bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Dec. 14, 2023
Abstract
Acinetobacter
baumannii
is
a
Gram-negative
opportunistic
pathogen
causing
infections
of
the
immunocompromised.
With
high
incidence
muti-drug
resistance,
carbapenem-resistant
A.
as
priority
1
designated
by
WHO.
The
current
literature
has
expertly
characterized
clinical
isolates
baumannii.
As
challenge
these
recently
been
classified
One
Health
issue,
we
set
out
to
explore
diversity
from
human
and
non-clinical
sources
such
agricultural
surface
water,
urban
streams,
various
effluents
wastewater-treatment
plants
tank
milk;
and,
importantly,
came
wide
geographic
distribution.
Phylogenomic
analysis
considering
almost
200
showed
that
our
diverse
well-differentiated
main
international
clones
.
We
discovered
novel
sequence
types
in
both
hospital
settings,
five
strains
overexpress
RND
efflux
pump
adeIJK
without
changes
susceptibility.
Further,
detected
bla
ADC-79
non-human
isolate
despite
its
sensitivity
all
antibiotics.
There
was
no
significant
differentiation
between
virulence
profiles
Galleria
mellonella
insect
model
suggesting
neither
dependent
on
origin
nor
isolation
source.
Detection
antibiotic
resistance
genes
suggests
may
act
genetic
reservoir
for
strains.
This
endorses
notion
order
combat
multi-drug
resistant
infection
caused
baumannii,
approach
required,
deeper
understanding
must
be
achieved.
Importance
global
crisis
silent
one.
More
more
bacteria
are
becoming
antibiotics
available
treatment,
leaving
options
remaining.
includes
shows
frequency
many
last-resort
drugs
carbapenem
colistin.
Research
focused
origin,
but
there
knowledge
gap
regarding
traits,
particularly,
how
become
notorious
today.
Antibiotic
have
animals,
environmental
locations
grass
soil.
such,
concern
which
health
humans,
animals
environment.
Thus,
truly
crisis,
need
understand
gene
reservoirs
this
under
continuum.
Repositories
NCBI
GenBank
Accession
numbers:
Bioproject
PRJNA819071,
Biosamples
SAMN26898552
-
SAMN26898587.
Applied and Environmental Microbiology,
Journal Year:
2024,
Volume and Issue:
90(2)
Published: Jan. 11, 2024
an
important
pathogen
known
for
its
widespread
antibiotic
resistance,
has
been
the
focus
of
extensive
research
within
genus,
primarily
involving
clinical
isolates.
Consequently,
data
on
environmental
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.
Microbiology Spectrum,
Journal Year:
2024,
Volume and Issue:
12(2)
Published: Jan. 10, 2024
Acinetobacter
baumannii
is
a
major
opportunistic
pathogen
causing
hospital-acquired
infections,
and
it
imperative
to
comprehend
its
evolutionary
epidemiological
dynamics
in
hospitals
prevent
control
nosocomial
transmission.
Here,
we
present
comprehensive
genomic
study
involving
the
sequencing
antibiotic
resistance
profiling
of
634
A.
strains
isolated
from
seven
intensive
care
units
(ICUs)
Chinese
general
hospital
over
2
consecutive
years.
Our
reveals
that
ST2
highly
dominant
(90.54%)
ICUs,
with
98.90%
exhibiting
multidrug
resistant
or
extensively
drug
resistant.
Phylogenetic
analyses
newly
sequenced
genomes
public
data
suggest
isolates
originated
outside
but
evolved
inside.
The
lineages
appear
be
stable,
9
28
identified
epidemic
clones
infecting
60%
affected
patients.
However,
outbreaks
two
have
been
observed
different
hospitals,
suggesting
significant
inter-hospital
transmission
chains.
By
coupling
patient
medical
records
divergence
ST2,
found
cross-ward
transfer
played
crucial
role
pathogen's
Additionally,
831
potential
adaptive
loci
44
associated
genes
by
grouping
comparing
prevalence.
Overall,
our
provides
contemporary
survey
on
epidemiology
evolution
large
hospital.
These
findings
shed
light
offers
valuable
information
for
prevention
therapy.IMPORTANCEThis
delved
into
scale,
spanning
both
an
extended
time
period
largest
sample
size
date.
Through
molecular
investigations
based
genomics,
can
directly
trace
origin
pathogen,
detecting
monitoring
infectious
diseases
timely
manner,
ensuring
health
safety.
In
addition,
this
also
collects
amount
detection
data,
which
helpful
phenotype
prediction
sequencing.
It
enables
patients
receive
personalized
treatment
quickly,
helps
doctors
select
antibiotics
more
accurately,
contributes
reducing
use
lowering
risk
development.
mSphere,
Journal Year:
2024,
Volume and Issue:
9(3)
Published: March 5, 2024
is
a
Gram-negative,
opportunistic
pathogen
that
causes
infections
in
the
immunocompromised.
With
high
incidence
of
muti-drug
resistance,
carbapenem-resistant
Journal of Innate Immunity,
Journal Year:
2025,
Volume and Issue:
17(1), P. 112 - 125
Published: Jan. 22, 2025
Introduction:
Acinetobacter
baumannii
is
a
gram-negative
opportunistic
bacterium
that
causes
life-threatening
infections
in
immunocompromised
hosts.
