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1.
Mountain research and development ; 42(2):p. D22-D31, 2022.
Article in English | ProQuest Central | ID: covidwho-2065237

ABSTRACT

The explosive volcanic eruptions of La Soufrière volcano, St Vincent and the Grenadines, in April 2021 caused the displacement of thousands of people, resulting in heavy disruption of livelihoods and economic activities, destruction of critical infrastructure, and volcanic ash deposits that affected the entire mountainous island of St Vincent and the neighboring island of Barbados. The resulting triple crisis in the region included volcanological risks, the prevailing COVID-19 pandemic, and hydrometeorological risks due to the approaching hurricane season. This article analyzes the scientific and operational activities that The University of the West Indies Seismic Research Centre undertook after effusive activity was detected in December 2020, as well as the actions taken during an official response mission of the United Nations, led by the Joint Environment Unit of the United Nations Environment Programme and the United Nations Office for the Coordination of Humanitarian Affairs in Geneva and upon request for international environmental assistance from the Government of St Vincent. It examines the interplay and collaboration between these 2 organizations and other disaster risk reduction agencies. The article also highlights how the interconnected, systemic nature of risks and disasters emphasizes the ultimate need for regional coordination and collaboration across sectors, including scientific monitoring networks, national, regional, and international emergency preparedness and response agencies, academia, and the private sector. The presented case study for elucidating the ongoing lahar hazard at La Soufrière volcano supports a long-term view for planning and mitigation in this challenging topography. This will help to ensure that the volcanic risks in the Caribbean region are appropriately considered a major component of the multihazard approach undertaken by national authorities and scientists to manage community safety and sustainable economic development through adequate means of disaster risk reduction and emergency preparedness.

2.
Elife ; 102021 10 25.
Article in English | MEDLINE | ID: covidwho-1485451

ABSTRACT

Severe acute respiratory syndrome (SARS)-CoV-2 infection leads to severe disease associated with cytokine storm, vascular dysfunction, coagulation, and progressive lung damage. It affects several vital organs, seemingly through a pathological effect on endothelial cells. The SARS-CoV-2 genome encodes 29 proteins, whose contribution to the disease manifestations, and especially endothelial complications, is unknown. We cloned and expressed 26 of these proteins in human cells and characterized the endothelial response to overexpression of each, individually. Whereas most proteins induced significant changes in endothelial permeability, nsp2, nsp5_c145a (catalytic dead mutant of nsp5), and nsp7 also reduced CD31, and increased von Willebrand factor expression and IL-6, suggesting endothelial dysfunction. Using propagation-based analysis of a protein-protein interaction (PPI) network, we predicted the endothelial proteins affected by the viral proteins that potentially mediate these effects. We further applied our PPI model to identify the role of each SARS-CoV-2 protein in other tissues affected by coronavirus disease (COVID-19). While validating the PPI network model, we found that the tight junction (TJ) proteins cadherin-5, ZO-1, and ß-catenin are affected by nsp2, nsp5_c145a, and nsp7 consistent with the model prediction. Overall, this work identifies the SARS-CoV-2 proteins that might be most detrimental in terms of endothelial dysfunction, thereby shedding light on vascular aspects of COVID-19.


Subject(s)
Capillary Permeability , Endothelium, Vascular/metabolism , Host-Pathogen Interactions , SARS-CoV-2/metabolism , Viral Proteins/metabolism , Animals , COVID-19/virology , Human Umbilical Vein Endothelial Cells , Humans , Protein Interaction Maps , Tight Junction Proteins/metabolism
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