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      The Obesity Paradox Predicts the Second Wave of COVID-19 to Be Severe in Western Countries

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          Abstract

          While COVID-19 infection and mortality rates are soaring in Western countries, Southeast Asian countries have successfully avoided the second wave of the SARS-CoV-2 pandemic despite high population density. We provide a biochemical hypothesis for the connection between low COVID-19 incidence, mortality rates, and high visceral adiposity in Southeast Asian populations. The SARS-CoV-2 virus uses angiotensin-converting enzyme 2 (ACE2) as a gateway into the human body. Although the highest expression levels of ACE2 are found in people’s visceral adipose tissue in Southeast Asia, this does not necessarily make them vulnerable to COVID-19. Hypothetically, high levels of visceral adiposity cause systemic inflammation, thus decreasing the ACE2 amount on the surface of both visceral adipocytes and alveolar epithelial type 2 cells in the lungs. Extra weight gained during the pandemic is expected to increase visceral adipose tissue in Southeast Asians, further decreasing the ACE2 pool. In contrast, weight gain can increase local inflammation in fat depots in Western people, leading to worse COVID-related outcomes. Because of the biological mechanisms associated with fat accumulation, inflammation, and their differential expression in Southeast Asian and Western populations, the second wave of the pandemic may be more severe in Western countries, while Southeast Asians may benefit from their higher visceral fat depots.

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          Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus

          Spike (S) proteins of coronaviruses, including the coronavirus that causes severe acute respiratory syndrome (SARS), associate with cellular receptors to mediate infection of their target cells 1,2 . Here we identify a metallopeptidase, angiotensin-converting enzyme 2 (ACE2) 3,4 , isolated from SARS coronavirus (SARS-CoV)-permissive Vero E6 cells, that efficiently binds the S1 domain of the SARS-CoV S protein. We found that a soluble form of ACE2, but not of the related enzyme ACE1, blocked association of the S1 domain with Vero E6 cells. 293T cells transfected with ACE2, but not those transfected with human immunodeficiency virus-1 receptors, formed multinucleated syncytia with cells expressing S protein. Furthermore, SARS-CoV replicated efficiently on ACE2-transfected but not mock-transfected 293T cells. Finally, anti-ACE2 but not anti-ACE1 antibody blocked viral replication on Vero E6 cells. Together our data indicate that ACE2 is a functional receptor for SARS-CoV. Supplementary information The online version of this article (doi:10.1038/nature02145) contains supplementary material, which is available to authorized users.
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            Cytokine release syndrome in severe COVID-19

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              Neuropilin-1 facilitates SARS-CoV-2 cell entry and infectivity

              Another host factor for SARS-CoV-2 Virus-host interactions determine cellular entry and spreading in tissues. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the earlier SARS-CoV use angiotensin-converting enzyme 2 (ACE2) as a receptor; however, their tissue tropism differs, raising the possibility that additional host factors are involved. The spike protein of SARS-CoV-2 contains a cleavage site for the protease furin that is absent from SARS-CoV (see the Perspective by Kielian). Cantuti-Castelvetri et al. now show that neuropilin-1 (NRP1), which is known to bind furin-cleaved substrates, potentiates SARS-CoV-2 infectivity. NRP1 is abundantly expressed in the respiratory and olfactory epithelium, with highest expression in endothelial and epithelial cells. Daly et al. found that the furin-cleaved S1 fragment of the spike protein binds directly to cell surface NRP1 and blocking this interaction with a small-molecule inhibitor or monoclonal antibodies reduced viral infection in cell culture. Understanding the role of NRP1 in SARS-CoV-2 infection may suggest potential targets for future antiviral therapeutics. Science, this issue p. 856, p. 861; see also p. 765
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Environ Res Public Health
                Int J Environ Res Public Health
                ijerph
                International Journal of Environmental Research and Public Health
                MDPI
                1661-7827
                1660-4601
                25 January 2021
                February 2021
                : 18
                : 3
                : 1029
                Affiliations
                [1 ]Department of Biotechnology, Daugavpils University, LV5401 Daugavpils, Latvia; ronalds.krams@ 123456student.emu.ee (R.K.); tatjana.krama@ 123456du.lv (T.K.)
                [2 ]Institute of Ecology and Earth Sciences, University of Tartu, EE51014 Tartu, Estonia
                [3 ]Department of Zoology and Animal Ecology, Faculty of Biology, University of Latvia, LV1004 Riga, Latvia
                [4 ]Institute of Molecular and Cell Biology, University of Tartu, EE51010 Tartu, Estonia; priit.joers@ 123456ut.ee
                [5 ]School of Psychology, University of Auckland, 1142 Auckland, New Zealand; s.luoto@ 123456auckland.ac.nz
                [6 ]Institute of Biosciences, Vilnius University, 10257 Vilnius, Lithuania; giedrius.trakimas@ 123456gf.vu.lt
                [7 ]Department of Surgery, Riga Stradins University, LV1007 Riga, Latvia; vilnis.lietuvietis@ 123456icloud.com
                [8 ]Riga East Clinical University Hospital, LV1010 Riga, Latvia
                [9 ]Department of Anatomy and Physiology, Daugavpils University, LV5401 Daugavpils, Latvia; irena.kaminska@ 123456du.lv
                [10 ]Department of Biology, Section of Ecology, University of Turku, FI-20014 Turku, Finland; mjranta@ 123456utu.fi
                Author notes
                [* ]Correspondence: indrikis.krams@ 123456ut.ee
                Author information
                https://orcid.org/0000-0001-7150-4108
                https://orcid.org/0000-0002-3904-3994
                https://orcid.org/0000-0001-6294-0194
                Article
                ijerph-18-01029
                10.3390/ijerph18031029
                7908102
                33503828
                a9ebabb2-9f33-4ed6-abfe-688827f1c6eb
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 18 December 2020
                : 22 January 2021
                Categories
                Perspective

                Public health
                covid-19,visceral adipose tissue,systemic inflammation,sars-cov-2,ace2,weight gain,second wave,quarantine-15

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