Vietnam Journal of Biotechnology,
Journal Year:
2023,
Volume and Issue:
21(4), P. 621 - 635
Published: Dec. 30, 2023
The
SARS-CoV-2
virus
is
the
primary
agent
responsible
for
ongoing
COVID-19
pandemic,
leading
to
loss
of
millions
lives
worldwide.
In
2023,
pandemic's
impact
primarily
driven
by
Omicron
variant,
which
features
many
unique
mutations
compared
previously
identified
variants.
Through
analysis
network
variants
collected
in
Vietnam,
we
determined
expected
have
high
transmission
efficiency
and
positive
influence
before
studying
on
structural
behavior
spike
proteins
their
affinity
with
hACE2.
Our
computational
indicates
that
these
not
only
exhibit
a
significantly
higher
binding
than
Wildtype
but
also
demonstrate
increased
free
energy
among
This
enhanced
variant
reflected
stability
hACE2
structure
Wildtype.
study
further
elucidates
specific
contributions
point
energy.
Notably,
such
as
W152R,
F157L,
G257S,
S371F,
S373P,
S375F,
T376A,
D405N,
N440K,
S477N,
T478K,
E484A,
Q493R,
Q498R,
N501Y,
D614G,
N679K,
P681H,
N764K,
D796Y,
N969K
were
found
increasing
Omicron's
protein
complex
Expert Review of Vaccines,
Journal Year:
2024,
Volume and Issue:
23(1), P. 510 - 522
Published: April 24, 2024
COVID-19
was
an
unprecedented
challenge
worldwide;
however,
disease
epidemiology
has
evolved,
and
no
longer
constitutes
a
public
health
emergency
of
international
concern.
Nonetheless,
remains
global
threat
uncertainties
remain,
including
definition
the
end
pandemic
transition
to
endemicity,
understanding
true
rates
SARS-CoV-2
infection/transmission.
Cell Death and Disease,
Journal Year:
2024,
Volume and Issue:
15(6)
Published: June 28, 2024
Abstract
SARS-CoV-2
infection
is
initiated
by
Spike
glycoprotein
binding
to
the
human
angiotensin-converting
enzyme
2
(ACE2)
receptor
via
its
domain.
Blocking
this
interaction
has
been
proven
be
an
effective
approach
inhibit
virus
infection.
Here
we
report
discovery
of
a
neutralizing
nanobody
named
VHH60,
which
was
directly
produced
from
engineering
library
based
on
commercialized
within
very
short
period.
VHH60
competes
with
ACE2
bind
domain
protein
at
S
351
,
470-471
and
493-494
as
determined
structural
analysis,
affinity
2.56
nM.
It
inhibits
infections
both
ancestral
strain
pseudotyped
viruses
harboring
wildtype,
key
mutations
or
variants
nanomolar
level.
Furthermore,
suppressed
propagation
50-fold
better
protected
mice
death
for
twice
long
control
group
after
nasal
in
vivo.
Therefore,
not
only
powerful
promising
profile
disease
but
also
provides
evidence
highly
rapid
generating
therapeutic
nanobodies.
Deleted Journal,
Journal Year:
2024,
Volume and Issue:
6(15), P. 324 - 331
Published: Jan. 1, 2024
Introduction
In
the
first
half
of
2023,
a
global
shift
was
observed
towards
predominance
XBB
variants.
China
faced
significant
epidemic
between
late
2022
and
early
2023
due
to
Omicron
subvariants
BA.5.2
BF.7.
This
study
aims
depict
evolving
variant
distribution
among
provincial-level
administrative
divisions
(PLADs)
in
explore
factors
driving
replacement.
Methods
Sequences
from
local
imported
coronavirus
disease
2019
(COVID-19)
cases
recorded
January
1
June
30,
were
included.
The
analyzed
changing
viral
variants
assessed
how
prior
dominance
specific
variants,
subvariants,
influenced
prevalence
replacement
variant.
Results
A
total
56,486
sequences
obtained
cases,
8,669
cases.
Starting
April,
there
with
varying
PLADs.
PLADs
previously
high
BF.7,
rise
delayed.
positive
correlation
found
proportions
March
April.
pattern
differed
within
same
PLAD.
No
differences
noted
rates
subvariants.
Conclusions
timing
various
correlating
closely
Biosensors,
Journal Year:
2025,
Volume and Issue:
15(3), P. 198 - 198
Published: March 20, 2025
Viral
infectious
diseases
pose
a
serious
threat
to
global
public
health
due
their
high
transmissibility,
rapid
mutation
rates,
and
limited
treatment
options.
