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       #Post#: 70--------------------------------------------------
       Coronaviruses
       By: gsgs Date: February 7, 2020, 9:21 pm
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       “There is some evidence that people can be reinfected with the
       four coronaviruses
       and that there is no long-lasting immunity,”
       SARS has a molecular proofreading system that reduces its
       mutation rate, and the
       new coronavirus’s similarity to SARS at the genomic level
       suggests it does, too.
       “That makes the mutation rate much, much lower than for flu or
       HIV,” Farzan said.
  HTML https://www.statnews.com/2020/02/04/two-scenarios-if-new-coronavirus-isnt-contained/
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       Thus nsp14-ExoN is essential for replication fidelity, and
       likely serves either as a direct
       mediator or regulator of a more complex RNA proofreading
       machine, a process previously
       unprecedented in RNA virus biology. E
       The discovery of a protein distinct from a viral RdRp that
       regulates replication fidelity also
       raises the possibility that RNA genome replication fidelity may
       be adaptable to differing
       replication environments and selective pressures, rather than
       being a fixed determinant.
       Proofreading Exoribonuclease.
       Coronaviruses genome also encodes a protein called a replicase
       which allows
       the RNA viral genome to be transcribed into new RNA copies
       using the host cell's machinery.
       The replicase is the first protein to be made; once the gene
       encoding the replicase
       is translated, translation is stopped by a stop codon.
       This is known as a nested transcript. When the mRNA transcript
       only encodes
       one gene, it is monocistronic.
       A coronavirus non-structural protein provides extra fidelity to
       replication because it
       confers a proofreading function,[9] which is lacking in
       RNA-dependent RNA
       polymerase enzymes alone.
       Sexton NR, Smith EC, Blanc H, Vignuzzi M, Peersen OB, Denison MR
       (August 2016).
       "Homology-Based Identification of a Mutation in the Coronavirus
       RNA-Dependent RNA
       Polymerase That Confers Resistance to Multiple Mutagens".
       Journal of Virology. 90 (16): 7415–7428.
       doi:10.1128/JVI.00080-16. PMC 4984655. PMID 27279608.
       CoVs encode a proofreading exonuclease in nonstructural protein
       14(nsp14-ExoN),
       which confers a greater-than-10
       fold increase in fidelity compared to other RNA viruses. It is
       unknown to what extent the CoV
       polymerase (nsp12-RdRp) participates in replication fidelity
       multiproteinreplicase-proofreadingcomplex.
       Proofreading-deficient coronaviruses adapt for increased fitness
       over long-term passage
       without reversion of exoribonuclease-inactivating mutations
       Alanine replacement of the motif I residues (AA-E-D; four
       nucleotide substitutions) in
       murine hepatitis virus (MHV) and severe acute respiratory
       syndrome (SARS)-CoV yields
       viable mutants with impaired replication and fitness, increased
       mutation rates, and attenuated
       virulence in vivo. Despite these impairments, MHV- and SARS-CoV
       ExoN motif I AA mutants
       (ExoN-AA) have not reverted at motif I in diverse in vitro and
       in vivo environments, suggesting
       that profound fitness barriers prevent motif I reversion
       The Amazing Diversity of Nidoviruses
       #Post#: 268--------------------------------------------------
       Re: Coronaviruses
       By: gsgs Date: December 26, 2020, 11:52 pm
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       human non-sars-like Coronaviruses at genbank , release 239.0 :
       1394, Human coronavirus OC43
       907, Human coronavirus NL63
       424, Human coronavirus 229E
       415, Human coronavirus HKU1
       195, unidentified human coronavirus
       6, Human enteric coronavirus 4408
       4, Human coronavirus Feline-like Hu142
       2, Human betacoronavirus 2c Jordan-N3/2012
       2, Human betacoronavirus 2c EMC/2012
       1, Human group 1 coronavirus associated with pneumonia
       1, Human enteric coronavirus strain 4408
       1, Human coronavirus type 5
       1, Human coronavirus NO/2708/04
       1, Human coronavirus NO/1917/04
       1, Human coronavirus NO/1055/04
       1, Human coronavirus NO/0867/04
       1, Human coronavirus NO/0848/04
       1, Human coronavirus NO/0835/04
       1, Human coronavirus NO/0749/04
       1, Human coronavirus NO/0733/05
       1, Human coronavirus NO/0643/05
       1, Human coronavirus NO/0398/05
       1, Human coronavirus NO/0341/04
       1, Human coronavirus NO/0193/05
       1, Human coronavirus NO/0053/04
       1, Human coronavirus NO/0023/05
       1, Human coronavirus NO/0003/05
       1, Human coronavirus 3363/2000/NL
       1, Human coronavirus 1196/2001/NL
       1, Human betacoronavirus 2c England-Qatar/2012
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