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Antibiotic Resistance in Campylobacter : Emergence, Transmission and Persistence

https://doi.org/10.2217/17460913.4.2.189

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What this work says

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

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Development of resistance to quinolones in five patients with campylobacteriosis treated with norfloxacin or ciprofloxacin

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[37] Systems of experimental genetics for Campylobacter species

inferredcites →https://doi.org/10.1016/0168-1605(95)00044-kopenalex-snapshot

Culture media for the isolation of campylobacters

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Role ofdprAin transformation ofCampylobacter jejuni

inferredcites →https://doi.org/10.1016/j.ijantimicag.2003.12.008openalex-snapshot

Relative contribution of target gene mutation and efflux to fluoroquinolone and erythromycin resistance, in French poultry and pig isolates of Campylobacter coli

inferredcites →https://doi.org/10.1016/j.ijantimicag.2005.08.019openalex-snapshot

An investigation of the molecular mechanisms contributing to high-level erythromycin resistance in Campylobacter

inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2005.04.029openalex-snapshot

Antimicrobial resistance among Campylobacter jejuni isolated from raw poultry meat at retail level in Denmark

inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2007.01.006openalex-snapshot

Campylobacters as zoonotic pathogens: A food production perspective

inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2007.03.012openalex-snapshot

Mechanisms of erythromycin resistance of Campylobacter spp. isolated from food, animals and humans

inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2007.07.040openalex-snapshot

Antimicrobial resistance of 114 porcine isolates of Campylobacter coli

inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2008.09.005openalex-snapshot

Antimicrobial resistance of Campylobacter coli isolates from swine

inferredcites →https://doi.org/10.1016/j.micinf.2005.12.030openalex-snapshot

The epidemiology of antibiotic resistance in Campylobacter

inferredcites →https://doi.org/10.1016/j.micinf.2005.12.032openalex-snapshot

Mechanisms of fluoroquinolone and macrolide resistance in Campylobacter spp.

inferredcites →https://doi.org/10.1016/j.vetmic.2006.08.011openalex-snapshot

Antimicrobial susceptibility patterns of thermotolerant Campylobacter strains isolated from food animals in Ethiopia

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β-Lactam resistance and β-lactamases in bacteria of animal origin

inferredcites →https://doi.org/10.1016/s0168-1605(02)00314-8openalex-snapshot

Occurrence and resistance to antibiotics of Campylobacter jejuni and Campylobacter coli in animals and meat in northeastern Italy

inferredcites →https://doi.org/10.1016/s0732-8893(03)00154-8openalex-snapshot

Antimicrobial susceptibility trends in Campylobacter jejuni and Campylobacter coli isolated from a rural Egyptian pediatric population with diarrhea

inferredcites →https://doi.org/10.1017/s0950268806006200openalex-snapshot

Antibiotic resistance of retail food and human Campylobacter isolates on the island of Ireland from 2001–2002

inferredcites →https://doi.org/10.1038/35001088openalex-snapshot

The genome sequence of the food-borne pathogen Campylobacter jejuni reveals hypervariable sequences

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Genetic basis of quinolone resistance and epidemiology of resistant and susceptible isolates of porcine Campylobacter coli strains

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Generation of Campylobacter jejuni genetic diversity in vivo

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/10.1086/319760openalex-snapshot

Campylobacter jejuni Infections: Update on Emerging Issues and Trends

inferredcites →https://doi.org/10.1086/339195openalex-snapshot

Ciprofloxacin Resistance inCampylobacter jejuniEvolves Rapidly in Chickens Treated with Fluoroquinolones

inferredcites →https://doi.org/10.1086/509936openalex-snapshot

The Health Burden of Campylobacter Infection and the Impact of Antimicrobial Resistance: Playing Chicken

inferredcites →https://doi.org/10.1089/10766290152652800openalex-snapshot

Single or Double Mutational Alterations of GyrA Associated with Fluoroquinolone Resistance in Campylobacter jejuni and Campylobacter coli

inferredcites →https://doi.org/10.1089/10766290260469606openalex-snapshot

Selection and Characterization of Fluoroquinolone-Resistant Mutants of Campylobacter jejuni Using Enrofloxacin

inferredcites →https://doi.org/10.1089/1076629041310127openalex-snapshot

Characterization of Plasmid-Mediated aphA - 3 Kanamycin Resistance in Campylobacter jejuni

inferredcites →https://doi.org/10.1089/mdr.2005.11.40openalex-snapshot

Detection of Mutations Associated with Macrolide Resistance in Thermophilic Campylobacter spp. by Real-Time PCR

inferredcites →https://doi.org/10.1093/emboj/cdg093openalex-snapshot

Mechanism of Tet(O)‐mediated tetracycline resistance

inferredcites →https://doi.org/10.1093/infdis/165.4.667openalex-snapshot

High-Level Quinolone Resistance in Clinical Isolates of Campylobacter jejuni

inferredcites →https://doi.org/10.1093/jac/35.1.173openalex-snapshot

Incidence and transmission of antibiotic resistance in Campylobacter jejuni and Campylobacter coli

inferredcites →https://doi.org/10.1093/jac/36.1.259openalex-snapshot

A placebo controlled evaluation of lomefloxacin in the treatment of bacterial diarrhoea in the community

inferredcites →https://doi.org/10.1093/jac/36.4.738openalex-snapshot

Mobile rRNA methylase genes in Campylobacter (Wotinella) rectus

inferredcites →https://doi.org/10.1093/jac/dkg033openalex-snapshot

Fluoroquinolone resistance in Campylobacter species from man and animals: detection of mutations in topoisomerase genes

inferredcites →https://doi.org/10.1093/jac/dkg402openalex-snapshot

Rapid selection of quinolone resistance in Campylobacter jejuni but not in Escherichia coli in individually housed broilers

inferredcites →https://doi.org/10.1093/jac/dkg489openalex-snapshot

Multidrug resistance in Campylobacter jejuni strains collected from Finnish patients during 1995-2000

inferredcites →https://doi.org/10.1093/jac/dkh150openalex-snapshot

Emergence of fluoroquinolone resistance in the native Campylobacter coli population of pigs exposed to enrofloxacin

inferredcites →https://doi.org/10.1093/jac/dkh193openalex-snapshot

Molecular characterization of class 1 integrons from Irish thermophilic Campylobacter spp.

