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Arcobacter, what is known and unknown about a potential foodborne zoonotic agent!
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/mcpr.2000.0290openalex-snapshot
Multiplex PCR detection of Campylobacter jejuni and Arcobacter butzleri in food products
inferredcites →https://doi.org/10.1007/s00248-002-1063-7openalex-snapshot
Bacterial 16S rRNA Gene Analysis Revealed That Bacteria Related to Arcobacter spp. Constitute an Abundant and Common Component of the Oyster Microbiota (Tiostrea chilensis)
inferredcites →https://doi.org/10.1016/0378-1097(96)84202-9openalex-snapshot
Immunochemical characterization of a haemagglutinating antigen of Arcobacter spp.
inferredcites →https://doi.org/10.1016/j.resmic.2004.04.011openalex-snapshot
Occurrence and strain diversity of Arcobacter species isolated from healthy Belgian pigs
inferredcites →https://doi.org/10.1016/j.resmic.2004.05.011openalex-snapshot
Survival and injury of Arcobacter after artificial inoculation into drinking water
inferredcites →https://doi.org/10.1016/j.vetmic.2004.11.002openalex-snapshot
Prevalence, enumeration and strain variation of Arcobacter species in the faeces of healthy cattle in Belgium
inferredcites →https://doi.org/10.1016/j.vetmic.2005.11.051openalex-snapshot
Potential routes of acquisition of Arcobacter species by piglets
inferredcites →https://doi.org/10.1016/j.watres.2004.03.004openalex-snapshot
The occurrence of campylobacters in water sources in South Africa
inferredcites →https://doi.org/10.1016/s0034-5288(18)32825-xopenalex-snapshot
Designation of aerotolerant Campylobacter-like organisms from porcine and bovine abortions to the genus Campylobacter
inferredcites →https://doi.org/10.1016/s0163-4453(95)80031-xopenalex-snapshot
Isolation of Arcobacter butzleri from a neonate with bacteraemia
inferredcites →https://doi.org/10.1016/s0168-1605(02)00163-0openalex-snapshot
The prevalence of Arcobacter spp. on chicken carcasses sold in retail markets in Turkey, and identification of the isolates using SDS-PAGE
inferredcites →https://doi.org/10.1016/s0168-1605(02)00197-6openalex-snapshot
One-step polymerase chain reaction-based typing of Arcobacter species
inferredcites →https://doi.org/10.1016/s0168-1605(03)00322-2openalex-snapshot
Prevalence of Arcobacter species in retail meats and antimicrobial susceptibility of the isolates in Japan
inferredcites →https://doi.org/10.1016/s0168-1605(03)00328-3openalex-snapshot
Isolation and characterisation of Arcobacter butzleri from meat
inferredcites →https://doi.org/10.1016/s0378-1097(00)00461-4openalex-snapshot
Development of a multiplex PCR assay for the simultaneous detection and identification of Arcobacter butzleri, Arcobacter cryaerophilus and Arcobacter skirrowii
inferredcites →https://doi.org/10.1016/s0378-1097(03)00840-1openalex-snapshot
Isolation ofArcobacterspecies from animal feces
inferredcites →https://doi.org/10.1016/s0378-1135(01)00503-xopenalex-snapshot
Prevalence and diversity of Arcobacter spp. isolated from the internal organs of spontaneous porcine abortions in Denmark
inferredcites →https://doi.org/10.1016/s0378-1135(02)00312-7openalex-snapshot
Distribution of Arcobacter species among livestock in Japan
inferredcites →https://doi.org/10.1016/s0378-1135(97)00106-5openalex-snapshot
Classification of Arcobacter species isolated from aborted pig fetuses and sows with reproductive problems in Brazil
inferredcites →https://doi.org/10.1016/s0378-1135(97)00151-xopenalex-snapshot
Multiplex PCR for the identification of Arcobacter and differentiation of Arcobacter butzleri from other arcobacters
inferredcites →https://doi.org/10.1016/s0732-8893(01)00261-9openalex-snapshot
Identification of Arcobacter cryaerophilus isolated from a traffic accident victim with bacteremia by 16S ribosomal RNA gene sequencing
inferredcites →https://doi.org/10.1016/s0740-0020(02)00172-7openalex-snapshot
Adherence of environmental Arcobacter butzleri and Vibrio spp. isolates to epithelial cells in vitro
inferredcites →https://doi.org/10.1016/s0924-8579(03)00004-9openalex-snapshot
In vitro susceptibility of Arcobacter butzleri and Arcobacter cryaerophilus to different antimicrobial agents
inferredcites →https://doi.org/10.1016/s0934-8859(99)80048-0openalex-snapshot
Occurrence, Removal and Seasonal Variation of Thermophilic Campylobacters and Arcobacter in Sewage Sludge
inferredcites →https://doi.org/10.1016/s0966-842x(96)10085-8openalex-snapshot
DNA gyrase as a drug target
inferredcites →https://doi.org/10.1046/j.1365-2672.1997.00277.xopenalex-snapshot
The prevalence of campylobacters and arcobacters in broiler chickens
inferredcites →https://doi.org/10.1046/j.1365-2672.1998.00437.xopenalex-snapshot
Diversity and prevalence of Arcobacter spp. in broiler chickens
inferredcites →https://doi.org/10.1046/j.1365-2672.1999.00483.xopenalex-snapshot
Isolation ofArcobacter butzlerifrom ground water
inferredcites →https://doi.org/10.1046/j.1365-2672.2003.02100.xopenalex-snapshot
Differentiation of Arcobacter species by numerical analysis of AFLP profiles and description of a novel Arcobacter from pig abortions and turkey faeces
inferredcites →https://doi.org/10.1046/j.1472-765x.2001.01025.xopenalex-snapshot
Susceptibility of Arcobacter butzleri isolates to 23 antimicrobial agents
inferredcites →https://doi.org/10.1086/514923openalex-snapshot
Bacterial Topoisomerases, Anti‐Topoisomerases, and Anti‐Topoisomerase Resistance
inferredcites →https://doi.org/10.1089/mdr.2004.10.243openalex-snapshot
Antimicrobial Susceptibility Patterns of Arcobacter butzleri and Arcobacter cryaerophilus Strains Isolated from Humans and Broilers
inferredcites →https://doi.org/10.1093/infdis/163.5.1062openalex-snapshot
Isolation of Group 2 Aerotolerant Campylobacter Species from Thai Children with Diarrhea
inferredcites →https://doi.org/10.1093/ps/78.4.536openalex-snapshot
Natural and experimental infections of Arcobacter in poultry
inferredcites →https://doi.org/10.1093/ps/82.12.1898openalex-snapshot
Comparison of sampling techniques for detection of Arcobacter butzleri from chickens
inferredcites →https://doi.org/10.1099/00207713-33-3-605openalex-snapshot
Campylobacter nitrofigilis sp. nov., a Nitrogen-Fixing Bacterium Associated with Roots of Spartina alterniflora Loisel
inferredcites →https://doi.org/10.1099/00207713-41-1-88openalex-snapshot
Revision of Campylobacter, Helicobacter, and Wolinella Taxonomy: Emendation of Generic Descriptions and Proposal of Arcobacter gen. nov.
