Diagnostics,
Journal Year:
2022,
Volume and Issue:
12(9), P. 2219 - 2219
Published: Sept. 14, 2022
We
report
two
cases
of
SARS-CoV-2
recombinant
variant
XE
detected
in
nasopharyngeal
swabs
(NPS)
hospitalized
patients
with
no
evident
epidemiological
link
Lazio,
Central
Italy.
Whole-Genome
Sequencing
(WGS)
performed
on
an
Ion
Torrent
GSS5
platform
according
to
Italian
flash
surveys
showed
genomes
corresponding
the
PANGOLIN
unclassified
lineage
and
Nextclade
clade.
Further
analyses
were
then
carried
out
investigate
more
deeply
genetic
characteristics
these
XE-like
sequences.
When
phylogenetic
trees,
by
using
IQ-TREE,
built
splitting
genome
into
regions
putative
recombination
site,
upstream
downstream
seen
be
clustered
near
BA.1
BA.2
sequences,
respectively.
However,
our
sequences
separately,
a
significant
bootstrap,
from
classified
European
strains,
although
site
between
was
identified
at
nucleotide
11556
RDP4
software,
consistent
breakpoint.
These
findings
show
risk
introduction
novel
variants
existence
phylogenetically
separated,
that
could
make
their
exact
taxonomy
difficult.
It
follows
need
for
continued
surveillance
WGS.
Journal of Medical Virology,
Journal Year:
2022,
Volume and Issue:
95(2)
Published: Dec. 30, 2022
Emerging
evidence
suggests
the
oral
and
upper
respiratory
microbiota
may
play
important
roles
in
modulating
host
immune
responses
to
viral
infection.
As
microbiome
be
involved
pathophysiology
of
coronavirus
disease
2019
(COVID-19),
we
investigated
associations
between
nasopharyngeal
COVID-19
severity.
We
collected
saliva
(n
=
78)
swab
66)
samples
from
a
cohort
characterized
microbiomes
using
16S
ribosomal
RNA
gene
sequencing.
also
examined
salivary
age,
symptoms,
blood
cytokines.
Severe
acute
syndrome
2
(SARS-CoV-2)
infection
status,
but
not
severity,
was
associated
with
community-level
differences
microbiomes.
Salivary
alpha
diversity
negatively
correlated
age
were
fever
diarrhea.
Oral
Bifidobacterium,
Lactobacillus,
Solobacterium
depleted
patients
severe
COVID-19.
Nasopharyngeal
Paracoccus
while
Proteus,
Cupravidus,
Lactobacillus
increased
Further
analysis
revealed
that
abundance
Bifidobacterium
plasma
concentrations
known
biomarkers
interleukin
17F
monocyte
chemoattractant
protein-1.
Our
results
suggest
severity
is
relative
certain
bacterial
taxa.
Letters in Applied Microbiology,
Journal Year:
2024,
Volume and Issue:
77(8)
Published: July 30, 2024
Abstract
Since
the
emergence
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2),
new
variants
with
enhanced
transmissibility
and
pathogenicity
have
surfaced.
The
World
Health
Organization
has
designated
five
such
variants—Alpha
(B.1.1.7),
Beta
(B.1.351),
Gamma
(P.1),
Delta
(B.1.617.2),
Omicron
(B.1.1.529)—as
concern.
Each
variant
exhibits
distinct
characteristics,
many
displaying
a
combination
point
mutations
insertions/deletions
(indels).
These
genetic
alterations,
including
mutations,
recombinations,
rearrangements,
contribute
to
strains
that
may
exhibit
modified
phenotypes.
However,
identifying
recombinant
forms
can
be
challenging
due
their
resemblance
other
lineages.
It
is
critical
monitor
evolution
variants,
particularly
in
light
potential
for
vaccine-resistant
accelerated
propagation.
Recombination
played
pivotal
role
development
certain
SARS-CoV-2
as
XA,
XD,
XF,
XE,
XBB,
among
others.
This
report
delves
into
significance
recombination
especially
sublineages,
underscoring
necessity
continuous
surveillance
genome
identify
newly
emerged
variants.
Vaccines,
Journal Year:
2023,
Volume and Issue:
12(1), P. 5 - 5
Published: Dec. 20, 2023
The
new
coronavirus
infection
causes
severe
respiratory
failure
following
tract
with
acute
syndrome-related
(SARS-CoV-2).
