Antibiotics,
Journal Year:
2023,
Volume and Issue:
12(4), P. 739 - 739
Published: April 12, 2023
Infections
caused
by
resistant
strains
of
Acinetobacter
baumannii
are
now
a
global
problem
that
requires
the
immediate
development
new
antimicrobial
drugs.
Combination
therapy
is
one
strategies
used
to
solve
this
problem.
Based
on
information,
purpose
study
was
determine
whether
quercetin
(QUE),
in
combination
with
three
antibiotics,
effective
against
colistin-resistant
A.
(ColR-Ab).
The
effects
QUE
colistin
(COL),
amikacin
(AMK),
and
meropenem
(MEM)
were
evaluated
according
checkerboard
synergy
test.
combinations
+
COL
AMK
showed
synergistic
activity
ColR-Ab
FICI
values
range
0.1875-0.5
0.1875-0.2825,
respectively.
A
4-
16-fold
decrease
MIC
16-
64-fold
detected.
Synergistic
confirmed
time-kill
test,
these
found
be
bactericidal
at
end
24
h.
According
spectrophotometric
measurements,
induced
membrane
damage,
leading
leakage
nucleic
acids.
Cell
lysis
cell
death
SEM
observations.
detected
offers
an
opportunity
for
future
treatment
potential
infections
strains.
Heliyon,
Journal Year:
2023,
Volume and Issue:
9(7), P. e17657 - e17657
Published: June 26, 2023
Over
the
past
decade,
numerous
publications
have
emerged
in
literature
focusing
on
inhibition
of
quorum
sensing
(QS)
by
plant
extracts
and
phenolic
compounds.
However,
there
is
still
a
scarcity
studies
that
delve
into
specific
mechanisms
which
these
compounds
inhibit
QS.
Thus,
our
question
whether
can
QS
or
indirect
manner
to
elucidate
underlying
involved.
This
study
focused
most
studied
system,
namely,
auto-inducer
(AI-1)
type
QS,
represented
N-acyl-homoserine
lactone
(AHL)
signals
AHL-mediated
responses.
Here,
we
analyzed
recent
order
understand
how
act
at
cellular
level,
sub-inhibitory
concentrations,
evaluated
they
may
act.
The
biotechnological
application
inhibitors
holds
promising
prospects
for
pharmaceutical
food
industries,
serving
as
adjunct
therapies
prevention
biofilms
various
surfaces.
Catalysts,
Journal Year:
2023,
Volume and Issue:
13(2), P. 443 - 443
Published: Feb. 18, 2023
Jania
rubens
red
seaweed
has
various
bioactive
compounds
that
can
be
used
for
several
medicinal
and
pharmaceutical
applications.
In
this
study,
we
investigate
the
antidiabetic,
anti-inflammatory,
antioxidant
competency
of
polyphenolic
extract
(JRPE)
by
assessing
their
interactions
with
α-amylase,
lipase,
trypsin
enzymes.
HPLC
analysis
revealed
dominance
twelve
compounds.
We
performed
computational
using
as
target
proteins
polyphenols
to
explore
activities
based
on
predicted
modes
binding
sites
following
molecular
modeling
analysis.
The
docking
demonstrated
a
good
affinity
score
noticeable
compositions
rubens.
highest
α-amylase
(PDB:
4W93)
were
kaempferol,
quercetin,
chlorogenic
acid,
−8.4,
−8.8
−8
kcal/mol,
respectively.
Similarly,
lipase
1LPB)
high
scores
−7.1,
−7.4,
−7.2
kcal/mol
Furthermore,
4DOQ)
results,
acid
−7.2,
−7.1
findings
verified
in
vitro
evaluations,
manifesting
comparable
results.
Overall,
these
enlighten
JRPE
properties
different
diabetics’
enzymes
could
further
studied
vivo
investigations
diabetes
treatment.
Pharmaceuticals,
Journal Year:
2023,
Volume and Issue:
16(11), P. 1531 - 1531
Published: Oct. 30, 2023
Bacterial
and
fungal
biofilm
has
increased
antibiotic
resistance
plays
an
essential
role
in
many
persistent
diseases.
Biofilm-associated
chronic
infections
are
difficult
to
treat
reduce
the
efficacy
of
medical
devices.
This
global
problem
prompted
extensive
research
find
alternative
strategies
fight
microbial
infections.
Plant
bioactive
metabolites
with
antibiofilm
activity
known
be
potential
resources
alleviate
this
problem.
The
phytochemical
screening
some
medicinal
plants
showed
different
active
groups,
such
as
stilbenes,
tannins,
alkaloids,
terpenes,
polyphenolics,
flavonoids,
lignans,
quinones,
coumarins.
