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  • 2015-2019  (79)
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  • 1
    Publication Date: 2015-12-19
    Description: The deep-sea hypersaline anoxic basins (DHABs) of the Mediterranean (water depth ~3500 m) are some of the most extreme oceanic habitats known. Brines of DHABs are nearly saturated with salt, leading many to su...
    Electronic ISSN: 1741-7007
    Topics: Biology
    Published by BioMed Central
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  • 2
    Publication Date: 2016-02-06
    Description: SH3 and multiple ankyrin repeat domains 3 (SHANK3) haploinsufficiency is causative for the neurological features of Phelan-McDermid syndrome (PMDS), including a high risk of autism spectrum disorder (ASD). We used unbiased, quantitative proteomics to identify changes in the phosphoproteome of Shank3-deficient neurons. Down-regulation of protein kinase B (PKB/Akt)-mammalian target of rapamycin complex 1 (mTORC1) signaling resulted from enhanced phosphorylation and activation of serine/threonine protein phosphatase 2A (PP2A) regulatory subunit, B56beta, due to increased steady-state levels of its kinase, Cdc2-like kinase 2 (CLK2). Pharmacological and genetic activation of Akt or inhibition of CLK2 relieved synaptic deficits in Shank3-deficient and PMDS patient-derived neurons. CLK2 inhibition also restored normal sociability in a Shank3-deficient mouse model. Our study thereby provides a novel mechanistic and potentially therapeutic understanding of deregulated signaling downstream of Shank3 deficiency.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bidinosti, Michael -- Botta, Paolo -- Kruttner, Sebastian -- Proenca, Catia C -- Stoehr, Natacha -- Bernhard, Mario -- Fruh, Isabelle -- Mueller, Matthias -- Bonenfant, Debora -- Voshol, Hans -- Carbone, Walter -- Neal, Sarah J -- McTighe, Stephanie M -- Roma, Guglielmo -- Dolmetsch, Ricardo E -- Porter, Jeffrey A -- Caroni, Pico -- Bouwmeester, Tewis -- Luthi, Andreas -- Galimberti, Ivan -- New York, N.Y. -- Science. 2016 Mar 11;351(6278):1199-203. doi: 10.1126/science.aad5487. Epub 2016 Feb 4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Developmental Molecular Pathways, Novartis Institutes for Biomedical Research, Basel, Switzerland. ; Friedrich Miescher Institute, Basel, Switzerland. ; Analytical Sciences and Imaging, Novartis Institutes for Biomedical Research, Basel, Switzerland. ; Neuroscience, Novartis Institutes for Biomedical Research, Cambridge, USA. ; Developmental Molecular Pathways, Novartis Institutes for Biomedical Research, Basel, Switzerland. ivan.galimberti@novartis.com.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26847545" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Autism Spectrum Disorder/*drug therapy/enzymology/genetics ; Chromosome Deletion ; Chromosome Disorders/genetics ; Chromosomes, Human, Pair 22/genetics ; Disease Models, Animal ; Down-Regulation ; Gene Knockdown Techniques ; Humans ; Insulin-Like Growth Factor I/metabolism ; Mice ; Molecular Sequence Data ; Multiprotein Complexes/metabolism ; Nerve Tissue Proteins/*genetics ; Neurons/enzymology ; Phosphorylation ; Protein Phosphatase 2/metabolism ; Protein-Serine-Threonine Kinases/*antagonists & inhibitors/metabolism ; Protein-Tyrosine Kinases/*antagonists & inhibitors/metabolism ; Proteomics ; Proto-Oncogene Proteins c-akt/genetics/metabolism ; Rats ; Signal Transduction ; TOR Serine-Threonine Kinases/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2016-10-26
    Description: Gene expression profiling of microbial activities and interactions in sediments under haloclines of E. Mediterranean deep hypersaline anoxic basins The ISME Journal 10, 2643 (November 2016). doi:10.1038/ismej.2016.58 Authors: Virginia P Edgcomb, Maria G Pachiadaki, Paraskevi Mara, Konstantinos A Kormas, Edward R Leadbetter & Joan M Bernhard
    Print ISSN: 1751-7362
    Electronic ISSN: 1751-7370
    Topics: Biology
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  • 4
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    PANGAEA
    In:  Supplement to: Thiele, Stefan; Fuchs, Bernhard M; Amann, Rudolf; Iversen, Morten Hvitfeldt; Wommack, K Eric (2015): Colonization in the Photic Zone and Subsequent Changes during Sinking Determine Bacterial Community Composition in Marine Snow. Applied and Environmental Microbiology, 81(4), 1463-1471, https://doi.org/10.1128/AEM.02570-14
    Publication Date: 2023-03-03
