Virology Journal,
Journal Year:
2024,
Volume and Issue:
21(1)
Published: Jan. 4, 2024
Abstract
Background
The
COVID-19
pandemic,
caused
by
the
Severe
Acute
Respiratory
Syndrome
Coronavirus
2
virus,
emerged
in
late
2019
and
spready
globally.
Many
effects
of
infection
with
this
pathogen
are
still
unknown,
both
chronic
repeated
producing
novel
pathologies.
Case
presentation
An
immunocompromised
patient
presented
infection.
had
history
Hodgkin’s
lymphoma,
treated
chemotherapy
stem
cell
transplant.
During
course
their
treatment,
eleven
respiratory
samples
from
were
analyzed
whole-genome
sequencing
followed
lineage
identification.
Whole-genome
virus
present
over
time
revealed
that
at
various
timepoints
harboured
three
different
lineages
virus.
was
initially
infected
B.1.1.176
before
coinfection
BA.1.
When
coinfected
BA.1,
viral
populations
found
approximately
equal
proportions
within
based
on
read
abundance.
Upon
further
sampling,
during
final
two
to
be
BA.2.9.
eventually
developed
failure
died.
Conclusions
This
case
study
shows
an
example
changes
can
happen
who
is
multiple
times.
Furthermore,
demonstrates
how
simultaneous
lead
unclear
assignment
standard
methods,
which
resolved
investigation.
analyzing
reinfection
cases,
care
must
taken
properly
identify
present.
Journal of Medical Virology,
Journal Year:
2022,
Volume and Issue:
95(1)
Published: Sept. 13, 2022
As
of
November
2021,
several
SARS-CoV-2
variants
appeared
and
became
dominant
epidemic
strains
in
many
countries,
including
five
concern
(VOCs)
Alpha,
Beta,
Gamma,
Delta,
Omicron
defined
by
the
World
Health
Organization
during
COVID-19
pandemic.
August
2022,
is
classified
into
main
lineages,
BA.1,
BA.2,
BA.3,
BA.4,
BA.5
some
sublineages
(BA.1.1,
BA.2.12.1,
BA.2.11,
BA.2.75,
BA.4.6)
(https://www.gisaid.org/).
Compared
to
previous
VOCs
(Alpha,
Delta),
all
lineages
have
most
highly
mutations
spike
protein,
with
50
accumulated
throughout
genome.
Early
data
indicated
that
BA.2
sublineage
had
higher
infectivity
more
immune
escape
than
early
wild-type
(WT)
strain,
VOCs,
BA.1.
Recently,
global
surveillance
suggest
a
transmissibility
BA.4/BA.5
BA.1.1
becoming
strain
countries
globally.
Cell Reports,
Journal Year:
2023,
Volume and Issue:
42(12), P. 113444 - 113444
Published: Nov. 18, 2023
The
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
Omicron
variant
of
concern,
first
identified
in
November
2021,
rapidly
spread
worldwide
and
diversified
into
several
subvariants.
spike
(S)
protein
accumulated
an
unprecedented
number
sequence
changes
relative
to
previous
variants.
In
this
review,
we
discuss
how
S
structural
features
modulate
host
cell
receptor
binding,
virus
entry,
immune
evasion
highlight
these
differentiate
from
We
also
examine
key
properties
track
across
the
still-evolving
subvariants
importance
continuing
surveillance
evolution
over
time.
Genes,
Journal Year:
2023,
Volume and Issue:
14(2), P. 407 - 407
Published: Feb. 4, 2023
The
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
produced
diverse
molecular
variants
during
its
recent
expansion
in
humans
that
caused
different
transmissibility
and
severity
of
the
associated
disease
as
well
resistance
to
monoclonal
antibodies
polyclonal
sera,
among
other
treatments.
In
order
understand
causes
consequences
observed
SARS-CoV-2
diversity,
a
variety
studies
investigated
evolution
this
virus
humans.
general,
evolves
with
moderate
rate
evolution,
10
Medicine,
Journal Year:
2023,
Volume and Issue:
102(51), P. e36714 - e36714
Published: Dec. 22, 2023
Nirmatrelvir
plus
ritonavir
(Paxlovid)
have
been
used
in
the
treatment
of
adult
patients
with
mild-to-moderate
coronavirus
disease
2019
(COVID-19).
