TY - JOUR A1 - Schreiber, Frank A1 - Zimmermann, M. A1 - Escrig, S. A1 - Lavik, G. A1 - Kuypers, M.M.M. A1 - Meibom, A. A1 - Ackermann, M. T1 - Substrate and electron donor limitation induce phenotypic heterogeneity in different metabolic activities in a green sulphur bacterium JF - Environmental Microbiology Reports N2 - Populations of genetically identical cells can display marked variation in phenotypic traits; such variation is termed phenotypic heterogeneity. Here, we investigate the effect of substrate and electron donor limitation on phenotypic heterogeneity in N2 and CO2 fixation in the green sulphur bacterium Chlorobium phaeobacteroides. We grew populations in chemostats and batch cultures and used stable isotope labelling combined with nanometer‐scale secondary ion mass spectrometry (NanoSIMS) to quantify phenotypic heterogeneity. Experiments in H2S (i.e. electron donor) limited chemostats show that varying levels of NH4+ limitation induce heterogeneity in N2 fixation. Comparison of phenotypic heterogeneity between chemostats and batch (unlimited for H2S) populations indicates that electron donor limitation drives heterogeneity in N2 and CO2 fixation. Our results demonstrate that phenotypic heterogeneity in a certain metabolic activity can be driven by different modes of limitation and that heterogeneity can emerge in different metabolic processes upon the same mode of limitation. In conclusion, our data suggest that limitation is a general driver of phenotypic heterogeneity in microbial populations. KW - NanoSIMS KW - Phenotypic heterogeneity PY - 2018 UR - https://onlinelibrary.wiley.com/doi/abs/10.1111/1758-2229.12616 DO - https://doi.org/10.1111/1758-2229.12616 SN - 1758-2229 VL - 10 IS - 2 SP - 179 EP - 183 PB - John Wiley & Sons Ltd AN - OPUS4-44596 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schreiber, Frank T1 - Phenotypic diversity in microbial metabolism and antimicrobial resistance N2 - Most microorganisms live in environments where nutrients are limited and fluctuate over time. Cells respond to nutrient fluctuations by sensing and adapting their physiological state. Recent studies suggest phenotypic heterogeneity in isogenic populations as an alternative strategy in fluctuating environments, where a subpopulation of cells express a function that allows growth under conditions that might arise in the future. It is unknown how environmental factors such as nutrient limitation shape phenotypic heterogeneity in metabolism and whether this allows cells to respond to nutrient fluctuations. Here, we show that substrate limitation increases phenotypic heterogeneity in metabolism, and this heterogeneity allows cells to cope with substrate fluctuations. We subjected the N2-fixing bacterium Klebsiella oxytoca to different levels of substrate limitation and substrate shifts, and obtained time-resolved single-cell measurements of metabolic activities using nanometre-scale secondary ion mass spectrometry (NanoSIMS). We found that the level of NH4+ limitation shapes phenotypic heterogeneity in N2 fixation. In turn, the N2 fixation rate of single cells during NH4+ limitation correlates positively with their growth rate after a shift to NH4+ depletion, experimentally demonstrating the benefit of heterogeneity. The results indicate that phenotypic heterogeneity is a general solution to two important ecological challenges - nutrient limitation and fluctuations - that many microorganisms face. Currently, we use NanoSIMS to develop a new approach that defines functionally-relevant, phenotypic biodiversity in microbial systems. In the last part of my presentation, I will highlight why the concept of phenotypic diversity is relevant for the understanding of antimicrobial resistance. T2 - Berlin Seminar for Resistance Research at FU Berlin Veterinary Medicine CY - Berlin, Germany DA - 01.03.2018 KW - Antimicrobial Resistance KW - Metabolism KW - Phenotypic diversity PY - 2018 AN - OPUS4-44597 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Marchant, H. K. A1 - Tegetmeyer, H. E. A1 - Ahmerkamp, S. A1 - Holtappels, M. A1 - Lavik, G. A1 - Graf, J. A1 - Schreiber, Frank A1 - Mussmann, M. A1 - Strous, M. A1 - Kuypers, M. M. M. T1 - Metabolic specialization of denitrifiers in permeable sediments controls N2O emissions JF - Environmental Microbiology N2 - Coastal oceans receive large amounts of anthropogenic fixed nitrogen (N), most of which is denitrified in the sediment before reaching the open ocean. Sandy sediments, which are common in coastal regions, seem to play an important role in catalysing this N‐loss. Permeable sediments are characterized by advective porewater transport, which supplies high fluxes of organic matter into the sediment, but