Molecular characterization of SARS-CoV-2 nucleocapsid protein
Yanping Huang,
No information about this author
Junkai Chen,
No information about this author
Siwei Chen
No information about this author
et al.
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2024,
Volume and Issue:
14
Published: May 23, 2024
Corona
Virus
Disease
2019
(COVID-19)
is
a
highly
prevalent
and
potent
infectious
disease
caused
by
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2).
Until
now,
the
world
still
endeavoring
to
develop
new
ways
diagnose
treat
COVID-19.
At
present,
clinical
prevention
treatment
of
COVID-19
mainly
targets
spike
protein
on
surface
SRAS-CoV-2.
However,
with
continuous
emergence
SARS-CoV-2
Variants
concern
(VOC),
targeting
therapy
shows
high
degree
limitation.
The
Nucleocapsid
Protein
(N
protein)
conserved
in
virus
evolution
involved
key
process
viral
infection
assembly.
It
most
expressed
structural
after
humans
has
immunogenicity.
Therefore,
N
as
factor
replication
basic
research
application
great
potential
value.
This
article
reviews
progress
structure
biological
function
protein,
diagnosis
drug
order
promote
researchers’
further
understanding
lay
theoretical
foundation
for
possible
outbreak
sudden
diseases
future.
Language: Английский
Revolutionizing SARS-CoV-2 omicron variant detection: Towards faster and more reliable methods
Dan Li,
No information about this author
Cai Sun,
No information about this author
Pengfei Zhuang
No information about this author
et al.
Talanta,
Journal Year:
2023,
Volume and Issue:
266, P. 124937 - 124937
Published: July 12, 2023
Language: Английский
Validation of the United States Isolation Termination Criteria Using Virus Culture Results of the Omicron Variant in Japan
Journal of Infection and Chemotherapy,
Journal Year:
2025,
Volume and Issue:
unknown, P. 102714 - 102714
Published: April 1, 2025
Language: Английский
Recent Advances in Enzyme‐Mediated Rolling Circle Replication Technology Empowering Virus Detection
Min Du,
No information about this author
Juncheng Liu,
No information about this author
Guangshuai Teng
No information about this author
et al.
Chinese Journal of Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 11, 2025
Comprehensive
Summary
The
prevalence
and
spread
of
viral
infectious
diseases
pose
a
grave
threat
to
global
public
health,
particularly
resulting
in
significant
number
casualties.
To
curb
the
diseases,
virus
testing
is
one
efficient
economical
means,
among
which
nucleic
acid
detection
has
advantage
detecting
infections
at
an
early
stage,
even
before
symptoms
appear.
Rolling
circle
replication
representative
enzyme‐mediated
isothermal
amplification
technology,
characterized
by
its
mild
reaction
conditions,
no
need
for
temperature
control
equipment,
high
efficiency.
This
review
provides
conceptual
overview
latest
advances
rolling
(RCR)
their
applications
detection,
focusing
on
molecular
design
principles
different
application
scenarios.
first
part
briefly
describes
significance
advantages
RCR
detection.
second
elaborates
principle
preparation
strategy
derivative
technologies.
third
focuses
various
scenarios
In
end,
we
provide
perspective
innovation
improving
accuracy
specificity
cope
with
challenges
that
may
arise
future.
Language: Английский
Pathogen Discovery in the Post-COVID Era
Pathogens,
Journal Year:
2024,
Volume and Issue:
13(1), P. 51 - 51
Published: Jan. 5, 2024
Pathogen
discovery
plays
a
crucial
role
in
the
fields
of
infectious
diseases,
clinical
microbiology,
and
public
health.
During
past
four
years,
global
response
to
COVID-19
pandemic
highlighted
importance
early
accurate
identification
novel
pathogens
for
effective
management
prevention
outbreaks.
The
post-COVID
era
has
ushered
new
phase
disease
research,
marked
by
accelerated
advancements
pathogen
discovery.
This
review
encapsulates
recent
innovations
paradigm
shifts
that
have
reshaped
landscape
pandemic.
