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suck abstract from ncbi


10.1038/s42003-020-01370-w

http://scihub22266oqcxt.onion/10.1038/s42003-020-01370-w
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33110195!7591510!33110195
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suck abstract from ncbi

pmid33110195      Commun+Biol 2020 ; 3 (1): 641
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  • Comparative ACE2 variation and primate COVID-19 risk #MMPMID33110195
  • Melin AD; Janiak MC; Marrone F 3rd; Arora PS; Higham JP
  • Commun Biol 2020[Oct]; 3 (1): 641 PMID33110195show ga
  • The emergence of SARS-CoV-2 has caused over a million human deaths and massive global disruption. The viral infection may also represent a threat to our closest living relatives, nonhuman primates. The contact surface of the host cell receptor, ACE2, displays amino acid residues that are critical for virus recognition, and variations at these critical residues modulate infection susceptibility. Infection studies have shown that some primate species develop COVID-19-like symptoms; however, the susceptibility of most primates is unknown. Here, we show that all apes and African and Asian monkeys (catarrhines), exhibit the same set of twelve key amino acid residues as human ACE2. Monkeys in the Americas, and some tarsiers, lemurs and lorisoids, differ at critical contact residues, and protein modeling predicts that these differences should greatly reduce SARS-CoV-2 binding affinity. Other lemurs are predicted to be closer to catarrhines in their susceptibility. Our study suggests that apes and African and Asian monkeys, and some lemurs, are likely to be highly susceptible to SARS-CoV-2. Urgent actions have been undertaken to limit the exposure of great apes to humans, and similar efforts may be necessary for many other primate species.
  • |Amino Acid Sequence[MESH]
  • |Amino Acid Substitution[MESH]
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Animals[MESH]
  • |Betacoronavirus/*pathogenicity/physiology[MESH]
  • |Biological Evolution[MESH]
  • |COVID-19[MESH]
  • |Chiroptera/genetics[MESH]
  • |Conserved Sequence[MESH]
  • |Coronavirus Infections/epidemiology/transmission/*veterinary[MESH]
  • |Genetic Predisposition to Disease[MESH]
  • |Host Specificity/*genetics[MESH]
  • |Mammals/genetics[MESH]
  • |Models, Molecular[MESH]
  • |Mutation, Missense[MESH]
  • |Pandemics/*veterinary[MESH]
  • |Peptidyl-Dipeptidase A/chemistry/*genetics[MESH]
  • |Phylogeny[MESH]
  • |Pneumonia, Viral/epidemiology/transmission/*veterinary[MESH]
  • |Point Mutation[MESH]
  • |Primate Diseases/*enzymology/virology[MESH]
  • |Primates/*genetics[MESH]
  • |Protein Binding[MESH]
  • |Protein Conformation[MESH]
  • |Receptors, Virus/*genetics[MESH]
  • |Risk[MESH]
  • |SARS-CoV-2[MESH]
  • |Sequence Alignment[MESH]
  • |Sequence Homology, Amino Acid[MESH]
  • |Species Specificity[MESH]


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