scholarly article | Q13442814 |
P50 | author | David L Swerdlow | Q92482004 |
Patricia M Griffin | Q124220349 | ||
P2093 | author name string | Josefa M Rangel | |
Collen Crowe | |||
Phyllis H Sparling | |||
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P433 | issue | 4 | |
P921 | main subject | United States of America | Q30 |
epidemiology | Q133805 | ||
Escherichia coli | Q25419 | ||
P304 | page(s) | 603-609 | |
P577 | publication date | 2005-04-01 | |
P1433 | published in | Emerging Infectious Diseases | Q5235761 |
P1476 | title | Epidemiology of Escherichia coli O157:H7 outbreaks, United States, 1982-2002. | |
P478 | volume | 11 |
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Q38991233 | Multilocus genotypic characterization of Escherichia coli O157:H7 recovered from food sources. |
Q50044300 | Multiplex PCR assay for the detection and quantification of Campylobacter spp., Escherichia coli O157:H7, and Salmonella serotypes in water samples |
Q36395663 | Multiplicity of Salmonella entry mechanisms, a new paradigm for Salmonella pathogenesis. |
Q40323901 | Multistate Outbreak of Escherichia coli O157:H7 Infections Associated with Consumption of Fresh Spinach: United States, 2006. |
Q91868270 | Multistate Outbreaks of Foodborne Illness in the United States Associated With Fresh Produce From 2010 to 2017 |
Q58057326 | Multistate outbreak of Escherichia coli O157:H7 infections associated with a national fast-food chain, 2006: a study incorporating epidemiological and food source traceback results |
Q41734054 | N-acyl-homoserine lactones-producing bacteria protect plants against plant and human pathogens |
Q35558488 | NAIL: Nucleic Acid detection using Isotachophoresis and Loop-mediated isothermal amplification |
Q50215614 | National Survey of Shiga Toxin-Producing Escherichia coli Serotypes O26, O45, O103, O111, O121, O145, and O157 in Australian Beef Cattle Feces. |
Q51244295 | National patterns of Escherichia coli O157 infections, USA, 1996-2011. |
Q57915159 | Naturally Occurring Water Pollutants |
Q28389146 | Naturally resident and exogenously applied T4-like and T5-like bacteriophages can reduce Escherichia coli O157:H7 levels in sheep guts |
Q55416818 | Non-pathogenic Escherichia coli Enhance Stx2a Production of E. coli O157:H7 Through Both bamA-Dependent and Independent Mechanisms. |
Q51006284 | Norovirus Outbreak Associated With a Natural Lake Used for Recreation-Oregon, 2014. |
Q41231125 | Norovirus outbreak associated with a natural lake used for recreation - Oregon, 2014. |
Q39896145 | Novel cell-based method to detect Shiga toxin 2 from Escherichia coli O157:H7 and inhibitors of toxin activity |
Q27500362 | O-antigen and Virulence Profiling of Shiga Toxin-Producing Escherichia coli by a Rapid and Cost–Effective DNA Microarray Colorimetric Method |
Q39879431 | Occurrence and antibiotic resistance of Escherichia coli O157:H7 in a watershed in north-central Indiana |
Q41070016 | Occurrence of virulence gene signatures associated with diarrhoeagenic and non-diarrhoeagenic pathovars of Escherichia coli isolates from some selected rivers in South-Western Nigeria |
Q40072954 | Occurrence of virulence genes associated with Diarrheagenic pathotypes in Escherichia coli isolates from surface water. |
Q37643869 | Oral intoxication of mice with Shiga toxin type 2a (Stx2a) and protection by anti-Stx2a monoclonal antibody 11E10. |
Q42233868 | Outbreaks of non-O157 Shiga toxin-producing Escherichia coli infection: USA. |
Q33712512 | Pathogenesis of Escherichia coli O157:H7 strain 86-24 following oral infection of BALB/c mice with an intact commensal flora |
Q94464356 | Pathogenomes of Atypical Non-shigatoxigenic Escherichia coli NSF/SF O157:H7/NM: Comprehensive Phylogenomic Analysis Using Closed Genomes |
