A review of feline infectious peritonitis virus: molecular biology, immunopathogenesis, clinical aspects, and vaccination
Identifieur interne : 000922 ( Istex/Corpus ); précédent : 000921; suivant : 000923A review of feline infectious peritonitis virus: molecular biology, immunopathogenesis, clinical aspects, and vaccination
Auteurs : Christopher W. OlsenSource :
- Veterinary Microbiology [ 0378-1135 ] ; 1993.
English descriptors
- Teeft :
- Acad, Antigenic, Antigenic homology, Antigenic relationship, Antigenic sites, Baines, Baric, Barlough, Bovine, Bovine coronavirus, Boyle, Callebaut, Canine coronaviruses, Cats inoculated, Cell culture, Cheetah, Cleavage, Clinical aspects, Clinical disease, Clinical signs, Corapi, Coronavirus, Coronavirus transcription, Coronaviruses, Correa, Cvlps, Delmas, Dengue, Dengue virus infection, Enhancement, Enjuanes, Enteric, Enteric coronavirus, Enteric disease, Epitope, Evermann, Experimental infection, Experimental inoculation, Fecv, Fecv genome, Feline, Feline coronavirus, Feline coronavirus infection, Feline coronaviruses, Feline enteric coronavirus, Feline macrophages, Fipv, Fipv challenge, Fipv infection, Fipv infections, Fipv infectivity, Fipv review, Fipv strains, Fipv vaccine, Fiscus, Gaskell, Gastroenteritis, Gastroenteritis virus, Genome, Gerber, Glycoprotein, Groot, Halstead, Harbour, Hayashi, Hepatitis, Hohdatsu, Homology, Horzinek, Human coronavirus, Human immunodeficiency virus type, Immune, Immune complexes, Immunodeficiency, Immunol, Infection, Infection enhancement, Infectious bronchitis virus, Infectious peritonitis virus, Infectivity, Interferon, Laude, Leader sequence, Lenstra, Mabs, Macrophage, Major histocompatability, Makino, Microbiol, Molecular biology, Monoclonal, Monoclonal antibodies, Montefiori, Morens, Mouse hepatitis virus, Mrna, Mrna levels, Murine, Murine coronavirus, Neutralizing, Nucleocapsid, Olsen, Other species, Pathogenesis, Peplomer, Peplomer glycoprotein, Peplomer protein, Peritonitis, Peritonitis virus, Plasma membrane, Polymerase, Polypeptide, Porcine, Porcine coronavirus, Porterfield, Prcv, Primary structure, Proc, Protein, Proteolytic cleavage, Putative, Receptor, Recombinant, Recombinant vaccinia virus, Recombinant vaccinia viruses, Recombination, Replication, Rna, Sequence analysis, Seropositive, Seropositive kittens, Serum antibodies, Sethna, Signal sequence, Simian immunodeficiency virus, Small intestine, Snijder, Spaan, Spike, Spike protein, Stoddart, Stohlman, Sturman, Survival times, Teramoto, Tgev, Transcription, Transmissible, Transmissible gastroenteritis coronavirus, Transmissible gastroenteritis virus, Unpublished data, Vaccine, Vaccinia, Vennema, Viral, Viral envelope, Virion, Virol, Virology, Virulent, Virulent fipv, Virus, Virus infection, Virus infectivity, Wege, Weiss.
Abstract
Abstract: Feline infectious peritontis (FIP) has been an elusive and frustrating problem for veterinary practitioners and cat breeders for many years. Over the last several years, reports have begun to elucidate aspects of the molecular biology of the causal virus (FIPV). These papers complement a rapidly growing base of knowledge concerning the molecular organization and replication of coronaviruses in general. The fascinating immunopathogenesis of FIPV infection and the virus' interaction with macrophages has also been the subject of several recent papers. It is now clear that FIPV may be of interest to scientists other than veterinary virologists since its pathogenesis may provide a useful model system for other viruses whose infectivity is enhanced in the presence of virus-specific antibody. With these advances and the recent release of the first commercially-available FIPV vaccine, it is appropriate to review what is known about the organization and replication of coronaviruses and the pathogenesis of FIPV infection.
