Other Positive-Strand RNA Viruses
Identifieur interne : 000785 ( Pmc/Corpus ); précédent : 000784; suivant : 000786Other Positive-Strand RNA Viruses
Auteurs : Wang-Shick RyuSource :
- Molecular Virology of Human Pathogenic Viruses ; 2016.
Abstract
Three miscellaneous positive-strand RNA viruses are described briefly with an emphasis on the genome structure: caliciviruses, togaviruses, and coronaviruses. Unlike those described in the two preceding chapters, these RNA viruses possess one or more subgenomic RNAs, besides the full-length genomic RNA. These subgenomic RNAs are all positioned to the 3′ side of the RNA genome and encode structural proteins. Importantly, viruses belonging to these three RNA virus families have become a global public health concern. Noroviruses, a prototype of calicivirus, are responsible for almost all viral gastroenteritis outbreaks worldwide. Moreover, some newly emerging viruses belong to togaviruses and coronaviruses. Chikungunya virus, an emerging virus that caused an outbreak in Africa during 2004–2006, belongs to the togavirus family. Severe acute respiratory syndrome (SARS) coronavirus and Middle-East respiratory syndrome (MERS) coronavirus, which caused 2003 SARS outbreak in China and 2014 MERS outbreak in the Middle East, belong to the coronavirus family.
Url:
DOI: 10.1016/B978-0-12-800838-6.00013-8
PubMed: NONE
PubMed Central: 7149767
Links to Exploration step
PMC:7149767Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Other Positive-Strand RNA Viruses</title><author><name sortKey="Ryu, Wang Shick" sort="Ryu, Wang Shick" uniqKey="Ryu W" first="Wang-Shick" last="Ryu">Wang-Shick Ryu</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmc">7149767</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149767</idno><idno type="RBID">PMC:7149767</idno><idno type="doi">10.1016/B978-0-12-800838-6.00013-8</idno><idno type="pmid">NONE</idno><date when="2016">2016</date><idno type="wicri:Area/Pmc/Corpus">000785</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000785</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Other Positive-Strand RNA Viruses</title><author><name sortKey="Ryu, Wang Shick" sort="Ryu, Wang Shick" uniqKey="Ryu W" first="Wang-Shick" last="Ryu">Wang-Shick Ryu</name></author></analytic><series><title level="j">Molecular Virology of Human Pathogenic Viruses</title><imprint><date when="2016">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Three miscellaneous positive-strand RNA viruses are described briefly with an emphasis on the genome structure: caliciviruses, togaviruses, and coronaviruses. Unlike those described in the two preceding chapters, these RNA viruses possess one or more subgenomic RNAs, besides the full-length genomic RNA. These subgenomic RNAs are all positioned to the 3′ side of the RNA genome and encode structural proteins. Importantly, viruses belonging to these three RNA virus families have become a global public health concern. Noroviruses, a prototype of calicivirus, are responsible for almost all viral gastroenteritis outbreaks worldwide. Moreover, some newly emerging viruses belong to togaviruses and coronaviruses. Chikungunya virus, an emerging virus that caused an outbreak in Africa during 2004–2006, belongs to the togavirus family. Severe acute respiratory syndrome (SARS) coronavirus and Middle-East respiratory syndrome (MERS) coronavirus, which caused 2003 SARS outbreak in China and 2014 MERS outbreak in the Middle East, belong to the coronavirus family.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Jones, M K" uniqKey="Jones M">M.K. Jones</name></author><author><name sortKey="Watanabe, M" uniqKey="Watanabe M">M. Watanabe</name></author><author><name sortKey="Zhu, S" uniqKey="Zhu S">S. Zhu</name></author><author><name sortKey="Graves, C L" uniqKey="Graves C">C.L. Graves</name></author><author><name sortKey="Keyes, L R" uniqKey="Keyes L">L.R. Keyes</name></author><author><name sortKey="Grau, K R" uniqKey="Grau K">K.R. Grau</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Karst, S M" uniqKey="Karst S">S.M. Karst</name></author><author><name sortKey="Wobus, C E" uniqKey="Wobus C">C.E. Wobus</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Li, W" uniqKey="Li W">W. Li</name></author><author><name sortKey="Moore, M J" uniqKey="Moore M">M.J. Moore</name></author><author><name sortKey="Vasilieva, N" uniqKey="Vasilieva N">N. Vasilieva</name></author><author><name sortKey="Sui, J" uniqKey="Sui J">J. Sui</name></author><author><name sortKey="Wong, S K" uniqKey="Wong