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      A study on the effect of natural products against the transmission of B.1.1.529 Omicron

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          Abstract

          Background

          The recent outbreak of the Coronavirus pandemic resulted in a successful vaccination program launched by the World Health Organization. However, a large population is still unvaccinated, leading to the emergence of mutated strains like alpha, beta, delta, and B.1.1.529 (Omicron). Recent reports from the World Health Organization raised concerns about the Omicron variant, which emerged in South Africa during a surge in COVID-19 cases in November 2021. Vaccines are not proven completely effective or safe against Omicron, leading to clinical trials for combating infection by the mutated virus. The absence of suitable pharmaceuticals has led scientists and clinicians to search for alternative and supplementary therapies, including dietary patterns, to reduce the effect of mutated strains.

          Main body

          This review analyzed Coronavirus aetiology, epidemiology, and natural products for combating Omicron. Although the literature search did not include keywords related to in silico or computational research, in silico investigations were emphasized in this study. Molecular docking was implemented to compare the interaction between natural products and Chloroquine with the ACE2 receptor protein amino acid residues of Omicron. The global Omicron infection proceeding SARS-CoV-2 vaccination was also elucidated. The docking results suggest that DGCG may bind to the ACE2 receptor three times more effectively than standard chloroquine.

          Conclusion

          The emergence of the Omicron variant has highlighted the need for alternative therapies to reduce the impact of mutated strains. The current review suggests that natural products such as DGCG may be effective in binding to the ACE2 receptor and combating the Omicron variant, however, further research is required to validate the results of this study and explore the potential of natural products to mitigate COVID-19.

          Graphical abstract

          Highlights

          • There are 32 mutations in the spike of the Omicron variant.

          • Non-SARS-COV-2 vaccinated individuals accelerate transmission of Omicron variant.

          • Effect of mutation in transmissibility of Omicron.

          • In vitro docking of natural products enhances patient immunity against Omicron virus.

          • High consumption of foods rich in bioactive substances (polyphenols and vitamins) protects against Omicron infection.

          • DGCG could bind to ACE2 receptor three times more effective than standard chloroquine.

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          Most cited references169

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          Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation

          Structure of the nCoV trimeric spike The World Health Organization has declared the outbreak of a novel coronavirus (2019-nCoV) to be a public health emergency of international concern. The virus binds to host cells through its trimeric spike glycoprotein, making this protein a key target for potential therapies and diagnostics. Wrapp et al. determined a 3.5-angstrom-resolution structure of the 2019-nCoV trimeric spike protein by cryo–electron microscopy. Using biophysical assays, the authors show that this protein binds at least 10 times more tightly than the corresponding spike protein of severe acute respiratory syndrome (SARS)–CoV to their common host cell receptor. They also tested three antibodies known to bind to the SARS-CoV spike protein but did not detect binding to the 2019-nCoV spike protein. These studies provide valuable information to guide the development of medical counter-measures for 2019-nCoV. Science, this issue p. 1260
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            OpenSAFELY: factors associated with COVID-19 death in 17 million patients

            COVID-19 has rapidly impacted on mortality worldwide. 1 There is unprecedented urgency to understand who is most at risk of severe outcomes, requiring new approaches for timely analysis of large datasets. Working on behalf of NHS England we created OpenSAFELY: a secure health analytics platform covering 40% of all patients in England, holding patient data within the existing data centre of a major primary care electronic health records vendor. Primary care records of 17,278,392 adults were pseudonymously linked to 10,926 COVID-19 related deaths. COVID-19 related death was associated with: being male (hazard ratio 1.59, 95%CI 1.53-1.65); older age and deprivation (both with a strong gradient); diabetes; severe asthma; and various other medical conditions. Compared to people with white ethnicity, black and South Asian people were at higher risk even after adjustment for other factors (HR 1.48, 1.29-1.69 and 1.45, 1.32-1.58 respectively). We have quantified a range of clinical risk factors for COVID-19 related death in the largest cohort study conducted by any country to date. OpenSAFELY is rapidly adding further patients’ records; we will update and extend results regularly.
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              Structural basis for the recognition of SARS-CoV-2 by full-length human ACE2