inferredcites →https://doi.org/10.1099/00207713-41-3-451openalex-snapshot
Proposal for a New Family, Campylobacteraceae
inferredcites →https://doi.org/10.1099/00207713-42-3-344openalex-snapshot
Polyphasic Taxonomic Study of the Emended Genus Arcobacter with Arcobacter butzleri comb. nov. and Arcobacter skirrowii sp. nov., an Aerotolerant Bacterium Isolated from Veterinary Specimens
inferredcites →https://doi.org/10.1099/ijs.0.63103-0openalex-snapshot
Arcobacter cibarius sp. nov., isolated from broiler carcasses
inferredcites →https://doi.org/10.1099/ijs.0.63581-0openalex-snapshot
Arcobacter halophilus sp. nov., the first obligate halophile in the genus Arcobacter
inferredcites →https://doi.org/10.1111/j.1348-0421.2004.tb03548.xopenalex-snapshot
Isolation and Phylogenetic Analysis of Arcobacter Spp. in Ground Chicken Meat and Environmental Water in Japan and Thailand
inferredcites →https://doi.org/10.1111/j.1472-765x.1996.tb00030.xopenalex-snapshot
A selective medium for the isolation of Arcobacter from meats
inferredcites →https://doi.org/10.1111/j.1472-765x.2004.01494.xopenalex-snapshot
Investigation of arcobacters in meat and faecal samples of clinically healthy cattle in Turkey
inferredcites →https://doi.org/10.1128/9781555815554.ch1openalex-snapshot
Taxonomy of the Family Campylobacteraceae
inferredcites →https://doi.org/10.1128/aem.66.5.1994-2000.2000openalex-snapshot
Fecal Shedding ofCampylobacterandArcobacterspp. in Dairy Cattle
inferredcites →https://doi.org/10.1128/aem.69.2.1181-1186.2003openalex-snapshot
Specific Detection of Arcobacter and Campylobacter Strains in Water and Sewage by PCR and Fluorescent In Situ Hybridization
inferredcites →https://doi.org/10.1128/aem.70.3.1271-1276.2004openalex-snapshot
Detection of Arcobacter spp. in the Coastal Environment of the Mediterranean Sea
inferredcites →https://doi.org/10.1128/iai.61.5.2220-2223.1993openalex-snapshot
Arcobacter (Campylobacter) butzleri-associated diarrheal illness in a nonhuman primate population
inferredcites →https://doi.org/10.1128/iai.64.6.2295-2299.1996openalex-snapshot
Infection of cesarean-derived colostrum-deprived 1-day-old piglets with Arcobacter butzleri, Arcobacter cryaerophilus, and Arcobacter skirrowii
inferredcites →https://doi.org/10.1128/jcm.26.12.2469-2473.1988openalex-snapshot
Campylobacter cryaerophila isolated from a human
inferredcites →https://doi.org/10.1128/jcm.30.9.2335-2337.1992openalex-snapshot
Outbreak of recurrent abdominal cramps associated with Arcobacter butzleri in an Italian school
inferredcites →https://doi.org/10.1128/jcm.35.2.489-491.1997openalex-snapshot
Bacteremia caused by Arcobacter cryaerophilus 1B
inferredcites →https://doi.org/10.1128/jcm.39.4.1654-1656.2001openalex-snapshot
Susceptibility of Arcobacter butzleri, Arcobacter cryaerophilus , and Arcobacter skirrowii to Antimicrobial Agents Used in Selective Media
inferredcites →https://doi.org/10.1128/jcm.42.4.1851-1852.2004openalex-snapshot
Isolation of Arcobacter skirrowii from a Patient with Chronic Diarrhea
inferredcites →https://doi.org/10.1136/mp.55.3.182openalex-snapshot
Identification by 16S ribosomal RNA gene sequencing of Arcobacter butzleri bacteraemia in a patient with acute gangrenous appendicitis
inferredcites →https://doi.org/10.1136/vr.100.21.451openalex-snapshot
Isolation of Spirillum/Vibrio-like organisms from bovine fetuses
inferredcites →https://doi.org/10.1136/vr.102.5.106-aopenalex-snapshot
Isolation of spirillum-like organisms from pig fetuses
inferredcites →https://doi.org/10.1136/vr.110.10.229openalex-snapshot
Mastitis in dairy cows associated with an aerotolerant campylobacter
inferredcites →https://doi.org/10.1177/104063879600800208openalex-snapshot
Phenotypic and Ribosomal RNA Characterization of Arcobacter Species Isolated from Porcine Aborted Fetuses
inferredcites →https://doi.org/10.1177/104063879901100513openalex-snapshot
Arcobacter Cryaerophilus and Arcobacter Butzleri Isolated from Preputial Fluid of Boars and Fattening Pigs in Brazil
inferredcites →https://doi.org/10.1258/002367799780578499openalex-snapshot
Arcobacter butzleri isolated from a diarrhoeic non-human primate
inferredcites →https://doi.org/10.1590/s0074-02761995000500018openalex-snapshot
Toxigenic and invasive capacities: possible pathogenic mechanisms in Arcobacter cryaerophilus
inferredcites →https://doi.org/10.3201/eid1202.050570openalex-snapshot
Arcobacter butzleri: Underestimated Enteropathogen
inferredcites →https://doi.org/10.4315/0362-028x-64.5.645openalex-snapshot
Genotypic Variation among Arcobacter Isolates from a Farrow-to-Finish Swine Facility
inferredcites →https://doi.org/10.4315/0362-028x-65.11.1789openalex-snapshot
Arcobacter Isolates from Various Sources
inferredcites →https://doi.org/10.4315/0362-028x-65.12.1849openalex-snapshot
Determination of the Occurrence of Arcobacter butzleri in Beef and Dairy Cattle from Texas by Various Isolation Methods
inferredcites →https://doi.org/10.4315/0362-028x-65.8.1233openalex-snapshot
Occurrence and Distribution of Arcobacter Species in Poultry Processing
inferredcites →https://doi.org/10.4315/0362-028x-65.8.1240openalex-snapshot
Attachment of Arcobacter butzleri, a New Waterborne Pathogen, to Water Distribution Pipe Surfaces
inferredcites →https://doi.org/10.4315/0362-028x-66.3.364openalex-snapshot
Molecular Characterization of Arcobacter Isolates Collected in a Poultry Slaughterhouse
inferredcites →https://doi.org/10.4315/0362-028x-66.8.1374openalex-snapshot
Isolation of Arcobacter spp. from Retail Meats and Cytotoxic Effects of Isolates against Vero Cells
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4001256openalex-extracted
Arcobacter Butzleri in an AIDS Patient: A Case Report
inferred← citeshttps://doi.org/10.2139/ssrn.4750685openalex-extracted
Impacts of Nanopolystyrene and/or Phoxim Exposure on the Intestinal Histopathology, Intestinal Microbiota, and Metabolome in Eriocheir Sinensis
inferred← citeshttps://doi.org/10.1002/2052-2975.35openalex-snapshot
A severe case of persistent diarrhoea associated with Arcobacter cryaerophilus but attributed to Campylobacter sp. and a review of the clinical incidence of Arcobacter spp
inferred← citeshttps://doi.org/10.1002/9781118308035.ch44openalex-snapshot
Emerging Bacterial Food‐Borne Pathogens and Methods of Detection
inferred← citeshttps://doi.org/10.1002/9781119139188.ch4openalex-snapshot
