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Host Cell and SARS-CoV-2-Associated Molecular Structures and Factors as Potential Therapeutic Targets
Coronavirus disease 19 (COVID-19) is caused by an enveloped, positive-sense, single-stranded RNA virus, referred to as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which belongs to the realm Riboviria, order Nidovirales, family Coronaviridae, genus Betacoronavirus and the species Se...
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Published in: | Cells (Basel, Switzerland) Switzerland), 2021-09, Vol.10 (9), p.2427 |
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creator | Chaudhary, Jitendra Kumar Yadav, Rohitash Chaudhary, Pankaj Kumar Maurya, Anurag Roshan, Rakesh Azam, Faizul Mehta, Jyoti Handu, Shailendra Prasad, Ramasare Jain, Neeraj Pandey, Avaneesh Kumar Dhamija, Puneet |
description | Coronavirus disease 19 (COVID-19) is caused by an enveloped, positive-sense, single-stranded RNA virus, referred to as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which belongs to the realm Riboviria, order Nidovirales, family Coronaviridae, genus Betacoronavirus and the species Severe acute respiratory syndrome-related coronavirus. This viral disease is characterized by a myriad of varying symptoms, such as pyrexia, cough, hemoptysis, dyspnoea, diarrhea, muscle soreness, dysosmia, lymphopenia and dysgeusia amongst others. The virus mainly infects humans, various other mammals, avian species and some other companion livestock. SARS-CoV-2 cellular entry is primarily accomplished by molecular interaction between the virus’s spike (S) protein and the host cell surface receptor, angiotensin-converting enzyme 2 (ACE2), although other host cell-associated receptors/factors, such as neuropilin 1 (NRP-1) and neuropilin 2 (NRP-2), C-type lectin receptors (CLRs), as well as proteases such as TMPRSS2 (transmembrane serine protease 2) and furin, might also play a crucial role in infection, tropism, pathogenesis and clinical outcome. Furthermore, several structural and non-structural proteins of the virus themselves are very critical in determining the clinical outcome following infection. Considering such critical role(s) of the abovementioned host cell receptors, associated proteases/factors and virus structural/non-structural proteins (NSPs), it may be quite prudent to therapeutically target them through a multipronged clinical regimen to combat the disease. |
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This viral disease is characterized by a myriad of varying symptoms, such as pyrexia, cough, hemoptysis, dyspnoea, diarrhea, muscle soreness, dysosmia, lymphopenia and dysgeusia amongst others. The virus mainly infects humans, various other mammals, avian species and some other companion livestock. SARS-CoV-2 cellular entry is primarily accomplished by molecular interaction between the virus’s spike (S) protein and the host cell surface receptor, angiotensin-converting enzyme 2 (ACE2), although other host cell-associated receptors/factors, such as neuropilin 1 (NRP-1) and neuropilin 2 (NRP-2), C-type lectin receptors (CLRs), as well as proteases such as TMPRSS2 (transmembrane serine protease 2) and furin, might also play a crucial role in infection, tropism, pathogenesis and clinical outcome. Furthermore, several structural and non-structural proteins of the virus themselves are very critical in determining the clinical outcome following infection. Considering such critical role(s) of the abovementioned host cell receptors, associated proteases/factors and virus structural/non-structural proteins (NSPs), it may be quite prudent to therapeutically target them through a multipronged clinical regimen to combat the disease.