S">S.K. Wong</name></author><author><name sortKey="Berne, M A" uniqKey="Berne M">M.A. Berne</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Raj, V S" uniqKey="Raj V">V.S. Raj</name></author><author><name sortKey="Mou, H" uniqKey="Mou H">H. Mou</name></author><author><name sortKey="Smits, S L" uniqKey="Smits S">S.L. Smits</name></author><author><name sortKey="Dekkers, D H" uniqKey="Dekkers D">D.H. Dekkers</name></author><author><name sortKey="Muller, M A" uniqKey="Muller M">M.A. Muller</name></author><author><name sortKey="Dijkman, R" uniqKey="Dijkman R">R. Dijkman</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zust, R" uniqKey="Zust R">R. Zust</name></author><author><name sortKey="Cervantes Barragan, L" uniqKey="Cervantes Barragan L">L. Cervantes-Barragan</name></author><author><name sortKey="Habjan, M" uniqKey="Habjan M">M. Habjan</name></author><author><name sortKey="Maier, R" uniqKey="Maier R">R. Maier</name></author><author><name sortKey="Neuman, B W" uniqKey="Neuman B">B.W. Neuman</name></author><author><name sortKey="Ziebuhr, J" uniqKey="Ziebuhr J">J. Ziebuhr</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="chapter-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Molecular Virology of Human Pathogenic Viruses</journal-id><journal-title-group><journal-title>Molecular Virology of Human Pathogenic Viruses</journal-title></journal-title-group></journal-meta><article-meta><article-id pub-id-type="pmc">7149767</article-id><article-id pub-id-type="publisher-id">B978-0-12-800838-6.00013-8</article-id><article-id pub-id-type="doi">10.1016/B978-0-12-800838-6.00013-8</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Other Positive-Strand RNA Viruses</article-title></title-group><contrib-group><contrib contrib-type="author" id="au0010"><name><surname>Ryu</surname><given-names>Wang-Shick</given-names></name></contrib></contrib-group><aff id="aff1">Department of Biochemistry, Yonsei University, Seoul, Korea</aff><pub-date pub-type="pmc-release"><day>6</day><month>5</month><year>2016</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><year>2017</year></pub-date><pub-date pub-type="epub"><day>6</day><month>5</month><year>2016</year></pub-date><fpage>177</fpage><lpage>184</lpage><permissions><copyright-statement>Copyright © 2017 Elsevier Inc. All rights reserved.</copyright-statement><copyright-year>2017</copyright-year><copyright-holder>Elsevier Inc.</copyright-holder><license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p></license></permissions><abstract id="ab0010"><p>Three miscellaneous positive-strand RNA viruses are described briefly with an emphasis on the genome structure: caliciviruses, togaviruses, and coronaviruses. Unlike those described in the two preceding chapters, these RNA viruses possess one or more subgenomic RNAs, besides the full-length genomic RNA. These subgenomic RNAs are all positioned to the 3′ side of the RNA genome and encode structural proteins. Importantly, viruses belonging to these three RNA virus families have become a global public health concern. Noroviruses, a prototype of calicivirus, are responsible for almost all viral gastroenteritis outbreaks worldwide. Moreover, some newly emerging viruses belong to togaviruses and coronaviruses. Chikungunya virus, an emerging virus that caused an outbreak in Africa during 2004–2006, belongs to the togavirus family. Severe acute respiratory syndrome (SARS) coronavirus and Middle-East respiratory syndrome (MERS) coronavirus, which caused 2003 SARS outbreak in China and 2014 MERS outbreak in the Middle East, belong to the coronavirus family.</p></abstract><kwd-group id="kys0010"><title>Keywords</title><kwd>Alphavirus</kwd><kwd>calicivirus</kwd><kwd>coronavirus</kwd><kwd>MERS-CoV</kwd><kwd>norovirus</kwd><kwd>SARS-CoV</kwd><kwd>sindbis virus</kwd><kwd>togavirus</kwd></kwd-group></article-meta></front><body><p id="p0050">In the two preceding chapters, picornaviruses and flaviviruses were covered. Besides these two positive-strand RNA viruses, caliciviruses, togaviruses, and coronaviruses are also clinically important human pathogens. Here, these positive-strand RNA viruses will be covered only briefly with an emphasis on classification and the genome features.</p><sec id="s0010"><label>13.1</label><title>Calicivivirus</title><p id="p0055">Caliciviruses<xref rid="fn1" ref-type="fn">1</xref>(family Caliciviridae) are similar to picornaviruses in many respects. Caliciviruses are small (35–40 nm), nonenveloped, and icosahedral viruses that possess a positive-strand RNA genome of 7–8 kb. Caliciviruses are important human and veterinary pathogens which are associated with a broad spectrum of diseases in their hosts. Here, norovirus, a prototype of calicivirus and the causative agent of nonbacterial gastroenteritis in humans, will be covered.