Arcobacter spp. in Food Chain—From Culture to Omics
inferred← citeshttps://doi.org/10.1002/jsfa.6401openalex-snapshot
Genus‐specific PCR assay for screening Arcobacter spp. in chicken meat
inferred← citeshttps://doi.org/10.1002/mbo3.1106openalex-snapshot
Detection of Arcobacter species in different intestinal compartments of broiler chicken during slaughter and processing
inferred← citeshttps://doi.org/10.1002/mbo3.890openalex-snapshot
Diversity, enumeration, and isolation of Arcobacter spp. in the giant abalone, Haliotis gigantea
inferred← citeshttps://doi.org/10.1002/vms3.800openalex-snapshot
Genotyping, antibiotic resistance and prevalence of Arcobacter species in milk and dairy products
inferred← citeshttps://doi.org/10.1007/978-3-319-29907-5_11openalex-snapshot
Non-jejuni/coli Campylobacter Species and Related Organisms in Poultry, and Their Relevance in Human and Animal Disease
inferred← citeshttps://doi.org/10.1007/978-3-642-39044-9_274openalex-snapshot
The Family Campylobacteraceae
inferred← citeshttps://doi.org/10.1007/s00248-015-0583-xopenalex-snapshot
Antibiotics, Antibiotic Resistance Genes, and Bacterial Community Composition in Fresh Water Aquaculture Environment in China
inferred← citeshttps://doi.org/10.1007/s00284-015-0883-xopenalex-snapshot
Isolation and Identification of Arcobacter spp. by Multiplex PCR from Water Sources in Kars Region
inferred← citeshttps://doi.org/10.1007/s00343-022-1431-8openalex-snapshot
Spatial-temporal dynamics of bacterioplankton communities in the breeding area of large yellow croaker Larimichthys crocea in Sansha Bay, China
inferred← citeshttps://doi.org/10.1007/s00580-014-1981-zopenalex-snapshot
Distribution of Salmonella, Arcobacter, and thermophilic Campylobacter spp. among Persian fallow deer (Dama mesopotamica) population in Dasht-e-Arzhan Wildlife refuge, southern Iran
inferred← citeshttps://doi.org/10.1007/s10482-007-9153-7openalex-snapshot
Prevalence of Arcobacter species in market-weight commercial turkeys
inferred← citeshttps://doi.org/10.1007/s11250-017-1262-3openalex-snapshot
Arcobacter spp. in fecal samples from Brazilian farmed caimans (Caiman yacare, Daudin 1802)
inferred← citeshttps://doi.org/10.1007/s11356-015-5786-7openalex-snapshot
Bacterial community composition of an urban river in the North West Province, South Africa, in relation to physico-chemical water quality
inferred← citeshttps://doi.org/10.1007/s12161-011-9343-9openalex-snapshot
Current Status on Arcobacter Research: An Update on DNA-Based Identification and Typing Methodologies
inferred← citeshttps://doi.org/10.1007/s12223-015-0395-xopenalex-snapshot
Modified isolation method of Arcobacter spp. from different environmental and food samples
inferred← citeshttps://doi.org/10.1007/s12223-016-0460-0openalex-snapshot
Isolation and identification of Arcobacter species from environmental and drinking water samples
inferred← citeshttps://doi.org/10.1007/s13213-015-1092-3openalex-snapshot
Incidence of Arcobacter spp. in fresh seafood from retail markets in Mumbai, India
inferred← citeshttps://doi.org/10.1007/s40009-016-0484-7openalex-snapshot
Characterization of Arcobacter butzleri Cryptic Plasmid pDWAN from Human Isolate
inferred← citeshttps://doi.org/10.1016/b978-0-12-374186-8.00007-0openalex-snapshot
Produce Contamination by Other Wildlife
inferred← citeshttps://doi.org/10.1016/b978-0-12-378612-8.00083-4openalex-snapshot
Bacteria: Arcobacter
inferred← citeshttps://doi.org/10.1016/b978-0-12-384731-7.00047-7openalex-snapshot
MICROBIOLOGICAL SAFETY OF MEAT | Emerging Pathogens
inferred← citeshttps://doi.org/10.1016/b978-0-12-404611-5.00008-7openalex-snapshot
Produce Contamination by Other Wildlife
inferred← citeshttps://doi.org/10.1016/b978-0-12-800245-2.00012-5openalex-snapshot
Arcobacter Species
inferred← citeshttps://doi.org/10.1016/b978-0-444-52512-3.00049-8openalex-snapshot
Food Safety: Emerging Pathogens
inferred← citeshttps://doi.org/10.1016/bs.afnr.2016.12.009openalex-snapshot
Pathogens of Food Animals
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2011.05.028openalex-snapshot
Characterization of a biofilm bacterium from a recirculation system for European lobster (Homarus gammarus)
inferred← citeshttps://doi.org/10.1016/j.aquatox.2024.107168openalex-snapshot
Impacts of nanopolystyrene and/or phoxim exposure at environmentally relevant concentrations on the intestinal histopathology, intestinal microbiota, and metabolome in Eriocheir sinensis
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2010.06.011openalex-snapshot
Characterization of an anaerobic population digesting a model substrate for maize in the presence of trace metals
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.125105openalex-snapshot
Effects of cadmium on intestinal histology and microbiota in freshwater crayfish (Procambarus clarkii)
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.128130openalex-snapshot
Effescts of acute diclofenac exposure on intestinal histology, antioxidant defense, and microbiota in freshwater crayfish (Procambarus clarkii)
inferred← citeshttps://doi.org/10.1016/j.cimid.2015.12.002openalex-snapshot
Occurrence and antimicrobial resistance of emergent Arcobacter spp. isolated from cattle and sheep in Iran
inferred← citeshttps://doi.org/10.1016/j.diagmicrobio.2007.09.019openalex-snapshot
A new 16S rDNA-RFLP method for the discrimination of the accepted species of Arcobacter
inferred← citeshttps://doi.org/10.1016/j.envpol.2021.116639openalex-snapshot
Characteristics of bacterial community structure and function associated with nutrients and heavy metals in coastal aquaculture area
inferred← citeshttps://doi.org/10.1016/j.fm.2013.02.001openalex-snapshot
Heat stress adaptation induces cross-protection against lethal acid stress conditions in Arcobacter butzleri but not in Campylobacter jejuni
inferred← citeshttps://doi.org/10.1016/j.fm.2013.09.005openalex-snapshot
A microbial spoilage profile of half shell Pacific oysters (Crassostrea gigas) and Sydney rock oysters (Saccostrea glomerata)
inferred← citeshttps://doi.org/10.1016/j.fm.2015.07.015openalex-snapshot
Prevalence of ten putative virulence genes in the emerging foodborne pathogen Arcobacter isolated from food products
inferred← citeshttps://doi.org/10.1016/j.fm.2018.09.008openalex-snapshot
