Acinetobacter baumannii’s lifestyle includes soil-dwelling colonization of decaying plant material and airborne spread
Loading...
Official URL
Full text at PDC
Publication date
2026
Advisors (or tutors)
Editors
Journal Title
Journal ISSN
Volume Title
Publisher
Springer Nature
Citation
Wilharm, G., Skiebe, E., Michalska, A., Higgins, P. G., Weber, K., Schaudinn, C., Neugebauer, C., Görlitz, K., Meimers, G., Rizova, Y., Blaschke, U., Heider, C., Cuny, C., Drewes, S., Heuser, E., Jeske, K., Jacob, J., Ulrich, R. G., Bocheński, M., et al. (2026). Acinetobacter baumannii’s lifestyle includes soil-dwelling colonization of decaying plant material and airborne spread. Nature Communications , 17(1). https://doi.org/10.1038/S41467-026-70072-4
Abstract
Acinetobacter baumannii is a Gram-negative nosocomial pathogen that is notorious for its rapid development of antibiotic resistance. However, its ecology and evolution outside hospital settings remain poorly defined. Here, we demonstrate that the natural lifestyle of A. baumannii includes soil-dwelling and airborne dissemination, which helps explaining its adaptability and tolerance to desiccation, radiation and antibiotics, and thus its predisposition to establish within hospitals. Starting from white stork nestlings previously discovered as a reservoir, we studied food chains and associated environments and identified soil and decaying plants as habitats. We demonstrate that sterilized plant material is rapidly colonized by airborne A. baumannii. A set of 401 genomes were sequenced and compared to publicly available genomes, revealing numerous links between wildlife isolates and hospital strains, and disclosing intercontinental dispersal. Our pan-genome estimate of the species (~51,000 gene families) more than doubles that of previous studies. Our data further suggest massive radiation of the species early after its emergence, possibly fostered by human activity since the Neolithic. Now, it is possible to study the ecology and evolution of A. baumannii in nature at an unprecedented temporal and spatial resolution and to elucidate the adaptive evolution of environmental bacteria towards multidrug-resistant opportunistic pathogens.
Description
We thank colleagues at the central DNA sequencing lab of the Robert Koch Institute for technical assistance. G.W. & P.G.H. acknowledge financial support from the Deutsche Forschungsgemeinschaft (DFG-FOR 2251). A.M. acknowledges financial support from a traineeship within the ERASMUS+ Program (agreement no. 20/ SMP/2015/16). The collection of rats was funded by Deutsches Zentrum für Infektionsforschung (DZIF), thematic translational Unit (TTU) “Emerging Infections” to R.G.U.; the collection of other rodents was commissioned and funded by the Federal Environment Agency (UBA) within the Environment Research Plan of the German Federal Ministry for the Environment, Nature Conservation, Building and Nuclear Safety (J.J., grant numbers 3716484310 and 3714674070). This publication made use of the Acinetobacter baumannii MLST website (http://pubmlst.org/abaumannii/) hosted at the University of Oxford144. The development of this site has been funded by the Wellcome Trust. Open Access funding enabled and organized by Projekt DEAL.







