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Variability of antibiotic susceptibility and toxin production of Staphylococcus aureus strains isolated from skin, soft tissue, and bone related infections.
[pyomyositis]
Staphylococcus
aureus
is
an
opportunistic
commensal
bacterium
that
mostly
colonizes
the
skin
and
soft
tissues
.
The
pathogenicity
of
S
.
aureus
is
due
to
both
its
ability
to
resist
antibiotics
,
and
the
production
of
toxins
.
Here
,
we
characterize
a
group
of
genes
responsible
for
toxin
production
and
antibiotic
resistance
of
S
.
aureus
strains
isolated
from
skin
,
soft
tissue
,
and
bone
related
infections
.
A
total
of
136
S
.
aureus
strains
were
collected
from
five
different
types
of
infection
:
furuncles
,
pyomyositis
,
abscesses
,
Buruli
ulcers
,
and
osteomyelitis
,
from
hospital
admissions
and
out-patients
in
Benin
.
All
strains
were
resistant
to
benzyl
penicillin
,
while
25
%
were
resistant
to
methicillin
,
and
all
showed
sensitivity
to
vancomycin
.
Panton
-
Valentine
leukocidin
(
PVL
)
was
the
most
commonly
produced
virulence
factor
(
70
%
)
,
followed
by
staphylococcal
enterotoxin
B
(
44
%
)
.
Exfoliative
toxin
B
was
produced
by
1
.
3
%
of
the
strains
,
and
was
only
found
in
isolates
from
Buruli
ulcers
.
The
tsst-
1
,
sec
,
and
seh
genes
were
rarely
detected
(
≤
1
%
)
.
This
study
provides
new
insight
into
the
prevalence
of
toxin
and
antibiotic
resistance
genes
in
S
.
aureus
strains
responsible
for
skin
,
soft
tissue
,
and
bone
infections
.
Our
results
showed
that
PVL
was
strongly
associated
with
pyomyositis
and
osteomyelitis
,
and
that
there
is
a
high
prevalence
of
PVL-MRSA
skin
infections
in
Benin
.
Diseases
Validation
Diseases presenting
"and"
symptom
achondroplasia
adrenomyeloneuropathy
aniridia
carcinoma of the gallbladder
cutaneous mastocytosis
cystinuria
esophageal squamous cell carcinoma
harlequin ichthyosis
hodgkin lymphoma, classical
hydrocephalus with stenosis of the aqueduct of sylvius
kallmann syndrome
liposarcoma
locked-in syndrome
neonatal adrenoleukodystrophy
omenn syndrome
oral submucous fibrosis
pleomorphic liposarcoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
sneddon syndrome
triple a syndrome
trochlear dysplasia
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