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Reduced Permeability to Rifampicin by Capsular Thickening as a Mechanism of Antibiotic Persistence in Mycobacterium tuberculosis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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The Role of Bacterial Polysaccharide Capsules as Virulence Factors
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Triple-layered structure of mycobacterial cell wall: Evidence for the existence of a polysaccharide-rich outer layer in 18 mycobacterial species
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Cell walls of mycobacteria and related organisms; Chemistry and immunostimulant properties
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Physiological roles of trehalose in bacteria and yeasts: a comparative analysis
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Antibiotic resistance mechanisms in M. tuberculosis: an update
inferredcites →https://doi.org/10.1007/s13213-013-0758-yopenalex-snapshot
Zeta potential as a measure of the surface charge of mycobacterial cells
inferredcites →https://doi.org/10.1016/j.cell.2011.02.022openalex-snapshot
Drug Tolerance in Replicating Mycobacteria Mediated by a Macrophage-Induced Efflux Mechanism
inferredcites →https://doi.org/10.1016/j.molcel.2010.01.003openalex-snapshot
Sublethal Antibiotic Treatment Leads to Multidrug Resistance via Radical-Induced Mutagenesis
inferredcites →https://doi.org/10.1016/s0008-6215(00)84676-5openalex-snapshot
Specificity in the interaction of direct dyes with polysaccharides
inferredcites →https://doi.org/10.1016/s0065-2911(09)05502-7openalex-snapshot
Physiology of Mycobacteria
inferredcites →https://doi.org/10.1016/s0167-7012(00)00224-4openalex-snapshot
Status of methods for assessing bacterial cell surface charge properties based on zeta potential measurements
inferredcites →https://doi.org/10.1016/s0966-842x(01)02238-7openalex-snapshot
Mycobacterial persistence: adaptation to a changing environment
inferredcites →https://doi.org/10.1021/acsinfecdis.5b00148openalex-snapshot
Cell-Envelope Remodeling as a Determinant of Phenotypic Antibacterial Tolerance in Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1038/ja.2015.52openalex-snapshot
Activity of lipophilic and hydrophilic drugs against dormant and replicating Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1038/s41579-018-0013-4openalex-snapshot
Metabolic principles of persistence and pathogenicity in Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1042/bj20020615openalex-snapshot
Overexpression and functional characterization of an ABC (ATP-binding cassette) transporter encoded by the genes drrA and drrB of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1042/bj2970351openalex-snapshot
Structural features of the exocellular polysaccharides of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1054/tuld.1998.0200openalex-snapshot
The capsule of Mycobacterium tuberculosis and its implications for pathogenicity
inferredcites →https://doi.org/10.1074/jbc.m610183200openalex-snapshot
The Mycobacterium tuberculosis Cell-surface Glycoprotein Apa as a Potential Adhesin to Colonize Target Cells via the Innate Immune System Pulmonary C-type Lectin Surfactant Protein A
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RESPONSE OF CULTURED MACROPHAGES TO MYCOBACTERIUM TUBERCULOSIS , WITH OBSERVATIONS ON FUSION OF LYSOSOMES WITH PHAGOSOMES
inferredcites →https://doi.org/10.1093/glycob/cwg047openalex-snapshot
New insights on trehalose: a multifunctional molecule
inferredcites →https://doi.org/10.1093/jac/1.4.363openalex-snapshot
The role of the bacterial cell envelope in antibiotic resistance
inferredcites →https://doi.org/10.1093/jac/10.5.368openalex-snapshot
Antibiotic penetration through bacterial capsules and exopolysaccharides
inferredcites →https://doi.org/10.1093/jac/45.2.159openalex-snapshot
Accumulation of rifampicin by Mycobacterium aurum, Mycobacterium smegmatis and Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1097/01.inf.0000437878.87561.f3openalex-snapshot
Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1099/00221287-129-7-2315openalex-snapshot
Electron Microscopic Observations of Cell Division in Mycobacterium vaccae V1
inferredcites →https://doi.org/10.1099/13500872-141-7-1609openalex-snapshot
Molecular composition of the outermost capsular material of the tubercle bacillus
inferredcites →https://doi.org/10.1099/mic.0.2008/022301-0openalex-snapshot
Capsule polysaccharide is a bacterial decoy for antimicrobial peptides
inferredcites →https://doi.org/10.1111/j.1348-0421.2003.tb03394.xopenalex-snapshot
Comparative Studies of the Cell Structures of Mycobacterium leprae and M. tuberculosis Using the Electron Microscopy Freeze‐Substitution Technique
inferredcites →https://doi.org/10.1111/j.1574-6968.1980.tb05599.xopenalex-snapshot
Adherence of bacteria to hydrocarbons: A simple method for measuring cell-surface hydrophobicity
inferredcites →https://doi.org/10.1111/j.1574-6968.1994.tb07194.xopenalex-snapshot
Mycobacterial cell wall: Structure and role in natural resistance to antibiotics