</p><p id="p0060"><italic>Classification</italic>: Caliciviruses comprise four genera (<xref rid="t0010" ref-type="table">Table 13.1</xref>). Norwalk virus, a member of the genus <italic>Norovirus</italic>, causes epidemic gastroenteritis. Sapporovirus, a member of the genus <italic>Sapovirus</italic>, also causes epidemic gastroenteritis. Besides human caliciviruses, two veterinary caliciviruses are found. Rabbit hemorrhagic disease virus (RHDV), a member of the genus <italic>Lagovirus</italic>, is associated with a fatal liver disease in rabbits. Feline calicivirus (FCV), a member of the genus <italic>Vesivirus</italic>, causes respiratory disease in cats.<table-wrap position="float" id="t0010"><label>Table 13.1</label><caption><p>Classification of Calicivirus</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Genus/Species</th><th>Acronym</th><th>Host</th><th>Transmission</th><th>Disease</th></tr></thead><tbody><tr><td>Norovirus/Norwalk virus</td><td>NoV</td><td>Humans</td><td>Fecal-oral</td><td>Epidemic gastroenteritis</td></tr><tr><td>Sapovirus/Sapporovirus</td><td>SV</td><td>Humans, pigs</td><td>Fecal-oral</td><td>Epidemic gastroenteritis</td></tr><tr><td>Vesivirus/Feline calicivirus</td><td>FCV</td><td>Cats</td><td>Contact</td><td>Respiratory disease</td></tr><tr><td>Lagovirus/Rabbit hemorrhagic disease virus</td><td>RHDV</td><td>Rabbits</td><td>Fecal-oral</td><td>Hemorrhages</td></tr></tbody></table></table-wrap></p><sec id="s0015"><label>13.1.1</label><title>Norovirus</title><p id="p0065"><italic>Norovirus</italic><xref rid="fn2" ref-type="fn">2</xref>represents a prototype of calicivirus. Noroviruses are the causative agents of nonbacterial gastroenteritis in humans and are responsible for almost all viral gastroenteritis outbreaks worldwide.</p><p id="p0070"><italic>Epidemiology</italic>: Noroviruses are transmitted via the oral-fecal route due to contaminated water and food, or directly from person to person. They are extremely contagious. Transmission can be aerosolized when those stricken with the illness vomit, or when a toilet flushes with vomit or diarrhea in it; infection can occur by eating food or breathing air near an episode of vomiting, even if cleaned up. The viruses continue to be shed after symptoms have subsided and shedding can still be detected many weeks after infection.</p><p id="p0075">Noroviruses are responsible for over 50% of gastroenteritis worldwide (<xref rid="f0010" ref-type="fig">Fig. 13.1</xref>). Each year, human noroviruses cause at least around 267 million episodes and over 200,000 deaths in developing nations as well as approximately 900,000 cases of pediatric gastroenteritis in industrialized nations. Even in the United States, they cause over 20,000 episodes and 300 deaths. Shellfishes (oysters in particular), which are often consumed uncooked, are frequently the source of infection. Oysters act as a filter to concentrate the virus particles present in sea water. Symptoms include vomiting, diarrhea, and dehydration. No vaccine or antiviral drugs are yet available.<fig id="f0010"><label>Figure 13.1</label><caption><p>Norovius particle.</p><p>(Left) A cross section of norovirus capsid particle of 38 nm in diameter. VPg is linked to 5′ terminus of the positive-strand RNA genome. The capsid is an icosahedral particles having <italic>T</italic>=3 symmetry. (Right) The electron microscopic image of norovirus particles.</p></caption><graphic xlink:href="f13-01-9780128008386"></graphic></fig></p><p id="p0080"><italic>Genome Structure</italic>: The RNA genome of norovirus is fundamentally similar to that of picornaviruses, except that a <italic>subgenomic RNA</italic><xref rid="fn3" ref-type="fn">3</xref>is expressed (<xref rid="f0015" ref-type="fig">Fig. 13.2</xref>). <italic>VPg</italic> (virion protein genome-linked) is covalently linked to both the genomic and the subgenomic RNAs. The ORF1 polyprotein encoded by the genomic RNA encodes nonstructural proteins such as 3CL<sup>PRO</sup> and RdRp that are essential for viral RNA replication. On the other hand, the subgenomic RNA encodes the structural proteins such as VP1 and VP2. Unlike picornaviruses, internal ribosome entry site (IRES) element is not found in the 5′ NCR. Instead, the VPg recruits eIF4E, a cap-binding translation initiation factor, to initiate translation (<xref rid="b0010" ref-type="boxed-text">Box 13.1</xref>). In other words, the VPg substitutes for the cap structure in recruiting host translation factors.