A decade after SARS: strategies for controlling emerging coronaviruses
Identifieur interne : 002069 ( Main/Exploration ); précédent : 002068; suivant : 002070A decade after SARS: strategies for controlling emerging coronaviruses
Auteurs : Rachel L. Graham ; Eric F. Donaldson ; Ralph S. BaricSource :
- Nature Reviews. Microbiology [ 1740-1526 ] ; 2013.
Descripteurs français
- KwdFr :
- Coronavirus (génétique), Coronavirus (isolement et purification), Coronavirus (pathogénicité), Coronavirus (physiologie), Découverte de médicament (tendances), Humains, Infections à coronavirus (), Infections à coronavirus (épidémiologie), Maladies transmissibles émergentes (), Maladies transmissibles émergentes (épidémiologie), Récepteurs viraux (métabolisme), Tropisme viral, Vaccins antiviraux (immunologie), Vaccins antiviraux (isolement et purification).
- MESH :
- génétique : Coronavirus.
- immunologie : Vaccins antiviraux.
- isolement et purification : Coronavirus, Vaccins antiviraux.
- métabolisme : Récepteurs viraux.
- pathogénicité : Coronavirus.
- physiologie : Coronavirus.
- tendances : Découverte de médicament.
- épidémiologie : Infections à coronavirus, Maladies transmissibles émergentes.
- Humains, Infections à coronavirus, Maladies transmissibles émergentes, Tropisme viral.
English descriptors
- KwdEn :
- Communicable Diseases, Emerging (epidemiology), Communicable Diseases, Emerging (prevention & control), Coronavirus (genetics), Coronavirus (isolation & purification), Coronavirus (pathogenicity), Coronavirus (physiology), Coronavirus Infections (epidemiology), Coronavirus Infections (prevention & control), Drug Discovery (trends), Humans, Receptors, Virus (metabolism), Viral Tropism, Viral Vaccines (immunology), Viral Vaccines (isolation & purification).
- MESH :
- chemical , immunology : Viral Vaccines.
- chemical , isolation & purification : Viral Vaccines.
- chemical , metabolism : Receptors, Virus.
- epidemiology : Communicable Diseases, Emerging, Coronavirus Infections.
- genetics : Coronavirus.
- isolation & purification : Coronavirus.
- pathogenicity : Coronavirus.
- physiology : Coronavirus.
- prevention & control : Communicable Diseases, Emerging, Coronavirus Infections.
- trends : Drug Discovery.
- Humans, Viral Tropism.
Abstract
Two highly pathogenic human coronaviruses, severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV), have emerged in the past decade. The lack of any clinically approved antiviral treatments or vaccines for either virus emphasizes the importance of the design of effective therapeutics and preventives. Bats have been implicated as reservoirs of both SARS-CoV and MERS-CoV as well as related viruses and other human coronaviruses (HCoVs), such as HCoV-229E and HCoV-NL63. The dispersion of bat species over much of the globe probably enhances their potential to act as reservoirs for pathogens, some of which are extremely virulent and potentially lethal to other animals and humans. Multiple animal models for SARS-CoV infection exist, although mouse models have been the most thoroughly characterized. Mouse-adapted SARS-CoV is capable of causing pathology that is representative of human infections in both young and aged animals. Small animal models for MERS-CoV infection have not yet been reported, although the possibility of further ongoing selection in the receptor-binding sequence in the spike protein or other sequences that are important for host specificity might contribute to this limitation. A mild disease phenotype that can include either localized or widespread pneumonia is observed in inoculated macaques. Multiple vaccine strategies have been attempted with coronaviruses, mostly (but not exclusively) targeting the spike glycoprotein. Successful live-attenuated vaccines have utilized reverse genetic strategies to delete the envelope protein or inactivate the exonuclease activity of non-structural protein 14 (nsp14) . MERS-CoV, similarly to SARS-CoV in 2003, has the potential to have a profound impact on the human population; however, its low penetrance thus far suggests that the virus might either ultimately fail to develop a niche in humans or it might still be adapting to human hosts and that the worst of its effects are yet to come. Coronavirus phylogeny shows an incredible diversity in antigenic variants, which leads to limited cross-protection against infection with different strains, even within a phylogenetic subcluster. Consequently, the risk of introducing novel coronaviruses into naive human and animal populations remains high.