Q53163131 | Persistence of Escherichia coli O157:H7 and Total Escherichia coli in Feces and Feedlot Surface Manure from Cattle Fed Diets with and without Corn or Sorghum Wet Distillers Grains with Solubles. |
Q42121963 | Persistence, transmission, and virulence characteristics of Aeromonas strains in a duckweed aquaculture-based hospital sewage water recycling plant in Bangladesh |
Q34641686 | Phenotypic and Genotypic Characterization of Escherichia coli Isolated from Untreated Surface Waters |
Q35081075 | Phenotypic and genotypic characterization of biofilm forming capabilities in non-O157 Shiga toxin-producing Escherichia coli strains |
Q42119862 | Phylogenetically related Argentinean and Australian Escherichia coli O157 isolates are distinguished by virulence clades and alternative Shiga toxin 1 and 2 prophages |
Q37396989 | Physiological Response of Escherichia coli O157:H7 Sakai to Dynamic Changes in Temperature and Water Activity as Experienced during Carcass Chilling |
Q57972024 | Plasma membrane profiling during enterohemorrhagic E. coli infection reveals that the metalloprotease StcE cleaves CD55 from host epithelial surfaces |
Q39472250 | Plasmids from Shiga Toxin-Producing Escherichia coli Strains with Rare Enterohemolysin Gene (ehxA) Subtypes Reveal Pathogenicity Potential and Display a Novel Evolutionary Path |
Q30466776 | Portable microfluidic chip for detection of Escherichia coli in produce and blood |
Q41998662 | Potentiating the Heat Inactivation of Escherichia coli O157:H7 in Ground Beef Patties by Natural Antimicrobials |
Q35965328 | Presence of pathogenic Escherichia coli is correlated with bacterial community diversity and composition on pre-harvest cattle hides |
Q54414278 | Prevalence and concentration of Verotoxigenic Escherichia coli O157:H7 in adult sheep at slaughter from Italy. |
Q64910219 | Prevalence and concentration of stx+ E. coli and E. coli O157 in bovine manure from Florida farms. |
Q39894339 | Prevalence and occurrence of zoonotic bacterial pathogens in surface waters determined by quantitative PCR. |
Q36970605 | Prevalence and relatedness of Escherichia coli O157:H7 strains in the feces and on the hides and carcasses of U.S. meat goats at slaughter |
Q37301713 | Prevalence of Escherichia coli O157:H7 in organically and naturally raised beef cattle |
Q38864851 | Prevalence of Escherichia coli O157:H7 on hides and faeces of ruminants at slaughter in two major abattoirs in Nigeria |
Q41093307 | Prevalence of Virulence Genes Associated with Diarrheagenic Pathotypes of Escherichia coli Isolates from Water, Sediment, Fish, and Crab in Aby Lagoon, Côte d'Ivoire |
Q37263266 | Prevalence of hemolysin genes and comparison of ehxA subtype patterns in Shiga toxin-producing Escherichia coli (STEC) and non-STEC strains from clinical, food, and animal sources |
Q33498153 | Primary and secondary cases in Escherichia coli O157 outbreaks: a statistical analysis |
Q37248054 | Quantification of plasmid DNA reference materials for Shiga toxin-producing Escherichia coli based on UV, HR-ICP-MS and digital PCR. |
Q42637879 | Rapid detection of Shiga toxin-producing Escherichia coli by optical immunoassay. |
Q34375210 | Recent advances in understanding enteric pathogenic Escherichia coli. |
Q35673972 | Reduced Toxicity of Shiga Toxin (Stx) Type 2c in Mice Compared to Stx2d Is Associated with Instability of Stx2c Holotoxin. |
Q42120477 | Reduction of Escherichia coli O157:H7 shedding in cattle by addition of chitosan microparticles to feed |
Q40086175 | Review: Comparison of the Effectiveness of Decontaminating Strategies for Fresh Fruits and Vegetables and Related Limitations |
Q57541958 | Risk Factors for E. coli O157 and Cryptosporidiosis Infection in Individuals in the Karst Valleys of East Tennessee, USA |
