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Interplay of Mycobacterium abscessus and Pseudomonas aeruginosa in coinfection: Biofilm Dynamics and Host Immune Response

https://doi.org/10.1101/2024.01.22.576702

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What this work says

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

inferredcites →https://doi.org/10.1002/9780471729259.mc06e01s25openalex-snapshot

Growth and Laboratory Maintenance of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1002/9780471729259.mc10d01s18openalex-snapshot

Laboratory Maintenance of Mycobacterium abscessus

inferredcites →https://doi.org/10.1002/ppul.24129openalex-snapshot

Inflammation in cystic fibrosis: An update

inferredcites →https://doi.org/10.1007/978-981-10-6141-7_16openalex-snapshot

Pseudomonas aeruginosa and Its Arsenal of Proteases: Weapons to Battle the Host

inferredcites →https://doi.org/10.1007/s00253-014-5792-6openalex-snapshot

Insect antimicrobial peptides and their applications

inferredcites →https://doi.org/10.1007/s10096-013-1876-yopenalex-snapshot

Pseudomonas aeruginosa infection in cystic fibrosis lung disease and new perspectives of treatment: a review

inferredcites →https://doi.org/10.1007/s12602-017-9267-9openalex-snapshot

The Inhibition Effect of Lactobacilli Against Growth and Biofilm Formation of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1016/j.ccm.2014.11.003openalex-snapshot

Nontuberculous Mycobacterial Infections in Cystic Fibrosis

inferredcites →https://doi.org/10.1016/j.dci.2009.08.014openalex-snapshot

Nitric oxide is an essential component of the hemocyte-mediated mosquito immune response against bacteria

inferredcites →https://doi.org/10.1016/j.dci.2009.10.004openalex-snapshot

The role of lysozyme in the prophenoloxidase activation system of Manduca sexta: An in vitro approach

inferredcites →https://doi.org/10.1016/j.dci.2012.06.012openalex-snapshot

Manduca sexta gloverin binds microbial components and is active against bacteria and fungi

inferredcites →https://doi.org/10.1016/j.femsle.2004.12.024openalex-snapshot

Apolipophorin III is a substrate for protease IV fromPseudomonas aeruginosa

inferredcites →https://doi.org/10.1016/j.ijmm.2018.03.003openalex-snapshot

Non-Tuberculous Mycobacteria multispecies biofilms in cystic fibrosis: development of an in vitro Mycobacterium abscessus and Pseudomonas aeruginosa dual species biofilm model

inferredcites →https://doi.org/10.1016/j.jcf.2004.06.006openalex-snapshot

Cytokines and inflammatory mediators in cystic fibrosis

inferredcites →https://doi.org/10.1016/j.jcf.2005.05.005openalex-snapshot

Infection and inflammation in cystic fibrosis: A short review

inferredcites →https://doi.org/10.1016/j.jcf.2005.05.010openalex-snapshot

Anti-inflammatory therapy in cystic fibrosis

inferredcites →https://doi.org/10.1016/j.jcf.2009.12.001openalex-snapshot

Chronic Mycobacterium abscessus infection and lung function decline in cystic fibrosis

inferredcites →https://doi.org/10.1016/j.jcf.2010.03.008openalex-snapshot

Lung transplantation in patients with cystic fibrosis and Mycobacterium abscessus infection

inferredcites →https://doi.org/10.1016/j.jcf.2012.07.003openalex-snapshot

Innate immunity in cystic fibrosis lung disease

inferredcites →https://doi.org/10.1016/j.jcf.2013.01.001openalex-snapshot

Cystic fibrosis CFBE41o‐ cells contain TLR1 SNP I602S and fail to respond to Mycobacterium abscessus

inferredcites →https://doi.org/10.1016/j.jcf.2020.09.007openalex-snapshot

Trends in nontuberculous mycobacteria infection in children and young people with cystic fibrosis

inferredcites →https://doi.org/10.1016/j.jcf.2021.04.012openalex-snapshot

Microbial interaction: Prevotella spp. reduce P. aeruginosa induced inflammation in cystic fibrosis bronchial epithelial cells

