The effects of leaching from alkaline red mud on soil biota: modelling the conditions after the Hungarian red mud disaster

A soil column experiment was set up to investigate the effect of red mud from Ajka (Hungary) on a typical soil profile from the concerned area. The chemical changes caused by the leachate of the red mud and the effects of these changes on living organisms were assessed. Ecotoxicological tests with Vibrio fischeri, Sinapis alba and Folsomia candida were performed and the number of aerobic heterotrophic microorganisms was determined. The total, plant available, exchangeable and water soluble fractions of Na, Mo, Cu, and Cr increased in the soil mostly due to their leaching from the red mud layer and partly to the increase of the pH and DOC concentration. The chemical changes had significant effects on the test organisms only in the 0 – 30 cm soil layer except for F. candida that had a lower survival rate also in the 30 – 50 cm soil layer. There were no severe toxic effects detected on the test organisms. Furthermore in case of the aerobic heterotrophic cell number and S. alba germination a stimulating effect was revealed. However, the red mud itself was toxic, therefore the performed ecotoxicology tests have justified the removal of red mud from the soil surface after the disaster

Dengue Virus Capsid Protein Binds Core Histones and Inhibits Nucleosome Formation in Human Liver Cells

Dengue virus (DENV) is a member of the Flaviviridae and a globally (re)emerging pathogen that causes serious human disease. There is no specific antiviral or vaccine for dengue virus infection. Flavivirus capsid (C) is a structural protein responsible for gathering the viral RNA into a nucleocapsid that forms the core of a mature virus particle. Flaviviral replication is known to occur in the cytoplasm yet a large portion of capsid protein localizes to the nucleus during infection. The reasons for the nuclear presences of capsid are not completely understood. Here, we expressed mature DENV C in a tandem affinity purification assay to identify potential binding partners in human liver cells. DENV C targeted the four core histones, H2A, H2B, H3 and H4. DENV C bound recombinant histones in solution and colocalized with histones in the nucleus and cytoplasm of liver cells during DENV infection. We show that DENV C acts as a histone mimic, forming heterodimers with core histones, binding DNA and disrupting nucleosome formation. We also demonstrate that DENV infection increases the amounts of core histones in livers cells, which may be a cellular response to C binding away the histone proteins. Infection with DENV additionally alters levels of H2A phosphorylation in a time-dependent manner. The interactions of C and histones add an interesting new role for the presence of C in the nucleus during DENV infection