Fat(al) attraction: Picornaviruses Usurp Lipid Transfer at Membrane Contact Sites to Create Replication Organelles.
Identifieur interne : 002C30 ( Ncbi/Merge ); précédent : 002C29; suivant : 002C31Fat(al) attraction: Picornaviruses Usurp Lipid Transfer at Membrane Contact Sites to Create Replication Organelles.
Auteurs : Hilde M. Van Der Schaar [Pays-Bas] ; Cristina M. Dorobantu [Pays-Bas] ; Lucian Albulescu [Pays-Bas] ; Jeroen R P M. Strating [Pays-Bas] ; Frank J M. Van Kuppeveld [Pays-Bas]Source :
- Trends in microbiology [ 1878-4380 ] ; 2016.
Descripteurs français
- KwdFr :
- MESH :
- croissance et développement : Enterovirus.
- génétique : Génome viral, Réplication virale.
- métabolisme : Enterovirus.
- pathogénicité : Enterovirus.
- physiologie : Métabolisme des lipides, Réplication virale.
- virologie : Membranes intracellulaires.
- Humains, Lipides.
English descriptors
- KwdEn :
- MESH :
- chemical : Lipids.
- genetics : Genome, Viral, Virus Replication.
- growth & development : Enterovirus.
- metabolism : Enterovirus.
- pathogenicity : Enterovirus.
- physiology : Lipid Metabolism, Virus Replication.
- virology : Intracellular Membranes.
- Humans.
Abstract
All viruses that carry a positive-sense RNA genome (+RNA), such as picornaviruses, hepatitis C virus, dengue virus, and SARS- and MERS-coronavirus, confiscate intracellular membranes of the host cell to generate new compartments (i.e., replication organelles) for amplification of their genome. Replication organelles (ROs) are membranous structures that not only harbor viral proteins but also contain a specific array of hijacked host factors that create a unique lipid microenvironment optimal for genome replication. While some lipids may be locally synthesized de novo, other lipids are shuttled towards ROs. In picornavirus-infected cells, lipids are exchanged at membrane contact sites between ROs and other organelles. In this paper, we review recent advances in our understanding of how picornaviruses exploit host membrane contact site machinery to generate ROs, a mechanism that is used by some other +RNA viruses as well.
DOI: 10.1016/j.tim.2016.02.017
PubMed: 27020598
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pubmed:27020598Le document en format XML
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Van Der Schaar</name><affiliation wicri:level="4"><nlm:affiliation>Department of Infectious Diseases & Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.</nlm:affiliation><country xml:lang="fr">Pays-Bas</country><wicri:regionArea>Department of Infectious Diseases & Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Utrecht</wicri:regionArea><placeName><settlement type="city">Utrecht</settlement><region nuts="2" type="province">Utrecht (province)</region></placeName><orgName type="university">Université d'Utrecht</orgName></affiliation></author><author><name sortKey="Dorobantu, Cristina M" sort="Dorobantu, Cristina M" uniqKey="Dorobantu C" first="Cristina M" last="Dorobantu">Cristina M. 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Van Kuppeveld</name><affiliation wicri:level="4"><nlm:affiliation>Department of Infectious Diseases & Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands. Electronic address: f.j.m.vankuppeveld@uu.nl.</nlm:affiliation><country xml:lang="fr">Pays-Bas</country><wicri:regionArea>Department of Infectious Diseases & Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Utrecht</wicri:regionArea><placeName><settlement type="city">Utrecht</settlement><region nuts="2" type="province">Utrecht (province)</region></placeName><orgName type="university">Université d'Utrecht</orgName></affiliation></author></analytic><series><title level="j">Trends in microbiology</title><idno type="eISSN">1878-4380</idno><imprint><date when="2016" type="published">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Enterovirus (growth & development)</term><term>Enterovirus (metabolism)</term><term>Enterovirus (pathogenicity)</term><term>Genome, Viral (genetics)</term><term>Humans</term><term>Intracellular Membranes (virology)</term><term>Lipid Metabolism (physiology)</term><term>Lipids</term><term>Virus Replication (genetics)</term><term>Virus Replication (physiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Enterovirus (croissance et développement)</term><term>Enterovirus (métabolisme)</term><term>Enterovirus (pathogénicité)</term><term>Génome viral (génétique)</term><term>Humains</term><term>Lipides</term><term>Membranes intracellulaires (virologie)</term><term>Métabolisme des lipides (physiologie)</term><term>Réplication virale (génétique)</term><term>Réplication virale (physiologie)</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Lipids</term></keywords><keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr"><term>Enterovirus</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Genome, Viral</term><term>Virus Replication</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Enterovirus</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Génome viral</term><term>Réplication virale</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Enterovirus</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Enterovirus</term></keywords><keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en"><term>Enterovirus</term></keywords><keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr"><term>Enterovirus</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Métabolisme