On the public citation graph

The European Union summary report on antimicrobial resistance in zoonotic and indicator bacteria from humans, animals and food in 2017

https://doi.org/10.2903/j.efsa.2019.5598
0 signed · 439 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/emmm.201202413openalex-snapshot
Whole genome sequencing identifies zoonotic transmission of MRSA isolates with the novel mecA homologue mecC
inferredcites →https://doi.org/10.1016/j.cimid.2015.02.003openalex-snapshot
Higher resistance of Campylobacter coli compared to Campylobacter jejuni at chicken slaughterhouse
inferredcites →https://doi.org/10.1016/j.cmi.2015.05.022openalex-snapshot
Contemporary resistance trends and mechanisms for the old antibiotics colistin, temocillin, fosfomycin, mecillinam and nitrofurantoin
inferredcites →https://doi.org/10.1016/j.cmi.2017.01.013openalex-snapshot
Extended-spectrum β-lactamase/AmpC- and carbapenemase-producing Enterobacteriaceae in animals: a threat for humans?
inferredcites →https://doi.org/10.1016/j.cmi.2018.04.004openalex-snapshot
Carbapenem-resistant Enterobacteriaceae in wildlife, food-producing, and companion animals: a systematic review
inferredcites →https://doi.org/10.1016/j.fm.2016.03.004openalex-snapshot
Prevalence, antimicrobial susceptibility and molecular typing of Methicillin-Resistant Staphylococcus aureus (MRSA) in bulk tank milk from southern Italy
inferredcites →https://doi.org/10.1016/j.fm.2016.10.028openalex-snapshot
Prevalence and quantification of thermophilic Campylobacter spp. in Italian retail poultry meat: Analysis of influencing factors
inferredcites →https://doi.org/10.1016/j.fm.2018.01.018openalex-snapshot
Use of whole-genome sequencing for Campylobacter surveillance from NARMS retail poultry in the United States in 2015
inferredcites →https://doi.org/10.1016/j.ijantimicag.2016.06.025openalex-snapshot
Extended-spectrum β-lactamase-producing Salmonella enterica serovar Infantis from humans in Italy
inferredcites →https://doi.org/10.1016/j.ijantimicag.2016.09.016openalex-snapshot
Colistin use and colistin resistance in bacteria from animals
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2018.05.001openalex-snapshot
Emerging high-level ciprofloxacin resistance and molecular basis of resistance in Salmonella enterica from humans, food and animals
inferredcites →https://doi.org/10.1016/j.ijmm.2014.08.002openalex-snapshot
New patterns of methicillin-resistant Staphylococcus aureus (MRSA) clones, community-associated MRSA genotypes behave like healthcare-associated MRSA genotypes within hospitals, Argentina
inferredcites →https://doi.org/10.1016/j.jiac.2016.11.011openalex-snapshot
Molecular epidemiological analysis of human- and chicken-derived isolates of Campylobacter jejuni in Japan using next-generation sequencing
inferredcites →https://doi.org/10.1016/j.plasmid.2016.06.001openalex-snapshot
Novel plasmid conferring kanamycin and tetracycline resistance in the turkey-derived Campylobacter jejuni strain 11601MD
inferredcites →https://doi.org/10.1016/j.tim.2013.11.003openalex-snapshot
The emergence of mecC methicillin-resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1016/j.vetmic.2013.11.022openalex-snapshot
Identification and characterization of methicillin-resistant Staphylococcus aureus (MRSA) from Austrian companion animals and horses
inferredcites →https://doi.org/10.1016/j.vetmic.2014.02.001openalex-snapshot
An emerging public health problem: Acquired carbapenemase-producing microorganisms are present in food-producing animals, their environment, companion animals and wild birds
inferredcites →https://doi.org/10.1016/j.vetmic.2015.02.031openalex-snapshot
Prevalence of the immune evasion gene cluster in Staphylococcus aureus CC398
inferredcites →https://doi.org/10.1016/j.vetmic.2015.05.010openalex-snapshot
Methicillin-resistant Staphylococcus aureus (MRSA) is associated with low within-herd prevalence of intra-mammary infections in dairy cows: Genotyping of isolates
inferredcites →https://doi.org/10.1016/j.vetmic.2015.09.001openalex-snapshot
Comparative genome analysis of IncHI2 VIM-1 carbapenemase-encoding plasmids of Escherichia coli and Salmonella enterica isolated from a livestock farm in Germany
inferredcites →https://doi.org/10.1016/j.vetmic.2015.11.030openalex-snapshot
Prevalence of carbapenemase producing Enterobacteriaceae isolated from German pig-fattening farms during the years 2011–2013
inferredcites →https://doi.org/10.1016/j.vetmic.2015.12.007openalex-snapshot
Longitudinal study on the colonisation and transmission of methicillin-resistant Staphylococcus aureus in pig farms
inferredcites →https://doi.org/10.1016/j.vetmic.2016.04.026openalex-snapshot
Spread and persistence of VIM-1 Carbapenemase-producing Enterobacteriaceae in three German swine farms in 2011 and 2012
inferredcites →https://doi.org/10.1016/j.vetmic.2016.05.021openalex-snapshot
Simultaneous occurrence of MRSA and ESBL-producing Enterobacteriaceae on pig farms and in nasal and stool samples from farmers
inferredcites →https://doi.org/10.1016/j.vetmic.2016.11.013openalex-snapshot
Antimicrobial resistance at the interface of human and veterinary medicine
inferredcites →https://doi.org/10.1016/j.vetmic.2017.06.004openalex-snapshot
High occurrence of mecC -MRSA in wild hedgehogs ( Erinaceus europaeus ) in Sweden
inferredcites →https://doi.org/10.1016/s1369-5274(99)80053-8openalex-snapshot
The role of short sequence repeats in epidemiologic typing
inferredcites →https://doi.org/10.1016/s1473-3099(11)70126-8openalex-snapshot
Meticillin-resistant Staphylococcus aureus with a novel mecA homologue in human and bovine populations in the UK and Denmark: a descriptive study
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/10.1017/s0950268812000568openalex-snapshot
Estimating the true incidence of campylobacteriosis and salmonellosis in the European Union, 2009
inferredcites →https://doi.org/10.1017/s0950268812002166openalex-snapshot
Community incidence of pathogen-specific gastroenteritis: reconstructing the surveillance pyramid for seven pathogens in seven European Union member states
inferredcites →https://doi.org/10.1038/ismej.2015.149openalex-snapshot
Rapid host switching in generalist Campylobacter strains erodes the signal for tracing human infections
inferredcites →https://doi.org/10.1038/nmicrobiol.2016.260openalex-snapshot
Comprehensive resistome analysis reveals the prevalence of NDM and MCR-1 in Chinese poultry production
inferredcites →https://doi.org/10.1038/s41598-017-05227-xopenalex-snapshot
A combined case-control and molecular source attribution study of human Campylobacter infections in Germany, 2011–2014
inferredcites →https://doi.org/10.1038/srep20939openalex-snapshot
Human Campylobacteriosis in Luxembourg, 2010–2013: A Case-Control Study Combined with Multilocus Sequence Typing for Source Attribution and Risk Factor Analysis
inferredcites →https://doi.org/10.1073/pnas.0408966102openalex-snapshot
Enhanced in vivo fitness of fluoroquinolone-resistant Campylobacter jejuni in the absence of antibiotic selection pressure
inferredcites →https://doi.org/10.1080/10408398.2015.1119798openalex-snapshot
Effect of Antimicrobial Use in Agricultural Animals on Drug-resistant Foodborne Campylobacteriosis in Humans: A Systematic Literature Review
inferredcites →https://doi.org/10.1089/107662904323047745openalex-snapshot
Characterization of β-Lactamases Responsible for Resistance to Extended-Spectrum Cephalosporins in Escherichia coli and Salmonella enterica Strains from Food-Producing Animals in the United Kingdom
inferredcites →https://doi.org/10.1089/fpd.2009.0354openalex-snapshot
Contribution of the Multidrug Efflux Transporter CmeABC to Antibiotic Resistance in Different Campylobacter Species
inferredcites →https://doi.org/10.1089/fpd.2011.1015openalex-snapshot
Tentative Colistin Epidemiological Cut-Off Value for Salmonella spp.