inferredcites →https://doi.org/10.1016/j.jinsphys.2021.104239openalex-snapshot

A comparison of the production of antimicrobial peptides and proteins by Galleria mellonella larvae in response to infection with two Pseudomonas aeruginosa strains differing in the profile of secreted proteases

inferredcites →https://doi.org/10.1016/j.jip.2007.06.003openalex-snapshot

Changes in Galleria mellonella apolipophorin III level during Pseudomonas aeruginosa infection

inferredcites →https://doi.org/10.1016/j.jip.2023.107975openalex-snapshot

Investigating bacterial infections in Galleria mellonella larvae: Insights into pathogen dissemination and behavior

inferredcites →https://doi.org/10.1016/j.nbt.2021.02.003openalex-snapshot

Easily applicable modifications to electroporation conditions improve the transformation efficiency rates for rough morphotypes of fast-growing mycobacteria

inferredcites →https://doi.org/10.1016/j.pupt.2007.12.001openalex-snapshot

Pseudomonas aeruginosa biofilm formation in the cystic fibrosis airway

inferredcites →https://doi.org/10.1016/j.tcsw.2021.100051openalex-snapshot

Mycobacterium abscessus biofilms produce an extracellular matrix and have a distinct mycolic acid profile

inferredcites →https://doi.org/10.1016/s0022-1910(02)00096-3openalex-snapshot

Apolipophorin-III affects the activity of the haemocytes of Galleria mellonella larvae

inferredcites →https://doi.org/10.1016/s0140-6736(09)60327-5openalex-snapshot

Cystic fibrosis

inferredcites →https://doi.org/10.1038/s41598-017-14051-2openalex-snapshot

A single point mutation in class III ribonucleotide reductase promoter renders Pseudomonas aeruginosa PAO1 inefficient for anaerobic growth and infection

inferredcites →https://doi.org/10.1038/s41598-021-84525-xopenalex-snapshot

Mycobacterium abscessus biofilms have viscoelastic properties which may contribute to their recalcitrance in chronic pulmonary infections

inferredcites →https://doi.org/10.1042/bj20031923openalex-snapshot

Cloning and expression of an inhibitor of microbial metalloproteinases from insects contributing to innate immunity

inferredcites →https://doi.org/10.1073/pnas.1321390111openalex-snapshot

Mycobacterium abscessus cording prevents phagocytosis and promotes abscess formation

inferredcites →https://doi.org/10.1073/pnas.1605477113openalex-snapshot

Deletion of a dehydratase important for intracellular growth and cording renders rough Mycobacterium abscessus avirulent

inferredcites →https://doi.org/10.1073/pnas.1914830117openalex-snapshot

Iron sequestration by transferrin 1 mediates nutritional immunity in Drosophila melanogaster

inferredcites →https://doi.org/10.1074/jbc.270.50.29923openalex-snapshot

Moricin, a Novel Type of Antibacterial Peptide Isolated from the Silkworm, Bombyx mori

inferredcites →https://doi.org/10.1080/19336950.2018.1502585openalex-snapshot

Cystic fibrosis transmembrane conductance regulator (CFTR): Making an ion channel out of an active transporter structure

inferredcites →https://doi.org/10.1080/21505594.2018.1491255openalex-snapshot

Galleria mellonella - a novel infection model for the Mycobacterium tuberculosis complex

inferredcites →https://doi.org/10.1080/21505594.2020.1787034openalex-snapshot

Differential adaptability between reference strains and clinical isolates of Pseudomonas aeruginosa into the lung epithelium intracellular lifestyle

inferredcites →https://doi.org/10.1086/504381openalex-snapshot

Infections Due to Rapidly Growing Mycobacteria

inferredcites →https://doi.org/10.1093/cid/cir399openalex-snapshot

Inflammatory Responses to Individual Microorganisms in the Lungs of Children With Cystic Fibrosis

