Viruses,
Год журнала:
2025,
Номер
17(5), С. 623 - 623
Опубликована: Апрель 26, 2025
Acinetobacter
baumannii
and
Klebsiella
pneumoniae
are
significant
nosocomial
pathogens
worldwide.
In
this
study,
the
general
characterization
of
A.
K.
isolates
obtained
from
blood
intensive
care
unit
patients
multidisciplinary
scientific
practical
center
emergency
medicine
January
to
September
2024
was
performed.
Prophage
regions
prophage-derived
tailspike
polysaccharide-depolymerizing
or
-modifying
enzymes
within
these
were
identified
characterized
in
detail
using
a
refined
workflow.
The
protocol,
encompassing
comprehensive
survey
all
predicted
bacterial
proteins,
revealed
an
average
6.0
prophage
per
genome,
including
putatively
derived
filamentous
phages,
4.8
isolate.
Analysis
putative
indicated
that
most
related
previously
isolated,
yet
unclassified,
temperate
phages
infecting
pneumoniae.
However,
certain
sequences
likely
originated
representing
novel
groups
comparatively
distant
known
phages.
Expert Review of Anti-infective Therapy,
Год журнала:
2024,
Номер
22(1-3), С. 25 - 43
Опубликована: Янв. 18, 2024
Introduction
Klebsiella
pneumoniae
is
a
major
agent
of
healthcare-associated
infections
and
cause
some
community-acquired
infections,
including
severe
bacteremic
associated
with
metastatic
abscesses
in
liver
other
organs.
Clinical
relevance
compounded
by
its
outstanding
propensity
to
evolve
antibiotic
resistance.
In
particular,
the
emergence
dissemination
carbapenem
resistance
K.
has
posed
challenge
due
few
residual
treatment
options,
which
have
only
recently
been
expanded
new
agents.
The
epidemiological
success
carbapenem-resistant
(CR-Kp)
mainly
linked
clonal
lineages
that
produce
carbapenem-hydrolyzing
enzymes
(carbapenemases)
encoded
plasmids.
Frontiers in Microbiology,
Год журнала:
2023,
Номер
14
Опубликована: Ноя. 30, 2023
Hypervirulence
and
carbapenem-resistant
have
emerged
as
two
distinct
evolutionary
pathotypes
of
Klebsiella
pneumoniae,
with
both
reaching
their
epidemic
success
posing
a
great
threat
to
public
health.
However,
the
boundaries
separating
these
fade,
we
assist
worrisome
convergence
in
certain
high-risk
clones,
causing
hospital
outbreaks
challenging
every
therapeutic
option
available.
To
better
understand
basic
biology
pathogens,
this
review
aimed
describe
virulence
factors
distribution
worldwide
among
highly
virulent
or
hypervirulent
K.
pneumoniae
strains,
well
interplay
strains
carbapenemase
produced
sequence
type
such
strains.
As
witness
shift
healthcare
settings
where
are
beginning
emerge
replace
classical
understanding
is
urgently
needed
for
immediate
appropriate
response.
The
emergence
of
hypervirulence
(hv)
and
carbapenem
resistance
(CR)
as
distinct
evolutionary
directions
for
Klebsiella
pneumoniae
presents
a
significant
threat
in
clinical
settings.
However,
recent
years,
there
has
been
growing
identification
K.
strains
that
integrate
both
phenotypes,
resulting
severe
outcomes.
Carbapenem-resistant
hypervirulent
(CRhvKP)
typically
emerges
through
the
acquisition
plasmids
carrying
either
virulence
or
CR-encoded
genes
by
carbapenem-resistant
pneumoniae.
Furthermore,
hybrid
plasmid
can
confer
combination
CR
hv.
CRhvKP
cause
variety
infections,
including
pneumonia,
urinary
tract
bloodstream
liver
abscesses,
other
related
conditions.
While
sequence
type
11
(ST11)
dominates
majority
China,
molecular
factors
responsible
success
ST11
largely
remain
unknown.
Here,
we
provide
an
overview
current
understanding
variation
distribution
crucial
determinants,
mechanisms
driving
merging
hv
CR,
potential
influencing
epidemiological
CRhvKP.
This
research
aims
to
contribute
comprehensive
complexities
surrounding
It
is
imperative
underscore
development
therapies,
precision
medicine,
vaccine
strategies
pivotal
approaches
effectively
combating
Considering
widespread
prevalence
CRhvKP,
prioritized,
multifaceted
approach
encompassing
infection
control,
active
surveillance,
innovative
therapeutics
essential.
Infection and Drug Resistance,
Год журнала:
2025,
Номер
Volume 18, С. 1339 - 1354
Опубликована: Март 1, 2025
Abstract:
Klebsiella
spp
.
are
ubiquitous
gram-negative
bacteria,
commonly
present
in
natural
environments
and
as
part
of
the
human
microbiota.
is
involved
occurrence
development
many
diseases,
effective
antibiotics
for
it
have
attracted
attention
researchers.
In
recent
years,
its
multi-drug
resistance,
particularly
to
carbapenems
β-lactam
antibiotics,
has
posed
significant
challenges
clinical
treatment.
Therefore,
a
comprehensive
understanding
resistance
mechanisms
,
along
with
enhancement
detection
methods,
crucial
effectively
controlling
spread
drug-resistant
strains
guiding
individualized
This
paper
systematically
reviews
epidemiological
characteristics,
mechanisms,
treatment
strategies
aiming
provide
new
insights
management
this
pathogen.
Keywords:
drug
method,
β-lactam,
Antibiotics,
Год журнала:
2025,
Номер
14(3), С. 223 - 223
Опубликована: Фев. 21, 2025
Background/Objectives:
The
incidence
of
Ceftazidime/Avibactam
(CZA)-resistant
Klebsiella
pneumoniae
isolate
co-producing
carbapenemase
2
(KPC-2)
and
Vietnamese
extended-spectrum
β-lactamase
25
(VEB-25)
has
been
on
the
rise
in
Greece
over
past
five
years.
This
study
investigates
isolation
ST323
K.
isolates
co-resistant
to
CZA
cefiderocol
(FDC)
from
colonized
infected
patients
a
single
hospital
Athens.
Methods:
CZA-resistant
strains
were
isolated
5
ICU
27
December
2023
22
January
2024.
Antimicrobial
susceptibility
was
tested
against
panel
agents.
Whole-genome
sequencing
carried
out
identify
acquired
resistance
genes
mutations
that
associated
with
FDC
resistance.
Results:
belonged
harbored
blaKPC-2
blaVEB-25.
had
minimum
inhibitory
concentration
(MIC)
>256
mg/L
for
32
FDC,
due
disrupted
catecholate
siderophore
receptor
Fiu.
blaVEB-25
located
an
IncC
non-conjugative
plasmid
~14
kb
multidrug
(MDR)
region
comprising
15
further
genes.
Transformation
studies
showed
blaVEB-25-carrying
provided
most
β-lactams
tested,
including
CZA.
remained
susceptible
carbapenems,
imipenem/relebactam,
meropenem/vaborbactam.
citrate-dependent
iron
(III)
uptake
system
(fecIRABCDE),
which
increased
MIC
≤0.08
mg/L.
Conclusions:
gene
plasmids
are
important
contributors
spread
key
antibiotic
Strict
infection
control
measures
must
be
elaborated
upon
prevent
extensively
drug-resistant
organisms
such
as
those
described
here.
Frontiers in Cellular and Infection Microbiology,
Год журнала:
2025,
Номер
15
Опубликована: Фев. 14, 2025
Carbapenem-resistant
hypervirulent
Klebsiella
pneumoniae
(CRhvKP)
poses
a
significant
global
health
threat
due
to
its
enhanced
virulence
and
resistance.
This
study
analyzed
5,036
publicly
available
K.
genomes
from
China
(2005–2023),
identifying
1,538
CRhvKP
genomes,
accounting
for
44.6%
of
carbapenem-resistant
isolates
69.5%
isolates.
Predominant
carbapenemases
included
bla
KPC
(92.1%),
with
an
increasing
prevalence
NDM
OXA-48-like
genes.
