Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Evaluation of a PCR-restriction fragment length polymorphism (PCR-RFLP) assay for molecular epidemiological study of Shiga toxin-producing Escherichia coli.

The Journal of veterinary medical science - 1 Jul 2011

Sugimoto Norihiko, Shima Kensuke, Hinenoya Atsushi, Asakura Masahiro, Matsuhisa Akio, Watanabe Haruo, Yamasaki Shinji

Abstract excerpt

In this study, we have evaluated our recently developed polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay for the molecular subtyping of Shiga toxin-producing Escherichia coli (STEC). A total of 200 STEC strains including O157 (n=100), O26 (n=50), O111 (n=10), and non-O26/O111/O157 (n=40) serogroups isolated during 2005-2006 in Japan, which were identified to be clonally...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to DNA, Bacterial
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Molecular Epidemiology

Share to O Antigens

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Share to Shiga-Toxigenic Escherichia coli

Source

Identifiers

PMID: 21321474
DOI: 10.1292/jvms.11-0008

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evaluation of a PCR-restriction fragment length polymorphism (PCR-RFLP) assay for molecular epidemiological study of Shiga toxin-producing Escherichia coli.PMID 21321474Read ↗

Development of a PCR-based method for specific identification of genotypic markers of shiga toxin-producing Escherichia coli strains.Semantic proximity Read ↗

Detection of E. coli O157:H7 and Shigella dysenteriae toxins in clinical samples by PCR-ELISASemantic proximity Read ↗

Genetic typing of shiga toxin 2 variants of Escherichia coli by PCR-restriction fragment length polymorphism analysis.Semantic proximity Read ↗

Phylogenetic analysis and Shiga toxin production profiling of Shiga toxin-producing/enterohemorrhagic Escherichia coli clinical isolates.Semantic proximity Read ↗

Detection and Characterization of Shiga Toxigenic <i>Escherichia coli</i> by Using Multiplex PCR Assays for <i>stx</i> <sub>1</sub> , <i>stx</i> <sub>2</sub> , <i>eaeA</i> , Enterohemorrhagic <i>E. coli hlyA</i> , <i>rfb</i> <sub>O111</sub> , and <i>rfb</i> <sub>O157</sub>Semantic proximity Read ↗

Detection by 5′-nuclease PCR of Shiga-toxin producing Escherichia coli O26, O55, O91, O103, O111, O113, O145 and O157:H7, associated with the world's most frequent clinical casesSemantic proximity Read ↗

Direct Detection of Shiga Toxigenic Escherichia coli Strains Belonging to Serogroups O111, O157, and O113 by Multiplex PCRSemantic proximity Read ↗

Pathogenic Factors and Recent Study on the Rapid Detection of Shiga Toxin-Producing Escherichia coli (STEC)Semantic proximity Read ↗

Rapid Detection of Shiga Toxin-Producing Bacteria in Feces by Multiplex PCR with Molecular Beacons on the Smart CyclerSemantic proximity Read ↗

O-antigen and virulence profiling of shiga toxin-producing Escherichia coli by a rapid and cost-effective DNA microarray colorimetric method.Semantic proximity Read ↗

Molecular risk assessment and epidemiological typing of Shiga toxin-producing Escherichia coli by using a novel PCR binary typing system.Semantic proximity Read ↗

Methods for genotyping verotoxin-producing Escherichia coli.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.