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Non-clonal emergence of colistin resistance associated with mutations in the BasRS two-component system in Escherichia coli bloodstream isolates
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1 of the 70 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-11): 10.1001/jama.2014.7247 (notice 2017-04-18).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jama.2014.7247openalex-snapshot
Effects of Decontamination of the Oropharynx and Intestinal Tract on Antibiotic Resistance in ICUs
inferredcites →https://doi.org/10.1002/bip.22095openalex-snapshot
Biophysical characterization of polymyxin b interaction with LPS aggregates and membrane model systems
inferredcites →https://doi.org/10.1007/978-1-4939-7060-5_5openalex-snapshot
Inverse PCR for Point Mutation Introduction
inferredcites →https://doi.org/10.1016/j.drudis.2018.07.004openalex-snapshot
MCR-1: a promising target for structure-based design of inhibitors to tackle polymyxin resistance
inferredcites →https://doi.org/10.1016/j.drup.2010.05.002openalex-snapshot
Resistance to polymyxins: Mechanisms, frequency and treatment options
inferredcites →https://doi.org/10.1016/j.ijantimicag.2014.07.020openalex-snapshot
Worldwide emergence of colistin resistance in Klebsiella pneumoniae from healthy humans and patients in Lao PDR, Thailand, Israel, Nigeria and France owing to inactivation of the PhoP/PhoQ regulator mgrB: an epidemiological and molecular study
inferredcites →https://doi.org/10.1016/j.ijantimicag.2015.11.009openalex-snapshot
Emergence of colistin-resistant bacteria in humans without colistin usage: a new worry and cause for vigilance
inferredcites →https://doi.org/10.1016/j.ijantimicag.2016.06.023openalex-snapshot
Molecular mechanisms of polymyxin resistance: knowns and unknowns
inferredcites →https://doi.org/10.1016/j.ijmm.2014.12.007openalex-snapshot
Intraprotein signal transduction by HAMP domains: A balancing act
inferredcites →https://doi.org/10.1016/j.jgar.2019.07.002openalex-snapshot
IncX4 plasmids harbouring mcr-1 genes: Further dissemination
inferredcites →https://doi.org/10.1016/j.tibs.2019.06.002openalex-snapshot
Genetic and Biochemical Mechanisms for Bacterial Lipid A Modifiers Associated with Polymyxin Resistance
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1016/s1473-3099(15)00424-7openalex-snapshot
Emergence of plasmid-mediated colistin resistance mechanism MCR-1 in animals and human beings in China: a microbiological and molecular biological study
inferredcites →https://doi.org/10.1021/jm900999hopenalex-snapshot
Structure−Activity Relationships of Polymyxin Antibiotics
inferredcites →https://doi.org/10.1038/msb4100050openalex-snapshot
Construction of Escherichia coli K‐12 in‐frame, single‐gene knockout mutants: the Keio collection
inferredcites →https://doi.org/10.1038/nature07830openalex-snapshot
The structural basis of lipopolysaccharide recognition by the TLR4–MD-2 complex
inferredcites →https://doi.org/10.1038/s41467-018-03205-zopenalex-snapshot
The global distribution and spread of the mobilized colistin resistance gene mcr-1
inferredcites →https://doi.org/10.1038/s41598-017-05167-6openalex-snapshot
An allelic variant of the PmrB sensor kinase responsible for colistin resistance in an Escherichia coli strain of clinical origin
inferredcites →https://doi.org/10.1073/pnas.0406038101openalex-snapshot
Phenotypic differences between Salmonella and Escherichia coli resulting from the disparate regulation of homologous genes
inferredcites →https://doi.org/10.1073/pnas.1508820112openalex-snapshot
Deciphering tissue-induced Klebsiella pneumoniae lipid A structure
inferredcites →https://doi.org/10.1073/pnas.1717295115openalex-snapshot
Global increase and geographic convergence in antibiotic consumption between 2000 and 2015
inferredcites →https://doi.org/10.1074/jbc.m106962200openalex-snapshot
Accumulation of a Polyisoprene-linked Amino Sugar in Polymyxin-resistant Salmonella typhimurium andEscherichia coli