inferredcites →https://doi.org/10.1089/fpd.2016.2186openalex-snapshot
Antimicrobial Resistance of Campylobacter Species Isolated from Broilers in Live Bird Markets in Shanghai, China
inferredcites →https://doi.org/10.1089/fpd.2016.2223openalex-snapshot
The Molecular Mechanisms of Ciprofloxacin Resistance in Clinical Campylobacter jejuni and Their Genotyping Characteristics in Beijing, China
inferredcites →https://doi.org/10.1089/fpd.2018.2477openalex-snapshot
Lack of Evidence for erm (B) Infiltration Into Erythromycin-Resistant Campylobacter coli and Campylobacter jejuni from Commercial Turkey Production in Eastern North Carolina: A Major Turkey-Growing Region in the United States
inferredcites →https://doi.org/10.1089/mdr.2015.0161openalex-snapshot
Antimicrobial Drug Resistance and Molecular Typing of Salmonella enterica Serovar Rissen from Different Sources
inferredcites →https://doi.org/10.1089/mdr.2017.0198openalex-snapshot
Extended-Spectrum β-Lactamase, AmpC, and MBL-Producing Gram-Negative Bacteria on Fresh Vegetables and Ready-to-Eat Salads Sold in Local Markets
inferredcites →https://doi.org/10.1093/cid/ciw475openalex-snapshot
World Health Organization Ranking of Antimicrobials According to Their Importance in Human Medicine: A Critical Step for Developing Risk Management Strategies to Control Antimicrobial Resistance From Food Animal Production
inferredcites →https://doi.org/10.1093/cid/ciw532openalex-snapshot
Evidence for Human Adaptation and Foodborne Transmission of Livestock-Associated Methicillin-Resistant Staphylococcus aureus : Table 1.
inferredcites →https://doi.org/10.1093/cid/ciw552openalex-snapshot
Methicillin-ResistantStaphylococcus aureusCC398 in Humans and Pigs in Norway: A “One Health” Perspective on Introduction and Transmission
inferredcites →https://doi.org/10.1093/cid/ciy034openalex-snapshot
A Nosocomial Foodborne Outbreak of a VIM Carbapenemase-Expressing Citrobacter freundii
inferredcites →https://doi.org/10.1093/jac/dkg312openalex-snapshot
European harmonization of MIC breakpoints for antimicrobial susceptibility testing of bacteria
inferredcites →https://doi.org/10.1093/jac/dkp241openalex-snapshot
Methicillin-resistant Staphylococcus aureus strain USA300: origin and epidemiology
inferredcites →https://doi.org/10.1093/jac/dkp361openalex-snapshot
Emergence of extended-spectrum -lactamases and AmpC-type -lactamases in human Salmonella isolated in Spain from 2001 to 2005
inferredcites →https://doi.org/10.1093/jac/dkq415openalex-snapshot
Escherichia coli O25b-ST131: a pandemic, multiresistant, community-associated strain
inferredcites →https://doi.org/10.1093/jac/dkr115openalex-snapshot
Molecular characterization of spa type t127, sequence type 1 methicillin-resistant Staphylococcus aureus from pigs
inferredcites →https://doi.org/10.1093/jac/dkt259openalex-snapshot
Emergence of OXA-48 carbapenemase-producing Escherichia coli and Klebsiella pneumoniae in dogs
inferredcites →https://doi.org/10.1093/jac/dkt392openalex-snapshot
Carbapenemase-producing Enterobacteriaceae and non-Enterobacteriaceae from animals and the environment: an emerging public health risk of our own making?
inferredcites →https://doi.org/10.1093/jac/dkt492openalex-snapshot
Report of ribosomal RNA methylase gene erm(B) in multidrug-resistant Campylobacter coli
inferredcites →https://doi.org/10.1093/jac/dkv001openalex-snapshot
Novel gentamicin resistance genes in Campylobacter isolated from humans and retail meats in the USA
inferredcites →https://doi.org/10.1093/jac/dkv383openalex-snapshot
Description of anerm(B)-carryingCampylobacter coliisolate in Europe
inferredcites →https://doi.org/10.1093/jac/dkw274openalex-snapshot
Transferable resistance to colistin: a new but old threat: Table 1.
inferredcites →https://doi.org/10.1093/jac/dkw389openalex-snapshot
Report ofmecC-carrying MRSA in domestic swine
inferredcites →https://doi.org/10.1093/jac/dkw479openalex-snapshot
Recurrent detection of VIM-1-producingEscherichia coliclone in German pig production
inferredcites →https://doi.org/10.1093/jac/dkx023openalex-snapshot
Emergence of a plasmid-borne multidrug resistance gene cfr(C) in foodborne pathogen Campylobacter
inferredcites →https://doi.org/10.1093/jac/dkx101openalex-snapshot
VIM-1-producing Salmonella Infantis isolated from swine and minced pork meat in Germany
inferredcites →https://doi.org/10.1111/1462-2920.12351openalex-snapshot
A unique megaplasmid contributes to stress tolerance and pathogenicity of an emergent S almonella enterica serovar Infantis strain
inferredcites →https://doi.org/10.1111/1469-0691.12036openalex-snapshot
Epidemiology of methicillin-resistant Staphylococcus aureus carrying the novel mecC gene in Denmark corroborates a zoonotic reservoir with transmission to humans
inferredcites →https://doi.org/10.1111/j.1469-0691.2011.03570.xopenalex-snapshot
Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance
inferredcites →https://doi.org/10.1111/j.1574-6968.2010.02151.xopenalex-snapshot
Variations in spa types found in consecutive MRSA isolates from the same patients
inferredcites →https://doi.org/10.1111/jam.13135openalex-snapshot
Molecular subtyping and erythromycin resistance ofCampylobacterin China
inferredcites →https://doi.org/10.1111/nyas.12830openalex-snapshot
Mechanisms of drug resistance: quinolone resistance
inferredcites →https://doi.org/10.1111/zph.12144openalex-snapshot
Comparative Phenotypic and Genotypic Analyses ofSalmonellaRissen that Originated from Food Animals in Thailand and United States
inferredcites →https://doi.org/10.1128/aac.00112-17openalex-snapshot
High Prevalence and Predominance of the aph(2″)-If Gene Conferring Aminoglycoside Resistance in Campylobacter
inferredcites →https://doi.org/10.1128/aac.00187-11openalex-snapshot
Detection of Staphylococcal Cassette Chromosome mec Type XI Carrying Highly Divergent mecA , mecI , mecR1 , blaZ , and ccr Genes in Human Clinical Isolates of Clonal Complex 130 Methicillin-Resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aac.00294-09openalex-snapshot
Characterization of the Plasmid-Borne Quinolone Resistance Gene qnrB19 in S almonella enterica Serovar Typhimurium
inferredcites →https://doi.org/10.1128/aac.00398-18openalex-snapshot
Enterobacter cloacae Complex Isolated from Shrimps from Vietnam Carrying bla IMI-1 Resistant to Carbapenems but Not Cephalosporins
inferredcites →https://doi.org/10.1128/aac.00488-17openalex-snapshot
Comparative Analysis of Extended-Spectrum-β-Lactamase CTX-M-65-Producing Salmonella enterica Serovar Infantis Isolates from Humans, Food Animals, and Retail Chickens in the United States
inferredcites →https://doi.org/10.1128/aac.00809-12openalex-snapshot
Identification of a Novel Genomic Island Conferring Resistance to Multiple Aminoglycoside Antibiotics in Campylobacter coli
inferredcites →https://doi.org/10.1128/aac.00997-08openalex-snapshot
qnrD , a Novel Gene Conferring Transferable Quinolone Resistance in Salmonella enterica Serovar Kentucky and Bovismorbificans Strains of Human Origin
inferredcites →https://doi.org/10.1128/aac.01013-16openalex-snapshot
Chromosome-Based bla OXA-48 -Like Variants in Shewanella Species Isolates from Food-Producing Animals, Fish, and the Aquatic Environment
inferredcites →https://doi.org/10.1128/aac.01103-15openalex-snapshot
Constitutive and Inducible Expression of the rRNA Methylase Gene erm (B) in Campylobacter
inferredcites →https://doi.org/10.1128/aac.01298-16openalex-snapshot
Carbapenemase-Producing Enterobacteriaceae Recovered from the Environment of a Swine Farrow-to-Finish Operation in the United States
inferredcites →https://doi.org/10.1128/aac.01603-16openalex-snapshot
Decreased Susceptibility to Tigecycline Mediated by a Mutation in mlaA in Escherichia coli Strains
inferredcites →https://doi.org/10.1128/aac.01803-16openalex-snapshot
Occurrence of mcr-1 in Colistin-Resistant Salmonella enterica Isolates Recovered from Humans and Animals in Italy, 2012 to 2015
inferredcites →https://doi.org/10.1128/aac.02615-17openalex-snapshot
Report of erm (B) + Campylobacter jejuni in the United States