also leads to fluctuations in oxygen and nitrate concentrations. Little is known about how the denitrifying communities in these sediments are adapted to such fluctuations. Our combined results indicate that denitrification in eutrophied sandy sediments from the world's largest tidal flat system, the Wadden Sea, is carried out by different groups of microorganisms. This segregation leads to the formation of N2O which is advectively transported to the overlying waters and thereby emitted to the atmosphere. At the same time, the production of N2O within the sediment supports a subset of Flavobacteriia which appear to be specialized on N2O reduction. If the mechanisms shown here are active in other coastal zones, then denitrification in eutrophied sandy sediments may substantially contribute to current marine N2O emissions. KW - Nitrous oxide KW - Denitrification KW - Cross-feeding PY - 2018 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-463061 UR - https://onlinelibrary.wiley.com/doi/full/10.1111/1462-2920.14385 DO - https://doi.org/10.1111/1462-2920.14385 SN - 1462-2920 SN - 1462-2912 VL - 20 IS - 12 SP - 4486 EP - 4502 PB - John Wiley & Sons Ltd AN - OPUS4-46306 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schreiber, Frank T1 - Phenotypic diversity in microbial metabolism and antimicrobial resistance N2 - Phenotypic dicersty can emerge in microbial metabolic activties and in persistence against antimicrobials. In this talk, I present two examples of phenotypic heterogeneity and discuss how they might be related. T2 - Workshop on Bacterial adaptation to antimicrobials: environmental, evolutionary and mechanistic aspects CY - FU Berlin, Germany DA - 17.04.2018 KW - Antimicrobial resistance KW - Metabolism KW - Phenotypic diversity PY - 2018 AN - OPUS4-46271 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schreiber, Frank T1 - Resistance selection on antimicrobial surfaces N2 - Antimicrobial surfaces are widely used to reduce the number of bacteria residing in the indoor environment. In this talk, I discuss the risk how these surfaces can lead to the selection of antimicrobial resistant bacteria. T2 - Cost action workshop Amici - Antimicrobial Coatings Applied in Healthcare Settings – Efficacy Testing CY - BAM Unter den Eichen, Berlin, Germany DA - 07.06.2018 KW - Antimicrobial resistance KW - Antimicrobial surfaces KW - Cross-resistance PY - 2018 AN - OPUS4-46272 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schreiber, Frank T1 - Single-cell trait-based biodiversity in microbial communities N2 - A fundamental question in ecology is how biodiversity affects ecosystem function. Biodiversity is commonly estimated based on genetic variation. We investigated a new approach that defines and measures biodiversity in complex microbial communities. We used the variation in multiple functionally-relevant, phenotypic traits measured in parallel in single cells as a metric for microbial phenotypic diversity. We studied phenotypic diversity and ecosystem functioning throughout different photosynthetic layers dominated by divergent microbial communities in the gradient of Lago di Cadagno. We determined genetic diversity by 16S and 18S amplicon sequencing and bulk ecosystem functioning (photosynthesis). In addition, we determined phenotypic diversity using single-cell technologies such as nanometer-scale secondary ion mass spectrometry (NanoSIMS) correlated with confocal laser scanning microscopy (CLSM) and scanning flow-cytometry. We measured functional trait variation between individuals in 13CO2 fixation, 15NH4+ uptake, and variation in physio-morphological cell traits, such as cell size, shape, and auto-fluorescence for various pigments related to photosynthesis. We used the distances between individuals in a multidimensional trait space to derive phenotypic trait-based diversity indices, such as trait richness, trait evenness, and trait divergence. We find that phenotypic trait divergence associates with ecosystem functioning, whereas genetic diversity does not. Including activity-based, single-cell phenotypic measurements with NanoSIMS provided an additional accuracy to the trait-based diversity assessment and allowed us to formulate hypotheses on the mechanisms that shape the correlation between phenotypic diversity and eco-system function. Together, our results show that phenotypic diversity is a meaningful concept to measure microbial biodiversity and associate it with ecosystem functioning. T2 - 17th International Symposium on Microbial Ecology (ISME 17) CY - Leipzig, Germany DA - 12.08.2018 KW - Trait-based ecology KW - Phenotypic diversity KW - Lake Cadagno PY - 2018 AN - OPUS4-46273 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -