bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Aug. 16, 2023
Traditional
antiviral
therapies
often
have
limited
effectiveness
due
to
toxicity
and
development
of
drug
resistance.
Host-based
antivirals,
while
an
alternative,
may
lead
non-specific
effects.
Recent
evidence
shows
that
virus-infected
cells
can
be
selectively
eliminated
by
targeting
synthetic
lethal
(SL)
partners
proteins
disrupted
viral
infection.
Thus,
we
hypothesized
genes
depleted
in
CRISPR
KO
screens
enriched
SL
altered
To
investigate
this,
established
a
computational
pipeline
predicting
targets
infections.
First,
identified
SARS-CoV-2-induced
changes
gene
products
via
large
compendium
omics
data.
Second,
for
each
product.
Last,
screened
data
required
cell
viability
infected
cells.
Despite
differences
virus-induced
alterations
detected
various
data,
they
share
many
predicted
targets,
with
significant
enrichment
KO-depleted
datasets.
Comparing
from
SARS-CoV-2
influenza
infections,
found
possible
broad-spectrum,
host-based
targets.
This
suggests
are
replete
common
their
relationship
virus-altered
states
such
revealed
analysis
datasets
predictions.
EBioMedicine,
Journal Year:
2023,
Volume and Issue:
94, P. 104731 - 104731
Published: July 22, 2023
The
clinical
outcomes
of
SARS-CoV-2
infection
vary
in
severity,
potentially
influenced
by
the
resident
human
microbiota.
There
is
limited
consensus
on
conserved
microbiome
changes
response
to
infection,
with
many
studies
focusing
severely
ill
individuals.
This
study
aimed
assess
variation
upper
respiratory
tract
using
saliva
specimens
a
cohort
individuals
primarily
mild
moderate
disease.
Deleted Journal,
Journal Year:
2024,
Volume and Issue:
1(1)
Published: Jan. 1, 2024
Traditional
antiviral
therapies
often
have
limited
effectiveness
due
to
toxicity
and
the
emergence
of
drug
resistance.
Host-based
antivirals
are
an
alternative,
but
can
cause
nonspecific
effects.
Recent
evidence
shows
that
virus-infected
cells
be
selectively
eliminated
by
targeting
synthetic
lethal
(SL)
partners
proteins
disrupted
viral
infection.
Thus,
we
hypothesized
genes
depleted
in
CRISPR
knockout
(KO)
screens
may
enriched
SL
altered
To
investigate
this,
established
a
computational
pipeline
predicting
targets.
First,
identified
SARS-CoV-2-induced
changes
gene
products
via
large
compendium
omics
data.
Second,
for
each
product.
Last,
screened
KO
data
required
cell
viability
infected
cells.
Despite
differences
virus-induced
alterations
detected
various
data,
they
share
many
predicted
targets,
with
significant
enrichment
KO-depleted
datasets.
Our
comparison
SARS-CoV-2
influenza
infection
revealed
potential
broad-spectrum,
host-based
This
suggests
replete
common
targets
their
relationship
virus-altered
states
such
from
analysis
datasets
predictions.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: April 11, 2024
Abstract
The
death
of
coronavirus
disease
2019
(COVID-19)
is
primarily
due
to
from
critically
ill
patients,
especially
ARDS
complications
caused
by
SARS-CoV-2.
Therefore,
it
essential
contribute
an
in-depth
understanding
the
pathogenesis
and
identify
biomarkers
for
predicting
patients
at
molecular
level.
Immunogenic
cell
(ICD),
as
a
specific
variant
regulatory
driven
stress,
can
induce
adaptive
immune
responses
against
antigens
in
host.
Studies
have
confirmed
that
both
innate
pathways
are
involved
SARS-CoV-2
infection.
However,
role
ICD
severe
COVID-19
has
rarely
been
explored.
In
this
study,
we
systematically
evaluated
ICD-related
genes
COVID-19.
We
conducted
consensus
clustering,
infiltration
analysis,
functional
enrichment
analysis
based
on
differentially
expressed
genes.
results
showed
characteristics
were
altered
non-severe
addition,
used
multiple
machine
learning
methods
screen
five
risk
(KLF5,
NSUN7,
APH1B,
GRB10
CD4),
which
predict
severity.
Finally,
constructed
nomogram
classification
recognition
model,
validated
model
with
external
data
sets.