Q54450910 | Risk factors for sporadic Shiga toxin-producing Escherichia coli O157 infections in FoodNet sites, 1999-2000. |
Q33379409 | Risk factors for sporadic Shiga toxin-producing Escherichia coli infections in children, Argentina |
Q33426758 | Risk of haemolytic uraemic syndrome caused by shiga-toxin-producing Escherichia coli infection in adult women in Japan |
Q37033120 | Role of RpoS in the virulence of Citrobacter rodentium |
Q35880433 | Saltelli Global Sensitivity Analysis and Simulation Modelling to Identify Intervention Strategies to Reduce the Prevalence of Escherichia coli O157 Contaminated Beef Carcasses |
Q41411543 | Same-day detection of Escherichia coli O157:H7 from spinach by using electrochemiluminescent and cytometric bead array biosensors |
Q37387719 | Scientific status summary |
Q47262383 | Screening for host proteins interacting with Escherichia coli O157:H7 EspF using bimolecular fluorescence complementation |
Q30496798 | Sensing Escherichia coli O157:H7 via frequency shift through a self-assembled monolayer based QCM immunosensor. |
Q35041070 | Sequences of two related multiple antibiotic resistance virulence plasmids sharing a unique IS26-related molecular signature isolated from different Escherichia coli pathotypes from different hosts |
Q36705833 | Shiga Toxin (Stx) Type 1a Reduces the Oral Toxicity of Stx Type 2a |
Q41669177 | Shiga Toxin Therapeutics: Beyond Neutralization. |
Q92882569 | Shiga Toxin-Associated Hemolytic Uremic Syndrome: A Narrative Review |
Q47102102 | Shiga Toxin-Producing Escherichia coli O157 Shedding Dynamics in an Australian Beef Herd |
Q26752966 | Shiga Toxins as Multi-Functional Proteins: Induction of Host Cellular Stress Responses, Role in Pathogenesis and Therapeutic Applications |
Q35003696 | Shiga toxin 2-induced endoplasmic reticulum stress is minimized by activated protein C but does not correlate with lethal kidney injury. |
Q33402959 | Shiga toxin in enterohemorrhagic E.coli: regulation and novel anti-virulence strategies |
Q90402100 | Shiga toxin producing Escherichia coli-associated diarrhea and hemolytic uremic syndrome in young children in Romania |
Q90458378 | Shiga toxin sub-type 2a increases the efficiency of Escherichia coli O157 transmission between animals and restricts epithelial regeneration in bovine enteroids |
Q33411533 | Shiga toxin-producing Escherichia coli O157 is more likely to lead to hospitalization and death than non-O157 serogroups--except O104 |
Q38991230 | Shiga toxin-producing Escherichia coli from raw milk cheese in Egypt: prevalence, molecular characterization and survival to stress conditions. |
Q90299808 | Shiga toxin-producing Escherichia coli in British Columbia, 2011-2017: Analysis to inform exclusion guidelines |
Q34000479 | Shiga toxin-producing Escherichia coli in swine: the public health perspective |
Q34775764 | Shiga toxin-producing Escherichia coli in yaks (Bos grunniens) from the Qinghai-Tibetan Plateau, China |
Q33381863 | Shiga toxin-producing Escherichia coli serogroups in food and patients, Germany |
Q37021485 | Shiga toxin-producing Escherichia coli: factors involved in virulence and cattle colonization |
Q33404640 | Shiga toxins and the pathophysiology of hemolytic uremic syndrome in humans and animals |
Q54290985 | Simultaneous enrichment and optical detection of low levels of stressed Escherichia coli O157:H7 in food matrices. |
Q28289657 | Slugs: potential novel vectors of Escherichia coli O157. |
Q54458579 | Soil survival of Escherichia coli O157:H7 acquired by a child from garden soil recently fertilized with cattle manure. |
Q41925990 | Sorbitol-Fermenting Enterohemorrhagic Escherichia coli O157:H- Isolates from Czech Patients with Novel Plasmid Composition Not Previously Seen in German Isolates |