inferredcites →https://doi.org/10.1093/jac/dki040openalex-snapshot

Tetracycline resistance of Australian Campylobacter jejuni and Campylobacter coli isolates

inferredcites →https://doi.org/10.1093/jac/dki253openalex-snapshot

Molecular basis of macrolide resistance in Campylobacter: role of efflux pumps and target mutations

inferredcites →https://doi.org/10.1093/jac/dki292openalex-snapshot

Involvement of the CmeABC efflux pump in the macrolide resistance of Campylobacter coli

inferredcites →https://doi.org/10.1093/jac/dkl210openalex-snapshot

Macrolide resistance in Campylobacter jejuni and Campylobacter coli

inferredcites →https://doi.org/10.1093/jac/dkl412openalex-snapshot

Role of the CmeABC efflux pump in the emergence of fluoroquinolone-resistant Campylobacter under selection pressure

inferredcites →https://doi.org/10.1093/jac/dkm024openalex-snapshot

Antibiotic resistance in Campylobacter jejuni and Campylobacter coli isolated from poultry in the South-East Queensland region

inferredcites →https://doi.org/10.1093/jac/dkm300openalex-snapshot

Macrolide-resistant Campylobacter: the meat of the matter

inferredcites →https://doi.org/10.1099/jmm.0.47103-0openalex-snapshot

Role of the plasmid-encoded tet(O) gene in tetracycline-resistant clinical isolates of Campylobacter jejuni and Campylobacter coli

inferredcites →https://doi.org/10.1099/mic.0.26531-0openalex-snapshot

Variation of the natural transformation frequency of Campylobacter jejuni in liquid shake culture

inferredcites →https://doi.org/10.1099/mic.0.27112-0openalex-snapshot

Nucleotide sequences and comparison of two large conjugative plasmids from different Campylobacter species

inferredcites →https://doi.org/10.1111/j.1365-2672.2004.02278.xopenalex-snapshot

Characterization of erythromycin resistance in Campylobacter coli and Campylobacter jejuni isolated from pig offal in New Zealand

inferredcites →https://doi.org/10.1111/j.1365-2672.2004.02306.xopenalex-snapshot

Evidence for natural horizontal transfer of tetO gene between Campylobacter jejuni strains in chickens

inferredcites →https://doi.org/10.1111/j.1365-2672.2005.02712.xopenalex-snapshot

Campylobacter susceptibility to ciprofloxacin and corresponding fluoroquinolone concentrations within the gastrointestinal tracts of chickens*

inferredcites →https://doi.org/10.1111/j.1365-2672.2006.03189.xopenalex-snapshot

Prevalence and antimicrobial resistance of Campylobacter in US dairy cattle

inferredcites →https://doi.org/10.1111/j.1462-2920.2007.01351.xopenalex-snapshot

Bacteriophage influence Campylobacter jejuni types populating broiler chickens

inferredcites →https://doi.org/10.1111/j.1469-0691.2006.01643.xopenalex-snapshot

Regional and seasonal differences in incidence and antibiotic resistance of Campylobacter from a nationwide surveillance study in The Netherlands: an overview of 2000–2004

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Antibiotic resistance and resistance mechanisms inCampylobacter jejuniandCampylobacter coli

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Prevalence ofCampylobacter jejuniand its Resistance to Antibiotics in Poultry in the Czech Republic

inferredcites →https://doi.org/10.1128/9781555815554.ch14openalex-snapshot

Mechanisms of Antibiotic Resistance in Campylobacter

inferredcites →https://doi.org/10.1128/9781555815554.ch36openalex-snapshot

Transmission of Antibiotic Resistance from Food Animals to Humans

inferredcites →https://doi.org/10.1128/9781555815554.ch6openalex-snapshot

Clinical Aspects ofCampylobacter jejuniandCampylobacter coliInfections

inferredcites →https://doi.org/10.1128/aac.00450-08openalex-snapshot

Development, Stability, and Molecular Mechanisms of Macrolide Resistance in Campylobacter jejuni

inferredcites →https://doi.org/10.1128/aac.00616-06openalex-snapshot

Synergy between Efflux Pump CmeABC and Modifications in Ribosomal Proteins L4 and L22 in Conferring Macrolide Resistance in Campylobacter jejuni and Campylobacter coli

inferredcites →https://doi.org/10.1128/aac.01411-06openalex-snapshot

Effect of Macrolide Usage on Emergence of Erythromycin-Resistant Campylobacter Isolates in Chickens

inferredcites →https://doi.org/10.1128/aac.01592-06openalex-snapshot

Contribution of the CmeABC Efflux Pump to Macrolide and Tetracycline Resistance in Campylobacter jejuni

inferredcites →https://doi.org/10.1128/aac.01607-07openalex-snapshot

Role of Cj1211 in Natural Transformation and Transfer of Antibiotic Resistance Determinants inCampylobacter jejuni

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Characterization of tetracycline resistance plasmids from Campylobacter jejuni and Campylobacter coli

inferredcites →https://doi.org/10.1128/aac.32.8.1107openalex-snapshot

Mechanisms of antibiotic resistance in Campylobacter species

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Class 1 Integron-Associated Tobramycin-Gentamicin Resistance in Campylobacter jejuni Isolated from the Broiler Chicken House Environment

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CmeABC Functions as a Multidrug Efflux System in Campylobacter jejuni

inferredcites →https://doi.org/10.1128/aac.47.1.390-394.2003openalex-snapshot

In Vivo Selection of Campylobacter Isolates with High Levels of Fluoroquinolone Resistance Associated with gyrA Mutations and the Function of the CmeABC Efflux Pump

inferredcites →https://doi.org/10.1128/aac.47.12.3675-3681.2003openalex-snapshot

Ribosomal Protection Proteins and Their Mechanism ofTetracyclineResistance

inferredcites →https://doi.org/10.1128/aac.47.12.3825-3830.2003openalex-snapshot

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inferredcites →https://doi.org/10.1128/aac.47.6.2027-2029.2003openalex-snapshot

Antimicrobial Resistance of Campylobacter jejuni subsp. jejuni Strains Isolated from Humans in 1998 to 2001 in Montreal, Canada

inferredcites →https://doi.org/10.1128/aac.47.9.2946-2950.2003openalex-snapshot

In Vitro Activities of New Fluoroquinolones against Campylobacter jejuni and Campylobacter coli Isolates Obtained from Humans in 1980 to 1982 and 1997 to 2001

inferredcites →https://doi.org/10.1128/aac.49.2.699-707.2005openalex-snapshot

Incidence and Mechanism of Ciprofloxacin Resistance in Campylobacter spp. Isolated from Commercial Poultry Flocks in the United Kingdom before, during, and after Fluoroquinolone Treatment

inferredcites →https://doi.org/10.1128/aac.49.6.2454-2459.2005openalex-snapshot

Mosaic Structure of a Multiple-Drug-Resistant, Conjugative Plasmid from Campylobacter jejuni

inferredcites →https://doi.org/10.1128/aac.49.7.2753-2759.2005openalex-snapshot

Macrolide Resistance in Campylobacter jejuni and Campylobacter coli : Molecular Mechanism and Stability of the Resistance Phenotype

inferredcites →https://doi.org/10.1128/aac.49.8.3347-3354.2005openalex-snapshot

Role of Efflux Pumps and Topoisomerase Mutations in Fluoroquinolone Resistance in Campylobacter jejuni and Campylobacter coli

inferredcites →https://doi.org/10.1128/aem.02579-06openalex-snapshot

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inferredcites →https://doi.org/10.1128/aem.69.8.4511-4518.2003openalex-snapshot