inferredcites →https://doi.org/10.1128/aac.02822-15openalex-snapshot
A Highly Macrolide-Resistant Campylobacter jejuni Strain with Rare A2074T Mutations in 23S rRNA Genes
inferredcites →https://doi.org/10.1128/aac.03039-14openalex-snapshot
Emergence of Multidrug-Resistant Campylobacter Species Isolates with a Horizontally Acquired rRNA Methylase
inferredcites →https://doi.org/10.1128/aem.00934-16openalex-snapshot
Molecular Epidemiology of Campylobacter coli Strains Isolated from Different Sources in New Zealand between 2005 and 2014
inferredcites →https://doi.org/10.1128/cmr.00116-14openalex-snapshot
The Role of Epidemic Resistance Plasmids and International High-Risk Clones in the Spread of Multidrug-Resistant Enterobacteriaceae
inferredcites →https://doi.org/10.1128/jb.187.13.4401-4409.2005openalex-snapshot
The Genomic Island SGI1, Containing the Multiple Antibiotic Resistance Region ofSalmonella entericaSerovar Typhimurium DT104 or Variants of It, Is Widely Distributed in OtherS. entericaSerovars
inferredcites →https://doi.org/10.1128/jcm.00390-18openalex-snapshot
Whole-Genome Sequence Analysis of Multidrug-Resistant Campylobacter Isolates: a Focus on Aminoglycoside Resistance Determinants
inferredcites →https://doi.org/10.1128/jcm.00417-13openalex-snapshot
Detection of Epidemic USA300 Community-Associated Methicillin-Resistant Staphylococcus aureus Strains by Use of a Single Allele-Specific PCR Assay Targeting a Novel Polymorphism of Staphylococcus aureus pbp3
inferredcites →https://doi.org/10.1128/jcm.01287-15openalex-snapshot
Development of a Pefloxacin Disk Diffusion Method for Detection of Fluoroquinolone-Resistant Salmonella enterica
inferredcites →https://doi.org/10.1128/jcm.43.10.5164-5170.2005openalex-snapshot
Molecular Epidemiology of Methicillin-Resistant Staphylococcus aureus in Zurich, Switzerland (2003): Prevalence of Type IV SCC mec and a New SCC mec Element Associated with Isolates from Intravenous Drug Users
inferredcites →https://doi.org/10.1128/mbio.01543-16openalex-snapshot
Emergence of a Potent Multidrug Efflux Pump Variant That Enhances Campylobacter Resistance to Multiple Antibiotics
inferredcites →https://doi.org/10.1136/oemed-2011-100069openalex-snapshot
Livestock-associated MRSA ST398 carriage in pig slaughterhouse workers related to quantitative environmental exposure
inferredcites →https://doi.org/10.1155/2015/141475openalex-snapshot
Population Structure and Oxacillin Resistance ofStaphylococcus aureusfrom Pigs and Pork Meat in South-West of Poland
inferredcites →https://doi.org/10.1155/2018/4526576openalex-snapshot
Molecular Basis of Macrolide Resistance inCampylobacterStrains Isolated from Poultry in South Korea
inferredcites →https://doi.org/10.1186/1471-2458-14-147openalex-snapshot
Measuring underreporting and under-ascertainment in infectious disease datasets: a comparison of methods
inferredcites →https://doi.org/10.1186/s13756-016-0105-8openalex-snapshot
New dominant spa type t2741 in livestock-associated MRSA (CC398-MRSA-V) in Finnish fattening pigs at slaughter
inferredcites →https://doi.org/10.1371/journal.pone.0010990openalex-snapshot
Methicillin Resistant Staphylococcus aureus ST398 in Veal Calf Farming: Human MRSA Carriage Related with Animal Antimicrobial Usage and Farm Hygiene
inferredcites →https://doi.org/10.1371/journal.pone.0017936openalex-snapshot
A Field Guide to Pandemic, Epidemic and Sporadic Clones of Methicillin-Resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1371/journal.pone.0048280openalex-snapshot
Discovery of blaOXA-199, a Chromosome-Based blaOXA-48-Like Variant, in Shewanella xiamenensis
inferredcites →https://doi.org/10.1371/journal.pone.0053738openalex-snapshot
Isolation and Characterization of Methicillin-Resistant Staphylococcus aureus from Pork Farms and Visiting Veterinary Students
inferredcites →https://doi.org/10.1371/journal.pone.0144802openalex-snapshot
Emergence of a Clonal Lineage of Multidrug-Resistant ESBL-Producing Salmonella Infantis Transmitted from Broilers and Broiler Meat to Humans in Italy between 2011 and 2014
inferredcites →https://doi.org/10.2217/17460913.4.2.189openalex-snapshot
Antibiotic Resistance in Campylobacter : Emergence, Transmission and Persistence
inferredcites →https://doi.org/10.26226/morressier.56d6be73d462b80296c9732aopenalex-snapshot
Selective enrichment of ESBL, AmpC and carbapenemase producing E. coli in meat and cecal samples - additional validation for poultry samples
inferredcites →https://doi.org/10.2807/1560-7917.es.2016.21.26.30270openalex-snapshot
MCR-1 in multidrug-resistant and copper-tolerant clinically relevant Salmonella 1,4,[5],12:i:- and S. Rissen clones in Portugal, 2011 to 2015
inferredcites →https://doi.org/10.2807/1560-7917.es.2016.21.6.30135openalex-snapshot
Prevalence of mcr-1 in commensal Escherichia coli from French livestock, 2007 to 2014
inferredcites →https://doi.org/10.2807/1560-7917.es.2017.22.28.30573openalex-snapshot
Evaluation of a widely used culture-based method for detection of livestock-associated meticillin-resistant Staphylococcus aureus (MRSA), Denmark and Norway, 2014 to 2016
inferredcites →https://doi.org/10.2807/1560-7917.es.2017.22.44.16-00696openalex-snapshot
Livestock-associated meticillin-resistant Staphylococcus aureus (MRSA) among human MRSA isolates, European Union/European Economic Area countries, 2013
inferredcites →https://doi.org/10.2807/ese.15.22.19580-enopenalex-snapshot
Multiresistant Salmonella enterica serovar 4,[5],12:i:- in Europe: a new pandemic strain?
inferredcites →https://doi.org/10.2807/esm.09.10.00478-enopenalex-snapshot
The European Centre for Disease Prevention and Control
inferredcites →https://doi.org/10.2903/j.efsa.2008.141ropenalex-snapshot
Report from the Task Force on Zoonoses Data Collection including guidance for harmonized monitoring and reporting of antimicrobial resistance in commensal Escherichia coli and Enterococcus spp. from food animals
inferredcites →https://doi.org/10.2903/j.efsa.2009.1372openalex-snapshot
Joint Opinion on antimicrobial resistance (AMR) focused on zoonotic infections
inferredcites →https://doi.org/10.2903/j.efsa.2011.2322openalex-snapshot
Scientific Opinion on the public health risks of bacterial strains producing extended-spectrum β-lactamases and/or AmpC β-lactamases in food and food-producing animals
inferredcites →https://doi.org/10.2903/j.efsa.2012.2587openalex-snapshot
Technical specifications for the analysis and reporting of data on antimicrobial resistance (AMR) in the European Union Summary Report
inferredcites →https://doi.org/10.2903/j.efsa.2012.2897openalex-snapshot
Technical specifications on the harmonised monitoring and reporting of antimicrobial resistance in methicillin‐resistant Staphylococcus aureus in food‐producing animals and food
inferredcites →https://doi.org/10.2903/j.efsa.2013.3501openalex-snapshot
Scientific Opinion on Carbapenem resistance in food animal ecosystems
inferredcites →https://doi.org/10.2903/j.efsa.2014.3590openalex-snapshot
The European Union Summary Report on antimicrobial resistance in zoonotic and indicator bacteria from humans, animals and food in 2012
inferredcites →https://doi.org/10.2903/j.efsa.2015.3991openalex-snapshot
The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2013
inferredcites →https://doi.org/10.2903/j.efsa.2016.4380openalex-snapshot
The European Union summary report on antimicrobial resistance in zoonotic and indicator bacteria from humans, animals and food in 2014
inferredcites →https://doi.org/10.2903/j.efsa.2017.4694openalex-snapshot
The European Union summary report on antimicrobial resistance in zoonotic and indicator bacteria from humans, animals and food in 2015
inferredcites →https://doi.org/10.2903/j.efsa.2017.4872openalex-snapshot
ECDC/EFSA/EMA second joint report on the integrated analysis of the consumption of antimicrobial agents and occurrence of antimicrobial resistance in bacteria from humans and food‐producing animals
inferredcites →https://doi.org/10.2903/j.efsa.2018.5182openalex-snapshot
The European Union summary report on antimicrobial resistance in zoonotic and indicator bacteria from humans, animals and food in 2016