<fig id="f0015"><label>Figure 13.2</label><caption><p>RNA genome structure of norovirus.</p><p>In addition to the genomic RNA, norovirus has a subgenomic RNA. The VPg is covalently linked to the 5′ termini of both the genomic and the subgenomic RNAs. The ORF1 polyprotein is later processed to form six individual proteins by a virus-encoded 3CL<sup>PRO</sup> protease. RdRp, RNA-dependent RNA polymerase.</p></caption><graphic xlink:href="f13-02-9780128008386"></graphic></fig><boxed-text id="b0010"><label>Box 13.1</label><caption><title>VPg of Norovirus in Translation</title></caption><p id="p0010">VPg is linked to the 5′ terminus of norovirus RNAs, which is a reminiscent of picornavirus. However, unlike picornavirus, the IRES element, which is essential for the cap-independent translation, is not present in the 5′ NCR of norovirus RNAs. An immediate question is then how norovirus genome RNA is translated. Surprisingly, it was found that VPg has the ability to bind eIF4E and, in doing so, it facilitates the translation initiation of viral RNAs in eIF4E-dependent manner. In other words, VPg substitutes the role of the cap structure of eukaryotic mRNAs in recruiting eIF4E, a cap-binding protein. Overall, norovirus co-opts the cellular eIF4E-dependent translation mechanism via a novel VPg-eIF4E interaction.<fig id="f0040"><caption><p>Translation initiation factors associated with norovirus RNA.</p><p>eIF4F=eIF4A+eIF4G+eIF4E.</p></caption><graphic xlink:href="u13-01-9780128008386"></graphic></fig></p></boxed-text></p><p id="p0085"><italic>Cultivation in Cell Culture:</italic> The investigation on human norovirus has been hampered by the lack of cell lines that support the virus infection. Since human norovirus has remained uncultivable, the studies on viral genome replication could be performed only by transfection of viral genomic RNA into appropriate cells. Recently, major progress in norovirus research was made by a successful demonstration of a human norovirus infection in a cell culture (see <xref rid="fr0015" ref-type="sec">Journal Club</xref>). Successful establishment of an in vitro cultivation system of human norovirus will facilitate the development of prophylatic vaccine and antivirals.</p><p id="p0090"><italic>Animal Model:</italic> Animal model for human norovirus infection is not yet available. Murine norovirus was recently discovered and will be explored as an animal model for human norovirus.</p></sec></sec><sec id="s0020"><label>13.2</label><title>Togavirus</title><p id="p0095">Togaviruses (family Togaviridae) are enveloped and icosahedral viruses that possess a positive-sense single-strand RNA genome of 11 kb. Members of this family are frequently referred to as alphaviruses, a genus of this family.</p><p id="p0100">Sindbis virus and Semliki Forest virus (SFV) have been extensively studied as the prototype of togaviruses, since these viruses are only weakly pathogenic to human.</p><p id="p0105"><italic>Classification</italic>: Family Togaviridae is constituted by two genera: genus <italic>Alphavirus</italic> and genus <italic>Rubivirus</italic> (<xref rid="t0015" ref-type="table">Table 13.2</xref>). Chikungunya virus, an emerging virus, is an important human pathogen belonging to the genus <italic>Alphavirus</italic>. Togaviruses are important veterinary pathogens, and are transmitted via mosquitoes. Some of them are zoonotic viruses, including Venezuelan equine encephalitis virus (VEEV). Rubella virus is the only member of togavirus family that causes significant disease in human—German measles.<table-wrap position="float" id="t0015"><label>Table 13.2</label><caption><p>Classification of Togavirus</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Genus/Species</th><th>Vertebrate Hosts</th><th>Invertebrate Host</th><th>Geographic Distribution</th><th>Human Disease</th></tr></thead><tbody><tr><td colspan="5">Alphavirus</td></tr><tr><td>Sindbis virus (SINV)</td><td>Birds</td><td>Mosquitoes</td><td>Africa, Australia, Middle East</td><td>Fever, arthritis, rash</td></tr><tr><td>Semliki Forest virus (SFV)</td><td>Birds, rodents, primates</td><td>Mosquitoes</td><td>Africa</td><td>Fever, encephalitis</td></tr><tr><td>Venezuelan equine encephalitis virus (VEEV)</td><td>Birds, horses, human</td><td>Mosquitoes</td><td>North America, South