des lipides</term><term>Réplication virale</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Lipid Metabolism</term><term>Virus Replication</term></keywords><keywords scheme="MESH" qualifier="virologie" xml:lang="fr"><term>Membranes intracellulaires</term></keywords><keywords scheme="MESH" qualifier="virology" xml:lang="en"><term>Intracellular Membranes</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Humans</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Humains</term><term>Lipides</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">All viruses that carry a positive-sense RNA genome (+RNA), such as picornaviruses, hepatitis C virus, dengue virus, and SARS- and MERS-coronavirus, confiscate intracellular membranes of the host cell to generate new compartments (i.e., replication organelles) for amplification of their genome. Replication organelles (ROs) are membranous structures that not only harbor viral proteins but also contain a specific array of hijacked host factors that create a unique lipid microenvironment optimal for genome replication. While some lipids may be locally synthesized de novo, other lipids are shuttled towards ROs. In picornavirus-infected cells, lipids are exchanged at membrane contact sites between ROs and other organelles. In this paper, we review recent advances in our understanding of how picornaviruses exploit host membrane contact site machinery to generate ROs, a mechanism that is used by some other +RNA viruses as well.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">27020598</PMID><DateCompleted><Year>2017</Year><Month>11</Month><Day>16</Day></DateCompleted><DateRevised><Year>2020</Year><Month>04</Month><Day>09</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1878-4380</ISSN><JournalIssue CitedMedium="Internet"><Volume>24</Volume><Issue>7</Issue><PubDate><Year>2016</Year><Month>07</Month></PubDate></JournalIssue><Title>Trends in microbiology</Title><ISOAbbreviation>Trends Microbiol.</ISOAbbreviation></Journal><ArticleTitle>Fat(al) attraction: Picornaviruses Usurp Lipid Transfer at Membrane Contact Sites to Create Replication Organelles.</ArticleTitle><Pagination><MedlinePgn>535-546</MedlinePgn></Pagination><ELocationID EIdType="pii" ValidYN="Y">S0966-842X(16)00054-8</ELocationID><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.tim.2016.02.017</ELocationID><Abstract><AbstractText>All viruses that carry a positive-sense RNA genome (+RNA), such as picornaviruses, hepatitis C virus, dengue virus, and SARS- and MERS-coronavirus, confiscate intracellular membranes of the host cell to generate new compartments (i.e., replication organelles) for amplification of their genome. Replication organelles (ROs) are membranous structures that not only harbor viral proteins but also contain a specific array of hijacked host factors that create a unique lipid microenvironment optimal for genome replication. While some lipids may be locally synthesized de novo, other lipids are shuttled towards ROs. In picornavirus-infected cells, lipids are exchanged at membrane contact sites between ROs and other organelles. In this paper, we review recent advances in our understanding of how picornaviruses exploit host membrane contact site machinery to generate ROs, a mechanism that is used by some other +RNA viruses as well.</AbstractText><CopyrightInformation>Copyright © 2016 Elsevier Ltd. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>van der Schaar</LastName><ForeName>Hilde M</ForeName><Initials>HM</Initials><AffiliationInfo><Affiliation>Department of Infectious Diseases & Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Dorobantu</LastName><ForeName>Cristina M</ForeName><Initials>CM</Initials><AffiliationInfo><Affiliation>Department of Infectious Diseases & Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Albulescu</LastName><ForeName>Lucian</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Department of Infectious Diseases & Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Strating</LastName><ForeName>Jeroen R P M</ForeName><Initials>JRPM</Initials><AffiliationInfo><Affiliation>Department of Infectious Diseases & Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>van Kuppeveld</LastName><ForeName>Frank J M</ForeName><Initials>FJM</Initials><AffiliationInfo><Affiliation>Department of Infectious Diseases & Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands. Electronic address: f.j.m.vankuppeveld@uu.nl.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2016</Year><Month>03</Month><Day>22</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Trends Microbiol</MedlineTA><NlmUniqueID>9310916</NlmUniqueID><ISSNLinking>0966-842X</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008055">Lipids</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D004770" MajorTopicYN="N">Enterovirus</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016679" MajorTopicYN="N">Genome, Viral</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007425" MajorTopicYN="N">Intracellular Membranes</DescriptorName><QualifierName UI="Q000821" MajorTopicYN="Y">virology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D050356" MajorTopicYN="N">Lipid Metabolism</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008055" MajorTopicYN="N">Lipids</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014779" MajorTopicYN="N">Virus 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