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    Has Epizootic Become Enzootic? Evidence for a Fundamental Change in the Infection Dynamics of Highly Pathogenic Avian Influenza in Europe, 2021

    mBio

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    mbio.00609-22.pdf (1.014MB)
    Data
    2022
    Autor
    Pohlmann, Anne
    King, Jacqueline
    Fusaro, Alice
    Zecchin, Bianca
    Banyard, Ashley C.
    Brown, Ian H.
    Byrne, Alexander M. P.
    Beerens, Nancy
    Liang, Yuan
    Heutink, Rene
    Harders, Frank
    James, Joe
    Reid, Scott M.
    Hansen, Rowena D. E.
    Lewis, Nicola S.
    Hjulsager, Charlotte
    Larsen, Lars E.
    Zohari, Siamak
    Anderson, Kristofer
    Bröjer, Caroline
    Nagy, Alexander
    SavIc, Vladimir
    van Borm, Steven
    Steensels, Mieke
    Briand, Francois-Xavier
    Święton, Edyta
    Śmietanka, Krzysztof
    Grund, Christian
    Beer, Martin
    Harder, Timm
    Metadane
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    Streszczenie
    This study presents a multi-compound method for the determination of 20 pharmacologically active dyes from 5 different chemical classes in environmental water samples. These compounds, including triphenylmethane dyes (malachite green, crystal violet, brilliant green, ethyl violet, methyl violet 2B, pararosaniline, victoria blue B, victoria blue R, victoria pure blue BO), phenothiazine dyes (methylene blue, azure A, azure B, azure C, new methylene blue, thionine), phenoxazine dye (nile blue A), acridine dyes (acriflavine, proflavine) and xanthene dyes (rhodamine B, rhodamine 6G) constitute pharmacologically active substances (PASs). For the optimisation of sample preparation, different solid-phase extraction (SPE) sorbents and a wide range of pH (from 2 to 12) of water samples were tested. Finally, water samples were preconcentrated and cleaned up on diol SPE cartridges. Extracts were analysed by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) operating in the positive electrospray ionisation (ESI+) mode. The chromatographic separation of the 20 pharmacologically active dyes was achieved within 5 min by using a pentafluorophenyl (F5) analytical column and mobile phases of ammonium acetate buffer (0.05 M, pH = 3.5) and acetonitrile with gradient elution. The developed method was validated proving to be suitable for the determination of all tested compounds. Limits of quantification were 0.01–0.1 μg/l, are sensitive enough to quantify very low concentration levels of the dyes in environmental water samples. The obtained recovery values for all tested analytes were between 71.2 and 104.9% with a good RSD, less than 14 % at all fortification levels. The application of the developed method to water samples allows the detection of dyes such as crystal violet, rhodamine B, and methyl violet in two wastewater samples in concentration ran ge from 0.017 to 0.0043 μg/l).
    URI
    https://journals.asm.org/doi/epub/10.1128/mbio.00609-22
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    DSpace software copyright © 2002-2016  DuraSpace
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