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Comparison of Escherichia coli isolates implicated in human urinary tract infection and avian colibacillosis

https://doi.org/10.1099/mic.0.27499-0
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What this work says

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

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Discriminant Analysis and Statistical Pattern Recognition
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Multivariate Statistical Methods
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Adhesins, Serum Resistance and Cytolysins of E. Coli- Genetic Structure and Role in Pathogenicity
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Cloning and DNA sequence of plasmid determinant iss, coding for increased serum survival and surface exclusion, which has homology with lambda DNA
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Bacterial pathogenesis: A molecular approach
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[10] Storing, shipping, and maintaining records on bacterial strains
inferredcites →https://doi.org/10.1016/b978-012677530-3/50291-9openalex-snapshot
Escherichia coli in Urinary Tract Infections
inferredcites →https://doi.org/10.1016/s0002-9343(02)01054-9openalex-snapshot
Epidemiology of urinary tract infections: incidence, morbidity, and economic costs
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Escherichia coli Infection in Poultry
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Pathogenicity islands of uropathogenic E. coli and the evolution of virulence
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Medical and economic impact of extraintestinal infections due to Escherichia coli: focus on an increasingly important endemic problem
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Direct transmission of Escherichia coli from poultry to humans
inferredcites →https://doi.org/10.1023/a:1022854902700openalex-snapshot
Resistance to Serum Complement, iss, and Virulence of Avian Escherichia coli
inferredcites →https://doi.org/10.1038/260040a0openalex-snapshot
Spread of antibiotic-resistant plasmids from chicken to chicken and from chicken to man
inferredcites →https://doi.org/10.1038/279778a0openalex-snapshot
Cloned fragments of the plasmid ColV,I-K94 specifying virulence and serum resistance
inferredcites →https://doi.org/10.1051/vetres:2004057openalex-snapshot
Characterizing the APEC pathotype
inferredcites →https://doi.org/10.1056/nejmoa011265openalex-snapshot
Widespread Distribution of Urinary Tract Infections Caused by a Multidrug-ResistantEscherichia coliClonal Group
inferredcites →https://doi.org/10.1073/pnas.0737682100openalex-snapshot
Salmochelins, siderophores of Salmonella enterica and uropathogenic Escherichia coli strains, are recognized by the outer membrane receptor IroN
inferredcites →https://doi.org/10.1073/pnas.74.11.5104openalex-snapshot
Cell--cell interactions in conjugating Escherichia coli: role of traT protein in surface exclusion.
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Cluster analysis and display of genome-wide expression patterns
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Virulence-associated genes in avian pathogenic (APEC) isolated from internal organs of poultry having died from colibacillosis
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Applied Discriminant Analysis
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Extended Virulence Genotypes of Escherichia coli Strains from Patients with Urosepsis in Relation to Phylogeny and Host Compromise
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Proposal for a New Inclusive Designation for Extraintestinal Pathogenic Isolates ofEscherichia coli:ExPEC
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High‐Pathogenicity Island ofYersinia pestisin Enterobacteriaceae Isolated from Blood Cultures and Urine Samples: Prevalence and Functional Expression
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Phylogenetic Distribution of Extraintestinal Virulence‐Associated Traits inEscherichia coli
inferredcites →https://doi.org/10.1086/342301openalex-snapshot
Concurrent Fecal Colonization with Extraintestinal PathogenicEscherichia coliin a Homosexual Man with Recurrent Urinary Tract Infection and in His Male Sex Partner
inferredcites →https://doi.org/10.1086/514007openalex-snapshot
Transmission of Uropathogens between Sex Partners
inferredcites →https://doi.org/10.1093/infdis/173.4.920openalex-snapshot
A Novel Multiply Primed Polymerase Chain Reaction Assay for Identification of Variant papG Genes Encoding the Gal( 1-4)Gal-Binding PapG Adhesins of Escherichia coli
inferredcites →https://doi.org/10.1093/jac/47.6.763openalex-snapshot
Antibiotic resistance of faecal Escherichia coli in poultry, poultry farmers and poultry slaughterers
inferredcites →https://doi.org/10.1093/jac/49.3.497openalex-snapshot
Antibiotic resistance of faecal enterococci in poultry, poultry farmers and poultry slaughterers
inferredcites →https://doi.org/10.1097/00010694-193902000-00006openalex-snapshot
Statistical Methods
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Virulence factors of uropathogens
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The Colonization of the Human Gut by Antibiotic Resistant Escherichia coli from Chickens
inferredcites →https://doi.org/10.1128/aac.47.7.2161-2168.2003openalex-snapshot
Isolation and Molecular Characterization of Nalidixic Acid-Resistant Extraintestinal Pathogenic Escherichia coli from Retail Chicken Products
