Viruses,
Journal Year:
2021,
Volume and Issue:
14(1), P. 23 - 23
Published: Dec. 23, 2021
Severe
Acute
Respiratory
Syndrome
Coronavirus
2
(SARS-CoV-2)
quickly
spread
worldwide
following
its
emergence
in
Wuhan,
China,
and
hit
pandemic
levels.
Its
tremendous
incidence
favoured
the
of
viral
variants.
The
current
genome
diversity
SARS-CoV-2
has
a
clear
impact
on
epidemiology
clinical
practice,
especially
regarding
transmission
rates
effectiveness
vaccines.
In
this
study,
we
evaluated
replication
different
isolates
representing
virus
genotypes
which
have
been
isolated
throughout
pandemic.
We
used
three
distinct
cell
lines,
including
Vero
E6
cells
originating
from
monkeys;
Caco-2
cells,
an
intestinal
epithelium
line
humans;
Calu-3
pulmonary
also
humans.
RT-qPCR
to
replicate
by
quantifying
released
culture
supernatant
infected
cells.
found
that
similarly
but
show
very
replicative
capacities
This
was
highlighted
for
lineages
B.1.1.7,
B.1.351
P.1,
are
considered
be
variants
concern.
These
results
underscore
importance
evaluation
characterisation
each
isolate
order
establish
patterns
before
performing
tests,
consideration
ideal
genotype-cell
type
pair
assay.
Clinical Infectious Diseases,
Journal Year:
2021,
Volume and Issue:
74(10), P. 1722 - 1728
Published: Aug. 6, 2021
Abstract
Background
Multiple
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
superspreading
events
suggest
that
aerosols
play
an
important
role
in
driving
the
disease
2019
(COVID-19)
pandemic.
To
better
understand
how
airborne
SARS-CoV-2
transmission
occurs,
we
sought
to
determine
viral
loads
within
coarse
(>5
μm)
and
fine
(≤5
produced
when
breathing,
talking,
singing.
Methods
Using
a
G-II
exhaled
breath
collector,
measured
RNA
emitted
by
COVID-19
patients
during
30
minutes
of
15
Results
Thirteen
participants
(59%)
detectable
levels
aerosols,
including
3
asymptomatic
1
presymptomatic
patient.
Viral
ranged
from
63–5821
N
gene
copies
per
expiratory
activity
participant,
with
high
person-to-person
variation.
Patients
earlier
illness
were
more
likely
emit
RNA.
Two
participants,
sampled
on
day
illness,
accounted
for
52%
total
load.
Overall,
94%
talking
Interestingly,
7
virus
than
constituted
85%
load
detected
our
study.
Virus
cultures
negative.
Conclusions
Fine
singing
contain
may
significant
transmission.
Exposure
especially
indoors,
should
be
mitigated.
Isolating
viable
aerosol
samples
remains
challenging;
whether
this
can
easily
accomplished
emerging
variants
is
urgent
enquiry
necessitating
larger-scale
studies.
Clinical Infectious Diseases,
Journal Year:
2021,
Volume and Issue:
75(1), P. e241 - e248
Published: Sept. 11, 2021
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
epidemiology
implicates
airborne
transmission;
aerosol
infectiousness
and
impacts
of
masks
variants
on
shedding
are
not
well
understood.
Interface Focus,
Journal Year:
2022,
Volume and Issue:
12(2)
Published: Feb. 11, 2022
The
COVID-19
pandemic
is
the
most
severe
caused
by
a
respiratory
virus
since
1918
influenza
pandemic.
As
case
with
other
viruses,
three
modes
of
transmission
have
been
invoked:
contact
(direct
and
through
fomites),
large
droplets
aerosols.
This
narrative
review
makes
that
aerosol
an
important
mode
for
COVID-19,
reviewing
studies
about
bioaerosol
physiology,
detection
infectious
SARS-CoV-2
in
exhaled
bioaerosols,
prolonged
infectivity
persistence
aerosols
created
laboratory,
air
samples,
investigation
outbreaks
manifest
involvement
aerosols,
animal
model
experiments.
joins
A
as
proven
capacity
can
be
spread
route.
has
profound
implications
control
current
future
preparedness.
PLoS Pathogens,
Journal Year:
2021,
Volume and Issue:
17(6), P. e1009644 - e1009644
Published: June 17, 2021
Coronavirus
infection
induces
the
unfolded
protein
response
(UPR),
a
cellular
signalling
pathway
composed
of
three
branches,
triggered
by
proteins
in
endoplasmic
reticulum
(ER)
due
to
high
ER
load.
We
have
used
RNA
sequencing
and
ribosome
profiling
investigate
holistically
transcriptional
translational
murine
hepatitis
virus
(MHV),
often
as
model
for
Betacoronavirus
genus
which
recently
emerged
SARS-CoV-2
also
belongs.
found
UPR
be
amongst
most
significantly
up-regulated
pathways
MHV
infection.