Prevalence of pathogenic Arcobacter species in South Korea: Comparison of two protocols for isolating the bacteria from foods and examination of nine putative virulence genes
inferred← citeshttps://doi.org/10.1016/j.fm.2019.103403openalex-snapshot
Large genetic diversity of Arcobacter butzleri isolated from raw milk in Southern Italy
inferred← citeshttps://doi.org/10.1016/j.foodcont.2010.11.004openalex-snapshot
Prevalence of Arcobacter spp. on chicken meat at retail markets and in farm chickens in Selangor, Malaysia
inferred← citeshttps://doi.org/10.1016/j.foodcont.2021.108100openalex-snapshot
Detection of Arcobacter spp. in environmental and food samples collected in industrial and artisanal sheep's milk cheese-making plants
inferred← citeshttps://doi.org/10.1016/j.foodcont.2021.108139openalex-snapshot
Prevalence and pathogenic potential of Arcobacter spp. isolated from edible bivalve molluscs in Sardinia
inferred← citeshttps://doi.org/10.1016/j.foodcont.2021.108177openalex-snapshot
Prevalence of Arcobacter: From farm to retail – A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.fsi.2018.09.076openalex-snapshot
White spot syndrome virus (WSSV) infection impacts intestinal microbiota composition and function in Litopenaeus vannamei
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2009.02.017openalex-snapshot
Growth and survival at chiller temperatures of Arcobacter butzleri
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2010.11.018openalex-snapshot
Study of Arcobacter spp. contamination in fresh lettuces detected by different cultural and molecular methods
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2013.01.003openalex-snapshot
Genetic diversity, antibiotic resistance and biofilm-forming ability of Arcobacter butzleri isolated from poultry and environment from a Portuguese slaughterhouse
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2014.07.006openalex-snapshot
Prevalence and antimicrobial susceptibility of Arcobacter species in cow milk, water buffalo milk and fresh village cheese
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2014.08.030openalex-snapshot
Co-occurrence of free-living protozoa and foodborne pathogens on dishcloths: Implications for food safety
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2014.09.012openalex-snapshot
Multilocus sequence typing reveals genetic diversity of foodborne Arcobacter butzleri isolates in the North of Spain
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2016.05.018openalex-snapshot
Isolation and characterization of Arcobacter spp. from fresh seafood and the aquatic environment
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2017.01.006openalex-snapshot
Occurrence of Arcobacter spp. and correlation with the bacterial indicator of faecal contamination Escherichia coli in bivalve molluscs from the Central Adriatic, Italy
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2017.10.005openalex-snapshot
Virulence genotypes and antimicrobial susceptibility patterns of Arcobacter butzleri isolated from seafood and its environment
inferred← citeshttps://doi.org/10.1016/j.jare.2019.05.004openalex-snapshot
Vetiver and Dictyosphaerium sp. co-culture for the removal of nutrients and ecological inactivation of pathogens in swine wastewater
inferred← citeshttps://doi.org/10.1016/j.jclepro.2023.136480openalex-snapshot
Novel iron-carbon micro-electrolysis-anoxic/oxic biofilter system for enhanced treatment of tetracycline wastewater: Significant reduction of antibiotic-resistant and pathogenic bacteria
inferred← citeshttps://doi.org/10.1016/j.jenvman.2019.109992openalex-snapshot
Development of efficient electroactive biofilm in urine-fed microbial fuel cell cascades for bioelectricity generation
inferred← citeshttps://doi.org/10.1016/j.jgar.2017.01.006openalex-snapshot
Susceptibility to 18 drugs and multidrug resistance of Arcobacter isolates from different sources within the Czech Republic
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.131761openalex-snapshot
Persistence of antibiotic resistance from animal agricultural effluents to surface water revealed by genome-centric metagenomics
inferred← citeshttps://doi.org/10.1016/j.lwt.2017.03.052openalex-snapshot
The prevalence of major foodborne pathogens in ready-to-eat chicken meat samples sold in retail markets in Turkey and the molecular characterization of the recovered isolates
inferred← citeshttps://doi.org/10.1016/j.marenvres.2020.104979openalex-snapshot
Effects of holding time on the diversity and composition of potential pathogenic bacteria in ship ballast water
inferred← citeshttps://doi.org/10.1016/j.micpath.2013.10.003openalex-snapshot
Occurrence of six virulence-associated genes in Arcobacter species isolated from various sources in Shiraz, Southern Iran
inferred← citeshttps://doi.org/10.1016/j.micpath.2020.104649openalex-snapshot
Resistance rate and novel virulence factor determinants of Arcobacter spp., from cattle fresh meat products from Iraq
inferred← citeshttps://doi.org/10.1016/j.micpath.2024.106810openalex-snapshot
Investigation of Aliarcobacter spp. and Campylobacter spp. in uterine contents of cows: Antibacterial susceptibility and phylogenetic analysis of the isolates
inferred← citeshttps://doi.org/10.1016/j.mimet.2010.01.009openalex-snapshot
Identification of five human and mammal associated Arcobacter species by a novel multiplex-PCR assay
inferred← citeshttps://doi.org/10.1016/j.mimet.2015.12.017openalex-snapshot
Development and evaluation of multiplex PCR assays for rapid detection of virulence-associated genes in Arcobacter species
inferred← citeshttps://doi.org/10.1016/j.psj.2021.101157openalex-snapshot
Mapping foodborne pathogen contamination throughout the conventional and alternative poultry supply chains
inferred← citeshttps://doi.org/10.1016/j.rineng.2023.101623openalex-snapshot
Characterization of biofilm bacterial communities in rural drainage system ancillary facilities
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.05.105openalex-snapshot
Next-generation sequencing identification of pathogenic bacterial genes and their relationship with fecal indicator bacteria in different water sources in the Kathmandu Valley, Nepal
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.12.178openalex-snapshot
Do the Escherichia coli European Union shellfish safety standards predict the presence of Arcobacter spp., a potential zoonotic pathogen?
