Enterobacter
bugandensis
(1
isolado,
0,65%),
Burkholderia
cepacia
(13
isolados,
8,45%),
Proteus
mirabilis
Klebsiella
variicola
(2
1,30%),
Escherichia
coli
Serratia
marcescens
(5
3,25%),
Morganella
morganii
1,30%)
e
Elizabethkingia
miricola
0,65%).Especificamente,
17
cepas
(11,5%),
incluindo
K.
pneumoniae
(7
isolados),
P.
aeruginosa
A.
baumannii
(4
isolados)
E.
isolado),
apresentaram
um
perfil
de
resistência
a
carbapenêmicos
e/ou
cefalosporinas
amplo
espectro,
como
determinado
pelo
método
disco-difusão.Essas
foram
submetidas
à
sequenciamento
pela
plataforma
Illumina
NextSeq.A
análise
genômica
revelou
resistoma
para
beta-lactâmicos
(blaKPC-2,
blaCTX-M-14,
blaCTX-M-15),
aminoglicosídeos
(oqxA,
oqxB,
qnrE1
aac
(6')
-Ib-cr)
quinolonas
(gyrA-83I
parC-80I)
Adicionalmente,
identificados
clones
internacionais
alto
risco,
ST11,
ST16,
ST17
ST437,
ST244
ST671,
ST79
ST730,
ST1193.Genes
exoU
toxA,
relacionados
com
alta
virulência
o
sistema
secreção
tipo
III,
em
uma
cepa
aeruginosa,
enquanto
genes
responsáveis
produção
dos
sideróforos
enterobactina
(ent)
aerobactina
(iuc/iut)
detectados
baumannii.Uma
limitação
do
presente
estudo
é
ausência
dados
clínicos
pacientes.Nossos
resultados
sugerem
que
pacientes
COVID-19
são
suscetíveis
serem
colonizados
adquirir
infecções
secundárias
por
endêmicos
hospitais
brasileiros.Essa
condição
pode
contribuir
prognóstico
desfavorável
da
infecção
COVID-19.
Drug Resistance Updates,
Journal Year:
2024,
Volume and Issue:
74, P. 101083 - 101083
Published: March 29, 2024
Carbapenem-resistant
Klebsiella
pneumonia
(CRKP)
is
a
global
threat
that
varies
by
region.
The
distribution,
evolution,
and
clinical
implications
of
the
ST11
CRKP
clone
remain
obscure.
We
conducted
multicenter
molecular
epidemiological
survey
using
isolates
obtained
from
28
provinces
municipalities
across
China
between
2011
2021.
integrated
sequences
public
databases
performed
genetic
epidemiology
analysis
CRKP.
Among
CRKP,
KL64
serotypes
exhibited
considerable
expansion,
increasing
1.54%
to
46.08%
Combining
our
data
with
databases,
phylogenetic
phylogeography
analyses
indicated
appeared
in
Americas
1996
spread
worldwide,
key
clones
progressing
China's
southeastern
coast
inland
2010.
Global
showed
has
evolved
virulent,
resistant
clade
notable
regional
spread.
Single-nucleotide
polymorphism
(SNP)
identified
BMPPS
(bmr3,
mltC,
pyrB,
ppsC,
sdaC)
as
marker
for
this
clade.
SNP
associated
high
mortality
strong
anti-phagocytic
competitive
traits
vitro.
high-risk
subclone
expansion
potential
survival
advantages,
probably
owing
factors.
Pharmaceuticals,
Journal Year:
2024,
Volume and Issue:
17(9), P. 1206 - 1206
Published: Sept. 12, 2024
The
rise
of
antibiotic
resistance
and
the
dwindling
antimicrobial
pipeline
have
emerged
as
significant
threats
to
public
health.
emergence
carbapenem-resistant
hLife,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 1, 2024
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.
BMC Infectious Diseases,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: Jan. 3, 2025
In
clinical
practice,
the
emergence
of
ST11-K64
carbapenem-resistant
Klebsiella
pneumoniae
(ST11-K64
CRKP)
has
become
increasingly
alarming.
Despite
this
trend,
limited
research
been
conducted
to
elucidate
and
molecular
characteristics
these
strains.
This
study
aimed
comprehensively
investigate
characteristics,
antimicrobial
resistance
patterns,
virulence-associated
genes,
epidemiology
CRKP
in
Southwest
China.
A
retrospective
analysis
was
performed
on
patients
infected
with
(CRKP)
a
tertiary
care
hospital
between
July
2021
May
2022.
total
69
strains
were
isolated,
data
collected
for
detailed
analysis.
Laboratory
assessments
included
susceptibility
testing,
hypermucoviscosity
string
genotypic
characterization
virulence
multi-locus
sequence
typing.
Statistical
analyses
using
SPSS,
significance
set
at
P
<
0.05.
Among
isolates,
36
(52.2%)
identified
as
CRKP.
Hematological
diseases
less
associated
infection
compared
non-ST11-K64
(P
=
0.012).
However,
central
intravenous
catheter
use
0.001),
mechanical
ventilation
0.002),
tracheal
intubation
0.006),
tracheotomy
0.041)
significantly
more
common
cases.
Resistance
rates
amikacin
gentamicin
0.004),
tobramycin
0.034),
sulfamethoxazole
0.001)
higher
Additionally,
resistance-associated
genes
such
blaKPC−2
including
rmpA
iucA
rmpA2
iutA
detected
Furthermore,
ST11-K47
CRKP,
harbored
0.007),
0.003).