inferredcites →https://doi.org/10.2903/j.efsa.2018.5500openalex-snapshot
The European Union summary report on trends and sources of zoonoses, zoonotic agents and food‐borne outbreaks in 2017
inferredcites →https://doi.org/10.2903/j.efsa.2019.5598openalex-snapshot
The European Union summary report on antimicrobial resistance in zoonotic and indicator bacteria from humans, animals and food in 2017
inferredcites →https://doi.org/10.2903/j.efsa.2020.6007openalex-snapshot
The European Union Summary Report on Antimicrobial Resistance in zoonotic and indicator bacteria from humans, animals and food in 2017/2018
inferredcites →https://doi.org/10.2903/j.efsa.2021.6490openalex-snapshot
The European Union Summary Report on Antimicrobial Resistance in zoonotic and indicator bacteria from humans, animals and food in 2018/2019
inferredcites →https://doi.org/10.3168/jds.2016-10912openalex-snapshot
Methicillin-resistant and methicillin-susceptible Staphylococcus aureus in dairy sheep and in-contact humans: An intra-farm study
inferredcites →https://doi.org/10.3201/eid1512.090378openalex-snapshot
Novel Lineage of Methicillin-ResistantStaphylococcus aureus, Hong Kong
inferredcites →https://doi.org/10.3201/eid2312.170883openalex-snapshot
High Rate of MCR-1–Producing Escherichia coli and Klebsiella pneumoniae among Pigs, Portugal
inferredcites →https://doi.org/10.3389/fmicb.2013.00057openalex-snapshot
Transmission Dynamics of Methicillin-Resistant Staphylococcus aureus in Pigs
inferredcites →https://doi.org/10.3389/fmicb.2013.00395openalex-snapshot
The global establishment of a highly-fluoroquinolone resistant Salmonella enterica serotype Kentucky ST198 strain
inferredcites →https://doi.org/10.3389/fmicb.2014.00643openalex-snapshot
Mechanisms of polymyxin resistance: acquired and intrinsic resistance in bacteria
inferredcites →https://doi.org/10.3389/fmicb.2017.02240openalex-snapshot
Genome Comparison of Erythromycin Resistant Campylobacter from Turkeys Identifies Hosts and Pathways for Horizontal Spread of erm(B) Genes
inferredcites →https://doi.org/10.3390/toxins9050161openalex-snapshot
Molecular Epidemiology of Methicillin-Resistant and Methicillin-Susceptible Staphylococcus aureus in the Ovine Dairy Chain and in Farm-Related Humans
inferredcites →https://doi.org/10.3390/vetsci5020040openalex-snapshot
Resistance to Carbapenems in Non-Typhoidal Salmonella enterica Serovars from Humans, Animals and Food
inferredcites →https://doi.org/10.4315/0362-028x.jfp-13-035openalex-snapshot
Prevalence and Antimicrobial Resistance of Campylobacter spp. Isolated from Poultry Carcasses in Poland

What points at this work

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

inferred← backgroundhttps://doi.org/10.5281/zenodo.2585938zenodo-depositor-declared
inferred← citeshttps://doi.org/10.1002/advs.202103388openalex-snapshot
A Survey of Chinese Pig Farms and Human Healthcare Isolates Reveals Separate Human and Animal Methicillin‐Resistant Staphylococcus aureus Populations
inferred← citeshttps://doi.org/10.1002/fsn3.1319openalex-snapshot
Microbial load and antibiotic resistance in raw beef preparations from northwest Spain
inferred← citeshttps://doi.org/10.1002/vetr.10openalex-snapshot
Characterisation and mapping of the surveillance system for antimicrobial resistance and antimicrobial use in the United Kingdom
inferred← citeshttps://doi.org/10.1002/vetr.302openalex-snapshot
Influence of farm management on the dynamics of Salmonella enterica serovar Infantis shedding and antibiotic resistance during the growing period of broiler chickens
inferred← citeshttps://doi.org/10.1002/vms3.1315openalex-snapshot
Prevalence of colistin resistance and antibacterial resistance in commensal Escherichia coli from chickens: An assessment of the impact of regulatory intervention in South Africa
inferred← citeshttps://doi.org/10.1002/vms3.685openalex-snapshot
Is Salmonella enterica shared between wildlife and cattle in cattle farming areas? An 11‐year retrospective study in Tokachi district, Hokkaido, Japan
inferred← citeshttps://doi.org/10.1007/978-3-030-46721-0_4openalex-snapshot
Use of Antimicrobials in Practice (Targeted on Cattle, Pigs, Poultry, Horses)
inferred← citeshttps://doi.org/10.1007/978-3-032-16540-4_1openalex-snapshot
Introduction to Antimicrobial Resistance (AMR)
inferred← citeshttps://doi.org/10.1007/s00253-019-10017-8openalex-snapshot
Degradation and transformation of fluoroquinolones by microorganisms with special emphasis on ciprofloxacin
inferred← citeshttps://doi.org/10.1007/s00284-022-02900-xopenalex-snapshot
Salmonella Broiler Meat’s Contamination in Tunisia: Prevalence, Serotypes, Antimicrobial Resistance and Molecular Characterization of Isolated Strains
inferred← citeshttps://doi.org/10.1007/s00430-024-00790-3openalex-snapshot
Lipopolysaccharide with long O-antigen is crucial for Salmonella Enteritidis to evade complement activity and to facilitate bacterial survival in vivo in the Galleria mellonella infection model
inferred← citeshttps://doi.org/10.1007/s11101-020-09669-6openalex-snapshot
Anti-adhesion activity of phytochemicals to prevent Campylobacter jejuni biofilm formation on abiotic surfaces
inferred← citeshttps://doi.org/10.1007/s11259-021-09801-7openalex-snapshot
Characterization of antibiotic resistance in Escherichia coli isolates from Black-headed gulls (Larus ridibundus) present in the city of Novi Sad, Serbia
inferred← citeshttps://doi.org/10.1007/s12011-023-04032-0openalex-snapshot
Antibiotic Residues and Zinc Concentrations in the Livers and Kidneys of Portuguese Piglets—Relationship to Antibiotic and Zinc Resistance in Intestinal Escherichia coli
inferred← citeshttps://doi.org/10.1007/s12161-020-01916-yopenalex-snapshot
Development and Validation of a Multi-detection Confirmatory Method for Antibiotics Determination in Piglet Kidneys by UHPLC-TOF-MS According Commission Decision 2002/657/EC
inferred← citeshttps://doi.org/10.1007/s12223-026-01607-xopenalex-snapshot
Global research trends, thematic evolution, and one health implications of ESBL-producing Escherichia coli: a bibliometric and science mapping analysis, 2001–2025
inferred← citeshttps://doi.org/10.1007/s42770-025-01780-0openalex-snapshot
Molecular detection and prevalence of colistin-resistant Escherichia coli in poultry and humans: a one health perspective
inferred← citeshttps://doi.org/10.1016/b978-0-12-818030-3.00007-6openalex-snapshot
Antimicrobial resistance in farm environments
inferred← citeshttps://doi.org/10.1016/j.addr.2021.114078openalex-snapshot
Overcoming the rising incidence and evolving mechanisms of antibiotic resistance by novel drug delivery approaches – An overview
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2023.739768openalex-snapshot
Integrons from Aeromonas isolates collected from fish: A global indicator of antimicrobial resistance and anthropic pollution
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.134529openalex-snapshot
Impacts of farmland application of antibiotic-contaminated manures on the occurrence of antibiotic residues and antibiotic resistance genes in soil: A meta-analysis study
inferred← citeshttps://doi.org/10.1016/j.cimid.2021.101700openalex-snapshot
Respiratory microbiota of healthy broilers can act as reservoirs for multidrug-resistant Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.cmi.2019.11.015openalex-snapshot
Changing epidemiology of invasive non-typhoid Salmonella infection: a nationwide population-based registry study
inferred← citeshttps://doi.org/10.1016/j.crfs.2022.03.005openalex-snapshot
Prevalence and antimicrobial resistance of Campylobacter jejuni and C. coli identified in a slaughterhouse in Argentina
inferred← citeshttps://doi.org/10.1016/j.eng.2019.10.013openalex-snapshot
Presence and Antimicrobial Susceptibility of RE-cmeABC-Positive Campylobacter Isolated from Food-Producing Animals, 2014–2016
inferred← citeshttps://doi.org/10.1016/j.fm.2019.03.009openalex-snapshot
Evolution of Campylobacter jejuni of poultry origin in Brazil
inferred← citeshttps://doi.org/10.1016/j.fm.2022.104112openalex-snapshot