Recent
outbreaks
of
such
as
plague,
monkeypox,
avian
influenza,
coronavirus
disease
2019
(COVID-19)
have
underscored
the
urgent
need
for
efficient
diagnostic
surveillance
technologies.
Focusing
on
viral
that
seriously
threaten
human
health,
this
review
summarizes
analyzes
detection
techniques
from
perspective
combining
prevention
advice,
discusses
applications
in
improving
sensitivity
specificity.
One
major
innovations
is
systematic
integration
advanced
biorecognition
technologies,
bionanosensors,
test
strips,
microfluidic
platforms,
along
with
exploration
artificial
intelligence
virus
detection.
These
technologies
address
limitations
traditional
methods
enable
real-time
monitoring
early
warning
outbreaks.
By
analyzing
application
these
pathogens,
new
insights
are
provided
development
next-generation
tools
emerging
re-emerging
threats.
In
addition,
we
analyze
current
progress
developed
vaccines,
vaccine
research
provide
ideas
future
control
development,
call
attention
Journal of Virology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 24, 2025
ABSTRACT
Defective
genomes
are
part
of
SARS-CoV-2
quasispecies.
High-resolution,
ultra-deep
sequencing
bulk
RNA
from
viral
populations
does
not
distinguish
mutations,
insertions,
and
deletions
in
viable
those
defective
genomes.
To
quantify
infectious
variant
progeny,
virus
four
individual
plaques
(biological
clones)
a
preparation
isolate
USA-WA1/2020,
formed
on
Vero
E6
cell
monolayers,
was
subjected
to
further
biological
cloning
yield
9
second-generation
15
third-generation
sub-clones.
Consensus
genomic
sequences
the
clones
sub-clones
included
an
average
2.8
variations
per
genome,
relative
consensus
sequence
parental
USA-WA1/2020
virus.
This
value
is
6.5-fold
lower
than
estimates
for
other
viruses
such
as
bacteriophage
Qβ,
foot-and-mouth
disease
virus,
or
hepatitis
C
culture.
The
mutant
spectrum
complexity
nsp12
(polymerase)-
spike
(S)-coding
region
unique
progeny
each
10
sub-clones;
they
shared
2.4%
total
164
different
mutations
scored
3,719
residues
that
were
screened.
presence
minority
out-of-frame
revealed
ease
genome
production
genome.
Several
low-frequency
point
clade-discordant
typical
but
served
define
future
clades.
Implications
adaptability
COVID-19
control
heterogeneity
generation
complex
spectra
discussed.
IMPORTANCE
Sequencing
means
identify
located
distinction
particularly
important
populations,
SARS-CoV-2,
contain
large
proportions
By
sub-clones,
we
quantified
complement
be
exhibited
by
viruses.
difference
may
due
reduced
mutation
rate
limited
tolerance
coronavirus
incorporate
remain
functional
combination
both
influences.
suggests
limitations
occupation
space
SARS-CoV-2.
However,
rapidly
generated
suggest
aptness
confront
selective
constraints.
Pathogens,
Journal Year:
2024,
Volume and Issue:
13(4), P. 272 - 272
Published: March 23, 2024
Since
November
2021,
Omicron
has
emerged
as
the
dominant
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
variant,
and
its
sublineages
continue
to
appear
one
after
another,
significantly
reducing
effectiveness
of
existing
therapeutic
neutralizing
antibodies
(NAbs).
It
is
urgent
develop
effective
NAbs
against
circulating
variants.
Here,
we
isolated
receptor
binding
domain
(RBD)-specific
single
memory
B
cells
via
flow
cytometry
from
a
COVID-19
convalescent.
The
antibody
variable
region
genes
heavy
chain
(VHs)
light
(VLs)
were
amplified
cloned
into
expression
vectors.
After
expression,
ELISA
screening
activity
detection,
obtained
an
IGHV3-53-encoded
RBD-targeting
cross-neutralizing
D6,
whose
VL
originated
IGKV1-9*01
germlines.
D6
could
potently
neutralize
variants
(BA.1,
BA.2,
BA.4/5
BF.7),
with
IC50
values
less
than
0.04
μg/mL,
ability
XBB
was
reduced
but
still
effective.
KD
RBD
prototype
BA.1
both
1.0
×
10−12
M.
protein
structure
D6-RBD
model
indicates
that
interacts
external
subdomain
belongs
RBD-1
community.
sufficient
contact
deep
interaction
HCDR3
LCDR3
may
be
crucial
reason
for
activity.
sorting
analysis
mAb
will
provide
important
information
development
anti-COVID-19
reagents.
