Evidence map›Paper›PMID 31477105›Full record

ArticleBMC veterinary research2019

Comparison of the phylogenetic analysis of PFGE profiles and the characteristic of virulence genes in clinical and reptile associated Salmonella strains.

Bartłomiej Dudek, Marta Książczyk, Eva Krzyżewska, Klaudia Rogala, Maciej Kuczkowski, Anna Woźniak-Biel, Kamila Korzekwa, Agnieszka Korzeniowska-Kowal, Radosław Ratajszczak, Alina Wieliczko and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  7. The vertical transmission ofOne health (Amsterdam, Netherlands) · 2023
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  8. Molecular Characterization ofAnimals : an open access journal from MDPI · 2022
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  9. Comparison of Virulence Patterns BetweenFrontiers in veterinary science · 2022
    Article
  10. Article
  11. Microorganisms · 2021
    Article
  12. Subtyping β-lactamase-producingIranian journal of basic medical sciences · 2021
    Article
  13. Zoonotic potential and prevalence ofInfection ecology & epidemiology · 2021
    Review
  14. Article
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

12 authors at 4 institutions in 1 country.

Bartłomiej DudekDepartment of Microbiology, Faculty of Biological Sciences, University of Wrocław, 51-148, Wrocław, Poland.
Marta KsiążczykDepartment of Microbiology, Faculty of Biological Sciences, University of Wrocław, 51-148, Wrocław, Poland.
Eva KrzyżewskaDepartment of Immunology of Infectious Diseases, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 53-114, Wrocław, Poland.
Klaudia RogalaDepartment of Immunology of Infectious Diseases, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 53-114, Wrocław, Poland.
Maciej KuczkowskiDepartment of Epizootiology and Clinic of Birds and Exotic Animals, Wrocław University of Environmental and Life Sciences, 50-366, Wrocław, Poland.
Anna Woźniak-BielDepartment of Epizootiology and Clinic of Birds and Exotic Animals, Wrocław University of Environmental and Life Sciences, 50-366, Wrocław, Poland.
Kamila KorzekwaDepartment of Microbiology, Faculty of Biological Sciences, University of Wrocław, 51-148, Wrocław, Poland.
Agnieszka Korzeniowska-KowalDepartment of Immunology of Infectious Diseases, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 53-114, Wrocław, Poland.
Radosław RatajszczakWrocław ZOO, 51-618, Wrocław, Poland.
Alina WieliczkoDepartment of Epizootiology and Clinic of Birds and Exotic Animals, Wrocław University of Environmental and Life Sciences, 50-366, Wrocław, Poland.
Jacek RybkaDepartment of Immunology of Infectious Diseases, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 53-114, Wrocław, Poland.
Gabriela Bugla-PłoskońskaDepartment of Microbiology, Faculty of Biological Sciences, University of Wrocław, 51-148, Wrocław, Poland. gabriela.bugla-ploskonska@uwr.edu.pl.ORCID http://orcid.org/0000-0002-1222-201X
Ludwik Hirszfeld Institute of Immunology and Experimental Therapy · PLUniversity of Wrocław · PLWrocław University of Environmental and Life Sciences · PLWrocław Zoo · PL

Funding

Narodowe Centrum Nauki DEC-2013/11/N/NZ9/00069
6 · The paper itself

Abstract

backgroundSalmonella is generally considered as a human pathogen causing typhoid fever and gastrointestinal infections called salmonellosis, with S. Enteritidis and S. Typhimurium strains as the main causative agents. Salmonella enterica strains have a wide host array including humans, birds, pigs, horses, dogs, cats, reptiles, amphibians and insects. Up to 90% of reptiles are the carriers of one or more serovars of Salmonella. Extraintestinal bacterial infections associated with reptiles pose serious health threat to humans. The import of exotic species of reptiles as pet animals to Europe correlates with the emergence of Salmonella serotypes, which not found previously in European countries. The presented study is a new report about Salmonella serotypes associated with exotic reptiles in Poland. The goal of this research was to examine the zoonotic potential of Salmonella strains isolated from reptiles by comparative analysis with S. Enteritidis strains occurring in human population and causing salmonellosis.

resultsThe main findings of our work show that exotic reptiles are asymptomatic carriers of Salmonella serovars other than correlated with salmonellosis in humans (S. Enteritidis, S. Typhimurium). Among the isolated Salmonella strains we identified serovars that have not been reported earlier in Poland, for example belonging to subspecies diarizonae and salamae. Restriction analysis with Pulsed-field Gel Electrophoresis (PFGE), showed a great diversity among Salmonella strains isolated from reptiles. Almost all tested strains had distinct restriction patterns. While S. Enteritidis strains were quite homogeneous in term of phylogenetic relations. Most of the tested VGs were common for the two tested groups of Salmonella strains.

conclusionsThe obtained results show that Salmonella strains isolated from reptiles share most of virulence genes with the S. Enteritidis strains and exhibit a greater phylogenetic diversity than the tested S. Enteritidis population.

Indexed as

Electrophoresis, Gel, Pulsed-FieldAnimalsCarrier StateChromatography, GasDNA, BacterialGenotypeHumansReptilesSalmonella entericaSalmonella InfectionsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTandem Mass SpectrometryVirulenceZoonosesDNA, BacterialPFGE profilesRASSalmonellaZoonotic potential

Identifiers

PMID31477105
PMCPMC6721270
OpenAlexW2970972084

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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.