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SARS-CoV-2: Receptor and Co-receptor Tropism Probability
The recent pandemic which arose from China, is caused by a pathogenic virus named “severe acute respiratory syndrome-related coronavirus-2 (SARS-CoV-2)”. Its rapid global expansion has inflicted an extreme public health concern. The attachment of receptor-binding domains (RBD) of the spike proteins...
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Published in: | Current microbiology 2022-05, Vol.79 (5), p.133-133, Article 133 |
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container_title | Current microbiology |
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description | The recent pandemic which arose from China, is caused by a pathogenic virus named “severe acute respiratory syndrome-related coronavirus-2 (SARS-CoV-2)”. Its rapid global expansion has inflicted an extreme public health concern. The attachment of receptor-binding domains (RBD) of the spike proteins (S) to the host cell’s membrane, with or without the help of other cellular components such as proteases and especially co-receptors, is required for the first stage of its pathogenesis. In addition to humans, angiotensin-converting enzyme 2 (ACE2) is found on a wide range of vertebrate host’s cellular surface. SARS-CoV-2 has a broad spectrum of tropism; thus, it can infect a vast range of tissues, organs, and hosts; even though the surface amino acids of the spike protein conflict in the receptor-binding region. Due to the heterogeneous ACE2 distribution and the presence of different domains on the SARS-CoV-2 spike protein for binding, the virus entry into diverse host cell types may depend on the host cells’ receptor presentation with or without co-receptors. This review investigates multiple current types of receptor and co-receptor tropisms, with other molecular factors alongside their respective mechanisms, which facilitate the binding and entry of SARS-CoV-2 into the cells, extending the severity of the coronavirus disease 2019 (COVID-19). Understanding the pathogenesis of COVID-19 from this perspective can effectively help prevent this disease and provide more potent treatment strategies, particularly in vulnerable people with various cellular-level susceptibilities. |
doi_str_mv | 10.1007/s00284-022-02807-7 |
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Its rapid global expansion has inflicted an extreme public health concern. The attachment of receptor-binding domains (RBD) of the spike proteins (S) to the host cell’s membrane, with or without the help of other cellular components such as proteases and especially co-receptors, is required for the first stage of its pathogenesis. In addition to humans, angiotensin-converting enzyme 2 (ACE2) is found on a wide range of vertebrate host’s cellular surface. SARS-CoV-2 has a broad spectrum of tropism; thus, it can infect a vast range of tissues, organs, and hosts; even though the surface amino acids of the spike protein conflict in the receptor-binding region. Due to the heterogeneous ACE2 distribution and the presence of different domains on the SARS-CoV-2 spike protein for binding, the virus entry into diverse host cell types may depend on the host cells’ receptor presentation with or without co-receptors. This review investigates multiple current types of receptor and co-receptor tropisms, with other molecular factors alongside their respective mechanisms, which facilitate the binding and entry of SARS-CoV-2 into the cells, extending the severity of the coronavirus disease 2019 (COVID-19). Understanding the pathogenesis of COVID-19 from this perspective can effectively help prevent this disease and provide more potent treatment strategies, particularly in vulnerable people with various cellular-level susceptibilities.