    Description: Due to sampling difficulties, little is known about microbial communities associated with sinking marine snow in the twilight zone. A drifting sediment trap was equipped with a viscous cryogel and deployed to collect intact marine snow from depths of 100 and 400 m off Cape Blanc (Mauritania). Marine snow aggregates were fixed and washed in situ to prevent changes in microbial community composition and to enable subsequent analysis using catalyzed reporter deposition fluorescence in situ hybridization (CARD-FISH). The attached microbial communities collected at 100 m were similar to the free-living community at the depth of the fluorescence maximum (20 m) but different from those at other depths (150, 400, 550, and 700 m). Therefore, the attached microbial community seemed to be "inherited" from that at the fluorescence maximum. The attached microbial community structure at 400 m differed from that of the attached community at 100 m and from that of any free-living community at the tested depths, except that collected near the sediment at 700 m. The differences between the particle-associated communities at 400 m and 100 m appeared to be due to internal changes in the attached microbial community rather than de novo colonization, detachment, or grazing during the sinking of marine snow. The new sampling method presented here will facilitate future investigations into the mechanisms that shape the bacterial community within sinking marine snow, leading to better understanding of the mechanisms which regulate biogeochemical cycling of settling organic matter.
    Keywords: Center for Marine Environmental Sciences; MARUM
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 5
    Publication Date: 2023-07-06
    Description: Spring phytoplankton blooms contribute significantly to global marine primary production. A large fraction of the bloom derived organic matter is available to heterotrophic bacteria in the form of polysaccharides. We analyzed changes in the modes of polysaccharide utilization (selfish uptake and extracellular hydrolysis) during a spring phytoplankton bloom using fluorescently labelled polysaccharide incubations coupled with 16s rRNA sequencing and fluorescence in situ hybridization. We found that in the early bloom phases there was high selfish activity of simple polysaccharides (laminarin) and low extracellular hydrolysis rates of a limited range of polysaccharides. During the course of the bloom both the selfish uptake and extracellular hydrolysis rates increased but only for a limited range of substrates. At the late bloom phase a wide range of substrate was extracellularly hydrolyzed and the level of selfish uptake decreased. We found that during a spring phytoplankton bloom the mode of substrate utilization depended on both the substrates structural complexity and the composition of the heterotrophic community related to the bloom phase.
    Keywords: Alteromonadales, substrate stained; Alteromonadales, targeted with ALT1413 oligonucleiotide FISH-Probe; Bacterioplankton; Bacteroidetes, substrate stained; Bacteroidetes, targeted with CF319a oligonucliotide FISH-Probe; DATE/TIME; DEPTH, water; Device type; Experiment day; Fluorescence in situ hybridization (FISH); German Bight, North Sea; HelgolandRoads_site; Kabeltonne; Microbial abundance, cells; Sample code/label; Sample ID; Size; Substrate type; Volume
    Type: Dataset
    Format: text/tab-separated-values, 1448 data points
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  • 6
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    PANGAEA
    In:  Supplement to: Reintjes, Greta; Arnosti, Carol; Fuchs, Bernhard M; Amann, Rudolf (2019): Selfish, sharing and scavenging bacteria in the Atlantic Ocean: a biogeographical study of bacterial substrate utilisation. The ISME Journal, 13(5), 1119-1132, https://doi.org/10.1038/s41396-018-0326-3
    Publication Date: 2023-07-10
    Description: A large fraction of the organic matter fixed in the oceans is transformed and remineralised by marine heterotrophic microorganisms. They, therefore, play a critical role in the marine carbon cycle. In this study, we set out to identify the roles played by individual heterotrophic bacteria in the degradation of high molecular weight polysaccharides. At five sites in the Atlantic Ocean, we investigated the processing of organic matter in microbial communities by tracking the changes in community composition (fluorescence in situ hybridisation (FISH), 16S rRNA tag sequencing) in substrate incubation using a defined concentration of a known fluorescently labelled polysaccharide (FLA-laminarin, FLA-xylan, and FLA-chondroitin sulfate). Additionally, we tracked the dynamics of substrate processing (selfish uptake and extracellular hydrolysis) within the microbial communities between sites. We found that the same substrate was processed in different ways by different members of a pelagic microbial community which points to significant follow-on effects for carbon cycling.
