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Prevalence, Virulence, and Antimicrobial Resistance of Campylobacter jejuni and Campylobacter coli in White Stork Ciconia ciconia in Poland

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

inferredcites →https://doi.org/10.1007/s10344-004-0052-1openalex-snapshot
Campylobacter, salmonella and chlamydia in free-living birds of Croatia
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A one-step microbial DNA extraction method using “Chelex 100” suitable for gene amplification
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Prevalence of virulence-associated genes and cytolethal distending toxin production in Campylobacter spp. isolated in Italy
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.jinf.2007.11.001openalex-snapshot
Human infections associated with wild birds
inferredcites →https://doi.org/10.1016/j.vetmic.2011.03.002openalex-snapshot
Campylobacter jejuni, Campylobacter coli, and cytolethal distending toxin (CDT) genes in common teals (Anas crecca)
inferredcites →https://doi.org/10.1016/j.watres.2010.10.001openalex-snapshot
Molecular subtypes of Campylobacter spp., Salmonella enterica, and Escherichia coli O157:H7 isolated from faecal and surface water samples in the Oldman River watershed, Alberta, Canada
inferredcites →https://doi.org/10.1016/s0140-6736(95)90318-6openalex-snapshot
Bird attacks on milk bottles and campylobacter infection
inferredcites →https://doi.org/10.1017/s0950268806006583openalex-snapshot
Is the major increase in notified campylobacteriosis in New Zealand real?
inferredcites →https://doi.org/10.1046/j.1365-2672.1999.00924.xopenalex-snapshot
Distribution and seasonality of microbial indicators and thermophilic campylobacters in two freshwater bathing sites on the River Lune in northwest England
inferredcites →https://doi.org/10.1046/j.1365-2672.2001.01355.xopenalex-snapshot
Campylobacters in water, sewage and the environment
inferredcites →https://doi.org/10.1046/j.1365-2672.2001.01357.xopenalex-snapshot
Current epidemiological issues in human campylobacteriosis
inferredcites →https://doi.org/10.1046/j.1365-2672.2003.01926.xopenalex-snapshot
PCR detection of seven virulence and toxin genes of Campylobacter jejuni and Campylobacter coli isolates from Danish pigs and cattle and cytolethal distending toxin production of the isolates
inferredcites →https://doi.org/10.1093/cid/cir249openalex-snapshot
Outbreak of Campylobacteriosis Associated With Consumption of Raw Peas
inferredcites →https://doi.org/10.1099/0022-1317-50-12-1087openalex-snapshot
Prevalence of cytolethal distending toxin (cdt) genes and CDT production in Campylobacter spp. isolated from Danish broilers
inferredcites →https://doi.org/10.1099/jmm.0.45988-0openalex-snapshot
Prevalence of potential virulence markers in Polish Campylobacter jejuni and Campylobacter coli isolates obtained from hospitalized children and from chicken carcasses
inferredcites →https://doi.org/10.1111/j.1365-2672.2006.03090.xopenalex-snapshot
Species diversity of campylobacteria in a wild bird community in Sweden
inferredcites →https://doi.org/10.1111/j.1574-6968.2007.00935.xopenalex-snapshot
Antibiotic resistance and resistance mechanisms inCampylobacter jejuniandCampylobacter coli
inferredcites →https://doi.org/10.1128/9781555815554.ch9openalex-snapshot
Epidemiology of Campylobacter jejuni Infections in Industrialized Nations
inferredcites →https://doi.org/10.1128/aem.01979-08openalex-snapshot
Molecular Epidemiology of Campylobacter jejuni Isolates from Wild-Bird Fecal Material in Children's Playgrounds
inferredcites →https://doi.org/10.1128/aem.02458-08openalex-snapshot
Molecular Epidemiology and Characterization of Campylobacter spp. Isolated from Wild Bird Populations in Northern England
inferredcites →https://doi.org/10.1128/aem.02491-07openalex-snapshot
Comparison of Campylobacter Populations in Wild Geese with Those in Starlings and Free-Range Poultry on the Same Farm
inferredcites →https://doi.org/10.1128/aem.45.2.375-380.1983openalex-snapshot
Avian wildlife reservoir of Campylobacter fetus subsp. jejuni, Yersinia spp., and Salmonella spp. in Norway
inferredcites →https://doi.org/10.1128/aem.68.12.5911-5917.2002openalex-snapshot