Primarily,
we
summarize
latest
technology
innovations,
applications,
causation
proving
strategies
enable
rapid
both
acute
historical
infections.
We
also
explored
significance
trends
approaches
being
employed
implementation
from
various
environmental
samples.
Furthermore,
emphasize
collaborative
nature
response,
which
led
establishment
networks
Language: Английский
Rapid detection of SARS-CoV-2 RNA using a one-step fast multiplex RT-PCR coupled to lateral flow immunoassay
BMC Infectious Diseases,
Journal Year:
2024,
Volume and Issue:
24(1)
Published: Dec. 18, 2024
The
COVID-19
has
put
emphasis
on
pivotal
needs
for
diagnosis
and
surveillance
worldwide,
with
the
subsequent
shortage
of
diagnostic
reagents
kits.
Therefore,
it
become
strategic
countries
to
access
diagnostics,
expand
testing
capacity,
develop
their
own
capabilities
alternative
rapid
accurate
nucleic
acid
diagnostics
that
are
at
lower
costs.
Here,
we
propose
a
visual
SARS-CoV-2
detection
using
one-step
fast
multiplex
reverse
transcription-PCR
(RT-PCR)
amplification
coupled
lateral
flow
immunoassay
PCRD
device
(Abingdon
Health,
UK).
We
developed
various
simplex
fast-PCRs
screening
sets
primer
pairs
newly
designed
or
selected
from
literature
validated
WHO
targeting
S,
N,
E,
RdRp
ORF1ab
genes.
retained
primers
showing
specific
stable
assess
suitability
PCRD.
Thus,
RT-PCR
amplifications
were
performed
primers.
They
doubly
labeled
Fam
Biotin
Dig
allow
amplicons
PCR
Detection
(PCRD)
device,
looking
lack
interaction
(or
dimers)
test-lines
in
negative
no
RNA
controls.
set
up
all
assays
RNAs
isolated
patients'
nasopharyngeal
swabs.
used
two
assays,
different
viral
genomic
regions
(N
E)
PCRD,
assay
(where
both
differently
engaged)
amplicons'
device.
evaluated
this
novel
50
positive
samples
compared
its
performance
results
quantitative
(RT-qPCR)
diagnosing
patients,
here
considered
as
standard
tests.
new
achieved
sensitivity
88%
(44/50)
specificity
98%
(49/50).
All
patients
who
presented
Ct
values
than
33
our
assay.
Except
one
patient,
those
above
returned
results.
Our
have
brought
proof
principle
usefulness
RT-
specific,
sensitive,
without
requiring
costly
laboratory
equipment,
thus,
reduced
costs
format
prone
be
deployed
when
resources
limited.
This
offers
viable
points
need.
Language: Английский
Molecular Point‐of‐Care Assay Development: Design and Considerations
Ashley Hassman,
No information about this author
Colby Rouchka,
No information about this author
Diego Sunino
No information about this author
et al.
Current Protocols,
Journal Year:
2024,
Volume and Issue:
4(6)
Published: June 1, 2024
Abstract
Molecular
diagnostic
point‐of‐care
(MDx
POC)
testing
is
gaining
momentum
and
increasingly
important
for
infectious
disease
detection
monitoring,
as
well
other
areas
such
oncology.
has
traditionally
required
high‐complexity
laboratories.
Laboratory
complexity
determined
by
utilizing
the
Clinical
Improvement
Amendments
of
1988
(CLIA)
Categorization
Criteria
scorecard,
seven
criteria
that
are
scored
on
a
scale
one
to
three.
Previously,
most
commercially
available
(POC)
tests
use
analytes
technologies
were
not
found
be
highly
complex
CLIA
scoring
system.
However,
during
COVID‐19
pandemic,
MDx
POC
became
much
more
prominent.
Utilization
pandemic
demonstrated
applications
can
have
outstanding
advantages
compared
non‐molecular
tests.
This
article
introduces
students,
technologists,
researchers,
others,
providing
general
algorithm
test
development.
an
introductory,
step‐by‐step
decision
tree
defining
molecular
device
meeting
functional
requirements
desired
application.