    Keywords: Abundance; Alteromonadales, substrate stained; Alteromonadales, targeted with ALT1413 oligonucleiotide FISH-Probe; AMT22-46; ATM22; ATM22_JC079_CTD-24; ATM22_JC079_CTD-38; ATM22_JC079_CTD-57; ATM22_JC079_CTD-8; Bacteroidetes, substrate stained; Bacteroidetes, targeted with CF319a oligonucliotide FISH-Probe; Catenovulum, substrate stained; Catenovulum, targets with CAT653 oligonucleotide FISH-Probe; CTD/Rosette; CTD-RO; Date/Time of event; DEPTH, water; Event label; Experiment day; Fluorescence in situ hybridization (FISH); James Cook; JC079; JC079-04; JC079-12; JC079-19; JC079-28; JC079-46; Latitude of event; Longitude of event; Microbial abundance, cells; Optional event label; Planctomycetes, substrate stained; Planctomycetes, targeted with PLA46 oligonucliotide FISH-Probe; Sample ID; Substrate type
    Type: Dataset
    Format: text/tab-separated-values, 3490 data points
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  • 7
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    PANGAEA
    In:  Supplement to: Martínez-Pérez, Clara; Mohr, Wiebke; Löscher, Carolin R; Dekaezemacker, Julien; Littmann, Sten; Yilmaz, Pelin; Lehnen, Christina; Fuchs, Bernhard M; Lavik, Gaute; Schmitz, Ruth A; LaRoche, Julie; Kuypers, Marcel MM (2016): The small unicellular diazotrophic symbiont, UCYN-A, is a key player in the marine nitrogen cycle. Nature Microbiology, 1, 16163, https://doi.org/10.1038/nmicrobiol.2016.163
    Publication Date: 2023-10-28
    Description: Microbial dinitrogen (N2) fixation, the nitrogenase enzyme-catalysed reduction of N2 gas into biologically available ammonia, is the main source of new nitrogen (N) in the ocean. For more than 50 years, oceanic N2 fixation has mainly been attributed to the activity of the colonial cyanobacterium Trichodesmium. Other smaller N2-fixing microorganisms (diazotrophs)--in particular the unicellular cyanobacteria group A (UCYN-A)--are, however, abundant enough to potentially contribute significantly to N2 fixation in the surface waters of the oceans. Despite their abundance, the contribution of UCYN-A to oceanic N2 fixation has so far not been directly quantified. Here, we show that in one of the main areas of oceanic N2 fixation, the tropical North Atlantic7, the symbiotic cyanobacterium UCYN-A contributed to N2 fixation similarly to Trichodesmium. Two types of UCYN-A, UCYN-A1 and -A2, were observed to live in symbioses with specific eukaryotic algae. Single-cell analyses showed that both algae-UCYN-A symbioses actively fixed N2, contributing ~20% to N2 fixation in the tropical North Atlantic, revealing their significance in this region. These symbioses had growth rates five to ten times higher than Trichodesmium, implying a rapid transfer of UCYN-A-fixed N into the food web that might significantly raise their actual contribution to N2 fixation. Our analysis of global 16S rRNA gene databases showed that UCYN-A occurs in surface waters from the Arctic to the Antarctic Circle and thus probably contributes to N2 fixation in a much larger oceanic area than previously thought. Based on their high rates of N2 fixation and cosmopolitan distribution, we hypothesize that UCYN-A plays a major, but currently overlooked role in the oceanic N cycle.
