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Co-Selection of Resistance to Antibiotics, Biocides and Heavy Metals, and Its Relevance to Foodborne Pathogens
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ffj.1967openalex-snapshot
Essential oils and aromatic plants in animal feeding – a European perspective. A review.
inferredcites →https://doi.org/10.1007/s00248-007-9303-5openalex-snapshot
Spatial Analysis of Antibiotic Resistance Along Metal Contaminated Streams
inferredcites →https://doi.org/10.1007/s00253-015-6749-0openalex-snapshot
Survival in amoeba—a major selection pressure on the presence of bacterial copper and zinc resistance determinants? Identification of a “copper pathogenicity island”
inferredcites →https://doi.org/10.1016/0140-6736(93)90526-mopenalex-snapshot
Triclosan-resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1016/0162-0134(94)00082-lopenalex-snapshot
Metal ion interaction with penicillins— part VII: Mixed-ligand complex formation of cobalt(II), nickel(II), copper(II), and zinc(II) with amplicillin and nucleic bases
inferredcites →https://doi.org/10.1016/0195-6701(83)90003-8openalex-snapshot
Genetics of drug resistance in methicillin-resistant Staphylococcus aureus from Australian hospitals
inferredcites →https://doi.org/10.1016/0195-6701(87)90027-2openalex-snapshot
A hospital outbreak caused by a chlorhexidine and antibiotic-resistant Proteus mirabilis
inferredcites →https://doi.org/10.1016/0378-1097(92)90405-dopenalex-snapshot
Metal ion-catalysed hydrolysis of ampicillin in microbiological growth media
inferredcites →https://doi.org/10.1016/0378-1097(94)00493-bopenalex-snapshot
vanA-mediated high-level glycopeptide resistance in Enterococcus faecium from animal husbandry
inferredcites →https://doi.org/10.1016/0964-8305(95)00055-0openalex-snapshot
A brief history of heat, chemical and radiation preservation and disinfection
inferredcites →https://doi.org/10.1016/0964-8305(95)00056-9openalex-snapshot
Mechanisms of bacterial resistance to biocides
inferredcites →https://doi.org/10.1016/j.burns.2014.09.009openalex-snapshot
Silver in medicine: A brief history BC 335 to present
inferredcites →https://doi.org/10.1016/j.diagmicrobio.2014.06.002openalex-snapshot
Erythromycin- and copper-resistant Enterococcus hirae from marine sediment and co-transfer of erm(B) and tcrB to human Enterococcus faecalis
inferredcites →https://doi.org/10.1016/j.envres.2012.01.002openalex-snapshot
Heavy metals in liquid pig manure in light of bacterial antimicrobial resistance
inferredcites →https://doi.org/10.1016/j.femsle.2004.04.049openalex-snapshot
Low level of cross-resistance between triclosan and antibiotics in Escherichia coli K-12 and E. coli O55 compared to E. coli O157
inferredcites →https://doi.org/10.1016/j.foodcont.2009.02.011openalex-snapshot
Comparison of antibiotic resistance patterns in Listeria monocytogenes and Salmonella enterica strains pre-exposed and exposed to poultry decontaminants
inferredcites →https://doi.org/10.1016/j.foodcont.2012.01.018openalex-snapshot
The potential for biocide tolerance in Escherichia coli and its impact on the response to food processing stresses
inferredcites →https://doi.org/10.1016/j.foodcont.2013.08.041openalex-snapshot
Antimicrobial resistance determinants in antibiotic and biocide-resistant gram-negative bacteria from organic foods
inferredcites →https://doi.org/10.1016/j.foodcont.2013.11.046openalex-snapshot
Effect of sub-lethal concentrations of biocides on the susceptibility to antibiotics of multi-drug resistant Salmonella enterica strains
inferredcites →https://doi.org/10.1016/j.foodres.2011.02.002openalex-snapshot
Control of Salmonella in food related environments by chemical disinfection
inferredcites →https://doi.org/10.1016/j.foodres.2014.07.049openalex-snapshot
The sub-species characterization and antimicrobial resistance of Listeria monocytogenes isolated from domestic and imported food products from 2004 to 2011
inferredcites →https://doi.org/10.1016/j.ibiod.2005.11.002openalex-snapshot
Chloroxylenol- and triclosan-tolerant bacteria from industrial sources—susceptibility to antibiotics and other biocides
inferredcites →https://doi.org/10.1016/j.ijantimicag.2004.07.016openalex-snapshot
Mechanisms of resistance in Salmonella enterica adapted to erythromycin, benzalkonium chloride and triclosan
inferredcites →https://doi.org/10.1016/j.ijantimicag.2010.04.012openalex-snapshot
Prevalence of decreased susceptibility to triclosan in Salmonella enterica isolates from animals and humans and association with multiple drug resistance
inferredcites →https://doi.org/10.1016/j.ijantimicag.2012.01.011openalex-snapshot
Emergence of resistance to antibacterial agents: the role of quaternary ammonium compounds—a critical review
inferredcites →https://doi.org/10.1016/j.ijantimicag.2015.01.013openalex-snapshot
Metal tolerance in emerging clinically relevant multidrug-resistant Salmonella enterica serotype 4,[5],12:i:− clones circulating in Europe
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2006.08.008openalex-snapshot
Efflux pump activity in fluoroquinolone and tetracycline resistant Salmonella and E. coli implicated in reduced susceptibility to household antimicrobial cleaning agents
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2009.10.002openalex-snapshot