Prevalence of Campylobacter jejuni , Campylobacter lari , and Campylobacter coli in Different Ecological Guilds and Taxa of Migrating Birds
inferredcites →https://doi.org/10.1128/aem.69.3.1391-1396.2003openalex-snapshot
Detection and Typing of Campylobacter jejuni and Campylobacter coli and Analysis of Indicator Organisms in Three Waterborne Outbreaks in Finland
inferredcites →https://doi.org/10.1128/aem.71.5.2438-2441.2005openalex-snapshot
Antimicrobial Resistance Profiles of Campylobacter jejuni Isolates from Wild Birds in Sweden
inferredcites →https://doi.org/10.1128/iai.68.12.7137-7140.2000openalex-snapshot
DNA Rearrangements in the Flagellin Locus of an flaA Mutant of Campylobacter jejuni during Colonization of Chicken Ceca
inferredcites →https://doi.org/10.1128/jcm.31.6.1531-1536.1993openalex-snapshot
Flagellin gene typing of Campylobacter jejuni by restriction fragment length polymorphism analysis
inferredcites →https://doi.org/10.1128/jcm.37.3.510-517.1999openalex-snapshot
Identification of the Enteropathogens Campylobacter jejuni and Campylobacter coli Based on the cadF Virulence Gene and Its Product
inferredcites →https://doi.org/10.1128/jcm.39.4.1353-1359.2001openalex-snapshot
Molecular Characterization of Invasive and Noninvasive Campylobacter jejuni and Campylobacter coli Isolates
inferredcites →https://doi.org/10.1128/jcm.41.1.330-336.2003openalex-snapshot
Evaluation of 11 PCR Assays for Species-Level Identification of Campylobacter jejuni and Campylobacter coli
inferredcites →https://doi.org/10.1186/2046-0481-64-6openalex-snapshot
Genotypic characterisation and cluster analysis of Campylobacter jejuniisolates from domestic pets, human clinical cases and retail food
inferredcites →https://doi.org/10.1292/jvms.71.1247openalex-snapshot
Age-Dependent Variation of Virulence-Associated Genes Retained in Campylobacter jejuni Isolated from Chickens in a Poultry Farm
inferredcites →https://doi.org/10.1675/1524-4695(2005)028[0378:eowlal]2.0.co;2openalex-snapshot
Effect of Water Level and Livestock on the Productivity and Numbers of Breeding White Storks
inferredcites →https://doi.org/10.17221/6016-vetmedopenalex-snapshot
Prevalence, antimicrobial resistance, and molecular characterization of Campylobacter jejuni and C. coli isolated from retail raw meat in Poland
inferredcites →https://doi.org/10.2105/ajph.76.4.424openalex-snapshot
Epidemic campylobacteriosis associated with a community water supply.
inferredcites →https://doi.org/10.2307/1591142openalex-snapshot
Prevalence of Campylobacter jejuni in Selected Domestic and Wild Birds in Louisiana
inferredcites →https://doi.org/10.2478/pjvs-2013-0016openalex-snapshot
Prevalence of Campylobacter jejuni and Campylobacter coli species in cats and dogs from Bydgoszcz (Poland) region
inferredcites →https://doi.org/10.2754/avb201180010019openalex-snapshot
Molecular characterization of Campylobacter spp. isolated from poultry faeces and carcasses in Poland
inferredcites →https://doi.org/10.2903/j.efsa.2011.2105openalex-snapshot
Scientific Opinion on Campylobacter in broiler meat production: control options and performance objectives and/or targets at different stages of the food chain
inferredcites →https://doi.org/10.2903/j.efsa.2013.3129openalex-snapshot
The European Union Summary Report on Trends and Sources of Zoonoses, Zoonotic Agents and Food‐borne Outbreaks in 2011
inferredcites →https://doi.org/10.2903/j.efsa.2013.3196openalex-snapshot
The European Union Summary Report on antimicrobial resistance in zoonotic and indicator bacteria from humans, animals and food in 2011
inferredcites →https://doi.org/10.3389/fmicb.2011.00200openalex-snapshot
Campylobacter spp. as a Foodborne Pathogen: A Review
inferredcites →https://doi.org/10.4315/0362-028x-71.3.602openalex-snapshot
Comparison of Antimicrobial Resistance of Campylobacter jejuni and Campylobacter coli Isolated from Humans and Chicken Carcasses in Poland
inferredcites →https://doi.org/10.7589/0090-3558-47.3.750openalex-snapshot
Prevalence of Campylobacter in Wild Birds of the Mid-Atlantic Region, USA
inferredcites →https://doi.org/10.7589/2011-10-287openalex-snapshot
CHARACTERIZATION OF CAMPYLOBACTER FROM RESIDENT CANADA GEESE IN AN URBAN ENVIRONMENT