inferredcites →https://doi.org/10.1093/jac/37.6.1077openalex-snapshot

Antimicrobial activity of cecropins

inferredcites →https://doi.org/10.1101/cshperspect.a009589openalex-snapshot

CFTR, Mucins, and Mucus Obstruction in Cystic Fibrosis

inferredcites →https://doi.org/10.1101/cshperspect.a028241openalex-snapshot

Cilia and Mucociliary Clearance

inferredcites →https://doi.org/10.1111/1744-7917.12325openalex-snapshot

Immunity of the greater wax mothGalleria mellonella

inferredcites →https://doi.org/10.1126/science.abi5695openalex-snapshot

Mycobacterium abscessus in cystic fibrosis

inferredcites →https://doi.org/10.1128/aac.01547-19openalex-snapshot

Antimicrobial Treatment Provides a Competitive Advantage to Mycobacterium abscessus in a Dual-Species Biofilm with Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1128/aac.01782-17openalex-snapshot

Mycobacterium abscessus Smooth and Rough Morphotypes Form Antimicrobial-Tolerant Biofilm Phenotypes but Are Killed by Acetic Acid

inferredcites →https://doi.org/10.1128/aac.02539-17openalex-snapshot

Establishment and Validation of Galleria mellonella as a Novel Model Organism To Study Mycobacterium abscessus Infection, Pathogenesis, and Treatment

inferredcites →https://doi.org/10.1128/cmr.00138-18openalex-snapshot

Cystic Fibrosis and Pseudomonas aeruginosa: the Host-Microbe Interface

inferredcites →https://doi.org/10.1128/iai.00098-16openalex-snapshot

Role of Iron Uptake Systems in Pseudomonas aeruginosa Virulence and Airway Infection

inferredcites →https://doi.org/10.1128/iai.00411-17openalex-snapshot

Biofilms and Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1128/iai.00621-09openalex-snapshot

Pathogenicity Islands PAPI-1 and PAPI-2 Contribute Individually and Synergistically to the Virulence of Pseudomonas aeruginosa Strain PA14

inferredcites →https://doi.org/10.1128/iai.73.7.4161-4170.2005openalex-snapshot

Superoxide Production in Galleria mellonella Hemocytes: Identification of Proteins Homologous to the NADPH Oxidase Complex of Human Neutrophils

inferredcites →https://doi.org/10.1128/jb.182.13.3843-3845.2000openalex-snapshot

Positive Correlation between Virulence of Pseudomonas aeruginosa Mutants in Mice and Insects

inferredcites →https://doi.org/10.1128/mbio.02205-20openalex-snapshot

Intracellular Density of Wolbachia Is Mediated by Host Autophagy and the Bacterial Cytoplasmic Incompatibility Gene cifB in a Cell Type-Dependent Manner in Drosophila melanogaster

inferredcites →https://doi.org/10.1128/spectrum.02471-22openalex-snapshot

Surface Dependent Inhibition of Mycobacterium abscessus by Diverse Pseudomonas aeruginosa Strains

inferredcites →https://doi.org/10.1152/ajplung.2001.280.3.l493openalex-snapshot

Proinflammatory cytokine responses toP. aeruginosainfection in human airway epithelial cell lines

inferredcites →https://doi.org/10.1159/000481524openalex-snapshot

Nitric Oxide Mediates Insect Cellular Immunity via Phospholipase A2 Activation

inferredcites →https://doi.org/10.1164/rccm.201303-0429ocopenalex-snapshot

Survival Benefit of Lung Transplant for Cystic Fibrosis since Lung Allocation Score Implementation

inferredcites →https://doi.org/10.1165/rcmb.2017-0321tropenalex-snapshot

Pseudomonas aeruginosa Biofilms: Host Response and Clinical Implications in Lung Infections

inferredcites →https://doi.org/10.1186/1471-2164-12-1openalex-snapshot

Venom gland transcriptomes of two elapid snakes (Bungarus multicinctus and Naja atra) and evolution of toxin genes

inferredcites →https://doi.org/10.1186/1755-7682-1-24openalex-snapshot

Pulmonary bacterial pathogens in cystic fibrosis patients and antibiotic therapy: a tool for the health workers

inferredcites →https://doi.org/10.1371/journal.pone.0029148openalex-snapshot

Mycobacterium abscessus Glycopeptidolipid Prevents Respiratory Epithelial TLR2 Signaling as Measured by HβD2 Gene Expression and IL-8 Release