The
complement
system
critical
mechanism
of
innate
immunity
protects
the
human
body
from
bacterial
infections.
Complement
activation
leads
to
deposition
membrane
attack
complex
(MAC),
which
can
directly
lyse
bacteria.
However,
A.
has
developed
evasion
mechanisms
protect
itself
complement.
Methods:
was
investigated
by
flow
cytometry
and
Western
blotting.
Soluble
MAC
formation
assessed
ELISA.
Bacterial
serum
resistance
determined
SYTOX
Green
Assay.
Galleria
mellonella
used
as
an
infection
model.
Genome
sequencing
revealed
virulence
genes
carried
isolates.
Results:
We
examined
clinical
isolates
found
11
with
5
without
deposition.
Trypsinization
MAC-positive
significantly
reduced
MAC,
indicating
incorrect
insertion,
consistent
lack
lysis
these
strains.
MAC-negative
inhibited
alternative
pathway
were
more
serum-resistant.
These
strains
also
virulent
G.
Whole
genome
genes,
both
differed
capsule
type.
Importantly,
correlation
observed
between
inhibition
type
(e.g.,
locus
KL171)
bacteria,
while
KL230)
associated
increased
sensitivity
MAC-mediated
lysis.
Conclusion:
Our
findings
suggest
relationship
type,
resistance,
host
baumannii.
Journal of Infection and Public Health,
Journal Year:
2025,
Volume and Issue:
unknown, P. 102739 - 102739
Published: March 1, 2025
The
prevalence
of
multidrug-resistant
Acinetobacter
baumannii
(MDRA)
has
rapidly
increased
and
is
linked
to
severe
nosocomial
infections.
MDRA
outbreaks
in
a
Japanese
hospital
were
analysed
using
whole-genome
sequencing.
Antibiotic
susceptibility
testing
was
performed
on
clinical
isolates
from
hospitalised
patients
before
during
the
2009
2010
outbreaks.
Whole-genome
sequencing
conducted
identify
acquired
antibiotic-resistance
genes
genetic
mutations.
Clinical
A.
resistant
β-lactams
(broad-spectrum
cephalosporins
carbapenems),
aminoglycosides,
chloramphenicol,
fosfomycin,
fluoroquinolones,
tetracyclines,
trimethoprim-sulfamethoxazole.
harboured
aac(6')-Ib-cr,
abaF,
armA,
blaADC-30,
blaTEM-1,
blaOXA-82,
or
both
blaOXA-66
blaOXA-23,
catB8,
mphE,
msrE,
tet(B).
blaOXA-82
recombinationally
multiplied.
Quinolone
resistance
also
associated
with
gyrA
S81L
parC
S84L
belonged
Oxford
sequence
type
(ST)
208
Pasteur
ST2.
Three
15
developed
an
extensively
drug-resistant
(XDR)
phenotype,
two
adeS
mutation.
We
identified
molecular
markers
three
XDR
one
MDR
isolate
provided
genomic
description
virulence,
as
well
origins
isolates.
are
closely
related
ST208
ST2,
Asia
Australia.
concern
community
settings
Western
Pacific
region.
Carbohydrate Research,
Journal Year:
2024,
Volume and Issue:
538, P. 109097 - 109097
Published: March 24, 2024
The
structure
of
the
K141
type
capsular
polysaccharide
(CPS)
produced
by
Acinetobacter
baumannii
KZ1106,
a
clinical
isolate
recovered
from
Kazakhstan
in
2016,
was
established
sugar
analyses
and
one-
two-dimensional
Infection Genetics and Evolution,
Journal Year:
2024,
Volume and Issue:
123, P. 105642 - 105642
Published: July 14, 2024
Nosocomial
outbreaks
caused
by
carbapenem-resistant
Acinetobacter
baumannii
(CRAB)
strains
are
rapidly
emerging
worldwide
and
cause
for
concern.
Herein,
we
aimed
to
describe
the
genomic
characteristics
of
CRAB
isolated
from
two
hospitals
in
China
2023.
The
A.
isolates
were
mainly
collected
ICU
sputum
(71.43%,
15/21),
followed
urine
(14.29%,
3/21).
Twenty-one
possessed
a
multidrug-resistant
(MDR)
profile,
whole-genome
sequencing
showed
that
they
all
carried
bla
Microbiology Spectrum,
Journal Year:
2023,
Volume and Issue:
11(6)
Published: Nov. 17, 2023
Bacteriophage
show
promise
for
the
treatment
of
Acinetobacter
baumannii
infections
that
resist
all
therapeutically
suitable
antibiotics.
Many
tail-spike
depolymerases
encoded
by
phage
are
able
to
degrade
A.
capsular
polysaccharide
(CPS)
exhibit
specificity
linkage
present
between
K-units
make
up
CPS
polymers.
This
is
formed
a
specific
Wzy
polymerase,
and
ability
predict
this
using
sequence-based
methods
identify
at
K
locus
could
assist
with
selection
therapy.
However,
little
known
about
polymerase
enzymes.
Here,
we
describe
can
accommodate
two
different
but
similar
sugars
as
one
residues
it
links
cleave
both
types
bond
forms.