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  1. Article ; Online: The kinetics of SARS-CoV-2 viremia in COVID-19 patients receiving remdesivir.

    Krifors, Anders / Karlsson, Linda / Ekman, Martin / Lorant, Camilla / Skorup, Paul

    European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology

    2023  Volume 42, Issue 8, Page(s) 951–958

    Abstract: Detection of SARS-CoV-2 RNA in serum, viremia, has been linked to disease severity and outcome. The kinetics of viremia in patients receiving remdesivir has not been thoroughly studied and could help predict treatment response and outcome. We ... ...

    Abstract Detection of SARS-CoV-2 RNA in serum, viremia, has been linked to disease severity and outcome. The kinetics of viremia in patients receiving remdesivir has not been thoroughly studied and could help predict treatment response and outcome. We investigated the kinetics of SARS-CoV-2 viremia and factors associated with baseline viremia, viral clearance and 30-day mortality in patients receiving remdesivir. An observational study including 378 hospitalised patients (median age 67 years, 67% male) sampled with serum SARS-CoV-2 RT-PCR within ± 24 h of initiation of remdesivir treatment. Baseline viremia was present in 206 (54%) patients with a median Ct value of 35.3 (IQR = 33.3-37.1). In patients with baseline viremia, the estimated probability of viral clearance was 72% by day 5. Ct values decreased significantly during remdesivir treatment for viremic patients, indicating an increase in viral load. In total, 44 patients (12%) died within 30 days, and mortality was significantly associated with viremia at baseline (OR = 2.45, p = 0.01) and lack of viral clearance by day 5 (OR = 4.8, p =  < 0.01). Viral clearance was not associated with any individual risk factor. Viremia appears to be a prognostic marker before and during remedesivir treatment. The resolution of viremia was similar to patients not receiving remdesivir in other studies, and the decrease in Ct values during treatment questions the antiviral capacity of remdesivir in vivo. Prospective studies are warranted to confirm our findings.
    MeSH term(s) Humans ; Male ; Aged ; Female ; COVID-19 ; SARS-CoV-2 ; Kinetics ; Viremia/drug therapy ; RNA, Viral ; COVID-19 Drug Treatment ; Antiviral Agents/therapeutic use
    Chemical Substances remdesivir (3QKI37EEHE) ; RNA, Viral ; Antiviral Agents
    Language English
    Publishing date 2023-05-27
    Publishing country Germany
    Document type Observational Study ; Journal Article
    ZDB-ID 603155-9
    ISSN 1435-4373 ; 0934-9723 ; 0722-2211
    ISSN (online) 1435-4373
    ISSN 0934-9723 ; 0722-2211
    DOI 10.1007/s10096-023-04627-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Bed and rise times during the Age of Enlightenment: A case report.

    van Egmond, Lieve / Ekman, Martin / Benedict, Christian

    Journal of sleep research

    2019  Volume 28, Issue 6, Page(s) e12862

    Abstract: Studies have shown that our modern electrical lighting environment reduces naturally occurring seasonal variations in sleep-wake rhythms, such as longer sleep during the winter versus summer. However, less is known about how timing and duration of sleep ... ...

    Abstract Studies have shown that our modern electrical lighting environment reduces naturally occurring seasonal variations in sleep-wake rhythms, such as longer sleep during the winter versus summer. However, less is known about how timing and duration of sleep were affected by the seasons in the premodern era, before the invention of electrical lighting. The Swedish researcher Olof Hiorter collected and documented geophysical data every hour during wakefulness in Uppsala, Sweden, between December 1746 and November 1747. In this way, his bed and rise times could be approximated. The data revealed that Hiorter's rise times occurred around 1 hr before sunrise in winter versus 1 hr after sunrise in summer. No such association was observed between the time of sunset and Hiorter's bedtimes. Finally, the time in bed was about 3.5-4 hr shorter in summer compared to winter. This 273-year-old case report suggests that time in bed and rise times of people from the premodern era exhibited seasonal variations.
    MeSH term(s) Humans ; Male ; Middle Aged ; Circadian Rhythm/physiology ; History, 18th Century ; Lighting/trends ; Seasons ; Sleep/physiology ; Sweden ; Wakefulness/physiology
    Language English
    Publishing date 2019-04-22
    Publishing country England
    Document type Historical Article ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1122722-9
    ISSN 1365-2869 ; 0962-1105
    ISSN (online) 1365-2869
    ISSN 0962-1105
    DOI 10.1111/jsr.12862
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book: The changing level of the Baltic Sea during 300 years

