Whole-genome sequencing of Acinetobacter baumannii clinical isolates from a tertiary hospital in Terengganu, Malaysia (2011–2020), revealed the predominance of the Global Clone 2 lineage
Nurul Saidah Din,
No information about this author
Farahiyah Mohd. Rani,
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Ahmed Ghazi Alattraqchi
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et al.
Microbial Genomics,
Journal Year:
2025,
Volume and Issue:
11(2)
Published: Feb. 5, 2025
Carbapenem-resistant
Acinetobacter
baumannii
is
recognized
by
the
World
Health
Organization
(WHO)
as
one
of
top
priority
pathogens.
Despite
its
public
health
importance,
genomic
data
clinical
isolates
from
Malaysia
remain
scarce.
In
this
study,
whole-genome
sequencing
was
performed
on
126
A
.
collected
main
tertiary
hospital
in
state
Terengganu,
Malaysia,
over
a
10-year
period
(2011–2020).
Antimicrobial
susceptibilities
determined
for
20
antibiotics
belonging
to
8
classes
showed
that
77.0%
(
n
=97/126)
were
categorized
multidrug
resistant
(MDR),
with
all
MDR
being
carbapenem
resistant.
Multilocus
sequence
typing
analysis
Terengganu
A.
into
34
Pasteur
and
44
Oxford
types
(STs),
ST2
Global
Clone
2
lineage
identified
dominant
ST
=76/126;
60.3%).
The
could
be
subdivided
six
STs
majority
ST195
=35)
ST208
=17).
Various
antimicrobial
resistance
genes
bla
OXA-23
-encoded
carbapenemase
predominant
acquired
gene
=90/126;
71.4%).
Plasmid-encoded
rep
nearly
=122/126;
96.8%)
Rep_3
family
=121).
virulence
factors
identified,
highlighting
pathogenic
nature
bacterium.
Only
14/126
(11.1%)
positive
carriage
CRISPR-Cas
arrays
none
prevalent
harbouring
them.
This
study
provided
snapshot
obtained
single
healthcare
centre
predominance
closely
related
lineage,
indicating
entrenchment
clone
hospital.
Language: Английский
Surface-mediated bacteriophage defense incurs fitness tradeoffs for interbacterial antagonism
Chia-En Tsai,
No information about this author
F. Y. Wang,
No information about this author
Chih‐Wen Yang
No information about this author
et al.
The EMBO Journal,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Language: Английский
Environmental and clinical impacts of antibiotics’ sub-minimum inhibitory concentrations on the development of resistance in acinetobacter baumannii
Bipin Yadav,
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Dilip D Karad,
No information about this author
Kiran R. Kharat
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et al.
The Science of The Total Environment,
Journal Year:
2025,
Volume and Issue:
979, P. 179521 - 179521
Published: April 27, 2025
Language: Английский
Comprehensive Approaches to Combatting Acinetobacter baumannii Biofilms: From Biofilm Structure to Phage-Based Therapies
Ilona Grygiel,
No information about this author
Olaf Bajrak,
No information about this author
Michał Wójcicki
No information about this author
et al.
Antibiotics,
Journal Year:
2024,
Volume and Issue:
13(11), P. 1064 - 1064
Published: Nov. 8, 2024
Acinetobacter
baumannii—a
multidrug-resistant
(MDR)
pathogen
that
causes,
for
example,
skin
and
soft
tissue
wounds;
urinary
tract
infections;
pneumonia;
bacteremia;
endocarditis,
particularly
due
to
its
ability
form
robust
biofilms—poses
a
significant
challenge
in
clinical
settings.
This
structure
protects
the
bacteria
from
immune
responses
antibiotic
treatments,
making
infections
difficult
eradicate.
Given
rise
resistance,
alternative
therapeutic
approaches
are
urgently
needed.
Bacteriophage-based
strategies
have
emerged
as
promising
solution
combating
A.
baumannii
biofilms.
