Research Square (Research Square),
Journal Year:
2021,
Volume and Issue:
unknown
Published: Sept. 17, 2021
Abstract
The
animal
reservoir
of
SARS-CoV-2
is
unknown
despite
reports
various
SARS-CoV-2-related
viruses
in
Asian
Rhinolophus
bats,
including
the
closest
virus
from
R.
affinis,
RaTG13.
Several
studies
have
suggested
involvement
pangolin
coronaviruses
emergence.
presents
a
mosaic
genome,
to
which
different
progenitors
contribute.
spike
sequence
determines
binding
affinity
and
accessibility
its
receptor-binding
domain
(RBD)
cellular
angiotensin-converting
enzyme
2
(ACE2)
receptor
responsible
for
host
range.
progenitor
bat
genetically
close
able
enter
human
cells
through
ACE2
pathway
not
yet
been
identified,
though
they
would
be
key
understanding
origin
epidemics.
Here
we
show
that
such
indeed
circulate
cave
bats
living
limestone
karstic
terrain
North
Laos,
within
Indochinese
peninsula.
We
found
RBDs
these
differ
by
only
one
or
two
residues,
bind
as
efficiently
hACE2
protein
Wuhan
strain
isolated
early
cases,
mediate
hACE2-dependent
entry
into
cells,
inhibited
antibodies
neutralizing
SARS-CoV-2.
None
harbors
furin
cleavage
site
spike.
Our
findings
therefore
indicate
bat-borne
SARS-CoV-2-like
potentially
infectious
humans
spp.
Cell & Bioscience,
Journal Year:
2021,
Volume and Issue:
11(1)
Published: July 19, 2021
Abstract
SARS-CoV-2
is
an
extremely
contagious
respiratory
virus
causing
adult
atypical
pneumonia
COVID-19
with
severe
acute
syndrome
(SARS).
has
a
single-stranded,
positive-sense
RNA
(+RNA)
genome
of
~
29.9
kb
and
exhibits
significant
genetic
shift
from
different
isolates.
After
entering
the
susceptible
cells
expressing
both
ACE2
TMPRSS2,
directly
functions
as
mRNA
to
translate
two
polyproteins
ORF1a
ORF1b
region,
which
are
cleaved
by
viral
proteases
into
sixteen
non-structural
proteins
(nsp1-16)
initiate
replication
transcription.
The
also
encodes
four
structural
(S,
E,
M
N)
up
six
accessory
(3a,
6,
7a,
7b,
8,
9b)
proteins,
but
their
translation
requires
newly
synthesized
individual
subgenomic
RNAs
(sgRNA)
in
infected
cells.
Synthesis
full-length
genomic
(gRNA)
sgRNAs
conducted
inside
double-membrane
vesicles
(DMVs)
transcription
complex
(RTC),
comprises
nsp7,
nsp8,
nsp9,
nsp12,
nsp13
short
primer.
To
produce
sgRNAs,
RTC
starts
synthesis
highly
structured
gRNA
3'
end
switches
template
at
various
regulatory
sequence
(TRS
B
)
sites
along
body
probably
mediated
long-distance
RNA–RNA
interaction.
TRS
motif
5'
leader
L
responsible
for
interaction
upstream
each
ORF
skipping
between
them
sgRNAs.
Abundance
depend
on
location
read-through
efficiency
.
Although
more
studies
needed,
unprecedented
pandemic
taught
world
painful
lesson
that
invest
proactively
prepare
future
emergence
other
types
coronaviruses
any
possible
biological
horrors.
Nature Reviews Microbiology,
Journal Year:
2021,
Volume and Issue:
20(5), P. 299 - 314
Published: Nov. 19, 2021
In
the
past
two
decades,
three
coronaviruses
with
ancestral
origins
in
bats
have
emerged
and
caused
widespread
outbreaks
humans,
including
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2).
Since
first
SARS
epidemic
2002–2003,
appreciation
of
as
key
hosts
zoonotic
has
advanced
rapidly.
More
than
4,000
sequences
from
14
bat
families
been
identified,
yet
true
diversity
is
probably
much
greater.
Given
that
are
likely
evolutionary
source
for
several
human
coronaviruses,
strains
cause
mild
upper
tract
disease,
their
role
historic
future
pandemics
requires
ongoing
investigation.