Tests for determining in-use concentrations of antibiotics and disinfectants are based on entirely different concepts: “Resistance” has different meanings
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2012.11.006openalex-snapshot
Development of antimicrobial resistance in Campylobacter jejuni and Campylobacter coli adapted to biocides
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2012.12.028openalex-snapshot
Biocide tolerance in bacteria
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2014.04.021openalex-snapshot
Biocide and antibiotic susceptibility of Salmonella isolates obtained before and after cleaning at six Danish pig slaughterhouses
inferredcites →https://doi.org/10.1016/j.ijmm.2009.11.002openalex-snapshot
Emergence of methicillin-resistant Staphylococcus aureus (MRSA) in different animal species
inferredcites →https://doi.org/10.1016/j.ijmm.2013.06.004openalex-snapshot
The broader context of antibiotic resistance: Zinc feed supplementation of piglets increases the proportion of multi-resistant Escherichia coli in vivo
inferredcites →https://doi.org/10.1016/j.jhin.2011.06.008openalex-snapshot
Effect of higher minimum inhibitory concentrations of quaternary ammonium compounds in clinical E. coli isolates on antibiotic susceptibilities and clinical outcomes
inferredcites →https://doi.org/10.1016/j.jprot.2012.12.025openalex-snapshot
Proteomic and phenotypic analysis of triclosan tolerant verocytotoxigenic Escherichia coli O157:H19
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/j.prevetmed.2014.02.010openalex-snapshot
Effects of chlortetracycline and copper supplementation on antimicrobial resistance of fecal Escherichia coli from weaned pigs
inferredcites →https://doi.org/10.1016/j.tim.2006.02.006openalex-snapshot
Co-selection of antibiotic and metal resistance
inferredcites →https://doi.org/10.1016/j.vetmic.2004.01.013openalex-snapshot
Susceptibility of different bacterial species isolated from food animals to copper sulphate, zinc chloride and antimicrobial substances used for disinfection
inferredcites →https://doi.org/10.1016/j.vetmic.2005.01.013openalex-snapshot
Possible associations between Salmonella persistence in poultry houses and resistance to commonly used disinfectants and a putative role of mar
inferredcites →https://doi.org/10.1016/j.vetmic.2009.09.025openalex-snapshot
spa type distribution in Staphylococcus aureus originating from pigs, cattle and poultry
inferredcites →https://doi.org/10.1016/j.vetmic.2009.10.021openalex-snapshot
Decreased susceptibility to zinc chloride is associated with methicillin resistant Staphylococcus aureus CC398 in Danish swine
inferredcites →https://doi.org/10.1016/j.vetmic.2010.09.002openalex-snapshot
Antimicrobial and heavy metal resistance in commensal enterococci isolated from pigs
inferredcites →https://doi.org/10.1016/j.vetmic.2011.05.025openalex-snapshot
Effects of tetracycline and zinc on selection of methicillin-resistant Staphylococcus aureus (MRSA) sequence type 398 in pigs
inferredcites →https://doi.org/10.1016/j.vetmic.2012.01.030openalex-snapshot
Resistance to phenicol compounds following adaptation to quaternary ammonium compounds in Escherichia coli
inferredcites →https://doi.org/10.1016/j.vetmic.2014.09.023openalex-snapshot
Author's response: Critique of paper on ‘Effects of tetracycline and zinc on selection of methicillin-resistant Staphylococcus aureus (MRSA) sequence type 398 in pigs’
inferredcites →https://doi.org/10.1016/s0048-9697(03)00139-6openalex-snapshot
An inventory of heavy metals inputs to agricultural soils in England and Wales
inferredcites →https://doi.org/10.1016/s0168-6445(03)00047-0openalex-snapshot
Bacterial silver resistance: molecular biology and uses and misuses of silver compounds
inferredcites →https://doi.org/10.1016/s0168-6445(03)00049-4openalex-snapshot
Escherichia colimechanisms of copper homeostasis in a changing environment
inferredcites →https://doi.org/10.1016/s0168-6445(03)00053-6openalex-snapshot
Copper homeostasis inEnterococcus hirae
inferredcites →https://doi.org/10.1016/s0195-6701(99)90424-3openalex-snapshot
Antibiotic and biocide resistance in methicillin-resistant staphylococcus aureus and vancomycin-resistant enterococcus
inferredcites →https://doi.org/10.1016/s0378-1097(03)00099-5openalex-snapshot
Exposure ofSalmonellaEnteritidis to chlorine or food preservatives increases susceptibility to antibiotics
inferredcites →https://doi.org/10.1016/s0378-1097(03)00305-7openalex-snapshot
Corrigendum to “Exposure of Salmonella Enteritidis to chlorine or food preservatives increases susceptibility to antibiotics” [FEMS Microbiol. Lett. 220 (2003) 181–186]
inferredcites →https://doi.org/10.1016/s0378-1097(98)00347-4openalex-snapshot
Overexpression of marA, soxS, or acrAB produces resistance to triclosan in laboratory and clinical strains of Escherichia coli
inferredcites →https://doi.org/10.1016/s0964-8305(01)00037-3openalex-snapshot
Biocide tolerance and the harbingers of doom
inferredcites →https://doi.org/10.1016/s1473-3099(03)00833-8openalex-snapshot
Biocide use and antibiotic resistance: the relevance of laboratory findings to clinical and environmental situations
inferredcites →https://doi.org/10.1017/s0022029912000295openalex-snapshot