Q33382082 | Sorbitol-fermenting enterohaemorrhagic Escherichia coli O157:H- causes another outbreak of haemolytic uraemic syndrome in children. |
Q36497522 | Standardized Escherichia coli O157:H7 Exposure Studies in Cattle Provide Evidence that Bovine Factors Do Not Drive Increased Summertime Colonization |
Q27651305 | Structural mechanism of WASP activation by the enterohaemorrhagic E. coli effector EspFU |
Q90396133 | Surveillance for enterotoxigenic & enteropathogenic Escherichia coli isolates from animal source foods in Northwest Iran |
Q43354512 | Survey of antimicrobial effects of beef carcass intervention treatments in very small state-inspected slaughter plants |
Q33506514 | Survival and spread of Shiga toxin-producing Escherichia coli in alpine pasture grasslands |
Q38728032 | Synthesis of New Fluoro-Benzimidazole Derivatives as an Approach towards the Discovery of Novel Intestinal Antiseptic Drug Candidates |
Q28389976 | T4-Like genome organization of the Escherichia coli O157:H7 lytic phage AR1 |
Q37182771 | The Accessory Genome of Shiga Toxin-Producing Escherichia coli Defines a Persistent Colonization Type in Cattle |
Q33403986 | The CsgA and Lpp proteins of an Escherichia coli O157:H7 strain affect HEp-2 cell invasion, motility, and biofilm formation |
Q39840825 | The Escherichia coli O157:H7 EhaB autotransporter protein binds to laminin and collagen I and induces a serum IgA response in O157:H7 challenged cattle |
Q92683941 | The Escherichia coli O157:H7 carbon starvation-inducible lipoprotein Slp contributes to initial adherence in vitro via the human polymeric immunoglobulin receptor |
Q42363836 | The EspF N-Terminal of Enterohemorrhagic Escherichia coli O157:H7 EDL933w Imparts Stronger Toxicity Effects on HT-29 Cells than the C-Terminal |
Q34571628 | The N-terminal domain of EspF induces host cell apoptosis after infection with enterohaemorrhagic Escherichia coli O157:H7. |
Q87105810 | The Pepsin Hydrolysate of Bovine Lactoferrin Causes a Collapse of the Membrane Potential in Escherichia coli O157:H7 |
Q34360129 | The Salmonella effector protein SpvC, a phosphothreonine lyase is functional in plant cells |
Q37254093 | The Use of a Novel NanoLuc -Based Reporter Phage for the Detection of Escherichia coli O157:H7. |
Q41394032 | The acyl-homoserine lactone synthase YenI from Yersinia enterocolitica modulates virulence gene expression in enterohemorrhagic Escherichia coli O157:H7. |
Q46086165 | The antimicrobial effects of glucosinolates and their respective enzymatic hydrolysis products on bacteria isolated from the human intestinal tract. |
Q33954309 | The effect of handwashing at recommended times with water alone and with soap on child diarrhea in rural Bangladesh: an observational study |
Q33422389 | The epidemiology, microbiology and clinical impact of Shiga toxin-producing Escherichia coli in England, 2009-2012. |
Q35589090 | The evolution of metabolic networks of E. coli |
Q30396972 | The global burden of bacterial and viral zoonotic infections |
Q37387779 | The growing burden of foodborne outbreaks due to contaminated fresh produce: risks and opportunities |
Q33541689 | The impact of biofilm growth on transport of Escherichia coli O157:H7 in sand |
Q51165453 | The influence of melatonin on growth of E. coli O157:H7 in pure culture and exogenous melatonin on faecal shedding of E. coli O157:H7 in experimentally infected wethers. |
Q37125274 | The microcosm mediates the persistence of shiga toxin-producing Escherichia coli in freshwater ecosystems |
Q43451353 | The nitric oxide reductase of enterohaemorrhagic Escherichia coli plays an important role for the survival within macrophages |