We
review
integrate
information
on
bat–coronavirus
interactions
at
molecular,
tissue,
host
population
levels.
identify
critical
gaps
knowledge
which
relate
to
spillover
pandemic
risk,
pathways
spillover,
infection
dynamics
within
reservoir
hosts,
prior
adaptation
intermediate
transmission
viral
genotypes
or
traits
predict
capacity
potential.
Filling
these
may
help
prevent
next
pandemic.
Bats
harbour
a
multitude
owing
wide
distribution
prime
emerging
viruses.
Ruiz-Aravena,
McKee
colleagues
analyse
currently
available
discuss
recent
potential
spillovers.
Science,
Journal Year:
2022,
Volume and Issue:
377(6606)
Published: July 5, 2022
To
combat
future
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
variants
and
spillovers
of
SARS-like
betacoronaviruses
(sarbecoviruses)
threatening
global
health,
we
designed
mosaic
nanoparticles
that
present
randomly
arranged
sarbecovirus
spike
receptor-binding
domains
(RBDs)
to
elicit
antibodies
against
epitopes
are
conserved
relatively
occluded
rather
than
variable,
immunodominant,
exposed.
We
compared
immune
responses
elicited
by
mosaic-8
(SARS-CoV-2
seven
animal
sarbecoviruses)
homotypic
(only
SARS-CoV-2)
RBD
in
mice
macaques
observed
stronger
mismatched
(not
on
nanoparticles)
strains,
including
SARS-CoV
sarbecoviruses.
Mosaic-8
immunization
showed
equivalent
neutralization
SARS-CoV-2
variants,
Omicrons,
protected
from
challenges,
whereas
only
challenge.
Epitope
mapping
demonstrated
increased
targeting
after
immunization.
Together,
these
results
suggest
could
protect
spillovers.
Nature Communications,
Journal Year:
2021,
Volume and Issue:
12(1)
Published: Nov. 9, 2021
Abstract
Knowledge
of
the
origin
and
reservoir
coronavirus
responsible
for
ongoing
COVID-19
pandemic
is
still
fragmentary.
To
date,
closest
relatives
to
SARS-CoV-2
have
been
detected
in
Rhinolophus
bats
sampled
Yunnan
province,
China.
Here
we
describe
identification
related
coronaviruses
two
shameli
Cambodia
2010.
Metagenomic
sequencing
identifies
nearly
identical
viruses
sharing
92.6%
nucleotide
identity
with
SARS-CoV-2.
Most
genomic
regions
are
closely
SARS-CoV-2,
exception
a
region
spike,
which
not
compatible
human
ACE2-mediated
entry.
The
discovery
these
bat
species
found
China
indicates
that
much
wider
geographic
distribution
than
previously
reported,
suggests
Southeast
Asia
represents
key
area
consider
future
surveillance
coronaviruses.
Genome Biology and Evolution,
Journal Year:
2022,
Volume and Issue:
14(2)
Published: Feb. 1, 2022
Abstract
The
lack
of
an
identifiable
intermediate
host
species
for
the
proximal
animal
ancestor
SARS-CoV-2,
and
large
geographical
distance
between
Wuhan
where
closest
evolutionary
related
coronaviruses
circulating
in
horseshoe
bats
(members
Sarbecovirus
subgenus)
have
been
identified,
is
fueling
speculation
on
natural
origins
SARS-CoV-2.
We
performed
a
comprehensive
phylogenetic
study
SARS-CoV-2
all
bat
pangolin
sarbecoviruses
sampled
so
far.
Determining
likely
recombination
events
reveals
highly
reticulate
history
within
this
group
coronaviruses.
Distribution
inferred
nonrandom
with
evidence
that
Spike,
main
target
humoral
immunity,
beside
hotspot
driving
antigenic
shift
ancestry
sarbecoviruses.
Coupled
geographic
ranges
their
hosts
sampling
locations,
across
southern
China,
into
Southeast
Asia,
we
confirm
bats,
Rhinolophus,
are
reservoir
progenitor.
By
tracing
recombinant
sequence
patterns,
conclude
there
has
relatively
recent
movement
cocirculation
these
viruses’
ancestors,
extending
China
Asia
over
last
100
years.
direct
to
not
yet
sampled,
since
known
relatives
collected
Yunnan
shared
common
approximately
40
years
ago.
Our
analysis
highlights
need
dramatically
more
wildlife
to:
1)
pinpoint
exact
SARS-CoV-2’s
progenitor,
2)
facilitated
transmission
from
humans
(if
one),
3)
survey
extent
diversity
sarbecoviruses’
phylogeny
present
high
risk
future
spillovers.