Isolation and Characterization of Campylobacter Bacteriophages from Retail Poultry

inferredcites →https://doi.org/10.1128/aem.70.3.1442-1447.2004openalex-snapshot

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inferredcites →https://doi.org/10.1128/aem.70.7.3877-3883.2004openalex-snapshot

Longitudinal Study of Campylobacter jejuni Bacteriophages and Their Hosts from Broiler Chickens

inferredcites →https://doi.org/10.1128/aem.71.7.4108-4111.2005openalex-snapshot

Prevalence and Antimicrobial Resistance of Campylobacter spp. and Salmonella Serovars in Organic Chickens from Maryland Retail Stores

inferredcites →https://doi.org/10.1128/aem.72.2.1316-1321.2006openalex-snapshot

Natural Transformation-Mediated Transfer of Erythromycin Resistance in Campylobacter coli Strains from Turkeys and Swine

inferredcites →https://doi.org/10.1128/aem.72.5.3600-3607.2006openalex-snapshot

Effect of Conventional and Organic Production Practices on the Prevalence and Antimicrobial Resistance of Campylobacter spp. in Poultry

inferredcites →https://doi.org/10.1128/iai.68.8.4384-4390.2000openalex-snapshot

Involvement of a Plasmid in Virulence of Campylobacter jejuni 81-176

inferredcites →https://doi.org/10.1128/jb.01012-07openalex-snapshot

Cj0011c, a Periplasmic Single- and Double-Stranded DNA-Binding Protein, Contributes to Natural Transformation in Campylobacter jejuni

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Characterization and expression of a cloned tetracycline resistance determinant from Campylobacter jejuni plasmid pUA466

inferredcites →https://doi.org/10.1128/jb.185.18.5408-5418.2003openalex-snapshot

Natural Transformation of Campylobacter jejuni Requires Components of a Type II Secretion System

inferredcites →https://doi.org/10.1128/jb.186.19.6508-6514.2004openalex-snapshot

N-Linked Protein Glycosylation Is Required for Full Competence in Campylobacter jejuni 81-176

inferredcites →https://doi.org/10.1128/jcm.01456-06openalex-snapshot

Conjugative Transfer of Chromosomally Encoded Antibiotic Resistance from Helicobacter pylori to Campylobacter jejuni

inferredcites →https://doi.org/10.1128/jcm.42.7.3321-3323.2004openalex-snapshot

Genetic Relatedness and Quinolone Resistance of Campylobacter jejuni Strains Isolated in 2002 in Hong Kong

inferredcites →https://doi.org/10.1136/vr.151.11.317openalex-snapshot

Trends in antimicrobial susceptibility among isolates of Campylobacter species in Ireland and the emergence of resistance to ciprofloxacin

inferredcites →https://doi.org/10.1186/1471-2180-7-90openalex-snapshot

Characterization of Campylobacter phages including analysis of host range by selected Campylobacter Penner serotypes

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The Persistence of Fluoroquinolone-Resistant Campylobacter in Poultry Production

inferredcites →https://doi.org/10.1289/ehp.7647openalex-snapshot

Fluoroquinolone-Resistant Campylobacter Isolates from Conventional and Antibiotic-Free Chicken Products

inferredcites →https://doi.org/10.1371/journal.pbio.0030015openalex-snapshot

Major Structural Differences and Novel Potential Virulence Mechanisms from the Genomes of Multiple Campylobacter Species

inferredcites →https://doi.org/10.1371/journal.ppat.0030119openalex-snapshot

Genome Dynamics of Campylobacter jejuni in Response to Bacteriophage Predation

inferredcites →https://doi.org/10.1371/journal.ppat.1000083openalex-snapshot

Key Role of Mfd in the Development of Fluoroquinolone Resistance in Campylobacter jejuni

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98th General Meeting of the American Society for Microbiology

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Prevalence of Tetracycline-Resistant Campylobacter in Organic Broilers During a Production Cycle

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Human campylobacteriosis: a challenge for the veterinary profession

inferredcites →https://doi.org/10.3109/00365549209054659openalex-snapshot

Rapid Emergence of Quinolone Resistance in Campylobacter jejuni in Patients Treated with Norfloxacin

inferredcites →https://doi.org/10.3201/eid0701.010104openalex-snapshot

Quinolone and Macrolide Resistance in Campylobacter jejuni and C. coli: Resistance Mechanisms and Trends in Human Isolates

inferredcites →https://doi.org/10.3201/eid0802.010145openalex-snapshot

Comparative Antibiotic Resistance of Diarrheal Pathogens from Vietnam and Thailand, 1996-1999

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Increasing Fluoroquinolone Resistance inCampylobacter jejuni,Pennsylvania, USA,1982–20011

inferredcites →https://doi.org/10.3201/eid1006.030635openalex-snapshot

Antimicrobial Resistance amongCampylobacterStrains, United States, 1997–2001

inferredcites →https://doi.org/10.3201/eid1106.041052openalex-snapshot

pVir and Bloody Diarrhea inCampylobacter jejuniEnteritis

inferredcites →https://doi.org/10.3201/eid1302.060587openalex-snapshot

Campylobacter Antimicrobial Drug Resistance among Humans, Broiler Chickens, and Pigs, France

inferredcites →https://doi.org/10.33321/cdi.2003.27.27openalex-snapshot

Antibiotic resistance in Campylobacter jejuni isolated from humans in the Hunter Region, New South Wales

inferredcites →https://doi.org/10.4269/ajtmh.2003.68.666openalex-snapshot

ANTIMICROBIAL RESISTANCE OF BACTERIAL PATHOGENS ASSOCIATED WITH DIARRHEAL PATIENTS IN INDONESIA

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Prevalence and Antimicrobial Resistance of Campylobacter in Antimicrobial-Free and Conventional Pig Production Systems

inferredcites →https://doi.org/10.4315/0362-028x-70.3.729openalex-snapshot

Comparison of Antimicrobial Resistance of Campylobacter jejuni Isolated from Humans, Chickens, Raw Milk, and Environmental Water in Québec

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Prevalence and Antibiotic Resistance of Campylobacter spp. Isolated from Chicken Meat, Pork, and Beef in Korea, from 2001 to 2006

inferredcites →https://doi.org/10.4315/0362-028x-70.8.1945openalex-snapshot

Development of Macrolide-Resistant Campylobacter in Broilers Administered Subtherapeutic or Therapeutic Concentrations of Tylosin

inferredcites →https://doi.org/10.7883/yoken.jjid.2007.1openalex-snapshot

Pattern of Antibiotic Susceptibility in Campylobacter jejuni Isolates of Human and Poultry Origin

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Isolation and Drug-Resistant Patterns of Campylobacter Strains Cultured from Diarrheic Children in Tehran

What points at this work

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

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Impact of mutations in DNA gyrase genes on quinolone resistance in Campylobacter jejuni