America</td><td>Fever, encephalitis</td></tr><tr><td>Western equine encephalitis virus (WEEV)</td><td>Birds, horses</td><td>Mosquitoes</td><td>North America, South America</td><td>Fever, encephalitis</td></tr><tr><td>Chikungunya virus (CHIKV)</td><td>Primates</td><td>Mosquitoes</td><td>Africa, SE Asia</td><td>Fever, arthritis, rash</td></tr><tr><td colspan="5">Rubivirus</td></tr><tr><td>Rubella virus</td><td>Human</td><td></td><td>German measles</td><td></td></tr></tbody></table></table-wrap></p><p id="p0110"><italic>Epidemiology</italic>: Togaviruses are largely transmitted via mosquitoes. Chikungunya virus, an emerging virus, caused a massive outbreak in some countries in Africa including Kenya and Madagascar in 2004–2006. VEEV, a zoonotic virus, could infect birds, horses, and human. VEEV infection causes rash, fever, and encephalitis. Rubella virus, that causes German measles in human, is unique among togaviruses in that it is not transmitted via mosquitoes.</p><p id="p0115"><italic>Virion Structure</italic>: Togavirus virions are small (70–80 nm), enveloped, icosahedral capsid inside (<xref rid="f0020" ref-type="fig">Fig. 13.3</xref>). Togavirus virion structure stands out in that not only the capsid but also the envelope has an icosahedral symmetric structure. Indeed, 240 molecules of E1/E2 dimer form an icosahedral structure having <italic>T</italic>=4 symmetry. Likewise, 240 molecules of capsid proteins form an icosahedral structure having <italic>T</italic>=4 symmetry. Togavirus is unprecedented in that the envelope as well as the capsid has a symmetric structure (see Fig. 2.9).<fig id="f0020"><label>Figure 13.3</label><caption><p>Sindbis virus particle.</p><p>Cross-section view of sindbis virus particle. Note that trimers of the E1/E2 dimer envelope glycoproteins are tightly associated with the capsid proteins, revealing a parallel symmetric arrangement of envelope glycoproteins.</p></caption><graphic xlink:href="f13-03-9780128008386"></graphic></fig></p><p id="p0120"><italic>Genome Structure</italic>: Togavirus genome is a positive-strand RNA of 11 kb (<xref rid="f0025" ref-type="fig">Fig. 13.4</xref>). In addition to the genomic RNA that encodes a polyprotein for nonstructural proteins, a subgenomic RNA is expressed that encodes a polyprotein for structural proteins. The 5′ terminus of RNA is capped, whereas the 3′ terminus is polyadenylated. Note that the capping at the 5′ terminus is facilitated by the viral capping enzyme (ie, nsP1) (see Box 16.3). The polyproteins are processed into individual proteins either by viral protease (ie, nsP2 protease) or by host proteases such as signal peptidase and furin.<fig id="f0025"><label>Figure 13.4</label><caption><p>RNA genome structure of sindbis virus.</p><p>In addition to the genomic RNA, sindbis virus has a subgenomic RNA. The nonstructural proteins are translated from the genomic RNA, while the structural proteins are translated from the subgenomic RNA. The cleavage sites of polyproteins are denoted by symbols of respective proteases. RdRp, RNA-dependent RNA polymerase.</p></caption><graphic xlink:href="f13-04-9780128008386"></graphic></fig></p></sec><sec id="s0025"><label>13.3</label><title>Coronavirus</title><p id="p0125">Coronaviruses<xref rid="fn4" ref-type="fn">4</xref>(family Coronaviridae) are enveloped, spherical, and about 120 nm in diameter and possess a single-strand RNA genome of approximately 30 kb.</p><p id="p0130">Mouse hepatitis virus (MHV) is a prototype of coronavirus. MHV outbreak in animal laboratory facilities represents a serious concern. In some cases, the facility has to be closed for many years until reuse. On the other hand, human coronavirus has been considered clinically unimportant, until <italic>SARS</italic> (severe acute respiratory syndrome) coronavirus was discovered in 2003, as a newly emerging virus. More recently, the <italic>MERS</italic> (Middle-East respiratory syndrome) outbreak in the Middle East has drawn attention to human coronaviruses again (see Fig. 21.11).</p><p id="p0135"><italic>Classification</italic>: Family Coronaviridae is subdivided into three genera: alpha, beta, and gamma coronaviruses (<xref rid="t0020" ref-type="table">Table 13.3</xref>). SARS-coronavirus (SARS-CoV) and MERS-coronavirus (MERS-CoV) are classified as <italic>Beta coronavirus</italic>.