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- Zwicker, J., et al.
(författare)
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Evidence for archaeal methanogenesis within veins at the onshore serpentinite-hosted Chimaera seeps, Turkey
- 2018
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Ingår i: Chemical Geology. - : Elsevier BV. - 0009-2541. ; , s. 567-580
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Tidskriftsartikel (refereegranskat)abstract
- Serpentinite-hosted ecosystems are potential sites where life may first have evolved on Earth. Serpentinization reactions produce strongly reducing and highly alkaline fluids that are typified by high concentrations of molecular hydrogen (H2) and methane (CH4), which can be used as an energy source by chemosynthetic life. Low-temperature serpentinization at slow-spreading mid-ocean ridges provides an ideal environment for rich microbial communities. Similar environments have also been discovered on land, where present-day low temperature serpentinization occurs during the circulation of groundwater through exposed ophiolites, triggering the production of CH4 and H2, as well as the precipitation of secondary carbonate minerals. The rock samples analyzed here are from the Chimaera seeps in Turkey, representing serpentinized peridotites that are cross-cut by veins composed of brucite and hydromagnesite. Hydromagnesite features a mean δ13C value of −19.8‰ caused by kinetic isotope fractionation during air-groundwater exchange of CO2, followed by CO2 hydroxylation to bicarbonate within the groundwater. Geochemical modeling revealed that mixing of Mg- and Ca-rich groundwaters is required for hydromagnesite formation at the expense of brucite. Within the carbonate-hydroxide veins the lipid biomarkers pentamethylicosane (PMI) and squalane with δ13C values of +10‰ and +14‰, respectively, and unsaturated derivatives thereof were identified. Archaeol, sn2-hydroxyarchaeol, and sn3-hydroxyarchaeol are other prominent archaeal biomarkers in the veins, also revealing high δ13C values from +6 to +13‰. These isotope patterns combined with the absence of crocetane – a biomarker for methanotrophic archaea – reveal that the microbial communities of the Chimaera seeps performed methanogenesis from a CO2-limited pool rather than methanotrophy. Moreover, bacterial dialkyl glycerol diethers (DAGEs) with unusually high δ13C values (−9 to −2‰) and minor monoalkyl glycerol monoethers (MAGEs) were identified, suggesting that bacterial sulfate reduction is also active at the Chimaera site. This study reveals that archaeal methanogenesis and bacterial sulfate reduction may be prominent at onshore peridotite-hosted sites, and that biogenic CH4 may contribute to abiotic CH4 emissions from terrestrial seeps.
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- Bostrom, E. A., et al.
(författare)
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Increased Eotaxin and MCP-1 Levels in Serum from Individuals with Periodontitis and in Human Gingival Fibroblasts Exposed to Pro-Inflammatory Cytokines
- 2015
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Ingår i: Plos One. - : Public Library of Science (PLoS). - 1932-6203. ; 10:8
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Tidskriftsartikel (refereegranskat)abstract
- Periodontitis is a chronic inflammatory disease of tooth supporting tissues resulting in periodontal tissue destruction, which may ultimately lead to tooth loss. The disease is characterized by continuous leukocyte infiltration, likely mediated by local chemokine production but the pathogenic mechanisms are not fully elucidated. There are no reliable serologic biomarkers for the diagnosis of periodontitis, which is today based solely on the degree of local tissue destruction, and there is no available biological treatment tool. Prompted by the increasing interest in periodontitis and systemic inflammatory mediators we mapped serum cytokine and chemokine levels from periodontitis subjects and healthy controls. We used multivariate partial least squares (PLS) modeling and identified monocyte chemoattractant protein-1 (MCP-1) and eotaxin as clearly associated with periodontitis along with C-reactive protein (CRP), years of smoking and age, whereas the number of remaining teeth was associated with being healthy. Moreover, body mass index correlated significantly with serum MCP-1 and CRP, but not with eotaxin. We detected higher MCP-1 protein levels in inflamed gingival connective tissue compared to healthy but the eotaxin levels were undetectable. Primary human gingival fibroblasts displayed strongly increased expression of MCP-1 and eotaxin mRNA and protein when challenged with tumor necrosis factor-alpha (TNF-alpha and interleukin-1 beta (IL-1 beta), key mediators of periodontal inflammation. We also demonstrated that the upregulated chemokine expression was dependent on the NF-kappa B pathway. In summary, we identify higher levels of CRP, eotaxin and MCP-1 in serum of periodontitis patients. This, together with our finding that both CRP and MCP-1 correlates with BMI points towards an increased systemic inflammatory load in patients with periodontitis and high BMI. Targeting eotaxin and MCP-1 in periodontitis may result in reduced leukocyte infiltration and inflammation in periodontitis and maybe prevent tooth loss.
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