inferred← citeshttps://doi.org/10.1016/j.smallrumres.2011.02.004openalex-snapshot
Small ruminants as carriers of the emerging foodborne pathogen Arcobacter on small and medium farms
inferred← citeshttps://doi.org/10.1016/j.syapm.2010.10.001openalex-snapshot
Arcobacter molluscorum sp. nov., a new species isolated from shellfish
inferred← citeshttps://doi.org/10.1016/j.syapm.2011.04.004openalex-snapshot
Arcobacter ellisii sp. nov., isolated from mussels
inferred← citeshttps://doi.org/10.1016/j.syapm.2012.01.002openalex-snapshot
Arcobacter bivalviorum sp. nov. and Arcobacter venerupis sp. nov., new species isolated from shellfish
inferred← citeshttps://doi.org/10.1016/j.syapm.2013.02.003openalex-snapshot
Occurrence and genetic diversity of Arcobacter spp. in a spinach-processing plant and evaluation of two Arcobacter-specific quantitative PCR assays
inferred← citeshttps://doi.org/10.1016/j.syapm.2015.12.002openalex-snapshot
Identification, characterization and description of Arcobacter faecis sp. nov., isolated from a human waste septic tank
inferred← citeshttps://doi.org/10.1016/j.syapm.2020.126091openalex-snapshot
Aliarcobacter vitoriensis sp. nov., isolated from carrot and urban wastewater
inferred← citeshttps://doi.org/10.1016/j.tifs.2011.01.010openalex-snapshot
Arcobacter – An emerging threat to animals and animal origin food products?
inferred← citeshttps://doi.org/10.1016/j.vetmic.2012.05.037openalex-snapshot
Genetic characterization of Arcobacter isolates from various sources
inferred← citeshttps://doi.org/10.1016/j.vetmic.2016.04.016openalex-snapshot
The first experimental research on the pathogenicity of Arcobacter butzleri in zebrafish
inferred← citeshttps://doi.org/10.1016/j.watres.2010.04.002openalex-snapshot
Occurrence and diversity of Arcobacter spp. along the Llobregat River catchment, at sewage effluents and in a drinking water treatment plant
inferred← citeshttps://doi.org/10.1016/j.watres.2010.06.030openalex-snapshot
Molecular detection of pathogens in water – The pros and cons of molecular techniques
inferred← citeshttps://doi.org/10.1017/s095026881300160xopenalex-snapshot
Temporal and farm-management-associated variation in faecal pat prevalence ofArcobacterspp. in ruminants
inferred← citeshttps://doi.org/10.1021/acs.est.2c02312openalex-snapshot
Bacterial and Chemical Evidence of Coastal Water Pollution from the Tijuana River in Sea Spray Aerosol
inferred← citeshttps://doi.org/10.1038/s41598-020-71442-8openalex-snapshot
Improved culture enrichment broth for isolation of Arcobacter-like species from the marine environment
inferred← citeshttps://doi.org/10.1038/srep41395openalex-snapshot
Microbial shifts in the porcine distal gut in response to diets supplemented with Enterococcus Faecalis as alternatives to antibiotics
inferred← citeshttps://doi.org/10.1080/00071668.2013.878783openalex-snapshot
Prevalence and antimicrobial resistance ofArcobacterspecies isolated from poultry meat in Iran
inferred← citeshttps://doi.org/10.1080/00071668.2014.971223openalex-snapshot
Occurrence ofArcobacterin Iranian poultry and slaughterhouse samples implicates contamination by processing equipment and procedures
inferred← citeshttps://doi.org/10.1080/01652176.2017.1323355openalex-snapshot
Arcobacter : an emerging food-borne zoonotic pathogen, its public health concerns and advances in diagnosis and control – a comprehensive review
inferred← citeshttps://doi.org/10.1089/fpd.2006.0077openalex-snapshot
Prevalence of Foodborne Microorganisms in Retail Foods in Thailand
inferred← citeshttps://doi.org/10.1089/fpd.2009.0368openalex-snapshot
Rapid and Accurate Detection of Arcobacter Contamination in Commercial Chicken Products and Wastewater Samples by Real-Time Polymerase Chain Reaction
inferred← citeshttps://doi.org/10.1089/fpd.2012.1184openalex-snapshot
Spatial Distribution of the Emerging Foodborne Pathogen Arcobacter in the Gastrointestinal Tract of Pigs
inferred← citeshttps://doi.org/10.1089/fpd.2012.1307openalex-snapshot
An Outbreak of Foodborne Illness Among Attendees of a Wedding Reception in Wisconsin Likely Caused by Arcobacter butzleri
inferred← citeshttps://doi.org/10.1089/fpd.2013.1485openalex-snapshot
Survival of Arcobacter butzleri During Production and Storage of Artisan Water Buffalo Mozzarella Cheese
inferred← citeshttps://doi.org/10.1089/fpd.2013.1661openalex-snapshot
Towards a Typing Strategy for Arcobacter Species Isolated from Humans and Animals and Assessment of the In Vitro Genomic Stability
inferred← citeshttps://doi.org/10.1089/jmf.2010.0001openalex-snapshot
Inhibitory Effects of Some Plant Essential Oils Against Arcobacter butzleri and Potential for Rosemary Oil as a Natural Food Preservative
inferred← citeshttps://doi.org/10.1093/jambio/lxac037openalex-snapshot
Arcobacter species in milk contamination: a prevalence-based systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1099/ijs.0.000318openalex-snapshot
Arcobacter lanthieri sp. nov., isolated from pig and dairy cattle manure
inferred← citeshttps://doi.org/10.1099/ijs.0.003749-0openalex-snapshot
Arcobacter mytili sp. nov., an indoxyl acetate-hydrolysis-negative bacterium isolated from mussels
inferred← citeshttps://doi.org/10.1099/ijs.0.025668-0openalex-snapshot
Arcobacter defluvii sp. nov., isolated from sewage samples
inferred← citeshttps://doi.org/10.1099/ijsem.0.001809openalex-snapshot
Arcobacter lekithochrous sp. nov., isolated from a molluscan hatchery
inferred← citeshttps://doi.org/10.1101/2021.12.08.471852openalex-snapshot
Microbiome Analysis of Gut Bacterial Communities of Healthy and Diseased Malaysian Mahseer ( Tor tambroides )
