Angiotensin-converting
enzyme
2
(ACE2)
and
the
transmembrane
serine
protease
(TMPRSS2)
are
recognized
as
entry
proteins
of
severe
acute
respiratory
syndrome
coronavirus
(SARS-CoV-2),
recently
their
Single
Nucleotide
Polymorphisms
(SNP)
have
been
studied
in
different
populations
to
elucidate
impact
on
disease.
The
aim
this
study
was
evaluate
genetic
SNP
ACE2
(rs35803318)
TMPRSS2
(rs2070788)
genes
COVID-19
patients
from
Northeast
Brazil
compared
with
global
populations,
well
expression
quantitative
trait
locus
(eQTL).
For
(rs35803318),
we
found
92.6%
CC,
3.4%
CT,
4.0%
TT
genotype
carriers
SARS-CoV-2-positive
patients.
Surprisingly,
only
frequencies
were
not
Hardy-Weinberg
equilibrium.
rs2070788,
22.3%
GG,
50.7%
AG,
27%
AA
loci
(eQTLs)
revealed
that
rs35803318
associated
an
altered
PIR
gene
expression,
rs2070788
eQTLs
association
lung
tissue.
No
significant
identified
between
distribution
SNPs
'patient's
outcome.
In
conclusion,
our
results
suggest
may
be
protective
factors
for
including
Brazilian
population,
since
presence
does
affect
outcome
described
by
other
studies.
Frontiers in Medicine,
Journal Year:
2024,
Volume and Issue:
11
Published: Aug. 12, 2024
Introduction
Host
genetic
variations
have
been
identified
as
potential
influencers
of
COVID-19
infection.
This
study
aimed
to
examine
the
association
between
transmembrane
serine
protease
type
2
(
TMPRSS2
)
rs2070788
single
nucleotide
polymorphism
(SNP)
and
prognosis
in
Iranian
populations.
Method
case-control
was
performed
on
756
patients
59
healthy
individuals
across
Iran.
Clinical
data,
blood
samples,
presence
rs2070788:
G>A
SNP
were
determined
using
T-ARMS-PCR.
Additionally,
serum
levels
tumor
necrosis
factor
α
(TNF-α),
C-reactive
protein
(CRP),
interleukin-6
(IL-6),
IL-1β
evaluated
collected
samples.
Results
No
significant
found
genotypes
allele
frequencies
susceptibility
or
mortality
from
However,
we
observed
a
substantial
increase
IL-6
CRP
associated
with
severity
COVID-19,
while
no
such
trend
for
TNF-α.
showed
considerable
rise
TNF-α
exclusively
TT
genotype
compared
controls.
Conclusion
In
this
conducted
multiple
cities
Iran,
mortality.
Frontiers in Medicine,
Journal Year:
2024,
Volume and Issue:
11
Published: Dec. 18, 2024
ACE2
and
TMPRSS2
represent
the
major
gateways
for
SARS-CoV-2
cell
entry.
The
presence
of
functional
genetic
polymorphisms
that
affect
gene
expression
may
risk
severe
form
COVID-19
its
fatal
outcome.
Life Science Alliance,
Journal Year:
2023,
Volume and Issue:
6(8), P. e202201813 - e202201813
Published: May 19, 2023
Many
viruses
require
proteolytic
activation
of
their
envelope
proteins
for
infectivity,
and
relevant
host
proteases
provide
promising
drug
targets.
The
transmembrane
serine
protease
2
(TMPRSS2)
has
been
identified
as
a
major
activating
influenza
A
virus
(IAV)
various
coronaviruses
(CoV).
Increased
TMPRSS2
expression
associated
with
higher
risk
severe
infection
enhanced
susceptibility
to
SARS-CoV-2.
Here,
we
found
that
Legionella
pneumophila
stimulates
the
increased
TMPRSS2-mRNA
in
Calu-3
human
airway
cells.
We
flagellin
dominant
structural
component
inducing
expression.
flagellin-induced
increase
was
not
observed
at
this
magnitude
other
virus-activating
proteases.
also
significantly
by
LPS,
Pam3Cys,
Streptococcus
pneumoniae
,
although
less
pronounced.
Multicycle
replication
H1N1pdm
H3N2
IAV
but
SARS-CoV-2
SARS-CoV
treatment.
Our
data
suggest
bacteria,
particularly
flagellated
up-regulate
cells
and,
thereby,
may
support
upon
co-infections.
In
addition,
our
indicate
physiological
role
antimicrobial
response.
Angiotensin-converting
enzyme
2
(ACE2)
and
the
transmembrane
serine
protease
(TMPRSS2)
are
recognized
as
entry
proteins
of
severe
acute
respiratory
syndrome
coronavirus
(SARS-CoV-2),
recently
their
Single
Nucleotide
Polymorphisms
(SNP)
have
been
studied
in
different
populations
to
elucidate
impact
on
disease.
The
aim
this
study
was
evaluate
genetic
SNP
ACE2
(rs35803318)
TMPRSS2
(rs2070788)
genes
COVID-19
patients
from
Northeast
Brazil
compared
with
global
populations,
well
expression
quantitative
trait
locus
(eQTL).
For
(rs35803318),
we
found
92.6%
CC,
3.4%
CT,
4.0%
TT
genotype
carriers
SARS-CoV-2-positive
patients.
Surprisingly,
only
frequencies
were
not
Hardy-Weinberg
equilibrium.
rs2070788,
22.3%
GG,
50.7%
AG,
27%
AA
loci
(eQTLs)
revealed
that
rs35803318
associated
an
altered
PIR
gene
expression,
rs2070788
eQTLs
association
lung
tissue.
No
significant
identified
between
distribution
SNPs
'patient's
outcome.
In
conclusion,
our
results
suggest
may
be
protective
factors
for
including
Brazilian
population,
since
presence
does
affect
outcome
described
by
other
studies.