Research Square (Research Square),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Oct. 24, 2023
Abstract
The
global
prevalence
of
the
XBB
lineage
presents
a
formidable
challenge
posed
by
recombinant
SARS-CoV-2
virus.
understanding
SARS-CoV-2's
recombination
preference
assumes
utmost
significance
in
predicting
future
variants
and
adequately
preparing
for
subsequent
pandemics.
Thus,
an
urgent
need
arises
to
establish
comprehensive
landscape
concerning
recombinants
worldwide
elucidate
their
evolutionary
mechanisms.
However,
initial
step,
involving
detection
potential
from
vast
pool
over
ten
million
sequences,
significant
obstacle.
In
this
study,
we
present
CovRecomb,
lightweight
methodology
specifically
designed
effectively
identify
dissect
interlineage
recombinants.
Leveraging
successfully
detected
135,567
putative
across
entirety
14.5
accessed
genomes.
These
could
be
classified
into
1,451
distinct
events,
which
206
demonstrated
transmission
spanning
multiple
countries,
continents,
or
globally.
Hotspot
regions
were
identified
six
specific
areas,
with
particular
prominence
observed
latter
halves
N-terminal
domain
receptor-binding
within
spike
(S)
gene.
Epidemiological
investigations
revealed
extensive
events
occurring
among
different
(sub)lineages,
independent
frequencies.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: April 17, 2024
Abstract
Recombination
is
a
key
molecular
mechanism
for
the
evolution
and
adaptation
of
viruses.
The
first
recombinant
SARS-CoV-2
genomes
were
recognized
in
2021;
as
today,
more
than
ninety
lineages
are
designated
recombinant.
In
wake
COVID-19
pandemic,
several
methods
detecting
recombination
have
been
proposed;
however,
none
could
faithfully
confirm
manual
analyses
by
experts
field.
We
hereby
present
RecombinHunt,
an
original
data-driven
method
identification
genomes,
capable
recognizing
(or
lineages)
with
one
or
two
breakpoints
high
accuracy
within
reduced
turn-around
times.
ReconbinHunt
shows
specificity
sensitivity,
compares
favorably
other
state-of-the-art
methods,
confirms
experts.
RecombinHunt
identifies
viral
from
recent
monkeypox
epidemic
concordance
manually
curated
experts,
suggesting
that
our
approach
robust
can
be
applied
to
any
epidemic/pandemic
virus.
The Lancet Microbe,
Journal Year:
2024,
Volume and Issue:
5(2), P. e173 - e180
Published: Jan. 21, 2024
BackgroundWhole-genome
sequencing
(WGS)
is
the
gold
standard
diagnostic
tool
to
identify
and
genetically
characterise
emerging
pathogen
mutations
(variants),
but
cost,
capacity,
timeliness
limit
its
use
when
large
populations
need
rapidly
assessing.
We
assessed
potential
of
genotyping
assays
provide
accurate
timely
variant
information
at
scale
by
retrospectively
examining
surveillance
for
SARS-CoV-2
variants
in
England
between
March
September,
2021,
were
used
widely
detection.MethodsWe
chose
a
panel
four
RT-PCR
detect
circulating
SARS-COV-2
developed
decision
algorithm
assign
probable
samples
using
assay
results.
extracted
data
from
UK
Health
Security
Agency
databases
115
934
SARS-CoV-2-positive
(March
1–Sept
6,
2021)
was
available
both
WGS.
By
comparing
WGS
result,
we
calculated
accuracy
metrics
(ie,
sensitivity,
specificity,
positive
predictive
value
[PPV])
time
difference
sample
collection
date
availability
information.
number
with
assigned
or
WGS,
both,
over
time.FindingsGenotyping
an
initial
(April
10–May
11,
2021
data)
key
assignment:
sensitivities
PPVs
0·99
(95%
CI
0·99–0·99)
alpha,
1·00
(1·00–1·00)
beta,
0·91
(0·80–1·00)
gamma
variants;
specificities
0·97
(0·96–0·98),
(1·00–1·00),
respectively.
A
subsequent
longer
period
(May
27–Sept
remained
0·74–1·00)
0·98
(0·98–0·99)
delta,
0·93
(0·81–1·00)
0·96
(0·96–0·97),
respectively;
0·83
(0·62–1·00),
0·78
(0·59–0·97),
Genotyping
produced
median
3
days
(IQR
2–4)
after
date,
which
faster
than
(9
[8–11]).