    Ekman, Martin

    a clue to understanding the earth

    2009  

    Author's details Martin Ekman
    Language English
    Size 155 S, Ill., graph. Darst.
    Publisher Summer Institute for Historical Geophysics
    Publishing place Godby
    Document type Book
    ISBN 9789529252411 ; 9529252412
    Database Former special subject collection: coastal and deep sea fishing

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  4. Article ; Online: High abundance and expression of transposases in bacteria from the Baltic Sea.

    Vigil-Stenman, Theoden / Ininbergs, Karolina / Bergman, Birgitta / Ekman, Martin

    The ISME journal

    2017  Volume 11, Issue 11, Page(s) 2611–2623

    Abstract: Transposases are mobile genetic elements suggested to have an important role in bacterial genome plasticity and host adaptation but their transcriptional activity in natural bacterial communities is largely unexplored. Here we analyzed metagenomes and - ... ...

    Abstract Transposases are mobile genetic elements suggested to have an important role in bacterial genome plasticity and host adaptation but their transcriptional activity in natural bacterial communities is largely unexplored. Here we analyzed metagenomes and -transcriptomes of size fractionated (0.1-0.8, 0.8-3.0 and 3.0-200 μm) bacterial communities from the brackish Baltic Sea, and adjacent marine waters. The Baltic Sea transposase levels, up to 1.7% of bacterial genes and 2% of bacterial transcripts, were considerably higher than in marine waters and similar to levels reported for extreme environments. Large variations in expression were found between transposase families and groups of bacteria, with a two-fold higher transcription in Cyanobacteria than in any other phylum. The community-level results were corroborated at the genus level by Synechococcus transposases reaching up to 5.2% of genes and 6.9% of transcripts, which is in contrast to marine Synechococcus that largely lack these genes. Levels peaked in Synechococcus from the largest size fraction, suggesting high frequencies of lateral gene transfer and high genome plasticity in colony-forming picocyanobacteria. Together, the results support an elevated rate of transposition-based genome change and adaptation in bacterial populations of the Baltic Sea, and possibly also of other highly dynamic estuarine waters.
    MeSH term(s) Bacteria/classification ; Bacteria/enzymology ; Bacteria/genetics ; Bacteria/isolation & purification ; Bacterial Proteins/genetics ; Bacterial Proteins/metabolism ; Baltic States ; Gene Transfer, Horizontal ; Genome, Bacterial ; Metagenome ; Phylogeny ; Seawater/microbiology ; Transposases/genetics ; Transposases/metabolism
    Chemical Substances Bacterial Proteins ; Transposases (EC 2.7.7.-)
    Language English
    Publishing date 2017-07-21
    Publishing country England
    Document type Journal Article
    ZDB-ID 2406536-5
    ISSN 1751-7370 ; 1751-7362
    ISSN (online) 1751-7370
    ISSN 1751-7362
    DOI 10.1038/ismej.2017.114
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Microbial metagenomics in the Baltic Sea: Recent advancements and prospects for environmental monitoring.

    Ininbergs, Karolina / Bergman, Birgitta / Larsson, John / Ekman, Martin

    Ambio

    2015  Volume 44 Suppl 3, Page(s) 439–450

    Abstract: Metagenomics refers to the analysis of DNA from a whole community. Metagenomic sequencing of environmental DNA has greatly improved our knowledge of the identity and function of microorganisms in aquatic, terrestrial, and human biomes. Although open ... ...

