A Comparative Review of Animal Models of Middle East Respiratory Syndrome Coronavirus Infection.
Identifieur interne : 001413 ( Main/Exploration ); précédent : 001412; suivant : 001414A Comparative Review of Animal Models of Middle East Respiratory Syndrome Coronavirus Infection.
Auteurs : L. Baseler [États-Unis] ; E. De Wit [États-Unis] ; H. Feldmann [Indonésie]Source :
- Veterinary pathology [ 1544-2217 ] ; 2016.
Descripteurs français
- KwdFr :
- Animaux, Callithrix, Coronavirus du syndrome respiratoire du Moyen-Orient (génétique), Coronavirus du syndrome respiratoire du Moyen-Orient (pathogénicité), Dipeptidyl peptidase 4 (génétique), Humains, Infections à coronavirus (anatomopathologie), Infections à coronavirus (virologie), Lapins, Macaca mulatta, Modèles animaux de maladie humaine, Souris, Souris transgéniques.
- MESH :
- anatomopathologie : Infections à coronavirus.
- génétique : Coronavirus du syndrome respiratoire du Moyen-Orient, Dipeptidyl peptidase 4.
- pathogénicité : Coronavirus du syndrome respiratoire du Moyen-Orient.
- virologie : Infections à coronavirus.
- Animaux, Callithrix, Humains, Lapins, Macaca mulatta, Modèles animaux de maladie humaine, Souris, Souris transgéniques.
English descriptors
- KwdEn :
- Animals, Callithrix, Coronavirus Infections (pathology), Coronavirus Infections (virology), Dipeptidyl Peptidase 4 (genetics), Disease Models, Animal, Humans, Macaca mulatta, Mice, Mice, Transgenic, Middle East Respiratory Syndrome Coronavirus (genetics), Middle East Respiratory Syndrome Coronavirus (pathogenicity), Rabbits.
- MESH :
- chemical , genetics : Dipeptidyl Peptidase 4.
- genetics : Middle East Respiratory Syndrome Coronavirus.
- pathogenicity : Middle East Respiratory Syndrome Coronavirus.
- pathology : Coronavirus Infections.
- virology : Coronavirus Infections.
- Animals, Callithrix, Disease Models, Animal, Humans, Macaca mulatta, Mice, Mice, Transgenic, Rabbits.
Abstract
Middle East respiratory syndrome coronavirus (MERS-CoV) was initially isolated from a Saudi Arabian man with fatal pneumonia. Since the original case in 2012, MERS-CoV infections have been reported in >1500 humans, and the case fatality rate is currently 35%. This lineage C betacoronavirus has been reported to cause a wide range of disease severity in humans, ranging from asymptomatic to progressive fatal pneumonia that may be accompanied by renal or multiorgan failure. Although the clinical presentation of human MERS-CoV infection has been documented, many facets of this emerging disease are still unknown and could be studied with animal models. Several animal models of MERS-CoV have been developed, including New Zealand white rabbits, transduced or transgenic mice that express human dipeptidyl peptidase 4, rhesus macaques, and common marmosets. This review provides an overview of the current state of knowledge on human MERS-CoV infections, the probable origin of MERS-CoV, and the available animal models of MERS-CoV infection. Evaluation of the benefits and limitations of these models will aid in appropriate model selection for studying viral pathogenesis and transmission, as well as for testing vaccines and antivirals against MERS-CoV.
DOI: 10.1177/0300985815620845
PubMed: 26869154
Affiliations:
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Baseler</name><affiliation wicri:level="2"><nlm:affiliation>Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA Department of Comparative Pathobiology, Purdue University, West Lafayette, IN, USA Department of Veterinary Medicine and Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA Department of Comparative Pathobiology, Purdue University, West Lafayette, IN, USA Department of Veterinary Medicine and Surgery, University of Texas MD Anderson Cancer Center, Houston, TX</wicri:regionArea><placeName><region type="state">Texas</region></placeName></affiliation></author><author><name sortKey="De Wit, E" sort="De Wit, E" uniqKey="De Wit E" first="E" last="De Wit">E. De Wit</name><affiliation wicri:level="2"><nlm:affiliation>Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT</wicri:regionArea><placeName><region type="state">Montana</region></placeName></affiliation></author><author><name sortKey="Feldmann, H" sort="Feldmann, H" uniqKey="Feldmann H" first="H" last="Feldmann">H. 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Since the original case in 2012, MERS-CoV infections have been reported in >1500 humans, and the case fatality rate is currently 35%. This lineage C betacoronavirus has been reported to cause a wide range of disease severity in humans, ranging from asymptomatic to progressive fatal pneumonia that may be accompanied by renal or multiorgan failure. Although the clinical presentation of human MERS-CoV infection has been documented, many facets of this emerging disease are still unknown and could be studied with animal models. Several animal models of MERS-CoV have been developed, including New Zealand white rabbits, transduced or transgenic mice that express human dipeptidyl peptidase 4, rhesus macaques, and common marmosets. This review provides an overview of the current state of knowledge on human MERS-CoV infections, the probable origin of MERS-CoV, and the available animal models of MERS-CoV infection. Evaluation of the benefits and limitations of these models will aid in appropriate model selection for studying viral pathogenesis and transmission, as well as for testing vaccines and antivirals against MERS-CoV. </div></front></TEI><affiliations><list><country><li>Indonésie</li><li>États-Unis</li></country><region><li>Montana</li><li>Texas</li></region></list><tree><country name="États-Unis"><region name="Texas"><name sortKey="Baseler, L" sort="Baseler, L" uniqKey="Baseler L" first="L" last="Baseler">L. Baseler</name></region><name sortKey="De Wit, E" sort="De Wit, E" uniqKey="De Wit E" first="E" last="De Wit">E. De Wit</name></country><country name="Indonésie"><noRegion><name sortKey="Feldmann, H" sort="Feldmann, H" uniqKey="Feldmann H" first="H" last="Feldmann">H. Feldmann</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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