The online version of this article (doi:10.1038/nrmicro3143) contains supplementary material, which is available to authorized users.
Url:
DOI: 10.1038/nrmicro3143
PubMed: 24217413
PubMed Central: 5147543
Affiliations:
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Le document en format XML
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Microbiology</title><idno type="ISSN">1740-1526</idno><idno type="eISSN">1740-1534</idno><imprint><date when="2013">2013</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Communicable Diseases, Emerging (epidemiology)</term><term>Communicable Diseases, Emerging (prevention & control)</term><term>Coronavirus (genetics)</term><term>Coronavirus (isolation & purification)</term><term>Coronavirus (pathogenicity)</term><term>Coronavirus (physiology)</term><term>Coronavirus Infections (epidemiology)</term><term>Coronavirus Infections (prevention & control)</term><term>Drug Discovery (trends)</term><term>Humans</term><term>Receptors, Virus (metabolism)</term><term>Viral Tropism</term><term>Viral Vaccines (immunology)</term><term>Viral Vaccines (isolation & purification)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Coronavirus (génétique)</term><term>Coronavirus (isolement et purification)</term><term>Coronavirus (pathogénicité)</term><term>Coronavirus (physiologie)</term><term>Découverte de médicament (tendances)</term><term>Humains</term><term>Infections à coronavirus ()</term><term>Infections à coronavirus (épidémiologie)</term><term>Maladies transmissibles émergentes ()</term><term>Maladies transmissibles émergentes (épidémiologie)</term><term>Récepteurs viraux (métabolisme)</term><term>Tropisme viral</term><term>Vaccins antiviraux (immunologie)</term><term>Vaccins antiviraux (isolement et purification)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en"><term>Viral Vaccines</term></keywords><keywords scheme="MESH" type="chemical" qualifier="isolation & purification" xml:lang="en"><term>Viral Vaccines</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Receptors, Virus</term></keywords><keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Communicable Diseases, Emerging</term><term>Coronavirus Infections</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Coronavirus</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Coronavirus</term></keywords><keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Vaccins antiviraux</term></keywords><keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en"><term>Coronavirus</term></keywords><keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr"><term>Coronavirus</term><term>Vaccins antiviraux</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Récepteurs viraux</term></keywords><keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en"><term>Coronavirus</term></keywords><keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr"><term>Coronavirus</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Coronavirus</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Coronavirus</term></keywords><keywords scheme="MESH" qualifier="prevention & control" xml:lang="en"><term>Communicable Diseases, Emerging</term><term>Coronavirus Infections</term></keywords><keywords scheme="MESH" qualifier="tendances" xml:lang="fr"><term>Découverte de médicament</term></keywords><keywords scheme="MESH" qualifier="trends" xml:lang="en"><term>Drug Discovery</term></keywords><keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr"><term>Infections à coronavirus</term><term>Maladies transmissibles émergentes</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Humans</term><term>Viral Tropism</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Humains</term><term>Infections à coronavirus</term><term>Maladies transmissibles émergentes</term><term>Tropisme viral</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><title>Key Points</title><p id="Par4"><list list-type="bullet"><list-item><p id="Par5">Two highly pathogenic human coronaviruses, severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV), have emerged in the past decade. The lack of any clinically approved antiviral treatments or vaccines for either virus emphasizes the importance of the design of effective therapeutics and preventives.</p></list-item><list-item><p id="Par6">Bats have been implicated as reservoirs of both SARS-CoV and MERS-CoV as well as related viruses and other human coronaviruses (HCoVs), such as HCoV-229E and HCoV-NL63. The dispersion of bat species over much of the globe probably enhances their potential to act as reservoirs for pathogens, some of which are extremely virulent and potentially lethal to other animals and humans.