Antibodies,
Journal Year:
2022,
Volume and Issue:
11(4), P. 68 - 68
Published: Oct. 25, 2022
We
investigated
the
short
sequences
involving
Omicron
21K
and
21L
variants
to
reveal
any
possible
molecular
mimicry-associated
autoimmunity
risks
changes
in
those.
first
identified
common
6mers
of
viral
human
protein
present
for
both
mutant
(Omicron)
nonmutant
(SARS-CoV-2)
versions
same
sequence
then
predicted
binding
affinities
those
HLA
supertype
representatives.
evaluated
change
potential
risk,
through
comparative
assessment
their
similar
peptides
with
allele.
This
is
lost
new,
or
de
novo,
associated
mutations
variants.
Accordingly,
e.g.,
affinity
virus-similar
Ig
heavy
chain
junction
regions
shifted
from
HLA-B*15:01
HLA-A*01:01
allele
at
sequences.
Additionally,
different
proteins
sharing
SARS-CoV-2
mutation
sites
interest
HLA-B*07:02
allele,
such
as
respective
sequences,
were
lost.
Among
all,
novel
risk
appeared
be
prominent
HLA-A*24:02
HLA-B*27:05
serotypes
upon
infection
21L.
Associated
disease,
pathway,
tissue
expression
data
supported
new
serotypes,
while
could
have
been
diminished,
HLA-A*03:01
retained,
individuals
infected
under
study.
These
are
likely
affect
complications
related
cross-reactions
influencing
relevant
Journal of Medical Virology,
Journal Year:
2023,
Volume and Issue:
95(2)
Published: Jan. 31, 2023
The
newly
emerging
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
Omicron
BA.2.75
and
BA.2.76
subvariants
contained
35
29
additional
mutations
in
its
spike
(S)
protein
compared
with
the
reference
SARS-CoV-2
genome,
respectively.
Here,
we
measured
evasion
degree
of
BA.1,
BA.2,
BA.4,
BA.5,
BA.2.75,
from
neutralizing
immunity
people
previously
infected
BA.1
determined
effect
vaccination
on
immune
evasion,
titers
antibodies
serums
between
infection
convalescence.
Results
showed
that
neutralization
patients
different
statuses
BA.1/BA.2
breakthrough
decreased
evolution
to
BA.2.76.
This
study
also
indicated
existing
vaccines
could
no
longer
provide
effective
protection,
especially
for
subvariants.
Therefore,
against
epidemic
strains
should
be
designed
specifically.
In
future,
can
not
only
focus
current
strains,
but
predict
design
new
potential
mutant
strains.
At
same
time,
combine
virus
strains'
characteristics
develop
protective
measures
colonization
areas,
such
as
nasal
protection
spray.
Besides,
further
studies
Y248N
mutation
subvariant
were
necessary
explore
contribution
enhanced
ability.
BMC Public Health,
Journal Year:
2024,
Volume and Issue:
24(1)
Published: Feb. 22, 2024
Abstract
Background
SARS-CoV-2
infections
usually
cause
immune
dysregulation
in
the
human
body.
Studies
of
immunological
changes
resulting
from
coinfections
with
Mycobacterium
tuberculosis
(
Mtb
)
or
HIV
are
limited.
Methods
We
conducted
a
retrospective
study
focusing
on
patients
COVID-19.
A
total
550
infected
were
enrolled
our
and
categorized
into
four
groups
based
presence
coinfections;
166
Delta-infected
patients,
among
whom
103
had
no
coinfections,
52
who
coinfected
,
11
HIV,
384
Omicron-infected
patients.
By
collecting
data
epidemiologic
information,
laboratory
findings,
treatments,
clinical
outcomes,
we
analyzed
compared
characteristics.
Results
Compared
those
Delta
group,
median
white
blood
cell,
CD4
+
T-cell
B-cell
counts
lower
group
group.
Except
for
Omicron
more
than
half
three
abnormal
chest
CT
findings.
Among
groups,
there
significant
differences
any
cytokines.
disease
duration
LOS
longer
For
unvaccinated
number
B
cells
T
was
that
difference
duration.
