Scientia Pharmaceutica,
Journal Year:
2024,
Volume and Issue:
93(1), P. 2 - 2
Published: Dec. 26, 2024
Although
COVID-19
is
not
a
pandemic
anymore,
the
virus
frequently
mutates,
resulting
in
new
strains
and
presenting
global
public
health
challenges.
The
lack
of
oral
antiviral
drugs
makes
it
difficult
to
treat
him,
which
creation
broadly
acting
antivirals
necessary
fight
current
next
epidemics
viruses.
Using
molecular
docking
approach,
118
compounds
derived
from
marine
organisms
92
previously
synthesized
were
screened
assess
their
binding
affinity
for
main
protease
papain-like
enzymes
SARS-CoV-2.
best
candidates
xanthene,
benzoxazole,
coumarin
classes
identified.
Marine-derived
showed
slightly
better
potential
as
enzyme
inhibitors,
though
affinities
similar,
with
displaying
values
between
0.2
0.4
mM.
Xanthenes,
among
both
origin
compounds,
emerged
most
promising
scaffolds
further
research
inhibitors.
was
found
be
more
druggable
than
protease.
Additionally,
all
top
met
criteria
various
drug-likeness
properties,
indicating
good
bioavailability
low
risk
adverse
effects.
This
provides
valuable
insights
into
comparative
coumarin,
benzoxazole
classes,
highlighting
vitro
vivo
studies.
Immunity Inflammation and Disease,
Journal Year:
2023,
Volume and Issue:
11(9)
Published: Sept. 1, 2023
Abstract
Introduction
The
novel
coronavirus
infectious
disease
2019
(COVID‐19)
which
is
caused
by
severe
acute
respiratory
syndrome
2
(SARS‐CoV‐2)
has
emerged
as
a
gigantic
problem.
lung
the
major
target
organ
of
SARS‐CoV‐2
and
some
its
variants
like
Delta
Omicron
variant
adapted
in
such
way
that
these
can
significantly
damage
this
vital
body.
These
raised
few
eyebrows
outbreaks
have
been
seen
vaccinated
population.
Patients
develop
illnesses
eventually
prove
fatal
unless
treated
early.
Main
Body
Studies
shown
causes
release
pro‐inflammatory
cytokines
interleukin
(IL)‐6,
IL‐1β
tumor
necrosis
factor
(TNF)‐α
are
mediators
inflammation,
damage,
fever,
fibrosis.
Additionally,
various
chemokines
found
to
play
an
important
role
progression.
A
plethora
“cytokine
storm”
observed
cases
infection
leading
distress
(ARDS)
pneumonia
may
fatal.
To
counteract
cytokine
storm‐inducing
several
promising
immunomodulatory
approaches
being
investigated
numerous
clinical
trials.
However,
benefits
using
strategies
should
outweigh
risks
involved
use
certain
immunosuppressive
might
lead
host
susceptible
secondary
bacterial
infections.
Conclusion
present
review
discusses
manage
inflammation
COVID‐19
serve
potential
therapeutic
options
future
lifesaving.
International Journal of Biological Macromolecules,
Journal Year:
2024,
Volume and Issue:
266, P. 131054 - 131054
Published: March 24, 2024
The
surveillance
of
COVID-19
pandemic
has
led
to
the
determination
millions
genome
sequences
SARS-CoV-2
virus,
with
accumulation
a
wealth
information
never
collected
before
for
an
infectious
disease.
Exploring
retrieved
from
GISAID
database
reporting
at
that
time
>13
million
sequences,
we
classified
141,639
unique
missense
mutations
detected
in
first
two-and-a-half
years
(up
October
2022)
pandemic.
Notably,
our
analysis
indicates
98.2
%
all
possible
conservative
amino
acid
replacements
occurred.
Even
non-conservative
were
highly
represented
(73.9
%).
For
significant
number
residues
(3
%),
other
nineteen
acids
have
been
observed.
These
observations
strongly
indicate
that,
this
interval,
virus
explored
alternatives
terms
sites
its
polypeptide
chain
and
those
are
not
observed
severely
affect
integrity.
implications
present
findings
go
well
beyond
structural
biology
as
huge
amount
here
may
be
valuable
elucidation
sequence-structure-function
relationships
proteins.
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(9), P. e29909 - e29909
Published: April 21, 2024
According
to
information
from
the
World
Health
Organization,
world
has
experienced
about
430
million
cases
of
COVID-19,
a
world-wide
health
crisis
caused
by
SARS-CoV-2
virus.
This
outbreak,
originating
China
in
2019,
led
nearly
6
deaths
worldwide.
As
number
confirmed
infections
continues
rise,
need
for
cutting-edge
techniques
that
can
detect
early
and
accurately
become
more
critical.
To
address
this,
Federal
Drug
Administration
(FDA)
issued
emergency
use
authorizations
(EUAs)
wide
range
diagnostic
tools.
These
include
tests
based
on
detecting
nucleic
acids
antigen-antibody
reactions.
The
quantitative
real-time
reverse
transcription
PCR
(qRT-PCR)
assay
stands
out
as
gold
standard
virus
detection.
