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Projekt Druckansicht

Phänotypische Heterogenität und Populationsdynamik in Biofilmen

Antragstellerin Professorin Dr. Erika Kothe, seit 7/2017
Fachliche Zuordnung Mikrobielle Ökologie und Angewandte Mikrobiologie
Stoffwechselphysiologie, Biochemie und Genetik der Mikroorganismen
Förderung Förderung von 2015 bis 2019
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 276408659
 
Erstellungsjahr 2019

Zusammenfassung der Projektergebnisse

The aim of the SPP was to characterize phenotypic heterogeneity and sociobiology of bacterial populations. Our project fully followed these aims and explored phenotypic heterogeneity and sociobiology of B. subtilis biofilms. While B. subtilis has become a widely studied model for the biofilm development field in the last decades, the social and experimental evolution aspects have been mainly explored within this DFG-funded project. The project was initiated by summarizing the knowledge on experimental evolution of laboratory biofilms, on bacterial differentiation and on the functions of biofilm matrix. This project has revealed how genetic division of labor benefits biofilm establishment, while being sensitive to evolution of individuality in a longer time scale. Interestingly, the benefit from genetic division of labor (i.e. the separation of matrix production to genetically distinct cells) surpasses the advantage resulted from phenotypic heterogeneity in expression of biofilm matrix components. The project discovered genetic differentiation in experimentally evolved biofilm populations of B. subtilis and demonstrated that such genetic differentiation promotes higher productivity of biofilms. To explore the influence of phenotypic heterogeneity on sociobiology of biofilms, this project described how temporal and spatial heterogeneity of matrix production determines biofilm robustness. The project also examined the ability of cheaters to exploit the biofilm matrix. While mutants lacking both matrix components could not incorporate into the biofilm produced by the wild type biofilms, their abundance was influenced by de novo competition explained through bacteriophages. In contrast, mutant strains that lacked only one of the matrix components could incorporate into the biofilm produced by the wild type cells and shift phenotypic heterogeneity in these matrix producing cells. The project promoted collaborations with numerous researchers providing different expertise, including theoretical modeling biofilm imaging, biofilm biophysics, protein biophysics, genomics, electron microscopy, and evolution. Finally, the obtained results were summarized in a review publication within the SPP special issue.

Projektbezogene Publikationen (Auswahl)

 
 

Zusatzinformationen

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