<table-wrap position="float" id="t0020"><label>Table 13.3</label><caption><p>Classification of Coronavirus</p></caption><table frame="hsides" rules="groups"><thead><tr><th>Genus</th><th>Virus Species</th><th>Host</th><th>Disease</th></tr></thead><tbody><tr><td rowspan="3">Alpha Coronavirus</td><td>Human coronavirus-229E</td><td>Human</td><td>Colds, pneumonia</td></tr><tr><td>Human coronavirus-NL63</td><td>Human</td><td>Colds, pneumonia</td></tr><tr><td>Transmissible gastroenteritis virus (TGEV)</td><td>Swine</td><td>Gastroenteritis</td></tr><tr><td rowspan="4">Beta Coronavirus</td><td>Mouse hepatitis virus (MHV)</td><td>Rodents</td><td>Hepatitis</td></tr><tr><td>Human coronavirus-HKU1</td><td>Human</td><td>Pneumonia</td></tr><tr><td>SARS-coronavirus (SARS-CoV)</td><td>Human</td><td>Pneumonia, Gastroenteritis</td></tr><tr><td>MERS-coronavirus (MERS-CoV)</td><td>Human, Camel</td><td>Respiratory infection</td></tr><tr><td>Gamma Coronavirus</td><td>Avian infectious bronchitis virus (AIBV)</td><td>Avian</td><td>Kidney infection</td></tr></tbody></table></table-wrap></p><p id="p0140"><italic>Epidemiology</italic>: Human coronaviruses were known to cause only mild respiratory infections, until the SARS outbreak. The SARS-CoV outbreak that occurred in 2003 has drawn attention, since it was fatal, causing SARS (see below). Moreover, a novel human coronavirus, MERS-CoV, is responsible for a new emerging respiratory infection that occurred in 2012 in Middle East countries, including Saudi Arabia (see Fig. 21.11).</p><p id="p0145"><italic>Virion Structure</italic>: Coronaviruses are enveloped and contain a large helical nucleocapsid inside (<xref rid="f0030" ref-type="fig">Fig. 13.5</xref>). The viral envelope is studded with spike glycoprotein trimer (S), hemagglutinin-esterase dimer (HE), membrane protein (M), and envelope protein (E). In particular, the protruding spike protein (S) characterizes the crown shaped virion, which it was named after. “Corona” (crown) refers to the characteristic appearance of virions under electron microscopy with a fringe of large, bulbous surface projections creating an image reminiscent of the solar corona.<fig id="f0030"><label>Figure 13.5</label><caption><p>Coronavirus particle.</p><p>(A) Envelope proteins are denoted: spike glycoprotein (S), hemagglutinin-esterase (HE), and membrane protein (M), enveloped small membrane pentamer (E), and nucleocapsid protein (N). A large helical nucleocapsid (N) inside encircles the viral RNA genome. (B) Electron microscopy of SARS-CoV. Coronaviruses are a group of viruses that have a halo, or crown-like (corona) appearance when viewed under an electron microscope.</p></caption><graphic xlink:href="f13-05-9780128008386"></graphic></fig></p><p id="p0150"><italic>Genome Structure</italic>: The genome of coronavirus represents a large single-strand RNA of 27–32 kb (<xref rid="f0035" ref-type="fig">Fig. 13.6</xref>). It is the largest RNA genome among animal RNA viruses. The ORF1a and ORF1ab are translated as polyproteins, which are subsequently processed to 16 nonstructural proteins. In addition to the large genomic RNA, coronaviruses have eight subgenomic RNAs, each of them encoding one structural protein. In particular, the S (spike) envelope glycoprotein binds to the host cell receptor and determines tissue tropism and host range.<fig id="f0035"><label>Figure 13.6</label><caption><p>RNA genome structure of coronavirus.</p><p>In addition to the large genomic RNA, coronavirus has eight subgenomic RNAs. The genomic RNA encodes two ORFs: ORF1a and ORF1b. The ORF1b is translated as an ORF1a-ORF1b fusion protein following a frame-shift (denoted by an <italic>asterisk</italic>). Each subgenomic RNA encodes one protein, as denoted by a <italic>box</italic>: spike glycoprotein (S), hemagglutinin-esterase (HE), membrane protein (M), enveloped small membrane pentamer (E), and nucleocapsid protein (N).</p></caption><graphic xlink:href="f13-06-9780128008386"></graphic></fig></p><p id="p0155"><italic>SARS-CoV</italic>: SARS outbreak first occurred in Southern China (including Hong Kong), and spread to South East Asia and Northern America within a few weeks (see Fig. 21.10). The initial casualty and media hype made the public paranoid, canceling overseas travel and international meetings. SARS outbreaks resulted in over 8000 infections and 700 deaths in 20 countries. It turned out that bats were the reservoir for SARS-CoV. It is believed that bat coronavirus had acquired the ability to infect human, extending the host range, by having a few mutations in the spike protein. Recently, <italic>ACE</italic> (angiotensin-converting enzyme 2) was identified as the cellular receptor for virus entry of SARS-CoV to human infection.
