Chiang Mai Journal of Science,
Journal Year:
2023,
Volume and Issue:
51(1), P. 1 - 13
Published: Dec. 25, 2023
Eleutherine
bulbosa
is
a
plant
commonly
employed
in
traditional
medicine
across
various
tropical
regions,
including
Thailand.
The
aim
of
this
study
was
to
identify
the
phytochemical
constituents
E.
bulbosa,
evaluate
inhibitory
effects
on
skin
fungal
and
bacterial
pathogens,
examine
anti-inflammatory
cytotoxic
properties
extracts
obtained
from
bulbs
through
n-Hexane,
EtOAc,
EtOH
extraction
methods.
Agar
diffusion,
MIC,
MBC
assays
were
determine
fungistatic,
bacteriostatic,
bactericidal
activities.
EtOAc
extract
demonstrated
highest
inhibition
against
strains
when
compared
other
solvents.
results
revealed
that
exhibited
potent
anti-fungal
effect
T.
rubrum
(the
zones
=
35.00
±
0.00
mm)
comparable
Ketoconazole
34.33
1.16
mm).
antibacterial
activity
S.
pyogenes
observed,
with
zone
diameter
23.00
1.00
mm,
while
lowest
MIC
values
recorded
at
19.53
78.12
μg/ml,
respectively.
Additionally,
we
significant
extracted
n-Hexane
NO
production
LPS-stimulated
RAW
264.7
cells
solvent
extracts.
This
occurred
without
affecting
cell
viability
concentration
range
6.25
25
μg/ml.
Moreover,
less
affected
fibroblasts
suggests
may
be
useful
preventing
inflammatory
diseases
mediated
by
excessive
low
toxicity
normal
cells.
Phytochemical
screening
indicated
presence
compounds
biological
activities
alkaloids,
flavonoids,
phenols,
tannins
all
different
These
findings
suggest
bulb
possess
beneficial
hold
potential
for
further
development
as
new
natural
source
multifunctional
therapeutic
agents,
which
are
safe
effective
broad
spectrum
infectious
microorganisms
also
potentially
reduce
inflammation
associated
an
infection
caused
microorganisms.
Frontiers in Microbiology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 7, 2025
Introduction
Hypervirulent
and
multidrug-resistant
Klebsiella
pneumoniae
(hvKP
MDR-KP)
are
significant
public
health
threats.
This
study
aimed
to
isolate
a
lytic
bacteriophage
targeting
these
high-risk
strains,
systematically
characterize
its
biological
properties,
genomic
features,
therapeutic
efficacy,
establish
foundation
for
clinical
phage
therapy
novel
antimicrobial
development.
Methods
The
vB_Kp_XP4
was
isolated
from
river
water
using
the
double-layer
agar
plate
method
with
clinically
strain
P4
as
host.
Morphology
analyzed
via
transmission
electron
microscopy
(TEM).
Host
range,
pH,
thermal
stability
were
assessed
spot
assays
OD
630
measurements.
One-step
growth
curves
determined
latent
period
burst
size.
Whole-genome
sequencing
phylogenetic
analysis
performed.
Therapeutic
efficacy
safety
evaluated
in
Galleria
mellonella
infection
model.
Results
TEM
revealed
Phage
tailed
an
icosahedral
head
long,
flexible
tail.
It
lysed
hvKP
(carrying
rmp
,
peg
iuc
iro
genes)
MDR-KP
(resistant
carbapenems,
fluoroquinolones,
etc.),
optimal
MOI
of
0.1
<10
minutes.
Stability
maintained
at
pH
4–11
≤70°C.
linear
double-stranded
DNA
genome
44,344
bp
G+C
content
53.80%.
comprised
54
coding
sequences
lacked
lysogenic,
virulence,
or
antibiotic
resistance
genes.
Phylogenetic
positioned
species
within
genus
Drulisvirus
family
Autographiviridae
.
In
model,
prolonged
survival
P4-infected
larvae
(
P
<
0.001)
Conclusion
exhibits
high
stability,
specificity,
potent
activity,
no
undesirable
genes,
demonstrating
effective
vivo
suggest
potential
applications
against
infections.
presence
multiple
halos
during
plaque
formation
further
enhances
research
value.
complete
sequence
has
been
submitted
GenBank
under
accession
number
PP663283.
Journal of Biomedical Science,
Journal Year:
2025,
Volume and Issue:
32(1)
Published: March 22, 2025
Abstract
Backgrounds
Endolysins
are
promising
alternatives
to
antibiotics
because
they
can
lyse
bacterial
cells
rapidly
with
a
low
risk
of
resistance
development,
however,
their
effectiveness
against
Gram-negative
bacteria
is
hindered
by
the
presence
outer
membrane
present
in
bacteria.