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Identification of Outer Membrane Vesicles as a New Vehicle Mediating Antibiotic Resistance Gene Transfer in Campylobacter

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Antibiotic resistance mediated by site‐specific mutations in the multidrug efflux transporter CmeB of zoonotic pathogen Campylobacter

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Crystal structure of the Campylobacter jejuni CmeC outer membrane channel

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Problematic Groups of Multidrug-Resistant Bacteria and Their Resistance Mechanisms

inferred← citeshttps://doi.org/10.1007/978-981-13-9871-1_4openalex-snapshot

Antibiotic Resistance in Campylobacter jejuni: Mechanism, Status, and Public Health Significance

inferred← citeshttps://doi.org/10.1007/978-981-16-9723-4_16-1openalex-snapshot

Antimicrobial Resistance in Food-Borne Campylobacter spp.

inferred← citeshttps://doi.org/10.1007/978-981-19-9279-7_16openalex-snapshot

Antimicrobial Resistance in Food-Borne Campylobacter spp.

inferred← citeshttps://doi.org/10.1007/978-981-95-6615-0_23openalex-snapshot

Campylobacter Infections

inferred← citeshttps://doi.org/10.1007/978-981-96-1885-9_21openalex-snapshot

Insights into Campylobacter Biofilm Architecture: A Molecular Perspective

inferred← citeshttps://doi.org/10.1007/s00284-016-1134-5openalex-snapshot

The Influence of Prior Modes of Growth, Temperature, Medium, and Substrate Surface on Biofilm Formation by Antibiotic-Resistant Campylobacter jejuni

inferred← citeshttps://doi.org/10.1007/s10123-019-00062-8openalex-snapshot

Pulsed-field gel electrophoresis fingerprinting of Campylobacter jejuni and Campylobacter coli strains isolated from clinical specimens, Iran

inferred← citeshttps://doi.org/10.1007/s10156-012-0471-yopenalex-snapshot

Bloodstream infection caused by Campylobacter lari

inferred← citeshttps://doi.org/10.1007/s12088-024-01199-5openalex-snapshot

Diagnosis of Campylobacter spp. Isolates and Their Antimicrobial Susceptibility Patterns

inferred← citeshttps://doi.org/10.1007/s13538-026-02034-6openalex-snapshot

Assessing Intervention Strategies to Mitigate Campylobacteriosis Dynamics: An Optimal Control Analysis and Applications

inferred← citeshttps://doi.org/10.1016/b978-0-08-100596-5.00984-7openalex-snapshot

Campylobacter spp.

inferred← citeshttps://doi.org/10.1016/b978-0-12-374407-4.00390-3openalex-snapshot

Pathogens in Milk | Campylobacter spp.

inferred← citeshttps://doi.org/10.1016/b978-0-12-381366-4.00012-2openalex-snapshot

Digestive System Diseases of Nonhuman Primates

inferred← citeshttps://doi.org/10.1016/b978-0-12-397169-2.00067-6openalex-snapshot

Campylobacter

inferred← citeshttps://doi.org/10.1016/b978-0-12-409548-9.11418-6openalex-snapshot

Environmental Reservoirs of Antimicrobial Resistance of Foodborne Pathogens

inferred← citeshttps://doi.org/10.1016/b978-0-12-415846-7.00004-4openalex-snapshot

Campylobacter

inferred← citeshttps://doi.org/10.1016/b978-0-12-801214-7.00004-1openalex-snapshot

Antimicrobial Resistance and Campylobacter jejuni and C. coli

inferred← citeshttps://doi.org/10.1016/b978-0-12-811444-5.00005-1openalex-snapshot

Campylobacteriosis: An Emerging Infectious Foodborne Disease

inferred← citeshttps://doi.org/10.1016/b978-0-12-818619-0.00075-7openalex-snapshot

Campylobacter

inferred← citeshttps://doi.org/10.1016/b978-0-12-823426-6.00003-6openalex-snapshot

Atomic force microscopy as multifunctional microbial imaging and characterization platform

inferred← citeshttps://doi.org/10.1016/b978-0-323-40181-4.00163-8openalex-snapshot

Campylobacter jejuni and Campylobacter coli

inferred← citeshttps://doi.org/10.1016/b978-0-323-75608-2.00163-4openalex-snapshot

Campylobacter jejuni and Campylobacter coli

inferred← citeshttps://doi.org/10.1016/b978-0-323-82763-8.00046-7openalex-snapshot

Approach to Patients With Gastrointestinal Tract Infections and Food Poisoning

inferred← citeshttps://doi.org/10.1016/b978-0-443-33702-4.00005-0openalex-snapshot

Epidemiology of antimicrobial resistance in human and veterinary practices: 2014–24

inferred← citeshttps://doi.org/10.1016/b978-0-443-33702-4.00013-xopenalex-snapshot

Recent updates on an alternative approach to tackle antimicrobial resistance: Secondary metabolites from natural sources

inferred← citeshttps://doi.org/10.1016/b978-0-7020-3468-8.50169-3openalex-snapshot

Campylobacter jejuni and Campylobacter coli

inferred← citeshttps://doi.org/10.1016/b978-1-4377-2702-9.00165-3openalex-snapshot

Campylobacter jejuni and Campylobacter coli

inferred← citeshttps://doi.org/10.1016/b978-84-9113-949-2.00110-4openalex-snapshot

10.1016/b978-84-9113-949-2.00110-4

inferred← citeshttps://doi.org/10.1016/bs.aambs.2018.01.001openalex-snapshot

Antimicrobial Resistance in Campylobacter Species: Mechanisms and Genomic Epidemiology

inferred← citeshttps://doi.org/10.1016/bs.afnr.2016.12.009openalex-snapshot

Pathogens of Food Animals

inferred← citeshttps://doi.org/10.1016/bs.afnr.2018.04.004openalex-snapshot

Antimicrobial Resistance in the Food Chain in the European Union

inferred← citeshttps://doi.org/10.1016/bs.afnr.2018.04.005openalex-snapshot

Campylobacter in the Food Chain

inferred← citeshttps://doi.org/10.1016/j.ajem.2018.12.019openalex-snapshot

Multiplex polymerase chain reaction test to diagnose infectious diarrhea in the emergency department

inferred← citeshttps://doi.org/10.1016/j.antinf.2016.09.004openalex-snapshot

Infections à Campylobacter : tableaux cliniques, prise en charge diagnostique et thérapeutique

inferred← citeshttps://doi.org/10.1016/j.antinf.2016.09.005openalex-snapshot

Infections à Campylobacter : épidémiologie, facteurs de virulence, résistance aux antibiotiques

inferred← citeshttps://doi.org/10.1016/j.carres.2012.11.017openalex-snapshot

The design of a capsule polysaccharide conjugate vaccine against Campylobacter jejuni serotype HS15