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Rapid and Simple Determination of the Escherichia coli Phylogenetic Group
inferredcites →https://doi.org/10.1128/cmr.4.1.80openalex-snapshot
Virulence factors in Escherichia coli urinary tract infection
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Plasmid-determined resistance to serum bactericidal activity: a major outer membrane protein, the traT gene product, is responsible for plasmid-specified serum resistance in Escherichia coli
inferredcites →https://doi.org/10.1128/iai.35.2.654-659.1982openalex-snapshot
Further characterization of complement resistance conferred on Escherichia coli by the plasmid genes traT of R100 and iss of ColV,I-K94
inferredcites →https://doi.org/10.1128/iai.62.4.1369-1380.1994openalex-snapshot
Isolation and characterization of a gene involved in hemagglutination by an avian pathogenic Escherichia coli strain
inferredcites →https://doi.org/10.1128/iai.66.2.480-485.1998openalex-snapshot
Prevalence of the “High-Pathogenicity Island” of Yersinia Species among Escherichia coli Strains That Are Pathogenic to Humans
inferredcites →https://doi.org/10.1128/iai.67.10.5306-5314.1999openalex-snapshot
Identification of Genes in an Extraintestinal Isolate of Escherichia coli with Increased Expression after Exposure to Human Urine
inferredcites →https://doi.org/10.1128/iai.68.4.2096-2101.2000openalex-snapshot
Identification of Regions of the Escherichia coli Chromosome Specific for Neonatal Meningitis-Associated Strains
inferredcites →https://doi.org/10.1128/iai.68.6.3327-3336.2000openalex-snapshot
Evidence of Commonality between Canine and Human Extraintestinal PathogenicEscherichia coliStrains That ExpresspapGAllele III
inferredcites →https://doi.org/10.1128/iai.69.10.6209-6216.2001openalex-snapshot
Identification of a New Iron-Regulated Virulence Gene, ireA , in an Extraintestinal Pathogenic Isolate of Escherichia coli
inferredcites →https://doi.org/10.1128/iai.69.7.4248-4256.2001openalex-snapshot
S-Fimbria-Encoding Determinant sfa I Is Located on Pathogenicity Island III 536 of Uropathogenic Escherichia coli Strain 536
inferredcites →https://doi.org/10.1128/iai.70.11.6365-6372.2002openalex-snapshot
Genetic Structure and Distribution of Four Pathogenicity Islands (PAI I 536 to PAI IV 536 ) of Uropathogenic Escherichia coli Strain 536
inferredcites →https://doi.org/10.1128/iai.70.12.7156-7160.2002openalex-snapshot
IroN Functions as a Siderophore Receptor and Is a Urovirulence Factor in an Extraintestinal Pathogenic Isolate of Escherichia coli
inferredcites →https://doi.org/10.1128/iai.70.9.5335-5337.2002openalex-snapshot
Yersinia High-Pathogenicity Island Contributes to Virulence in Escherichia coli Causing Extraintestinal Infections
inferredcites →https://doi.org/10.1128/iai.71.4.1919-1928.2003openalex-snapshot
Contribution of the Shigella flexneri Sit, Iuc, and Feo Iron Acquisition Systems to Iron Acquisition In Vitro and in Cultured Cells
inferredcites →https://doi.org/10.1128/iai.71.6.3285-3293.2003openalex-snapshot
Characterization of an iroBCDEN Gene Cluster on a Transmissible Plasmid of Uropathogenic Escherichia coli : Evidence for Horizontal Transfer of a Chromosomal Virulence Factor
inferredcites →https://doi.org/10.1128/jb.165.2.570-578.1986openalex-snapshot
Aerobactin biosynthesis and transport genes of plasmid ColV-K30 in Escherichia coli K-12
inferredcites →https://doi.org/10.1128/jb.167.1.350-355.1986openalex-snapshot
Characterization of iucA and iucC genes of the aerobactin system of plasmid ColV-K30 in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.169.6.2466-2470.1987openalex-snapshot
Four plasmid genes are required for colicin V synthesis, export, and immunity
inferredcites →https://doi.org/10.1128/jb.172.2.648-652.1990openalex-snapshot
Colicin cleavage by OmpT protease during both entry into and release from Escherichia coli cells
inferredcites →https://doi.org/10.1128/jb.180.3.538-546.1998openalex-snapshot
The Yersiniabactin Biosynthetic Gene Cluster of Yersinia enterocolitica : Organization and Siderophore-Dependent Regulation
inferredcites →https://doi.org/10.1128/jcm.35.5.1066-1070.1997openalex-snapshot
Molecular characterization of the gene encoding H antigen in Escherichia coli and development of a PCR-restriction fragment length polymorphism test for identification of E. coli O157:H7 and O157:NM
inferredcites →https://doi.org/10.1515/9783110809817.1openalex-snapshot
1 User’s guide
inferredcites →https://doi.org/10.1637/0005-2086(2002)046[0342:loissg]2.0.co;2openalex-snapshot
Location of Increased Serum Survival Gene and Selected Virulence Traits on a Conjugative R Plasmid in an Avian Escherichia coli Isolate
inferredcites →https://doi.org/10.1637/7030openalex-snapshot
Characterizing Avian Escherichia coli Isolates with Multiplex Polymerase Chain Reaction
inferredcites →https://doi.org/10.1637/7121openalex-snapshot
Multiple Antimicrobial Resistance Region of a Putative Virulence Plasmid from an Escherichia coli Isolate Incriminated in Avian Colibacillosis
inferredcites →https://doi.org/10.2307/1592504openalex-snapshot
Complement Resistance-Related Traits among Escherichia coli Isolates from Apparently Healthy Birds and Birds with Colibacillosis
inferredcites →https://doi.org/10.2307/1592582openalex-snapshot
The Occurrence of Ambient Temperature-Regulated Adhesins, Curli, and the Temperature-Sensitive Hemagglutinin Tsh among Avian Escherichia coli
inferredcites →https://doi.org/10.2307/2290355openalex-snapshot
Discriminant Analysis and Statistical Pattern Recognition.