This
study
aimed
to
evaluate
impact
Paxlovid
on
in-hospital
outcomes
and
post-COVID-19
condition
Chinese
infected
severe
acute
respiratory
syndrome
2
(SARS-CoV-2)
Omicron
variant.This
non-randomized
clinical
controlled
trial
recruited
SARS-CoV-2
variant
from
designated
hospital
for
treating
COVID-19
between
November
5
28,
2022,
Shijiazhuang,
China.
Participants
were
administered
(300
mg
nirmatrelvir
100
orally)
or
standard
treatment.
The
primary
outcome
was
nucleic
acid
shedding
time
condition.A
total
320
included,
mean
age
29.10
±
7.34
years
old.
Two
hundred
received
Paxlovid.
Compared
group,
those
group
had
a
significantly
shorter
(3.26
1.80
vs
7.75
3.68
days,
P
<
.001),
days
until
negative
swab
test
(1.74
1.15
5.33
2.91,
first
symptoms
resolution
(4.86
1.62
7.45
2.63,
higher
rate
within
3
[138
(70.77%)
14
(11.67%),
.001],
[174
(89.23%)
26
(21.67%),
7
[185
(94.87%)
78
(65.00%),
less
likely
[32
(18.60%)
30
(31.57%),
=
.016].
There
no
significant
difference
duration
(43.00
26.00
49.00
26.34
.354)
groups.Compared
treatment,
reduced
time,
test,
resolution,
as
well
improved
condition.
Continuous
emergence
of
the
Omicron
variant,
along
with
its
subvariants,
has
caused
an
increasing
number
infections,
reinfections,
and
vaccine-breakthrough
seriously
threatening
human
health.
Recently,
several
new
such
as
BA.5,
BA.2.75,
BA.4.6,
BF.7,
bearing
distinct
mutation
profiles
in
their
spike
(S)
proteins,
have
significantly
increased
capacity
to
evade
vaccine-induced
immunity
shown
enhanced
infectivity
transmissibility,
quickly
becoming
dominant
sublineages.
In
this
study,
we
found
S
proteins
these
subvariants
2-
4-fold
more
efficient
membrane
fusion
kinetics
than
that
original
variant
(BA.1),
indicating
novel
might
possess
pathogenicity.
We
also
identified
peptide-based
pan-CoV
inhibitors,
EK1
EK1C4,
showed
equal
efficacy
against
mediated
by
noted
infection
pseudoviruses.
Additionally,
either
immune
sera
induced
wild-type
(WT)
SARS-CoV-2
RBD-based
vaccine
or
BA.2
convalescent
potent
synergism
both
WT
various
further
suggesting
EK1-based
inhibitors
are
promising
candidates
for
development
clinical
antiviral
agents
currently
circulating
subvariants.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: May 9, 2023
Abstract
Mucosal
immunity
plays
a
significant
role
in
the
first-line
defense
against
viruses
transmitted
and
infected
through
respiratory
system,
such
as
SARS-CoV-2.
However,
lack
of
effective
safe
adjuvants
currently
limits
development
COVID-19
mucosal
vaccines.
In
current
study,
we
prepare
an
intranasal
vaccine
containing
cationic
crosslinked
carbon
dots
(CCD)
SARS-CoV-2
antigen,
RBD-HR
with
spontaneous
antigen
particlization.
Intranasal
immunization
CCD/RBD-HR
induces
high
levels
antibodies
broad-spectrum
neutralization
authentic
viruses/pseudoviruses
Omicron-included
variants
protects
immunized
female
BALB/c
mice
from
Omicron
infection.
Despite
strong
systemic
cellular
immune
response
stimulation,
also
potent
determined
by
generation
tissue-resident
T
cells
lungs
airway.