To
confirm
extend
these
observations,
we
show
experimentally
induction
all
branches
both
MHV-
SARS-CoV-2-infected
cells.
Over-expression
ORF8
or
S
alone
is
itself
sufficient
induce
UPR.
Remarkably,
pharmacological
inhibition
greatly
reduced
replication
SARS-CoV-2,
revealing
importance
this
successful
coronavirus
replication.
This
was
particularly
striking
when
IRE1α
ATF6
were
inhibited,
reducing
virion
release
(~1,000-fold).
Together,
data
highlight
promising
antiviral
target
combat
International Journal of Molecular Sciences,
Journal Year:
2021,
Volume and Issue:
22(14), P. 7425 - 7425
Published: July 10, 2021
The
emergence
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
presents
significant
social,
economic
and
political
challenges
worldwide.
SARS-CoV-2
has
caused
over
3.5
million
deaths
since
late
2019.
Mutations
in
the
spike
(S)
glycoprotein
are
particular
concern
because
it
harbours
domain
which
recognises
angiotensin-converting
enzyme
(ACE2)
receptor
is
target
for
neutralising
antibodies.
S
protein
may
induce
alterations
surface
structures,
changing
conformational
B-cell
epitopes
leading
to
a
potential
reduction
vaccine
efficacy.
Here,
we
summarise
how
more
important
variants
SARS-CoV-2,
include
cluster
5,
lineages
B.1.1.7
(Alpha
variant),
B.1.351
(Beta),
P.1
(B.1.1.28/Gamma),
B.1.427/B.1.429
(Epsilon),
B.1.526
(Iota)
B.1.617.2
(Delta)
confer
mutations
their
respective
proteins
enhance
viral
fitness
by
improving
binding
affinity
ACE2
lead
an
increase
infectivity
transmission.
We
further
discuss
these
provide
resistance
against
immune
responses,
either
acquired
naturally
or
induced
vaccination.
This
information
will
be
valuable
guiding
development
vaccines
other
therapeutics
protection
ongoing
disease
2019
(COVID-19)
pandemic.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2021,
Volume and Issue:
unknown
Published: July 19, 2021
Abstract
Background
Multiple
SARS-CoV-2
superspreading
events
suggest
that
aerosols
play
an
important
role
in
driving
the
COVID-19
pandemic.
However,
detailed
roles
of
coarse
(>5μm)
and
fine
(≤5μm)
respiratory
produced
when
breathing,
talking,
singing
are
not
well-understood.
Methods
Using
a
G-II
exhaled
breath
collector,
we
measured
viral
RNA
emitted
by
patients
during
30
minutes
15
singing.
Results
Among
22
study
participants,
13
(59%)
detectable
levels
aerosols,
including
3
asymptomatic
1
presymptomatic
patient.
Viral
loads
ranged
from
63–5,821
N
gene
copies
per
expiratory
activity
Patients
earlier
illness
were
more
likely
to
emit
RNA,
differed
significantly
between
The
largest
proportion
was
(53%),
followed
talking
(41%)
breathing
(6%).
Overall,
constituted
85%
load
detected
our
study.
Virus
cultures
negative.
Conclusions
Fine
contain
than
may
significant
transmission
SARS-CoV-2.
Exposure
should
be
mitigated,
especially
indoor
environments
where
airborne
is
occur.
Isolating
viable
aerosol
samples
remains
challenging,
whether
this
can
easily
accomplished
for
emerging
variants
enquiry
future
studies.
Key
Points
We
sampled
discovered
generated
Antiviral Research,
Journal Year:
2021,
Volume and Issue:
192, P. 105122 - 105122
Published: June 26, 2021
There
are,
besides
remdesivir,
no
approved
antivirals
for
the
treatment
of
SARS-CoV-2
infections.
To
aid
in
search
against
this
virus,
we
explored
use
human
tracheal
airway
epithelial
cells
(HtAEC)
and
small
(HsAEC)
grown
at
air-liquid
interface
(ALI).
These
cultures
were
infected
apical
side
with
one
two
different
isolates.
Each
virus
was
shown
to
replicate
high
titers
extended
periods
time
(at
least
8
days)
and,
particular
an
isolate
D614G
spike
(S)
protein
did
so
more
efficiently
35
°C
than
37
°C.
The
effect
a
selected
panel
reference
drugs
that
added
culture
medium
basolateral
system
explored.
Remdesivir,
GS-441524
(the
parent
nucleoside
remdesivir),
EIDD-1931
molnupiravir)
IFN
(β1
λ1)
all
resulted
dose-dependent
inhibition
viral
RNA
infectious
collected
side.
However,
AT-511
free
base
form
AT-527
currently
clinical
testing)
failed
inhibit
replication
these
vitro
primary
cell
models.
Together,
results
provide
further
studies
aimed
selecting
inhibitors
preclinical
development.