Cell Host & Microbe,
Journal Year:
2021,
Volume and Issue:
29(12), P. 1788 - 1801.e6
Published: Nov. 13, 2021
Previous
work
found
that
the
co-occurring
mutations
R203K/G204R
on
SARS-CoV-2
nucleocapsid
(N)
protein
are
increasing
in
frequency
among
emerging
variants
of
concern
or
interest.
Through
a
combination
silico
analyses,
this
study
demonstrates
adaptive,
while
large-scale
phylogenetic
analyses
indicate
associate
with
emergence
high-transmissibility
lineage
B.1.1.7.
Competition
experiments
suggest
203K/204R
possess
replication
advantage
over
preceding
R203/G204
variants,
possibly
related
to
ribonucleocapsid
(RNP)
assembly.
Moreover,
virus
shows
increased
infectivity
human
lung
cells
and
hamsters.
Accordingly,
we
observe
positive
association
between
COVID-19
severity
sample
203K/204R.
Our
suggests
contribute
transmission
virulence
select
variants.
In
addition
spike
protein,
important
for
viral
spreading
during
pandemic.
Cell,
Journal Year:
2022,
Volume and Issue:
185(3), P. 467 - 484.e15
Published: Jan. 4, 2022
On
24th
November
2021,
the
sequence
of
a
new
SARS-CoV-2
viral
isolate
Omicron-B.1.1.529
was
announced,
containing
far
more
mutations
in
Spike
(S)
than
previously
reported
variants.
Neutralization
titers
Omicron
by
sera
from
vaccinees
and
convalescent
subjects
infected
with
early
pandemic
Alpha,
Beta,
Gamma,
or
Delta
are
substantially
reduced,
failed
to
neutralize.
Titers
against
boosted
third
vaccine
doses
high
both
vaccinated
individuals
those
Delta.
Mutations
knock
out
reduce
neutralization
most
large
panel
potent
monoclonal
antibodies
under
commercial
development.
S
has
structural
changes
earlier
viruses
uses
that
confer
tight
binding
ACE2
unleash
evolution
driven
immune
escape.
This
leads
number
site
rebalances
receptor
affinity
viruses.
Cell,
Journal Year:
2021,
Volume and Issue:
184(16), P. 4220 - 4236.e13
Published: June 17, 2021
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
has
undergone
progressive
change,
with
variants
conferring
advantage
rapidly
becoming
dominant
lineages,
e.g.,
B.1.617.
With
apparent
increased
transmissibility,
variant
B.1.617.2
contributed
to
the
current
wave
of
infection
ravaging
Indian
subcontinent
and
been
designated
a
concern
in
United
Kingdom.
Here
we
study
ability
monoclonal
antibodies
convalescent
vaccine
sera
neutralize
B.1.617.1
B.1.617.2,
complement
this
structural
analyses
Fab/receptor
binding
domain
(RBD)
complexes,
map
antigenic
space
variants.
Neutralization
both
viruses
is
reduced
compared
ancestral
Wuhan-related
strains,
but
there
no
evidence
widespread
antibody
escape
as
seen
B.1.351.
However,
B.1.351
P.1
showed
markedly
more
reduction
neutralization
suggesting
that
individuals
infected
previously
by
these
may
be
susceptible
reinfection
B.1.617.2.
This
observation
provides
important
new
insights
for
immunization
policy
future
vaccines
non-immune
populations.
Cell,
Journal Year:
2022,
Volume and Issue:
185(14), P. 2422 - 2433.e13
Published: June 9, 2022
The
Omicron
lineage
of
SARS-CoV-2,
which
was
first
described
in
November
2021,
spread
rapidly
to
become
globally
dominant
and
has
split
into
a
number
sublineages.
BA.1
dominated
the
initial
wave
but
been
replaced
by
BA.2
many
countries.
Recent
sequencing
from
South
Africa's
Gauteng
region
uncovered
two
new
sublineages,
BA.4
BA.5,
are
taking
over
locally,
driving
wave.
BA.5
contain
identical
spike
sequences,
although
closely
related
BA.2,
they
further
mutations
receptor-binding
domain
their
spikes.
Here,
we
study
neutralization
BA.4/5
using
range
vaccine
naturally
immune
serum
panels
monoclonal
antibodies.
shows
reduced
individuals
vaccinated
with
triple
doses
AstraZeneca
or
Pfizer
compared
BA.2.
Furthermore,
breakthrough
infections,
there
are,
likewise,
significant
reductions
BA.4/5,
raising
possibility
repeat
infections.
New England Journal of Medicine,
Journal Year:
2021,
Volume and Issue:
385(6), P. 562 - 566
Published: Aug. 4, 2021
SARS-CoV-2
and
Immunosuppression
In
this
article,
the
authors
discuss
challenges
of
infection
in
patients
with
a
weakened
immune
system,
including
potential
implications
regardin...
Cell Reports,
Journal Year:
2022,
Volume and Issue:
39(7), P. 110812 - 110812
Published: April 25, 2022
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)-neutralizing
monoclonal
antibodies
(mAbs)
can
reduce
the
risk
of
hospitalization
from
disease
2019
(COVID-19)
when
administered
early.
However,
SARS-CoV-2
variants
concern
(VOCs)
have
negatively
affected
therapeutic
use
some
authorized
mAbs.
Using
a
high-throughput
B
cell
screening
pipeline,
we
isolated
LY-CoV1404
(bebtelovimab),
highly
potent
spike
glycoprotein
receptor
binding
domain
(RBD)-specific
antibody.
potently
neutralizes
authentic
SARS-CoV-2,
B.1.1.7,
B.1.351,
and
B.1.617.2.
In
pseudovirus
neutralization
studies,
variants,
including
B.1.617.2,
B.1.427/B.1.429,
P.1,
B.1.526,
B.1.1.529,
BA.2
subvariant.
Structural
analysis
reveals
that
contact
residues
epitope
are
conserved,
except
for
N439
N501.
The
neutralizing
activity
is
unaffected
by
most
common
mutations
at
these
positions
(N439K
N501Y).
broad
relatively
conserved
suggest
has
potential
to
be
an
effective
agent
treat
all
known
variants.
Nature,
Journal Year:
2021,
Volume and Issue:
596(7873), P. 495 - 504
Published: July 8, 2021
There
is
a
realistic
expectation
that
the
global
effort
in
vaccination
will
bring
pandemic
caused
by
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
under
control.
Nonetheless,
uncertainties
remain
about
type
of
long-term
association
virus
establish
with
human
population
and,
particular,
whether
disease
2019
(COVID-19)
become
an
endemic
disease.
Although
trajectory
difficult
to
predict,
conditions,
concepts
and
variables
influence
this
transition
can
be
anticipated.
Persistence
SARS-CoV-2
as
virus,
perhaps
seasonal
epidemic
peaks,
may
fuelled
pockets
susceptible
individuals
waning
immunity
after
infection
or
vaccination,
changes
through
antigenic
drift
diminish
protection
re-entries
from
zoonotic
reservoirs.
Here
we
review
relevant
observations
previous
epidemics
discuss
potential
evolution
it
adapts
during
persistent
transmission
presence
level
immunity.
Lack
effective
surveillance
adequate
response
could
enable
emergence
new
patterns
SARS-CoV-2.
are
key
pieces
data
urgently
needed
order
make
good
decisions;
outline
these
propose
way
forward.
This
Perspective
discusses
possible
future
infection,
development
variants,
spread
implications
for
vaccine
deployment
consequences
issues
policy.