Q50055430 | The prevalence of Escherichia coli O157:H7 fecal shedding in feedlot pens is affected by the water-to-cattle ratio: A randomized controlled trial |
Q35088435 | The relationship between lay and technical views of Escherichia coli O157 risk. |
Q92006957 | The transcriptome analysis of the Arabidopsis thaliana in response to the Vibrio vulnificus by RNA-sequencing |
Q26860229 | The unexhausted potential of E. coli |
Q40254824 | The utility of multiple molecular methods including whole genome sequencing as tools to differentiate Escherichia coli O157:H7 outbreaks |
Q35105318 | Top-down proteomic identification of Shiga toxin 2 subtypes from Shiga toxin-producing Escherichia coli by matrix-assisted laser desorption ionization-tandem time of flight mass spectrometry |
Q34326000 | Towards a pathogenic Escherichia coli detection platform using multiplex SYBR®Green Real-time PCR methods and high resolution melting analysis. |
Q57927658 | Toxigenic properties and stx phage characterization of Escherichia coli O157 isolated from animal sources in a developing country setting |
Q39410377 | Transcriptome analysis of Escherichia coli O157:H7 exposed to lysates of lettuce leaves. |
Q37365283 | Transcriptomic response of Escherichia coli O157:H7 to oxidative stress |
Q43344044 | Translocation and cross-contamination of E. coli O157 in beef eye-of-round subprimal cuts processed with high-pressure needleless injection |
Q36308310 | Twenty-Two Years of U.S. Meat and Poultry Product Recalls: Implications for Food Safety and Food Waste |
Q36465208 | Two or more enteropathogens are associated with diarrhoea in Mexican children |
Q92353572 | Unexpected Prevalence of eae-Positive Escherichia coli in the Animas River, Durango, Colorado |
Q41478376 | Use of copper cast alloys to control Escherichia coli O157 cross-contamination during food processing |
Q35796066 | Using comparative genomics for inquiry-based learning to dissect virulence of Escherichia coli O157:H7 and Yersinia pestis |
Q41953952 | Vaccination with type III secreted proteins leads to decreased shedding in calves after experimental infection with Escherichia coli O157. |
Q59259149 | Variation in acid resistance among enterohaemorrhagic Escherichia coli in a simulated gastric environment |
Q33378926 | Variation in virulence among clades of Escherichia coli O157:H7 associated with disease outbreaks |
Q37467549 | Verocytotoxin-producing Escherichia coli (VTEC). |
Q38588986 | Verotoxigenic Escherichia coli transmission in Ireland: a review of notified outbreaks, 2004-2012. |
Q37002416 | Virulence Gene Profiles and Clonal Relationships of Escherichia coli O26:H11 Isolates from Feedlot Cattle as Determined by Whole-Genome Sequencing |
Q64097014 | Virulence gene profiles and phylogeny of Shiga toxin-positive Escherichia coli strains isolated from FDA regulated foods during 2010-2017 |
Q41441329 | What Role Does Mycobacterium avium subsp. paratuberculosis Play in Crohn's Disease? |
Q58699815 | Whole genome shotgun sequencing revealed highly polymorphic genome regions and genes in Escherichia coli O157:H7 isolates collected from a single feedlot |
Q43847337 | Whole-Genome Sequencing: Opportunities and Challenges for Public Health, Food-borne Outbreak Investigations, and the Global Food Supply |
Q34821019 | Widespread acquisition of antimicrobial resistance among Campylobacter isolates from UK retail poultry and evidence for clonal expansion of resistant lineages |
Q43096103 | σ(N) -dependent control of acid resistance and the locus of enterocyte effacement in enterohemorrhagic Escherichia coli is activated by acetyl phosphate in a manner requiring flagellar regulator FlhDC and the σ(S) antagonist FliZ. |
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