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    On the ecology of Acinetobacter baumannii – jet stream rider and opportunist by nature (2024)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Wilharm, Gottfried
    Skiebe, Evelyn
    Łopińska, Andżelina
    Higgins, Paul G.
    Weber, Kristin
    Schaudinn, Christoph
    Neugebauer, Christof
    Görlitz, Katharina
    Meimers, Gideon
    Rizova, Yana
    Blaschke, Ulrike
    Heider, Christine
    Cuny, Christiane
    Drewes, Stephan
    Heuser, Elisa
    Jeske, Kathrin
    Jacob, Jens
    Ulrich, Rainer G.
    Bochenski, Marcin
    Kasprzak, Mariusz
    Burda, Ewa
    Ciepliński, Mateusz
    Kaługa, Ireneusz
    Jankowiak, Łukasz
    Aguirre, José I.
    López-García, Alejandro
    Höfle, Ursula
    Jagiello, Zuzanna
    Tobółka, Marcin
    Janic, Bartosz
    Zieliński, Piotr
    Kamiński, Maciej
    Frisch, Johannes
    Siekiera, Joachim
    Wendel, Andreas F.
    Brauner, Paul
    Jäckel, Udo
    Kaatz, Michael
    Müller, Stefanie (WE 7)
    Lübke-Becker, Antina (WE 7)
    Wieler, Lothar H (WE 7)
    von Wachsmann, Johanna
    Thrukonda, Lakshmipriya
    Helal, Mustafa
    Epping, Lennard
    Wolf, Silver A.
    Semmler, Torsten
    Jerzak, Leszek
    Quelle
    bioRxiv beta : the preprint server for biology
    Bandzählung: PrePrint!
    Seiten: 1 – 55
    ISSN: 2692-8205
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://www.biorxiv.org/content/10.1101/2024.01.15.572815v1
    DOI: 10.1101/2024.01.15.572815
    Kontakt
    Institut für Mikrobiologie und Tierseuchen

    Robert-von-Ostertag-Str. 7-13
    14163 Berlin
    +49 30 838 51843 / 66949
    mikrobiologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    The natural reservoirs of the nosocomial pathogen Acinetobacter baumannii are not well defined. We previously identified white storks as a model system to study the ecology of A. baumannii. Having screened more than 1,300 white stork nestlings over a period of six years across different regions of Poland and Germany (overall isolation rate of ∼29.5%), including food chain analyses and environmental samplings, we come up with a detailed picture of the dynamics and diversity of A. baumannii in their natural habitats. Adult storks, rather than being stably colonized with strains of A. baumannii which are successively transferred to their offspring, instead initially encounter these bacteria while foraging. Among their common food sources, consisting of earthworms, small mammals, and insects, we identified earthworms as a potential source of A. baumannii, but more so the associated soil as well as plant roots. Through this, hotspot soil and compost habitats were identified which enable population dynamics to be studied over the course of the year. We demonstrate that sterilized plant material is rapidly colonized by airborne A. baumannii suggesting they patrol to search for novel habitats, being opportunist by nature. The prevalence of A. baumannii exhibited a strong seasonality and peaked during summer. The strains we collected in Poland and Germany represent more than 50% of the worldwide known diversity in terms of the intrinsic OXA-51-like β-lactamase. A set of ∼400 genomes was determined and compared to a diverse set of publicly available genomes. Our pan-genome estimate of the species (∼51,000 unique genes) more than doubles the amount proposed by previous studies. Core-genome based phylogenetic analyses illustrated numerous links between wildlife isolates and hospital strains, including ancient as well as recent intercontinental transfer. Our data further suggest massive radiation within the species early after its emergence, matching with human activity during the Neolithic. Deforestation in particular seemed to set the stage for this bloom as we found that forests do not provide conducive conditions for the proliferation of A. baumannii. In contrast, wet and nutrient-rich soil alongside rivers sampled during the summer can yield an isolation rate of ∼30%. Linking published work on the interaction between A. baumannii and fungi and on aspergillosis as a major cause of mortality in white stork nestlings to our findings, we hypothesized that fungi and A. baumannii share a long history of coevolution. Interaction studies revealed the capability of A. baumannii to adhere to fungal spores and to suppress spore germination. Taken together, the intrinsic resistance endowment and potential to acquire antibiotic resistance can be explained by coevolution with antibiotic-producing fungi and other microorganisms within soil, and resistance to desiccation stress and radiation can be interpreted in the light of intercontinental hitchhiking through fungal spores.