Url:
DOI: 10.1016/0378-1135(93)90126-R
Links to Exploration step
ISTEX:C02E3D04DC26FF1397E9425551D3E91696D7A8F7Le document en format XML
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Over the last several years, reports have begun to elucidate aspects of the molecular biology of the causal virus (FIPV). These papers complement a rapidly growing base of knowledge concerning the molecular organization and replication of coronaviruses in general. The fascinating immunopathogenesis of FIPV infection and the virus' interaction with macrophages has also been the subject of several recent papers. It is now clear that FIPV may be of interest to scientists other than veterinary virologists since its pathogenesis may provide a useful model system for other viruses whose infectivity is enhanced in the presence of virus-specific antibody. With these advances and the recent release of the first commercially-available FIPV vaccine, it is appropriate to review what is known about the organization and replication of coronaviruses and the pathogenesis of FIPV 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cleavage</json:string><json:string>cleavage</json:string></teeft></keywords><author><json:item><name>Christopher W. Olsen</name><affiliations><json:string>Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, USA</json:string></affiliations></json:item></author><arkIstex>ark:/67375/6H6-PRWLRKPQ-7</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>Full-length article</json:string></originalGenre><abstract>Abstract: Feline infectious peritontis (FIP) has been an elusive and frustrating problem for veterinary practitioners and cat breeders for many years. Over the last several years, reports have begun to elucidate aspects of the molecular biology of the causal virus (FIPV). These papers complement a rapidly growing base of knowledge concerning the molecular organization and replication of coronaviruses in general. The fascinating immunopathogenesis of FIPV infection and the virus' interaction with macrophages has also been the subject of several recent papers. It is now clear that FIPV may be of interest to scientists other than veterinary virologists since its pathogenesis may provide a useful model system for other viruses whose infectivity is enhanced in the presence of virus-specific antibody. With these advances and the recent release of the first commercially-available FIPV vaccine, it is appropriate to review what is known about the organization and replication of coronaviruses and the pathogenesis of FIPV infection.</abstract><qualityIndicators><score>8.836</score><pdfWordCount>16713</pdfWordCount><pdfCharCount>101990</pdfCharCount><pdfVersion>1.2</pdfVersion><pdfPageCount>37</pdfPageCount><pdfPageSize>468 x 677 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractWordCount>153</abstractWordCount><abstractCharCount>1037</abstractCharCount><keywordCount>0</keywordCount></qualityIndicators><title>A review of feline infectious peritonitis virus: molecular biology, immunopathogenesis, clinical aspects, and vaccination</title><pmid><json:string>8236772</json:string></pmid><pii><json:string>0378-1135(93)90126-R</json:string></pii><genre><json:string>research-article</json:string></genre><serie><title>Proc. Natl. Acad. Sci. USA</title><language><json:string>unknown</json:string></language><volume>88</volume><pages><first>9593</first><last>9597</last></pages></serie><host><title>Veterinary Microbiology</title><language><json:string>unknown</json:string></language><publicationDate>1993</publicationDate><issn><json:string>0378-1135</json:string></issn><pii><json:string>S0378-1135(00)X0210-6</json:string></pii><volume>36</volume><issue>1–2</issue><pages><first>1</first><last>37</last></pages><genre><json:string>journal</json:string></genre></host><namedEntities><unitex><date><json:string>1979</json:string><json:string>1970</json:string><json:string>1986</json:string><json:string>1964</json:string><json:string>1993</json:string><json:string>1960s</json:string><json:string>1983</json:string><json:string>1984</json:string></date><geogName><json:string>Murray</json:string><json:string>Semliki</json:string></geogName><orgName></orgName><orgName_funder></orgName_funder><orgName_provider></orgName_provider><persName><json:string>Van 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and Scott, 1981 c</json:string><json:string>Pieris and Porterfield, 1981</json:string><json:string>Banerjee, 1987</json:string><json:string>Halstead, 1989</json:string><json:string>Reynolds