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.2023 Jan 20;18(1):e0280810.
doi: 10.1371/journal.pone.0280810. eCollection 2023.

A comprehensive analysis of chemical and biological pollutants (natural and anthropogenic origin) of soil and dandelion (Taraxacum officinale) samples

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A comprehensive analysis of chemical and biological pollutants (natural and anthropogenic origin) of soil and dandelion (Taraxacum officinale) samples

Mieczysława Irena Boguś et al. PLoS One..

Abstract

A range of analytical methods (GC-MS, LC-MS, voltammetry, microbiological and microscopic techniques, PCR) was used to assay a range of potential chemical and biological contaminants in soil and dandelion samples. The results provide the first comprehensive safety analysis of dandelion as a herbal product. Samples were collected from three different sites in Poland where the local population collects dandelion plants for their own consumption: Rudenka (a mountain meadow in the European Ecological Network of Natura 2000 protection area, free of agrotechnical treatments for over 30 years), Warszawa 1 (dense single-family housing with heavy traffic), and Warszawa 2 (recreation area with heavy traffic near a coal-fired heat and power plant). The assays of heavy metals and other chemical pollutants (PAHs, PCBs, dioxins, pesticides, mycotoxins) confirm that all collected soil and dandelion samples were chemically pure; however, 95 species of pathogenic bacteria were detected, including "carnivorous" Vibrio vulnificus, zoonotic Pasteurella pneumotropica, Pasteurella canis, Staphylococcus pseudintermedius, Staphylococcus lentus and Francisella tularensis as well as 14 species of pathogenic fungi and one protozoan parasite (Giardia intestinalis). The discovery of septicemia agents V. vulnificus, Fusobacterium mortiferum and Rahnella aquatilis in the soil surrounding dandelion roots and in the flowers, G. intestinalis in dandelion leaves and roots samples, all collected in Warsaw, is highly disturbing. This finding underlines the need for increased caution when collecting dandelion in densely populated areas with a large population of pets. Thorough washing of the harvested plants is necessary before using them for consumption, especially in the case of making salads from fresh dandelion leaves, which is becoming increasingly popular among people leading healthy and an environmentally friendly lifestyle.

Copyright: © 2023 Boguś et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Heavy metal detection inTaraxacum officinale flowers collected in Warszawa 2.
(A) Co and Ni determined by adsorptive cathodic stripping voltammetry (AdCSV) at hanging mercury dropping electrode (HMDE); (B) Tl determined by anodic stripping voltammetry (ASV) at hanging mercury dropping electrode (HMDE); (C) Zn, Cd, Pb and Cu determined by anodic stripping voltammetry (ASV) at hanging mercury dropping electrode (HMDE).
Fig 2
Fig 2. The total ion current (TIC) chromatograms of: (A) PAH standards, (B) PCB standards, (C) dioxins’ standards, (D) pesticide standards, (E) soil sample collected in Rudenka.
List of standards used, their retention times (RT) and limits of detection (LOD) is presented in S1 Table.
Fig 3
Fig 3. Examples of pathogenic bacteria detected inTaraxacum officinale and soil samples.
Scale bars: 10 μm.
Fig 4
Fig 4. Fungi detected inTaraxacum officinale and soil samples.
(A) macroscopic view of fungal colony, (B) microscopic image of the fungus. Scale bars: 20 μm.
Fig 5
Fig 5. Detection of parasites’ DNA inTaraxacum officinale samples.
(A) Helminth Test, 1—H2O, 2—dried dandelion leaves (Rudenka), 3—Oxyuridae sp. (eggs), 4—Echinococcus sp. (adult), 5—Taenia sp. (eggs), 6—Trichuris sp. (eggs), 7—Fasciola hepatica (adult), 8—Toxocara cati (adult); (B) Helminth Test, M—Marker DNA, 1- dried dandelion leaves (Warszawa 1), 2—dried dandelion leaves (Warszawa 2), 3—dried dandelion flowers (Warszawa 2), 6—Echinococcus sp. (adult), 7—Toxocara cati (adult), 8—Dipylidium caninum (adult), 9—Fasciola hepatica (adult), 10—Taenia taeniaeformis (eggs), 11—Toxocara canis (eggs), 12—Oxyuridae sp. (eggs), 13—H2O; (C) Giardia Test, 1—H2O, M—Marker DNA, 2—dried dandelion leaves (Warszawa 2), 3—dried dandelion flowers (Warszawa 2), 4—dried dandelion leaves (Rudenka), 5—dried dandelion flowers (Rudenka). DNA marker—100 bp DNA Ladder (Novazym).
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References

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This work was supported by the Marshal’s Office of the Mazowieckie Voivodeship grant RPMA.01.02.00-14-5626/16 to the Biomibo company and by the National Science Center grant 2020/39/O/NZ6/00447 to MIB. There was no additional external funding received for this study. Biomibo covered the cost of the salaries of its employees (MIB, AC-G, LS, EM), provided support in the purchase of chemicals, and made laboratory equipment available for all authors. The specific roles of the authors are articulated in the ‘author contributions’ section. The funders had no role in study design, data collection, analysis and interpretation, decision to publish, or preparation of the manuscript. For the purpose of Open Access, the authors haves applied a CC-BY public copyright license to any Author Accepted Manuscript (AAM) version arising from this submission.

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