</p></list-item><list-item><p id="Par7">Multiple animal models for SARS-CoV infection exist, although mouse models have been the most thoroughly characterized. Mouse-adapted SARS-CoV is capable of causing pathology that is representative of human infections in both young and aged animals.</p></list-item><list-item><p id="Par8">Small animal models for MERS-CoV infection have not yet been reported, although the possibility of further ongoing selection in the receptor-binding sequence in the spike protein or other sequences that are important for host specificity might contribute to this limitation. A mild disease phenotype that can include either localized or widespread pneumonia is observed in inoculated macaques.</p></list-item><list-item><p id="Par9">Multiple vaccine strategies have been attempted with coronaviruses, mostly (but not exclusively) targeting the spike glycoprotein. Successful live-attenuated vaccines have utilized reverse genetic strategies to delete the envelope protein or inactivate the exonuclease activity of non-structural protein 14 (nsp14) .</p></list-item><list-item><p id="Par10">MERS-CoV, similarly to SARS-CoV in 2003, has the potential to have a profound impact on the human population; however, its low penetrance thus far suggests that the virus might either ultimately fail to develop a niche in humans or it might still be adapting to human hosts and that the worst of its effects are yet to come.</p></list-item><list-item><p id="Par11">Coronavirus phylogeny shows an incredible diversity in antigenic variants, which leads to limited cross-protection against infection with different strains, even within a phylogenetic subcluster. Consequently, the risk of introducing novel coronaviruses into naive human and animal populations remains high.</p></list-item></list></p><sec><title>Supplementary information</title><p>The online version of this article (doi:10.1038/nrmicro3143) contains supplementary material, which is available to authorized users.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Zhong, N" uniqKey="Zhong N">N Zhong</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Peiris, Js" uniqKey="Peiris J">JS Peiris</name></author><author><name sortKey="Guan, Y" uniqKey="Guan Y">Y Guan</name></author><author><name sortKey="Yuen, Ky" uniqKey="Yuen K">KY Yuen</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Cherry, Jd" uniqKey="Cherry J">JD Cherry</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Anthony, Sj" uniqKey="Anthony S">SJ Anthony</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Woo, Pc" uniqKey="Woo P">PC Woo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Lau, Sk" uniqKey="Lau S">SK Lau</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Pfefferle, S" uniqKey="Pfefferle S">S Pfefferle</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Chu, Dk" uniqKey="Chu D">DK Chu</name></author><author><name sortKey="Peiris, Js" uniqKey="Peiris J">JS Peiris</name></author><author><name sortKey="Chen, H" uniqKey="Chen H">H Chen</name></author><author><name sortKey="Guan, Y" uniqKey="Guan Y">Y Guan</name></author><author><name sortKey="Poon, Ll" uniqKey="Poon L">LL Poon</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Woo, Pc" uniqKey="Woo P">PC Woo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Tang, Xc" 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Mj" uniqKey="Cameron M">MJ Cameron</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Tang, Nl" uniqKey="Tang N">NL Tang</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Reghunathan, R" uniqKey="Reghunathan R">R Reghunathan</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Jiang, Y" uniqKey="Jiang Y">Y Jiang</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Tsushima, K" uniqKey="Tsushima K">K Tsushima</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Li, Ts" uniqKey="Li T">TS Li</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Gralinski, Le" uniqKey="Gralinski L">LE Gralinski</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Graham, Rl" uniqKey="Graham R">RL Graham</name></author><author><name sortKey="Baric, Rs" uniqKey="Baric R">RS Baric</name></author></analytic></biblStruct><biblStruct></biblStruct></listBibl></div1></back></TEI><affiliations><list></list><tree><noCountry><name sortKey="Baric, Ralph S" sort="Baric, Ralph S" uniqKey="Baric R" first="Ralph S." last="Baric">Ralph S. Baric</name><name sortKey="Donaldson, Eric F" sort="Donaldson, Eric F" uniqKey="Donaldson E" first="Eric F." last="Donaldson">Eric F. Donaldson</name><name sortKey="Graham, Rachel L" sort="Graham, Rachel L" uniqKey="Graham R" first="Rachel L." last="Graham">Rachel L. Graham</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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