Synergistic
effects
can
observed
interaction
between
plant
compounds
conventional
drugs.
review
analyses
summarises
current
knowledge
on
synergistic
combination
antimicrobials
against
biofilms
Staphylococcus
aureus,
Pseudomonas
aeruginosa,
Candida
albicans.
synergism
modify
inhibit
mechanisms
acquired
resistance,
undesirable
effects,
obtain
appropriate
therapeutic
effect
at
lower
doses.
A
deeper
these
combinations
their
possible
targets
is
needed
develop
next-generation
novel
and/or
improve
drug-resistant
attributed
biofilm.
Chemical Physics Impact,
Journal Year:
2024,
Volume and Issue:
8, P. 100501 - 100501
Published: Feb. 2, 2024
This
study
aims
to
determine
the
antibacterial
efficacy
of
a
bioactive
phytochemical
quercetin
(QUR),
compared
reference
antibiotic
ciprofloxacin
(CIP),
using
in
vitro
and
silico
approaches.
Following
molecular
docking,
QUR
showed
strong
affinity
druggable
targets
from
bacteria:
Sortase
B,
Toxic
Shock
Syndrome
Toxin-1,
Multidrug
Efflux
Pump
AdeJ
LasR,
with
binding
energies
-6.9
–
-10.3
kcal/mol.
CIP
displayed
-7.3
-7.4
kcal/mol
against
target
proteins.
had
stronger
MEPJ
(binding
energy:
-8.1
kcal/mol)
LasR
kcal/mol),
having
kcal/mol,
respectively.
Molecular
dynamics
simulation
validated
formation
complex
QUR,
which
was
energetically
more
stable
LasR-CIP
complex.
Disc
diffusion
method,
nutrient
agar
medium,
demonstrated
activity
both
gram-negative
(Acinetobacter
baumannii,
Escherichia
coli,
Pseudomonas
aeruginosa)
gram-positive
(Staphylococcus
aureus,
Streptococcus
pneumonia)
bacteria
zone
diameter
inhibition
10
23
mm
7
21
mm,
synergistic
effect,
growth
inhibitory
index
(GII)
values
0.65
1.15,
combined
PIP.
QUR-CEF
combination
synergy
E.
P.
aeruginosa,
S.
pneumoniae
GIIs
0.60
0.73.
Pharmacokinetics
studies
through
for
revealed
acceptable
parametric
values,
comparable
that
CIP.
Thus,
current
integrated
analysis
authenticated
as
lead
molecule
combat
bacterial
infections,
alone
or
conventionally
used
antibiotics
(PIP
CEF).
For
further
validation
our
results,
clinical
experiments
are
suggested.
Journal of Materials Chemistry B,
Journal Year:
2024,
Volume and Issue:
12(11), P. 2894 - 2904
Published: Jan. 1, 2024
Lysine
and
fatty
acid-tethered
amphiphilic
copolymers
exhibited
potent
antibacterial
activity
against
Gram-positive
(
B.
subtilis
)
Gram-negative
E.
coli
bacteria
with
side
chain
degradability
in
the
presence
of
an
enzyme
pH.
Frontiers in Microbiology,
Journal Year:
2021,
Volume and Issue:
12
Published: Sept. 14, 2021
The
emergence
of
multidrug-resistant
bacteria
stimulates
the
search
for
new
substitutes
to
traditional
antimicrobial
agents,
especially
molecules
with
antivirulence
properties,
such
as
those
that
interfere
quorum
sensing
(QS).
This
study
aimed
evaluate
potential
phenolic
compounds
QS
inhibition
in
a
biosensor
strain
(
Chromobacterium
violaceum
)
and
three
foodborne
bacterial
species
Aeromonas
hydrophila
,
Salmonella
enterica
serovar
Montevideo,
Serratia
marcescens
).
Initially,
an
silico
molecular
docking
was
performed
select
greatest
inhibition,
using
structural
variants
CviR
regulator
C.
target.
Curcumin,
capsaicin,
resveratrol,
gallic
acid,
phloridizin
presented
good
affinity
at
least
four
variants.
These
were
tested
activity,
biofilm
formation,
anti-QS
activity.
activity
when
combined
kanamycin
also
assessed.
resveratrol
inhibited
up
50%
violacein
production
by
.
Biofilm
formation
80%
A.
capsaicin
curcumin
40%
S.
Montevideo
60%
Curcumin
completely
swarming
motility
Additionally,
increased
sensitivity
kanamycin.
results
indicate
concentrations
low
6μM
are
inhibitors
besides
having
properties
higher
concentrations,
encouraging
applications
food
pharmaceutical
industries.
Natural Product Reports,
Journal Year:
2021,
Volume and Issue:
39(2), P. 231 - 248
Published: Aug. 19, 2021
Since
the
early
1970s,
375
natural
products
have
been
identified
from
members
of
fungus-farming
termite
symbiosis,
and
this
review
summarises
discusses
ecological
implications
presence
vast
chemical
repertoire.