    Keywords: Center for Marine Environmental Sciences; Climate - Biogeochemistry Interactions in the Tropical Ocean; MARUM; SFB754
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 8
    Publication Date: 2024-02-23
    Description: A process of global importance in carbon cycling is the remineralization of algae biomass by heterotrophic bacteria, most notably during massive marine algae blooms. Such blooms can trigger secondary blooms of planktonic bacteria that consist of swift successions of distinct bacterial clades, most prominently members of the Flavobacteriia, Gammaproteobacteria and the alphaproteobacterial Roseobacter clade. This study explores such successions during spring phytoplankton blooms in the southern North Sea (German Bight) for four consecutive years. The surface water samples were taken at Helgoland Island about 40 km offshore in the southeastern North Sea in the German Bight at the station 'Kabeltonne' (54° 11.3' N, 7° 54.0' E) between the main island and the minor island, Düne (German for 'dune') using small research vessels (http://www.awi.de/en/expedition/ships/more-ships.html). Water depths at this site fluctuate from 6 to 10 m over the tidal cycle. Samples were processed as described previously (Teeling et al., 2012; doi:10.7554/eLife.11888.001) in the laboratory of the Biological Station Helgoland within less than two hours after sampling. Assessment of absolute cell numbers and bacterioplankton community composition was carried out as described previously (Thiele et al., 2011; doi:10.1016/B978-0-444-53199-5.00056-7). To obtain total cell numbers, DNA of formaldehyde fixed cells filtered on 0.2 mm pore sized filters was stained with 4',6-diamidino-2-phenylindole (DAPI). Fluorescently labeled cells were subsequently counted on filter sections using an epifluores-cence microscope. Likewise, bacterioplankton community composition was assessed by catalyzedreporter deposition fluorescence in situ hybridization (CARD-FISH) of formaldehyde fixed cells on 0.2 mm pore sized filters.
    Keywords: Actinobacteria, targeted with HGC69a oligonucleotides FISH-probe; Alphaproteobacteria, targeted with ALF968 oligonucleotides FISH-probe; Alteromonas/Colwellia, targeted with Alt1413 oligonucleotide FISH-probe; Archaea, targed with ARCH915 oligonucleotide FISH-probe; Bacteria, targed with EUB338(I-III) oligonucleotide FISH-probe; Bacterioplankton; Balneatrix, targeted with Bal731 oligonucleotides FISH-probe; Betaproteobacteria, targeted with BET42a oligonucleotides FISH-probe; Catalysed reporter deposition-fluorescence in situ hybridization (CARD-FISH); Crenarchaeota marine group I, targeted with Cren554 oligonucleotide FISH-probe; Cytophaga-Flavobacterium cluster, targeted with CF319a oligonucleotide FISH-probe; DATE/TIME; DEPTH, water; Epifluorescence microscopy after DAPI staining; Euryarchaeota marine group II, targeted with Eury806 oligonucleotide FISH-probe; Formosa, targeted with FORM181A oligonucleotides FISH-probe; Formosa, targeted with FORM181B oligonucleotides FISH-probe; Gammaproteobacteria, targeted with Gam42a oligonucleotide FISH-probe; German Bight, North Sea; Glaciecola, targeted with Glac227 oligonucleotides FISH-probe; HelgolandRoads_bacterioplankton_2009-2012; Julian day; Kabeltonne; Marinoscillum, targeted with CYT-734 oligonucleotides FISH-probe; NAC11-7 clade, targeted with NAC11-7-1030 oligonucleotides FISH-probe; Non-bacteria control, targeted with NON338 oligonucleotides FISH-probe; NOR5 clade, targeted with NOR5-730 oligonucleotides FISH-probe; NS3a clade, targeted with NS3a-840 oligonucleotides FISH-probe; NS5 clade, targeted with NS5/DE2-471 oligonucleotides FISH-probe; NS5 clade, targeted with NS5/VIS1-575 oligonucleotides FISH-probe; NS9 clade, targeted with NS9-664 oligonucleotides FISH-probe; OM182 clade, targeted with OM182-707 oligonucleotides FISH-probe; Pirellula group D, targeted with PirD1039 oligonucleotides FISH-probe; Planctomyce group A, targeted with PlaA1228 oligonucleotides FISH-probe; Planctomycete group B, targeted with uPlaB440 oligonucleotides FISH-probe; Planctomycetes, targeted