    Abstract Metagenomics refers to the analysis of DNA from a whole community. Metagenomic sequencing of environmental DNA has greatly improved our knowledge of the identity and function of microorganisms in aquatic, terrestrial, and human biomes. Although open oceans have been the primary focus of studies on aquatic microbes, coastal and brackish ecosystems are now being surveyed. Here, we review so far published studies on microbes in the Baltic Sea, one of the world's largest brackish water bodies, using high throughput sequencing of environmental DNA and RNA. Collectively the data illustrate that Baltic Sea microbes are unique and highly diverse, and well adapted to this brackish-water ecosystem, findings that represent a novel base-line knowledge necessary for monitoring purposes and a sustainable management. More specifically, the data relate to environmental drivers for microbial community composition and function, assessments of the microbial biodiversity, adaptations and role of microbes in the nitrogen cycle, and microbial genome assembly from metagenomic sequences. With these discoveries as background, prospects of using metagenomics for Baltic Sea environmental monitoring are discussed.
    MeSH term(s) Biodiversity ; Ecosystem ; Environmental Monitoring/methods ; Metagenomics/methods ; Oceans and Seas ; Seawater/microbiology
    Language English
    Publishing date 2015-05-29
    Publishing country Sweden
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 120759-3
    ISSN 1654-7209 ; 0044-7447
    ISSN (online) 1654-7209
    ISSN 0044-7447
    DOI 10.1007/s13280-015-0663-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Diverse roles of the GlcP glucose permease in free-living and symbiotic cyanobacteria.

    Picossi, Silvia / Flores, Enrique / Ekman, Martin

    Plant signaling & behavior

    2013  Volume 8, Issue 12, Page(s) e27416

    Abstract: Certain cyanobacteria can form symbiotic associations with plants, where the symbiont supplies the plant partner with nitrogen and in return obtains sugars. We recently showed that in the symbiotic cyanobacterium Nostoc punctiforme, a glucose specific ... ...

    Abstract Certain cyanobacteria can form symbiotic associations with plants, where the symbiont supplies the plant partner with nitrogen and in return obtains sugars. We recently showed that in the symbiotic cyanobacterium Nostoc punctiforme, a glucose specific permease, GlcP, is necessary for the symbiosis to be formed. Results presented here from growth yield measurements of mutant strains with inactivated or overexpressing sugar transporters suggest that GlcP could be induced by a symbiosis specific substance. We also discuss that the transporter may have a role other than nutritional once the symbiosis is established, i.e., during infection, and more specifically in the chemotaxis of the symbiont. Phylogenetic analysis shows that the distribution of GlcP among cyanobacteria is likely influenced by horizontal gene transfer, but also that it is not correlated with symbiotic competence. Instead, regulatory patterns of the transporter in Nostoc punctiforme likely constitute symbiosis specific adaptations.
    MeSH term(s) Chemotaxis/drug effects ; Evolution, Molecular ; Glucose/pharmacology ; Nostoc/cytology ; Nostoc/drug effects ; Nostoc/enzymology ; Nostoc/growth & development ; Phosphoenolpyruvate Sugar Phosphotransferase System/metabolism ; Phylogeny ; Symbiosis/drug effects
    Chemical Substances Phosphoenolpyruvate Sugar Phosphotransferase System (EC 2.7.1.-) ; phosphoenolpyruvate-glucose phosphotransferase (EC 2.7.1.-) ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2013-12-31
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1559-2324
    ISSN (online) 1559-2324
    DOI 10.4161/psb.27416
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Cellular and functional specificity among ferritin-like proteins in the multicellular cyanobacterium Nostoc punctiforme.

    Ekman, Martin / Sandh, Gustaf / Nenninger, Anja / Oliveira, Paulo / Stensjö, Karin

    Environmental microbiology

    2014  Volume 16, Issue 3, Page(s) 829–844

    Abstract: Ferritin-like proteins constitute a remarkably heterogeneous protein family, including ferritins, bacterioferritins and Dps proteins. The genome of the filamentous heterocyst-forming cyanobacterium Nostoc punctiforme encodes five ferritin-like proteins. ... ...