inferredcites →https://doi.org/10.1128/aac.01343-16openalex-snapshot
De Novo Emergence of Genetically Resistant Mutants of Mycobacterium tuberculosis from the Persistence Phase Cells Formed against Antituberculosis Drugs In Vitro
inferredcites →https://doi.org/10.1128/aac.02107-17openalex-snapshot
Verapamil Targets Membrane Energetics in Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1128/aac.11.5.773openalex-snapshot
Permeability Barrier to Rifampin in Mycobacteria
inferredcites →https://doi.org/10.1128/aac.40.3.646openalex-snapshot
Rifampin resistance in Neisseria meningitidis due to alterations in membrane permeability
inferredcites →https://doi.org/10.1128/aac.48.8.3175-3178.2004openalex-snapshot
Rv2686c-Rv2687c-Rv2688c, an ABC Fluoroquinolone Efflux Pump in Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1128/aac.50.2.428-438.2006openalex-snapshot
Novel Mechanism of Antibiotic Resistance Originating in Vancomycin-Intermediate Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aem.02211-08openalex-snapshot
Use of Calcofluor White for Detection, Identification, and Quantification of Phytoplanktonic Fungal Parasites
inferredcites →https://doi.org/10.1128/iai.13.3.776-781.1976openalex-snapshot
Adjuvant effect of cord factor, a mycobacterial lipid
inferredcites →https://doi.org/10.1128/iai.62.10.4495-4499.1994openalex-snapshot
Polysaccharide capsule-mediated resistance to opsonophagocytosis in Klebsiella pneumoniae
inferredcites →https://doi.org/10.1128/iai.70.5.2566-2575.2002openalex-snapshot
Glucan Is a Component of theMycobacterium tuberculosisSurface That Is Expressed In Vitro and In Vivo
inferredcites →https://doi.org/10.1128/iai.72.10.5676-5686.2004openalex-snapshot
The Glycan-Rich Outer Layer of the Cell Wall ofMycobacterium tuberculosisActs as an Antiphagocytic Capsule Limiting the Association of the Bacterium with Macrophages
inferredcites →https://doi.org/10.1128/iai.72.12.7107-7114.2004openalex-snapshot
Capsule Polysaccharide Mediates Bacterial Resistance to Antimicrobial Peptides
inferredcites →https://doi.org/10.1128/jb.06184-11openalex-snapshot
Unveiling Unusual Features of Formation of Septal Partition and Constriction in Mycobacteria—an Ultrastructural Study
inferredcites →https://doi.org/10.1128/jb.180.4.801-808.1998openalex-snapshot
Mycobacterial Stationary Phase Induced by Low Oxygen Tension: Cell Wall Thickening and Localization of the 16-Kilodalton α-Crystallin Homolog
inferredcites →https://doi.org/10.1128/jb.90.5.1438-1447.1965openalex-snapshot
Effect of Oleic Acid on Growth and Cell Structure of Mycobacteria
inferredcites →https://doi.org/10.1128/jcm.41.1.5-14.2003openalex-snapshot
Cell Wall Thickening Is a Common Feature of Vancomycin Resistance in Staphylococcus aureus
inferredcites →https://doi.org/10.1146/annurev-micro-091014-104121openalex-snapshot
Assembly of the Mycobacterial Cell Wall
inferredcites →https://doi.org/10.1164/rccm.201304-0650ocopenalex-snapshot
Acceleration of Tuberculosis Treatment by Adjunctive Therapy with Verapamil as an Efflux Inhibitor
inferredcites →https://doi.org/10.1242/jeb.01133openalex-snapshot
Role of trehalose phosphate synthase and trehalose during hypoxia: from flies to mammals
inferredcites →https://doi.org/10.1371/journal.pone.0087329openalex-snapshot
Non-Replicating Mycobacterium tuberculosis Elicits a Reduced Infectivity Profile with Corresponding Modifications to the Cell Wall and Extracellular Matrix
inferredcites →https://doi.org/10.1371/journal.pone.0116545openalex-snapshot
In Vitro Activity of Rifampicin and Verapamil Combination in Multidrug-Resistant Mycobacterium tuberculosis
inferredcites →https://doi.org/10.4049/jimmunol.0900768openalex-snapshot
Identification of Mycobacterial α-Glucan As a Novel Ligand for DC-SIGN: Involvement of Mycobacterial Capsular Polysaccharides in Host Immune Modulation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/463232openalex-snapshot
PerSort facilitates characterization and elimination of persister subpopulation in mycobacteria
inferred← citeshttps://doi.org/10.1128/msystems.01127-20openalex-snapshot
PerSort Facilitates Characterization and Elimination of Persister Subpopulation in Mycobacteria
inferred← citeshttps://doi.org/10.1134/s0003683820040110openalex-snapshot
Biogenic Polyamines Influence the Antibiotic Susceptibility and Cell-Surface Properties of Mycobacterium smegmatis
inferred← citeshttps://doi.org/10.1186/s12866-020-01802-xopenalex-snapshot
LipF increases rifampicin and streptomycin sensitivity in a Mycobacterium tuberculosis surrogate
inferred← citeshttps://doi.org/10.3389/fimmu.2021.703060openalex-snapshot
Understanding the Reciprocal Interplay Between Antibiotics and Host Immune System: How Can We Improve the Anti-Mycobacterial Activity of Current Drugs to Better Control Tuberculosis?
inferred← citeshttps://doi.org/10.3389/fmicb.2020.554795openalex-snapshot
Mycobacterium tuberculosis Cells Surviving in the Continued Presence of Bactericidal Concentrations of Rifampicin in vitro Develop Negatively Charged Thickened Capsular Outer Layer That Restricts Permeability to the Antibiotic
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