All
currently
approved
vaccines
are
administered
intramuscularly;
however,
intranasal
administration
enhances
mucosal
immunity,
facilitating
the
production
of
a
less
invasive
vaccine
fewer
adverse
events.
Herein,
recombinant
combining
SARS-CoV-2
spike
protein
receptor-binding
domain
(RBD),
or
S1
protein,
CpG-deoxyoligonucleotide
(ODN)
aluminum
hydroxide
(alum)
adjuvants
was
intranasally
subcutaneously
to
mice.
Serum-specific
IgG
titers,
IgA
titers
in
alveolar
lavage
fluid,
and
neutralizing
antibody
were
analyzed.
nasal
RBD
did
not
increase
serum
fluid.
However,
significant
observed
group
CpG-ODN
subcutaneous
alum.
levels
increased
significantly
fluid
only
after
CpG-ODN.
bronchoalveolar
higher
S1-CpG
than
every
other
group.
Hence,
CpG
adjuvant
might
represent
an
effective
candidate.
ImmunoHorizons,
Journal Year:
2024,
Volume and Issue:
8(2), P. 193 - 197
Published: Feb. 1, 2024
Abstract
Recent
research
has
highlighted
the
Omicron
variant’s
capacity
to
evade
immune
protection
conferred
by
wild-type
(WT)
mRNA
vaccines.
Despite
this
observation,
potential
involvement
of
antigenic
sin
phenomena
remains
unclear.
Our
hypothesis
posited
that
a
greater
number
prior
WT
vaccine
doses
might
lead
reduced
anti-Omicron
neutralization
Abs
following
infection.
To
investigate
this,
we
analyzed
blood
samples
from
human
participants
in
COVID-19
Occupational
Risk,
Seroprevalence,
and
Immunity
among
Paramedics
(CORSIP)
study
who
had
received
at
least
one
before
contracting
Omicron.
The
exposure
variable
was
vaccines
administered,
outcome
angiotensin-converting
enzyme
2
(ACE-2)
percent
inhibition
specific
BA.4/BA.5
Ag.
Contrary
expectations,
our
findings
revealed
more
WT-based
were
associated
with
an
enhanced
Omicron-specific
response.
ACS Infectious Diseases,
Journal Year:
2023,
Volume and Issue:
9(11), P. 2226 - 2251
Published: Oct. 18, 2023
The
latest
RNA
genomic
mutation
of
SARS-CoV-2
virus,
termed
the
Omicron
variant,
has
generated
a
stream
highly
contagious
and
antibody-resistant
strains,
which
in
turn
led
to
classifying
as
variant
concern.
We
systematically
collected
Raman
spectra
from
six
subvariants
available
Japan
(i.e.,
BA.1.18,
BA.2,
BA.4,
BA.5,
XE,
BA.2.75)
applied
machine-learning
algorithms
decrypt
their
structural
characteristics
at
molecular
scale.
Unique
fingerprints
sulfur-containing
amino
acid
rotamers,
purines
pyrimidines,
tyrosine
phenol
ring
configurations,
secondary
protein
structures
clearly
differentiated
subvariants.
These
spectral
characteristics,
were
linked
infectiousness,
transmissibility,
propensity
for
immune
evasion,
revealed
evolutionary
motifs
be
compared
with
outputs
studies.
availability
"metabolomic
snapshot",
was
then
translated
into
barcode
enable
prompt
subvariant
identification,
opened
way
rationalize
real-time
activity
variability.
As
proof
concept,
we
procedure
nasal
swab
sample
retrieved
patient
identified
its
by
coupling
commercially
magnetic
bead
technology
our
newly
developed
analyses.
Applied Biological Chemistry,
Journal Year:
2023,
Volume and Issue:
66(1)
Published: Dec. 13, 2023
Abstract
COVID-19
has
been
a
major
global
health
concern
for
the
past
three
years,
and
currently
we
are
still
experiencing
coronavirus
patients
in
following
years.
The
virus,
known
as
SARS-CoV-2,
shares
similar
genomic
identity
with
previous
viruses
such
SARS-CoV
MERS-CoV.
To
combat
pandemic,
modern
drugs
discovery
techniques
silico
experiments
docking
virtual
screening
have
employed
to
design
new
against
COVID-19.
However,
release
of
human
use
requires
two
safety
assessment
steps
consisting
preclinical
clinical
trials.
bypass
these
steps,
scientists
exploring
potential
repurposing
existing
treatment.