inferred← citeshttps://doi.org/10.1016/j.cimid.2021.101712openalex-snapshot

Prevalence and antimicrobial resistance of Campylobacter from wild birds of prey in Spain

inferred← citeshttps://doi.org/10.1016/j.cofs.2020.12.020openalex-snapshot

Whole genome sequencing of Campylobacter in agri-food surveillance

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115277openalex-snapshot

Nano-Selenium inhibited antibiotic resistance genes and virulence factors by suppressing bacterial selenocompound metabolism and chemotaxis pathways in animal manure

inferred← citeshttps://doi.org/10.1016/j.eimc.2013.07.014openalex-snapshot

Aplicación del análisis de los polimorfismos de los tamaños de los fragmentos de restricción del gen flaA amplificado por reacción en cadena de la polimerasa y resistotipo para identificar potenciales brotes de campilobacteriosis no diagnosticados en España

inferred← citeshttps://doi.org/10.1016/j.eimc.2014.02.012openalex-snapshot

Molecular epidemiology and antimicrobial susceptibility of Campylobacter coli clinical isolates

inferred← citeshttps://doi.org/10.1016/j.eimc.2015.06.015openalex-snapshot

Enteropatógenos y antibióticos

inferred← citeshttps://doi.org/10.1016/j.eimce.2015.06.002openalex-snapshot

Enteropathogens and antibiotics

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.envint.2018.05.040openalex-snapshot

Bacterial lineages putatively associated with the dissemination of antibiotic resistance genes in a full-scale urban wastewater treatment plant

inferred← citeshttps://doi.org/10.1016/j.foodcont.2013.01.035openalex-snapshot

Identification and antimicrobial resistance of Campylobacter species isolated from poultry meat in Khorasan province, Iran

inferred← citeshttps://doi.org/10.1016/j.foodcont.2013.12.016openalex-snapshot

Frequency of contamination and antimicrobial resistance of thermotolerant Campylobacter isolated from some broiler farms and slaughterhouses in the region of Algiers

inferred← citeshttps://doi.org/10.1016/j.foodcont.2014.03.039openalex-snapshot

Persistence of foodborne pathogens and their control in primary and secondary food production chains

inferred← citeshttps://doi.org/10.1016/j.foodcont.2014.09.016openalex-snapshot

Prevalence and antimicrobial resistance of Campylobacter species isolates in ducks and geese

inferred← citeshttps://doi.org/10.1016/j.foodcont.2015.10.013openalex-snapshot

Prevalence and antimicrobial resistance of Campylobacter spp. isolated from retail chicken and duck meat in South Korea

inferred← citeshttps://doi.org/10.1016/j.foodcont.2017.03.048openalex-snapshot

Prevalence and antimicrobial resistance patterns of Campylobacter spp. isolated from retail meat in Lahore, Pakistan

inferred← citeshttps://doi.org/10.1016/j.foodcont.2025.111846openalex-snapshot

Evaluating antimicrobial resistance in Campylobacter coli and Campylobacter jejuni isolated from market hogs and sows at U.S. slaughter plants (2013–2021): A longitudinal comparative analysis

inferred← citeshttps://doi.org/10.1016/j.heliyon.2019.e02814openalex-snapshot

Human campylobacteriosis: A public health concern of global importance

inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e28774openalex-snapshot

Spatiotemporal variations in the occurrence of Campylobacter species in the Bloukrans and Swartkops rivers, Eastern Cape, South Africa

inferred← citeshttps://doi.org/10.1016/j.idc.2012.06.002openalex-snapshot

Traveler’s Diarrhea

inferred← citeshttps://doi.org/10.1016/j.idcr.2019.e00555openalex-snapshot

Campylobacter jejuni bacteremia in a patient with asplenia and enteritis

inferred← citeshttps://doi.org/10.1016/j.ijantimicag.2019.09.022openalex-snapshot

Visible light as an inhibitor of Campylobacter jejuni

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.130388openalex-snapshot

Identification and functional characterization of putative ligand binding domain(s) of JlpA protein of Campylobacter jejuni

inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2009.01.033openalex-snapshot

EFSA's 12th Scientific Colloquium — Assessing health benefits of controlling Campylobacter in the food chain

inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2011.01.035openalex-snapshot

Antimicrobial resistance in Campylobacter coli isolated from pigs in two provinces of China

inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2012.04.020openalex-snapshot

Prevalence, quantification and antimicrobial resistance of Campylobacter spp. on chicken neck-skins at points of slaughter in 5 major cities located on 4 continents

inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2013.02.004openalex-snapshot

Occurrence and characteristics of fastidious Campylobacteraceae species in porcine samples

inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2015.06.006openalex-snapshot

Comparative analysis of antimicrobial resistance and genetic diversity of Campylobacter from broilers slaughtered in Poland

inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2020.108656openalex-snapshot

Prevalence, antibiotic resistance and genotypes of Campylobacter jejuni and Campylobacter coli isolated from chickens in Irbid governorate, Jordan

inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2020.109017openalex-snapshot

Prevalence and antimicrobial susceptibility of Campylobacter isolated from retail chickens in Thailand

inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2021.109440openalex-snapshot

Characterization and antimicrobial resistance of Campylobacter jejuni and Campylobacter coli isolated from chicken and pork

inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2025.111187openalex-snapshot

Multidrug-resistant, hyperaerotolerant, and aerobic growth of Campylobacter jejuni and C. coli in retail broiler chicken meat in Selangor, Malaysia

inferred← citeshttps://doi.org/10.1016/j.ijheh.2018.03.005openalex-snapshot

Pathogens transmitted in animal feces in low- and middle-income countries

inferred← citeshttps://doi.org/10.1016/j.ijheh.2020.113640openalex-snapshot

Seasonality of drinking water sources and the impact of drinking water source on enteric infections among children in Limpopo, South Africa

inferred← citeshttps://doi.org/10.1016/j.jgar.2014.07.001openalex-snapshot

WITHDRAWN: Identification of Campylobacter jejuni and determination of point mutations associated with macrolide resistance using a multiplex TaqMan MGB real-time PCR

inferred← citeshttps://doi.org/10.1016/j.jgar.2018.09.011openalex-snapshot

Antimicrobial susceptibility of clinical isolates of Campylobacter jejuni from New South Wales, Australia

inferred← citeshttps://doi.org/10.1016/j.jgar.2019.07.018openalex-snapshot

Transmission of multidrug-resistant Campylobacter jejuni to children from different sources in Pakistan

inferred← citeshttps://doi.org/10.1016/j.jgar.2025.05.008openalex-snapshot

Antimicrobial resistance in Campylobacter spp. focussing on C. jejuni and C. coli – A narrative review

inferred← citeshttps://doi.org/10.1016/j.jiac.2015.05.003openalex-snapshot

Characterization of Campylobacter jejuni DNA gyrase as the target of quinolones

inferred← citeshttps://doi.org/10.1016/j.jinf.2024.106265openalex-snapshot

Machine learning to attribute the source of Campylobacter infections in the United States: A retrospective analysis of national surveillance data

