Pathogens,
Journal Year:
2024,
Volume and Issue:
13(4), P. 338 - 338
Published: April 19, 2024
New
evidence
has
suggested
that
oral
and
gut
microflora
may
have
significant
impacts
on
the
predisposition,
development,
stability
of
obesity
in
adults
over
time-although
less
is
known
about
this
phenomenon
children.
Compared
with
healthy-weight
controls,
overweight
obese
adult
patients
are
now
to
harbor
specific
pathogens,
such
as
Nature Aging,
Journal Year:
2024,
Volume and Issue:
4(11), P. 1619 - 1634
Published: Aug. 14, 2024
Aging
is
a
complex
process
associated
with
nearly
all
diseases.
Understanding
the
molecular
changes
underlying
aging
and
identifying
therapeutic
targets
for
aging-related
diseases
are
crucial
increasing
healthspan.
Although
many
studies
have
explored
linear
during
aging,
prevalence
of
mortality
risk
accelerates
after
specific
time
points,
indicating
importance
studying
nonlinear
changes.
In
this
study,
we
performed
comprehensive
multi-omics
profiling
on
longitudinal
human
cohort
108
participants,
aged
between
25
years
75
years.
The
participants
resided
in
California,
United
States,
were
tracked
median
period
1.7
years,
maximum
follow-up
duration
6.8
analysis
revealed
consistent
patterns
markers
substantial
dysregulation
occurring
at
two
major
periods
approximately
44
60
chronological
age.
Distinct
molecules
functional
pathways
these
also
identified,
such
as
immune
regulation
carbohydrate
metabolism
that
shifted
60-year
transition
cardiovascular
disease,
lipid
alcohol
40-year
transition.
Overall,
research
demonstrates
functions
risks
change
nonlinearly
across
lifespan
provides
insights
into
biological
involved
Cell,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
The
factors
shaping
human
microbiome
variation
are
a
major
focus
of
biomedical
research.
While
other
fields
have
used
large
sequencing
compendia
to
extract
insights
requiring
otherwise
impractical
sample
sizes,
the
field
has
lacked
comparably
sized
resource
for
16S
rRNA
gene
amplicon
commonly
quantify
composition.
To
address
this
gap,
we
processed
168,464
publicly
available
gut
samples
with
uniform
pipeline.
We
use
compendium
evaluate
geographic
and
technical
effects
on
variation.
find
that
regions
such
as
Central
Southern
Asia
differ
significantly
from
more
thoroughly
characterized
microbiomes
Europe
Northern
America
composition
alone
can
be
predict
sample's
region
origin.
also
strong
associations
between
primers
DNA
extraction.
anticipate
growing
work,
Human
Microbiome
Compendium,
will
enable
advanced
applied
methodological
Gut Microbes,
Journal Year:
2025,
Volume and Issue:
17(1)
Published: Jan. 28, 2025
Hyperoxaluria,
including
primary
and
secondary
hyperoxaluria,
is
a
disorder
characterized
by
increased
urinary
oxalate
excretion
could
lead
to
recurrent
calcium
kidney
stones,
nephrocalcinosis
eventually
end
stage
renal
disease.
For
high
dietary
(HDOx)
or
its
precursors
intake
key
reason.
Recently,
accumulated
studies
highlight
the
important
role
of
gut
microbiota
in
regulation
homeostasis.
However,
underlying
mechanisms
involving
metabolite
disruptions
hyperoxaluria
remain
poorly
understood.
Here,
we
investigated
therapeutic
efficacy
fecal
transplantation
(FMT)
sourced
from
healthy
rats
fed
with
standard
pellet
diet
against
excretion,
damage
(CaOx)
crystal
depositions
via
using
rat
models.
We
observed
dose-dependent
increases
CaOx
due
accompanied
significant
reductions
diversity
shifts
Ruminococcaceae_UCG-014
Parasutterella
composition.
Metabolomic
analysis
validated
these
findings,
revealing
substantial
decreases
metabolites
associated
microbial
groups.
Transplanting
microbes
effectively
reduced
HDOx-induced
meanwhile
restoring
populations
their
metabolites.
Furthermore,
FMT
treatment
significantly
decrease
kidneys
via,
at
least
part,
upregulating
expressions
intestinal
barrier
proteins
transporters
intestine.
In
conclusion,
our
study
emphasizes
effectiveness
countering
related
These
findings
provide
insights
on
complex
connection
between
caused
microbiota,
offering
promising
avenues
for
targeted
strategies.
Journal of Translational Medicine,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Oct. 15, 2024
The
tumour
microenvironment
represents
a
novel
frontier
in
oncological
research.
Over
the
past
decade,
accumulating
evidence
has
underscored
importance
of
(TME),
including
cells,
stromal
immune
and
various
secreted
factors,
which
collectively
influence
growth,
invasion,
responses
to
therapeutic
agents.
Immune
cells
within
TME
are
now
widely
acknowledged
play
pivotal
roles
development
treatment.
While
some
perspectives
have
posited
that
facilitate
progression
confer
resistance
interventions,
contrasting
conclusions
also
exist.
Affirmative
negative
appear
be
context
dependent,
unified
consensus
yet
reached.
burgeoning
body
research
on
relationship
between
gut
microbiota
tumours
recent
years
led
growing
understanding.
Most
studies
indicated
specific
components
microbiota,
such
as
unique
bacterial
communities
or
secretory
diverse
regulating
TME,
thereby
influencing
prognosis
outcomes
cancer
treatments.
A
detailed
understanding
these
factors
could
provide
insights
into
therapy.
In
this
study,
we
aimed
synthesise
information
interactions
providing
an
in-depth
exploration
potential
guiding
implications
for
future
therapies.
Science Translational Medicine,
Journal Year:
2024,
Volume and Issue:
16(742)
Published: April 10, 2024
A
study
from
Long
et
al.
shows
that
many
pathogens
cause
surgical
site
infections
during
spine
surgery
come
the
patient’s
own
microbiome,
suggesting
a
paradigm
shift
in
understanding
of
questions
effectiveness
current
enhanced
sterility
and
antibiotic
protocols.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Sept. 26, 2024
Abstract
The
human
microbiome
emerges
as
a
promising
reservoir
for
diagnostic
markers
and
therapeutics.
Since
host-associated
microbiomes
at
various
body
sites
differ
diseases
do
not
occur
in
isolation,
comprehensive
analysis
strategy
highlighting
the
full
potential
of
should
include
diverse
specimen
types
diseases.
To
ensure
robust
data
quality
comparability
across
diseases,
we
employ
standardized
protocols
to
generate
sequencing
from
1931
prospectively
collected
specimens,
including
saliva,
plaque,
skin,
throat,
eye,
stool,
with
an
average
depth
5.3
gigabases.
Collected
515
patients,
these
samples
yield
3.7
metagenomes
per
patient.
Our
results
suggest
significant
microbial
variations
types,
unexpected
anatomical
sites.
We
identify
583
unexplored
species-level
genome
bins
(SGBs)
which
189
are
significantly
disease-associated.
Of
note,
existence
resistance
genes
one
was
indicative
same
other
specimens
Annotated
previously
undescribed
SGBs
collectively
harbor
28,315
biosynthetic
gene
clusters
(BGCs),
1050
correlations
combinatorial
approach
identifies
distinct
BGCs,
emphasizing
value
pan-body
pan-disease
microbiomics
source
therapeutic
strategies.