This
approach
involves
evaluating
antiviral
activity
previously
used
treating
respiratory
diseases
other
enveloped
HPV,
HSV,
HIV.
aim
this
study
is
review
drugs,
traditional
medicines,
active
secondary
metabolites
from
plant-based
natural
products
that
target
specific
protein
enzymes
related
SARS-CoV-2.
also
analyzes
chemical
structure
relationship
between
selected
molecules,
particularly
flavonol
groups,
ligands
proteins
or
sites
Jundishapur Journal of Microbiology,
Journal Year:
2024,
Volume and Issue:
16(11)
Published: Jan. 10, 2024
Background:
The
coronavirus
disease
2019
(COVID-19)
poses
a
threat
to
the
global
economy
and
public
health.
Mutations
in
spike
protein
of
virus
can
impact
functional
characteristics
effectiveness
vaccines.
Objectives:
This
study
aimed
analyze
mutations
three
key
regions
protein,
investigate
clinical
presentations,
assess
protective
immune
levels
healthcare
workers
(HCWs)
who
had
received
full
vaccine
doses
but
were
re-infected.
Methods:
In
this
cross-sectional
study,
49
breakthrough-infected
HCWs
included
from
November
2021
May
2022.
After
confirming
COVID-19
reinfection,
SARS-CoV-2
genome
was
extracted
using
ROJE
extraction
kit,
genetic
variation
analysis
performed
through
Sanger
sequencing.
Blood
samples
collected
with
prior
consent,
ELISA
tests
determine
antibody
levels.
Clinical
presentations
recorded,
independent
t-tests
revealed
no
significant
gender-based
differences
C-terminal
point
mutation.
Results:
75.5%
(37/49)
female
(P-value
<
0.05),
25
qualified
for
PCR
gene
observed
25,
10,
1
sequence(s)
domain,
N-terminal
RBD
S1
gene,
respectively.
correlation
patient's
gender,
age,
or
occupation,
they
significantly
more
prevalent
those
underlying
diseases.
63.3%
(31/49)
patients
high
very
IgG
levels,
none
undetectable
at
time
reinfection.
Loss
sense
smell
(69.4%
-
34/49),
sore
throat
(65.3%
32/49),
headache
(59.2%
29/49),
cough
(57.1%
28/49)
most
manifestations
(P
>
0.05)
HCWs,
aligning
pattern
symptoms
seen
Omicron
wave.
However,
loss
taste
showed
results
concerning
manifestation
0.05).
examination
presence
variant
majority
individuals.
Point
region
did
not
vary
based
on
type.
No
difference
between
types
symptoms.
Conclusions:
conclusion,
identified
reinfections
among
vaccinated
workers.
While
prevalent,
correlations
found
demographics
types.
Symptoms
resembled
variant,
notably
as
marker.
Detectable
post-reinfection
suggest
that
vaccine-induced
immunity
remains
robust.
Continuous
monitoring
variants
is
crucial
optimizing
vaccination
strategies
face
evolving
strains.
Pathogens,
Journal Year:
2023,
Volume and Issue:
12(8), P. 1017 - 1017
Published: Aug. 6, 2023
As
of
November
2021,
the
SARS-CoV-2
Omicron
variant
had
made
its
appearance,
gradually
replacing
predominant
Delta
variant.
Since
emergence,
has
been
continuously
evolving
through
more
than
500
strains,
most
which
belong
to
five
sub-variants
known
as
BA.1,
BA.2,
BA.3,
BA.4,
and
BA.5.
The
aim
this
study
was
develop
a
multiplex
polymerase
chain
reaction
(PCR)
that
will
be
able
distinguish
basic
in
rapid
specific
way.
Full
genome
sequences
strains
with
high
frequency
wide
geographical
distribution
were
retrieved
by
NCBI
Virus
ENA
databases.
These
compared
each
other
order
locate
single
nucleotide
polymorphisms
common
all
same
sub-variant.
should
also
capable
distinguishing
not
only
from
but
previously
circulating
variants
well.
Thus,
primers
targeting
characteristic
four
main
branches
BA.5
designed
according
principles
amplification
refractory
mutation
system
(ARMS)
ability
react
under
PCR
conditions.
According
our
results,
ARMS-multiplex
could
successfully
carry
corresponding
mutations.