</p><p id="p0160"><italic>MERS-CoV</italic>: MERS outbreak first occurred in the Middle East (mainly Saudi Arabia) in 2012, and spread to European countries in a limited manner (see Fig. 21.11). As of June 2015, MERS-CoV caused 1266 cases and 470 deaths reported in multiple countries. MERS-CoV cases have been reported in 23 countries, including Saudi Arabia, Malaysia, Jordan, Qatar, Egypt, the United States, and South Korea. The fatality of MERS-CoV is considerably higher than that of SARS-CoV, approaching 30%. It is speculated that the virus spreads from bats to human via dromedary camel (see Fig. 21.11). The risk of sustained person-to-person transmission appears to be very low. Recently, dipeptidyl peptidase 4 (DPP4 or also known as CD26) was identified as the cellular receptor for virus entry of MERS-CoV. Further, a mouse model for MERS-CoV infection was established that expresses the DPP4. It is hoped that the established mouse model will facilitate the development of a vaccine and antiviral drugs.</p></sec><sec id="s0030"><label>13.4</label><title>Perspectives</title><p id="p0165">In this chapter, three miscellaneous positive-strand DNA viruses are described. Noroviruses, a prototype of caliciviruses, are responsible for almost all viral gastroenteritis outbreaks worldwide. Nonetheless, no vaccine and antiviral drugs are available to control norovirus infection. The lack of susceptible cell lines and animal model for norovirus infection have imposed barriers to basic research until recently. A recent successful demonstration of human norovirus infection using B lymphocytes (see <xref rid="fr0015" ref-type="sec">Journal Club</xref>) deserves more attention in this regard. Such progress in norovirus infection system will greatly advance our understanding on the infection pathology of human norovirus and at the same time facilitate antiviral drug discovery and preventive vaccine development. Sindbis virus and SFV have been extensively studied as the prototype of togaviruses. Surveillance on zoonotic togaviruses, such as VEEV, has become more important. Finally, the emergence of deadly human coronaviruses—SARS-CoV and MERS-CoV—have bolstered research in these viral and often zoonotic pathogens. Accordingly, great advances, such as identification of host cell receptor, the establishment of reverse genetics, and small animal model for infection, have been made in the past decade.</p></sec><sec id="s0035"><label>13.5</label><title>Summary</title><p id="p0170"><list list-type="simple" id="li0020"><list-item id="u0020"><label>•</label><p id="p0175"><italic>Calicivirus</italic>: Noroviruses, the prototype of caliciviruses, are responsible for almost all viral gastroenteritis outbreaks worldwide.</p></list-item><list-item id="u0025"><label>•</label><p id="p0180"><italic>Togavirus</italic>: Sindbis virus and Semliki Forest virus (SFV) have been extensively studied as the prototype of togaviruses. Chikungunya virus, an emerging virus that caused an outbreak in Africa during 2004–2006, belongs to the togavirus family.</p></list-item><list-item id="u0030"><label>•</label><p id="p0185"><italic>Coronavirus</italic>: Coronaviruses possess the larger RNA genome of approximately 30 kb. SARS-coronavirus was discovered as a newly emerging virus that caused the 2003 SARS outbreak and 2012 MERS outbreak.</p></list-item></list></p></sec><sec id="s0040"><title>Study Questions</title><p id="p0190"><list list-type="simple" id="li0025"><list-item id="o0035"><label>13.1</label><p id="p0195">Consider that a novel positive-strand RNA virus was discovered. The RNA genome structure is organized similar to that of picornaviruses, encoding one large polyprotein. Moreover, a viral protein is covalently linked to the 5′ terminus of the RNA genome. (1) Please hypothesize the role of the 5′ terminus-linked viral protein. (2) How would you test your hypothesis?</p></list-item><list-item id="o0040"><label>13.2</label><p id="p0200">Sindbis virus has subgenomic RNA as well as genomic RNA. (1) State your hypothesis on the mechanism by which the subgenomic RNA is transcribed. (2) How would you test your hypothesis?</p></list-item></list></p></sec></body><back><ref-list id="fr0010"><title>Suggested Reading</title><ref id="fur1"><element-citation publication-type="journal" id="sbref1"><person-group person-group-type="author"><name><surname>Jones</surname><given-names>M.K.</given-names></name><name><surname>Watanabe</surname><given-names>M.</given-names></name><name><surname>Zhu</surname><given-names>S.</given-names></name><name><surname>Graves</surname><given-names>C.L.</given-names></name><name><surname>Keyes</surname><given-names>L.R.</given-names></name><name><surname>Grau</surname><given-names>K.R.</given-names></name></person-group><article-title>Enteric bacteria promote human and mouse norovirus infection of B cells</article-title><source>Science</source><volume>346</volume><issue>6210</issue><year>2014</year><fpage>755</fpage><lpage>759</lpage><pub-id pub-id-type="pmid">25378626</pub-id></element-citation></ref><ref id="fur2"><element-citation publication-type="journal" id="sbref2"><person-group person-group-type="author"><name><surname>Karst</surname><given-names>S.M.