Moreover,
not
only
activates
professional
antigen-presenting
(APCs),
dendritic
cells,
but
effectively
targets
nasal
epithelial
promotes
binding
via
sialic
acid,
surprisingly
provokes
cells.
We
demonstrate
that
CCD
is
promising
adjuvant
for
provoking
might
be
candidate
many
types
infectious
diseases,
including
COVID-19.
JAMA Network Open,
Journal Year:
2023,
Volume and Issue:
6(3), P. e235755 - e235755
Published: March 30, 2023
Importance
In
2022,
Omicron
variants
circulated
globally,
and
Urumqi,
China,
experienced
a
COVID-19
outbreak
seeded
by
BA.5
variants,
resulting
in
the
highest
number
of
infections
city’s
record
before
exit
zero
strategy.
Little
was
known
about
characteristics
mainland
China.
Objective
To
evaluate
transmission
effectiveness
inactivated
vaccine
(mainly
BBIBP-CorV)
against
their
transmission.
Design,
Setting,
Participants
This
cohort
study
conducted
using
data
from
an
Omicron-seeded
Urumqi
August
7
to
September
7,
2022.
included
all
individuals
with
confirmed
SARS-CoV-2
close
contacts
identified
between
2022
Urumqi.
Exposures
A
booster
dose
compared
vs
2
doses
(reference
level)
risk
factors
were
evaluated.
Main
Outcomes
Measures
Demographic
characteristics,
timeline
records
exposure
laboratory
testing
outcomes,
contact
tracing
history,
setting
obtained.
The
mean
variance
key
time-to-event
intervals
estimated
for
information.
Transmission
risks
patterns
assessed
under
different
disease-control
measures
settings.
multivariate
logistic
regression
models.
Results
Among
1139
diagnosed
(630
females
[55.3%];
[SD]
age,
37.4
[19.9]
years)
51
323
who
tested
negative
(26
299
[51.2%];
38.4
[16.0]
years),
means
generation
interval,
viral
shedding
period,
incubation
period
at
2.8
days
(95%
credible
interval
[CrI],
2.4-3.5
days),
6.7
CrI,
6.4-7.1
5.7
4.8-6.6
respectively.
Despite
tracing,
intensive
control
measures,
high
coverage
(980
[86.0%]
received
≥2
vaccine),
found
household
settings
(secondary
attack
rate,
14.7%;
95%
13.0%-16.5%)
younger
(aged
0-15
years;
secondary
2.5%;
1.9%-3.1%)
older
age
&gt;65
2.2%;
1.5%-3.0%)
groups.
Vaccine
variant
booster-dose
28.9%
7.7%-45.2%)
48.5%
23.9%-61.4%)
15-90
after
dose.
No
protective
outcome
detected
beyond
90
Conclusions
Relevance
revealed
as
they
evolved,
well
variants.
These
findings
suggest
importance
continuously
evaluating
emerging
Journal of Infection,
Journal Year:
2024,
Volume and Issue:
88(3), P. 106121 - 106121
Published: Feb. 16, 2024
The
COVID-19
pandemic,
caused
by
the
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2),
has
substantially
damaged
global
economy
and
human
health.
spike
(S)
protein
of
coronaviruses
plays
a
pivotal
role
in
viral
entry
binding
to
host
cell
receptors.
Additionally,
it
acts
as
primary
target
for
neutralizing
antibodies
those
infected
is
central
focus
currently
utilized
or
researched
vaccines.
During
virus's
adaptation
host,
S
SARS-CoV-2
undergone
significant
evolution.
As
pandemic
unfolded,
new
mutations
have
arisen
vanished,
giving
rise
distinctive
amino
acid
profiles
within
variant
concern
strains
SARS-CoV-2.
Notably,
many
these
changes
been
positively
selected,
leading
substantial
alterations
characteristics,
such
heightened
transmissibility
immune
evasion
capabilities.
This
review
aims
provide
an
overview
our
current
understanding
structural
implications
associated
with
key
These
research
findings
shed
light
on
intricate
dynamic
nature
evolution,
underscoring
importance
continuous
monitoring
analysis
genomes.