with Pla46 oligonucleotide FISH-probe; Polaribacter, targeted with POL740 oligonucleotides FISH-probe; Pseudoalteromonas, targeted with PSA184 oligonucleotide FISH-probe; Reinekea, targeted with REI731 oligonucleotides FISH-probe; Roseobacter clade, targeted with RCA1000 oligonucleotides FISH-probe; Roseobacter clade, targeted with ROS537 oligonucleotides FISH-probe; SAR11 clade, targeted with SAR11-441 oligonucleotide FISH-probe; SAR11 clade, targeted with SAR11-486 oligonucleotides FISH-probe; SAR324 clade, targeted with SAR324-1412 oligonucleotide FISH-probe; SAR86 clade, targeted with SAR86-1245 oligonucleotide FISH-probe; SAR92 clade, targeted with SAR92-627 oligonucleotides FISH-probe; Ulvibacter, targeted with ULV995 oligonucleotides FISH-probe; Vibrio, targeted with GV841 oligonucleotide FISH-probe; VIS6 clade, targeted with VIS6-814 oligonucleotides FISH-probe
    Type: Dataset
    Format: text/tab-separated-values, 5239 data points
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  • 9
    Publication Date: 2024-02-02
    Description: Fluorescence in situ hybridization (FISH) with 16S rRNA-targeted oligonucleotide probes was used to investigate the phylogenetic composition of the seven most abundant bacterial clades (determined by 16S rRNA tag sequencing) of the South Pacific Gyre (SPG). Seawater samples were collected aboard the RV Sonne SO-245 "UltraPac"cruise from Antofagasta, Chile (17.12.2015) to Wellington, New Zealand (28.01.2016). A total of 15 stations were sampled at multiple depths from surface (20 m) to ~5000 m. Total cell counts (TCC, by DAPI staining) and FISH were carried out as described in Bennke et al. (2016). DAPI and FISH stained cells were visualised and counted automatically using a fully automated image acquisition and cell enumeration system (Bennke et al., 2016). The cellular abundance of SAR11 clade, Prochlorococcus, AEGEAN-169 marine group, SAR86, SAR202, SAR324 and SAR406 were enumerated and are shown here in total (cell ml-1) and relative abundance (% TCC). For this study, a new probe specific for the AEGEAN-169 clade was designed and tested, based on the latest SILVA 16S rRNA database (refnr 128). We found that the microbial community within the SPG was highly similar to that of other oceanic gyres and showed a pronounced vertical distribution pattern. Two major differences which we observed, in comparison to previous studies of both the SPG and other oceanic Gyres, was a high abundance of the AEGEAN-169 marine group, a sister group of the SAR11 clade, and a low abundance of Prochlorococcus specifically in the surface waters of the central gyre.
    Keywords: Accession number, genetics; AEGEAN-169 marine group, targeted with the AEGEAN-169 mix oligonucleotide FISH-probes; Catalysed reporter deposition-fluorescence in situ hybridization (CARD-FISH); CTD/Rosette; CTD-RO; DEPTH, water; Event label; Flow cytometry; Microbial abundance, cells; Number; Prochlorococcus, targeted with PRO405 oligonucleotide FISH-probe; SAR11 mix oligonucleotide FISH-probes targeting SAR11 clade; SAR202 clade, targeted with SAR202-312R oligonucleotide FISH-probe; SAR324 clade, targeted with SAR324-1412 oligonucleotide FISH-probe; SAR406 clade, targeted with SAR406-97 oligonucleotide FISH-probe; SAR86 clade, targeted with SAR86-1245 oligonucleotide FISH-probe; SO245; SO245_10-1; SO245_1-1; SO245_11-1; SO245_12-2; SO245_13-1; SO245_14-2; SO245_15-13; SO245_2-2; SO245_3-1; SO245_4-1; SO245_5-1; SO245_6-1; SO245_7-4; SO245_8-1; SO245_9-1; Sonne_2; South Pacific Ocean; Station label; UltraPac, GEOTRACES
    Type: Dataset
    Format: text/tab-separated-values, 2922 data points
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  • 10
    Publication Date: 2024-02-02
    Keywords: 604; Alteromonas; Bacteroidetes; Center for Marine Environmental Sciences; Comment; DEPTH, water; GeoB15704-2; In situ pump; ISP; Maria S. Merian; MARUM; MSM18/1; Planctomycetes, cells; Pseudoalteromonas; Roseobacter; Synechococcus
    Type: Dataset
    Format: text/tab-separated-values, 49 data points
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