</given-names></name><name><surname>Wobus</surname><given-names>C.E.</given-names></name></person-group><article-title>A working model of how noroviruses infect the intestine</article-title><source>PLoS Pathog.</source><volume>11</volume><issue>2</issue><year>2015</year><fpage>e1004626</fpage><pub-id pub-id-type="pmid">25723501</pub-id></element-citation></ref><ref id="fur3"><element-citation publication-type="journal" id="sbref3"><person-group person-group-type="author"><name><surname>Li</surname><given-names>W.</given-names></name><name><surname>Moore</surname><given-names>M.J.</given-names></name><name><surname>Vasilieva</surname><given-names>N.</given-names></name><name><surname>Sui</surname><given-names>J.</given-names></name><name><surname>Wong</surname><given-names>S.K.</given-names></name><name><surname>Berne</surname><given-names>M.A.</given-names></name></person-group><article-title>Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus</article-title><source>Nature</source><volume>426</volume><issue>6965</issue><year>2003</year><fpage>450</fpage><lpage>454</lpage><pub-id pub-id-type="pmid">14647384</pub-id></element-citation></ref><ref id="fur4"><element-citation publication-type="journal" id="sbref4"><person-group person-group-type="author"><name><surname>Raj</surname><given-names>V.S.</given-names></name><name><surname>Mou</surname><given-names>H.</given-names></name><name><surname>Smits</surname><given-names>S.L.</given-names></name><name><surname>Dekkers</surname><given-names>D.H.</given-names></name><name><surname>Muller</surname><given-names>M.A.</given-names></name><name><surname>Dijkman</surname><given-names>R.</given-names></name></person-group><article-title>Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC</article-title><source>Nature</source><volume>495</volume><issue>7440</issue><year>2013</year><fpage>251</fpage><lpage>254</lpage><pub-id pub-id-type="pmid">23486063</pub-id></element-citation></ref><ref id="fur5"><element-citation publication-type="journal" id="sbref5"><person-group person-group-type="author"><name><surname>Zust</surname><given-names>R.</given-names></name><name><surname>Cervantes-Barragan</surname><given-names>L.</given-names></name><name><surname>Habjan</surname><given-names>M.</given-names></name><name><surname>Maier</surname><given-names>R.</given-names></name><name><surname>Neuman</surname><given-names>B.W.</given-names></name><name><surname>Ziebuhr</surname><given-names>J.</given-names></name></person-group><article-title>Ribose 2′-O-methylation provides a molecular signature for the distinction of self and non-self mRNA dependent on the RNA sensor Mda5</article-title><source>Nat. Immunol.</source><volume>12</volume><issue>2</issue><year>2011</year><fpage>137</fpage><lpage>143</lpage><pub-id pub-id-type="pmid">21217758</pub-id></element-citation></ref></ref-list><ref-list id="fr0015"><title>Journal Club</title><p id="p0205"><list list-type="simple" id="li0030"><list-item id="u0035"><label>•</label><p id="p0210">Jones, M.K., Watanabe, M., Zhu, S., et al., 2014. Enteric bacteria promote human and mouse norovirus infection of B cells. Science 346 (6210), 755–759.</p><p id="p0215">Highlight: The biggest hurdle in norovirus research has been that norovirus is not cultivatable in a cell culture. It has been speculated that noroviruses primarily target intestinal epithelial cells, which line the intestine and protect it from pathogens. Surprisingly, the authors here demonstrated that human norovirus can be propagated in B cells, with the help of enteric bacteria. It is an unprecedented finding that bacteria facilitates the virus infection.</p></list-item></list></p></ref-list><fn-group><fn id="fn1"><label>1.</label><p id="ntp0010"><bold>Calicivirus</bold> The term is derived from Greek word for “cup”-<italic>calyx</italic>.</p></fn><fn id="fn2"><label>2.</label><p id="ntp0015"><bold>Norovirus</bold> The norovirus was originally named the “Norwalk agent” after Norwalk, Ohio, in the United States, where an outbreak of acute gastroenteritis occurred among children at the elementary school in 1968. The virus was given the name “Norwalk virus.”</p></fn><fn id="fn3"><label>3.</label><p id="ntp0020"><bold>Coronavirus</bold> The name “coronavirus” is derived from the Latin <italic>corona</italic>, meaning crown or halo.</p></fn><fn id="fn4"><label>4.</label><p id="ntp0025"><bold>Subgenomic RNA</bold> It refers to a viral RNA that is smaller than the full-length viral RNA.</p></fn></fn-group></back></pmc></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/MersV1/Data/Pmc/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000785 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd -nk 000785 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Sante
|area= MersV1
|flux= Pmc
|étape= Corpus
|type= RBID
|clé= PMC:7149767
|texte= Other Positive-Strand RNA Viruses
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/RBID.i -Sk "pubmed:NONE" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd \
| NlmPubMed2Wicri -a MersV1
| This area was generated with Dilib version V0.6.33. |  |