inferred← citeshttps://doi.org/10.1109/icbbe.2010.5518027openalex-snapshot
Detection Analysis of Pathogenic Organisms in Municipal Sewage with PCR-Based 16S rDNA Technique
inferred← citeshttps://doi.org/10.1111/1462-2920.12553openalex-snapshot
Phage–bacteria network analysis and its implication for the understanding of coral disease
inferred← citeshttps://doi.org/10.1111/1462-2920.16025openalex-snapshot
Microbial community origin and fate through a rural wastewater treatment plant
inferred← citeshttps://doi.org/10.1111/1541-4337.12577openalex-snapshot
Arcobacter butzleri : Up‐to‐date taxonomy, ecology, and pathogenicity of an emerging pathogen
inferred← citeshttps://doi.org/10.1111/1750-3841.13997openalex-snapshot
Impact of Trans ‐Fats on Heat‐Shock Protein Expression and the Gut Microbiota Profile of Mice
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2009.04269.xopenalex-snapshot
Shedding ofCampylobacterspp. in Finnish cattle on dairy farms
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2009.04430.xopenalex-snapshot
Arcobacter contamination on pre- and post-chilled bovine carcasses and in minced beef at retail
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2007.01555.xopenalex-snapshot
Presence of Arcobacter spp. in environmental waters correlates with high levels of fecal pollution
inferred← citeshttps://doi.org/10.1111/j.1574-695x.2008.00405.xopenalex-snapshot
Arcobacterspp. possess two very short flagellins of which FlaA is essential for motility
inferred← citeshttps://doi.org/10.1111/j.1865-1682.2011.01221.xopenalex-snapshot
Prevalence of Arcobacter spp. in Humans, Animals and Foods of Animal Origin Including Sea Food from India
inferred← citeshttps://doi.org/10.1111/j.1865-1682.2012.01311.xopenalex-snapshot
Prevalence, Distribution and Antibiotic Resistance of EmergentArcobacterspp. from Clinically Healthy Cattle and Goats
inferred← citeshttps://doi.org/10.1111/jam.12977openalex-snapshot
Multilocus sequence typing of Arcobacter butzleri isolates collected from dairy plants and their products, and comparison with their PFGE types
inferred← citeshttps://doi.org/10.1111/jam.13597openalex-snapshot
Enhanced Single‐tube Multiplex PCR Assay for Detection and Identification of SixArcobacterSpecies
inferred← citeshttps://doi.org/10.1111/lam.13281openalex-snapshot
Occurrence, virulence gene and antimicrobial susceptibility profiles of Arcobacter sp . isolated from catla ( Catla catla ) in India
inferred← citeshttps://doi.org/10.1126/science.aal1956openalex-snapshot
Seagrass ecosystems reduce exposure to bacterial pathogens of humans, fishes, and invertebrates
inferred← citeshttps://doi.org/10.1128/9781555815554.ch7openalex-snapshot
Clinical Significance ofCampylobacterand Related Species Other ThanCampylobacter jejuniandCampylobacter coli
inferred← citeshttps://doi.org/10.1128/9781555816803.ch9openalex-snapshot
Arcobacter: an Opportunistic Human Food-Borne Pathogen?
inferred← citeshttps://doi.org/10.1128/aem.00181-18openalex-snapshot
Crown-of-Thorns Sea Star Acanthaster cf. solaris Has Tissue-Characteristic Microbiomes with Potential Roles in Health and Reproduction
inferred← citeshttps://doi.org/10.1128/aem.01073-13openalex-snapshot
Adherence to and Invasion of Human Intestinal Cells by Arcobacter Species and Their Virulence Genotypes
inferred← citeshttps://doi.org/10.1128/aem.01118-20openalex-snapshot
Search for Campylobacter spp. Reveals High Prevalence and Pronounced Genetic Diversity of Arcobacter butzleri in Floodwater Samples Associated with Hurricane Florence in North Carolina, USA
inferred← citeshttps://doi.org/10.1128/aem.02241-07openalex-snapshot
Survival of Gastric and Enterohepatic Helicobacter spp. in Water: Implications for Transmission
inferred← citeshttps://doi.org/10.1128/aem.02491-14openalex-snapshot
Arcobacter butzleri in Sheep Ricotta Cheese at Retail and Related Sources of Contamination in an Industrial Dairy Plant
inferred← citeshttps://doi.org/10.1128/aem.03014-13openalex-snapshot
Higher Water Temperature and Incubation under Aerobic and Microaerobic Conditions Increase the Recovery and Diversity of Arcobacter spp. from Shellfish
inferred← citeshttps://doi.org/10.1128/aem.08009-11openalex-snapshot
Arcobacter in Lake Erie Beach Waters: an Emerging Gastrointestinal Pathogen Linked with Human-Associated Fecal Contamination
inferred← citeshttps://doi.org/10.1128/cmr.00034-10openalex-snapshot
Taxonomy, Epidemiology, and Clinical Relevance of the Genus Arcobacter
inferred← citeshttps://doi.org/10.1128/genomea.01617-16openalex-snapshot
Complete Genome Sequence of Arcobacter sp. Strain LFT 1.7 Isolated from Great Scallop ( Pecten maximus ) Larvae
inferred← citeshttps://doi.org/10.1128/jcm.02883-13openalex-snapshot
Comparison of Conventional PCR, Multiplex PCR, and Loop-Mediated Isothermal Amplification Assays for Rapid Detection of Arcobacter Species
inferred← citeshttps://doi.org/10.1155/2015/956507openalex-snapshot
Genetic Diversity and Incidence of Virulence-Associated Genes ofArcobacter butzleriandArcobacter cryaerophilusIsolates from Pork, Beef, and Chicken Meat in Poland
inferred← citeshttps://doi.org/10.1155/2016/8132058openalex-snapshot
The Use of Two Culturing Methods in Parallel Reveals a High Prevalence and Diversity ofArcobacterspp. in a Wastewater Treatment Plant
inferred← citeshttps://doi.org/10.1155/2022/6983094openalex-snapshot
Arcobacter Butzleri in an AIDS Patient
inferred← citeshttps://doi.org/10.1186/1471-2180-9-196openalex-snapshot
First multi-locus sequence typing scheme for Arcobacter spp.