</description><identifier>ISSN: 0343-8651</identifier><identifier>EISSN: 1432-0991</identifier><identifier>DOI: 10.1007/s00284-022-02807-7</identifier><identifier>PMID: 35292865</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>ACE2 ; Amino acids ; Angiotensin ; Angiotensin-converting enzyme 2 ; Binding ; Biomedical and Life Sciences ; Biotechnology ; Coronaviruses ; COVID-19 ; Humans ; Life Sciences ; Microbiology ; Organs ; Pandemics ; Pathogenesis ; Peptidyl-dipeptidase A ; Peptidyl-Dipeptidase A - metabolism ; Probability ; Proteins ; Public health ; Receptors ; Receptors, Virus - genetics ; Receptors, Virus - metabolism ; Respiratory diseases ; Review ; Review Article ; SARS-CoV-2 ; Severe acute respiratory syndrome coronavirus 2 ; Spike Glycoprotein, Coronavirus ; Spike protein ; Tropism ; Vertebrates ; Viral diseases ; Viruses</subject><ispartof>Current microbiology, 2022-05, Vol.79 (5), p.133-133, Article 133</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022</rights><rights>2022. 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Its rapid global expansion has inflicted an extreme public health concern. The attachment of receptor-binding domains (RBD) of the spike proteins (S) to the host cell’s membrane, with or without the help of other cellular components such as proteases and especially co-receptors, is required for the first stage of its pathogenesis. In addition to humans, angiotensin-converting enzyme 2 (ACE2) is found on a wide range of vertebrate host’s cellular surface. SARS-CoV-2 has a broad spectrum of tropism; thus, it can infect a vast range of tissues, organs, and hosts; even though the surface amino acids of the spike protein conflict in the receptor-binding region. Due to the heterogeneous ACE2 distribution and the presence of different domains on the SARS-CoV-2 spike protein for binding, the virus entry into diverse host cell types may depend on the host cells’ receptor presentation with or without co-receptors. This review investigates multiple current types of receptor and co-receptor tropisms, with other molecular factors alongside their respective mechanisms, which facilitate the binding and entry of SARS-CoV-2 into the cells, extending the severity of the coronavirus disease 2019 (COVID-19). Understanding the pathogenesis of COVID-19 from this perspective can effectively help prevent this disease and provide more potent treatment strategies, particularly in vulnerable people with various cellular-level susceptibilities.</description><subject>ACE2</subject><subject>Amino acids</subject><subject>Angiotensin</subject><subject>Angiotensin-converting enzyme 2</subject><subject>Binding</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Microbiology</subject><subject>Organs</subject><subject>Pandemics</subject><subject>Pathogenesis</subject><subject>Peptidyl-dipeptidase A</subject><subject>Peptidyl-Dipeptidase A - metabolism</subject><subject>Probability</subject><subject>Proteins</subject><subject>Public health</subject><subject>Receptors</subject><subject>Receptors, Virus - genetics</subject><subject>Receptors, Virus - metabolism</subject><subject>Respiratory diseases</subject><subject>Review</subject><subject>Review Article</subject><subject>SARS-CoV-2</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Spike Glycoprotein, Coronavirus</subject><subject>Spike protein</subject><subject>Tropism</subject><subject>Vertebrates</subject><subject>Viral diseases</subject><subject>Viruses</subject><issn>0343-8651</issn><issn>1432-0991</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9UctKAzEUDaLY-vgBF1Jw4yZ6c5OZSVwIUnxBQfG1DZlMWkemk5pMBf_eaLU-Fi6ScHLOPfdeDiE7DA4YQHEYAVAKCojpSChosUL6TPAElWKrpA9ccCrzjPXIRoxPAAwVsHXS4xkqTESfyNuTm1s69A8UjwY3zrpZ58PAtNVg6Gn4wnfBz-o4HVwHX5qyburudYusjU0T3fbnu0nuz07vhhd0dHV-OTwZUSsK0VFhlZEW0UCZlTZN4BwHnmeIcpzLyoDMTPqvlK0MZgUKbpWz4xLSDXmCm-R44Tubl1NXWdd2wTR6FuqpCa_am1r_Ztr6UU_8i5YKucQsGex_GgT_PHex09M6Wtc0pnV-HjXmAkBInkGS7v2RPvl5aNN6ScUVQ87E-0S4UNngYwxuvByGgX4PRi-C0SkY_RGMLlLR7s81liVfSSQBXwhiotqJC9-9_7F9A-gfl2k</recordid><startdate>20220501</startdate><enddate>20220501</enddate><creator>Eslami, Narges</creator><creator>Aghbash, Parisa Shiri</creator><creator>Shamekh, Ali</creator><creator>Entezari-Maleki, Taher</creator><creator>Nahand, Javid Sadri</creator><creator>Sales, Abolfazl Jafari</creator><creator>Baghi, Hossein