In
(6%)
presented
greater
months
decreased
lymphocyte
IL17A
counts,
possibly
due
to
double
lungs
caused
by
M.
tuberculosis.
Conclusions
found
exhibited
LOS,
decrease
cells,
suggesting
these
related
function.
Changes
cytokine
levels
suggest
coinfection
does
not
result
response.
Importantly,
discovered
chronic
course
involving
infection.
mBio,
Journal Year:
2023,
Volume and Issue:
unknown
Published: June 5, 2023
ABSTRACT
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
is
continuously
evolving,
bringing
great
challenges
to
the
control
of
virus.
In
present
study,
we
investigated
characteristics
SARS-CoV-2
within-host
diversity
human
hosts
and
its
implications
for
immune
evasion
using
about
2,00,000
high-depth
next-generation
genome
sequencing
data
SARS-CoV-2.
A
total
44%
samples
showed
variations
(iSNVs),
average
number
iSNVs
in
with
iSNV
was
1.90.
C-to-U
dominant
substitution
pattern
iSNVs.
C-to-U/G-to-A
A-to-G/U-to-C
preferentially
occur
5′-CG-3′
5′-AU-3′
motifs,
respectively.
addition,
found
that
are
under
negative
selection.
About
15.6%
had
an
impact
on
content
CpG
dinucleotide
(CpG)
genomes.
We
detected
signatures
faster
loss
CpG-gaining
iSNVs,
possibly
resulting
from
zinc-finger
antiviral
protein-mediated
activities
targeting
CpG,
which
could
be
major
reason
depletion
consensus
The
non-synonymous
S
gene
can
largely
alter
protein’s
antigenic
features,
many
these
distributed
amino-terminal
domain
(NTD)
receptor-binding
(RBD).
These
results
suggest
interacts
actively
attempts
take
different
evolutionary
strategies
escape
innate
adaptive
immunity.
new
findings
further
deepen
widen
our
understanding
features
IMPORTANCE
(SARS-CoV-2),
causative
pathogen
disease
2019,
has
evolved
rapidly
since
it
discovered.
Recent
studies
have
pointed
out
some
mutations
protein
confer
ability
evade
system.
observed
sequences
decreased
over
time,
reflecting
adaptation
host.
significance
research
revealing
hosts,
identifying
causes
genomes,
exploring
potential
impacts
escape,
Viruses,
Journal Year:
2023,
Volume and Issue:
15(9), P. 1862 - 1862
Published: Aug. 31, 2023
The
COVID-19
pandemic
caused
by
the
SARS-CoV-2
virus
has
inflicted
significant
mortality
and
morbidity
worldwide.
Continuous
mutations
have
led
to
emergence
of
new
variants.
Omicron
BA.1
sub-lineage
prevailed
as
dominant
variant
globally
at
beginning
2022
but
was
subsequently
replaced
BA.2
in
numerous
countries.
Wastewater-based
epidemiology
(WBE)
offers
an
efficient
tool
for
capturing
viral
shedding
from
infected
individuals,
enabling
early
detection
potential
outbreaks
without
relying
solely
on
community
cooperation
clinical
testing
resources.
This
study
integrated
RT-qPCR
assays
detecting
general
its
variants
levels
wastewater
into
a
modified
triple
susceptible-infected-recovered-susceptible
(SIRS)
model.
observed,
replacing
presence
predecessor,
Delta
variant.
Comparative
analysis
between
data
SIRS
model
effectively
described
subsequent
waves,
with
decline
aligning
diminished
below
threshold
wastewater.
demonstrates
WBE
valuable
future
pandemics.
Furthermore,
analyzing
sensitivity
different
parameters,
we
are
able
deduce
real-life
values
cross-variant
immunity
probabilities,
emphasizing
asymmetry
their
strength.
Journal of Infection,
Journal Year:
2024,
Volume and Issue:
89(5), P. 106284 - 106284
Published: Sept. 26, 2024
Rapid
evolution
of
SARS-CoV-2
has
resulted
in
the
emergence
numerous
variants,
posing
significant
challenges
to
public
health
surveillance.