inferred← citeshttps://doi.org/10.1186/s12866-018-1357-7openalex-snapshot
Novel virulence, antibiotic resistance and toxin gene-specific PCR-based assays for rapid pathogenicity assessment of Arcobacter faecis and Arcobacter lanthieri
inferred← citeshttps://doi.org/10.1186/s12866-023-03119-xopenalex-snapshot
Pathogenicity assessment of Arcobacter butzleri isolated from Canadian agricultural surface water
inferred← citeshttps://doi.org/10.1264/jsme2.me18052openalex-snapshot
Development of a Quantitative PCR Assay for Arcobacter spp. and its Application to Environmental Water Samples
inferred← citeshttps://doi.org/10.12681/jhvms.27186openalex-snapshot
Antimicrobial susceptibility testing of Arcobacter butzleri and Arcobacter cryaerophilus isolated from buffalo milk with subclinical mastitis: A different approach
inferred← citeshttps://doi.org/10.13130/milesi-serena_phd2011-02-08openalex-snapshot
EMERGING PATHOGEN ARCOBACTER SPP. IN FOOD OF ANIMAL ORIGIN
inferred← citeshttps://doi.org/10.1371/journal.pone.0139402openalex-snapshot
Arcobacter butzleri Induce Colonic, Extra-Intestinal and Systemic Inflammatory Responses in Gnotobiotic IL-10 Deficient Mice in a Strain-Dependent Manner
inferred← citeshttps://doi.org/10.1371/journal.pone.0159685openalex-snapshot
The Immunopathogenic Potential of Arcobacter butzleri – Lessons from a Meta-Analysis of Murine Infection Studies
inferred← citeshttps://doi.org/10.1371/journal.pone.0180493openalex-snapshot
Characterization of the emerging zoonotic pathogen Arcobacter thereius by whole genome sequencing and comparative genomics
inferred← citeshttps://doi.org/10.1371/journal.pone.0278221openalex-snapshot
Identifying oral microbiome alterations in adult betel quid chewing population of Delhi, India
inferred← citeshttps://doi.org/10.1515/pjvs-2015-0008openalex-snapshot
Prevalence and antimicrobial resistance of Arcobacter butzleri and Arcobacter cryaerophilus isolates from retail meat in Lower Silesia region, Poland
inferred← citeshttps://doi.org/10.1533/9780857090508.4.465openalex-snapshot
Tracing pathogens in poultry and egg production and at the abattoir
inferred← citeshttps://doi.org/10.1556/1886.2015.00042openalex-snapshot
Toll-like receptor-4 dependent small intestinal immune responses following murine Arcobacter butzleri infection
inferred← citeshttps://doi.org/10.1556/1886.2016.00005openalex-snapshot
Intestinal expression of genes encoding inflammatory mediators and gelatinases during Arcobacter butzleri infection of gnotobiotic IL-10 deficient mice
inferred← citeshttps://doi.org/10.1556/1886.2016.00006openalex-snapshot
Toll-like receptor-4 dependent intestinal gene expression during Arcobacter butzleri infection of gnotobiotic IL-10 deficient mice
inferred← citeshttps://doi.org/10.15760/etd.3493openalex-snapshot
Uncovering Coxiella burnetii's Pathogenicity by Elucidating its Metabolism and Host Interactions
inferred← citeshttps://doi.org/10.1590/s1678-9946201658022openalex-snapshot
SURVIVAL CAPACITY OF Arcobacter butzleri INOCULATED IN POULTRY MEAT AT TWO DIFFERENT REFRIGERATION TEMPERATURES
inferred← citeshttps://doi.org/10.17169/refubium-17689openalex-snapshot
Prävalenz von Arcobacter spp. in Puten- und Schweinefleisch aus dem Berliner Einzelhandel und Vergleich von drei kulturellen Arcobacter-Nachweisverfahren
inferred← citeshttps://doi.org/10.17221/273/2015-vetmedopenalex-snapshot
Presence of Arcobacter species in pet cats and dogs in the Czech Republic
inferred← citeshttps://doi.org/10.17221/69/2016-vetmedopenalex-snapshot
Isolation and determination of antimicrobial resistance of Arcobacter species isolated from animal faeces in the Diyarbakir region of Turkey using the 16S rDNA-RFLP method
inferred← citeshttps://doi.org/10.20546/ijcmas.2019.812.237openalex-snapshot
Antibiotic Resistance of Arcobacter spp. Isolated from Sewage, Meat Shop and Fish Market Environment of Bareilly City
inferred← citeshttps://doi.org/10.21161/mjm.211329openalex-snapshot
Microbiome analysis of gut bacterial communities of healthy and diseased Malaysian mahseer (Tor tambroides) using 16S rRNA metagenomics approach
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1201703/v1openalex-snapshot
Persistence of Antibiotic Resistance from Agricultural Effluents to Surface Water Revealed in Metagenome Assembled Genomes
inferred← citeshttps://doi.org/10.21608/avmj.2015.170219openalex-snapshot
ARCOBACTER SPECIES AND THEIR RISKS IN SOME MEAT AND FISH WITH A SODIUM ACETATE AND SODIUM CHLORIDE INTERVENTION
inferred← citeshttps://doi.org/10.21608/scvmj.2013.78286openalex-snapshot
Isolation and Identification of Arcobacter species Recovered from Rabbits in Zagazig, Egypt
inferred← citeshttps://doi.org/10.22456/1679-9216.17066openalex-snapshot
Arcobacter butzleri strains isolated from different sources display adhesive capacity to epithelial cells in vitro
inferred← citeshttps://doi.org/10.2903/j.efsa.2014.3782openalex-snapshot
Scientific Opinion on the public health risks of table eggs due to deterioration and development of pathogens
inferred← citeshttps://doi.org/10.3109/1040841x.2014.954523openalex-snapshot
Insights in the pathogenesis and resistance ofArcobacter: A review
inferred← citeshttps://doi.org/10.3168/jds.2013-7682openalex-snapshot
Short communication: Occurrence of Arcobacter species in industrial dairy plants
inferred← citeshttps://doi.org/10.3201/eid2010.140433openalex-snapshot
Prevalence ofArcobacterSpecies among Humans, Belgium, 2008–2013
inferred← citeshttps://doi.org/10.3382/ps.2008-00092openalex-snapshot
The Presence of Arcobacter Species in Breeding Hens and Eggs from These Hens
inferred← citeshttps://doi.org/10.3382/ps/peu022openalex-snapshot
Development of an absorbance-based response model for monitoring the growth rates of Arcobacter butzleri as a function of temperature, pH, and NaCl concentration
inferred← citeshttps://doi.org/10.3389/fmicb.2019.01719openalex-snapshot