inferredcites →https://doi.org/10.1089/cmb.2012.0021openalex-snapshot
SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing
inferredcites →https://doi.org/10.1093/bioinformatics/8.3.275openalex-snapshot
The rapid generation of mutation data matrices from protein sequences
inferredcites →https://doi.org/10.1093/bioinformatics/btu153openalex-snapshot
Prokka: rapid prokaryotic genome annotation
inferredcites →https://doi.org/10.1093/bioinformatics/btu555openalex-snapshot
Poretools: a toolkit for analyzing nanopore sequence data
inferredcites →https://doi.org/10.1093/bioinformatics/btv195openalex-snapshot
PROVEAN web server: a tool to predict the functional effect of amino acid substitutions and indels
inferredcites →https://doi.org/10.1093/gbe/evt038openalex-snapshot
The Evolutionary Path to Extraintestinal Pathogenic, Drug-Resistant Escherichia coli Is Marked by Drastic Reduction in Detectable Recombination within the Core Genome
inferredcites →https://doi.org/10.1093/jac/48.suppl_1.5openalex-snapshot
Determination of minimum inhibitory concentrations
inferredcites →https://doi.org/10.1093/jac/dks261openalex-snapshot
Identification of acquired antimicrobial resistance genes
inferredcites →https://doi.org/10.1093/jac/dkz090openalex-snapshot
Colistin resistance in Parisian inpatient faecal Escherichia coli as the result of two distinct evolutionary pathways
inferredcites →https://doi.org/10.1093/molbev/mss236openalex-snapshot
The Rhizome of the Multidrug-Resistant Enterobacter aerogenes Genome Reveals How New “Killer Bugs” Are Created because of a Sympatric Lifestyle
inferredcites →https://doi.org/10.1093/molbev/mst197openalex-snapshot
MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0
inferredcites →https://doi.org/10.1093/nar/gkw408openalex-snapshot
ConSurf 2016: an improved methodology to estimate and visualize evolutionary conservation in macromolecules
inferredcites →https://doi.org/10.1093/nar/gkx922openalex-snapshot
20 years of the SMART protein domain annotation resource
inferredcites →https://doi.org/10.1097/qco.0b013e328332e672openalex-snapshot
Colistin in the 21st century
inferredcites →https://doi.org/10.1099/ijs.0.02475-0openalex-snapshot
Escherichia albertii sp. nov., a diarrhoeagenic species isolated from stool specimens of Bangladeshi children
inferredcites →https://doi.org/10.1099/ijsem.0.001572openalex-snapshot
Enterobacter aerogenes Hormaeche and Edwards 1960 (Approved Lists 1980) and Klebsiella mobilis Bascomb et al. 1971 (Approved Lists 1980) share the same nomenclatural type (ATCC 13048) on the Approved Lists and are homotypic synonyms, with consequences for the name Klebsiella mobilis Bascomb et al.…
inferredcites →https://doi.org/10.1101/781724openalex-snapshot
Escherichia ruysiae sp. nov., isolated from an international traveller
inferredcites →https://doi.org/10.1101/gr.216606.116openalex-snapshot
Systematic longitudinal survey of invasive Escherichia coli in England demonstrates a stable population structure only transiently disturbed by the emergence of ST131
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07115.xopenalex-snapshot
MicA sRNA links the PhoP regulon to cell envelope stress
inferredcites →https://doi.org/10.1128/aac.00864-18openalex-snapshot
Contribution of Novel Amino Acid Alterations in PmrA or PmrB to Colistin Resistance in mcr -Negative Escherichia coli Clinical Isolates, Including Major Multidrug-Resistant Lineages O25b:H4-ST131- H 30Rx and Non-x
inferredcites →https://doi.org/10.1128/aac.01016-08openalex-snapshot
Genetic Analysis of Colistin Resistance in Salmonella enterica Serovar Typhimurium
inferredcites →https://doi.org/10.1128/aac.01344-16openalex-snapshot
Genomic Characterization of Colistin Heteroresistance in Klebsiella pneumoniae during a Nosocomial Outbreak
inferredcites →https://doi.org/10.1128/aac.01480-13openalex-snapshot
In Vivo Emergence of Colistin Resistance in Klebsiella pneumoniae Producing KPC-Type Carbapenemases Mediated by Insertional Inactivation of the PhoQ/PhoP mgrB Regulator