    Abstract Ferritin-like proteins constitute a remarkably heterogeneous protein family, including ferritins, bacterioferritins and Dps proteins. The genome of the filamentous heterocyst-forming cyanobacterium Nostoc punctiforme encodes five ferritin-like proteins. In the present paper, we report a multidimensional characterization of these proteins. Our phylogenetic and bioinformatics analyses suggest both structural and physiological differences among the ferritin-like proteins. The expression of these five genes responded differently to hydrogen peroxide treatment, with a significantly higher rise in transcript level for Npun_F3730 as compared with the other four genes. A specific role for Npun_F3730 in the cells tolerance against hydrogen peroxide was also supported by the inactivation of Npun_F3730, Npun_R5701 and Npun_R6212; among these, only the ΔNpun_F3730 strain showed an increased sensitivity to hydrogen peroxide compared with wild type. Analysis of promoter-GFP reporter fusions of the ferritin-like genes indicated that Npun_F3730 and Npun_R5701 were expressed in all cell types of a diazotrophic culture, while Npun_F6212 was expressed specifically in heterocysts. Our study provides the first comprehensive analysis combining functional differentiation and cellular specificity within this important group of proteins in a multicellular cyanobacterium.
    MeSH term(s) Amino Acid Sequence ; Computational Biology ; Ferritins/genetics ; Ferritins/metabolism ; Gene Expression Regulation, Bacterial/drug effects ; Green Fluorescent Proteins/genetics ; Green Fluorescent Proteins/metabolism ; Hydrogen Peroxide/pharmacology ; Iron/metabolism ; Nostoc/classification ; Nostoc/drug effects ; Nostoc/genetics ; Nostoc/metabolism ; Oxidants/pharmacology ; Phylogeny ; Sequence Alignment
    Chemical Substances Oxidants ; Green Fluorescent Proteins (147336-22-9) ; Ferritins (9007-73-2) ; Hydrogen Peroxide (BBX060AN9V) ; Iron (E1UOL152H7)
    Language English
    Publishing date 2014-03
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2020213-1
    ISSN 1462-2920 ; 1462-2912
    ISSN (online) 1462-2920
    ISSN 1462-2912
    DOI 10.1111/1462-2920.12233
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Massive and rapid COVID-19 testing is feasible by extraction-free SARS-CoV-2 RT-qPCR

    Smyrlaki, Ioanna / Ekman, Martin / Vondracek, Martin / Papanicoloau, Natali / Lentini, Antonio / Aarum, Johan / Muradrasoli, Shaman / Albert, Jan / Högberg, Björn / Reinius, Björn

    Abstract: Coronavirus disease 2019 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The most widely used method of COVID-19 diagnostics is a reverse transcription quantitative polymerase chain reaction (RT-qPCR) assay, ... ...

    Abstract Coronavirus disease 2019 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The most widely used method of COVID-19 diagnostics is a reverse transcription quantitative polymerase chain reaction (RT-qPCR) assay, detecting the presence of SARS-CoV-2 RNA in patient samples, typically from nasopharyngeal swabs. The RNA extraction is a major bottleneck in current COVID-19 testing, in terms of turn-around, logistics, component availability and cost, which delays or completely precludes COVID-19 diagnostics in many settings. Efforts to simplify the current methods are important, as increased diagnostic availability and efficiency is expected to benefit patient care and infection control. Here, we describe methods to circumvent RNA extraction in COVID-19 testing by performing RT-qPCR directly on heat-inactivated subject samples as well as samples lysed with readily available detergents. Our data, including cross-comparisons with clinically diagnosed patient samples, suggest that direct RT-qPCR is a viable option to extraction-based COVID-19 diagnostics. We argue that significant savings in terms of time and cost can be achieved by embracing RNA-extraction-free protocols, that feeds directly into the established PCR-based testing pipeline. This could aid the expansion of COVID-19 testing.
    Keywords covid19
    Publisher MedRxiv; WHO
    Document type Article ; Online
    DOI 10.1101/2020.04.17.20067348
    Database COVID19

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  9. Article ; Online: Massive and rapid COVID-19 testing is feasible by extraction-free SARS-CoV-2 RT-qPCR

    Smyrlaki, Ioanna / Ekman, Martin / Vondracek, Martin / Papanicoloau, Natali / Lentini, Antonio / Aarum, Johan / Muradrasoli, Shaman / Albert, Jan / Högberg, Björn / Reinius, Björn

    medRxiv

    Abstract: Coronavirus disease 2019 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The most widely used method of COVID-19 diagnostics is a reverse transcription quantitative polymerase chain reaction (RT-qPCR) assay, ... ...

