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Biology subjects

Dannborg, M.

Publications and source records attributed to Dannborg, M..

3 recordsLinked to original sources

Introducing a gastric microbial model community

Persistent colonization by Helicobacter pylori in the stomach is connected to the development of different gastric pathologies including gastric cancer. Around half of the worlds population is estimated to be colonized by H. pylori, but few develop symptoms. The bacterium dominates the gastric mucosa of individuals who are H. pylori-positive by conventional testing, however, low abundances of H. pylori have also been detected in individuals who test negative, suggesting low-level colonization The factors driving the predominance of H. pylori within the gastric microbiota remain unclear, as are its interactions with the gastric microbiota. Yet these interactions may offer important insights into the organisms colonization success and its role in disease. In this study, we developed a gastric microbial model community, consisting of five species with high abundance and prevalence in gastric samples based on transcriptional data: H. pylori, Escherichia coli, Pseudomonas aeruginosa, Streptococcus salivarius, and Lactobacillus kalixensis. We established growth parameters and methods to track species abundance in vitro. Our results show that H. pylori growth is partly inhibited in pair-wise cultures with all other community members, except with L. kalixensis. This inhibition can to a certain extent be explained by resource competition, pH modulation of the medium, and the initial inoculum ratio of the members. The gastric microbial model community will allow dissection of the genetic mechanisms behind H. pylori interactions with other members of the gastric microbiota, and how these interactions influence H. pylori pathogenesis, providing a non-invasive, low resource model for future studies of the gastric microbiome.

microbiology↗

Seal milk oligosaccharides rival human milk complexity and exhibit functional dynamics during lactation

Breast milk oligosaccharides are crucial for neonatal development and health. Yet most milk research focuses on humans, or domesticated mammals that are historically poor in milk oligosaccharide complexity. Here, we perform an exhaustive mass spectrometry-driven structural characterization of milk oligosaccharides in a wild mammal, Atlantic grey seals (Halichoerus grypus), throughout their lactation period. Characterizing and quantifying 332 milk oligosaccharides, including 166 novel structures, we reveal seals to rival human milk in complexity, with seal free oligosaccharides reaching unprecedented 28 monosaccharides in size. Glycomics and metabolomics time course analysis establishes a concerted regulatory process reshaping the seal milk glycome throughout lactation,similar as in human milk. Functional analysis of herein newly characterized structures reveals anti-biofilm effects and immunomodulatory functions of seal milk oligosaccharides. We envision these findings to overturn long-held assumptions about milk complexity of non-human mammals and enable insights into the functional relevance of complex carbohydrates in breast milk.

biochemistry↗

The generation of plasma cells and CD27-IgD- B cells during Hantavirus infection are associated with distinct pathological findings

Human hantavirus infections can cause hemorrhagic fever with renal syndrome (HFRS), major signs of the disease being thrombocytopenia and transient kidney dysfunction. By a comprehensive and longitudinal study of circulating B cells, we demonstrate that these two pathologies associate with distinct effects on the humoral immune system during HFRS. Low thrombocyte counts strongly associated with an abnormal frequency of plasmablasts in circulation, whereas kidney dysfunction was indicative of an accumulation of CD27- B cells and plasmablasts. Finally, we provide evidence that high levels of extracellular ATP in circulation during HFRS correlates with shedding of surface CD27 on B cells via a metallomatrix proteinase-8-mediated mechanism. Since extracellular ATP is known to regulate kidney function, our study reveals a link between kidney dysfunction and the generation of CD27-IgD- B cells, and a potential molecular target for treatment of the symptomatic phase of HFRS.

immunology↗