cwbe coordinatez:
101
8333809
8837211
8703087
8731316
8731359
8736604

ABSOLUT
KYBERIA
permissions
you: r,
system: public
net: yes

neurons

stats|by_visit|by_K
source
tiamat
K|my_K|given_K
last
commanders
polls

total descendants::1
total children::1
show[ 2 | 3] flat
mea culpa & You got my K




0000010108333809088372110870308708731316087313590873660408736624
himself
 himself      07.04.2020 - 14:08:15 (modif: 07.04.2020 - 14:08:28) [1K] , level: 1, UP   NEW !!CONTENT CHANGED!!
Tu je ku téme ďaľší pekný šupa článok. Ešte teplý.

https://www.biorxiv.org/content/10.1101/2020.03.30.015008v1

Key Points

- RaTG13 is the closest available bat virus to SARS-CoV-2; a sub-lineage of these bat viruses is able to infect humans. Two sister lineages of the RaTG13/SARS-CoV-2 lineage infect Malayan pangolins.

- The sarbecoviruses show a pattern of deep recombination events, indicating that there are high levels of co-infection in horseshoe bats and that the viral pool can generate novel allele combinations and substantial genetic diversity; the sarbecoviruses are efficient ‘explorers’ of phenotype space.

- The SARS-CoV-2 lineage is not a recent recombinant, at least not involving any of the bat or pangolin viruses sampled to date.

- Non-recombinant regions of the sarbecoviruses can be identified, allowing for phylogenetic inference and dating to be performed. We constructed three such regions using different methods.

- We estimate that RaTG13 and SARS-CoV-2 diverged 40 to 70 years ago. There is a diverse unsampled reservoir of generalist viruses established in horseshoe bats.

- While an intermediate host responsible for the zoonotic event cannot be ruled out, the relevant evolution for spillover to humans very likely occurred in horseshoe bats.