Through
molecular-level
investigations,
we
can
attain
deeper
insights
into
adaptive
offering
valuable
guidance
designing
vaccines
developing
antiviral
drugs
combat
ever-evolving
threats.
MedComm,
Journal Year:
2023,
Volume and Issue:
4(3)
Published: April 26, 2023
The
XBB.1.5
subvariant
has
drawn
great
attention
owing
to
its
exceptionality
in
immune
evasion
and
transmissibility.
Therefore,
it
is
essential
develop
a
universally
protective
coronavirus
disease
2019
vaccine
against
various
strains
of
Omicron,
especially
XBB.1.5.
In
this
study,
we
evaluated
compared
the
responses
induced
by
six
different
spike
protein
vaccines
targeting
ancestral
or
Omicron
severe
acute
respiratory
syndrome
2
(SARS-CoV-2)
mice.
We
found
that
spike-wild-type
immunization
high
titers
neutralizing
antibodies
(NAbs)
SARS-CoV-2.
However,
activity
subvariants
decreased
sharply
as
number
mutations
receptor-binding
domain
(RBD)
these
viruses
increased.
Spike-BA.5,
spike-BF.7,
spike-BQ.1.1
strong
NAbs
BA.5,
BF.7,
BQ.1,
BQ.1.1
but
were
poor
protecting
XBB
XBB.1.5,
which
have
more
RBD
mutations.
sharp
contrast,
spike-XBB.1.5
vaccination
can
activate
broadly
other
common
Omicron.
By
performing
correlation
analysis,
negatively
correlated
with
subvariants.
Vaccines
effectively
overcome
resistance
caused
accumulation
mutations,
making
most
promising
candidate
universal
variants.
Frontiers in Medicine,
Journal Year:
2023,
Volume and Issue:
9
Published: Jan. 9, 2023
The
multi-systemic
inflammation
as
a
result
of
COVID-19
can
persevere
long
after
the
initial
symptoms
illness
have
subsided.
These
effects
are
referred
to
Long-COVID.
Our
research
focused
on
contribution
Spike
protein
S1
subunit
SARS-CoV-2
(Spike
S1)
lung
mediated
by
NLRP3
inflammasome
machinery
and
cytokine
releases,
interleukin
6
(IL-6),
IL-1beta,
IL-18,
in
epithelial
cells.
This
study
has
attempted
identify
naturally-
occurring
agents
that
act
against
inflammation-related
long-COVID.
seed
meal
Perilla
frutescens
(P.
frutescens),
which
contains
two
major
dietary
polyphenols
(rosmarinic
acid
luteolin),
been
reported
exhibit
anti-inflammation
activities.
Therefore,
we
established
ethyl
acetate
fraction
P.
(PFEA)
determined
its
anti-inflammatory
exposure
A549
cells.PFEA
was
using
solvent-partitioned
extraction.
Rosmarinic
(Ra)
luteolin
(Lu)
PFEA
were
identified
HPLC
technique.
inhibitory
active
compounds
S1-induced
inflammatory
response
cells
RT-PCR
ELISA.
mechanistic
properties
Lu
western
blot
technique.PFEA
found
contain
Ra
(388.70
±
11.12
mg/g
extract)
(248.82
12.34
polyphenols.
Accordingly,
pre-treated
with
(12.5-100
μg/mL)
(2.5-20
prior
at
100
ng/mL.
dose-dependently
exhibited
upon
S1-exposed
through
IL-6,
IL-1β,
gene
suppressions,
well
IL-18
releases
statistical
significance
(p
<
0.05).
Importantly,
possesses
superior
when
compared
0.01).
Mechanistically,
effectively
attenuated
downregulation
JAK1/STAT3-inflammasome-dependent
pathway
evidenced
NLRP3,
ASC,
cleaved-caspase-1
components
modulating
phosphorylation
JAK1
STAT3
proteins
0.05).The
findings
suggested
modulate
signaling
cascades
regulate
during
incidence
Consequently,
may
be
introduced
potential
candidates
preventive
therapeutic
strategy
for
post-acute
sequelae
COVID-19.