Adaptation to benzalkonium chloride and ciprofloxacin affects biofilm formation potential, efflux pump and haemolysin activity of Escherichia coli of dairy origin
inferredcites →https://doi.org/10.1017/s0950268800067819openalex-snapshot
Pattern of antibiotic and heavy-metal ion resistance in recent hospital isolates ofStaphylococcus aureus
inferredcites →https://doi.org/10.1021/acs.est.5b00644openalex-snapshot
Distinguishing Effects of Ultraviolet Exposure and Chlorination on the Horizontal Transfer of Antibiotic Resistance Genes in Municipal Wastewater
inferredcites →https://doi.org/10.1021/es101798ropenalex-snapshot
Cu Exposure under Field Conditions Coselects for Antibiotic Resistance as Determined by a Novel Cultivation-Independent Bacterial Community Tolerance Assay
inferredcites →https://doi.org/10.1021/es401507kopenalex-snapshot
Long-Term Exposure to Benzalkonium Chloride Disinfectants Results in Change of Microbial Community Structure and Increased Antimicrobial Resistance
inferredcites →https://doi.org/10.1038/nature09354openalex-snapshot
Bacterial charity work leads to population-wide resistance
inferredcites →https://doi.org/10.1038/nchembio.1380openalex-snapshot
The multiple antibiotic resistance regulator MarR is a copper sensor in Escherichia coli
inferredcites →https://doi.org/10.1038/sj.jim.7000320openalex-snapshot
Chloroxylenol- and triclosan-tolerant bacteria from industrial sources
inferredcites →https://doi.org/10.1046/j.1365-2672.1997.00171.xopenalex-snapshot
Glutaraldehyde‐resistant Mycobacterium chelonae from endoscope washer disinfectors
inferredcites →https://doi.org/10.1046/j.1365-2672.2003.02140.xopenalex-snapshot
Cross-resistance to antibiotics of Escherichia coli adapted to benzalkonium chloride or exposed to stress-inducers
inferredcites →https://doi.org/10.1046/j.1365-2672.92.5s1.13.xopenalex-snapshot
Exploiting current understanding of antibiotic action for discovery of new drugs
inferredcites →https://doi.org/10.1046/j.1365-2672.92.5s1.15.xopenalex-snapshot
Significance of biocide usage and antimicrobial resistance in domiciliary environments
inferredcites →https://doi.org/10.1046/j.1365-2672.92.5s1.3.xopenalex-snapshot
Bacterial target sites for biocide action
inferredcites →https://doi.org/10.1046/j.1365-2672.92.5s1.5.xopenalex-snapshot
Biofilms in vitro and in vivo : do singular mechanisms imply cross-resistance?
inferredcites →https://doi.org/10.1046/j.1365-2672.92.5s1.8.xopenalex-snapshot
Mechanisms of bacterial biocide and antibiotic resistance
inferredcites →https://doi.org/10.1046/j.1469-0691.2000.00149.xopenalex-snapshot
Terminology relating to methods for the determination of susceptibility of bacteria to antimicrobial agents
inferredcites →https://doi.org/10.1051/vetres:2001122openalex-snapshot
Importance of integrons in the diffusion of resistance
inferredcites →https://doi.org/10.1080/03079457.2010.537303openalex-snapshot
Evaluation of commonly-used farm disinfectants in wet and dry models ofSalmonellafarm contamination
inferredcites →https://doi.org/10.1080/07853890701195262openalex-snapshot
Efflux pumps as antimicrobial resistance mechanisms
inferredcites →https://doi.org/10.1080/1120009x.2009.12030920openalex-snapshot
Bacterial Biocide Resistance
inferredcites →https://doi.org/10.1086/430063openalex-snapshot
Antiseptic "Resistance": Real or Perceived Threat?
inferredcites →https://doi.org/10.1086/647641openalex-snapshot
Susceptibility of Antibiotic-Susceptible and Antibiotic-Resistant Hospital Bacteria to Disinfectants
inferredcites →https://doi.org/10.1089/fpd.2006.0078openalex-snapshot
Antimicrobial Susceptibility of Listeria monocytogenes from Food Products
inferredcites →https://doi.org/10.1089/fpd.2011.1097openalex-snapshot
Evaluation of Bacterial Resistance to Essential Oils and Antibiotics After Exposure to Oregano and Cinnamon Essential Oils
inferredcites →https://doi.org/10.1089/fpd.2013.1635openalex-snapshot
Influence of the Treatment of Listeria monocytogenes and Salmonella enterica Serovar Typhimurium with Citral on the Efficacy of Various Antibiotics
inferredcites →https://doi.org/10.1089/fpd.2013.1724openalex-snapshot
Antibiotic Susceptibility in Benzalkonium Chloride-Resistant and -Susceptible Listeria monocytogenes Strains
inferredcites →https://doi.org/10.1089/mdr.2006.12.83openalex-snapshot
Triclosan and Antimicrobial Resistance in Bacteria: An Overview
inferredcites →https://doi.org/10.1089/mdr.2009.0120openalex-snapshot
Does the Wide Use of Quaternary Ammonium Compounds Enhance the Selection and Spread of Antimicrobial Resistance and Thus Threaten Our Health?
inferredcites →https://doi.org/10.1089/mdr.2012.0154openalex-snapshot
The Role of the qacA Gene in Mediating Resistance to Quaternary Ammonium Compounds
inferredcites →https://doi.org/10.1089/mdr.2012.0225openalex-snapshot
Resistant Mechanism Study of Benzalkonium Chloride Selected Salmonella Typhimurium Mutants
inferredcites →https://doi.org/10.1093/jac/46.1.11openalex-snapshot
Triclosan and antibiotic resistance in Staphylococcus aureus
inferredcites →https://doi.org/10.1093/jac/46.1.7openalex-snapshot
Epidemic Salmonella typhimurium DT 104--a truly international multiresistant clone
inferredcites →https://doi.org/10.1093/jac/49.1.11openalex-snapshot
Biocide abuse and antimicrobial resistance--a cause for concern?
