Cell Host & Microbe,
Год журнала:
2013,
Номер
14(5), С. 559 - 570
Опубликована: Ноя. 1, 2013
Microbial
exposure
following
birth
profoundly
impacts
mammalian
immune
system
development.
Microbiota
alterations
are
associated
with
increased
incidence
of
allergic
and
autoimmune
disorders
elevated
serum
IgE
as
a
hallmark.
The
previously
reported
abnormally
high
levels
in
germ-free
mice
suggests
that
immunoregulatory
signals
from
microbiota
required
to
control
basal
levels.
We
report
those
low-diversity
develop
early
life.
B
cells
neonatal
undergo
isotype
switching
at
mucosal
sites
CD4
T-cell-
IL-4-dependent
manner.
A
critical
level
microbial
diversity
is
order
inhibit
induction.
Elevated
lead
mast-cell-surface-bound
exaggerated
oral-induced
systemic
anaphylaxis.
Thus,
appropriate
intestinal
stimuli
during
life
for
inducing
an
network
protects
induction
sites.
Frontiers in Microbiology,
Год журнала:
2018,
Номер
9
Опубликована: Апрель 19, 2018
Lactobacillus
reuteri
(L.
reuteri)
is
a
well-studied
probiotic
bacterium
that
can
colonize
large
number
of
mammals.
In
humans,
L.
found
in
different
body
sites,
including
the
gastrointestinal
tract,
urinary
skin,
and
breast
milk.
The
abundance
varies
among
individuals.
Several
beneficial
effects
have
been
noted.
First,
produce
antimicrobial
molecules,
such
as
organic
acids,
ethanol,
reuterin.
Due
to
its
activity,
able
inhibit
colonization
pathogenic
microbes
remodel
commensal
microbiota
composition
host.
Second,
benefit
host
immune
system.
For
instance,
some
strains
reduce
production
pro-inflammatory
cytokines
while
promoting
regulatory
T
cell
development
function.
Third,
bearing
ability
strengthen
intestinal
barrier,
may
decrease
microbial
translocation
from
gut
lumen
tissues.
Microbial
across
epithelium
has
hypothesized
an
initiator
inflammation.
Therefore,
inflammatory
diseases,
those
located
well
remote
tissues,
be
ameliorated
by
increasing
reuteri.
Notably,
humans
past
decades
correlated
with
increase
incidences
diseases
over
same
period
time.
Direct
supplementation
or
prebiotic
modulation
attractive
preventive
and/or
therapeutic
avenue
against
diseases.
PLoS ONE,
Год журнала:
2016,
Номер
11(5), С. e0154090 - e0154090
Опубликована: Май 26, 2016
Intestinal
microbiota
changes
are
associated
with
the
development
of
obesity.
However,
studies
in
humans
have
generated
conflicting
results
due
to
high
inter-individual
heterogeneity
terms
diet,
age,
and
hormonal
factors,
largely
unexplored
influence
gender.
In
this
work,
we
aimed
identify
differential
gut
signatures
obesity,
as
a
function
gender
body
mass
index
(BMI).
Differences
bacterial
community
structure
were
analyzed
by
16S
sequencing
39
men
36
post-menopausal
women,
who
had
similar
dietary
background,
matched
age
stratified
according
BMI.
We
observed
that
abundance
Bacteroides
genus
was
lower
than
women
(P<0.001,
Q
=
0.002)
when
BMI
>
33.
fact,
decreased
an
increase
Q<0.001).
it
remained
unchanged
within
different
ranges
higher
presence
Veillonella
(84.6%
vs.
47.2%;
X2
test
P
0.001,
0.019)
Methanobrevibacter
genera
0.002,
0.026)
fecal
samples
compared
women.
also
Bilophila
regardless
(P
0.041).
Additionally,
after
correcting
for
sex,
66
taxa
at
level
found
be
plasma
lipids.
Microbiota
explained
31.17%
variation
BMI,
29.04%
triglycerides,
33.70%
high-density
lipoproteins,
46.86%
low-density
28.55%
total
cholesterol.
Our
suggest
may
differ
between
these
differences
influenced
grade
The
divergence
might
dominant
role
definition
prevalence
metabolic
intestinal
inflammatory
diseases.
ABSTRACT
Systemic
lupus
erythematosus
(SLE)
is
the
prototypical
systemic
autoimmune
disease
in
humans
and
characterized
by
presence
of
hyperactive
immune
cells
aberrant
antibody
responses
to
nuclear
cytoplasmic
antigens,
including
characteristic
anti–double-stranded
DNA
antibodies.
We
performed
a
cross-sectional
study
order
determine
if
an
SLE-associated
gut
dysbiosis
exists
patients
without
active
disease.
A
group
20
SLE
remission,
for
which
there
was
strict
inclusion
exclusion
criteria,
recruited,
we
used
optimized
Ion
Torrent
16S
rRNA
gene-based
analysis
protocol
decipher
fecal
microbial
profiles
these
compare
them
with
those
age-
sex-matched
healthy
control
subjects.
found
diversity
be
comparable
based
on
Shannon’s
index.
However,
saw
significantly
lower
Firmicutes
/
Bacteroidetes
ratio
individuals
(median
ratio,
1.97)
than
subjects
4.86;
P
<
0.002).
corroborated
quantitative
PCR
analysis.
Notably,
decrease
some
families
also
detected.
This
reflected,
silico
functional
inference,
overrepresentation
oxidative
phosphorylation
glycan
utilization
pathways
patient
microbiota.
IMPORTANCE
Growing
evidence
suggests
that
microbiota
might
impact
symptoms
progression
diseases.
how
why
this
community
influences
remains
elucidated.
first
report
describing
intestinal
dysbiosis,
it
contributes
understanding
interplay
between
host
disorders.
Cell Host & Microbe,
Год журнала:
2013,
Номер
14(5), С. 559 - 570
Опубликована: Ноя. 1, 2013
Microbial
exposure
following
birth
profoundly
impacts
mammalian
immune
system
development.
Microbiota
alterations
are
associated
with
increased
incidence
of
allergic
and
autoimmune
disorders
elevated
serum
IgE
as
a
hallmark.
The
previously
reported
abnormally
high
levels
in
germ-free
mice
suggests
that
immunoregulatory
signals
from
microbiota
required
to
control
basal
levels.
We
report
those
low-diversity
develop
early
life.
B
cells
neonatal
undergo
isotype
switching
at
mucosal
sites
CD4
T-cell-
IL-4-dependent
manner.
A
critical
level
microbial
diversity
is
order
inhibit
induction.
Elevated
lead
mast-cell-surface-bound
exaggerated
oral-induced
systemic
anaphylaxis.
Thus,
appropriate
intestinal
stimuli
during
life
for
inducing
an
network
protects
induction
sites.