However,
despite
its
accuracy,
qRT-PCR
limitations,
such
complex
testing
protocols
risk
false
negatives,
which
drive
continuous
improvement
acid
serological
approaches.
emergence
highly
contagious
variants
coronavirus,
Alpha
(B.1.1.7),
Delta
(B.1.617.2),
Omicron
(B.1.1.529),
increased
specifically
identify
these
mutations.
article
explores
both
acid-based
assays,
assessing
performance
recently
approved
FDA
those
documented
scientific
research,
especially
identifying
new
coronavirus
strains.
Eurosurveillance,
Journal Year:
2025,
Volume and Issue:
30(10)
Published: March 13, 2025
Background
Evolution
of
SARS-CoV-2
is
continuous.
Aim
Between
01/2020
and
02/2022,
we
studied
variant
epidemiology,
evolution
association
with
COVID-19
severity.
Methods
In
nasopharyngeal
swabs
patients
(n
=
1,762)
from
France,
Italy,
Spain,
the
Netherlands,
was
investigated
by
reverse
transcription-quantitative
PCR
whole-genome
sequencing,
virus
variant/lineage
(NextStrain/Pangolin)
determined.
Patients’
demographic
clinical
details
were
recorded.
Associations
between
mild/moderate
or
severe
variants
patient
characteristics
assessed
logistic
regression.
Rates
genomic
locations
mutations,
as
well
quasi-species
distribution
(≥
2
heterogeneous
positions,
≥
50×
coverage)
estimated
based
on
1,332
high-quality
sequences.
Results
Overall,
11
clades
infected
1,762
study
median
age
59
years
(interquartile
range
(IQR):
45–73),
52.5%
925)
being
male.
total,
101
non-synonymous
substitutions/insertions
correlated
disease
prognosis
(severe,
n
27;
mild-to-moderate,
74).
Several
hotspots
(mutation
rates
85%)
occurred
in
Alpha,
Delta,
Omicron
concern
(VOCs)
but
none
pre-Alpha
strains.
Four
retained
across
all
variants,
including
spike:D614G.
Average
number
mutations
per
open-reading-frame
(ORF)
increased
spike
gene
(average
<
5
genome
January
2020
to
>
15
2022),
remained
stable
ORF1ab,
membrane,
nucleocapsid
genes.
Quasi-species
most
prevalent
20A/EU2
(48.9%),
20E/EU1
(48.6%),
20A
(38.8%),
21K/Omicron
(36.1%)
infections.
Immunocompromised
status
60
years),
while
associated
death
irrespective
(odds
ratio
(OR):
1.60–2.25;
p
≤
0.014),
did
not
affect
quasi-species’
prevalence
(p
0.05).
Conclusion
Specific
correlate
potentially
shaping
VOCs’
emergence
are
relevant
consider.
Vaccines,
Journal Year:
2025,
Volume and Issue:
13(4), P. 424 - 424
Published: April 17, 2025
Vaccination
has
been
instrumental
in
curbing
the
transmission
of
SARS-CoV-2
and
mitigating
severity
clinical
manifestations
associated
with
COVID-19.
Numerous
COVID-19
vaccines
have
developed
to
this
effect,
including
BioNTech-Pfizer
Moderna’s
mRNA
vaccines,
as
well
adenovirus
vector-based
such
Oxford–AstraZeneca.
However,
emergence
new
variants
subvariants
SARS-CoV-2,
characterized
by
enhanced
transmissibility
immune
evasion,
poses
significant
challenges
efficacy
current
vaccination
strategies.
In
review,
we
aim
comprehensively
outline
landscape
emerging
concern
(VOCs)
sub-lineages
that
recently
surfaced
post-pandemic
years.
We
assess
effectiveness
existing
their
booster
doses,
against
these
subvariants,
BA.2-derived
sub-lineages,
XBB
BA.2.86
(Pirola).
Furthermore,
discuss
latest
advancements
vaccine
technology,
multivalent
pan-coronavirus
approaches,
along
development
several
next-generation
coronavirus
exosome-based,
virus-like
particle
(VLP),
mucosal,
nanomaterial-based
vaccines.
Finally,
highlight
key
critical
areas
for
future
research
address
evolving
threat
develop
strategies
combating
viral
threats,
thereby
improving
preparedness
pandemics.
Frontiers in Molecular Biosciences,
Journal Year:
2023,
Volume and Issue:
10
Published: Nov. 2, 2023
Coronavirus
disease
2019
(COVID-19),
caused
by
the
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2),
is
a
major
global
health
concern
associated
with
millions
of
fatalities
worldwide.
Mutant
variants
virus
have
further
exacerbated
COVID-19
mortality
and
infection
rates,
emphasizing
urgent
need
for
effective
preventive
strategies.
Understanding
viral
mechanism
crucial
developing
therapeutics
vaccines.
The
entry
SARS-CoV-2
into
host
cells
key
step
in
pathway
has
been
targeted
drug
development.
Despite
numerous
reviews
virus,
there
lack
comprehensive
focusing
on
structural
aspects
entry.
In
this
review,
we
analyze
changes
Spike
proteins
during
process,
dividing
process
prebinding,
receptor
binding,
proteolytic
cleavage,
membrane
fusion
steps.
By
understanding
atomic-scale
details
entry,
can
better
target
intervention
We
also
examine
impacts
mutations
proteins,
including
Omicron
variant,
Structural
information
provides
insights
effects
guide
development
Finally,
discuss
available
structure-based
approaches
Overall,
review
detailed
analysis
highlighting
its
significance
vaccines
against
COVID-19.
Therefore,
our
emphasizes
importance
combating
infection.