              How SARS-CoV-2 binds to human cells Scientists are racing to learn the secrets of severe acute respiratory syndrome–coronavirus 2 (SARS-CoV-2), which is the cause of the pandemic disease COVID-19. The first step in viral entry is the binding of the viral trimeric spike protein to the human receptor angiotensin-converting enzyme 2 (ACE2). Yan et al. present the structure of human ACE2 in complex with a membrane protein that it chaperones, B0AT1. In the context of this complex, ACE2 is a dimer. A further structure shows how the receptor binding domain of SARS-CoV-2 interacts with ACE2 and suggests that it is possible that two trimeric spike proteins bind to an ACE2 dimer. The structures provide a basis for the development of therapeutics targeting this crucial interaction. Science, this issue p. 1444
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                Author and article information

                Contributors
                samar.alkafas@science.tanta.edu.eg , samarsamy2017@yahoo.com
                GhoshS@ufs.ac.za , soumyaghosh@yahoo.com
                sara.139@sh-eng.menofia.edu.eg
                samah.loutfy@bue.edu.eg , samahloutfy@cu.edu.eg
                h.onyeaka@bham.ac.uk
                mohamed.hussien1@science.tanta.edu.eg , mohamed.hessien@fulbrightmail.org
                Journal
                Virol J
                Virol J
                Virology Journal
                BioMed Central (London )
                1743-422X
                25 August 2023
                25 August 2023
                2023
                : 20
                : 191
                Affiliations
                [1 ]GRID grid.412258.8, ISNI 0000 0000 9477 7793, Molecular Cell Biology Unit, Division of Biochemistry, Department of Chemistry, Faculty of Science, , Tanta University, ; Tanta, 31527 Egypt
                [2 ]Narcotic Research Department, National Center for Social and Criminological Research (NCSCR), Giza, 11561 Egypt
                [3 ]GRID grid.7155.6, ISNI 0000 0001 2260 6941, Biotechnology Department at Institute of Graduate Studies and Research, Alexandria University, ; Alexandria, Egypt
                [4 ]GRID grid.412258.8, ISNI 0000 0000 9477 7793, Botany Department, Faculty of Science, , Tanta University, ; Tanta, Egypt
                [5 ]GRID grid.412219.d, ISNI 0000 0001 2284 638X, Department of Genetics, Faculty of Natural and Agricultural Sciences, , University of the Free State, ; Bloemfontein, 9301 South Africa
                [6 ]GRID grid.411775.1, ISNI 0000 0004 0621 4712, Production Engineering and Mechanical Design Department, Faculty of Engineering, , Menofia University, ; Menofia, Egypt
                [7 ]GRID grid.411455.0, ISNI 0000 0001 2203 0321, Department of Agricultural and Food Engineering, Faculty of Agronomy, , Universidad Autónoma de Nuevo León, ; Francisco Villa S/N, Ex-Hacienda El Canadá, 66050 General Escobedo, Nuevo León Mexico
                [8 ]GRID grid.411230.5, ISNI 0000 0000 9296 6873, Department of Microbiology, Faculty of Medicine, , Ahvaz Jundishapur University of Medical Sciences, ; Ahvaz, Iran
                [9 ]GRID grid.7776.1, ISNI 0000 0004 0639 9286, Virology and Immunology Unit, Cancer Biology Department, National Cancer Institute, , Cairo University, ; Cairo, Egypt
                [10 ]GRID grid.440862.c, ISNI 0000 0004 0377 5514, Nanotechnology Research Center, , British University, ; Cairo, Egypt
                [11 ]GRID grid.6572.6, ISNI 0000 0004 1936 7486, School of Chemical Engineering, , University of Birmingham, ; Edgbaston, Birmingham, B15 2TT UK
                [12 ]GRID grid.412258.8, ISNI 0000 0000 9477 7793, Division of Biochemistry, Department of Chemistry, , Faculty of Science, Tanta University, ; Tanta, 31527, Egypt
                Article
                2160
                10.1186/s12985-023-02160-6
                10464336
                37626376
                a057b900-4774-4a9f-8c41-57c6e123b7a8
                © BioMed Central Ltd., part of Springer Nature 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 29 March 2023
                : 15 August 2023
                Funding
                Funded by: The Science, Technology & Innovation Funding Authority (STDF) in cooperation with the Egyptian Knowledge Bank (EKB)
                Funded by: Tanta University
                Categories
                Review
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2023

                Microbiology & Virology
                covid-19,omicron,natural product,in silico,vaccine,molecular docking
                Microbiology & Virology
                covid-19, omicron, natural product, in silico, vaccine, molecular docking

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