Evidence map›Paper›PMID 23483233›Full record

ArticleFrontiers in cellular and infection microbiology2013

Characterization of Shiga toxin-producing Escherichia coli O130:H11 and O178:H19 isolated from dairy cows.

Daniel Fernández, Alejandra Krüger, Rosana Polifroni, Ana V Bustamante, A Mariel Sanso, Analía I Etcheverría, Paula M A Lucchesi, Alberto E Parma, Nora L Padola

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Comparative genomics of Shiga toxin-producingFrontiers in veterinary science · 2025
    Article
  2. Detection and analysis of Shiga toxin producing and enteropathogenic Escherichia coli in cattle from Tierra del Fuego, Argentina.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2023
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Daniel FernándezLaboratorio de Inmunoquímica y Biotecnología, Facultad Ciencias Veterinarias, Centro de Investigaciones Veterinarias Tandil-Consejo Nacional de Investigaciones Científicas y Técnicas-Comisión de Investigaciones Científicas de la Provincia de Buenos Aires (CIVETAN-CONICET-CICPBA), Universidad Nacional del Centro de la Provincia de Buenos Aires Tandil, Argentina.
Alejandra Krüger
Rosana Polifroni
Ana V Bustamante
A Mariel Sanso
Analía I Etcheverría
Paula M A Lucchesi
Alberto E Parma
Nora L Padola
Universidad Nacional del Centro de la Provincia de Buenos Aires · ARConsejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Shiga toxin-producing E. coli (STEC) are isolated from human patients with bloody diarrhea, hemorrhagic colitis (HC), and hemolytic uremic syndrome (HUS). In the last years, the infections with non-O157 serotypes are increasing their frequency of association with human disease. STEC produce Shiga toxin (Stx) and other virulence factors that could contribute to human pathogenesis. Cattle are the main reservoir and the transmission to humans is through the consumption of undercooked meat, non-pasteurized dairy products, and vegetables or water contaminated with feces. We have previously determined that O130:H11 and O178:H19 serotypes were the most prevalent in dairy cows from Argentina. In the present study, 37 and 25 STEC isolates from dairy cows belonging to O130:H11 and O178:H19 serotypes, respectively, were characterized regarding to their cytotoxicity on Vero cells, stx subtypes, presence of sab and typing by multiple-locus variable-number tandem repeat analysis (MLVA). All strains demonstrated a cytotoxic effect, and in O130:H11 isolates, stx2EDL933 was the predominant subtype. In O178:H19 isolates the main stx2 subtype was stx2vha. The sab gene was detected in 65 and 24% of the isolates belonging to O130:H11 and O178:H19, respectively. Only one MLVA profile was identified among the O130:H11 isolates meanwhile 10 MLVA profiles were detected among the O178:H19 isolates which were grouped in two main clusters. In conclusion, our data show that O130:H11 and O178:H19 STEC isolates encode virulence factors associated with severe human disease and both serotypes should be considered for routinely testing. Our subtyping experiments showed that isolates could be distinguished based on the stx2 subtype and the presence/absence of sab gene, and for isolates belonging to O178:H19, also when the MLVA type was considered. However, MLVA subtyping of O130:H11 isolates will require the development of more specific markers.

Indexed as

AllelesAnimalsArgentinaCattleCell SurvivalChlorocebus aethiopsCluster AnalysisEscherichia coli InfectionsEscherichia coli ProteinsFemaleGenetic VariationGenotypeHumansMembrane Transport ProteinsSerotypingShiga-Toxigenic Escherichia coliEscherichia coli ProteinsMembrane Transport ProteinsSab protein, E coliShiga ToxinsVirulence Factorsdairy cattleMLVAShiga toxinSTEC

Identifiers

PMID23483233
PMCPMC3592196
OpenAlexW2106646376

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.