Evidence map›Paper›PMID 20581183›Full record

ArticleApplied and environmental microbiology2010

Rapid microarray-based genotyping of enterohemorrhagic Escherichia coli serotype O156:H25/H-/Hnt isolates from cattle and clonal relationship analysis.

Lutz Geue, Susann Schares, Birgit Mintel, Franz J Conraths, Elke Müller, Ralf Ehricht

Abstract read
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Article in Applied and environmental microbiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

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28citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

28 citing papers in PubMed.

  1. Article
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  3. Presence of β-Lactamase-producing Enterobacterales andInternational journal of molecular sciences · 2021
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  10. Variability in CharacterizingMicroorganisms · 2018
    Article
  11. Genetic makeup of Shiga toxin-producing Escherichia coli in relation to clinical symptoms and duration of shedding: a microarray analysis of isolates from Swedish children.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2017
    Article
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Lutz GeueFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Epidemiology, Seestrasse 55, Wusterhausen, Germany. lutz.geue@fli.bund.de
Susann Schares
Birgit Mintel
Franz J Conraths
Elke Müller
Ralf Ehricht

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since enterohemorrhagic Escherichia coli (EHEC) isolates of serogroup O156 have been obtained from human diarrhea patients and asymptomatic carriers, we studied cattle as a potential reservoir for these bacteria. E. coli isolates serotyped by agglutination as O156:H25/H-/Hnt strains (n = 32) were isolated from three cattle farms during a period of 21 months and characterized by rapid microarray-based genotyping. The serotyping by agglutination of the O156 isolates was not confirmed in some cases by the results of DNA-based serotyping as only 25 of the 32 isolates were conclusively identified as O156:H25. In the multilocus sequence typing (MLST) analysis, all EHEC O156:H25 isolates were characterized as sequence type 300 (ST300) and ST688, which differ by a single-nucleotide exchange in the purA gene. Oligonucleotide microarrays allow simultaneous detection of a wider range of EHEC-associated and other E. coli virulence markers than other methods. All O156:H25 isolates showed a wide spectrum of virulence factors typical for EHEC. The stx(1) genes combined with the EHEC hlyA (hlyA(EHEC)) gene, the eae gene of the zeta subtype, as well as numerous other virulence markers were present in all EHEC O156:H25 strains. The behavior of eight different cluster groups, including four that were EHEC O156:H25, was monitored in space and time. Variations in the O156 cluster groups were detected. The results of the cluster analysis suggest that some O156:H25 strains had the genetic potential for a long persistence in the host and on the farm, while other strains did not. As judged by their pattern of virulence markers, E. coli O156:H25 isolates of bovine origin may represent a considerable risk for human infection. Our results showed that the miniaturized E. coli oligonucleotide arrays are an excellent tool for the rapid detection of a large number of virulence markers.

Indexed as

Bacterial Typing TechniquesMicroarray AnalysisAnimalsCattleCattle DiseasesCluster AnalysisDNA, BacterialEnterohemorrhagic Escherichia coliEscherichia coli InfectionsEscherichia coli ProteinsGenotypeMolecular Sequence DataSequence Analysis, DNASerotypingVirulence FactorsDNA, BacterialEscherichia coli ProteinsVirulence Factors

Identifiers

PMID20581183
PMCPMC2918981

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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.