and Garwes, 1979</json:string><json:string>Ward, 1970</json:string><json:string>Pedersen, 1983b</json:string><json:string>Morens and Halstead, 1990</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/6H6-PRWLRKPQ-7</json:string></ark><categories><wos><json:string>1 - science</json:string><json:string>2 - veterinary sciences</json:string><json:string>2 - microbiology</json:string></wos><scienceMetrix><json:string>1 - applied sciences</json:string><json:string>2 - agriculture, fisheries & forestry</json:string><json:string>3 - veterinary sciences</json:string></scienceMetrix><scopus><json:string>1 - Health Sciences</json:string><json:string>2 - Veterinary</json:string><json:string>3 - General Veterinary</json:string><json:string>1 - Health 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medicales</json:string></inist></categories><publicationDate>1993</publicationDate><copyrightDate>1993</copyrightDate><doi><json:string>10.1016/0378-1135(93)90126-R</json:string></doi><id>C02E3D04DC26FF1397E9425551D3E91696D7A8F7</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-PRWLRKPQ-7/fulltext.pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-PRWLRKPQ-7/bundle.zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/ark:/67375/6H6-PRWLRKPQ-7/fulltext.tei"><teiHeader><fileDesc><titleStmt><title level="a">A review of feline infectious peritonitis virus: molecular biology, immunopathogenesis, clinical aspects, and vaccination</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher 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Olsen, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, 2015 Linden Drive West, Madison, WI, USA.</p></note><affiliation>Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, USA</affiliation></author><idno type="istex">C02E3D04DC26FF1397E9425551D3E91696D7A8F7</idno><idno type="ark">ark:/67375/6H6-PRWLRKPQ-7</idno><idno type="DOI">10.1016/0378-1135(93)90126-R</idno><idno type="PII">0378-1135(93)90126-R</idno></analytic><monogr><title level="j">Veterinary Microbiology</title><title level="j" type="abbrev">VETMIC</title><idno type="pISSN">0378-1135</idno><idno type="PII">S0378-1135(00)X0210-6</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1993"></date><biblScope unit="volume">36</biblScope><biblScope unit="issue">1–2</biblScope><biblScope unit="page" from="1">1</biblScope><biblScope unit="page" to="37">37</biblScope></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1993</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Abstract: Feline infectious peritontis (FIP) has been an elusive and frustrating problem for veterinary practitioners and cat breeders for many years. Over the last several years, reports have begun to elucidate aspects of the molecular biology of the causal virus (FIPV). These papers complement a rapidly growing base of knowledge concerning the molecular organization and replication of coronaviruses in general. The fascinating immunopathogenesis of FIPV infection and the virus' interaction with macrophages has also been the subject of several recent papers. It is now clear that FIPV may be of interest to scientists other than veterinary virologists since its pathogenesis may provide a useful model system for other viruses whose infectivity is enhanced in the presence of virus-specific antibody. With these advances and the recent release of the first commercially-available FIPV vaccine, it is appropriate to review what is known about the organization and replication of coronaviruses and the pathogenesis of FIPV infection.</p></abstract></profileDesc><revisionDesc><change when="1993">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-PRWLRKPQ-7/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier, elements deleted: tail"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="fla"><item-info><jid>VETMIC</jid><aid>9390126R</aid><ce:pii>0378-1135(93)90126-R</ce:pii><ce:doi>10.1016/0378-1135(93)90126-R</ce:doi><ce:copyright type="unknown" year="1993"></ce:copyright></item-info><head><ce:title>A review of feline infectious peritonitis virus: molecular biology, immunopathogenesis, clinical aspects, and vaccination</ce:title><ce:author-group><ce:author><ce:given-name>Christopher W.</ce:given-name><ce:surname>Olsen</ce:surname><ce:cross-ref refid="COR1"><ce:sup>∗</ce:sup></ce:cross-ref></ce:author><ce:affiliation><ce:textfn>Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, USA</ce:textfn></ce:affiliation><ce:correspondence id="COR1"><ce:label>∗</ce:label><ce:text>Correspondence to: C.W. Olsen, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, 2015 Linden Drive West, Madison, WI, USA.