Clinical
genome
sequencing,
while
valuable,
limitations
capturing
full
epidemiological
dynamics
circulating
variants
general
population.
This
study
aimed
monitor
variant
community
and
using
receptor-binding
domain
(RBD)
amplicon
sequencing
wastewater
samples.
The
COVID-19
pandemic
caused
by
the
SARS-CoV-2
virus
has
inflicted
significant
mortality
and
morbidity
worldwide.
Continuous
mutations
have
led
to
emergence
of
new
variants.
Omicron
BA.1
sub-lineage
prevailed
as
dominant
variant
globally
at
beginning
2022
but
was
subsequently
replaced
BA.2
in
numerous
countries.
Wastewater-based
epidemiology
(WBE)
offers
an
efficient
tool
for
capturing
viral
shedding
from
infected
individuals,
enabling
early
detection
potential
outbreaks
without
relying
solely
on
community
cooperation
clinical
testing
resources.
This
study
integrated
RT-qPCR
assays
detecting
general
its
variants
levels
wastewater
into
a
modified
triple
susceptible-infected-recovered-susceptible
(SIRS)
model.
Omicron-BA.1
observed,
replacing
presence
predecessor,
Delta
variant.
Comparative
analysis
between
data
SIRS
model
effectively
described
subsequent
waves,
with
decline
aligning
diminished
below
threshold
wastewater.
demonstrates
WBE
valuable
future
pandemics.
Furthermore,
analyzing
sensitivity
different
parameters,
we
are
able
deduce
real-life
values
cross-variant
immunity
probabilities,
emphasizing
asymmetry
their
strength.
Journal of Medical Virology,
Journal Year:
2023,
Volume and Issue:
95(3)
Published: March 1, 2023
Abstract
Novel
immune
escape
variants
have
emerged
as
severe
acute
respiratory
syndrome
coronavirus
2
(SARS‐CoV‐2)
continues
to
spread
worldwide.
Many
of
the
cause
breakthrough
infections
in
vaccinated
populations,
posing
great
challenges
current
antiviral
strategies
targeting
immunodominance
receptor‐binding
domain
within
spike
protein.
Here,
we
found
that
a
novel
broadly
neutralizing
monoclonal
antibody
(mAb),
G5,
provided
efficient
protection
against
SARS‐CoV‐2
concern
(VOCs)
vitro
and
vivo.
A
single
dose
mAb
G5
could
significantly
inhibit
viral
burden
mice
challenged
with
mouse‐adapted
or
Omicron
BA.1
variant,
well
body
weight
loss
cytokine
release
induced
by
SARS‐CoV‐2.
The
refined
epitope
recognized
was
identified
1148
FKEELDKYF
1156
stem
helix
subunit
S2.
In
addition,
human−mouse
chimeric
generated
based
on
variable
region
heavy
chain
VL
genes
G5.
Our
study
provides
broad
drug
candidate
VOCs
reveals
target
for
developing
pan‐SARS‐CoV‐2
vaccines.
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.
PLoS ONE,
Journal Year:
2024,
Volume and Issue:
19(10), P. e0312098 - e0312098
Published: Oct. 31, 2024
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
is
the
causative
agent
of
disease
19
(COVID-19).
SARS-CoV-2
infection
suppresses
host
innate
immunity
and
impairs
cell
viability.
Among
viral
proteins,
ORF6
exhibits
potent
interferon
(IFN)
antagonistic
activity
cellular
toxicity.
It
also
interacts
with
RNA
export
factor
RAE1,
which
bridges
nuclear
pore
complex
receptors,
suggesting
an
effect
on
export.
Using
Xenopus
oocyte
microinjection
system,
I
found
that
blocked
not
only
mRNA
but
spliceosomal
U
snRNA.
further
demonstrated
affects
interaction
between
RAE1
receptors
inhibits
binding
RAE1.
These
effects
may
cumulatively
block
several
classes
RNA.
binds
forms
oligomers.
findings
provide
insights
into
suppression
immune
responses
reduction
in
viability
caused
by
infection,
contributing
to
development
antiviral
drugs
targeting
ORF6.