Publications by authors named "E Tokarska-Pietrzak"

Article Synopsis
  • Isolation & Significance
  • : A rare antibiotic-resistant pathogen was isolated from a migratory mallard duck in central Europe, marking the first such finding in this species, which serves as a useful indicator for detecting pathogens and antibiotic resistance in the environment.
  • Genomic Analysis & Findings
  • : Advanced techniques like whole-genome sequencing and serosequencing revealed that this strain shares significant genetic similarities to those isolated from humans and food, highlighting possible transmission pathways.
  • Resistance & Pathogenicity
  • : The isolated strain contains 24 antibiotic resistance genes and six pathogenicity islands, indicating a potential risk to human health due to its virulence factors and genetic adaptations related to antibiotic resistance.
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The "One Health" approach increasingly demonstrates the global spread of pathogenic microorganisms and their antimicrobial resistance in the environment, both in animals and humans. subsp. is nowadays very often isolated from cold-blooded reptiles to a lesser extent from sheep, but unfortunately more and more often from humans.

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The bacterium Salmonella Uccle belongs to serotype O:54 in the Kauffmann'a-White scheme. Group O:54 is unique among the serogroups belonging to the genus Salmonella. Normally, the enzymes involved in the biosynthesis of the repeating units of somatic antigen are encoded by a set of genes, located in the region of the bacterial chromosome.

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Unlabelled: Phage typing carried out according to the well-defined schemes is still recommended as a standard, fast and inexpensive method for epidemiological investigations all over the world to control Salmonella infections. However, the method should be in the hands of well-trained staff. This means that it is generally limited to reference laboratories.

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The use of bacteriophages, instead of antibodies, in the ELISA-based detection of bacterial strains was tested. This procedure appeared to be efficient, and specific strains of Salmonella enterica and Escherichia coli could be detected. The sensitivity of the assay was about 10(5) bacterial cells/well (10(6)/ml), which is comparable with or outperforms other ELISA tests detecting intact bacterial cells without an enrichment step.

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