inferredcites →https://doi.org/10.2307/2344930openalex-snapshot
Multivariate Statistical Methods.
inferredcites →https://doi.org/10.2307/2533021openalex-snapshot
Applied Discriminant Analysis.

What points at this work

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

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Extraintestinal pathogenic Escherichia coli (ExPEC) of human and avian origin belonging to sequence type complex 95 (STC95) portray indistinguishable virulence features
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Acetoacetyl-CoA transferase ydiF regulates the biofilm formation of avian pathogenic Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.150539openalex-snapshot
Extended-spectrum β-lactamase (ESBL)-producing Escherichia coli survey in wild seabirds at a pristine atoll in the southern Atlantic Ocean, Brazil: First report of the O25b-ST131 clone harboring blaCTX-M-8
inferred← citeshttps://doi.org/10.1016/j.urology.2009.01.042openalex-snapshot
Prevalence of Virulence Factors and Antimicrobial Resistance of Uropathogenic Escherichia coli in Jiangsu Province (China)
inferred← citeshttps://doi.org/10.1016/j.vaccine.2022.12.057openalex-snapshot
Evaluation of immunogenicity and efficacy of the enterobactin conjugate vaccine in protecting chickens from colibacillosis
inferred← citeshttps://doi.org/10.1016/j.vetmic.2010.07.013openalex-snapshot
The extra-intestinal avian pathogenic Escherichia coli strain BEN2908 invades avian and human epithelial cells and survives intracellularly
inferred← citeshttps://doi.org/10.1016/j.vetmic.2012.04.015openalex-snapshot
IbeB is involved in the invasion and pathogenicity of avian pathogenic Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.vetmic.2012.11.008openalex-snapshot
Genetic diversity and virulence profiles of Escherichia coli causing salpingitis and peritonitis in broiler breeders
inferred← citeshttps://doi.org/10.1016/j.vetmic.2013.11.028openalex-snapshot
Population structure and virulence content of avian pathogenic Escherichia coli isolated from outbreaks in Sri Lanka
inferred← citeshttps://doi.org/10.1016/j.vetmic.2015.05.007openalex-snapshot
Genetic diversity of Escherichia coli isolates of animal and environmental origins from an integrated poultry production chain
inferred← citeshttps://doi.org/10.1016/j.vetmic.2016.04.011openalex-snapshot
Experimental induced avian E. coli salpingitis: Significant impact of strain and host factors on the clinical and pathological outcome
inferred← citeshttps://doi.org/10.1016/j.vetmic.2017.02.005openalex-snapshot
Determinants of virulence and of resistance to ceftiofur, gentamicin, and spectinomycin in clinical Escherichia coli from broiler chickens in Québec, Canada
inferred← citeshttps://doi.org/10.1016/j.vetmic.2019.108483openalex-snapshot
Avian-source mcr-1-positive Escherichia coli is phylogenetically diverse and shares virulence characteristics with E. coli causing human extra-intestinal infections
inferred← citeshttps://doi.org/10.1016/j.vetmic.2019.108506openalex-snapshot
Intestinal colonization of genotoxic Escherichia coli strains encoding colibactin and cytotoxic necrotizing factor in small mammal pets
inferred← citeshttps://doi.org/10.1016/j.vetmic.2020.108766openalex-snapshot
Genomic landscape of multi-drug resistant avian pathogenic Escherichia coli recovered from broilers
inferred← citeshttps://doi.org/10.1016/j.vetmic.2022.109358openalex-snapshot
O145 may be emerging as a predominant serogroup of Avian pathogenic Escherichia coli (APEC) in China
inferred← citeshttps://doi.org/10.1016/j.vetmic.2023.109914openalex-snapshot
Multicenter molecular investigation of recurrent Escherichia coli bacteriuria in dogs
inferred← citeshttps://doi.org/10.1016/j.yexmp.2008.03.007openalex-snapshot
Origins and virulence mechanisms of uropathogenic Escherichia coli
inferred← citeshttps://doi.org/10.1017/s0950268816000820openalex-snapshot
Escherichia coli type III secretion system 2 (ETT2) is widely distributed in avian pathogenic Escherichia coli isolates from Eastern China
inferred← citeshttps://doi.org/10.1021/acsinfecdis.7b00081openalex-snapshot
Identification of the Colicin V Bacteriocin Gene Cluster by Functional Screening of a Human Microbiome Metagenomic Library
inferred← citeshttps://doi.org/10.1021/es300292yopenalex-snapshot