inferred← citeshttps://doi.org/10.1016/j.jinf.2026.106695openalex-snapshot

Global frequency of Campylobacter-associated hospitalisations: A systematic review and meta-analyses

inferred← citeshttps://doi.org/10.1016/j.jmb.2016.09.021openalex-snapshot

MOMP from Campylobacter jejuni Is a Trimer of 18-Stranded β-Barrel Monomers with a Ca 2+ Ion Bound at the Constriction Zone

inferred← citeshttps://doi.org/10.1016/j.jmii.2021.07.001openalex-snapshot

Distribution of virulence and antibiotic resistance genes in Campylobacter jejuni and Campylobacter coli isolated from broiler chickens in Tunisia

inferred← citeshttps://doi.org/10.1016/j.lwt.2021.111202openalex-snapshot

Antimicrobial resistance genes and plasmids in Campylobacter jejuni from broiler production chain in Southern Brazil

inferred← citeshttps://doi.org/10.1016/j.micpath.2025.107796openalex-snapshot

Whole genome data analysis from a one health perspective reveals global landscape of antimicrobial resistance in Campylobacter jejuni over the past decade, revealing striking prevalence of aminoglycoside, tetracycline, and macrolide resistance genes in Asia

inferred← citeshttps://doi.org/10.1016/j.micres.2022.127149openalex-snapshot

Campylobacter biofilms

inferred← citeshttps://doi.org/10.1016/j.mimet.2013.06.021openalex-snapshot

Antimicrobial resistance in Campylobacter: Susceptibility testing methods and resistance trends

inferred← citeshttps://doi.org/10.1016/j.mimet.2013.06.024openalex-snapshot

Use of phages to control Campylobacter spp.

inferred← citeshttps://doi.org/10.1016/j.modpat.2023.100210openalex-snapshot

Infectious Mimics of Inflammatory Bowel Disease

inferred← citeshttps://doi.org/10.1016/j.nmni.2025.101687openalex-snapshot

Global prevalence of fluoroquinolone resistance in common Campylobacter species associated with human infections

inferred← citeshttps://doi.org/10.1016/j.parepi.2021.e00207openalex-snapshot

Prevalence of intestinal parasitic infections and Campylobacter spp. among children with gastrointestinal disorders in Tehran, Iran

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1016/j.prevetmed.2020.104935openalex-snapshot

Genotyping, virulence genes and antimicrobial resistance of Campylobacter spp.isolated during two seasonal periods in Spanish poultry farms

inferred← citeshttps://doi.org/10.1016/j.provac.2015.05.007openalex-snapshot

The Application of a Proteoliposome Adjuvant System in the Development of a Campylobacter Jejuni Vaccine

inferred← citeshttps://doi.org/10.1016/j.psj.2020.06.020openalex-snapshot

Carvacrol attenuates Campylobacter jejuni colonization factors and proteome critical for persistence in the chicken gut

inferred← citeshttps://doi.org/10.1016/j.psj.2020.11.079openalex-snapshot

Research Note: Antimicrobial resistance of Campylobacter species isolated from chickens near Ulaanbaatar city, Mongolia

inferred← citeshttps://doi.org/10.1016/j.psj.2022.102419openalex-snapshot

Prevalence, drug resistance spectrum and virulence gene analysis of Campylobacter jejuni in broiler farms in central Shanxi, China

inferred← citeshttps://doi.org/10.1016/j.psj.2023.102786openalex-snapshot

Avian campylobacteriosis, prevalence, sources, hazards, antibiotic resistance, poultry meat contamination, and control measures: a comprehensive review

inferred← citeshttps://doi.org/10.1016/j.psj.2024.103485openalex-snapshot

Molecular characterization of Campylobacter spp. isolates obtained from commercial broilers and native chickens in Southern Thailand using whole genome sequencing

inferred← citeshttps://doi.org/10.1016/j.psj.2025.105302openalex-snapshot

Phenotypic and whole genome-based characterization of antibiotic resistance of Campylobacter jejuni isolates from chicken livers

inferred← citeshttps://doi.org/10.1016/j.psj.2025.105657openalex-snapshot

Antimicrobial resistance patterns of Campylobacter jejuni isolated from retail raw chicken meat in Jordan

inferred← citeshttps://doi.org/10.1016/j.psj.2026.107484openalex-snapshot

Phenotypic and PCR-based analysis of antimicrobial resistance in heat-treated multidrug-resistant Salmonella spp. and Campylobacter jejuni isolated from raw chicken meat

inferred← citeshttps://doi.org/10.1016/j.tifs.2010.09.003openalex-snapshot

Campylobacter and its multi-resistance in the food chain

inferred← citeshttps://doi.org/10.1016/j.trsl.2020.04.009openalex-snapshot

New and alternative strategies for the prevention, control, and treatment of antibiotic-resistant Campylobacter

inferred← citeshttps://doi.org/10.1016/j.vetmic.2009.12.035openalex-snapshot

Prevalence and antimicrobial resistance of Campylobacter isolates in broilers from China

inferred← citeshttps://doi.org/10.1016/j.vetmic.2017.02.022openalex-snapshot

Dissemination of erm (B) and its associated multidrug-resistance genomic islands in Campylobacter from 2013 to 2015

inferred← citeshttps://doi.org/10.1016/j.vetmic.2020.108652openalex-snapshot

Tetracycline resistance transmission in Campylobacter is promoted at temperatures resembling the avian reservoir

inferred← citeshttps://doi.org/10.1016/s1773-035x(10)70508-6openalex-snapshot

Mécanismes et épidémiologie de la résistance aux fluoroquinolones en 2010

inferred← citeshttps://doi.org/10.1017/s0950268813003245openalex-snapshot

The evidence for clonal spreading of quinolone resistance with a particular clonal complex ofCampylobacter jejuni

inferred← citeshttps://doi.org/10.1017/s095026882200139xopenalex-snapshot

Characterisation of burden of illness measures associated with human (Fluoro)quinolone-resistant Campylobacter spp. infections – a scoping review

inferred← citeshttps://doi.org/10.1017/s0950268823000742openalex-snapshot

A scoping review of factors associated with antimicrobial-resistant Campylobacter species infections in humans

inferred← citeshttps://doi.org/10.1017/s0950268824000359openalex-snapshot

Monitoring antimicrobial resistance in Campylobacter isolates of chickens and turkeys at the slaughter establishment level across the United States, 2013–2021

inferred← citeshttps://doi.org/10.1017/s0950268824001511openalex-snapshot

Reducing antimicrobial use in livestock alone may be not sufficient to reduce antimicrobial resistance among human Campylobacter infections: an ecological study in the Netherlands

inferred← citeshttps://doi.org/10.1017/s1466252317000135openalex-snapshot

Antibiotic resistance trends and mechanisms in the foodborne pathogen,Campylobacter

