Frontiers in Cell and Developmental Biology,
Journal Year:
2022,
Volume and Issue:
10
Published: April 14, 2022
The
gut
microbiome
has
a
tremendous
influence
on
human
physiology,
including
the
nervous
system.
During
fetal
development,
initial
colonization
of
coincides
with
development
system
in
timely,
coordinated
manner.
Emerging
studies
suggest
an
active
involvement
and
its
metabolic
by-products
regulating
early
brain
development.
However,
any
disruption
during
this
developmental
process
can
negatively
impact
functionality,
leading
to
range
neurodevelopment
neuropsychiatric
disorders
(NPD).
In
review,
we
summarize
recent
evidence
as
how
association
major
neurodevelopmental
psychiatric
such
autism
spectrum
disorders,
attention-deficit
hyperactivity
disorder,
schizophrenia.
Further,
discuss
alterations
also
play
role
inducing
drug
resistance
affected
individuals.
We
propose
model
that
establishes
direct
link
dysbiosis
exacerbated
inflammatory
state,
functional
deficits
associated
NPD.
Based
existing
research,
framework
whereby
diet
intervention
boost
mental
wellness
subjects
call
for
further
research
better
understanding
mechanisms
govern
gut-brain
axis
may
lead
novel
approaches
study
pathophysiology
treatment
disorders.
Journal of Neurogastroenterology and Motility,
Journal Year:
2019,
Volume and Issue:
25(1), P. 48 - 60
Published: Jan. 10, 2019
Disturbances
along
the
brain-gut-microbiota
axis
may
significantly
contribute
to
pathogenesis
of
neurodegenerative
disorders.
Alzheimer's
disease
(AD)
is
most
frequent
cause
dementia
characterized
by
a
progressive
decline
in
cognitive
function
associated
with
formation
amyloid
beta
(Aβ)
plaques
and
neurofibrillary
tangles.
Alterations
gut
microbiota
composition
induce
increased
permeability
barrier
immune
activation
leading
systemic
inflammation,
which
turn
impair
blood-brain
promote
neuroinflammation,
neural
injury,
ultimately
neurodegeneration.
Recently,
Aβ
has
also
been
recognized
as
an
antimicrobial
peptide
participating
innate
response.
However,
dysregulated
state,
reveal
harmful
properties.
Importantly,
bacterial
amyloids
through
molecular
mimicry
elicit
cross-seeding
misfolding
microglial
priming.
The
seeding
propagation
occur
at
different
levels
axis.
potential
mechanisms
spreading
include
neuron-to-neuron
or
distal
neuron
spreading,
direct
crossing
via
other
cells
astrocytes,
fibroblasts,
microglia,
system
cells.
A
growing
body
experimental
clinical
data
confirms
key
role
dysbiosis
microbiota-host
interactions
convergence
gut-derived
inflammatory
response
together
aging
poor
diet
elderly
AD.
Modification
food-based
therapy
probiotic
supplementation
create
new
preventive
therapeutic
options
Journal of Alzheimer s Disease,
Journal Year:
2016,
Volume and Issue:
51(4), P. 979 - 984
Published: April 12, 2016
We
are
researchers
and
clinicians
working
on
Alzheimer’s
disease
(AD)
or
related
topics,
we
write
to
express
our
concern
that
one
particular
aspect
of
the
has
been
neglected,
even
thoug
...
Nutrition Reviews,
Journal Year:
2016,
Volume and Issue:
74(10), P. 624 - 634
Published: Sept. 15, 2016
It
has
been
hypothesized
that
alterations
in
the
composition
of
gut
microbiota
might
be
associated
with
onset
certain
human
pathologies,
such
as
Alzheimer
disease,
a
neurodegenerative
syndrome
cerebral
accumulation
amyloid-β
fibrils.
shown
bacteria
populating
can
release
significant
amounts
amyloids
and
lipopolysaccharides,
which
play
role
modulation
signaling
pathways
production
proinflammatory
cytokines
related
to
pathogenesis
disease.
Additionally,
nutrients
have
affect
well
formation
aggregation
amyloid-β.
This
suggests
modulating
microbiome
amyloidogenesis
through
specific
nutritional
interventions
prove
an
effective
strategy
prevent
or
reduce
risk
review
examines
possible
dissemination
amyloids,
regulation
gut–brain
axis,
potential
amyloidogenic
properties
bacteria,
impact
on
amyloid
relation
Transfusion,
Journal Year:
2016,
Volume and Issue:
56(5), P. 1138 - 1147
Published: Feb. 10, 2016
Recent
studies
have
revealed
that
the
blood
of
healthy
humans
is
not
as
sterile
previously
supposed.
The
objective
this
study
was
to
provide
a
comprehensive
description
microbiome
present
in
different
fractions
individuals.The
conducted
30
donors
French
national
collection
center
(Établissement
Français
du
Sang).
We
set
up
16S
rDNA
quantitative
polymerase
chain
reaction
assay
well
targeted
metagenomics
sequencing
pipeline
specifically
designed
analyze
microbiome,
which
we
used
on
whole
(buffy
coat
[BC],
red
cells
[RBCs],
and
plasma).Most
bacterial
DNA
located
BC
(93.74%),
RBCs
contain
more
(6.23%)
than
plasma
(0.03%).
distribution
for
each
fraction
spreads
over
relatively
broad
range
among
donors.
At
phylum
level,
mostly
from
Proteobacteria
(more
80%)
but
also
Actinobacteria,
Firmicutes,
Bacteroidetes.
deeper
taxonomic
levels,
there
are
striking
differences
between
profiles
fractions.We
demonstrate
diversified
exists
blood.
This
has
most
likely
an
important
physiologic
role
could
be
implicated
certain
transfusion-transmitted
infections.