The
flexibility
enabled
nine-times
increase
quantity
tested
this
method
(from
5000
45
000).InterpretationRT-PCR
are
suitable
high-throughput
could
complement
enabling
larger
testing
known
timelier
results,
important
implications
effective
public
health
responses
disease
control
globally,
especially
settings
low
capacity.
However,
choice
panels
highly
dependent
on
database
generated
new
spreading
rapidly.FundingUK
National
Institute
Research
Protection
Unit
Emergency
Preparedness
Response.
One Health,
Journal Year:
2023,
Volume and Issue:
16, P. 100536 - 100536
Published: April 6, 2023
Detection
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
viral
genome
in
wastewater
has
proven
to
be
useful
for
tracking
the
trends
virus
prevalence
within
community.
The
surveillance
also
provides
precise
and
early
detection
any
new
circulating
variants,
which
aids
response
outbreaks.
Site-specific
monitoring
SARS-CoV-2
variants
valuable
information
on
or
emerging
We
sequenced
genomic
RNA
viruses
present
samples
analyzed
as
well
other
a
period
one
year
account
seasonal
variations.
were
collected
from
Reno-Sparks
metropolitan
area
weekly
basis
between
November
2021
2022.
Samples
detect
levels
copies
identification.
This
study
confirmed
that
can
used
community
supports
wastewater-based
epidemiology
(WBE)
complement
clinical
testing
healthcare
effort.
Our
showed
persistence
throughout
compared
presence
viruses,
implicating
SARS-CoV-2's
broad
genetic
diversity
strength
persist
infect
susceptible
hosts.
Through
secondary
analysis,
we
further
identified
antimicrobial
resistance
(AMR)
genes
same
found
WBE
feasible
tool
AMR
monitoring.
Cellular and Molecular Life Sciences,
Journal Year:
2025,
Volume and Issue:
82(1)
Published: March 13, 2025
Abstract
Cellular
innate
immune
pathways
are
formidable
barriers
against
viral
invasion,
creating
an
environment
unfavorable
for
virus
replication.
Interferons
(IFNs)
play
a
crucial
role
in
driving
and
regulating
these
cell-intrinsic
antiviral
mechanisms
through
the
action
of
interferon-stimulated
genes
(ISGs).
The
host
IFN
response
obstructs
replication
at
every
stage,
prompting
viruses
to
evolve
various
strategies
counteract
or
evade
this
response.
Understanding
interplay
between
proteins
IFN-mediated
is
essential
developing
anti-inflammatory
strategies.
Human
coronaviruses
(HCoVs),
including
SARS-CoV-2,
MERS-CoV,
SARS-CoV,
seasonal
coronaviruses,
encode
range
that,
shared
distinct
mechanisms,
inhibit
responses.
Compounding
issue,
dysregulated
early
can
lead
hyper-inflammatory
reaction
later
infection,
resulting
severe
disease.
This
review
provides
brief
overview
HCoV
detailed
account
its
interaction
with
cellular
regulated
by
IFN.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: June 7, 2023
Abstract
Recombination
is
a
key
molecular
mechanism
for
the
evolution
and
adaptation
of
viruses.
The
first
recombinant
SARS-CoV-2
genomes
were
recognized
in
2021;
as
today,
more
than
ninety
lineages
are
designated
recombinant.
In
wake
COVID-19
pandemic,
several
methods
detecting
recombination
have
been
proposed;
however,
none
could
faithfully
confirm
manual
analyses
by
experts
field.
We
hereby
present
RecombinHunt,
novel,
automated
method
identification
recombinant/mosaic
purely
based
on
data-driven
approach.
RecombinHunt
compares
favorably
with
other
state-of-the-art
recognizes
(or
lineages)
one
or
two
breakpoints
high
accuracy,
within
reduced
turn-around
times
small
discrepancies
respect
to
expert
manually-curated
standard
nomenclature.
Strikingly,
applied
complete
collection
viral
sequences
from
recent
monkeypox
epidemic,
identifies
concordance
manually
curated
experts,
suggesting
that
our
approach
robust
can
be
any
epidemic/pandemic
virus.
conclusion,
represents
breakthrough
detection
pandemic/epidemic
scenarios
substantially
improve/advance
community-based
approaches
phylogenetic
analyses.
iScience,
Journal Year:
2023,
Volume and Issue:
26(11), P. 108299 - 108299
Published: Oct. 27, 2023
Additional
mutations
in
the
viral
Spike
protein
helped
BA.2.12.1
and
BA.4/5
SARS-CoV-2
Omicron
subvariants
to
outcompete
parental
BA.2
subvariant.