inferred← citeshttps://doi.org/10.1021/acs.biochem.2c00484openalex-snapshot

Functional Characterization of a HAD Phosphatase Involved in Capsular Polysaccharide Biosynthesis in Campylobacter jejuni

inferred← citeshttps://doi.org/10.1021/acs.biochem.5c00052openalex-snapshot

Identification and Functional Characterization of the Polymerizing Glycosyltransferase Required for the Transfer of d -Ribose to the d -GalfNAc Moiety of the Capsular Polysaccharide of Campylobacter jejuni

inferred← citeshttps://doi.org/10.1021/acs.jcim.3c00818openalex-snapshot

Kinetic Barrier to Enzyme Inhibition Is Manipulated by Dynamical Local Interactions in E. coli DHFR

inferred← citeshttps://doi.org/10.1021/acs.jmedchem.6b01869openalex-snapshot

Targeting Bacillosamine Biosynthesis in Bacterial Pathogens: Development of Inhibitors to a Bacterial Amino-Sugar Acetyltransferase from Campylobacter jejuni

inferred← citeshttps://doi.org/10.1021/acs.joc.8b02394openalex-snapshot

Total Synthesis of the Trisaccharide Antigen of the Campylobacter jejuni RM1221 Capsular Polysaccharide via de Novo Synthesis of the 6-Deoxy- d -manno-heptose Building Blocks

inferred← citeshttps://doi.org/10.1021/acsabm.9b00619openalex-snapshot

Antibacterial Amino Acid-Based Poly(ionic liquid) Membranes: Effects of Chirality, Chemical Bonding Type, and Application for MRSA Skin Infections

inferred← citeshttps://doi.org/10.1021/acschembio.8b00781openalex-snapshot

Transition-State Analogues of Campylobacter jejuni 5′-Methylthioadenosine Nucleosidase

inferred← citeshttps://doi.org/10.1021/bi401546ropenalex-snapshot

The Renaissance of Bacillosamine and Its Derivatives: Pathway Characterization and Implications in Pathogenicity

inferred← citeshttps://doi.org/10.1021/pr501061dopenalex-snapshot

Untargeted Metabolomic Profiling of Amphenicol-Resistant Campylobacter jejuni by Ultra-High-Performance Liquid Chromatography–Mass Spectrometry

inferred← citeshttps://doi.org/10.1038/ajg.2010.74openalex-snapshot

An Outbreak of Acute Bacterial Gastroenteritis Is Associated With an Increased Incidence of Irritable Bowel Syndrome in Children

inferred← citeshttps://doi.org/10.1038/ja.2013.20openalex-snapshot

Roles of the superoxide dismutase SodB and the catalase KatA in the antibiotic resistance of Campylobacter jejuni

inferred← citeshttps://doi.org/10.1038/ja.2015.26openalex-snapshot

Contribution of surface polysaccharides to the resistance of Campylobacter jejuni to antimicrobial phenolic compounds

inferred← citeshttps://doi.org/10.1038/s41467-017-00217-zopenalex-snapshot

Structures and transport dynamics of a Campylobacter jejuni multidrug efflux pump

inferred← citeshttps://doi.org/10.1038/s41591-019-0533-0openalex-snapshot

Gut microbiome alteration in MORDOR I: a community-randomized trial of mass azithromycin distribution

inferred← citeshttps://doi.org/10.1038/s41598-017-09593-4openalex-snapshot

Effects of low concentrations of erythromycin, penicillin, and virginiamycin on bacterial resistance development in vitro

inferred← citeshttps://doi.org/10.1038/s41598-017-17321-1openalex-snapshot

Integrated Genomic and Proteomic Analyses of High-level Chloramphenicol Resistance in Campylobacter jejuni

inferred← citeshttps://doi.org/10.1038/s41598-021-88318-0openalex-snapshot

Whole genome-based characterisation of antimicrobial resistance and genetic diversity in Campylobacter jejuni and Campylobacter coli from ruminants

inferred← citeshttps://doi.org/10.1039/d4tb01355gopenalex-snapshot

Purpose-built multicomponent supramolecular silver( i )-hydrogels as membrane-targeting broad-spectrum antibacterial agents against multidrug-resistant pathogens

inferred← citeshttps://doi.org/10.1074/jbc.m116.746404openalex-snapshot

Accumulation of Peptidoglycan O-Acetylation Leads to Altered Cell Wall Biochemistry and Negatively Impacts Pathogenesis Factors of Campylobacter jejuni

inferred← citeshttps://doi.org/10.1080/00071668.2019.1697426openalex-snapshot

Role of integrons in the proliferation of multiple drug resistance in selected bacteria occurring in poultry production

inferred← citeshttps://doi.org/10.1080/00071668.2020.1758300openalex-snapshot

Antimicrobial resistance of Campylobacter isolates recovered from broilers in the Republic of Ireland in 2017 and 2018: an update

inferred← citeshttps://doi.org/10.1080/00071668.2025.2494601openalex-snapshot

In vitro antimicrobial resistant pattern, plasmid profile and the survival of Campylobacter jejuni isolated from poultry sources

inferred← citeshttps://doi.org/10.1080/03079457.2012.734915openalex-snapshot

Molecular characterization and genotypic antimicrobial resistance analysis ofCampylobacter jejuniandCampylobacter coliisolated from broiler flocks in northern Italy

inferred← citeshttps://doi.org/10.1080/03079457.2015.1120272openalex-snapshot

Fluoroquinolone and macrolide resistance inCampylobacter jejuniisolated from broiler slaughterhouses in southern Brazil

inferred← citeshttps://doi.org/10.1080/03079457.2017.1315048openalex-snapshot

Prevalence of Campylobacter species in wild birds of South Korea

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1080/10495398.2021.1953514openalex-snapshot

Occurrence and antimicrobial resistance of Campylobacter isolates from broiler chicken and slaughter house environment in India

inferred← citeshttps://doi.org/10.1080/1120009x.2023.2267895openalex-snapshot

Antibiotic resistance in Campylobacter jejuni and Campylobacter coli: significant contribution of an RND type efflux pump in erythromycin resistance

inferred← citeshttps://doi.org/10.1080/23744235.2016.1258487openalex-snapshot

Campylobacter jejunistrains coresistant to tetracycline and ciprofloxacin in patients with gastroenteritis in Croatia

inferred← citeshttps://doi.org/10.1080/87559129.2025.2578312openalex-snapshot

Fluoroquinolone Resistance in Campylobacter Isolates from Broiler Meat: A Systematic Review and Meta-Analysis at a Global Scale

inferred← citeshttps://doi.org/10.1089/fpd.2009.0354openalex-snapshot

Contribution of the Multidrug Efflux Transporter CmeABC to Antibiotic Resistance in Different Campylobacter Species

inferred← citeshttps://doi.org/10.1089/fpd.2009.0505openalex-snapshot

Fluoroquinolone Resistance Detection in Campylobacter coli and Campylobacter jejuni by Luminex ® xMAP™ Technology

