredcites →https://doi.org/10.1371/journal.pone.0074963openalex-snapshot
Commensal Akkermansia muciniphila Exacerbates Gut Inflammation in Salmonella Typhimurium-Infected Gnotobiotic Mice
inferredcites →https://doi.org/10.1371/journal.pone.0096222openalex-snapshot
Sil: A Streptococcus iniae Bacteriocin with Dual Role as an Antimicrobial and an Immunomodulator That Inhibits Innate Immune Response and Promotes S. iniae Infection
inferredcites →https://doi.org/10.4161/gmic.32132openalex-snapshot
HIV-induced alteration in gut microbiota
inferredcites →https://doi.org/10.7554/elife.01202openalex-snapshot
Expansion of intestinal Prevotella copri correlates with enhanced susceptibility to arthritis

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.chom.2019.10.020openalex-snapshot
The Strange Case of Prevotella copri: Dr. Jekyll or Mr. Hyde?
inferred← citeshttps://doi.org/10.1038/s41467-021-21408-9openalex-snapshot
Lysates of Methylococcus capsulatus Bath induce a lean-like microbiota, intestinal FoxP3+RORγt+IL-17+ Tregs and improve metabolism
inferred← citeshttps://doi.org/10.3390/ijms22158141openalex-snapshot
Proteomic Characterization of Antibiotic Resistance in Listeria and Production of Antimicrobial and Virulence Factors
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