Large-scale genomic analysis reveals the pESI-like megaplasmid presence in Salmonella Agona, Muenchen, Schwarzengrund, and Senftenberg
inferred← citeshttps://doi.org/10.1016/j.foodchem.2022.132936openalex-snapshot
Promising energy transfer system between fuorine and nitrogen Co-doped graphene quantum dots and Rhodamine B for ratiometric and visual detection of doxycycline in food
inferred← citeshttps://doi.org/10.1016/j.foodchem.2023.137147openalex-snapshot
Selenium-based nanozyme as a fluorescence-enhanced probe and imaging for chlortetracycline in living cells and foods
inferred← citeshttps://doi.org/10.1016/j.foodcont.2024.111127openalex-snapshot
Systematic review and meta-analysis of the occurrence of ESBL-producing Escherichia coli and Salmonella spp. in foods of animal origin in Europe
inferred← citeshttps://doi.org/10.1016/j.foodres.2020.109424openalex-snapshot
Strain variability in biofilm formation: A food safety and quality perspective
inferred← citeshttps://doi.org/10.1016/j.foodres.2022.111007openalex-snapshot
Whole-genome sequencing analysis reveals pig as the main reservoir for persistent evolution of Salmonella enterica serovar Rissen causing human salmonellosis
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2019.108388openalex-snapshot
Characterization of antimicrobial resistance in lactobacilli and bifidobacteria used as probiotics or starter cultures based on integration of phenotypic and in silico data
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2019.108497openalex-snapshot
Mega-plasmid found worldwide confers multiple antimicrobial resistance in Salmonella Infantis of broiler origin in Russia
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2022.109736openalex-snapshot
Relevance of tracking the diversity of Escherichia coli pathotypes to reinforce food safety
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2023.110137openalex-snapshot
MLST genotypes and quinolone resistance profiles of Campylobacter jejuni isolates from various sources in Turkey
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2025.111577openalex-snapshot
Prevalence, antimicrobial resistance and virulence genes of Campylobacter isolated from retail duck meat in Southern China
inferred← citeshttps://doi.org/10.1016/j.jchromb.2020.122264openalex-snapshot
The use of ultra-high-pressure-liquid-chromatography tandem time-of-flight mass spectrometry as a confirmatory method in drug residue analysis: Application to the determination of antibiotics in piglet liver
inferred← citeshttps://doi.org/10.1016/j.jgar.2020.09.009openalex-snapshot
Identification of the first erm(B)-positive Campylobacter jejuni and Campylobacter coli associated with novel multidrug resistance genomic islands in Australia
inferred← citeshttps://doi.org/10.1016/j.livsci.2021.104530openalex-snapshot
An overview of the current trends in precision pig farming technologies
inferred← citeshttps://doi.org/10.1016/j.mimet.2022.106562openalex-snapshot
Current methodologies and future direction of Campylobacter isolation and detection from food matrices, clinical samples, and the agricultural environment
inferred← citeshttps://doi.org/10.1016/j.nmni.2023.101161openalex-snapshot
The battle against colistin-resistant E. coli and the need for a one health approach
inferred← citeshttps://doi.org/10.1016/j.onehlt.2020.100146openalex-snapshot
The state of One Health research across disciplines and sectors – a bibliometric analysis
inferred← citeshttps://doi.org/10.1016/j.onehlt.2021.100238openalex-snapshot
Drivers of ESBL-producing Escherichia coli dynamics in calf fattening farms: A modelling study
inferred← citeshttps://doi.org/10.1016/j.onehlt.2023.100639openalex-snapshot
Modelling the effects of antibiotic usage in livestock on human salmonellosis
inferred← citeshttps://doi.org/10.1016/j.onehlt.2024.100945openalex-snapshot
Investigating a propagation of emerging carbapenemase-producing Enterobacteriaceae in Dutch broiler production pyramid through stochastic simulation
inferred← citeshttps://doi.org/10.1016/j.pedneo.2020.03.017openalex-snapshot
Highly antimicrobial-resistant Nontyphoidal Salmonella from retail meats and clinical impact in children, Taiwan
inferred← citeshttps://doi.org/10.1016/j.plasmid.2018.09.010openalex-snapshot
Plasmid-mediated resistance is going wild
inferred← citeshttps://doi.org/10.1016/j.psj.2024.104380openalex-snapshot
Campylobacter jejuni from no antibiotics ever (NAE) broilers: prevalence, antibiotic resistance, and virulence genes analysis
inferred← citeshttps://doi.org/10.1016/j.rvsc.2022.09.037openalex-snapshot
A three-year evolution and comparison of the bla genes in pathogenic and non-pathogenic Escherichia coli isolated from young diarrheic and septicaemic calves in Belgium
inferred← citeshttps://doi.org/10.1016/j.rvsc.2024.105209openalex-snapshot
Investigation of Salmonella, hepatitis E virus (HEV) and viral indicators of fecal contamination in four Italian pig slaughterhouses, 2021–2022
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.153444openalex-snapshot
Zoonotic Campylobacter spp. and Salmonella spp. carried by wild boars in a metropolitan area: occurrence, antimicrobial susceptibility and public health relevance
inferred← citeshttps://doi.org/10.1016/j.vetmic.2020.108637openalex-snapshot
Decrease in fluoroquinolone use in French poultry and pig production and changes in resistance among E. coli and Campylobacter
inferred← citeshttps://doi.org/10.1016/j.vetmic.2022.109419openalex-snapshot
Antimicrobial susceptibility in E. coli and Pasteurellaceae at the beginning and at the end of the fattening process in veal calves: Comparing ‘outdoor veal calf’ and conventional operations
inferred← citeshttps://doi.org/10.1016/j.wasman.2020.01.031openalex-snapshot
Effects of the C/N ratio and moisture content on the survival of ESBL-producing Escherichia coli during chicken manure composting
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.5c00750openalex-snapshot
Assessing Campylobacter jejuni Extracellular Vesicle–Host Interaction Using a Microfluidic Platform with Caco-2 Spheroides-on-Chip
inferred← citeshttps://doi.org/10.1038/s41598-023-39588-3openalex-snapshot
Monitoring within-farm transmission dynamics of antimicrobial-resistant Campylobacter in dairy cattle using broth microdilution and long-read whole genome sequencing
inferred← citeshttps://doi.org/10.1038/s41598-024-76895-9openalex-snapshot
Identification and antimicrobial susceptibility profiles of Campylobacter isolated from camel at municipal abattoirs in eastern Ethiopia
inferred← citeshttps://doi.org/10.1080/00071668.2022.2126931openalex-snapshot
High frequency of non-susceptibility to ciprofloxacin in nontyphoid Salmonella recovered from Brazilian broiler chicken
inferred← citeshttps://doi.org/10.1080/00071668.2025.2451242openalex-snapshot
Comparison of pathogenicity factors of avian pathogenic and extraintestinal pathogenic Escherichia coli isolates originating from broiler chickens
inferred← citeshttps://doi.org/10.1080/22221751.2020.1821582openalex-snapshot
Genomic epidemiology of emerging ESBL-producing Salmonella Kentucky bla CTX-M-14b in Europe
inferred← citeshttps://doi.org/10.1089/fpd.2019.2738openalex-snapshot
Occurrence and Antimicrobial Susceptibility Profile of Salmonella spp. in Raw and Ready-To-Eat Foods and Campylobacter spp. in Retail Raw Chicken Meat in Transylvania, Romania
inferred← citeshttps://doi.org/10.1089/hs.2022.0111openalex-snapshot
Prevalence of Multidrug-Resistant Organisms in Healthy Adults in Shenzhen, China
inferred← citeshttps://doi.org/10.1089/mdr.2020.0082openalex-snapshot
Antimicrobial Resistance of Campylobacter spp. Causing Human Infection in Australia: An International Comparison
inferred← citeshttps://doi.org/10.1093/femsle/fnae066openalex-snapshot
Antibacterial mode of action of garviecin LG34 against Gram-negative bacterium Salmonella typhimurium
inferred← citeshttps://doi.org/10.1093/femsre/fuab049openalex-snapshot
Global colistin use: a review of the emergence of resistant Enterobacterales and the impact on their genetic basis.
