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Figured this is relevant given the current coronavirus outbreak in China (and spreading): https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)30251-8/fulltext
It discusses the study of the initial viral genomes and the associated phylogenetic analysis (study of evolutionary relationships) of the virus and insights that are gained from such analysis. In particular, it discusses the possibility that this virus uses the ACE2 receptor for binding (similar to SARS).
This appears to be confirmed in this subsequent paper: Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation
Thought this was another interesting example of how evolutionary biology is applied in real world situations to deal with real world problems.
The ten genome sequences of 2019-nCoV obtained from the nine patients were extremely similar, exhibiting more than 99·98% sequence identity. Notably, 2019-nCoV was closely related (with 88% identity) to two bat-derived severe acute respiratory syndrome (SARS)-like coronaviruses, bat-SL-CoVZC45 and bat-SL-CoVZXC21, collected in 2018 in Zhoushan, eastern China, but were more distant from SARS-CoV (about 79%) and MERS-CoV (about 50%). Phylogenetic analysis revealed that 2019-nCoV fell within the subgenus Sarbecovirus of the genus Betacoronavirus, with a relatively long branch length to its closest relatives bat-SL-CoVZC45 and bat-SL-CoVZXC21, and was genetically distinct from SARS-CoV.
It discusses the study of the initial viral genomes and the associated phylogenetic analysis (study of evolutionary relationships) of the virus and insights that are gained from such analysis. In particular, it discusses the possibility that this virus uses the ACE2 receptor for binding (similar to SARS).
This appears to be confirmed in this subsequent paper: Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation
Recent reports demonstrating that 2019-nCoV S and SARS-CoV S share the same functional host-cell receptor—angiotensin-converting enzyme 2 (ACE2) (22, 25–27)—prompted us to quantify the kinetics of this interaction by surface plasmon resonance (SPR). ACE2 bound to 2019-nCoV S ectodomain with ~15 nM affinity, which is approximately 10- to 20-fold higher affinity than ACE2 binding to SARS-CoV S (Fig. 3A and fig. S7) (14).
Thought this was another interesting example of how evolutionary biology is applied in real world situations to deal with real world problems.