Journal of Interferon & Cytokine Research,
Journal Year:
2024,
Volume and Issue:
44(7), P. 325 - 333
Published: April 1, 2024
India
saw
a
spike
in
COVID-19
cases
early
2023,
and
this
wave
of
infection
was
attributed
to
XBB
sublineages
SARS-CoV-2
Omicron
variant.
The
impact
significantly
shorter
with
low
burden
severe
or
hospitalization
as
compared
previous
variants
concern.
Although
combination
old
new
mutations
the
region
XBB.1.16
variant
led
drastic
reduction
ability
antibodies
from
prior
immunity
neutralize
virus,
additional
nonspike
suggested
possible
change
its
suppress
innate
immune
responses.
In
study,
we
tested
sensitivity
Delta,
BA.2.75,
interferon-β
(IFN-β)
treatment
found
that
most
sensitive
IFN-β.
We
next
serum
healthy
individuals
XBB.1.16.
showed
hybrid
maintained
but
significant
level
neutralizing
Therefore,
our
observations
indicated
both
because
natural
enhanced
IFNs
may
have
contributed
infections
India.
Frontiers research topics,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
it
is
a
pioneering
approach
to
the
world
of
academia,
radically
improving
way
scholarly
research
managed.The
grand
vision
Frontiers
where
all
people
have
an
equal
opportunity
seek,
share
and
generate
knowledge.Frontiers
provides
immediate
permanent
online
open
access
its
publications,
but
this
alone
not
enough
realize
our
goals.
journal
seriesThe
series
multi-tier
interdisciplinary
set
openaccess,
journals,
promising
paradigm
shift
from
current
review,
selection
dissemination
processes
in
academic
publishing.All
journals
are
driven
by
researchers
for
researchers;
therefore,
they
constitute
service
community.At
same
time,
operates
on
revolutionary
invention,
tiered
publishing
system,
initially
addressing
specific
communities
scholars,
gradually
climbing
up
broader
public
understanding,
thus
serving
interests
lay
society,
too.
Dedication
qualityEach
article
landmark
highest
quality,
thanks
genuinely
collaborative
interactions
between
authors
review
editors,
who
include
some
world's
best
academicians.Research
must
be
certified
peers
before
entering
stream
knowledge
that
may
eventually
reach
-and
shape
society;
only
applies
most
rigorous
unbiased
reviews.Frontiers
revolutionizes
freely
delivering
outstanding
research,
evaluated
with
no
bias
both
social
point
view.By
applying
advanced
information
technologies,
catapulting
into
new
generation.
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(23), P. 29716 - 29727
Published: May 30, 2024
The
emergence
of
XBB.1.16
has
gained
rapid
global
prominence.
Previous
studies
have
elucidated
that
the
infection
SARS-CoV-2
induces
alterations
in
mitochondrial
integrity
host
cells,
subsequently
influencing
cellular
response
to
infection.
In
this
study,
we
compared
differences
infectivity
and
pathogenicity
between
parental
Omicron
sublineages
BA.1
BA.2
assessed
their
impact
on
mitochondria.
Our
findings
suggest
that,
comparison
with
BA.2,
exhibits
more
efficient
spike
protein
cleavage,
mediating
syncytia
formation,
mild
mitochondriopathy,
less
pathogenicity.
Altogether,
our
investigations
based
mutation
key
sites,
exhibited
enhanced
but
lower
This
will
help
us
further
investigate
biological
functions
sites.
The
Omicron
variant
of
SARS-CoV-2,
which
is
a
cause
concern,
has
various
mutations
in
its
spike
protein.
This
protein
responsible
for
both
viral
infection
and
immunity.
We
have
analyzed
particular
sub-lineage
Omicron,
designated
XBB,
undergone
structural
functional
changes
as
response
to
the
African
selection
pressures.
Using
molecular
modeling,
we
compared
S
structures
XBB
discovered
that
reduced
receptor-binding
domain
(RBD)
because
loss
some
β-sheets.
change
may
result
an
increased
affinity
towards
human
angiotensin-converting
enzyme
2
(hACE2)
receptor.
also
conducted
recombination
analysis
sequences
using
Fast
Unconstrained
Bayesian
Approximation
(FUBAR)
Recombination
Detection
Program
4
(RDP
4).
Our
detected
signals
positive
N-terminal
(NTD)
S1
subunit,
contains
antibody-binding
epitopes,
RBD,
involved
entry.
findings
reveal
adaptation
Africa
potential
implications
pathogenesis