An Attempt to Identify the Likely Sources of Escherichia coli Harboring Toxin Genes in Rainwater Tanks
inferred← citeshttps://doi.org/10.1038/ismej.2007.52openalex-snapshot
Culture independent analysis of ileal mucosa reveals a selective increase in invasive Escherichia coli of novel phylogeny relative to depletion of Clostridiales in Crohn's disease involving the ileum
inferred← citeshttps://doi.org/10.1038/s41598-018-23962-7openalex-snapshot
Poultry hatcheries as potential reservoirs for antimicrobial-resistant Escherichia coli: A risk to public health and food safety
inferred← citeshttps://doi.org/10.1063/5.0172211openalex-snapshot
Virulence - associated E. Coli genes iss, felA, cvaC, Tsh, iuta and kpsII in avian respiratory issues isolated pathogenic E. Coli strains
inferred← citeshttps://doi.org/10.1080/00071668.2024.2368906openalex-snapshot
Occurrence, antibiotic resistance and molecular characterisation of Shiga toxin-producing Escherichia coli isolated from broiler chickens in Tunisia
inferred← citeshttps://doi.org/10.1080/03079450802216579openalex-snapshot
Molecular epidemiology of a reproductive tract-associated colibacillosis outbreak in a layer breeder flock associated with atypical avian pathogenicEscherichia coli
inferred← citeshttps://doi.org/10.1080/03079450802216652openalex-snapshot
Colibacillosis in poultry: unravelling the molecular basis of virulence of avian pathogenicEscherichia coliin their natural hosts
inferred← citeshttps://doi.org/10.1080/03079457.2010.495742openalex-snapshot
Distribution of serotypes and virulence-associated genes in pathogenicEscherichia coliisolated from ducks
inferred← citeshttps://doi.org/10.1080/03079457.2010.495744openalex-snapshot
Impact ofEscherichia colivaccine on parent stock mortality, first week mortality of broilers and population diversity ofE. coliin vaccinated flocks
inferred← citeshttps://doi.org/10.1080/03079457.2013.866213openalex-snapshot
The contribution of systemicEscherichia coliinfection to the early mortalities of commercial broiler chickens
inferred← citeshttps://doi.org/10.1080/03079457.2017.1349872openalex-snapshot
Pathological and microbiological investigations into cases of bacterial chondronecrosis and osteomyelitis in broiler poultry
inferred← citeshttps://doi.org/10.1080/03601234.2019.1608103openalex-snapshot
Antibiotic resistance and virulence factors of Escherichia coli from eagles and goshawks
inferred← citeshttps://doi.org/10.1080/10408410701647594openalex-snapshot
The Human/Animal Interface: Emergence and Resurgence of Zoonotic Infectious Diseases
inferred← citeshttps://doi.org/10.1080/17460913.2026.2719190openalex-snapshot
Genomic characterization of virulence and disinfectant resistant determinants in multidrug-resistant Escherichia coli and Klebsiella pneumoniae from urban wastewater treatment plants in Windhoek, Namibia
inferred← citeshttps://doi.org/10.1080/20477724.2018.1547542openalex-snapshot
Multiple antibiotic resistances and virulence markers of uropathogenicEscherichia colifrom Mexico
inferred← citeshttps://doi.org/10.1080/21505594.2018.1528844openalex-snapshot
Novel small molecule modulators of quorum sensing in avian pathogenic Escherichia coli (APEC)
inferred← citeshttps://doi.org/10.1080/21505594.2019.1624102openalex-snapshot
Three new serine-protease autotransporters of Enterobacteriaceae (SPATEs) from extra-intestinal pathogenic Escherichia coli and combined role of SPATEs for cytotoxicity and colonization of the mouse kidney
inferred← citeshttps://doi.org/10.1086/597423openalex-snapshot
Phylogenetic Background and Virulence Genotype of Ciprofloxacin‐Susceptible and Ciprofloxacin‐ResistantEscherichia coliStrains of Human and Avian Origin
inferred← citeshttps://doi.org/10.1088/1755-1315/848/1/012225openalex-snapshot
Etiological structure of pig colibacillosis on the territory of the Russian Federation
inferred← citeshttps://doi.org/10.1089/fpd.2007.0087openalex-snapshot
Extraintestinal Pathogenic Escherichia coli
inferred← citeshttps://doi.org/10.1089/fpd.2009.0266openalex-snapshot
Examination of the Source and Extended Virulence Genotypes of Escherichia coli Contaminating Retail Poultry Meat
inferred← citeshttps://doi.org/10.1089/fpd.2011.0961openalex-snapshot
Associations Between Multidrug Resistance, Plasmid Content, and Virulence Potential Among Extraintestinal Pathogenic and Commensal Escherichia coli from Humans and Poultry