Several
endolysins
amphipathic
helices
at
C-terminus
have
been
reported
intrinsic
antibacterial
activity
but
action
mechanism
not
fully
elucidated.
Methods
The
sequence
alignment
analysis
was
assessed
CLC
Main
workbench
7,
and
His-tagged
were
purified
affinity
chromatography.
Site-directed
mutagenesis
used
generate
mutations
endolysin
make
various
mutants.
muralytic
analyzed
using
turbidity
reduction
assay
activities
through
viable
cell
counting
assay.
Results
We
identified
two
endolysins,
LysTS3
LysTS6,
both
which
similar
sequences
structures
including
C-terminus.
LysTS6
exhibited
significantly
higher
compared
even
though
enzymes
membrane-permeabilized
Systematic
truncation
bioinformatic
these
revealed
major
difference
charge
on
surface
C-terminal
helices,
suggesting
possibility
that
this
helix
determine
could
enhance
replacing
Ala
156
Glu
160
lysine
alanine,
respectively,
amino
acid
residues
structurally
equivalent
positions
LysTS6.
A
boost
also
seen
LysSPN1S
LysJEP4
when
altered
be
more
positive
modification
surface-exposed
residues.
Conclusions
enhanced
adjusting
positive,
crucial
for
its
penetration
reach
peptidoglycan
layer
PLoS Pathogens,
Journal Year:
2025,
Volume and Issue:
21(4), P. e1012971 - e1012971
Published: April 8, 2025
Klebsiella
pneumoniae
(KP)
is
a
Gram-negative
bacterium
that
commonly
resides
in
the
human
gastrointestinal
tract
and
can
also
act
as
an
opportunistic
pathogen
cause
extra-intestinal
infections.
KP
poses
global
health
threat
because
it
causes
both
hospital-
community-acquired
infections
immune-competent
immunocompromised
hosts.
These
be
multidrug-resistant
and/or
hypervirulent,
making
difficult
to
treat
deadly.
In
absence
of
effective
treatments
for
recalcitrant
infections,
bacteriophage
(phage)
therapy
gaining
attention
promising
alternative.
this
review,
we
evaluate
epidemiology
epitope
diversity,
discuss
interactions
between
KP-targeting
phages
their
bacterial
hosts
from
eco-evolutionary
perspective,
summarize
recent
efforts
phage
treating
We
novel
approaches,
including
genetic
engineering
machine
learning,
initial
steps
toward
developing
precision
medicine
approach
emerging
dangerous
pathogen.
Viruses,
Journal Year:
2025,
Volume and Issue:
17(4), P. 560 - 560
Published: April 13, 2025
The
presented
in
silico
and
phylogenetic
analysis
of
putative
endolysins
potentially
produced
by
phages
infecting
uropathogenic
Escherichia
coli
(UPEC)
demonstrates
their
remarkable
diversity.
These
proteins
exhibit
significant
variations
sequence
length,
molecular
weight,
isoelectric
point,
stability,
as
well
diverse
functional
domains
determining
enzymatic
activity,
including
lysin,
lysozyme,
hydrolase,
amidase,
peptidase
functions.
Due
to
predicted
lytic
properties,
hold
great
promise
combating
UPEC
bacteria,
those
within
biofilms,
which
are
often
highly
resistant
conventional
treatments.
Despite
potential,
several
challenges
hinder
the
full
utilization
endolysins.
include
relatively
small
number
identified
proteins,
annotation
process,
scarcity
studies
evaluating
efficacy
vitro
vivo
against
Gram-negative
bacteria.
In
this
work,
we
emphasize
these
while
also
underlining
potential
an
effective
tool
infections.
Their
effectiveness
could
be
significantly
enhanced
when
combined
with
agents
that
disrupt
outer
membrane
making
them
a
promising
alternative
or
complement
existing
antimicrobial
strategies.
Further
research
is
necessary
fully
explore
therapeutic
potential.
Crystals,
Journal Year:
2025,
Volume and Issue:
15(5), P. 448 - 448
Published: May 9, 2025
Antibiotic
resistance
has
emerged
as
a
critical
global
public
health
challenge,
prompting
increased
interest
in
non-antibiotic
antimicrobial
strategies
such
bacteriophage-derived
endolysins.
Although
endolysins
possess
strong
lytic
potential,
their
application
to
Gram-negative
bacteria
remains
limited
due
the
outer
membrane
barrier.