Most
(93.6%)
carried
both
aerobactin
yersiniabactin
The
genetic
background
showed
high
diversity,
characterized
by
36
sequence
types
(STs)
22
capsule
types,
high-risk
endemic
STs
such
as
ST11,
ST15,
ST23
being
predominant.
demonstrated
virulence,
whereas
ST11
more
resistance
genes
but
minimal
presence
iroBCDN
A
core
genome
MLST
analysis
revealed
that
89.0%
clustered
into
131
clonal
groups,
indicating
widespread
dissemination,
particularly
in
eastern
China.
CR
hv
plasmids,
primarily
IncF,
IncH,
IncR
distinct
community
structures,
plasmids
demonstrating
higher
mobility
diversity.
Crucially,
we
identified
40
CR-hv
convergent
across
five
STs,
likely
resulting
plasmid
fusions,
which
have
become
increasingly
prevalent
over
the
last
decade.
Furthermore,
chromosomal
integration
KPC-2
was
detected,
underscoring
stable
inheritance
these
traits.
Class
1
Integrons
were
present
84.5%
strains,
most
notably
least
ST23.
These
integrons
harbored
confer
various
antibiotics,
including
IMP
VIM
,
their
content
varying
different
STs.
highlights
complexity,
rapid
China,
emphasizing
urgent
need
genomic
surveillance
targeted
interventions
mitigate
posed
multidrug-resistant
strains.
Background
Preliminary
unpublished
results
of
the
survey
carbapenem-
and/or
colistin-resistant
Enterobacterales
(CCRE
survey)
showed
expansion
carbapenemase-producing
Klebsiella
pneumoniae
(CPKP)
sequence
type
(ST)
39
in
12
15
participating
Greek
hospitals
2019.
Aim
We
conducted
a
rapid
to
determine
extent
spread
CPKP
high-risk
clones
2022
and
compare
distribution
circulating
these
since
2013.
Methods
analysed
whole
genome
sequences
epidemiological
data
310
K.
isolates
that
were
carbapenem-resistant
or
‘susceptible,
increased
exposure’
from
participated
European
Enterobacteriaceae
(EuSCAPE,
2013–2014),
CCRE
(2019)
national
follow-up
(2022)
including,
for
latter,
an
estimation
transmission
events.
Results
Five
STs
including
ST258/512
(n
=
101
isolates),
ST11
93),
ST39
56),
ST147
21)
ST323
13)
accounted
more
than
90%
dataset.
While
ST11,
have
been
detected
2013
2014,
KPC-2-producing
emerged
2019
2022,
respectively.
Based
on
defined
genetic
relatedness
cut-off,
44
within-hospital
events
identified
dataset,
with
having
at
least
one
event.
Conclusion
The
recent
emergence
new
healthcare
system
related
is
concern
highlights
need
molecular
surveillance
enhanced
infection
prevention
control
measures.
Journal of Global Antimicrobial Resistance,
Год журнала:
2024,
Номер
37, С. 24 - 27
Опубликована: Фев. 24, 2024
K.
pneumoniae
is
a
common
cause
of
severe
hospital-acquired
infections.
In
the
present
study,
we
have
characterised
whole-genome
two
ST437
belonging
to
clonal
complex
CC258.
The
sequencing
was
performed
by
MiSeq
Illumina,
with
2
×
300bp
paired-end
run.
ResFinder
4.4.2
used
detect
acquired
antimicrobial
resistance
genes
(ARGs)
and
chromosomal
mutations.
Mobile
genetic
elements
(plasmids
ISs)
were
identified
MobileElementFinder
v1.0.3.
genome
also
assigned
ST
using
MLST
2.0.9.
Virulence
factors
detected
Factor
Database
(VFDB).
KPNAQ_1/23
KPNAQ_2/23
strains,
isolated
from
urine
samples
hospitalised
patients,
showed
most
antibiotics,
including
ceftazidime-avibactam,
ceftolozane-tazobactam,
meropenem-vaborbactam
combinations.
Both
strains
susceptible
only
cefiderocol.
Multiple
mechanisms
identified.
Resistance
β-lactams
due
presence
NDM-5,
OXA-232,
CTX-M-15,
SHV-182
β-lactamases,
OmpK36
OmpK37
porin
fluoroquinolones
mediated
mutations
in
acrR,
oqxAB
efflux
pumps,
bifunctional
gene
aac(6')-Ib-cr.
different
virulence
makes
these
high-risk
clones.