inferred← citeshttps://doi.org/10.1093/jac/dkaa429openalex-snapshot
White Paper: Bridging the gap between surveillance data and antimicrobial stewardship in the animal sector—practical guidance from the JPIAMR ARCH and COMBACTE-MAGNET EPI-Net networks
inferred← citeshttps://doi.org/10.1093/jacamr/dlad119openalex-snapshot
MALDI-TOF MS combined with AUC method for tigecycline susceptibility testing in Escherichia coli
inferred← citeshttps://doi.org/10.1093/molbev/msac257openalex-snapshot
Antibiotic Cycling Affects Resistance Evolution Independently of Collateral Sensitivity
inferred← citeshttps://doi.org/10.1098/rspb.2023.1085openalex-snapshot
Global patterns and correlates in the emergence of antimicrobial resistance in humans
inferred← citeshttps://doi.org/10.1099/mgen.0.000455openalex-snapshot
Comprehensive screening of genomic and metagenomic data reveals a large diversity of tetracycline resistance genes
inferred← citeshttps://doi.org/10.1099/mgen.0.000630openalex-snapshot
A genomic epidemiological study shows that prevalence of antimicrobial resistance in Enterobacterales is associated with the livestock host, as well as antimicrobial usage
inferred← citeshttps://doi.org/10.1099/mgen.0.000773openalex-snapshot
Genomic characterization of multidrug-resistant Salmonella serovar Kentucky ST198 isolated in poultry flocks in Spain (2011–2017)
inferred← citeshttps://doi.org/10.1099/mgen.0.000782openalex-snapshot
Use of genomics to explore AMR persistence in an outdoor pig farm with low antimicrobial usage
inferred← citeshttps://doi.org/10.1099/mgen.0.001390openalex-snapshot
Methicillin-sensitive Staphylococcus aureus lineages contribute towards poor patient outcomes in orthopaedic device-related infections
inferred← citeshttps://doi.org/10.1101/2021.08.02.454852openalex-snapshot
A survey of Chinese pig farms and human healthcare isolates reveals separate human and animal MRSA populations
inferred← citeshttps://doi.org/10.1101/2022.09.29.22280519openalex-snapshot
Global patterns and correlates in the emergence of antimicrobial resistance in humans
inferred← citeshttps://doi.org/10.1111/1462-2920.14760openalex-snapshot
Gene pool transmission of multidrug resistance among Campylobacter from livestock, sewage and human disease
inferred← citeshttps://doi.org/10.1111/1462-2920.15016openalex-snapshot
Tolerance to arsenic contaminant among multidrug‐resistant and copper‐tolerant Salmonella successful clones is associated with diverse ars operons and genetic contexts
inferred← citeshttps://doi.org/10.1111/1758-2229.13287openalex-snapshot
Virulence factors of Salmonella spp. isolated from free‐living grass snakes Natrix natrix
inferred← citeshttps://doi.org/10.1111/risa.13998openalex-snapshot
Quantitative microbiological risk assessment of nontyphoidal Salmonella in ground pork in households in Chengdu, China
inferred← citeshttps://doi.org/10.1111/tbed.13346openalex-snapshot
Identifying emerging trends in antimicrobial resistance using Salmonella surveillance data in poultry in Spain
inferred← citeshttps://doi.org/10.1111/zph.12790openalex-snapshot
Effect of antimicrobial use and production system on Campylobacter spp., Staphylococcus spp. and Salmonella spp. resistance in Spanish swine: A cross‐sectional study
inferred← citeshttps://doi.org/10.1111/zph.12853openalex-snapshot
Campylobacter jejuni ST50, a pathogen of global importance: A comparative genomic analysis of isolates from Australia, Europe and North America
inferred← citeshttps://doi.org/10.1111/zph.12920openalex-snapshot
Assessing antimicrobial resistance occurrence in the Portuguese food system: Poultry, pigs and derived food, 2014–2018
inferred← citeshttps://doi.org/10.1126/science.aaw1944openalex-snapshot
Global trends in antimicrobial resistance in animals in low- and middle-income countries
inferred← citeshttps://doi.org/10.1128/aac.00092-20openalex-snapshot
Epidemiological Study on Prevalence, Serovar Diversity, Multidrug Resistance, and CTX-M-Type Extended-Spectrum β-Lactamases of Salmonella spp. from Patients with Diarrhea, Food of Animal Origin, and Pets in Several Provinces of China
inferred← citeshttps://doi.org/10.1128/aac.00272-23openalex-snapshot
Development of Meropenem Resistance in a Multidrug-Resistant Campylobacter coli Strain Causing Recurrent Bacteremia in a Hematological Malignancy Patient
inferred← citeshttps://doi.org/10.1128/aac.00671-21openalex-snapshot
Update on Shigella and Nontyphoidal Salmonella Antimicrobial Drug Resistance: Implications on Empirical Treatment of Acute Infectious Diarrhea in Cambodia
inferred← citeshttps://doi.org/10.1128/aac.00992-19openalex-snapshot
First Clinical Case ofIn VivoAcquisition of DHA-1 Plasmid-Mediated AmpC in a Salmonella enterica subsp.entericaIsolate
inferred← citeshttps://doi.org/10.1128/aem.00742-20openalex-snapshot
Prevalence of Cefotaxime-Resistant Escherichia coli Isolates from Healthy Cattle and Sheep in Northern Spain: Phenotypic and Genome-Based Characterization of Antimicrobial Susceptibility
inferred← citeshttps://doi.org/10.1128/aem.01499-19openalex-snapshot
Viability Quantitative PCR Utilizing Propidium Monoazide, Spheroplast Formation, and Campylobacter coli as a Bacterial Model
inferred← citeshttps://doi.org/10.1128/aem.01865-19openalex-snapshot
Methicillin-Resistant Staphylococcus aureus Strains in Swiss Pigs and Their Relation to Isolates from Farmers and Veterinarians
inferred← citeshttps://doi.org/10.1128/aem.02597-20openalex-snapshot
Method for Measuring Phenotypic Colistin Resistance in Escherichia coli Populations from Chicken Flocks
inferred← citeshttps://doi.org/10.1128/aem.02769-19openalex-snapshot
Dissemination of Quinolone-Resistant Escherichia coli in the Norwegian Broiler and Pig Production Chains and Possible Persistence in the Broiler Production Environment
inferred← citeshttps://doi.org/10.1128/mra.01269-19openalex-snapshot
Complete Circular Genome Sequence of a Multidrug-Resistant Escherichia coli Strain from Cuba Obtained with Nanopore and Illumina Hybrid Assembly
inferred← citeshttps://doi.org/10.1128/spectrum.00248-21openalex-snapshot
Genomic Epidemiology of Multidrug-Resistant Nontyphoidal Salmonella in Young Children Hospitalized for Gastroenteritis
inferred← citeshttps://doi.org/10.1128/spectrum.00251-22openalex-snapshot
Prevalence, Antimicrobial Resistance, and Molecular Characterization of Campylobacter Isolated from Broilers and Broiler Meat Raised without Antibiotics
inferred← citeshttps://doi.org/10.1134/s0003683825600174openalex-snapshot
Postbiotic S-layer Protein 2 from Human Lactobacillus crispatus 2029 Strain is a Natural Perforator of the Outer Membrane of Multi-drug Resistant Salmonella Enteritidis and a Protector of Intestinal Homeostasis in Humans and Animals
inferred← citeshttps://doi.org/10.11606/t.60.2020.tde-01072021-145546openalex-snapshot
Análise fenotípica e sequenciamento do genoma completo de linhagens de >i /i< isoladas de diversas fontes durante 16 anos no Brasil
inferred← citeshttps://doi.org/10.1177/20503121231175322openalex-snapshot
Antimicrobial resistance and virulence genes of invasive Salmonella enterica from children with bacteremia in north-central Nigeria
inferred← citeshttps://doi.org/10.1186/s12866-021-02160-yopenalex-snapshot
Population structure and uropathogenic potential of extended-spectrum cephalosporin-resistant Escherichia coli from retail chicken meat
inferred← citeshttps://doi.org/10.1186/s12917-021-02784-2openalex-snapshot
Assessing the role of livestock and sympatric wild ruminants in spreading antimicrobial resistant Campylobacter and Salmonella in alpine ecosystems
inferred← citeshttps://doi.org/10.1186/s12917-021-02810-3openalex-snapshot
Antimicrobial use and resistance in Escherichia coli from healthy food-producing animals in Guadeloupe
inferred← citeshttps://doi.org/10.1186/s12917-021-03070-xopenalex-snapshot
Search of antimicrobial lactic acid bacteria from Salmonella-negative dogs
inferred← citeshttps://doi.org/10.1186/s12917-022-03377-3openalex-snapshot
Patterns of antimicrobial resistance in Salmonella isolates from fattening pigs in Spain
inferred← citeshttps://doi.org/10.1186/s12985-019-1260-3openalex-snapshot
Veterinary use of bacteriophage therapy in intensively-reared livestock
inferred← citeshttps://doi.org/10.1186/s13620-019-0154-4openalex-snapshot
European perspectives on efforts to reduce antimicrobial usage in food animal production
inferred← citeshttps://doi.org/10.1186/s13620-021-00200-7openalex-snapshot
Livestock-associated methicillin-resistant Staphylococcus aureus (LA-MRSA) prevalence in humans in close contact with animals and measures to reduce on-farm colonisation
inferred← citeshttps://doi.org/10.1186/s40104-021-00570-6openalex-snapshot
Bacteriophage cocktail supplementation improves growth performance, gut microbiome and production traits in broiler chickens
