Brucella abortushijacks the host protein Slc2a1via the SepA effector to promote intracellular survival in macrophages
Yuanhao Yang,
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Youli Zu,
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Xin Wang
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et al.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 20, 2025
Abstract
Brucella
spp.
are
facultative
intracellular
bacteria
that
infect
and
induce
brucellosis
in
a
diverse
range
of
mammalian
hosts.
The
disease
causes
major
global
economic
losses
also
is
worldwide
threat
to
public
health
security.
Characterization
bacterial
host
factors
promote
survival
key
for
the
prevention
control
brucellosis.
In
this
study,
we
identified
proteins
involved
Brucella
abortus
A19
RAW264.7
macrophage
cells
by
liquid
chromatography-mass
spectrometry
macrophages
with
or
without
B.
infection.
functions
these
proteins,
signaling
pathways
which
participate,
domain
entries
enriched
subcellular
localization
differentially-expressed
were
deciphered.
Differential
protein
expression
revealed
Slc2a1,
Glycolytic
protein,
was
significantly
upregulated
infected
cells.
This
observation
confirmed
qRT-PCR
Western
blotting
studies.
role
Slc2a1
probed
overexpressing
knocking
down
SLC2A1
Overproduction
promoted
proliferation
whereas
knockdown
inhibited
bacterium.
Finally,
determined
Secreted
Effector
Protein
A
(SepA)
effector
enhanced
Thus,
stimulates
via
SepA
aid
environment
suggests
may
be
novel
antibacterial
target
combat
Language: Английский
(P)ppGpp synthetase Rel facilitates cellulose formation of biofilm by regulating glycosyltransferase in Brucella abortus
Xiao Fang Liu,
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Pingping Wang,
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Zheng Dong
No information about this author
et al.
International Journal of Biological Macromolecules,
Journal Year:
2025,
Volume and Issue:
unknown, P. 140022 - 140022
Published: Jan. 1, 2025
Language: Английский
What Is the Impact of Antibiotic Resistance Determinants on the Bacterial Death Rate?
Antibiotics,
Journal Year:
2025,
Volume and Issue:
14(2), P. 201 - 201
Published: Feb. 14, 2025
Objectives:
Antibiotic-resistant
bacteria
are
widespread,
with
resistance
arising
from
chromosomal
mutations
and
genes
located
in
the
chromosome
or
mobile
genetic
elements.
While
determinants
often
reduce
bacterial
growth
rates,
their
influence
on
death
under
bactericidal
antibiotics
remains
poorly
understood.
When
exposed
to
which
they
susceptible,
typically
undergo
a
two-phase
decline:
fast
initial
exponentially
decaying
phase,
followed
by
persistent
slow-decaying
phase.
This
study
examined
how
affect
rates
during
both
phases.
Methods:
We
analyzed
of
ampicillin-exposed
Escherichia
coli
populations
strains
sensitive
ampicillin
but
resistant
nalidixic
acid,
rifampicin,
both,
carrying
conjugative
plasmids
RN3
R702.
Results:
Single
mutants
acid
rifampicin
decayed
faster
than
cells
early
whereas
double-resistant
mutant
exhibited
prolonged
survival.
These
contrasting
impacts
suggest
epistatic
interactions
between
mutations.
Persistent-phase
for
did
not
differ
significantly
wild-type
cells.
In
contrast,
plasmid-carrying
displayed
distinct
dynamics:
R702
plasmid-bearing
showed
higher
persistent-phase
plasmid-free
cells,
while
lower
rates.
Conclusions:
Bactericidal
may
kill
other
more
effectively
Moreover,
epistasis
occur
when
different
same
cell,
impacting
potential
antibiotic
choice.
results
have
significant
implications
optimizing
eradication
protocols
clinical
settings,
as
well
animal
health
industrial
food
safety
management.
Language: Английский
Serine/threonine protein kinase mediates rifampicin resistance in Brucella melitensis through interacting with ribosomal protein RpsD and affecting antioxidant capacity
mSystems,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 5, 2024
ABSTRACT
Brucellosis,
a
zoonotic
disease,
has
re-emerged
in
both
humans
and
animals,
causing
significant
economic
losses
globally.
Recently,
an
increasing
number
of
rifampicin-resistant
Brucella
strains
have
been
isolated
worldwide
without
detectable
mutations
known
antibiotic
resistance
genes.
Here,
this
study
identified
the
deletion
serine/threonine
protein
kinase
(STPK)
gene
B.
melitensis
as
efficient
trigger
for
rifampicin
using
bioinformatics
predictions,
transposon
mutant
library,
mutation
strains.
Notably,
absence
STPK
could
increase
expression
ribosomal
proteins
genes
involved
sulfur
metabolism
reduced
glutathione,
decrease
NADPH
oxidase
activity
NADP
+
/NADPH
ratio,
which
is
associated
with
antioxidant
capacity
.
Moreover,
co-immunoprecipitation
revealed
that
efficiently
interact
RpsD,
possibly
altering
translation
riboswitch
expression.
These
findings
demonstrate
mediates
by
regulating
to
counteract
reactive
oxygen
species
induced
rifampicin.
Furthermore,
approaches
developed
provide
platform
screening
new
spp.,
or
its
pathway
can
serve
potential
target
drug
development
against
spp.
IMPORTANCE
New
via
predictions
whole-genome
mechanisms
,
function
interaction
proteins.
Language: Английский