</ce:text></ce:correspondence></ce:author-group><ce:date-accepted day="5" month="11" year="1992"></ce:date-accepted><ce:abstract><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para>Feline infectious peritontis (FIP) has been an elusive and frustrating problem for veterinary practitioners and cat breeders for many years. Over the last several years, reports have begun to elucidate aspects of the molecular biology of the causal virus (FIPV). These papers complement a rapidly growing base of knowledge concerning the molecular organization and replication of coronaviruses in general. The fascinating immunopathogenesis of FIPV infection and the virus' interaction with macrophages has also been the subject of several recent papers. It is now clear that FIPV may be of interest to scientists other than veterinary virologists since its pathogenesis may provide a useful model system for other viruses whose infectivity is enhanced in the presence of virus-specific antibody. With these advances and the recent release of the first commercially-available FIPV vaccine, it is appropriate to review what is known about the organization and replication of coronaviruses and the pathogenesis of FIPV infection.</ce:simple-para></ce:abstract-sec></ce:abstract></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo><title>A review of feline infectious peritonitis virus: molecular biology, immunopathogenesis, clinical aspects, and vaccination</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>A review of feline infectious peritonitis virus: molecular biology, immunopathogenesis, clinical aspects, and vaccination</title></titleInfo><name type="personal"><namePart type="given">Christopher W.</namePart><namePart type="family">Olsen</namePart><affiliation>Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, USA</affiliation><description>Correspondence to: C.W. Olsen, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, 2015 Linden Drive West, Madison, WI, USA.</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1993</dateIssued><copyrightDate encoding="w3cdtf">1993</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><abstract lang="en">Abstract: Feline infectious peritontis (FIP) has been an elusive and frustrating problem for veterinary practitioners and cat breeders for many years. Over the last several years, reports have begun to elucidate aspects of the molecular biology of the causal virus (FIPV). These papers complement a rapidly growing base of knowledge concerning the molecular organization and replication of coronaviruses in general. The fascinating immunopathogenesis of FIPV infection and the virus' interaction with macrophages has also been the subject of several recent papers. It is now clear that FIPV may be of interest to scientists other than veterinary virologists since its pathogenesis may provide a useful model system for other viruses whose infectivity is enhanced in the presence of virus-specific antibody. With these advances and the recent release of the first commercially-available FIPV vaccine, it is appropriate to review what is known about the organization and replication of coronaviruses and the pathogenesis of FIPV infection.</abstract><relatedItem type="host"><titleInfo><title>Veterinary Microbiology</title></titleInfo><titleInfo type="abbreviated"><title>VETMIC</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1993</dateIssued></originInfo><identifier type="ISSN">0378-1135</identifier><identifier type="PII">S0378-1135(00)X0210-6</identifier><part><date>1993</date><detail type="volume"><number>36</number><caption>vol.</caption></detail><detail type="issue"><number>1–2</number><caption>no.</caption></detail><extent unit="issue-pages"><start>1</start><end>196</end></extent><extent unit="pages"><start>1</start><end>37</end></extent></part></relatedItem><identifier type="istex">C02E3D04DC26FF1397E9425551D3E91696D7A8F7</identifier><identifier type="ark">ark:/67375/6H6-PRWLRKPQ-7</identifier><identifier type="DOI">10.1016/0378-1135(93)90126-R</identifier><identifier type="PII">0378-1135(93)90126-R</identifier><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-HKKZVM7B-M">elsevier</recordContentSource></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-PRWLRKPQ-7/record.json</uri></json:item></metadata></istex></record>Pour manipuler ce document sous Unix (Dilib)
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