inferred← citeshttps://doi.org/10.1186/s40104-022-00786-0openalex-snapshot
Production systems and important antimicrobial resistant-pathogenic bacteria in poultry: a review
inferred← citeshttps://doi.org/10.1186/s40168-020-00941-7openalex-snapshot
Antimicrobial use and production system shape the fecal, environmental, and slurry resistomes of pig farms
inferred← citeshttps://doi.org/10.1186/s40813-020-00166-yopenalex-snapshot
Quantification, description and international comparison of antimicrobial use on Irish pig farms
inferred← citeshttps://doi.org/10.1186/s40813-022-00255-0openalex-snapshot
Longitudinal study of the mcr-1 gene prevalence in Spanish food-producing pigs from 1998 to 2021 and its relationship with the use of polymyxins
inferred← citeshttps://doi.org/10.1186/s40813-025-00459-0openalex-snapshot
MRSA in pig farming: the emerging role of flies in antimicrobial resistance: a cross-sectional study
inferred← citeshttps://doi.org/10.12681/jhvms.25161openalex-snapshot
Whole issue
inferred← citeshttps://doi.org/10.12681/jhvms.25162openalex-snapshot
Determination of the ciprofloxacin-resistant Escherichia coli isolated from chicken meat in Turkey
inferred← citeshttps://doi.org/10.1371/journal.pbio.3001608openalex-snapshot
The expression of virulence genes increases membrane permeability and sensitivity to envelope stress in Salmonella Typhimurium
inferred← citeshttps://doi.org/10.1371/journal.pone.0223804openalex-snapshot
Antimicrobial resistance genotypes and phenotypes of Campylobacter jejuni isolated in Italy from humans, birds from wild and urban habitats, and poultry
inferred← citeshttps://doi.org/10.1371/journal.pone.0227833openalex-snapshot
Antimicrobial resistance patterns and molecular resistance markers of Campylobacter jejuni isolates from human diarrheal cases
inferred← citeshttps://doi.org/10.1371/journal.pone.0236889openalex-snapshot
Molecular characterization of Campylobacter spp. recovered from beef, chicken, lamb and pork products at retail in Australia
inferred← citeshttps://doi.org/10.1371/journal.pone.0242987openalex-snapshot
A metagenomic glimpse into the gut of wild and domestic animals: Quantification of antimicrobial resistance and more
inferred← citeshttps://doi.org/10.1371/journal.pone.0243772openalex-snapshot
Phenotypical antimicrobial resistance data of clinical and non-clinical Escherichia coli from poultry in Germany between 2014 and 2017
inferred← citeshttps://doi.org/10.1371/journal.pone.0265010openalex-snapshot
SPiNCAR: A systematic model to evaluate and guide actions for tackling AMR
inferred← citeshttps://doi.org/10.1371/journal.pone.0282254openalex-snapshot
Serotype distribution, trend of multidrug resistance and prevalence of β-lactamase resistance genes in human Salmonella isolates from clinical specimens in Guizhou, China
inferred← citeshttps://doi.org/10.1371/journal.pone.0301388openalex-snapshot
Antimicrobial resistance and genetic relatedness of Salmonella serotypes isolated from food, asymptomatic carriers, and clinical cases in Shiyan, China
inferred← citeshttps://doi.org/10.14202/vetworld.2020.2053-2061openalex-snapshot
Antimicrobial resistance of commensal Escherichia coli from food-producing animals in Russia
inferred← citeshttps://doi.org/10.14202/vetworld.2021.1020-1027openalex-snapshot
Antibiotic resistance of Escherichia coli and Salmonella spp. strains isolated from healthy poultry farms in the districts of Abidjan and Agnibilékrou (Côte d'Ivoire)
inferred← citeshttps://doi.org/10.14202/vetworld.2022.1515-1522openalex-snapshot
Characterization of plasmid-mediated quinolone resistance genes and extended-spectrum beta-lactamases in non-typhoidal Salmonella enterica isolated from broiler chickens
inferred← citeshttps://doi.org/10.14334/wartazoa.v32i1.2965openalex-snapshot
Antibiotic resistance in Escherichia coli from Animals, Food and Humans
inferred← citeshttps://doi.org/10.15789/2220-7619-doi-1506openalex-snapshot
Detection of international high-risk clones of food-borne pathogens Salmonella and Escherichia coli in the Russian Federation
inferred← citeshttps://doi.org/10.1787/83ccac56-enopenalex-snapshot
Assessing national action plans on antimicrobial resistance in animal production
inferred← citeshttps://doi.org/10.18002/10612/15058openalex-snapshot
Antimicrobial resistance in the Spanish swine production: Impact of the production system and the antimicrobial use = Resistencias antimicrobianas en la producción porcina española: impacto del sistema de producción y del uso de antibióticos
inferred← citeshttps://doi.org/10.18821/0869-2084-2019-64-10-620-626openalex-snapshot
ANTIMICROBIAL RESISTANCE AND CLINICAL SIGNIFICANT RESISTANCE MECHANISMS OF SALMONELLA ISOLATED IN 2014-2018 IN ST.PETERSBURG, RUSSIA
inferred← citeshttps://doi.org/10.18821/0869-2084-2020-65-10-638-644openalex-snapshot
Antimicrobial resistance of Escherichia coli, isolated from children’s intestinal microbiota
inferred← citeshttps://doi.org/10.18821/0869-2084-2020-65-5-308-315openalex-snapshot
CURRENT TRENDS IN THE DEVELOPMENT OF RESISTANCE TO CLINICALLY SIGNIFICANT ANTIBIOTICS IN SALMONELLA (REVIEW OF LITERATURE)
inferred← citeshttps://doi.org/10.21203/rs.3.rs-157826/v1openalex-snapshot
Plasmid-Mediated Resistance to Extended-Spectrum Cephalosporins and Resistance to Fluoroquinolones in Escherichia Coli Isolates from Black-headed Gulls (Larus Ridibundus)
inferred← citeshttps://doi.org/10.21307/pm-2019.58.3.259openalex-snapshot
Antibiotic Resistance Of Bacteria A Growing Threat For Animals And Public Health
inferred← citeshttps://doi.org/10.2147/idr.s237038openalex-snapshot
Monitoring Antimicrobial Resistance and Drug Usage in the Human and Livestock Sector and Foodborne Antimicrobial Resistance in Six European Countries
inferred← citeshttps://doi.org/10.2147/idr.s581416openalex-snapshot
Distribution of Pathogenic Bacteria and Changes in Drug Resistance of Urinary Tract Infections in Children in Southwest China, 2020–2024
inferred← citeshttps://doi.org/10.2147/ijn.s300428openalex-snapshot
Growth Inhibition of Gram-Positive and Gram-Negative Bacteria by Zinc Oxide Hedgehog Particles
inferred← citeshttps://doi.org/10.21521/mw.6603openalex-snapshot
Antimicrobial resistance: causes, consequences, diagnostic and therapeutic challenges in modern medicine
inferred← citeshttps://doi.org/10.21521/mw.6660openalex-snapshot
Antibiotic resistance patterns of chicken and human origin Campylobacter spp. in Turkey
inferred← citeshttps://doi.org/10.21608/ejhm.2022.269978openalex-snapshot
Detection of Some Virulence and Antibiotic Resistance Genes in Campylobacter jejuni isolated from Poultry and Human
inferred← citeshttps://doi.org/10.21608/mid.2022.163207.1404openalex-snapshot
Anti-biofilm Effect of Copper Oxide Nanoparticles, EDTA, and Kojic Acid on MDR-biofilm Forming Gram Negative Superbugs in Sohag University Hospitals, Egypt
inferred← citeshttps://doi.org/10.28933/ajmi-2020-02-2605openalex-snapshot
Prevalence and antibiotic resistance of Campylobacter coli and Campylobacter jejuni in Greek swine farms
inferred← citeshttps://doi.org/10.2903/j.efsa.2019.5709openalex-snapshot
Technical specifications on harmonised monitoring of antimicrobial resistance in zoonotic and indicator bacteria from food‐producing animals and food
inferred← citeshttps://doi.org/10.2903/j.efsa.2020.6007openalex-snapshot
The European Union Summary Report on Antimicrobial Resistance in zoonotic and indicator bacteria from humans, animals and food in 2017/2018
inferred← citeshttps://doi.org/10.2903/j.efsa.2020.e181108openalex-snapshot
Integration of computational tools, data analysis and social science into food safety risk assessment
inferred← citeshttps://doi.org/10.2903/j.efsa.2021.6490openalex-snapshot
The European Union Summary Report on Antimicrobial Resistance in zoonotic and indicator bacteria from humans, animals and food in 2018/2019
inferred← citeshttps://doi.org/10.2903/j.efsa.2022.7209openalex-snapshot
The European Union Summary Report on Antimicrobial Resistance in zoonotic and indicator bacteria from humans, animals and food in 2019–2020
inferred← citeshttps://doi.org/10.2903/j.efsa.2022.7620openalex-snapshot
Technical specifications for a baseline survey on the prevalence of methicillin‐resistant Staphylococcus aureus (MRSA) in pigs
inferred← citeshttps://doi.org/10.2903/j.efsa.2025.9336openalex-snapshot
Occurrence and spread of carbapenemase‐producing Enterobacterales (CPE) in the food chain in the EU/EFTA. Part 1: 2025 update
inferred← citeshttps://doi.org/10.30721/fsab2023.v6.i1.238openalex-snapshot
The role of food in the spread of the Methicillin – resistant Staphylococcus aureus (MRSA)
inferred← citeshttps://doi.org/10.32718/nvlvet9711openalex-snapshot