inferredcites →https://doi.org/10.1093/jac/dkf071openalex-snapshot
Biocide abuse and antimicrobial resistance: being clear about the issues
inferredcites →https://doi.org/10.1093/jac/dkg379openalex-snapshot
Prevalence of multiple antibiotic resistance in 443 Campylobacter spp. isolated from humans and animals
inferredcites →https://doi.org/10.1093/jac/dkh168openalex-snapshot
Selection for high-level resistance by chronic triclosan exposure is not universal
inferredcites →https://doi.org/10.1093/jac/dkh376openalex-snapshot
Effect of triclosan or a phenolic farm disinfectant on the selection of antibiotic-resistant Salmonella enterica
inferredcites →https://doi.org/10.1093/jac/dkl443openalex-snapshot
Habituation to sub-lethal concentrations of tea tree oil (Melaleuca alternifolia) is associated with reduced susceptibility to antibiotics in human pathogens
inferredcites →https://doi.org/10.1093/jac/dkm314openalex-snapshot
Prolonged treatment of Salmonella enterica serovar Typhimurium with commercial disinfectants selects for multiple antibiotic resistance, increased efflux and reduced invasiveness
inferredcites →https://doi.org/10.1093/jac/dkm359openalex-snapshot
Commonly used farm disinfectants can select for mutant Salmonella enterica serovar Typhimurium with decreased susceptibility to biocides and antibiotics without compromising virulence
inferredcites →https://doi.org/10.1093/jac/dkm363openalex-snapshot
Induction of multiple antibiotic resistance in Bacteroides fragilis by benzene and benzene-derived active compounds of commonly used analgesics, antiseptics and cleaning agents
inferredcites →https://doi.org/10.1093/jac/dkm415openalex-snapshot
Fitness and dissemination of disinfectant-selected multiple-antibiotic-resistant (MAR) strains of Salmonella enterica serovar Typhimurium in chickens
inferredcites →https://doi.org/10.1093/jac/dkr228openalex-snapshot
Leakage of emerging clinically relevant multidrug-resistant Salmonella clones from pig farms
inferredcites →https://doi.org/10.1093/jac/dkr311openalex-snapshot
Antibiotic and antiseptic resistance genes are linked on a novel mobile genetic element: Tn6087
inferredcites →https://doi.org/10.1093/jac/dks321openalex-snapshot
Molecular mechanisms of higher MICs of antibiotics and quaternary ammonium compounds for Escherichia coli isolated from bacteraemia
inferredcites →https://doi.org/10.1093/jac/dku197openalex-snapshot
Presence of disinfectant resistance genes in Escherichia coli isolated from retail meats in the USA
inferredcites →https://doi.org/10.1093/ps/84.9.1418openalex-snapshot
Effect of butyric acid on the performance and carcass yield of broiler chickens
inferredcites →https://doi.org/10.1099/0022-1317-50-10-919openalex-snapshot
Association between cyclohexane resistance in Salmonella of different serovars and increased resistance to multiple antibiotics, disinfectants and dyes
inferredcites →https://doi.org/10.1099/00222615-34-4-193openalex-snapshot
Genetic characterisation of resistance to metal ions in methicillin-resistant Staphylococcus aureus: elimination of resistance to cadmium, mercury and tetracycline with loss of methicillin resistance
inferredcites →https://doi.org/10.1099/jmm.0.003657-0openalex-snapshot
Development of triclosan and antibiotic resistance in Salmonella enterica serovar Typhimurium
inferredcites →https://doi.org/10.1099/mic.0.2008/021188-0openalex-snapshot
Multidrug efflux pump overexpression in Staphylococcus aureus after single and multiple in vitro exposures to biocides and dyes
inferredcites →https://doi.org/10.1111/1574-6941.12419openalex-snapshot
Temporal changes and the effect of subtherapeutic concentrations of antibiotics in the gut microbiota of swine
inferredcites →https://doi.org/10.1111/j.1365-2672.2004.02192.xopenalex-snapshot
National survey for Salmonella in pigs, cattle and sheep at slaughter in Great Britain (1999-2000)
inferredcites →https://doi.org/10.1111/j.1365-2672.2004.02488.xopenalex-snapshot
Farm disinfectants select for cyclohexane resistance, a marker of multiple antibiotic resistance, in Escherichia coli
inferredcites →https://doi.org/10.1111/j.1365-2672.2006.02811.xopenalex-snapshot
Effects of chronic triclosan exposure upon the antimicrobial susceptibility of 40 ex-situ environmental and human isolates
inferredcites →https://doi.org/10.1111/j.1365-2958.1994.tb01289.xopenalex-snapshot
Permeability of the cell wall of Mycobacterium smegmatis
inferredcites →https://doi.org/10.1111/j.1462-2920.2006.01091.xopenalex-snapshot
Coselection for microbial resistance to metals and antibiotics in freshwater microcosms
inferredcites →https://doi.org/10.1111/j.1469-0691.2010.03215.xopenalex-snapshot
Enterococcus research: recent developments and clinical challenges
inferredcites →https://doi.org/10.1111/j.1472-765x.2004.01650.xopenalex-snapshot
Copper amendment of agricultural soil selects for bacterial antibiotic resistance in the field
inferredcites →https://doi.org/10.1111/j.1574-6968.2004.tb09603.xopenalex-snapshot
Low level of cross-resistance between triclosan and antibiotics inEscherichia coliK-12 andE. coliO55 compared toE. coliO157
inferredcites →https://doi.org/10.1111/j.1574-6968.2006.00547.xopenalex-snapshot
