Highly infectious SARS-CoV pseudotyped virus reveals the cell tropism and its correlation with receptor expression.
Identifieur interne : 002B64 ( PubMed/Corpus ); précédent : 002B63; suivant : 002B65Highly infectious SARS-CoV pseudotyped virus reveals the cell tropism and its correlation with receptor expression.
Auteurs : Yuchun Nie ; Peigang Wang ; Xuanling Shi ; Guangwen Wang ; Jian Chen ; Aihua Zheng ; Wei Wang ; Zai Wang ; Xiuxia Qu ; Min Luo ; Lei Tan ; Xijun Song ; Xiaolei Yin ; Jianguo Chen ; Mingxiao Ding ; Hongkui DengSource :
- Biochemical and biophysical research communications [ 0006-291X ] ; 2004.
English descriptors
- KwdEn :
- Animals, Base Sequence, Carboxypeptidases (genetics), Carboxypeptidases (physiology), Cell Line, Chimera (genetics), Chlorocebus aethiops, DNA, Recombinant (genetics), Gene Expression, Genes, Viral, HIV (genetics), Humans, Hydrogen-Ion Concentration, Membrane Glycoproteins (genetics), Mice, Peptidyl-Dipeptidase A, Receptors, Virus (genetics), Receptors, Virus (physiology), SARS Virus (genetics), SARS Virus (pathogenicity), SARS Virus (physiology), Spike Glycoprotein, Coronavirus, Vero Cells, Viral Envelope Proteins (genetics), Virulence (genetics), Virulence (physiology), Virus Assembly.
- MESH :
- chemical , genetics : Carboxypeptidases, DNA, Recombinant, Membrane Glycoproteins, Receptors, Virus, Viral Envelope Proteins.
- chemical , physiology : Carboxypeptidases, Receptors, Virus.
- genetics : Chimera, HIV, SARS Virus, Virulence.
- pathogenicity : SARS Virus.
- physiology : SARS Virus, Virulence.
- Animals, Base Sequence, Cell Line, Chlorocebus aethiops, Gene Expression, Genes, Viral, Humans, Hydrogen-Ion Concentration, Mice, Peptidyl-Dipeptidase A, Spike Glycoprotein, Coronavirus, Vero Cells, Virus Assembly.
Abstract
Studies of SARS coronavirus (SARS-CoV)-the causative agent of severe acute respiratory syndrome (SARS)-have been hampered by its high transmission rate and the pathogenicity of this virus. To permit analysis of the host range and entry mechanism of SARS-CoV, we incorporated the humanized SARS-CoV spike (S) glycoprotein into HIV particles to generate a highly infectious SARS-CoV pseudotyped virus. The infection on Vero E6-a permissive cell line to SARS-CoV-could be neutralized by sera from convalescent SARS patients, and the entry was a pH-dependent process. With these highly infectious SARS-CoV pseudotypes, several cell lines derived from various tissues were revealed as susceptible to SARS-CoV, which were highly corresponding to the expression pattern of virus's receptor angiotensin-converting enzyme 2 (ACE2). In addition, we also demonstrated angiotensin 1 converting enzyme (ACE)-the homologue of ACE2 could not function as a receptor for SARS-CoV.