inferred← citeshttps://doi.org/10.1089/fpd.2013.1518openalex-snapshot
Evaluation of Virulence and Antimicrobial Resistance in Salmonella enterica Serovar Enteritidis Isolates from Humans and Chicken- and Egg-Associated Sources
inferred← citeshttps://doi.org/10.1089/fpd.2013.1533openalex-snapshot
Human and Avian Extraintestinal Pathogenic Escherichia coli : Infections, Zoonotic Risks, and Antibiotic Resistance Trends
inferred← citeshttps://doi.org/10.1089/fpd.2014.1815openalex-snapshot
Molecular Characterization and Clonal Relationships Among Escherichia coli Strains Isolated from Broiler Chickens with Colisepticemia
inferred← citeshttps://doi.org/10.1089/fpd.2014.1934openalex-snapshot
Prevalence of ColV Plasmid-Linked Genes and In Vivo Pathogenicity of Avian Strains of Escherichia coli
inferred← citeshttps://doi.org/10.1089/fpd.2021.0011openalex-snapshot
Prevalence and Molecular Characterization of Antimicrobial-Resistant Escherichia coli in Pig Farms, Slaughterhouses, and Terminal Markets in Henan Province of China
inferred← citeshttps://doi.org/10.1089/fpd.2023.0093openalex-snapshot
Phenotypic and Genotypic Characterizations of Antimicrobial-Resistant Escherichia coli Isolates from Diverse Retail Meat Samples in North Carolina During 2018–2019
inferred← citeshttps://doi.org/10.1089/mdr.2017.0149openalex-snapshot
High Prevalence of Extended-Spectrum β-Lactamase-Producing Enterobacteriaceae in Wild Fish from the Mediterranean Sea in Algeria
inferred← citeshttps://doi.org/10.1089/mdr.2019.0485openalex-snapshot
Distribution of Pathogenicity Island Markers and H-Antigen Types of Escherichia coli O25b/ST131 Isolates from Patients with Urinary Tract Infection in Iran
inferred← citeshttps://doi.org/10.1093/cid/cis502openalex-snapshot
Food-Borne Origins of Escherichia coli Causing Extraintestinal Infections
inferred← citeshttps://doi.org/10.1093/femsec/fix016openalex-snapshot
High frequency of B2 phylogroup among non-clonally related fecal Escherichia coli isolates from wild boars, including the lineage ST131
inferred← citeshttps://doi.org/10.1093/infdis/jis554openalex-snapshot
Escherichia coli-Mediated Impairment of Ureteric Contractility Is Uropathogenic E. coli Specific
inferred← citeshttps://doi.org/10.1093/jac/dkaa461openalex-snapshot
Prevalence and genomic analysis of ESBL-producingEscherichia coliin retail raw meats in Singapore
inferred← citeshttps://doi.org/10.1093/jac/dkm517openalex-snapshot
Imported chicken meat as a potential source of quinolone-resistant Escherichia coli producing extended-spectrum -lactamases in the UK
inferred← citeshttps://doi.org/10.1093/jac/dkr565openalex-snapshot
Escherichia coli of human and avian origin: detection of clonal groups associated with fluoroquinolone and multidrug resistance in Italy
inferred← citeshttps://doi.org/10.1093/jambio/lxad014openalex-snapshot
A compilation of virulence-associated genes that are frequently reported in avian pathogenicEscherichia coli(APEC) compared to otherE. coli
inferred← citeshttps://doi.org/10.1093/jambio/lxaf015openalex-snapshot
The pathogenicity traits of avian pathogenic Escherichia coli O25-ST131 associated with avian colibacillosis in Georgia poultry and their genotypic and phenotypic overlap with other extraintestinal pathogenic E. coli
inferred← citeshttps://doi.org/10.1093/lambio/ovac016openalex-snapshot
Extraintestinal pathogenic Escherichia coli (ExPEC) reservoirs, and antibiotics resistance trends: a one-health surveillance for risk analysis from “ farm-to-fork ”
inferred← citeshttps://doi.org/10.1097/olq.0b013e31823156a0openalex-snapshot
Sexually Transmitted Escherichia coli Urethritis and Orchiepididymitis
inferred← citeshttps://doi.org/10.1099/jmm.0.012088-0openalex-snapshot
Characterization of cytotoxic necrotizing factor 1-producing Escherichia coli strains from faeces of healthy macaques
inferred← citeshttps://doi.org/10.1099/jmm.0.033993-0openalex-snapshot
Microarray-based detection of extended virulence and antimicrobial resistance gene profiles in phylogroup B2 Escherichia coli of human, meat and animal origin
inferred← citeshttps://doi.org/10.1099/mgen.0.000250openalex-snapshot
Whole genome sequence analysis of Australian avian pathogenic Escherichia coli that carry the class 1 integrase gene