Current Pharmaceutical Biotechnology,
Journal Year:
2024,
Volume and Issue:
25(13), P. 1664 - 1692
Published: Oct. 1, 2024
Considering
the
limited
number
of
current
effective
treatments,
Multidrug-
Resistant
(MDR)
illnesses
have
grown
to
be
a
serious
concern
public
health.
It
has
become
necessary
look
for
new
antimicrobial
drugs
because
emergence
resistance
numerous
kinds
antibiotics.
The
use
flavonoids
is
one
phytotherapeutic
strategy
that
been
researched
as
potential
remedy
this
issue.
Secondary
plant
compounds
called
found
an
antibacterial
effect
against
resistant
microorganisms.
Nanomaterials,
Journal Year:
2022,
Volume and Issue:
12(10), P. 1648 - 1648
Published: May 12, 2022
This
paper
aimed
to
develop
two
types
of
support
materials
with
a
mesoporous
structure
mobile
crystalline
matter
(known
in
the
literature
as
MCM,
namely
MCM-41
and
MCM-48)
load
them
gallic
acid.
Soft
templating
methodology
was
chosen
for
preparation
structures-the
cylindrical
micelles
certain
structural
characteristics
being
formed
due
hydrophilic
hydrophobic
intermolecular
forces
which
occur
between
molecules
surfactants
(cetyltrimethylammonium
bromide-CTAB)
when
minimal
micellar
ionic
concentration
is
reached.
These
supports
were
loaded
acid
using
three
different
MCM-gallic
ratios
(1:0.41;
1:0.82
1:1.21)-and
their
characterizations
by
FTIR,
SEM,
XRD,
BET
drug
release
performed.
It
worth
mentioning
that
loading
carried
out
vacuum-assisted
methodology:
are
firstly
kept
under
vacuum
at
~0.1
barr
30
min
followed
addition
polyphenol
solutions.
The
solutions
adapted
such
final
volume
covered
wet
and-in
this
case-upon
reaching
normal
atmospheric
pressure,
solution
pushed
inside
pores,
thus
polyphenols
mainly
pores.
Based
on
SBET
data,
it
can
be
seen
specific
surface
area
decreased
considerably
increasing
ratio
acid;
3.07
4.25
times
MCM-48,
respectively.
sample
highest
content
further
evaluated
from
biological
point
view,
alone
or
association
amoxicillin
administration.
As
expected,
MCM-48
not
protective
against
infections-but,
acid,
potentiated
inhibition
recorded
tested
gram-negative
bacterial
strains.
Moreover,
important
mention
these
systems
efficient
recovery
gut
microbiota
after
exposure
antibiotics,
instance.
Heliyon,
Journal Year:
2023,
Volume and Issue:
9(3), P. e14152 - e14152
Published: Feb. 28, 2023
The
expression
of
many
virulence
genes
in
bacteria
is
regulated
by
quorum
sensing
(QS),
and
the
inhibition
this
mechanism
has
been
intensely
investigated.
N-acetylcysteine
(NAC)
good
antibacterial
activity
able
to
interfere
with
biofilm-related
respiratory
infections,
but
little
known
whether
compound
an
effect
on
bacterial
QS
communication.
This
work
aimed
evaluate
potential
NAC
as
a
inhibitor
(QSI)
Pseudomonas
aeruginosa
PAO1
through
silico
vitro
analyses,
well
combination
antibiotic
tobramycin.
Initially,
molecular
docking
analysis
was
performed
between
regulatory
proteins,
LasR
RhlR,
P.
NAC,
3-oxo-C12-HSL,
C4-HSL,
furanone
C30.
sub-inhibitory
concentration
determined
growth
curves.
Then,
we
tests
using
reporter
strains
lasB-gfp
rhlA-gfp,
QS-related
phenotypes.
Finally,
synergistic
tobramycin
calculated
fractional
inhibitory
concentrations
index
(FICi)
investigated
against
growth,
pigment
production,
biofilm
formation.
In
study,
bound
RhlR
proteins
similar
manner
AHL
cognate,
suggesting
that
it
may
be
bind
receptor
vivo.
biosensor
assay,
GFP
signal
turned
down
presence
at
1000,
500,
250,
125
μM
for
rhlA-gfp
(p
<
0.05),
effect.
Pyocyanin
rhamnolipids
decreased
0.05)
up
34
37%,
respectively,
μM.
Swarming
swimming
motilities
were
inhibited
250
10000
Additionally,
2500
reduced
NAC-tobramycin
showed
FICi
0.8,
best
2500–1.07
μM,
inhibiting
formation
60%,
besides
reducing
pyocyanin
pyoverdine
production.
Confocal
microscopy
images
revealed
stronger,
dense,
compact
control,
while
treated
became
thinner
more
dispersed.
Overall,
low
promising
anti-QS
properties
PAO1,
adding
its
already
antibiofilm
agent.