Growth Patterns of Two Marine Isolates: Adaptations to Substrate Patchiness?

ABSTRACT During bottle incubations of heterotrophic marine picoplankton, some bacterial groups are conspicuously favored. In an earlier investigation bacteria of the genusPseudoalteromonas rapidly multiplied in substrate-amended North Sea water, whereas the densities ofOceanospirillum changed little (H. Eilers, J. Pernthaler, and R. Amann, Appl. Environ. Microbiol. 66:4634–4640, 2000). We therefore studied the growth patterns of two isolates affiliating withPseudoalteromonas and Oceanospirillum in batch culture. Upon substrate resupply, Oceanospirillum lagged threefold longer than Pseudoalteromonas but reached more than fivefold-higher final cell density and biomass. A second, mobile morphotype was present in the starved Oceanospirillumpopulations with distinctly greater cell size, DNA and protein content, and 16S rRNA concentration. Contrasting cellular ribosome concentrations during stationary phase suggested basic differences in the growth responses of the two strains to a patchy environment. Therefore, we exposed the strains to different modes of substrate addition. During cocultivation on a single batch of substrates, the final cell densities of Oceanospirillum were reduced three times as much as those Pseudoalteromonas, compared to growth yields in pure cultures. In contrast, the gradual addition of substrates to stationary-phase cocultures was clearly disadvantageous for the Pseudoalteromonas population. Different growth responses to substrate gradients could thus be another facet affecting the competition between marine bacteria and may help to explain community shifts observed during enrichments.

[1]  C. E. Zobell Marine Microbiology, a Monograph on Hydrobacteriology , 2015 .

[2]  R. Amann,et al.  Succession of Pelagic Marine Bacteria during Enrichment: a Close Look at Cultivation-Induced Shifts , 2000, Applied and Environmental Microbiology.

[3]  J. Fuhrman,et al.  Marine Planktonic Archaea Take Up Amino Acids , 2000, Applied and Environmental Microbiology.

[4]  R. Amann,et al.  Culturability and In Situ Abundance of Pelagic Bacteria from the North Sea , 2000, Applied and Environmental Microbiology.

[5]  J. Pinhassi,et al.  Seasonal succession in marine bacterioplankton , 2000 .

[6]  Daniel B. Oerther,et al.  Monitoring Precursor 16S rRNAs ofAcinetobacter spp. in Activated Sludge Wastewater Treatment Systems , 2000, Applied and Environmental Microbiology.

[7]  R. Amann,et al.  Changes in community composition during dilution cultures of marine bacterioplankton as assessed by flow cytometric and molecular biological techniques. , 2000, Environmental microbiology.

[8]  P. Servais,et al.  Successional changes in the genetic diversity of a marine bacterial assemblage during confinement , 2000, Archives of Microbiology.

[9]  E. Sherr,et al.  Activity of marine bacteria under incubated and in situ conditions , 1999 .

[10]  Marcelino T. Suzuki Effect of protistan bacterivory on coastal bacterioplankton diversity , 1999 .

[11]  S. Kjelleberg,et al.  Marine Pseudoalteromonas species are associated with higher organisms and produce biologically active extracellular agents. , 1999, FEMS microbiology ecology.

[12]  Kemp,et al.  Small ribosomal RNA content in marine Proteobacteria during non-steady-state growth. , 1999, FEMS microbiology ecology.

[13]  J. Fuhrman,et al.  Significance of Size and Nucleic Acid Content Heterogeneity as Measured by Flow Cytometry in Natural Planktonic Bacteria , 1999, Applied and Environmental Microbiology.

[14]  R. Amann,et al.  Determination of Total Protein Content of Bacterial Cells by SYPRO Staining and Flow Cytometry , 1999, Applied and Environmental Microbiology.

[15]  B. Jørgensen,et al.  Photosynthesis, respiration, and carbon turnover in sinking marine snow from surface waters of Southern California Bight: Implications for the carbon cycle in the ocean. , 1999 .

[16]  J. Gasol,et al.  EFFECTS OF FILTRATION ON BACTERIAL ACTIVITY AND PICOPLANKTON COMMUNITY STRUCTURE AS ASSESSED BY FLOW CYTOMETRY , 1999 .

[17]  M. Höfle,et al.  Identification of Culturable Oligotrophic Bacteria within Naturally Occurring Bacterioplankton Communities of the Ligurian Sea by 16S rRNA Sequencing and Probing , 1999, Microbial Ecology.

