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Hansen, M. F.

Publications and source records attributed to Hansen, M. F..

4 recordsLinked to original sources

Biofilm compactness and spatial community composition determine bacterial phage-susceptibility

Bacteriophages (phages) are viruses that infect bacteria, often posing a threat to their survival. In recent years, research has shifted from studying bacteria-phage interactions in homogeneous, well-mixed environments to investigating more complex heterogeneous, structured communities, thereby more accurately reflecting bacterial life in natural and disease-associated settings. So far, these studies predominantly tested interactions of phages and single-species biofilms, despite the dominance of highly diverse biofilm communities in nature. Here, we investigated how different lytic phages spread in and infect a synthetic community composed of Escherichia coli, Kluyvera cryocrescens, and Vibrio anguillarum. We found that E. coli was protected from eradication by the T7-coliphage when embedded in a multispecies biofilm and covered by the two other species, where the V. anguillarum biofilm matrix was essential for protection of E. coli. The protective nature of the V. anguillarum matrix also ensured survival of K. cryocrescens exposed to the lytic kluyveraphage Lyn. V. anguillarum mutants lacking the matrix synthesis genes vpsMNOP or rbmC failed to protect E. coli despite forming biofilms. Labelling of phages indicated that these were not trapped in the matrix of the wildtype. Instead, advanced image analysis revealed that the mutants displayed biofilms with lower cell density, resulting in the E. coli clusters being less tightly surrounded by V. anguillarum cells, which opened gaps for phage entry. These findings highlight that community context and matrix composition play a major role in phage-bacteria dynamics.

microbiology↗

Reconciling the importance of minerals for propagation of antibiotic resistance genes in the environment

The role of mineral surfaces in environmental processes, particularly their influence on DNA preservation, biofilm formation, and genetic transfer, has garnered attention due to its implications for the spread of antibiotic resistance genes (ARg). Despite the recognized significance of mineral-mediated DNA transfer, this mechanism remains poorly understood. Here we investigate the intricate interplay between soil minerals, bacteria, and DNA, to better understand the mechanisms driving ARg propagation in natural environments. We here study the uptake of mineral adsorbed DNA into the natural competent bacteria b. subtilis and further explore the influence of minerals on the viability and subsequent biofilm formation of both b. subtilis and A. baylyi. We further adsorbed DNA to mineral surfaces and allowed biofilm formation while monitoring the propagation of the ARg through out the biofilms. All the results are set in context of mineral surface properties such as surface charge, charge densities and surface area. Our results showed that the surface properties of the mineral surfaces are highly influencing the transformation efficiencies, viability and biofilm formation where in particular a high number of positive charged surface sites enhance biofilm formation and viability and inhibit transformation. The influence of the mineral surfaces diminishes as the biofilm develops and propagation of mineral adsorbed ARg are seen widely across the mineral surfaces. Our results have implication for mitigations strategies and reconcile mineral surfaces as hot spots for the propagation of antibiotic resistance-which indeed can be driven by transformation in the absence of bacteria carrying the traits. In principle all it takes is one successful transfer event from a mineral adsorbed ARg.

microbiology↗

Fundamentals of biofilm formation in soil: From functionalized self-assembled monolayers to rewilding

Surface energy and surface charges play crucial roles in bacterial adhesion and biofilm formation, however the mechanisms underlying the bacteria-surface interaction, particularly on the formation of soil biofilms, remain unclear. In spite of considering the spatiotemporal dynamics of biofilm formation on different soil surfaces, we compared the impact of four different substrates on bacterial attachment and biofilm formation. The substrates were constituted of gold layer covered by NH2+, CH3, COO- and OH-terminated self-assembled monolayers (SAMS). Two soil habitat bacteria with different Gram barriers, Bacillus subtilis and Acinetobacter baylyi, were grown with incubation times of 6-72 h on each type of surfaces. Bacterial attachment and biofilm formation was assessed using metabolic activity of the cells adhered to the surfaces. The spatial distribution of adhere bacteria was visualized by scanning electron microscopy and confocal laser scanning microscopy. We also investigated whether the surface impacts the biofilm matrix composition. A general view of our results suggests a major influence of the surface chemistry on bacterial potential to form biofilms. The hydrophobic or positively charged substrates attract bacteria while a lack of attachment and biofilm formation on hydrophilic and negatively charged surfaces. This work points out the potential of surface treatments in the environment where it is intended to either repel or attract bacteria.

microbiology↗

Alanine cross-feeding determines Escherichia coli colony growth dynamics

Bacteria commonly live in spatially structured biofilm assemblages, which are encased by an extracellular matrix. Metabolic activity of the cells inside biofilms causes gradients in local environmental conditions, which leads to the emergence of physiologically differentiated subpopulations. Information about the properties and spatial arrangement of such metabolic subpopulations, as well as their interaction strength and interaction length scales are lacking, even for model systems like Escherichia coli colony biofilms grown on agar-solidified media. Here, we use an unbiased approach, based on temporal and spatial transcriptome and metabolome data acquired during E. coli colony biofilm growth, to study the spatial organization of metabolism. We discovered that alanine displays a unique pattern among amino acids and that alanine metabolism is spatially and temporally heterogeneous. At the anoxic base of the colony, where carbon and nitrogen sources are abundant, cells secrete alanine via the transporter AlaE. In contrast, cells utilize alanine as a carbon and nitrogen source in the oxic nutrient-deprived region at the colony mid-height, via the enzymes DadA and DadX. This spatially structured alanine cross-feeding influences cellular viability and growth in the cross-feeding-dependent region, which shapes the overall colony morphology. More generally, our results on this precisely controllable biofilm model system demonstrate a remarkable spatiotemporal complexity of metabolism in biofilms. A better characterization of the spatiotemporal metabolic heterogeneities and dependencies is essential for understanding the physiology, architecture, and function of biofilms.

microbiology↗