Unraveling the role of the nucleocapsid protein in SARS-CoV-2 pathogenesis: From viral life cycle to vaccine development
Yousra A. El‐Maradny,
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Moustafa A. Badawy,
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Kareem I. Mohamed
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et al.
International Journal of Biological Macromolecules,
Journal Year:
2024,
Volume and Issue:
279, P. 135201 - 135201
Published: Aug. 30, 2024
Language: Английский
Isolation and molecular characterization of an enteric isolate of the Genotype-Ia Bovine coronavirus with notable mutations in the receptor binding domain of the spike glycoprotein.
Virology,
Journal Year:
2024,
Volume and Issue:
603, P. 110313 - 110313
Published: Nov. 29, 2024
Language: Английский
Distinct roles of SARS-CoV-2 N protein and NFP in host cell response modulation
Hsin-Chi Lan,
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Baidong Hou,
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Shu-Ting Chang
No information about this author
et al.
Journal of Molecular Biology,
Journal Year:
2025,
Volume and Issue:
unknown, P. 169094 - 169094
Published: March 1, 2025
Language: Английский
Research Progress on the Structure and Function, Immune Escape Mechanism, Antiviral Drug Development Methods, and Clinical Use of SARS-CoV-2 Mpro
Molecules,
Journal Year:
2025,
Volume and Issue:
30(2), P. 351 - 351
Published: Jan. 16, 2025
The
three-year
COVID-19
pandemic
‘has’
caused
a
wide
range
of
medical,
social,
political,
and
financial
implications.
Since
the
end
2020,
various
mutations
variations
in
SARS-CoV-2
strains,
along
with
immune
escape
phenomenon,
have
emerged.
There
is
an
urgent
need
to
identify
relatively
stable
target
for
development
universal
vaccines
drugs
that
can
effectively
combat
both
strains
their
mutants.
Currently,
main
focus
treating
lies
disrupting
virus’s
life
cycle.
protease
(Mpro)
closely
associated
virus
replication
maturation
plays
crucial
role
early
stages
infection.
Consequently,
it
has
become
important
SARS-CoV-2-specific
drugs.
This
review
summarizes
recent
research
progress
on
novel
coronavirus’s
proteases,
including
pivotal
Mpro
cycle,
structure
catalytic
mechanism
Mpro,
self-maturation
escape,
current
methods
developing
antiviral
targeting
key
successfully
entered
clinical
trials.
aim
provide
researchers
involved
systematic
comprehensive
information.
Language: Английский
Isolation and molecular characterization of an enteric isolate of the Genotype-I Bovine coronavirus with notable mutations in the receptor binding domain of the spike glycoprotein and deletion downstream the RNA binding domain of the nucleocapsid protein
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 4, 2024
Abstract
Bovine
coronavirus
(BCoV)
continues
to
be
a
significant
threat
cattle
populations
despite
the
implementation
of
vaccination
programs.
The
continuous
circulation
BCoV
highlights
necessity
for
ongoing
genomic
surveillance
understand
better
virus’s
evolution
and
its
impact
on
health.
main
goal
this
study
was
do
isolation
perform
comprehensive
molecular
characterization
new
enteric
field
isolate
BCoV.
To
identify
any
genetic
elements
in
sequences
that
could
act
as
markers
infection
cattle.
achieve
these
objectives,
newly
identified
propagated
MDBK
cell
line
several
subsequent
blind
passages.
immunofluorescence
assay
verified
confirmation
virus
propagation.
We
plaque
purified
titrated
it
by
using
HRT-18
line.
examined
viral
protein
expression
SDS-PAGE
followed
Western
blot
BCoV/S
BCoV/N
antibodies.
Our
results
show
substantial
increase
genome
copy
number,
expression,
infectivity
with
culture
full-length
sequence
NGS
drafted.
vial
is
31
Kb
length.
has
typical
organization
(5’-UTR-Gene-
1-
HE-S-M-E-N-UTR-3’).
phylogenetic
analysis
based
nucleotide
(full-length
genome,
S,
HE,
N)
showed
BCoV-13
clustered
other
members
(genotype
I-i).
shows
synonymous
mutations
among
various
domains
S
glycoprotein,
especially
receptor
binding
domain.
found
nine
notable
deletions
immediately
downstream
RNA
domain
nucleocapsid
gene.
Further
gene
function
studies
are
encouraged
pathogenesis
immune
regulation/evasion.
This
research
enhances
our
understanding
genomics
contributes
improved
diagnostic
control
measures
infections
populations.
Language: Английский
Structural basis for the participation of the SARS-CoV-2 nucleocapsid protein in the template switch mechanism and genomic RNA reorganization
Journal of Biological Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown, P. 107834 - 107834
Published: Sept. 1, 2024
Language: Английский
Diagnostic utility of SARS-CoV-2 nucleocapsid antigenemia: a meta-analysis
Gregory L. Damhorst,
No information about this author
Sydney E Martin,
No information about this author
Eli Wilber
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et al.
Open Forum Infectious Diseases,
Journal Year:
2024,
Volume and Issue:
11(10)
Published: Sept. 27, 2024
Abstract
Background
Studies
of
the
diagnostic
performance
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
nucleocapsid
antigen
in
blood
(antigenemia)
have
reached
variable
conclusions.
The
potential
utility
antigenemia
measurements
as
a
clinical
test
needs
clarification.
Methods
We
performed
systematic
review
Pubmed,
Embase,
and
Scopus
through
July
15,
2023,
requested
source
data
from
corresponding
authors.
Results
Summary
sensitivity
16
studies
(4543
cases)
sampled
at
≤14
days
symptoms
was
0.83
(0.75–0.89),
specificity
0.98
(0.87–1.00)
6
(792
reverse
transcription
polymerase
chain
reaction–negative
controls).
for
paired
specimens
with
cycle
threshold
values
≤33
were
0.91
(0.85–0.95)
0.56
(0.39–0.73)
10
(612
individuals).
Source
1779
cases
reveal
that
>70%
weeks
following
symptom
onset,
which
persists
<10%
28
days.
available
suffer
heterogeneity,
Omicron-era
are
scarce.
Conclusions
Nucleocapsid
currently
has
limited
due
to
limitations
existing
lack
data.
Improved
study
designs
targeting
uses
screening,
surveillance,
complex
decision-making—especially
immunocompromised
patients—are
needed.
Language: Английский