Bannazadeh</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2513-5361</orcidid><orcidid>https://orcid.org/0000-0003-0749-9548</orcidid></search><sort><creationdate>20220501</creationdate><title>SARS-CoV-2: Receptor and Co-receptor Tropism Probability</title><author>Eslami, Narges ; Aghbash, Parisa Shiri ; Shamekh, Ali ; Entezari-Maleki, Taher ; Nahand, Javid Sadri ; Sales, Abolfazl Jafari ; Baghi, Hossein Bannazadeh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-4c9a8c22a0b5bc001ee30365228f68da085abc0d9cda257243c9ecfb09ec06243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>ACE2</topic><topic>Amino acids</topic><topic>Angiotensin</topic><topic>Angiotensin-converting enzyme 2</topic><topic>Binding</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Microbiology</topic><topic>Organs</topic><topic>Pandemics</topic><topic>Pathogenesis</topic><topic>Peptidyl-dipeptidase A</topic><topic>Peptidyl-Dipeptidase A - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Current microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eslami, Narges</au><au>Aghbash, Parisa Shiri</au><au>Shamekh, Ali</au><au>Entezari-Maleki, Taher</au><au>Nahand, Javid Sadri</au><au>Sales, Abolfazl Jafari</au><au>Baghi, Hossein Bannazadeh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SARS-CoV-2: Receptor and Co-receptor Tropism Probability</atitle><jtitle>Current microbiology</jtitle><stitle>Curr Microbiol</stitle><addtitle>Curr Microbiol</addtitle><date>2022-05-01</date><risdate>2022</risdate><volume>79</volume><issue>5</issue><spage>133</spage><epage>133</epage><pages>133-133</pages><artnum>133</artnum><issn>0343-8651</issn><eissn>1432-0991</eissn><abstract>The recent pandemic which arose from China, is caused by a pathogenic virus named “severe acute respiratory syndrome-related coronavirus-2 (SARS-CoV-2)”. Its rapid global expansion has inflicted an extreme public health concern. The attachment of receptor-binding domains (RBD) of the spike proteins (S) to the host cell’s membrane, with or without the help of other cellular components such as proteases and especially co-receptors, is required for the first stage of its pathogenesis. In addition to humans, angiotensin-converting enzyme 2 (ACE2) is found on a wide range of vertebrate host’s cellular surface. SARS-CoV-2 has a broad spectrum of tropism; thus, it can infect a vast range of tissues, organs, and hosts; even though the surface amino acids of the spike protein conflict in the receptor-binding region. Due to the heterogeneous ACE2 distribution and the presence of different domains on the SARS-CoV-2 spike protein for binding, the virus entry into diverse host cell types may depend on the host cells’ receptor presentation with or without co-receptors. This review investigates multiple current types of receptor and co-receptor tropisms, with other molecular factors alongside their respective mechanisms, which facilitate the binding and entry of SARS-CoV-2 into the cells, extending the severity of the coronavirus disease 2019 (COVID-19). Understanding the pathogenesis of COVID-19 from this perspective can effectively help prevent this disease and provide more potent treatment strategies, particularly in vulnerable people with various cellular-level susceptibilities.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>35292865</pmid><doi>10.1007/s00284-022-02807-7</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-2513-5361</orcidid><orcidid>https://orcid.org/0000-0003-0749-9548</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | ACE2 Amino acids Angiotensin Angiotensin-converting enzyme 2 Binding Biomedical and Life Sciences Biotechnology Coronaviruses COVID-19 Humans Life Sciences Microbiology Organs Pandemics Pathogenesis Peptidyl-dipeptidase A Peptidyl-Dipeptidase A - metabolism Probability Proteins Public health Receptors Receptors, Virus - genetics Receptors, Virus - metabolism Respiratory diseases Review Review Article SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 Spike Glycoprotein, Coronavirus Spike protein Tropism Vertebrates Viral diseases Viruses |
title | SARS-CoV-2: Receptor and Co-receptor Tropism Probability |
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