inferred← citeshttps://doi.org/10.1089/fpd.2010.0676openalex-snapshot

Rapid Detection of Point Mutations in Domain V of the 23S rRNA Gene in Erythromycin-Resistant Campylobacter Isolates by Pyrosequencing

inferred← citeshttps://doi.org/10.1089/fpd.2011.1042openalex-snapshot

Trend Analysis of Antimicrobial Resistance in Campylobacter jejuni and Campylobacter coli Isolated from Belgian Pork and Poultry Meat Products Using Surveillance Data of 2004–2009

inferred← citeshttps://doi.org/10.1089/fpd.2012.1127openalex-snapshot

Antimicrobial-Resistant Campylobacter in the Food Chain in Mexico

inferred← citeshttps://doi.org/10.1089/fpd.2012.1293openalex-snapshot

Molecular Epidemiology and Public Health Relevance of Campylobacter Isolated from Dairy Cattle and European Starlings in Ohio, USA

inferred← citeshttps://doi.org/10.1089/fpd.2015.2048openalex-snapshot

Typing of Campylobacter jejuni Isolated from Turkey by Genotypic Methods, Antimicrobial Susceptibility, and Virulence Gene Patterns: A Retrospective Study

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1089/fpd.2019.2707openalex-snapshot

Antimicrobial Resistance of Human Campylobacter Species Infections in Saskatchewan, Canada (1999–2006): A Historical Provincial Collection of All Reported Cases

inferred← citeshttps://doi.org/10.1089/fpd.2019.2770openalex-snapshot

Comparative Genomic Analysis of a Multidrug-Resistant Campylobacter jejuni Strain YH002 Isolated from Retail Beef Liver

inferred← citeshttps://doi.org/10.1089/fpd.2022.0043openalex-snapshot

Prevalence and Antimicrobial Resistance of Campylobacter spp. Isolated from Broilers Throughout the Supply Chain in Valencia, Spain

inferred← citeshttps://doi.org/10.1089/fpd.2023.0144openalex-snapshot

Virulence Genes, Antimicrobial Resistance, and Genotypes of Campylobacter jejuni Isolated from Chicken Slaughterhouses in South Korea

inferred← citeshttps://doi.org/10.1089/mdr.2010.0139openalex-snapshot

Fitness Cost of Fluoroquinolone Resistance in Campylobacter coli and Campylobacter jejuni

inferred← citeshttps://doi.org/10.1089/mdr.2012.0017openalex-snapshot

Effects of Efflux Pump Inhibitors on Erythromycin, Ciprofloxacin, and Tetracycline Resistance in Campylobacter spp. Isolates

inferred← citeshttps://doi.org/10.1089/mdr.2012.0160openalex-snapshot

Antimicrobial Susceptibilities of Campylobacter jejuni and Campylobacter coli Strains Isolated from Two Early Stages of Poultry Production

inferred← citeshttps://doi.org/10.1089/mdr.2013.0110openalex-snapshot

Antimicrobial Resistance of Campylobacter jejuni and Campylobacter coli from Poultry in Italy

inferred← citeshttps://doi.org/10.1089/mdr.2016.0249openalex-snapshot

High Prevalence of Resistance to Fluoroquinolones and Tetracycline Campylobacter Spp. Isolated from Poultry in Poland

inferred← citeshttps://doi.org/10.1089/mdr.2018.0455openalex-snapshot

Quinolone and Macrolide-Resistant Campylobacter jejuni in Pediatric Gastroenteritis Patients from Central Iran

inferred← citeshttps://doi.org/10.1089/vbz.2017.2116openalex-snapshot

Antimicrobial Susceptibility and Genotypic Characteristic of Campylobacter spp. Isolates from Free-Living Birds in Poland

inferred← citeshttps://doi.org/10.1093/cid/cir504openalex-snapshot

Antimicrobial Use: A Risk Factor or a Protective Factor for Acquiring Campylobacteriosis?

inferred← citeshttps://doi.org/10.1093/cid/cix1014openalex-snapshot

Rifaximin Fails to Prevent Campylobacteriosis in the Human Challenge Model: A Randomized, Double-Blind, Placebo-Controlled Trial

inferred← citeshttps://doi.org/10.1093/glycob/cwz082openalex-snapshot

N-glycosylation of the CmeABC multidrug efflux pump is needed for optimal function in Campylobacter jejuni

inferred← citeshttps://doi.org/10.1093/jac/dkp179openalex-snapshot

Risk factors for ciprofloxacin-resistant Campylobacter infection in Wales

inferred← citeshttps://doi.org/10.1093/jac/dkt242openalex-snapshot

Absence of class 1 and class 2 integrons among Campylobacter jejuni and Campylobacter coli isolated from poultry in Italy

inferred← citeshttps://doi.org/10.1093/jac/dkt381openalex-snapshot

Target optimization for peptide nucleic acid (PNA)-mediated antisense inhibition of the CmeABC multidrug efflux pump in Campylobacter jejuni

inferred← citeshttps://doi.org/10.1093/jac/dkt492openalex-snapshot

Report of ribosomal RNA methylase gene erm(B) in multidrug-resistant Campylobacter coli

inferred← citeshttps://doi.org/10.1093/jac/dku418openalex-snapshot

Characterization of the genetic environment of the ribosomal RNA methylase gene erm(B) in Campylobacter jejuni

inferred← citeshttps://doi.org/10.1093/jac/dku488openalex-snapshot

Identification of a novel fosXCC gene conferring fosfomycin resistance in Campylobacter

inferred← citeshttps://doi.org/10.1093/jac/dkv382openalex-snapshot

Species shift and multidrug resistance of Campylobacter from chicken and swine, China, 2008–14

inferred← citeshttps://doi.org/10.1093/jac/dkx023openalex-snapshot

Emergence of a plasmid-borne multidrug resistance gene cfr(C) in foodborne pathogen Campylobacter

inferred← citeshttps://doi.org/10.1093/jac/dky385openalex-snapshot

Antibiotic treatment of gastroenteritis in primary care

inferred← citeshttps://doi.org/10.1093/lambio/ovag031openalex-snapshot

Ecology and antimicrobial resistance of Campylobacter in wildlife: insights into specialist and generalist lineages and zoonotic potential

inferred← citeshttps://doi.org/10.1097/mog.0b013e3283413763openalex-snapshot

Update on human Campylobacter jejuni infections

inferred← citeshttps://doi.org/10.1097/qco.0000000000000570openalex-snapshot

A One Health approach to prevention, treatment, and control of campylobacteriosis

inferred← citeshttps://doi.org/10.1099/jmm.0.052316-0openalex-snapshot

Effects of efflux-pump inducers and genetic variation of the multidrug transporter cmeB in biocide resistance of Campylobacter jejuni and Campylobacter coli

inferred← citeshttps://doi.org/10.1099/mgen.0.000198openalex-snapshot

Trends in fluoroquinolone resistance in Campylobacter

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