Effect of triclosan onSalmonella typhimuriumat different growth stages and in biofilms
inferredcites →https://doi.org/10.1111/jam.12790openalex-snapshot
Effects of in-feed copper and tylosin supplementations on copper and antimicrobial resistance in faecal enterococci of feedlot cattle
inferredcites →https://doi.org/10.1111/lam.12216openalex-snapshot
Natural extracts stimulate membrane-associated mechanisms of resistance in Gram-negative bacteria
inferredcites →https://doi.org/10.1111/zph.12150openalex-snapshot
Zinc Oxide Therapy Increases Prevalence and Persistence of Methicillin‐Resistant Staphylococcus aureus in Pigs: A Randomized Controlled Trial
inferredcites →https://doi.org/10.1128/aac.00058-10openalex-snapshot
Cloning and Occurrence of czrC , a Gene Conferring Cadmium and Zinc Resistance in Methicillin-Resistant Staphylococcus aureus CC398 Isolates
inferredcites →https://doi.org/10.1128/aac.00171-13openalex-snapshot
Novel erm (T)-Carrying Multiresistance Plasmids from Porcine and Human Isolates of Methicillin-Resistant Staphylococcus aureus ST398 That Also Harbor Cadmium and Copper Resistance Determinants
inferredcites →https://doi.org/10.1128/aac.00460-11openalex-snapshot
Sublethal Triclosan Exposure Decreases Susceptibility to Gentamicin and Other Aminoglycosides in Listeria monocytogenes
inferredcites →https://doi.org/10.1128/aac.02266-13openalex-snapshot
Triclosan-Induced Aminoglycoside-Tolerant Listeria monocytogenes Isolates Can Appear as Small-Colony Variants
inferredcites →https://doi.org/10.1128/aac.32.6.932openalex-snapshot
Antiseptic and antibiotic resistance plasmid in Staphylococcus aureus that possesses ability to confer chlorhexidine and acrinol resistance
inferredcites →https://doi.org/10.1128/aac.37.4.761openalex-snapshot
The 3' conserved segment of integrons contains a gene associated with multidrug resistance to antiseptics and disinfectants
inferredcites →https://doi.org/10.1128/aac.42.8.2089openalex-snapshot
Overexpression of the marA or soxS Regulatory Gene in Clinical Topoisomerase Mutants of Escherichia coli
inferredcites →https://doi.org/10.1128/aac.44.1.10-13.2000openalex-snapshot
Ineffectiveness of Topoisomerase Mutations in Mediating Clinically Significant Fluoroquinolone Resistance in Escherichia coli in the Absence of the AcrAB Efflux Pump
inferredcites →https://doi.org/10.1128/aac.46.5.1410-1416.2002openalex-snapshot
tcrB, a Gene Conferring Transferable Copper Resistance inEnterococcus faecium: Occurrence, Transferability, and Linkage to Macrolide and Glycopeptide Resistance
inferredcites →https://doi.org/10.1128/aac.8.3.334openalex-snapshot
Effect of Surfactants on Antibiotic Resistance
inferredcites →https://doi.org/10.1128/aem.00036-15openalex-snapshot
Methicillin-Resistant Staphylococcus aureus in Commercial Swine Herds Is Associated with Disinfectant and Zinc Usage
inferredcites →https://doi.org/10.1128/aem.00418-14openalex-snapshot
Impact of UV and Peracetic Acid Disinfection on the Prevalence of Virulence and Antimicrobial Resistance Genes in Uropathogenic Escherichia coli in Wastewater Effluents
inferredcites →https://doi.org/10.1128/aem.01931-07openalex-snapshot
Phenotypic and Proteomic Characterization of Multiply Antibiotic-Resistant Variants ofSalmonella entericaSerovar Typhimurium Selected Following Exposure to Disinfectants
inferredcites →https://doi.org/10.1128/aem.02283-13openalex-snapshot
Exposure of Escherichia coli ATCC 12806 to Sublethal Concentrations of Food-Grade Biocides Influences Its Ability To Form Biofilm, Resistance to Antimicrobials, and Ultrastructure
inferredcites →https://doi.org/10.1128/aem.02979-05openalex-snapshot
Copper Resistance in Enterococcus faecium , Mediated by the tcrB Gene, Is Selected by Supplementation of Pig Feed with Copper Sulfate
inferredcites →https://doi.org/10.1128/aem.04283-13openalex-snapshot
In-Feed Use of Heavy Metal Micronutrients in U.S. Swine Production Systems and Its Role in Persistence of Multidrug-Resistant Salmonellae
inferredcites →https://doi.org/10.1128/aem.05941-11openalex-snapshot
Listeria monocytogenes Strains Selected on Ciprofloxacin or the Disinfectant Benzalkonium Chloride Exhibit Reduced Susceptibility to Ciprofloxacin, Gentamicin, Benzalkonium Chloride, and Other Toxic Compounds
inferredcites →https://doi.org/10.1128/aem.07534-11openalex-snapshot
Efficacy of Biocides Used in the Modern Food Industry To Control Salmonella enterica, and Links between Biocide Tolerance and Resistance to Clinically Relevant Antimicrobial Compounds
inferredcites →https://doi.org/10.1128/aem.68.8.4127-4129.2002openalex-snapshot
Antimicrobial Resistance among Enterococci from Pigs in Three European Countries
inferredcites →https://doi.org/10.1128/aem.72.5.3498-3503.2006openalex-snapshot
Role of Efflux Pumps in Adaptation and Resistance of Listeria monocytogenes to Benzalkonium Chloride
inferredcites →https://doi.org/10.1128/cmr.12.1.147openalex-snapshot
Antiseptics and Disinfectants: Activity, Action, and Resistance
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Efficacy of Chemical Interventions against Escherichia coli O157:H7 and Multidrug-Resistant and Antibiotic-Susceptible Salmonella on Inoculated Beef Trimmings