inferred← citeshttps://doi.org/10.1099/mgen.0.000385openalex-snapshot
Whole-genome sequence analysis of environmental Escherichia coli from the faeces of straw-necked ibis (Threskiornis spinicollis) nesting on inland wetlands
inferred← citeshttps://doi.org/10.1099/mic.0.024869-0openalex-snapshot
Comparison of virulence factors and expression of specific genes between uropathogenic Escherichia coli and avian pathogenic E. coli in a murine urinary tract infection model and a chicken challenge model
inferred← citeshttps://doi.org/10.1099/mic.0.2007/013086-0openalex-snapshot
A subset of mucosa-associated Escherichia coli isolates from patients with colon cancer, but not Crohn's disease, share pathogenicity islands with urinary pathogenic E. coli
inferred← citeshttps://doi.org/10.1099/mic.0.2007/015784-0openalex-snapshot
Characterization of a yjjQ mutant of avian pathogenic Escherichia coli (APEC)
inferred← citeshttps://doi.org/10.1099/mic.0.28682-0openalex-snapshot
A SitABCD homologue from an avian pathogenic Escherichia coli strain mediates transport of iron and manganese and resistance to hydrogen peroxide
inferred← citeshttps://doi.org/10.1101/2025.10.02.680073openalex-snapshot
Antimicrobial resistance and comparative genome analysis of high-risk Escherichia coli clones isolated from Egyptian children with diarrhoea
inferred← citeshttps://doi.org/10.1111/j.1365-2362.2008.01986.xopenalex-snapshot
Mechanisms and consequences of bladder cell invasion by uropathogenic Escherichia coli
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2006.03076.xopenalex-snapshot
Biofilm formation by avian Escherichia coli in relation to media, source and phylogeny
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2011.04978.xopenalex-snapshot
Escherichia coli from retail meats carry genes associated with uropathogenic Escherichia coli, but are weakly invasive in human bladder cell culture
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2008.01595.xopenalex-snapshot
ExPEC‐typical virulence‐associated genes correlate with successful colonization by intestinal E. coli in a small piglet group
inferred← citeshttps://doi.org/10.1111/j.1472-765x.2009.02717.xopenalex-snapshot
Distribution of integron-associated trimethoprim-sulfamethoxazole resistance determinants amongEscherichia colifrom humans and food-producing animals
inferred← citeshttps://doi.org/10.1111/j.1574-695x.2011.00797.xopenalex-snapshot
Escherichia colifrom animal reservoirs as a potential source of human extraintestinal pathogenicE. coli
inferred← citeshttps://doi.org/10.1111/j.1574-6968.2006.00392.xopenalex-snapshot
Unique DNA sequences of avian pathogenicEscherichia coliisolates as determined by genomic suppression subtractive hybridization
inferred← citeshttps://doi.org/10.1111/j.1758-2229.2009.00058.xopenalex-snapshot
Mallard ducks – a waterfowl species with high risk of distributing Escherichia coli pathogenic for humans
inferred← citeshttps://doi.org/10.1111/jam.12735openalex-snapshot
Origins and environmental mobility of antibiotic resistance genes, virulence factors and bacteria in a tidal creek's watershed
inferred← citeshttps://doi.org/10.1111/jam.14905openalex-snapshot
Poultry‐origin extraintestinal Escherichia coli strains carrying the traits associated with urinary tract infection, sepsis, meningitis and avian colibacillosis in India
inferred← citeshttps://doi.org/10.1111/jfs.12605openalex-snapshot
Evaluation of bulk tank raw milk and raw chicken meat samples as source of ESBL producing Escherichia coli in Turkey: Recent insights
inferred← citeshttps://doi.org/10.1111/lam.12349openalex-snapshot
Distribution of virulence genes and multiple drug‐resistant patterns amongst different phylogenetic groups of uropathogenic Escherichia coli isolated from patients with urinary tract infection
inferred← citeshttps://doi.org/10.1111/tbed.13755openalex-snapshot
Chicken‐source Escherichia coli within phylogroup F shares virulence genotypes and is closely related to extraintestinal pathogenic E. coli causing human infections
inferred← citeshttps://doi.org/10.1111/tbed.14678openalex-snapshot
Complete genomic analysis of ST117 lineage extraintestinal pathogenic Escherichia coli (ExPEC) to reveal multiple genetic determinants to drive its global transmission: ST117 E. coli as an emerging multidrug‐resistant foodborne ExPEC with zoonotic potential