Antimicrobial susceptibility of isolates of Salmonella enterica subsp. Enterica isolated in Ukraine during the period of 2014–2017
inferred← citeshttps://doi.org/10.33448/rsd-v11i12.34837openalex-snapshot
Resistência antimicrobiana da microbiota de queijos servidos em hospital oncológico do Rio de Janeiro-Brasil
inferred← citeshttps://doi.org/10.3389/fcimb.2020.00365openalex-snapshot
WGS-Based Prediction and Analysis of Antimicrobial Resistance in Campylobacter jejuni Isolates From Israel
inferred← citeshttps://doi.org/10.3389/fcimb.2020.592512openalex-snapshot
Genotyping and Antibiotic Resistance Traits in Campylobacter jejuni and coli From Pigs and Wild Boars in Italy
inferred← citeshttps://doi.org/10.3389/fimmu.2021.757909openalex-snapshot
Salmonella Infantis Delays the Death of Infected Epithelial Cells to Aggravate Bacterial Load by Intermittent Phosphorylation of Akt With SopB
inferred← citeshttps://doi.org/10.3389/fmicb.2019.02124openalex-snapshot
Low Dose Colonization of Broiler Chickens With ESBL-/AmpC- Producing Escherichia coli in a Seeder-Bird Model Independent of Antimicrobial Selection Pressure
inferred← citeshttps://doi.org/10.3389/fmicb.2020.00539openalex-snapshot
Comparative Genome Analysis of Hungarian and Global Strains of Salmonella Infantis
inferred← citeshttps://doi.org/10.3389/fmicb.2020.01678openalex-snapshot
ChromID® CARBA Agar Fails to Detect Carbapenem-Resistant Enterobacteriaceae With Slightly Reduced Susceptibility to Carbapenems
inferred← citeshttps://doi.org/10.3389/fmicb.2020.02012openalex-snapshot
Effects of Bifidobacterium longum Subsp. infantis CECT 7210 and Lactobacillus rhamnosus HN001, Combined or Not With Oligofructose-Enriched Inulin, on Weaned Pigs Orally Challenged With Salmonella Typhimurium
inferred← citeshttps://doi.org/10.3389/fmicb.2020.616032openalex-snapshot
Emergence and Spread of Different ESBL-Producing Salmonella enterica Serovars in Hospitalized Horses Sharing a Highly Transferable IncM2 CTX-M-3-Encoding Plasmid
inferred← citeshttps://doi.org/10.3389/fmicb.2021.591929openalex-snapshot
Salmonella Derby: A Comparative Genomic Analysis of Strains From Germany
inferred← citeshttps://doi.org/10.3389/fmicb.2021.596891openalex-snapshot
Estimation of the Prevalence of Antimicrobial Resistance in Badgers (Meles meles) and Foxes (Vulpes vulpes) in Northern Ireland
inferred← citeshttps://doi.org/10.3389/fmicb.2021.626774openalex-snapshot
Genomic Diversity and Virulence Potential of ESBL- and AmpC-β-Lactamase-Producing Escherichia coli Strains From Healthy Food Animals Across Europe
inferred← citeshttps://doi.org/10.3389/fmicb.2021.637771openalex-snapshot
Evaluation of Salmonella Serotype Prediction With Multiplex Nanopore Sequencing
inferred← citeshttps://doi.org/10.3389/fmicb.2021.656223openalex-snapshot
Antimicrobial Resistance Glides in the Sky—Free-Living Birds as a Reservoir of Resistant Escherichia coli With Zoonotic Potential
inferred← citeshttps://doi.org/10.3389/fmicb.2021.689262openalex-snapshot
Monitoring of Antimicrobial Resistance to Aminoglycosides and Macrolides in Campylobacter coli and Campylobacter jejuni From Healthy Livestock in Spain (2002–2018)
inferred← citeshttps://doi.org/10.3389/fmicb.2021.716185openalex-snapshot
Aminoglycoside Resistance and Possible Mechanisms in Campylobacter Spp. Isolated From Chicken and Swine in Jiangsu, China
inferred← citeshttps://doi.org/10.3389/fmicb.2021.802404openalex-snapshot
Genomic Analysis and Antimicrobial Resistance of Campylobacter jejuni and Campylobacter coli in Peru
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1016895openalex-snapshot
The hazard of carbapenemase (OXA-181)-producing Escherichia coli spreading in pig and veal calf holdings in Italy in the genomics era: Risk of spill over and spill back between humans and animals
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1042612openalex-snapshot
Mobile colistin resistance (MCR), extended-spectrum beta-lactamase (ESBL) and multidrug resistance monitoring in Escherichia coli (commensal and pathogenic) in pig farming: need of harmonized guidelines and clinical breakpoints
inferred← citeshttps://doi.org/10.3389/fmicb.2022.901192openalex-snapshot
Metaphenotypes associated with recurrent genomic lineages of Campylobacter jejuni responsible for human infections in Luxembourg
inferred← citeshttps://doi.org/10.3389/fmicb.2022.910616openalex-snapshot
Bacillus subtilis PS-216 Spores Supplemented in Broiler Chicken Drinking Water Reduce Campylobacter jejuni Colonization and Increases Weight Gain
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1357881openalex-snapshot
Genotypic and phenotypic analysis of Salmonella enterica serovar Derby, looking for clues explaining the impairment of egg isolates to cause human disease
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1478509openalex-snapshot
Editorial: Zoonotic antimicrobial resistance and virulence: one health integrated approaches to monitor and reduce food chain hazards
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1532036openalex-snapshot
Genomic analyses reveal presence of extensively drug-resistant Salmonella enterica serovars isolated from clinical samples in Guizhou province, China, 2019–2023
inferred← citeshttps://doi.org/10.3389/fmicb.2026.1875505openalex-snapshot
Genomic surveillance reveals escalating antimicrobial resistance and plasmid diversity in clinical Salmonella 1,4,[5],12:i:- ST34 isolates from Guizhou Province, China
inferred← citeshttps://doi.org/10.3389/fpubh.2023.1221351openalex-snapshot
Phenotypic and genotypic antimicrobial resistance correlation and plasmid characterization in Salmonella spp. isolates from Italy reveal high heterogeneity among serovars
inferred← citeshttps://doi.org/10.3389/fsufs.2022.819158openalex-snapshot
The UK Antimicrobial Resistance Strategy 2013–18: A Qualitative Study of International and Domestic Policy and Action Related to Livestock and the Food Chain
inferred← citeshttps://doi.org/10.3389/fvets.2019.00452openalex-snapshot
Raising Animals Without Antibiotics: U.S. Producer and Veterinarian Experiences and Opinions
inferred← citeshttps://doi.org/10.3389/fvets.2020.00345openalex-snapshot
Spatial Trends in Salmonella Infection in Pigs in Spain
inferred← citeshttps://doi.org/10.3389/fvets.2020.558793openalex-snapshot
Does the Use of Different Indicators to Benchmark Antimicrobial Use Affect Farm Ranking?
inferred← citeshttps://doi.org/10.3389/fvets.2020.613718openalex-snapshot
Pet Reptiles: A Potential Source of Transmission of Multidrug-Resistant Salmonella
inferred← citeshttps://doi.org/10.3389/fvets.2022.816279openalex-snapshot
Analysis of Antimicrobial Resistance in Non-typhoidal Salmonella Collected From Pork Retail Outlets and Slaughterhouses in Vietnam Using Whole Genome Sequencing
inferred← citeshttps://doi.org/10.3389/fvets.2026.1873052openalex-snapshot
Regional phenotypic surveillance of antimicrobial susceptibility in chicken-associated commensal Staphylococcus, Enterococcus, and Escherichia coli from Southern Transdanubia, Hungary
inferred← citeshttps://doi.org/10.3390/ani10030417openalex-snapshot
Antimicrobial use on Italian Pig Farms and its Relationship with Husbandry Practices
inferred← citeshttps://doi.org/10.3390/ani10040744openalex-snapshot
Pathotypes and Antimicrobial Susceptibility of Escherichia Coli Isolated from Wild Boar (Sus scrofa) in Tuscany
inferred← citeshttps://doi.org/10.3390/ani10122239openalex-snapshot
Escherichia coli as Commensal and Pathogenic Bacteria among Food-Producing Animals: Health Implications of Extended Spectrum β-Lactamase (ESBL) Production
inferred← citeshttps://doi.org/10.3390/ani11051339openalex-snapshot
Multidrug-Resistant Campylobacer jejuni on Swine Processing at a Slaughterhouse in Eastern Spain
inferred← citeshttps://doi.org/10.3390/ani11082394openalex-snapshot
Phenotypic and Molecular Patterns of Resistance among Campylobacter coli and Campylobacter jejuni Isolates, from Pig Farms
inferred← citeshttps://doi.org/10.3390/ani11113197openalex-snapshot
High Prevalence of Antibiotic-Resistant Escherichia coli Isolates from Retail Poultry Products in Spain
inferred← citeshttps://doi.org/10.3390/ani12131620openalex-snapshot
Salmonella Shedding in Slaughter Pigs and the Use of Esterified Formic Acid in the Drinking Water as a Potential Abattoir-Based Mitigation Measure
inferred← citeshttps://doi.org/10.3390/ani12233378openalex-snapshot
Role of Bacteriophages for Optimized Health and Production of Poultry
inferred← citeshttps://doi.org/10.3390/ani14060968openalex-snapshot
Pathogenic Bacteria in Free-Living Birds, and Its Public Health Significance
inferred← citeshttps://doi.org/10.3390/antibiotics10020148openalex-snapshot
Farnesane-Type Sesquiterpenoids with Antibiotic Activity from Chiliadenus lopadusanus
showing the first 199 of 301
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.