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Autor(en) / Beteiligte
Titel
Isolation of SARS-CoV-2-related coronavirus from Malayan pangolins
Ist Teil von
  • Nature (London), 2020-07, Vol.583 (7815), p.286-289
Ort / Verlag
London: Nature Publishing Group UK
Erscheinungsjahr
2020
Quelle
MEDLINE
Beschreibungen/Notizen
  • The current outbreak of coronavirus disease-2019 (COVID-19) poses unprecedented challenges to global health 1 . The new coronavirus responsible for this outbreak—severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)—shares high sequence identity to SARS-CoV and a bat coronavirus, RaTG13 2 . Although bats may be the reservoir host for a variety of coronaviruses 3 , 4 , it remains unknown whether SARS-CoV-2 has additional host species. Here we show that a coronavirus, which we name pangolin-CoV, isolated from a Malayan pangolin has 100%, 98.6%, 97.8% and 90.7% amino acid identity with SARS-CoV-2 in the E, M, N and S proteins, respectively. In particular, the receptor-binding domain of the S protein of pangolin-CoV is almost identical to that of SARS-CoV-2, with one difference in a noncritical amino acid. Our comparative genomic analysis suggests that SARS-CoV-2 may have originated in the recombination of a virus similar to pangolin-CoV with one similar to RaTG13. Pangolin-CoV was detected in 17 out of the 25 Malayan pangolins that we analysed. Infected pangolins showed clinical signs and histological changes, and circulating antibodies against pangolin-CoV reacted with the S protein of SARS-CoV-2. The isolation of a coronavirus from pangolins that is closely related to SARS-CoV-2 suggests that these animals have the potential to act as an intermediate host of SARS-CoV-2. This newly identified coronavirus from pangolins—the most-trafficked mammal in the illegal wildlife trade—could represent a future threat to public health if wildlife trade is not effectively controlled. A newly identified coronavirus found in Malayan pangolins shares considerable sequence identity with SARS-CoV-2, which suggests that the latter may have originated from a recombination event involving SARS-related coronaviruses from bats and pangolins.
Sprache
Englisch
Identifikatoren
ISSN: 0028-0836
eISSN: 1476-4687
DOI: 10.1038/s41586-020-2313-x
Titel-ID: cdi_proquest_miscellaneous_2400552604
Format
Schlagworte
14/28, 38/1, 38/77, 631/326/596/2078, 631/326/596/4130, 692/699/255/2514, Amino acids, Animals, Antibodies, Bats, Betacoronavirus - classification, Betacoronavirus - genetics, Betacoronavirus - isolation & purification, China, Chiroptera - virology, Chlorocebus aethiops, Coronaviridae, Coronavirus Envelope Proteins, Coronavirus Infections - epidemiology, Coronavirus Infections - pathology, Coronavirus Infections - transmission, Coronavirus Infections - veterinary, Coronavirus Infections - virology, Coronavirus M Proteins, Coronavirus Nucleocapsid Proteins, Coronaviruses, COVID-19, Disease Reservoirs - virology, Disease transmission, Enzymes, Eutheria - virology, Evolution, Molecular, Genes, Genome, Viral - genetics, Genomes, Genomic analysis, Genomics, Global health, Host Specificity, Humanities and Social Sciences, Humans, Lung - pathology, Lung - virology, Malaysia, Mammals, Middle East respiratory syndrome, multidisciplinary, Nucleocapsid Proteins - genetics, Outbreaks, Pandemics, Phosphoproteins, Phylogenetics, Phylogeny, Pneumonia, Viral - epidemiology, Pneumonia, Viral - transmission, Pneumonia, Viral - virology, Polymerase Chain Reaction, Proteins, Public health, Recombination, Recombination, Genetic, Respiratory diseases, SARS-CoV-2, Science, Science (multidisciplinary), Sequence Alignment, Sequence Analysis, RNA, Sequence Homology, Nucleic Acid, Severe acute respiratory syndrome coronavirus 2, Spike Glycoprotein, Coronavirus - genetics, Vero Cells, Viral diseases, Viral Envelope Proteins - genetics, Viral Matrix Proteins - genetics, Viruses, Wildlife, Wildlife trade, Zoonoses - transmission, Zoonoses - virology

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