inferredcites →https://doi.org/10.1128/aac.01574-15openalex-snapshot
Preservation of Acquired Colistin Resistance in Gram-Negative Bacteria
inferredcites →https://doi.org/10.1128/aac.05052-14openalex-snapshot
PmrD Is Required for Modifications to Escherichia coli Endotoxin That Promote Antimicrobial Resistance
inferredcites →https://doi.org/10.1128/cmr.00064-16openalex-snapshot
Polymyxins: Antibacterial Activity, Susceptibility Testing, and Resistance Mechanisms Encoded by Plasmids or Chromosomes
inferredcites →https://doi.org/10.1128/iai.05226-11openalex-snapshot
Analysis of the Networks Controlling the Antimicrobial-Peptide-Dependent Induction of Klebsiella pneumoniae Virulence Factors
inferredcites →https://doi.org/10.1128/jb.185.16.4956-4972.2003openalex-snapshot
Phenotype MicroArray Analysis of Escherichia coli K-12 Mutants with Deletions of All Two-Component Systems
inferredcites →https://doi.org/10.1128/jb.188.3.1180-1183.2006openalex-snapshot
A pmrA Constitutive Mutant Sensitizes Escherichia coli to Deoxycholic Acid
inferredcites →https://doi.org/10.1128/mbio.00347-16openalex-snapshot
Sequential Acquisition of Virulence and Fluoroquinolone Resistance Has Shaped the Evolution of Escherichia coli ST131
inferredcites →https://doi.org/10.1128/mbio.00644-19openalex-snapshot
Diversification of Colonization Factors in a Multidrug-Resistant Escherichia coli Lineage Evolving under Negative Frequency-Dependent Selection
inferredcites →https://doi.org/10.1128/mbio.02317-17openalex-snapshot
An Evolutionarily Conserved Mechanism for Intrinsic and Transferable Polymyxin Resistance
inferredcites →https://doi.org/10.1186/1471-2180-6-39openalex-snapshot
Fast, easy and efficient: site-specific insertion of transgenes into enterobacterial chromosomes using Tn7 without need for selection of the insertion event.
inferredcites →https://doi.org/10.1186/s13059-014-0524-xopenalex-snapshot
The Harvest suite for rapid core-genome alignment and visualization of thousands of intraspecific microbial genomes
inferredcites →https://doi.org/10.1186/s13099-017-0227-4openalex-snapshot
Colistin resistant Escherichia coli carrying mcr-1 in urban sludge samples: Dhaka, Bangladesh
inferredcites →https://doi.org/10.1194/jlr.d500014-jlr200openalex-snapshot
Microextraction of bacterial lipid A: easy and rapid method for mass spectrometric characterization
inferredcites →https://doi.org/10.1371/journal.pgen.1002184openalex-snapshot
Ancestral Genes Can Control the Ability of Horizontally Acquired Loci to Confer New Traits
inferredcites →https://doi.org/10.15252/emmm.201607336openalex-snapshot
A Klebsiella pneumoniae antibiotic resistance mechanism that subdues host defences and promotes virulence
inferredcites →https://doi.org/10.1592/phco.30.12.1279openalex-snapshot
Resurgence of Colistin: A Review of Resistance, Toxicity, Pharmacodynamics, and Dosing
inferredcites →https://doi.org/10.2144/96201bm08openalex-snapshot
Preparation of Electro-Competent E. coli Using Salt-Free Growth Medium
inferredcites →https://doi.org/10.3201/eid2206.151840openalex-snapshot
Rapid Detection of Polymyxin Resistance inEnterobacteriaceae
inferredcites →https://doi.org/10.3389/fcimb.2013.00003openalex-snapshot
Recognition of lipid A variants by the TLR4-MD-2 receptor complex
inferredcites →https://doi.org/10.3389/fmicb.2017.02262openalex-snapshot
Molecular Epidemiology and Colistin Resistant Mechanism of mcr-Positive and mcr-Negative Clinical Isolated Escherichia coli
inferredcites →https://doi.org/10.3389/fmicb.2017.02278openalex-snapshot
Characterization of Colistin-Resistant Escherichia coli Isolated from Diseased Pigs in France
inferredcites →https://doi.org/10.7554/elife.65836openalex-snapshot
Colistin kills bacteria by targeting lipopolysaccharide in the cytoplasmic membrane
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.mgene.2020.100708openalex-snapshot
Emergence of mcr- and fosA3-mediated colistin and fosfomycin resistance among carbapenem-resistant Acinetobacter baumannii in Iraq
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