</description><identifier>ISSN: 2073-4409</identifier><identifier>EISSN: 2073-4409</identifier><identifier>DOI: 10.3390/cells10092427</identifier><identifier>PMID: 34572076</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>ACE2 ; Angiotensin ; Angiotensin-converting enzyme 2 ; Cell surface ; coronavirus disease 19 ; Coronaviruses ; Cough ; COVID-19 ; Diarrhea ; Disease transmission ; Dyspnea ; Enzymes ; Epidemics ; Epigenetics ; Fever ; Furin ; Gene expression ; Genomes ; Hemoptysis ; Infections ; Livestock ; Lymphopenia ; Middle East respiratory syndrome ; Neuropilin ; Pandemics ; pathogenesis ; Peptidyl-dipeptidase A ; Proteins ; Respiration ; Review ; RNA polymerase ; RNA viruses ; SARS-CoV-2 ; Serine proteinase ; Severe acute respiratory syndrome coronavirus 2 ; Structural proteins ; therapeutic targeting ; Therapeutic targets ; Tropism ; Viral diseases ; Viral infections ; Viruses</subject><ispartof>Cells (Basel, Switzerland), 2021-09, Vol.10 (9), p.2427</ispartof><rights>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 (https://creativecommons.org/licenses/by/4.0/). 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This viral disease is characterized by a myriad of varying symptoms, such as pyrexia, cough, hemoptysis, dyspnoea, diarrhea, muscle soreness, dysosmia, lymphopenia and dysgeusia amongst others. The virus mainly infects humans, various other mammals, avian species and some other companion livestock. SARS-CoV-2 cellular entry is primarily accomplished by molecular interaction between the virus’s spike (S) protein and the host cell surface receptor, angiotensin-converting enzyme 2 (ACE2), although other host cell-associated receptors/factors, such as neuropilin 1 (NRP-1) and neuropilin 2 (NRP-2), C-type lectin receptors (CLRs), as well as proteases such as TMPRSS2 (transmembrane serine protease 2) and furin, might also play a crucial role in infection, tropism, pathogenesis and clinical outcome. Furthermore, several structural and non-structural proteins of the virus themselves are very critical in determining the clinical outcome following infection. Considering such critical role(s) of the abovementioned host cell receptors, associated proteases/factors and virus structural/non-structural proteins (NSPs), it may be quite prudent to therapeutically target them through a multipronged clinical regimen to combat the disease.</description><subject>ACE2</subject><subject>Angiotensin</subject><subject>Angiotensin-converting enzyme 2</subject><subject>Cell surface</subject><subject>coronavirus disease 19</subject><subject>Coronaviruses</subject><subject>Cough</subject><subject>COVID-19</subject><subject>Diarrhea</subject><subject>Disease transmission</subject><subject>Dyspnea</subject><subject>Enzymes</subject><subject>Epidemics</subject><subject>Epigenetics</subject><subject>Fever</subject><subject>Furin</subject><subject>Gene expression</subject><subject>Genomes</subject><subject>Hemoptysis</subject><subject>Infections</subject><subject>Livestock</subject><subject>Lymphopenia</subject><subject>Middle East respiratory syndrome</subject><subject>Neuropilin</subject><subject>Pandemics</subject><subject>pathogenesis</subject><subject>Peptidyl-dipeptidase A</subject><subject>Proteins</subject><subject>Respiration</subject><subject>Review</subject><subject>RNA polymerase</subject><subject>RNA viruses</subject><subject>SARS-CoV-2</subject><subject>Serine proteinase</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Structural proteins</subject><subject>therapeutic targeting</subject><subject>Therapeutic targets</subject><subject>Tropism</subject><subject>Viral diseases</subject><subject>Viral 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subjects | ACE2 Angiotensin Angiotensin-converting enzyme 2 Cell surface coronavirus disease 19 Coronaviruses Cough COVID-19 Diarrhea Disease transmission Dyspnea Enzymes Epidemics Epigenetics Fever Furin Gene expression Genomes Hemoptysis Infections Livestock Lymphopenia Middle East respiratory syndrome Neuropilin Pandemics pathogenesis Peptidyl-dipeptidase A Proteins Respiration Review RNA polymerase RNA viruses SARS-CoV-2 Serine proteinase Severe acute respiratory syndrome coronavirus 2 Structural proteins therapeutic targeting Therapeutic targets Tropism Viral diseases Viral infections Viruses |
title | Host Cell and SARS-CoV-2-Associated Molecular Structures and Factors as Potential Therapeutic Targets |
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