inferredcites →https://doi.org/10.1371/journal.pone.0117657openalex-snapshot

Mycobacterium abscessus Morphotype Comparison in a Murine Model

inferredcites →https://doi.org/10.1371/journal.ppat.1005258openalex-snapshot

Cystic Fibrosis Lung Infections: Polymicrobial, Complex, and Hard to Treat

inferredcites →https://doi.org/10.18388/abp.2016_1376openalex-snapshot

Expression if the insect metalloproteinase inhibitor IMPI in the fat body of Galleria mellonella exposed to infection with Beauveria bassiana

inferredcites →https://doi.org/10.2147/idr.s169789openalex-snapshot

Impact of concomitant nontuberculous mycobacteria and Pseudomonas aeruginosa isolates in non-cystic fibrosis bronchiectasis

inferredcites →https://doi.org/10.2217/fmb.10.125openalex-snapshot

Pseudomonas Aeruginosa Biofilms in Cystic fibrosis

inferredcites →https://doi.org/10.3389/fcimb.2020.00432openalex-snapshot

A TLR2-Activating Fraction From Mycobacterium abscessus Rough Variant Demonstrates Vaccine and Diagnostic Potential

inferredcites →https://doi.org/10.3389/fmicb.2016.01562openalex-snapshot

Mycobacteria Clumping Increase Their Capacity to Damage Macrophages

inferredcites →https://doi.org/10.3389/fmicb.2017.00339openalex-snapshot

Mycobacterium abscessus subsp. abscessus Is Capable of Degrading Pseudomonas aeruginosa Quinolone Signals

inferredcites →https://doi.org/10.3389/fmicb.2017.02039openalex-snapshot

A Novel TetR-Like Transcriptional Regulator Is Induced in Acid-Nitrosative Stress and Controls Expression of an Efflux Pump in Mycobacteria

inferredcites →https://doi.org/10.3389/fmicb.2017.02651openalex-snapshot

Mycobacterium Biofilms

inferredcites →https://doi.org/10.3389/fmicb.2018.01205openalex-snapshot

Aspergillus fumigatus Inhibits Pseudomonas aeruginosa in Co-culture: Implications of a Mutually Antagonistic Relationship on Virulence and Inflammation in the CF Airway

inferredcites →https://doi.org/10.3389/fphar.2021.573065openalex-snapshot

Enhancing Cystic Fibrosis Immune Regulation

inferredcites →https://doi.org/10.3389/fphys.2014.00252openalex-snapshot

Insect prophenoloxidase: the view beyond immunity

inferredcites →https://doi.org/10.3390/ijms20235868openalex-snapshot

Mycobacterium abscessus, an Emerging and Worrisome Pathogen among Cystic Fibrosis Patients

inferredcites →https://doi.org/10.3390/microorganisms11092244openalex-snapshot

A High-Throughput Microtiter Plate Screening Assay to Quantify and Differentiate Species in Dual-Species Biofilms

inferredcites →https://doi.org/10.3390/microorganisms8111798openalex-snapshot

Monitoring Gene Expression during a Galleria mellonella Bacterial Infection

inferredcites →https://doi.org/10.3390/v10080428openalex-snapshot

Mycobacteriophage Lysis Enzymes: Targeting the Mycobacterial Cell Envelope

inferredcites →https://doi.org/10.3791/4392openalex-snapshot

The Insect Galleria mellonella as a Powerful Infection Model to Investigate Bacterial Pathogenesis

inferredcites →https://doi.org/10.4161/viru.2.5.17811openalex-snapshot

Pre-exposure ofGalleria mellonellalarvae to different doses ofAspergillus fumigatusconidia causes differential activation of cellular and humoral immune responses

What points at this work

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

inferred← citeshttps://doi.org/10.3390/antibiotics13100926openalex-snapshot

Mycobacteriophages and Their Applications

inferred← citeshttps://doi.org/10.3390/microorganisms13010116openalex-snapshot

Pseudomonas aeruginosa pqs Quorum Sensing Mediates Interaction with Mycobacterium abscessus In Vitro

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