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Prevalence and Antimicrobial Resistance of Salmonella Isolates from Retail Meats in Indiana, USA
inferred← citeshttps://doi.org/10.1016/j.jgar.2021.08.001openalex-snapshot
Environmental antimicrobial resistance and its drivers: a potential threat to public health
inferred← citeshttps://doi.org/10.1016/j.jgar.2023.02.024openalex-snapshot
Genomic characterization of a multidrug-resistant Salmonella Rissen ST469 carrying blaCTX-M-55 gene and Tn6777 isolated from a paediatric patient in China
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.130898openalex-snapshot
Metagenomic analysis characterizes resistomes of an acidic, multimetal(loid)-enriched coal source mine drainage treatment system
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.134202openalex-snapshot
Emerging threat: Antimicrobial resistance proliferation during epidemics — A case study of the SARS-CoV-2 pandemic in South Brazil
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2026.141092openalex-snapshot
Urban habitat types modulate soil contamination and bacterial functional traits through antibiotic resistance genes and metal(loid) interactions
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2026.141522openalex-snapshot
Strategy selection for addressing antibiotic pollution in farmland soils based on the analysis of source apportionment and risk decomposition
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2026.141666openalex-snapshot
Transmission and migration of antibiotic resistance genes following agricultural fertilization in sloping croplands
inferred← citeshttps://doi.org/10.1016/j.jhin.2020.06.006openalex-snapshot
Selection of resistance by antimicrobial coatings in the healthcare setting
inferred← citeshttps://doi.org/10.1016/j.jhin.2024.05.006openalex-snapshot
Resistance or tolerance? Highlighting the need for precise terminology in the field of disinfection
inferred← citeshttps://doi.org/10.1016/j.jksus.2022.101979openalex-snapshot
The growing menace of drug resistant pathogens and recent strategies to overcome drug resistance: A review
inferred← citeshttps://doi.org/10.1016/j.jtemin.2023.100085openalex-snapshot
A review of the impact of dietary zinc on livestock health
inferred← citeshttps://doi.org/10.1016/j.lanmic.2025.101115openalex-snapshot
Does anticancer therapy directly contribute to antimicrobial resistance?
inferred← citeshttps://doi.org/10.1016/j.lwt.2026.119523openalex-snapshot
Unveiling antibiotic and biocide resistance genes in slaughterhouse environments: A One Health qPCR study
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.119206openalex-snapshot
Isolation and whole-genome sequencing of antibiotic-resistant bacteria revealed the reservoir for indigenous antibiotic resistance genes in the deepest ocean sediment of the Challenger Deep
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2026.119876openalex-snapshot
Multi-media antibiotics, intracellular and extracellular antibiotic resistance genes in marine protected areas of the South China Sea: Spatiotemporal distribution and multi-factor drivers of dissemination
inferred← citeshttps://doi.org/10.1016/j.meegid.2020.104437openalex-snapshot
Shewanella harboring antimicrobial and copper resistance genes in sea urchins (Paracentrotus lividus) from the Crozon peninsula (Brittany, France)
inferred← citeshttps://doi.org/10.1016/j.meegid.2025.105840openalex-snapshot
Deciphering the mobility, pathogenic hosts, and co-selection of antibiotic resistance genes in untreated wastewater from three different hospitals
inferred← citeshttps://doi.org/10.1016/j.micpath.2026.108429openalex-snapshot
Pan-genome analysis of methicillin-resistant Staphylococcus aureus PSU20 from a hospital in Thailand reveals insights into virulence, antibiotic resistance, and genetic diversity
inferred← citeshttps://doi.org/10.1016/j.micres.2025.128357openalex-snapshot
Global copper response of the soil bacterial predator Myxococcus xanthus and its contribution to antibiotic cross-resistance
inferred← citeshttps://doi.org/10.1016/j.mimet.2021.106174openalex-snapshot
Twenty-first century molecular methods for analyzing antimicrobial resistance in surface waters to support One Health assessments
inferred← citeshttps://doi.org/10.1016/j.nexres.2025.100284openalex-snapshot
Global cross-genome comparison of carbohydrate transporters in Staphylococcus aureus with distinct antimicrobial susceptibility profiles
inferred← citeshttps://doi.org/10.1016/j.onehlt.2021.100298openalex-snapshot
Antimicrobial resistance in wildlife and in the built environment in a wildlife rehabilitation center
inferred← citeshttps://doi.org/10.1016/j.plana.2025.100138openalex-snapshot
Biogenic CuO nanoparticles from Camellia sinensis and Pimpinella anisum plant extracts and their role as antimicrobial agents
inferred← citeshttps://doi.org/10.1016/j.psj.2020.10.045openalex-snapshot
Disinfectant and antimicrobial susceptibility studies of the foodborne pathogen Campylobacter jejuni isolated from the litter of broiler chicken houses
inferred← citeshttps://doi.org/10.1016/j.psj.2026.106528openalex-snapshot