inferred← citeshttps://doi.org/10.1128/9781555817404.ch10openalex-snapshot
Origin and Dissemination of Antimicrobial Resistance among UropathogenicEscherichia coli
inferred← citeshttps://doi.org/10.1128/9781555817404.ch11openalex-snapshot
Population Phylogenomics of Extraintestinal PathogenicEscherichia coli
inferred← citeshttps://doi.org/10.1128/9781555817404.ch9openalex-snapshot
Reservoirs of Extraintestinal PathogenicEscherichia coli
inferred← citeshttps://doi.org/10.1128/9781555818791.ch26openalex-snapshot
Escherichia coli O104:H4 Pathogenesis: An Enteroaggregative E. coli/Shiga Toxin-Producing E. coli Explosive Cocktail of High Virulence
inferred← citeshttps://doi.org/10.1128/aac.06001-11openalex-snapshot
Contribution of IncFII and Broad-Host IncA/C and IncN Plasmids to the Local Expansion and Diversification of Phylogroup B2 Escherichia coli ST131 Clones Carrying bla CTX-M-15 and qnrS1 Genes
inferred← citeshttps://doi.org/10.1128/aem.00760-07openalex-snapshot
Plasmid Replicon Typing of Commensal and Pathogenic Types of Escherichia coli Isolates
inferred← citeshttps://doi.org/10.1128/aem.00786-09openalex-snapshot
Antimicrobial Resistance-Conferring Plasmids with Similarity to Virulence Plasmids from Avian Pathogenic Escherichia coli Strains in Salmonella enterica Serovar Kentucky Isolates from Poultry
inferred← citeshttps://doi.org/10.1128/aem.01324-08openalex-snapshot
Intestine and Environment of the Chicken as Reservoirs for Extraintestinal Pathogenic Escherichia coli Strains with Zoonotic Potential
inferred← citeshttps://doi.org/10.1128/aem.01395-08openalex-snapshot
Comparison of Extraintestinal Pathogenic Escherichia coli Strains from Human and Avian Sources Reveals a Mixed Subset Representing Potential Zoonotic Pathogens
inferred← citeshttps://doi.org/10.1128/aem.01542-06openalex-snapshot
Autotransporter-Encoding Sequences Are Phylogenetically Distributed amongEscherichia coliClinical Isolates and Reference Strains
inferred← citeshttps://doi.org/10.1128/aem.01809-23openalex-snapshot
Anthropogenic contamination sources drive differences in antimicrobial-resistant Escherichia coli in three urban lakes
inferred← citeshttps://doi.org/10.1128/aem.02171-06openalex-snapshot
Plasmid Replicon Typing of Commensal and Pathogenic Escherichia coli Isolates
inferred← citeshttps://doi.org/10.1128/aem.02341-06openalex-snapshot
Detection and Identification by PCR of a Highly Virulent Phylogenetic Subgroup among Extraintestinal Pathogenic Escherichia coli B2 Strains
inferred← citeshttps://doi.org/10.1128/aem.02634-07openalex-snapshot
Evolution of the iss Gene in Escherichia coli
inferred← citeshttps://doi.org/10.1128/aem.03524-14openalex-snapshot
Zoonotic Potential of Escherichia coli Isolates from Retail Chicken Meat Products and Eggs
inferred← citeshttps://doi.org/10.1128/aem.07869-11openalex-snapshot
Genotypic and Phenotypic Traits That Distinguish Neonatal Meningitis-Associated Escherichia coli from Fecal E. coli Isolates of Healthy Human Hosts
inferred← citeshttps://doi.org/10.1128/ecosalplus.esp-0013-2020openalex-snapshot
Role of Plasmids in the Ecology and Evolution of “High-Risk” Extraintestinal Pathogenic Escherichia coli Clones
inferred← citeshttps://doi.org/10.1128/genomea.01611-15openalex-snapshot
Complete Genomic Sequence of an Avian Pathogenic Escherichia coli Strain of Serotype O7:HNT
inferred← citeshttps://doi.org/10.1128/iai.00334-08openalex-snapshot
Inactivation of ibeA and ibeT Results in Decreased Expression of Type 1 Fimbriae in Extraintestinal Pathogenic Escherichia coli Strain BEN2908
inferred← citeshttps://doi.org/10.1128/iai.00347-10openalex-snapshot
Avian-Pathogenic Escherichia coli Strains Are Similar to Neonatal Meningitis E. coli Strains and Are Able To Cause Meningitis in the Rat Model of Human Disease
inferred← citeshttps://doi.org/10.1128/iai.00363-06openalex-snapshot
Acquisition of Avian PathogenicEscherichia coliPlasmids by a CommensalE. coliIsolate Enhances Its Abilities To Kill Chicken Embryos, Grow in Human Urine, and Colonize the Murine Kidney
inferred← citeshttps://doi.org/10.1128/iai.00412-06openalex-snapshot
The BarA-UvrY Two-Component System Regulates Virulence in Avian Pathogenic Escherichia coli O78:K80:H9
inferred← citeshttps://doi.org/10.1128/iai.00455-08openalex-snapshot