This
study
provides
valuable
direction
exploration
progress
COVID-19,
helps
early
identification
cases
reduce
mortality.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(7), P. 1097 - 1097
Published: July 8, 2024
Viruses
often
pose
a
significant
threat
to
the
host
through
exploitation
of
cellular
machineries
for
their
own
benefit.
In
context
immune
responses,
myriad
factors
are
deployed
target
viral
RNAs
and
inhibit
protein
translation,
ultimately
hampering
replication.
Understanding
how
“non-self”
interact
with
translation
machinery
trigger
responses
would
help
in
development
treatment
strategies
infections.
this
review,
we
explore
interferon-stimulated
gene
products
RNA
order
induce
either
global
or
targeted
inhibition.
Viruses,
Journal Year:
2023,
Volume and Issue:
15(8), P. 1696 - 1696
Published: Aug. 5, 2023
Zoonotic
coronaviruses
infect
mammals
and
birds,
causing
pulmonary
gastrointestinal
infections.
Some
animal
coronaviruses,
such
as
the
porcine
epidemic
diarrhea
virus
(PEDV)
transmissible
gastroenteritis
(TGEV),
lead
to
severe
deaths.
Gastrointestinal
symptoms
were
also
found
in
COVID-19
SARS
patients.
However,
pathogenesis
of
coronavirus
diseases
remains
elusive.
In
this
study,
main
protease-induced
LPCAT3
cleavage
was
monitored
by
exogenous
gene
expression
protease
inhibitors,
related
regulation
confirmed
qRT-PCR
knockdown.
Interestingly,
plays
an
important
role
lipid
absorption
intestines.
The
Mpro
diarrhea,
PEDV
MERS-CoV,
but
not
HCoV-OC43
HCoV-HKU1,
which
could
induce
cleavage.
Mutagenesis
analysis
inhibitor
experiments
indicated
that
independent
catalytic
activity
Mpro.
Moreover,
cells
boosted
CHOP
GRP78
expression,
biomarkers
ER
stress.
Since
is
critical
for
intestines
malabsorption
may
diseases,
Mpro-induced
might
trigger
during
infection.
Nano Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 11, 2024
The
graphene
field-effect
transistor
(GFET)
biosensor
serves
as
a
foundational
platform
for
detecting
biomolecules,
offering
high
conductivity,
label-free
operation,
and
easy
integration.
These
features
have
garnered
significant
attention
in
biomarker
detection.
However,
the
presence
of
free
cations
solution
often
leads
to
electrostatic
shielding
negatively
charged
reducing
GFET
detection
sensitivity
(LOD
≥
1
fM).
Additionally,
limited
capacitance
change
restricts
its
use
response
signal.
This
study
introduces
cation
enrichment
electric
field
modulation
strategy
(CEEFMS)
enhance
Dirac
voltage
during
cation-enriched
rough
Nafion/graphene
FET
(CENG-FET)
achieves
RNA
at
aM
level.
Utilizing
total
shift
signals,
CENG-FET
demonstrates
wide
linear
range
from
pM.
findings
advance
dual-signal
strategies,
accidental
inaccuracies
biomolecular
sensing
paving
way
further
research.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Aug. 16, 2023
Traditional
antiviral
therapies
often
have
limited
effectiveness
due
to
toxicity
and
development
of
drug
resistance.
Host-based
antivirals,
while
an
alternative,
may
lead
non-specific
effects.
Recent
evidence
shows
that
virus-infected
cells
can
be
selectively
eliminated
by
targeting
synthetic
lethal
(SL)
partners
proteins
disrupted
viral
infection.
Thus,
we
hypothesized
genes
depleted
in
CRISPR
KO
screens
enriched
SL
altered
To
investigate
this,
established
a
computational
pipeline
predicting
targets
infections.
First,
identified
SARS-CoV-2-induced
changes
gene
products
via
large
compendium
omics
data.
Second,
for
each
product.
Last,
screened
data
required
cell
viability
infected
cells.
Despite
differences
virus-induced
alterations
detected
various
data,
they
share
many
predicted
targets,
with
significant
enrichment
KO-depleted
datasets.
Comparing
from
SARS-CoV-2
influenza
infections,
found
possible
broad-spectrum,
host-based
targets.
This
suggests
are
replete
common
their
relationship
virus-altered
states
such
revealed
analysis
datasets
predictions.