The
technical
considerations
driving
decision‐making
include
nucleic
acid
selection
method
(DNA,
RNA),
extraction
methods,
sample
preparation,
number
targets,
amplification
technology,
method.
scope
this
includes
neither
higher‐order
multiplexing,
nor
quantitative
analysis.
covers
key
application
considerations,
sensitivity,
specificity,
turnaround
time,
shipping/storage
requirements.
provides
overall
understanding
best
resources
practices
when
developing
assay
may
helpful
resource
readers
without
extensive
experience
those
who
already
familiar
with
want
increase
availability
at
POC.
©
2024
Wiley
Periodicals
LLC.
Language: Английский
Solid-State Nanopore Counting of Amplicons from Recombinase Polymerase Isothermal Amplification
Sensors & Diagnostics,
Journal Year:
2024,
Volume and Issue:
3(10), P. 1733 - 1742
Published: Jan. 1, 2024
A
nanopore-integrated
reverse-transcription
recombinase
polymerase
amplification-based
assay
is
employed
for
the
direct
electrical
detection
of
synthetic
SARS-CoV-2
RNA
amplicons.
Language: Английский
Rapid detection of SARS-CoV-2 RNA using a one-step fast multiplex RT-PCR coupled to lateral flow immunoassay
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 18, 2024
Abstract
Background
The
COVID-19
pandemics
has
put
emphasis
on
pivotal
needs
for
diagnosis
and
surveillance
worldwide,
with
the
subsequent
shortage
of
diagnostic
reagents
kits.
Therefore,
it
become
strategic
countries
to
be
able
access
diagnosis,
expand
it,
acquire
its
own
capacity
deploy
diagnostics
alternative
rapid
accurate
nucleic
acid
tests
that
are
at
lower
costs.
Here,
we
propose
a
visual
SARS-CoV-2
detection
using
one-step
fast
multiplex
reverse
transcription-PCR
(RT-PCR)
amplification
coupled
lateral
flow
immunoassay
PCRD
device
(Abingdon
Health,
UK).
Methods
Various
simplex
fast-PCRs
were
developed
screening
sets
primer
pairs
newly
designed
or
selected
from
literature
validated
WHO
tests,
targeting
S,
N,
E,
RdRp
ORF1ab
genes.
Primers
showing
specific
stable
retained
assess
their
suitability
PCRD.
Thus,
RT-PCR
amplifications
performed
primers.
They
doubly
labeled
Fam
Biotin
Dig
allow
amplicons
PCR
Detection
(PCRD)
device,
looking
lack
interaction
primers
(or
dimers)
test
lines
in
negative
no
RNA
controls.
All
assays
set
up
RNAs
isolated
patients’
nasopharyngeal
swabs.
Two
assays,
two
different
viral
genomic
regions
(
N
E)
PCRD,
used
assay
(where
both
differently
engaged)
amplicons’
device.
This
novel
method
was
evaluated
50
positive
samples
performance
compared
results
quantitative
(RT-qPCR)
diagnosing
patients,
here
considered
as
standard
methods.
Results
way,
new
showed
sensitivity
88%
(44/50)
specificity
98%
(49/50).
patients
who
presented
Ct
values
than
33
our
assay.
Except
one
patient,
those
greater
results.
Conclusion
Our
have
brought
proof
principle
usefulness
RT-
PCR
specific,
sensitive,
without
requiring
costly
laboratory
equipment,
thus
reduced
costs,
format
prone
deployed
when
resources
limited.
appears
good
points
need.
Language: Английский
Recent developments in isothermal amplification technology for rapid detection of SARS-CoV-2
Linlin Wang,
No information about this author
Ruizhe Tang,
No information about this author
Wentao Wang
No information about this author
et al.
Analytical Methods,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 16, 2024
The
latest
achievements
and
prospects
of
LAMP
RPA
in
the
rapid
detection
common
infectious
disease
pathogens
such
as
SARS-CoV-2
is
summarized.
Language: Английский