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

Using a commercial DiversiLab semiautomated repetitive sequence-based PCR typing technique for identification of Escherichia coli clone ST131 producing CTX-M-15.

Journal of clinical microbiology - 1 Apr 2009

Pitout Johann D D, Campbell Lorraine, Church Deirdre L, Wang Pauline W, Guttman David S, Gregson Daniel B

Abstract excerpt

A study was designed to evaluate the ability of the DiversiLab fingerprinting kit, a type of repetitive element PCR (rep-PCR), to identify Escherichia coli clone ST131 producing beta-lactamase CTX-M-15. A set of 53 nonduplicate isolates of extended-spectrum beta-lactamase-producing E. coli underw...

Read the complete abstract on PubMed

Topics

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

Share to Automation
Share to Bacterial Typing Techniques
Share to beta-Lactamases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cluster Analysis

Share to DNA, Bacterial

Share to DNA Fingerprinting

Share to Electrophoresis, Gel, Pulsed-Field

Share to Escherichia coli Infections

Source

Open in PubMed Open full text

Identifiers

PMID: 19204095
DOI: 10.1128/JCM.02265-08
PMCID: PMC2668328

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19204095-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Using a commercial DiversiLab semiautomated repetitive sequence-based PCR typing technique for identification of Escherichia coli clone ST131 producing CTX-M-15.PMID 19204095Read ↗

The epidemic of extended-spectrum-β-lactamase-producing Escherichia coli ST131 is driven by a single highly pathogenic subclone, H30-Rx.Semantic proximity Read ↗

Escherichia coli sequence type ST131 as the major cause of serious multidrug-resistant E. coli infections in the United States.Semantic proximity Read ↗

Real-time PCR for detection of the O25b-ST131 clone of Escherichia coli and its CTX-M-15-like extended-spectrum beta-lactamases.Semantic proximity Read ↗

Prevalence of O25b-ST131 clone among Escherichia coli strains producing CTX-M-15, CTX-M-14 and CTX-M-92 β-lactamases.Semantic proximity Read ↗

First Report of Prevalence of CTX-M-15-Producing Escherichia coli O25b/ST131 from Iran.Semantic proximity Read ↗

Detection of O25b-ST131 clone, CTX-M-1 and CTX-M-15 genes via real-time PCR in Escherichia coli strains in patients with UTIs obtained from a university hospital in IstanbulSemantic proximity Read ↗

Intercontinental emergence of Escherichia coli clone O25:H4-ST131 producing CTX-M-15.Semantic proximity Read ↗

Genotypic and phenotypic profiles of Escherichia coli isolates belonging to clinical sequence type 131 (ST131), clinical non-ST131, and fecal non-ST131 lineages from India.Semantic proximity Read ↗

Global dissemination of a multidrug resistant Escherichia coli clone.Semantic proximity Read ↗

Molecular Characteristics of Extended-Spectrum-β-Lactamase-Producing <i>Escherichia coli</i> Isolates Causing Bacteremia in the Calgary Health Region from 2000 to 2007: Emergence of Clone ST131 as a Cause of Community-Acquired InfectionsSemantic proximity Read ↗

Semi-automated rep-PCR for rapid differentiation of major clonal groups of Escherichia coli meningitis strains.Semantic proximity Read ↗

Turkey: a further country concerned by community-acquired Escherichia coli clone O25-ST131 producing CTX-M-15Semantic proximity Read ↗

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