PlyKp104
is
recently
identified
phage-derived
endolysin
that
exhibits
activity
against
without
aid
of
permeabilizers.
In
this
study,
crystal
structure
was
determined
at
resolution
1.85
Å.
consists
solely
catalytic
SLT
domain,
and
structure-based
analysis
revealed
putative
active
site
key
structural
features
associated
with
substrate
binding.
Comparative
homologous
structures
suggested
belongs
transglycosylase
family
1.
B-factor
hydrophobic
interaction
mapping
indicated
domain
high
stability,
supported
by
conserved
residues
clustered
motifs
I
II.
During
determination,
an
unidentified
electron
density
consistently
observed
near
neutral,
surface
region.
Its
shape
environment
suggest
presence
lipid-like
molecule,
implying
potential
lipid-binding
site.
These
findings
provide
insight
into
contribute
understanding
mechanisms
bacteria,
implications
for
future
protein
engineering
efforts.
European Journal of Microbiology and Immunology,
Journal Year:
2024,
Volume and Issue:
14(1), P. 1 - 12
Published: Jan. 23, 2024
Abstract
Pulmonary
infections
of
patients
with
cystic
fibrosis
(CF)
or
in
intensive
care
units
are
frequently
caused
by
the
Gram-negative
opportunistic
pathogen
Pseudomonas
aeruginosa.
Since
these
bacteria
commonly
inherently
multidrug-resistant
(MDR)
and
hence,
antibiotic
treatment
options
limited,
bacteriophages
may
provide
alternative
therapeutic
prophylactic
measures
combat
pneumonia
P.
aeruginosa
.
This
prompted
us
to
perform
a
comprehensive
literature
survey
current
knowledge
regarding
effects
phages
applied
against
pulmonary
infections.
The
included
23
studies
revealed
that
specific
lyse
eliminate
even
case
biofilm
production
vitro,
whereas
application
mice
men
resulted
mitigated
induced
clinical
signs
enhanced
survival.
Besides
distinct
host
immune
responses,
no
major
adverse
limiting
and/or
phage
were
noted.
However,
system
antibiotics
generate
synergies
due
mutable
sensitivity
In
conclusion,
results
summarized
this
review
evidence
constitute
promising
for
lung
MDR
Further
needed,
however,
underscore
efficacy
safety
aspects
infected
including
immune-compromised
individuals.
Applied and Environmental Microbiology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 30, 2024
ABSTRACT
Traditional
antibiotics
have
been
effective
in
many
cases.
However,
the
rise
multidrug-resistant
bacteria
has
diminished
their
therapeutic
efficacy,
signaling
dawn
of
an
era
beyond
antibiotics.
The
challenge
multidrug
resistance
Klebsiella
pneumoniae
is
particularly
critical,
with
increasing
global
mortality
and
rates.
Therefore,
development
alternative
therapies
to
urgently
needed.
Phages,
which
are
natural
predators
bacteria,
inherent
advantages.
comprehensive
information
on
K.
phages
lacking
current
literature.
This
review
aims
analyze
summarize
relevant
studies,
focusing
present
state
phage
therapy
for
infections.
includes
examination
treatment
methodologies,
associated
challenges,
strategies,
new
technologies,
clinical
trial
safety
regulatory
issues,
future
directions
development.
Enhancing
technology
crucial
addressing
evolving
threat
.
Current Opinion in Infectious Diseases,
Journal Year:
2023,
Volume and Issue:
36(6), P. 596 - 608
Published: Sept. 26, 2023
Purpose
of
review
To
update
the
management
severe
Acinetobacter
baumannii
infections
(ABI),
particularly
those
caused
by
multi-resistant
isolates.
Recent
findings
The
in
vitro
activity
various
antimicrobial
agents
potentially
helpful
treating
ABI
is
highly
variable
and
has
progressively
decreased
for
many
them,
limiting
current
therapeutic
options.
combination
more
than
one
drug
still
advisable
most
circumstances.
Ideally,
two
active
first-line
drugs
should
be
used.
Alternatively,
a
second-line
and,
if
this
not
possible,
or
combination.
emergence
new
such
as
Cefiderocol,
Sulbactam
Durlobactam,
Tetracyclines
offer
options
that
need
to
supported
clinical
evidence.
Summary
apparent
limitations
bacterium,
rapid
development
resistance,
serious
underlying
situation
cases
invite
search
alternatives
antibiotic
treatment,
promising
which
seems
bacteriophage
therapy.