Heparan sulfate is a binding molecule but not a receptor for CEACAM1-independent infection of murine coronavirus.
Identifieur interne : 001D49 ( PubMed/Corpus ); précédent : 001D48; suivant : 001D50Heparan sulfate is a binding molecule but not a receptor for CEACAM1-independent infection of murine coronavirus.
Auteurs : Rie Watanabe ; Stanley G. Sawicki ; Fumihiro TaguchiSource :
- Virology [ 0042-6822 ] ; 2007.
English descriptors
- KwdEn :
- Amino Acid Sequence, Animals, Binding Sites, Carcinoembryonic Antigen (physiology), Cell Line, Cell Membrane (virology), Coronavirus (classification), Coronavirus (pathogenicity), Coronavirus (physiology), Coronavirus Infections (physiopathology), Cricetinae, Heparitin Sulfate (metabolism), Kidney, Mice, Protein Binding, Receptors, Virus (physiology), Virulence.
- MESH :
- chemical , metabolism : Heparitin Sulfate.
- chemical , physiology : Carcinoembryonic Antigen, Receptors, Virus.
- classification : Coronavirus.
- pathogenicity : Coronavirus.
- physiology : Coronavirus.
- physiopathology : Coronavirus Infections.
- virology : Cell Membrane.
- Amino Acid Sequence, Animals, Binding Sites, Cell Line, Cricetinae, Kidney, Mice, Protein Binding, Virulence.
Abstract
A highly neurovirulent mouse hepatitis virus (MHV) JHMV strain (wt) with receptor (MHVR)-independent infection activity and its low-virulent mutant srr7 without such activity were found to attach to MHVR-negative, non-permissive BHK cells. To identify the molecule that interacts with JHMV, we focused on heparan sulfate (HS) since it works as a receptor of a mutant MHV-rec1 that infects in an MHVR-independent fashion. The present study indicates that HS interacts with both wt JHMV and srr7 but it does not function as an entry receptor as it apparently does for MHV-rec1. Furthermore, HS failed to serve as an entry receptor in the MHVR-independent infection of wt JHMV, indicating that HS is not a host factor that wt JHMV utilizes in an MHVR-independent infection.
DOI: 10.1016/j.virol.2007.06.034
PubMed: 17692355
Links to Exploration step
pubmed:17692355Le document en format XML
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<author><name sortKey="Watanabe, Rie" sort="Watanabe, Rie" uniqKey="Watanabe R" first="Rie" last="Watanabe">Rie Watanabe</name>
<affiliation><nlm:affiliation>Division of Viral Respiratory Diseases and SARS, Department of Virology III, National Institute of Infectious Diseases, Murayama Branch, 4-7-1 Gakuen, Musashi-Murayama, Tokyo 208-0011, Japan.</nlm:affiliation>
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<author><name sortKey="Sawicki, Stanley G" sort="Sawicki, Stanley G" uniqKey="Sawicki S" first="Stanley G" last="Sawicki">Stanley G. Sawicki</name>
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<author><name sortKey="Taguchi, Fumihiro" sort="Taguchi, Fumihiro" uniqKey="Taguchi F" first="Fumihiro" last="Taguchi">Fumihiro Taguchi</name>
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<affiliation><nlm:affiliation>Division of Viral Respiratory Diseases and SARS, Department of Virology III, National Institute of Infectious Diseases, Murayama Branch, 4-7-1 Gakuen, Musashi-Murayama, Tokyo 208-0011, Japan.</nlm:affiliation>
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<term>Animals</term>
<term>Binding Sites</term>
<term>Carcinoembryonic Antigen (physiology)</term>
<term>Cell Line</term>
<term>Cell Membrane (virology)</term>
<term>Coronavirus (classification)</term>
<term>Coronavirus (pathogenicity)</term>
<term>Coronavirus (physiology)</term>
<term>Coronavirus Infections (physiopathology)</term>
<term>Cricetinae</term>
<term>Heparitin Sulfate (metabolism)</term>
<term>Kidney</term>
<term>Mice</term>
<term>Protein Binding</term>
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<term>Virulence</term>
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<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Heparitin Sulfate</term>
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<term>Binding Sites</term>
<term>Cell Line</term>
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<front><div type="abstract" xml:lang="en">A highly neurovirulent mouse hepatitis virus (MHV) JHMV strain (wt) with receptor (MHVR)-independent infection activity and its low-virulent mutant srr7 without such activity were found to attach to MHVR-negative, non-permissive BHK cells. To identify the molecule that interacts with JHMV, we focused on heparan sulfate (HS) since it works as a receptor of a mutant MHV-rec1 that infects in an MHVR-independent fashion. The present study indicates that HS interacts with both wt JHMV and srr7 but it does not function as an entry receptor as it apparently does for MHV-rec1. Furthermore, HS failed to serve as an entry receptor in the MHVR-independent infection of wt JHMV, indicating that HS is not a host factor that wt JHMV utilizes in an MHVR-independent infection.</div>
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<Abstract><AbstractText>A highly neurovirulent mouse hepatitis virus (MHV) JHMV strain (wt) with receptor (MHVR)-independent infection activity and its low-virulent mutant srr7 without such activity were found to attach to MHVR-negative, non-permissive BHK cells. To identify the molecule that interacts with JHMV, we focused on heparan sulfate (HS) since it works as a receptor of a mutant MHV-rec1 that infects in an MHVR-independent fashion. The present study indicates that HS interacts with both wt JHMV and srr7 but it does not function as an entry receptor as it apparently does for MHV-rec1. Furthermore, HS failed to serve as an entry receptor in the MHVR-independent infection of wt JHMV, indicating that HS is not a host factor that wt JHMV utilizes in an MHVR-independent infection.</AbstractText>
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