Whole-genome sequencing reveals host factors underlying critical COVID-19

Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care1 or hospitalization2,3,4 after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes—including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)—in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease

An experimental investigation of behavior and hydrodynamics forces acting on a ship in shallow water

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Effect of surface chemistry on electrochemical storage of hydrogen in porous carbon materials

Porous carbon materials, with different porosities and surface chemistry have been prepared and characterized to obtain a better understanding of the mechanism of the electrochemical storage of hydrogen. The hydrogen storage capacity depends, not only on the porosity of the material, but also on the surface chemistry, which is a critical factor. The results show that the higher the amount of surface oxygen groups, the lower is the hydrogen uptake. Measurement of the number of active carbon sites shows the important role of the unsaturated carbon atoms in the process. In situ Raman spectroscopy has been used in order to further explore the structural changes in the carbon material during the charge–discharge processes. This technique has allowed us to observe the formation of the C(sp2)AH bonds during the cathodic process and its reversibility during the oxidation step.MEC and FEDER for financial support (Project CTQ2006-08958/PPQ) and Ministerio de Fomento (70012/t05-fomento05 project)

Purification, Expansion, and Multiple Fluorochrome Labeling of Cord Blood Hemopoietic Precursors: Preliminary Results

peer reviewedCD34-positive cells were isolated from a total of 23 cords using CellPro Ceprate columns. AIS MicroCellector flasks, and panning. The cells were (1) expanded in serum-free culture supplemented with a variety of combinations of cytokines and (2) immunophenotyped using multiple fluorochrome labeling. The results indicated that the avidin column produced the highest purity of CD34-positive cells, and that immature blast cells could be expanded in serum-free culture. Preliminary results suggested that the four fluorochrome labeling technique may provide useful information on the lineage commitment of cord blood precursor and blast cells