Specific Roles of the iroBCDEN Genes in Virulence of an Avian Pathogenic Escherichia coli O78 Strain and in Production of Salmochelins
inferred← citeshttps://doi.org/10.1128/iai.00531-10openalex-snapshot
The Type VI Secretion System Plays a Role in Type 1 Fimbria Expression and Pathogenesis of an Avian Pathogenic Escherichia coli Strain
inferred← citeshttps://doi.org/10.1128/iai.00688-16openalex-snapshot
Novel MicroRNA Involved in Host Response to Avian Pathogenic Escherichia coli Identified by Deep Sequencing and Integration Analysis
inferred← citeshttps://doi.org/10.1128/iai.00789-07openalex-snapshot
Contribution of the SitABCD, MntH, and FeoB Metal Transporters to the Virulence of Avian Pathogenic Escherichia coli O78 Strain χ7122
inferred← citeshttps://doi.org/10.1128/iai.00821-10openalex-snapshot
Effects of ibeA Deletion on Virulence and Biofilm Formation of Avian Pathogenic Escherichia coli
inferred← citeshttps://doi.org/10.1128/iai.01174-09openalex-snapshot
Sequence Analysis and Characterization of a Transferable Hybrid Plasmid Encoding Multidrug Resistance and Enabling Zoonotic Potential for Extraintestinal Escherichia coli
inferred← citeshttps://doi.org/10.1128/iai.74.1.744-749.2006openalex-snapshot
The pap Operon of Avian Pathogenic Escherichia coli Strain O1:K1 Is Located on a Novel Pathogenicity Island
inferred← citeshttps://doi.org/10.1128/jb.00204-06openalex-snapshot
Complete DNA Sequence of a ColBM Plasmid from Avian Pathogenic Escherichia coli Suggests that It Evolved from Closely Related ColV Virulence Plasmids
inferred← citeshttps://doi.org/10.1128/jb.00661-08openalex-snapshot
Insights into the Environmental Resistance Gene Pool from the Genome Sequence of the Multidrug-Resistant Environmental Isolate Escherichia coli SMS-3-5
inferred← citeshttps://doi.org/10.1128/jb.01717-08openalex-snapshot
Genomic Islands of Uropathogenic Escherichia coli Contribute to Virulence
inferred← citeshttps://doi.org/10.1128/jb.01726-06openalex-snapshot
The Genome Sequence of Avian PathogenicEscherichia coliStrain O1:K1:H7 Shares Strong Similarities with Human Extraintestinal PathogenicE. coliGenomes
inferred← citeshttps://doi.org/10.1128/jb.06375-11openalex-snapshot
Prevalence of Avian-Pathogenic Escherichia coli Strain O1 Genomic Islands among Extraintestinal and Commensal E. coli Isolates
inferred← citeshttps://doi.org/10.1128/jb.188.2.745-758.2006openalex-snapshot
DNA Sequence of a ColV Plasmid and Prevalence of Selected Plasmid-Encoded Virulence Genes among Avian Escherichia coli Strains
inferred← citeshttps://doi.org/10.1128/jcm.00037-07openalex-snapshot
Extraintestinal Pathogenic Escherichia coli Strains of Avian and Human Origin: Link between Phylogenetic Relationships and Common Virulence Patterns
inferred← citeshttps://doi.org/10.1128/jcm.00548-06openalex-snapshot
Common Virulence Factors and Genetic Relationships between O18:K1:H7 Escherichia coli Isolates of Human and Avian Origin
inferred← citeshttps://doi.org/10.1128/jcm.00788-18openalex-snapshot
Population Structure and Antimicrobial Resistance of Canine Uropathogenic Escherichia coli
inferred← citeshttps://doi.org/10.1128/jcm.00816-08openalex-snapshot
Identification of Minimal Predictors of Avian Pathogenic Escherichia coli Virulence for Use as a Rapid Diagnostic Tool
inferred← citeshttps://doi.org/10.1128/jcm.01488-07openalex-snapshot
Virulence Factors in Urinary Escherichia coli Strains: Phylogenetic Background and Quinolone and Fluoroquinolone Resistance
inferred← citeshttps://doi.org/10.1128/jcm.02086-12openalex-snapshot
Similarity and Divergence of Phylogenies, Antimicrobial Susceptibilities, and Virulence Factor Profiles of Escherichia coli Isolates Causing Recurrent Urinary Tract Infections That Persist or Result from Reinfection
inferred← citeshttps://doi.org/10.1128/mbio.00470-18openalex-snapshot
Escherichia coli ST131- H 22 as a Foodborne Uropathogen
inferred← citeshttps://doi.org/10.1128/mbio.03152-22openalex-snapshot
Genomic Island-Encoded Histidine Kinase and Response Regulator Coordinate Mannose Utilization with Virulence in Enterohemorrhagic Escherichia coli
inferred← citeshttps://doi.org/10.1128/microbiolspec.ame-0014-2020openalex-snapshot
Distinguishing Pathovars from Nonpathovars: Escherichia coli
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