Here,
we
determined
functional
impact
of
that
newly
emerged
(L452Q,
S704L)
(Δ69-70,
L452R,
F486V,
R493Q)
proteins.
Our
results
show
mutation
L452Q/R
or
F486V
typically
increases
R493Q
S704L
impair
Spike-mediated
infection.
In
combination,
changes
Δ69-70,
contribute
higher
infectiousness
fusogenicity
Spike.
L452R/Q
are
mainly
responsible
for
reduced
sensitivity
neutralizing
antibodies.
However,
combined
required
full
infectivity,
TMPRSS2
dependency,
immune
escape
Thus,
it
is
specific
combination
allows
increased
functionality
evasion,
which
helps
explain
temporary
dominance
pathogenicity
these
subvariants.
Virus Evolution,
Journal Year:
2024,
Volume and Issue:
10(1)
Published: Jan. 1, 2024
Abstract
The
global
prevalence
of
the
XBB
lineage
presents
a
formidable
challenge
posed
by
recombinant
SARS-CoV-2
virus.
understanding
SARS-CoV-2’s
recombination
preference
assumes
utmost
significance
in
predicting
future
variants
and
adequately
preparing
for
subsequent
pandemics.
Thus,
an
urgent
need
arises
to
establish
comprehensive
landscape
concerning
recombinants
worldwide
elucidate
their
evolutionary
mechanisms.
However,
initial
step,
involving
detection
potential
from
vast
pool
over
10
million
sequences,
significant
obstacle.
In
this
study,
we
present
CovRecomb,
lightweight
methodology
specifically
designed
effectively
identify
dissect
interlineage
recombinants.
Leveraging
successfully
detected
135,567
putative
across
entirety
14.5
accessed
genomes.
These
could
be
classified
into
1451
distinct
events,
which
206
demonstrated
transmission
spanning
multiple
countries,
continents,
or
globally.
Hotspot
regions
were
identified
six
specific
areas,
with
prominence
observed
latter
halves
N-terminal
domain
receptor-binding
within
spike
(S)
gene.
Epidemiological
investigations
revealed
extensive
events
occurring
among
different
(sub)lineages,
independent
frequencies.
Journal of Medical Virology,
Journal Year:
2023,
Volume and Issue:
95(10)
Published: Oct. 1, 2023
The
on-going
emergence
of
the
Omicron
BA.2.86
variant
is
one
major
events
in
SARS-CoV-2
genetic
evolution
that
remain
enigmatic
regarding
overall
virus
mutation
rate,
together
with
initial
variant,
BA.1.
Indeed,
genomes
lineage,
an
offspring
second
subvariant,
BA.2,
harbor
39
additional
mutations
spike
compared
to
this
ancestor.
Here
we
comment
on
phylogeny
BA.2.86,
positions,
and
frequencies
other
SARS-CoV-2,
its
spike,
structural
model
protein
concentrates
most
mutations.
PLoS ONE,
Journal Year:
2024,
Volume and Issue:
19(9), P. e0307873 - e0307873
Published: Sept. 19, 2024
Introduction
Epitopes
are
specific
structures
in
antigens
that
recognized
by
the
immune
system.
They
widely
used
context
of
immunology-related
applications,
such
as
vaccine
development,
drug
design,
and
diagnosis
/
treatment
prevention
disease.
The
SARS-CoV-2
virus
has
represented
main
point
interest
within
viral
genomic
surveillance
community
last
four
years.
Its
ability
to
mutate
acquire
new
characteristics
while
it
reorganizes
into
variants
been
analyzed
from
many
perspectives.
Understanding
how
epitopes
impacted
mutations
accumulate
on
protein
level
cannot
be
underrated.
Methods
With
a
focus
Omicron-named
lineages,
including
WHO-designated
Variants
Interest,
we
propose
workflow
for
data
retrieval,
integration,
analysis
pipeline
conducting
database-wide
study
impact
lineages’
characterizing
all
T
cell
B
linear
collected
Immune
Epitope
Database
(IEDB)
SARS-CoV-2.
Results
Our
allows
us
showcase
novel
qualitative
quantitative
results
1)
coverage
proteins
deposited
epitopes;
2)
distribution
mutated
across
Omicron
variants;
3)
epitopes.
discussed
based
type
epitope,
response
frequency
assays,
sample
size.
proposed
can
reproduced
at
any
time,
given
updated
variant
characterizations
IEDB,
thereby
guaranteeing
observe
landscape
mutations’
demand.
Conclusion
A
big
data-driven
one
provided
here
inform
next
policies
combatting
future
epidemic
viruses.