Poultry Proteus mirabilis in selected areas of Hunan, China: Resistance profiles and virulence genes
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.10.312openalex-snapshot
Antibiotics and common antibacterial biocides stimulate horizontal transfer of resistance at low concentrations
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2018.06.204openalex-snapshot
The effects of marine farm-scale sequentially integrated multi-trophic aquaculture systems on microbial community composition, prevalence of sulfonamide-resistant bacteria and sulfonamide resistance gene sul1
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.01.406openalex-snapshot
Antibiotic pollution in surface fresh waters: Occurrence and effects
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.146452openalex-snapshot
Characteristics of phytoplankton-zooplankton communities and the roles in the transmission of antibiotic resistance genes under the pressure of river contamination
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.154890openalex-snapshot
Spatiotemporal distribution of antimicrobial resistant organisms in different water environments in urban and rural settings of Bangladesh
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.159609openalex-snapshot
Impacts of dietary copper on the swine gut microbiome and antibiotic resistome
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.162148openalex-snapshot
Bacterial metal(loid) resistance genes (MRGs) and their variation and application in environment: A review
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.162330openalex-snapshot
Coal-source acid mine drainage reduced the soil multidrug-dominated antibiotic resistome but increased the heavy metal(loid) resistome and energy production-related metabolism
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.169567openalex-snapshot
Temporal variations of antimicrobial resistance genes in aerosols: A one-year monitoring at the puy de Dôme summit (Central France)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.174274openalex-snapshot
Arsenic behavior in soil-plant system under the manure application with the combination of antibiotic and roxarsone
inferred← citeshttps://doi.org/10.1016/j.tifs.2017.09.007openalex-snapshot
The agri-food chain and antimicrobial resistance: A review
inferred← citeshttps://doi.org/10.1016/j.tim.2017.04.010openalex-snapshot
At the Nexus of Antibiotics and Metals: The Impact of Cu and Zn on Antibiotic Activity and Resistance
inferred← citeshttps://doi.org/10.1016/j.tim.2018.03.004openalex-snapshot
Convergent Evolution in Intracellular Elements: Plasmids as Model Endosymbionts
inferred← citeshttps://doi.org/10.1016/j.vetmic.2021.109010openalex-snapshot
Genetic diversity of extended-spectrum cephalosporin resistance in Salmonella enterica and E. coli isolates in a single broiler chicken
inferred← citeshttps://doi.org/10.1016/j.vetmic.2024.110171openalex-snapshot
Prevalence and molecular characteristics of intestinal pathogenic Escherichia coli isolated from diarrheal pigs in Southern China
inferred← citeshttps://doi.org/10.1016/j.wasman.2025.115278openalex-snapshot
Investigating safety aspects of using insect farming to reduce pig and chicken wastes at semi-commercial and lab-scale
inferred← citeshttps://doi.org/10.1016/j.watres.2019.115073openalex-snapshot
Aromatic compounds lead to increased abundance of antibiotic resistance genes in wastewater treatment bioreactors
inferred← citeshttps://doi.org/10.1016/j.watres.2019.115229openalex-snapshot
Both silver ions and silver nanoparticles facilitate the horizontal transfer of plasmid-mediated antibiotic resistance genes
inferred← citeshttps://doi.org/10.1016/j.watres.2020.116127openalex-snapshot
Source tracking of antibiotic resistance genes in the environment — Challenges, progress, and prospects
inferred← citeshttps://doi.org/10.1016/j.watres.2025.123699openalex-snapshot
Unveiling the prevalence of metal resistance genes and their associations with antibiotic resistance genes in heavy metal-contaminated rivers
inferred← citeshttps://doi.org/10.1016/j.wroa.2026.100506openalex-snapshot
Impacts of wastewater treatment and the exposome on antibiotic resistance gene dynamics: Insights from Guadeloupe, a French Caribbean Island
inferred← citeshttps://doi.org/10.1016/s1002-0160(21)60089-9openalex-snapshot
Genomic characterization of multidrug-resistant extraintestinal pathogenic Escherichia coli isolated from grain culture soils
inferred← citeshttps://doi.org/10.1021/acs.est.1c02977openalex-snapshot
What Is the Role of the Environment in the Emergence of Novel Antibiotic Resistance Genes? A Modeling Approach
inferred← citeshttps://doi.org/10.1021/acs.est.2c00406openalex-snapshot
Triclosan is the Predominant Antibacterial Compound in Ontario Sewage Sludge
inferred← citeshttps://doi.org/10.1021/acs.est.2c01633openalex-snapshot
Characteristics of Wild Bird Resistomes and Dissemination of Antibiotic Resistance Genes in Interconnected Bird-Habitat Systems Revealed by Similarity of blaTEM Polymorphic Sequences
inferred← citeshttps://doi.org/10.1021/acs.est.3c06060openalex-snapshot
Understanding Stimulation of Conjugal Gene Transfer by Nonantibiotic Compounds: How Far Are We?