DOI: 10.1016/j.bbrc.2004.07.060
PubMed: 15358126
Links to Exploration step
pubmed:15358126Le document en format XML
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uniqKey="Nie Y" first="Yuchun" last="Nie">Yuchun Nie</name><affiliation><nlm:affiliation>Department of Cell Biology and Genetics, College of Life Sciences, Peking University, Beijing 100871, PR China.</nlm:affiliation></affiliation></author><author><name sortKey="Wang, Peigang" sort="Wang, Peigang" uniqKey="Wang P" first="Peigang" last="Wang">Peigang Wang</name></author><author><name sortKey="Shi, Xuanling" sort="Shi, Xuanling" uniqKey="Shi X" first="Xuanling" last="Shi">Xuanling Shi</name></author><author><name sortKey="Wang, Guangwen" sort="Wang, Guangwen" uniqKey="Wang G" first="Guangwen" last="Wang">Guangwen Wang</name></author><author><name sortKey="Chen, Jian" sort="Chen, Jian" uniqKey="Chen J" first="Jian" last="Chen">Jian Chen</name></author><author><name sortKey="Zheng, Aihua" sort="Zheng, Aihua" uniqKey="Zheng A" first="Aihua" last="Zheng">Aihua Zheng</name></author><author><name sortKey="Wang, Wei" sort="Wang, Wei" uniqKey="Wang W" first="Wei" last="Wang">Wei 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Ding</name></author><author><name sortKey="Deng, Hongkui" sort="Deng, Hongkui" uniqKey="Deng H" first="Hongkui" last="Deng">Hongkui Deng</name></author></analytic><series><title level="j">Biochemical and biophysical research communications</title><idno type="ISSN">0006-291X</idno><imprint><date when="2004" type="published">2004</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Base Sequence</term><term>Carboxypeptidases (genetics)</term><term>Carboxypeptidases (physiology)</term><term>Cell Line</term><term>Chimera (genetics)</term><term>Chlorocebus aethiops</term><term>DNA, Recombinant (genetics)</term><term>Gene Expression</term><term>Genes, Viral</term><term>HIV (genetics)</term><term>Humans</term><term>Hydrogen-Ion Concentration</term><term>Membrane Glycoproteins (genetics)</term><term>Mice</term><term>Peptidyl-Dipeptidase A</term><term>Receptors, Virus (genetics)</term><term>Receptors, Virus (physiology)</term><term>SARS Virus (genetics)</term><term>SARS Virus (pathogenicity)</term><term>SARS Virus (physiology)</term><term>Spike Glycoprotein, Coronavirus</term><term>Vero Cells</term><term>Viral Envelope Proteins (genetics)</term><term>Virulence (genetics)</term><term>Virulence (physiology)</term><term>Virus Assembly</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Carboxypeptidases</term><term>DNA, Recombinant</term><term>Membrane Glycoproteins</term><term>Receptors, Virus</term><term>Viral Envelope Proteins</term></keywords><keywords scheme="MESH" type="chemical" qualifier="physiology" xml:lang="en"><term>Carboxypeptidases</term><term>Receptors, Virus</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Chimera</term><term>HIV</term><term>SARS Virus</term><term>Virulence</term></keywords><keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en"><term>SARS Virus</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>SARS Virus</term><term>Virulence</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Base Sequence</term><term>Cell Line</term><term>Chlorocebus aethiops</term><term>Gene Expression</term><term>Genes, Viral</term><term>Humans</term><term>Hydrogen-Ion Concentration</term><term>Mice</term><term>Peptidyl-Dipeptidase A</term><term>Spike Glycoprotein, Coronavirus</term><term>Vero Cells</term><term>Virus Assembly</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Studies of SARS coronavirus (SARS-CoV)-the causative agent of severe acute respiratory syndrome (SARS)-have been hampered by its high transmission rate and the pathogenicity of this virus. To permit analysis of the host range and entry mechanism of SARS-CoV, we incorporated the humanized SARS-CoV spike (S) glycoprotein into HIV particles to generate a highly infectious SARS-CoV pseudotyped virus. The infection on Vero E6-a permissive cell line to SARS-CoV-could be neutralized by sera from convalescent SARS patients, and the entry was a pH-dependent process. With these highly infectious SARS-CoV pseudotypes, several cell lines derived from various tissues were revealed as susceptible to SARS-CoV, which were highly corresponding to the expression pattern of virus's receptor angiotensin-converting enzyme 2 (ACE2). In addition, we also demonstrated angiotensin 1 converting enzyme (ACE)-the homologue of ACE2 could not function as a receptor for SARS-CoV.