[18]  J. Antón,et al.  Diversity of Free-Living and Attached Bacteria in Offshore Western Mediterranean Waters as Depicted by Analysis of Genes Encoding 16S rRNA , 1999, Applied and Environmental Microbiology.

[19]  Mitchell,et al.  Microscale nutrient patches in planktonic habitats shown by chemotactic bacteria , 1998, Science.

[20]  Ricardo Cavicchioli,et al.  Implications of rRNA Operon Copy Number and Ribosome Content in the Marine Oligotrophic Ultramicrobacterium Sphingomonassp. Strain RB2256 , 1998, Applied and Environmental Microbiology.

[21]  Ying Chun Liu,et al.  Growth Rate Regulation of rRNA Content of a MarineSynechococcus (Cyanobacterium) Strain , 1998, Applied and Environmental Microbiology.

[22]  Farooq Azam,et al.  Microbial Control of Oceanic Carbon Flux: The Plot Thickens , 1998, Science.

[23]  M. Troussellier,et al.  Changes in Cellular States of the Marine Bacterium Deleya aquamarina under Starvation Conditions , 1997, Applied and environmental microbiology.

[24]  R. Prins,et al.  Oligotrophy and pelagic marine bacteria: Facts and fiction , 1997 .

[25]  J. Fuhrman,et al.  Determination of Active Marine Bacterioplankton: a Comparison of Universal 16S rRNA Probes, Autoradiography, and Nucleoid Staining , 1997, Applied and environmental microbiology.

[26]  J. Pernthaler,et al.  Cell-specific respiratory activity of aquatic bacteria studied with the tetrazolium reduction method, cyto-clear slides, and image analysis , 1997, Applied and environmental microbiology.

[27]  Frank Oliver Glöckner,et al.  An in situ hybridization protocol for detection and identification of planktonic bacteria , 1996 .

[28]  William K. W. Li,et al.  DNA distributions in planktonic bacteria stained with TOTO or TO‐PRO , 1995 .

[29]  K. Schleifer,et al.  Phylogenetic identification and in situ detection of individual microbial cells without cultivation. , 1995, Microbiological reviews.

[30]  S. Møller,et al.  Bacterial growth on surfaces: automated image analysis for quantification of growth rate-related parameters , 1995, Applied and environmental microbiology.

[31]  P. Lebaron,et al.  Flow cytometric analysis of the cellular DNA content of Salmonella typhimurium and Alteromonas haloplanktis during starvation and recovery in seawater , 1994, Applied and environmental microbiology.

[32]  R. Christen,et al.  Assessment of the state of activity of individual bacterial cells by hybridization with a ribosomal RNA targeted fluorescently labelled oligonucleotidic probe , 1994 .

[33]  J. LaRoche,et al.  Estimating the Growth Rate of Slowly Growing Marine Bacteria from RNA Content , 1993, Applied and environmental microbiology.

[34]  Egbert J. de Vries,et al.  Isolation of Typical Marine Bacteria by Dilution Culture: Growth, Maintenance, and Characteristics of Isolates under Laboratory Conditions , 1993, Applied and environmental microbiology.

[35]  E. Delong,et al.  Phylogenetic diversity of aggregate‐attached vs. free‐living marine bacterial assemblages , 1993 .

[36]  D A Stahl,et al.  Use of rRNA fluorescence in situ hybridization for measuring the activity of single cells in young and established biofilms , 1993, Applied and environmental microbiology.

[37]  B. Monger,et al.  Flow Cytometric Analysis of Marine Bacteria with Hoechst 33342 , 1993, Applied and environmental microbiology.

[38]  S. Kjelleberg,et al.  Ribosomes exist in large excess over the apparent demand for protein synthesis during carbon starvation in marine Vibrio sp. strain CCUG 15956 , 1992, Journal of bacteriology.

[39]  E. N. Buckley,et al.  Response of marine bacterioplankton to differential filtration and confinement , 1984, Applied and environmental microbiology.

[40]  R. Allen,et al.  Taxonomy of Aerobic Marine Eubacteria , 1972, Journal of bacteriology.

[41]  E. Stackebrandt,et al.  Microbial community dynamics in Mediterranean nutrient-enriched seawater mesocosms: changes in the genetic diversity of bacterial populations. , 2001, FEMS microbiology ecology.

[42]  S. Kjelleberg,et al.  Changes in cell morphology and motility in the marine Vibrio sp. strain S14 during conditions of starvation and recovery , 1997 .