    Abstract Coronavirus disease 2019 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The most widely used method of COVID-19 diagnostics is a reverse transcription quantitative polymerase chain reaction (RT-qPCR) assay, detecting the presence of SARS-CoV-2 RNA in patient samples, typically from nasopharyngeal swabs. The RNA extraction is a major bottleneck in current COVID-19 testing, in terms of turn-around, logistics, component availability and cost, which delays or completely precludes COVID-19 diagnostics in many settings. Efforts to simplify the current methods are important, as increased diagnostic availability and efficiency is expected to benefit patient care and infection control. Here, we describe methods to circumvent RNA extraction in COVID-19 testing by performing RT-qPCR directly on heat-inactivated subject samples as well as samples lysed with readily available detergents. Our data, including cross-comparisons with clinically diagnosed patient samples, suggest that direct RT-qPCR is a viable option to extraction-based COVID-19 diagnostics. We argue that significant savings in terms of time and cost can be achieved by embracing RNA-extraction-free protocols, that feeds directly into the established PCR-based testing pipeline. This could aid the expansion of COVID-19 testing.
    Keywords covid19
    Language English
    Publishing date 2020-04-18
    Publisher Cold Spring Harbor Laboratory Press
    Document type Article ; Online
    DOI 10.1101/2020.04.17.20067348
    Database COVID19

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  10. Article ; Online: Ecosystem-wide metagenomic binning enables prediction of ecological niches from genomes.

    Alneberg, Johannes / Bennke, Christin / Beier, Sara / Bunse, Carina / Quince, Christopher / Ininbergs, Karolina / Riemann, Lasse / Ekman, Martin / Jürgens, Klaus / Labrenz, Matthias / Pinhassi, Jarone / Andersson, Anders F

    Communications biology

    2020  Volume 3, Issue 1, Page(s) 119

    Abstract: The genome encodes the metabolic and functional capabilities of an organism and should be a major determinant of its ecological niche. Yet, it is unknown if the niche can be predicted directly from the genome. Here, we conduct metagenomic binning on 123 ... ...

    Abstract The genome encodes the metabolic and functional capabilities of an organism and should be a major determinant of its ecological niche. Yet, it is unknown if the niche can be predicted directly from the genome. Here, we conduct metagenomic binning on 123 water samples spanning major environmental gradients of the Baltic Sea. The resulting 1961 metagenome-assembled genomes represent 352 species-level clusters that correspond to 1/3 of the metagenome sequences of the prokaryotic size-fraction. By using machine-learning, the placement of a genome cluster along various niche gradients (salinity level, depth, size-fraction) could be predicted based solely on its functional genes. The same approach predicted the genomes' placement in a virtual niche-space that captures the highest variation in distribution patterns. The predictions generally outperformed those inferred from phylogenetic information. Our study demonstrates a strong link between genome and ecological niche and provides a conceptual framework for predictive ecology based on genomic data.
    MeSH term(s) Aquatic Organisms/genetics ; Archaea/genetics ; Bacteria/genetics ; Base Sequence ; Ecology ; Ecosystem ; Genome, Archaeal ; Genome, Bacterial ; Machine Learning ; Metagenome ; Metagenomics/methods ; Phylogeny ; Plankton/microbiology ; Sequence Analysis, DNA/methods
    Language English
    Publishing date 2020-03-13
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2399-3642
    ISSN (online) 2399-3642
    DOI 10.1038/s42003-020-0856-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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