inferred← citeshttps://doi.org/10.1021/acs.est.5b06348openalex-snapshot
Effect of Dust Storms on the Atmospheric Microbiome in the Eastern Mediterranean
inferred← citeshttps://doi.org/10.1021/acsestwater.5c00540openalex-snapshot
Free-Living Protozoa as Important Drivers of Antimicrobial Resistance in Engineered Water Systems and Their Ecological Niches
inferred← citeshttps://doi.org/10.1021/acsestwater.6c00558openalex-snapshot
Wastewater Resistance Dynamics: Antibiotic–Disinfectant Interaction Patterns, Surveillance, and Emerging Containment Strategies
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c03933openalex-snapshot
Amphiphilic Copolymer Thin Films with Short Fluoroalkyl Side Chains for Antibiofilm Properties at the Solid–Liquid–Air Interface
inferred← citeshttps://doi.org/10.1021/envhealth.5c00278openalex-snapshot
Resistance Gene Dynamics, Biogeochemical Coupling, and Ecological Risks in Sediments of Anthropogenically Impacted Lake Wetlands in China
inferred← citeshttps://doi.org/10.1038/ismej.2016.155openalex-snapshot
Co-occurrence of antibiotic and metal resistance genes revealed in complete genome collection
inferred← citeshttps://doi.org/10.1038/s41396-023-01514-wopenalex-snapshot
Oxytetracycline and heavy metals promote the migration of resistance genes in the intestinal microbiome by plasmid transfer
inferred← citeshttps://doi.org/10.1038/s41429-023-00649-4openalex-snapshot
Mechanisms of emerging resistance associated with non-antibiotic antimicrobial agents: a state-of-the-art review
inferred← citeshttps://doi.org/10.1038/s41467-020-19820-8openalex-snapshot
The structural basis of promiscuity in small multidrug resistance transporters
inferred← citeshttps://doi.org/10.1038/s41467-024-54459-9openalex-snapshot
Evidence of horizontal gene transfer and environmental selection impacting antibiotic resistance evolution in soil-dwelling Listeria
inferred← citeshttps://doi.org/10.1038/s41467-025-59758-3openalex-snapshot
A global atlas and drivers of antimicrobial resistance in Salmonella during 1900-2023
inferred← citeshttps://doi.org/10.1038/s41467-025-61055-yopenalex-snapshot
Phage-mediated peripheral kill-the-winner facilitates the maintenance of costly antibiotic resistance
inferred← citeshttps://doi.org/10.1038/s41522-025-00890-9openalex-snapshot
Microplastic biofilm as hotspots of antibiotic resistance genes and potential pathogens
inferred← citeshttps://doi.org/10.1038/s41545-023-00261-xopenalex-snapshot
Transition of antimicrobial resistome in wastewater treatment plants: impact of process configuration, geographical location and season
inferred← citeshttps://doi.org/10.1038/s41564-023-01474-zopenalex-snapshot
Systematic analyses identify modes of action of ten clinically relevant biocides and antibiotic antagonism in Acinetobacter baumannii
inferred← citeshttps://doi.org/10.1038/s41579-021-00649-xopenalex-snapshot
Antibiotic resistance in the environment
inferred← citeshttps://doi.org/10.1038/s41579-023-00958-3openalex-snapshot
Disinfectants and antiseptics: mechanisms of action and resistance
inferred← citeshttps://doi.org/10.1038/s41598-019-49464-8openalex-snapshot
Impact of cleaning and disinfection procedures on microbial ecology and Salmonella antimicrobial resistance in a pig slaughterhouse
inferred← citeshttps://doi.org/10.1038/s41598-020-77446-8openalex-snapshot
Antiseptic quaternary ammonium compound tolerance by gram-negative bacteria can be rapidly detected using an impermeant fluorescent dye-based assay
inferred← citeshttps://doi.org/10.1038/s41598-022-09689-6openalex-snapshot
Adsorptive colorimetric determination of chromium(VI) ions at ultratrace levels using amine functionalized mesoporous silica
inferred← citeshttps://doi.org/10.1038/s41598-023-42822-7openalex-snapshot
Recovery of the gut microbiome following enteric infection and persistence of antimicrobial resistance genes in specific microbial hosts
inferred← citeshttps://doi.org/10.1038/s41598-024-54738-xopenalex-snapshot
Impact of zinc supplementation on phenotypic antimicrobial resistance of fecal commensal bacteria from pre-weaned dairy calves
inferred← citeshttps://doi.org/10.1038/s41598-025-27034-5openalex-snapshot
High-throughput bacterial aggregation analysis in droplets
inferred← citeshttps://doi.org/10.1038/s41598-026-42583-zopenalex-snapshot
Third generation cephalosporin-resistant (3GCR) Escherichia coli and biocide-tolerant heterotrophic bacteria in irrigation water used in Capsicum annuum cultivation areas in Kosovo
inferred← citeshttps://doi.org/10.1038/s41893-018-0164-3openalex-snapshot
Antibiotic and pesticide susceptibility and the Anthropocene operating space
inferred← citeshttps://doi.org/10.1038/s44221-025-00514-8openalex-snapshot
Assessing antimicrobial resistance connectivity across One Health sectors
inferred← citeshttps://doi.org/10.1038/s44259-024-00026-7openalex-snapshot
Co-selection for antibiotic resistance by environmental contaminants
inferred← citeshttps://doi.org/10.1038/s44259-024-00042-7openalex-snapshot
Transition metal homoeostasis is key to metabolism and drug tolerance of Mycobacterium abscessus
inferred← citeshttps://doi.org/10.1038/s44259-025-00108-0openalex-snapshot
Reviewing the complexities of bacterial biocide susceptibility and in vitro biocide adaptation methodologies
inferred← citeshttps://doi.org/10.1038/srep25312openalex-snapshot
Co-spread of metal and antibiotic resistance within ST3-IncHI2 plasmids from E. coli isolates of food-producing animals
inferred← citeshttps://doi.org/10.1039/d3ew00356fopenalex-snapshot
Antibiotic resistance in urban stormwater: a review of the dissemination of resistance elements, their impact, and management opportunities
inferred← citeshttps://doi.org/10.1051/bioconf/202622806001openalex-snapshot
Biofilms and antimicrobial resistance: A hidden driver in the one health AMR crisis
inferred← citeshttps://doi.org/10.1080/00207233.2020.1719804openalex-snapshot
Occurrence of metal and antibiotic resistant Escherichia coli harbouring zntA and copA genes in selected surface water in Ibadan, South-west Nigeria
inferred← citeshttps://doi.org/10.1080/03079457.2022.2065969openalex-snapshot
Antimicrobial susceptibility, plasmid replicon typing, phylogenetic grouping, and virulence potential of avian pathogenic and faecal Escherichia coli isolated from meat chickens in Australia
inferred← citeshttps://doi.org/10.1080/08927014.2021.1955250openalex-snapshot
Plumbagin inhibits quorum sensing-regulated virulence and biofilms of Gram-negative bacteria:in vitroandin silicoinvestigations
inferred← citeshttps://doi.org/10.1080/10408398.2020.1798345openalex-snapshot
Antimicrobial resistance associated with the use of antimicrobial processing aids during poultry processing operations: cause for concern?
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