Phages,
which
viruses
specifically
infect
bacteria,
offer
targeted
effective
means
of
disrupting
biofilm
lysing
bacterial
cells.
review
explores
current
advancements
bacteriophage
therapy,
focusing
on
potential
treating
biofilm-related
infections.
We
described
mechanisms
by
phages
interact
with
biofilms,
challenges
phage
therapy
implementation,
being
developed
enhance
efficacy
(phage
cocktails,
engineered
phages,
combination
therapies
antibiotics).
Understanding
role
bacteriophages
both
disruption
inhibition
forming
could
pave
way
innovative
treatments
MDR
well
prevention
their
development.
Language: Английский
The Arms Race Between Actinobacillus pleuropneumoniae and Its Genetic Environment: A Comprehensive Analysis of Its Defensome and Mobile Genetic Elements
Molecular Microbiology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 3, 2025
ABSTRACT
Actinobacillus
pleuropneumoniae
is
the
causative
agent
of
pleuropneumonia
in
swine,
a
highly
contagious
and
economically
significant
disease.
The
genetic
variability
A.
complicates
disease
control
efforts,
as
it
enables
rapid
adaptation
to
various
stressors,
including
antimicrobial
treatments.
To
better
understand
molecular
mechanisms
underlying
this
adaptability,
we
investigated
role
bacterial
defensome
its
relationship
with
mobile
elements
(MGEs),
such
prophages,
plasmids,
integrative
conjugative
(ICEs).
Using
bioinformatic
tools,
identified
diverse
rich
,
an
average
16
different
defense
systems
per
strain.
We
found
that
CRISPR‐Cas
systems,
along
other
mechanisms,
are
actively
involved
restricting
entry
foreign
material,
playing
crucial
adaptation.
Additionally,
characterized
several
novel
prophages
examined
their
distribution
across
strains,
revealing
potential
contribution
bacterium's
evolutionary
success.
Our
findings
underscore
complex
interplay
between
MGEs,
shedding
light
on
how
maintains
diversity
while
also
safeguarding
itself
against
external
threats.
These
insights
provide
understanding
factors
influence
pathogen's
adaptability
highlight
avenues
for
more
effective
strategies.
Language: Английский
Surface-mediated Bacteriophage Defense Incurs Fitness Tradeoffs for Interbacterial Antagonism
Chia-En Tsai,
No information about this author
Fengqi Wang,
No information about this author
Chih-Wen Yang
No information about this author
et al.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 14, 2024
ABSTRACT
Bacteria
in
polymicrobial
habitats
are
constantly
exposed
to
biotic
threats
from
bacteriophages,
antagonistic
bacteria,
and
predatory
eukaryotes.
These
interactions
play
crucial
roles
shaping
the
evolution
physiology
of
bacteria.
To
survive,
bacteria
have
evolved
mechanisms
protect
themselves
such
attacks,
but
fitness
costs
resisting
one
threat
rendering
susceptible
others
remain
unappreciated.
Here,
we
examined
consequences
bacteriophage
resistance
Salmonella
enterica
,
revealing
that
phage-resistant
variants
exhibited
significant
loss
upon
co-culture
with
competitor
strains
display
varying
degrees
lipopolysaccharide
(LPS)
deficiency
increased
susceptibility
contact-dependent
interbacterial
antagonism,
as
type
VI
secretion
system
(T6SS).
Utilizing
mutational
analyses
atomic
force
microscopy,
show
long-modal
length
O-antigen
LPS
serves
a
protective
barrier
against
T6SS-mediated
intoxication.
Notably,
this
competitive
disadvantage
can
also
be
triggered
independently
by
phages
possessing
LPS-targeting
endoglycosidase
their
tail
spike
proteins,
which
actively
cleave
infection.
Our
findings
reveal
two
distinct
phage-mediated
modifications
modulate
competition,
shedding
light
on
dynamic
microbial
interplay
within
mixed
populations.
Language: Английский