Regulation of Respiratory Pathways in Campylobacterota: A Review
inferred← citeshttps://doi.org/10.3389/fmicb.2020.01549openalex-snapshot
Genomic Analysis and Antimicrobial Resistance of Aliarcobacter cryaerophilus Strains From German Water Poultry
inferred← citeshttps://doi.org/10.3389/fmicb.2020.617685openalex-snapshot
Antimicrobial Resistance and in silico Virulence Profiling of Aliarcobacter butzleri Strains From German Water Poultry
inferred← citeshttps://doi.org/10.3389/fmicb.2021.765091openalex-snapshot
Bacterial Indicators Are Ubiquitous Members of Pelagic Microbiome in Anthropogenically Impacted Coastal Ecosystem
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1035904openalex-snapshot
Pathogenic bacteria significantly increased under oxygen depletion in coastal waters: A continuous observation in the central Bohai Sea
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1141043openalex-snapshot
A longitudinal study to examine the influence of farming practices and environmental factors on pathogen prevalence using structural equation modeling
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1278268openalex-snapshot
Genomic diversity and taxonomic marker for Arcobacter species
inferred← citeshttps://doi.org/10.3390/antibiotics13070669openalex-snapshot
Arcobacteraceae: An Exploration of Antibiotic Resistance Featuring the Latest Research Updates
inferred← citeshttps://doi.org/10.3390/antiox11101944openalex-snapshot
Mercury Induced Tissue Damage, Redox Metabolism, Ion Transport, Apoptosis, and Intestinal Microbiota Change in Red Swamp Crayfish (Procambarus clarkii): Application of Multi-Omics Analysis in Risk Assessment of Hg
inferred← citeshttps://doi.org/10.3390/genes11091104openalex-snapshot
Aliarcobacter butzleri from Water Poultry: Insights into Antimicrobial Resistance, Virulence and Heavy Metal Resistance
inferred← citeshttps://doi.org/10.3390/ijerph15040708openalex-snapshot
Abundances of Clinically Relevant Antibiotic Resistance Genes and Bacterial Community Diversity in the Weihe River, China
inferred← citeshttps://doi.org/10.3390/ijms241713561openalex-snapshot
Marine Bacterioplankton Community Dynamics and Potentially Pathogenic Bacteria in Seawater around Jeju Island, South Korea, via Metabarcoding
inferred← citeshttps://doi.org/10.3390/microorganisms11051313openalex-snapshot
Comparison of the Diagnostic Accuracy of Three Real-Time PCR Assays for the Detection of Arcobacter butzleri in Human Stool Samples Targeting Different Genes in a Test Comparison without a Reference Standard
inferred← citeshttps://doi.org/10.3390/microorganisms12050965openalex-snapshot
Bioaerosol Sampling Devices and Pretreatment for Bacterial Characterization: Theoretical Differences and a Field Experience in a Wastewater Treatment Plant
inferred← citeshttps://doi.org/10.3390/microorganisms13071495openalex-snapshot
Molecular and Genetic Characterization of Arcobacter Species Isolated from Chicken Feces and Chicken Giblets from Grenada, West Indies
inferred← citeshttps://doi.org/10.3390/pathogens10111391openalex-snapshot
The Persistence of Bacterial Pathogens in Surface Water and Its Impact on Global Food Safety
inferred← citeshttps://doi.org/10.3390/pathogens8030110openalex-snapshot
Identification of 16S rRNA and Virulence-Associated Genes of Arcobacter in Water Samples in the Kathmandu Valley, Nepal
inferred← citeshttps://doi.org/10.3390/w14081266openalex-snapshot
A Review on the Prevalence of Arcobacter in Aquatic Environments
inferred← citeshttps://doi.org/10.3390/w7051825openalex-snapshot
Impact of Rural Domestic Wastewater Irrigation on the Physicochemical and Microbiological Properties of Pakchoi and Soil
inferred← citeshttps://doi.org/10.36440/recmvz.v20i1.38112openalex-snapshot
Gênero Arcobacter e Saúde Pública: revisão sobre sua importância na saúde humana, principais vias de transmissão e patogenicidade
inferred← citeshttps://doi.org/10.37201/req/060.2019openalex-snapshot
Arcobacter butzleri and intestinal colonization
inferred← citeshttps://doi.org/10.3906/vet-1602-7openalex-snapshot
Occurrence of Arcobacter in dogs and cats in Selangor,Malaysia, and associated risk factors
inferred← citeshttps://doi.org/10.3923/ajava.2014.452.466openalex-snapshot
Prevalence of Arcobacter spp. in Humans, Animals and Foods of Animal Origin in India Based on Cultural Isolation, Antibiogram, PCR and Multiplex PCR Detection
inferred← citeshttps://doi.org/10.3923/pjbs.2013.1076.1085openalex-snapshot
Food-borne Pathogens of Animal Origin-Diagnosis, Prevention, Control and Their Zoonotic Significance: A Review
inferred← citeshttps://doi.org/10.4067/s0301-732x2016000100001openalex-snapshot
Interaction between zoonotic bacteria and free living amoebas: A new angle of an epidemiological polyhedron of public health importance?
inferred← citeshttps://doi.org/10.4081/ijfs.2011.1.13openalex-snapshot
PRESENCE OF ARCOBACTER SPP. IN IN-LINE MILK FILTERS: AN EMERGING AND SIGNIFICANT MICROBIOLOGICAL HAZARD IN FOOD
inferred← citeshttps://doi.org/10.4081/ijfs.2015.4583openalex-snapshot
Detection of Arcobacter spp. in Mytilus galloprovincialis samples collected from Apulia region
inferred← citeshttps://doi.org/10.4081/ijfs.2018.7171openalex-snapshot
Detection of Arcobacter spp. in food products collected from Sicilia region: A preliminary study
inferred← citeshttps://doi.org/10.4081/mr.2016.6578openalex-snapshot
Prevalence and diversity of Arcobacter spp. in retail chicken meat in Turkey
inferred← citeshttps://doi.org/10.4315/0362-028x-70.2.341openalex-snapshot
Direct Detection and Identification of Arcobacter Species by Multiplex PCR in Chicken and Wastewater Samples from Spain
inferred← citeshttps://doi.org/10.4315/0362-028x-71.4.719openalex-snapshot
Prevalence and Diversity of Arcobacter spp. in the Czech Republic
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