What points at this work

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

inferred← citeshttps://doi.org/10.3897/oneeco.11.e200352zenodo-depositor-declared
The influence of landfill foraging: enteric helminths and bacteria in a population of White Stork (Ciconia ciconia) from central Spain
inferred← citeshttps://doi.org/10.1007/s10393-021-01540-0openalex-snapshot
Prevalence and Antibiotic Resistance of Campylobacter spp. in Urban and Rural Black-Headed Gulls Chroicocephalus ridibundus
inferred← citeshttps://doi.org/10.1007/s11356-019-07502-yopenalex-snapshot
Campylobacter in wintering great tits Parus major in Poland
inferred← citeshttps://doi.org/10.1016/j.foodcont.2016.04.051openalex-snapshot
Prevalence, antimicrobial resistance profiling and genetic diversity of Campylobacter jejuni and Campylobacter coli isolated from broilers at slaughter in China
inferred← citeshttps://doi.org/10.1016/j.foodcont.2019.04.038openalex-snapshot
Prevalence, antimicrobial resistance profiles and virulence-associated genes of thermophilic Campylobacter spp. isolated from ducks in a Chinese slaughterhouse
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2020.108641openalex-snapshot
Prevalence, genotypic diversity and detection of virulence genes in thermotolerant Campylobacter at different stages of the poultry meat supply chain
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.146872openalex-snapshot
Faecal microbiota and antibiotic resistance genes in migratory waterbirds with contrasting habitat use
inferred← citeshttps://doi.org/10.1021/acs.est.5c13743openalex-snapshot
Landfills as Hotspots of Multidrug Resistance Genes: Profiles, Drivers, and Hosts
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/cz/zoaa062openalex-snapshot
Not so black, not so white: differences in microorganism load of contiguous feathers from white stork chicks
inferred← citeshttps://doi.org/10.1128/spectrum.00990-25openalex-snapshot
Reassessing the role of wild birds in the spread of antibiotic resistance: the white stork as a model species in studying populations from Central European river valley
inferred← citeshttps://doi.org/10.1186/s12866-017-0991-9openalex-snapshot
Prevalence and antimicrobial resistance of Campylobacter jejuni and Campylobacter coli isolated from children and environmental sources in urban and suburban areas
inferred← citeshttps://doi.org/10.1292/jvms.22-0560openalex-snapshot
Anthropogenic threats to the reintroduced population of Oriental storks in Japan: analysis of the causes of injury and death of 153 storks from 2005 to 2021
inferred← citeshttps://doi.org/10.1371/journal.pone.0214705openalex-snapshot
Microbial metabolite deoxycholic acid shapes microbiota against Campylobacter jejuni chicken colonization
inferred← citeshttps://doi.org/10.15547/bjvm.2022-0073openalex-snapshot
Global systematic review and meta-analysis on foodborne thermotolerant Campylobacter prevalence in different species of poultry birds and associated sources of contamination
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1630008openalex-snapshot
Transcriptome-wide N6-methyladenosinem modifications analysis of chicken cecum in responding to Campylobacter jejuni inoculation
inferred← citeshttps://doi.org/10.3389/fmicb.2018.03186openalex-snapshot
Antimicrobial Susceptibility and Virulence Surveillance of Campylobacter spp. Isolated From Patients in Two Tertiary Medical Centers in Taiwan
inferred← citeshttps://doi.org/10.3389/fmicb.2020.01397openalex-snapshot
Foraging at Solid Urban Waste Disposal Sites as Risk Factor for Cephalosporin and Colistin Resistant Escherichia coli Carriage in White Storks (Ciconia ciconia)
inferred← citeshttps://doi.org/10.3390/ani13081334openalex-snapshot
A Systematic Review on the Role of Wildlife as Carriers and Spreaders of Campylobacter spp.
inferred← citeshttps://doi.org/10.3390/antibiotics12030520openalex-snapshot
Domestic Waste and Wastewaters as Potential Sources of Pharmaceuticals in Nestling White Storks (Ciconia ciconia)
inferred← citeshttps://doi.org/10.3390/pathogens10111387openalex-snapshot
Microbiota from Specific Pathogen-Free Mice Reduces Campylobacter jejuni Chicken Colonization
inferred← citeshttps://doi.org/10.3390/vetsci11050210openalex-snapshot
Exploring the Prevalence and Resistance of Campylobacter in Urban Bird Populations
inferred← citeshttps://doi.org/10.59463/rjvs.2026.1.09openalex-snapshot
White Storks (Ciconia ciconia) as Indicators of Environmental Antimicrobial Resistance: A Review of Microbiological Insights
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