In
regard,
amount
or
profile
monitored
improve
safety
supply.
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2017,
Volume and Issue:
7
Published: July 11, 2017
Although
the
potential
contribution
of
human
gastrointestinal
(GI)
tract
microbiome
to
health,
aging
and
disease
is
becoming
increasingly
acknowledged,
molecular
mechanics
signaling
pathways
just
how
this
accomplished
not
well
understood.
Major
bacterial
species
GI
tract,
such
as
abundant
Gram-negative
bacilli
Bacteroides
fragilis
(B.
fragilis)
Escherichia
coli
(E.
coli),
secrete
a
remarkably
complex
array
pro-inflammatory
neurotoxins
which,
when
released
from
confines
healthy
are
pathogenic
highly
detrimental
homeostatic
function
neurons
in
central
nervous
system
(CNS).
For
first
time
here
we
report
presence
lipopolysaccharide
(LPS)
brain
lysates
hippocampus
superior
temporal
lobe
neocortex
Alzheimer's
(AD)
brains.
Mean
LPS
levels
varied
2-fold
increases
3-fold
hippocampus,
AD
over
age-matched
controls,
however
some
samples
advanced
hippocampal
cases
exhibited
up
26-fold
increase
controls.
This
'Perspectives'
paper
will
further
highlight
very
recent
research
on
CNS,
update
current
findings
that
implicate
microbiome-derived
an
important
internal
contributor
inflammatory
degeneration
CNS.
Frontiers in Immunology,
Journal Year:
2018,
Volume and Issue:
9
Published: March 2, 2018
Uterine
microbiota
have
been
reported
under
various
conditions
and
populations,
however
it
is
uncertain
the
level
to
which
these
bacteria
are
residents
that
maintain
homeostasis,
tourists
readily
eliminated
or
invaders
contribute
human
disease.
This
review
provides
a
historical
timeline
summarizes
current
status
of
this
topic
with
aim
promoting
research
priorities
discussion
on
controversial
topic.
Discrepancies
exist
in
reports
uterine
critically
reviewed
examined.
Established
putative
routes
bacterial
seeding
uterus
interactions
distal
mucosal
sites
discussed.
Based
upon
literature
we
highlight
need
for
additional
robust
clinical
translational
studies
area.
In
addition,
discuss
necessity
investigating
host-microbiota
physiologic
functional
impact
local
endometrial
microenvironment
as
mechanisms
may
influence
poor
reproductive,
obstetric
gynecologic
health
outcomes
sequelae.
Nature Communications,
Journal Year:
2020,
Volume and Issue:
11(1)
Published: March 31, 2020
Abstract
Evidence
is
mounting
that
the
gut-brain
axis
plays
an
important
role
in
mental
diseases
fueling
mechanistic
investigations
to
provide
a
basis
for
future
targeted
interventions.
However,
shotgun
metagenomic
data
from
treatment-naïve
patients
are
scarce
hampering
comprehensive
analyses
of
complex
interaction
between
gut
microbiota
and
brain.
Here
we
explore
fecal
microbiome
based
on
90
medication-free
schizophrenia
81
controls
identify
microbial
species
classifier
distinguishing
with
area
under
receiver
operating
characteristic
curve
(AUC)
0.896,
replicate
microbiome-based
disease
45
(AUC
=
0.765).
Functional
potentials
associated
include
differences
short-chain
fatty
acids
synthesis,
tryptophan
metabolism,
synthesis/degradation
neurotransmitters.
Transplantation
schizophrenia-enriched
bacterium,
Streptococcus
vestibularis
,
appear
induces
deficits
social
behaviors,
alters
neurotransmitter
levels
peripheral
tissues
recipient
mice.
Our
findings
new
leads
further
cohort
studies
animal
models.
Frontiers in Aging Neuroscience,
Journal Year:
2018,
Volume and Issue:
10
Published: Feb. 22, 2018
This
review
proposes
that
LPS
(Lipopolysaccharide,
found
in
the
wall
of
all
Gram-negative
bacteria)
could
play
a
role
causing
sporadic
Alzheimer's
Disease
(AD).
is
based
part
upon
recent
studies
showing
that:
E
coli
bacteria
can
form
extracellular
amyloid;
bacterial-encoded
16S
rRNA
present
human
brains
with
over
70%
being
bacteria;
ultrastructural
analyses
have
shown
microbes
erythrocytes
AD
patients;
blood
levels
patients
are
3-fold
control;
combined
focal
cerebral
ischemia
and
hypoxia
produced
amyloid-like
plaques
myelin
injury
adult
rat
cortex.
Moreover,
bacterial
was
aging
control
brains,
though
were
much
higher
brains.
In
addition,
co-localized
amyloid
plaques,
peri-vascular
amyloid,
neurons,
oligodendrocytes
Based
postulate
caused
oligodendrocyte
injury,
degraded
Myelin
Basic
Protein
(dMBP)
to
be
compared
Immunofluorescence
showed
dMBP
β
(Aβ)
brain,
other
molecules
walls
vesicles
periventricular
white
matter.
These
data
led
hypothesis
acts
on
leukocyte
microglial
TLR4-CD14/TLR2
receptors
produce
NFĸB
mediated
increases
cytokines
which
increase
Aβ
levels,
damage
brain.
Since
Aβ1-42
also
an
agonist
for
TLR4
receptors,
this
vicious
cycle
accounts
relentless
progression
AD.
Thus,
LPS,
receptor
complex,
might
treatment
or
prevention
targets
Keywords:
disease,
Lipopolysaccharide,
Cytokines,
TLR4,
CD14,
Myelin,
MBP,
oligodendrocytes,
Amyloid
plaque,
perivascular