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">15358126</PMID><DateCompleted><Year>2004</Year><Month>10</Month><Day>14</Day></DateCompleted><DateRevised><Year>2020</Year><Month>04</Month><Day>15</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0006-291X</ISSN><JournalIssue CitedMedium="Print"><Volume>321</Volume><Issue>4</Issue><PubDate><Year>2004</Year><Month>Sep</Month><Day>03</Day></PubDate></JournalIssue><Title>Biochemical and biophysical research communications</Title><ISOAbbreviation>Biochem. Biophys. Res. Commun.</ISOAbbreviation></Journal><ArticleTitle>Highly infectious SARS-CoV pseudotyped virus reveals the cell tropism and its correlation with receptor expression.</ArticleTitle><Pagination><MedlinePgn>994-1000</MedlinePgn></Pagination><Abstract><AbstractText>Studies of SARS coronavirus (SARS-CoV)-the causative agent of severe acute respiratory syndrome (SARS)-have been hampered by its high transmission rate and the pathogenicity of this virus. To permit analysis of the host range and entry mechanism of SARS-CoV, we incorporated the humanized SARS-CoV spike (S) glycoprotein into HIV particles to generate a highly infectious SARS-CoV pseudotyped virus. The infection on Vero E6-a permissive cell line to SARS-CoV-could be neutralized by sera from convalescent SARS patients, and the entry was a pH-dependent process. With these highly infectious SARS-CoV pseudotypes, several cell lines derived from various tissues were revealed as susceptible to SARS-CoV, which were highly corresponding to the expression pattern of virus's receptor angiotensin-converting enzyme 2 (ACE2). In addition, we also demonstrated angiotensin 1 converting enzyme (ACE)-the homologue of ACE2 could not function as a receptor for SARS-CoV.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Nie</LastName><ForeName>Yuchun</ForeName><Initials>Y</Initials><AffiliationInfo><Affiliation>Department of Cell Biology and Genetics, College of Life Sciences, Peking University, Beijing 100871, PR China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Peigang</ForeName><Initials>P</Initials></Author><Author ValidYN="Y"><LastName>Shi</LastName><ForeName>Xuanling</ForeName><Initials>X</Initials></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Guangwen</ForeName><Initials>G</Initials></Author><Author ValidYN="Y"><LastName>Chen</LastName><ForeName>Jian</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Zheng</LastName><ForeName>Aihua</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Wei</ForeName><Initials>W</Initials></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Zai</ForeName><Initials>Z</Initials></Author><Author ValidYN="Y"><LastName>Qu</LastName><ForeName>Xiuxia</ForeName><Initials>X</Initials></Author><Author ValidYN="Y"><LastName>Luo</LastName><ForeName>Min</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Tan</LastName><ForeName>Lei</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><LastName>Song</LastName><ForeName>Xijun</ForeName><Initials>X</Initials></Author><Author ValidYN="Y"><LastName>Yin</LastName><ForeName>Xiaolei</ForeName><Initials>X</Initials></Author><Author ValidYN="Y"><LastName>Chen</LastName><ForeName>Jianguo</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Ding</LastName><ForeName>Mingxiao</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Deng</LastName><ForeName>Hongkui</ForeName><Initials>H</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Biochem Biophys Res Commun</MedlineTA><NlmUniqueID>0372516</NlmUniqueID><ISSNLinking>0006-291X</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D004274">DNA, Recombinant</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008562">Membrane Glycoproteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011991">Receptors, Virus</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D064370">Spike Glycoprotein, 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UI="D002268" MajorTopicYN="N">Carboxypeptidases</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002460" MajorTopicYN="N">Cell Line</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002678" MajorTopicYN="N">Chimera</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002522" MajorTopicYN="N">Chlorocebus aethiops</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004274" MajorTopicYN="N">DNA, Recombinant</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015870" MajorTopicYN="N">Gene Expression</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005814" MajorTopicYN="N">Genes, 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|area= SrasV1
|flux= PubMed
|étape= Corpus
|type= RBID
|clé= pubmed:15358126
|texte= Highly infectious SARS-CoV pseudotyped virus reveals the cell tropism and its correlation with receptor expression.
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/RBID.i -Sk "pubmed:15358126" \
| HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd \
| NlmPubMed2Wicri -a SrasV1
| This area was generated with Dilib version V0.6.33. |  |