MedComm,
Journal Year:
2025,
Volume and Issue:
6(2)
Published: Jan. 30, 2025
Inflammatory
bowel
diseases
(IBDs),
such
as
Crohn's
disease
(CD)
and
ulcerative
colitis
(UC),
represent
a
growing
global
health
concern.
Restoring
the
balance
of
gut
microbiota,
crucial
factor
in
intestinal
health,
offers
potential
for
treating
IBD.
DP7,
novel
antimicrobial
peptide
with
potent
antibacterial
activity,
was
investigated
its
anti-inflammatory
effects
dextran
sulfate
sodium
(DSS)-induced
UC
mouse
model.
DP7
significantly
ameliorated
key
parameters,
including
activity
index,
weight
loss,
shortened
colon
length,
while
preserving
colonic
epithelial
integrity
reducing
inflammatory
infiltration.
Further
analysis
revealed
targets
highlighting
significant
role
Muribaculaceae
bacteria
during
states.
To
further
explore
microbiota
DP7's
efficacy,
fecal
transplantation
(FMT)
performed
using
feces
from
DP7-treated
mice.
FMT
successfully
recipient
mice,
providing
evidence
microbiome
IBD
treatment
ability
to
modulate
therapeutic
benefit.
Moreover,
our
findings
suggest
that
modulation
immune
system
is
intricately
linked
complex
microbial
environment.
Our
demonstrate
effectively
mitigates
inflammation,
attenuates
barrier
dysfunction,
shapes
suggesting
agent
UC.
Microbiome,
Journal Year:
2024,
Volume and Issue:
12(1)
Published: Jan. 3, 2024
The
overgrowth
of
Desulfovibrio,
an
inflammation
promoting
flagellated
bacteria,
has
been
found
in
ulcerative
colitis
(UC)
patients.
However,
the
molecular
mechanism
remains
unestablished.
relative
abundance
Desulfovibrio
vulgaris
(D.
vulgaris)
stool
samples
UC
patients
was
detected.
Mice
were
treated
with
dextran
sulfate
sodium
to
induce
or
without
administration
D.
flagellin
(DVF),
and
severity
leucine-rich
repeat
containing
19
(LRRC19)
signaling
assessed.
interaction
between
DVF
LRRC19
identified
by
surface
plasmon
resonance
intestinal
organoid
culture.
Lrrc19-/-
Tlr5-/-
mice
used
investigate
indispensable
role
LRRC19.
Finally,
blockade
DVF-LRRC19
selected
through
virtual
screening
efficacy
enriched
fecal
correlated
disease
severity.
treatment
significantly
exacerbated
germ-free
conventional
mice.
Mechanistically,
could
interact
(rather
than
TLR5)
organoids,
then
production
pro-inflammatory
cytokines.
Lrrc19
knockdown
blunted
colitis.
Furthermore,
typhaneoside,
a
binding
interfaces,
blocked
dramatically
ameliorated
DVF-induced
promote
interaction.
Targeting
might
be
new
therapeutic
strategy
for
therapy.
Video
Abstract.
Gut Microbes,
Journal Year:
2024,
Volume and Issue:
16(1)
Published: March 25, 2024
Background
Inflammatory
bowel
disease
(IBD)
is
characterized
by
immune-mediated,
chronic
inflammation
of
the
intestinal
tract.
The
occurrence
IBD
driven
complex
interactions
multiple
factors.
objective
this
study
was
to
evaluate
therapeutic
effects
IAA
in
colitis.
MedComm,
Journal Year:
2025,
Volume and Issue:
6(2)
Published: Jan. 30, 2025
Inflammatory
bowel
diseases
(IBDs),
such
as
Crohn's
disease
(CD)
and
ulcerative
colitis
(UC),
represent
a
growing
global
health
concern.
Restoring
the
balance
of
gut
microbiota,
crucial
factor
in
intestinal
health,
offers
potential
for
treating
IBD.
DP7,
novel
antimicrobial
peptide
with
potent
antibacterial
activity,
was
investigated
its
anti-inflammatory
effects
dextran
sulfate
sodium
(DSS)-induced
UC
mouse
model.
DP7
significantly
ameliorated
key
parameters,
including
activity
index,
weight
loss,
shortened
colon
length,
while
preserving
colonic
epithelial
integrity
reducing
inflammatory
infiltration.
Further
analysis
revealed
targets
highlighting
significant
role
Muribaculaceae
bacteria
during
states.
To
further
explore
microbiota
DP7's
efficacy,
fecal
transplantation
(FMT)
performed
using
feces
from
DP7-treated
mice.
FMT
successfully
recipient
mice,
providing
evidence
microbiome
IBD
treatment
ability
to
modulate
therapeutic
benefit.
Moreover,
our
findings
suggest
that
modulation
immune
system
is
intricately
linked
complex
microbial
environment.
Our
demonstrate
effectively
mitigates
inflammation,
attenuates
barrier
dysfunction,
shapes
suggesting
agent
UC.