Our
findings
underscore
rising
prevalence
characterized
by
high
levels
presence
potent
genes.
strain
poses
significant
therapeutic
challenge,
necessitating
heightened
vigilance,
stringent
control
measures,
robust
management
strategies.
Communications Medicine,
Journal Year:
2025,
Volume and Issue:
5(1)
Published: March 11, 2025
Development
of
polymyxin
resistance
in
carbapenem-resistant
Klebsiella
pneumoniae
(CRKP)
poses
a
severe
challenge
to
public
health.
Here
we
aimed
perform
retrospective
study
prevalence
and
molecular
characteristics
polymyxin-resistant
CRKP
strains.
4455
clinical
strains
from
18
provinces
China
during
2000
2023
were
collected.
Polymyxin-resistant
subjected
antimicrobial
susceptibility
testing,
whole
genome
sequencing
bioinformatic
analysis.
Molecular
mechanisms
underlying
the
analyzed.
show
that
emerge
initially
2014,
such
then
increase
steadily
over
years,
reaching
rate
9.86%
2023.
In
total,
112
isolates
are
identified.
Antimicrobial
tests
all
resistant
commonly
used
antibiotics,
yet
most
remain
susceptible
only
ceftazidime-avibactam
tigecycline.
Predominant
mechanism
is
mutations
mgrB
(59/112),
which
involves
disruption
by
insertion
elements
as
ISKpn26
(20/59),
IS903B
(14/59),
ISKpn14
(9/59).
Phylogenetic
analysis
reveals
frequent
clonal
dissemination
within
same
hospital
even
among
different
hospitals
neighboring
provinces.
pLVPK-like
virulence
plasmids
detected
46
isolates,
therefore
categorized
hypervirulent
K.
may
cause
infections
with
high
mortality.
Our
results
highlight
transmission
hospitals.
Continuous
surveillance
should
be
implemented
prevent
further
settings
China.
Polymyxins
antibiotics
treat
do
not
respond
other
antibiotic
treatments.
These
described
multidrug-resistant
infections.
However,
an
increasing
number
cannot
successfully
treated
polymyxins
consequence
these
being
caused
bacteria
killed
treatment.
We
studied
had
across
20-year
period.
found
became
more
common
areas.
This
indicates
monitoring
undertaken
detect
presence
this
bacteria,
approaches
taken
spread
bacteria.
Xie,
Zhang
et
al.
conduct
epidemiological
They
find
Journal of Antimicrobial Chemotherapy,
Journal Year:
2024,
Volume and Issue:
79(9), P. 2292 - 2297
Published: July 13, 2024
Carbapenem-resistant
Klebsiella
pneumoniae
(CRKP)
is
a
major
nosocomial
infectious
pathogen
with
rapidly
increasing
prevalence.
The
genomic
epidemiological
characteristics
of
CRKP
nationwide,
especially
the
evolving
trends
within
predominant
clones,
should
be
evaluated
clearly.
Microbiology Spectrum,
Journal Year:
2023,
Volume and Issue:
11(2)
Published: March 27, 2023
Carbapenem-resistant
Klebsiella
pneumoniae
(CRKP)
is
a
major
severe
threat
for
human
health,
and
its
spread
largely
driven
by
few
dominant
lineages
defined
sequence
types
(ST)
capsular
(KL)
types.
ST11-KL64
one
such
lineage
that
particularly
common
in
China
but
also
has
worldwide
distribution.
However,
the
population
structure
origin
of
K.
remain
to
be
determined.
We
retrieved
all
genomes
(n
=
13,625,
as
June
2022)
from
NCBI,
comprising
730
strains.
Phylogenomic
analysis
core-genome
single-nucleotide
polymorphisms
identified
two
clades
(I
II)
plus
an
additional
singleton
ST11-KL64.
performed
dated
ancestral
reconstruction
using
BactDating
found
clade
I
likely
emerged
1989
Brazil,
while
II
around
2008
eastern
China.
then
investigated
phylogenomic
approach
combined
with
potential
recombination
regions.
hybrid
91.2%
(ca.
4.98
Mb)
chromosome
derived
ST11-KL15
8.8%
(483
kb)
acquired
ST147-KL64.
In
contrast,
was
ST11-KL47
swapping
157-kb
region
(3%
chromosome)
containing
capsule
gene
cluster
clonal
complex
1764
(CC1764)-KL64.
The
evolved
126-kb
I.
conclusion,
heterogenous
different
origins
countries
at
time
points.
IMPORTANCE
globally
associated
increased
lengths
hospital
stay
high
mortality
affected
patients.
CRKP
lineages,
including
ST11-KL64,
type
Here,
we
tested
hypothesis
single
genomic
performing
genome-based
study.
comprises
clades,
which
years.
particular,
have
KL64
various
sources.
Our
study
underscores
chromosomal
hot
spot
pneumoniae.
This
represents
evolutionary
mechanism
employed
some
bacteria
rapid
evolution
novel
accommodate
stress
survival.
Virulence,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: May 12, 2024
ST11
is
the
most
common
lineage
among
carbapenem-resistant
Klebsiella
pneumoniae
(CRKP)
infections
in
Asia.
Diverse
morphotypes
resulting
from
genetic
mutations
are
associated
with
significant
differences
microbial
characteristics
K.
isolates.
Here,
we
investigated
determinants
and
critical
distinct
of
CRKP.
An
ST11-KL47
CRKP
isolate
carrying
a
pLVPK-like
virulence
plasmid
was
isolated
patient
bloodstream
infection;
had
"mcsw"
morphotype.
Two
("ntrd"
"msdw")
were
derived
this
strain
during
vitro
passage.
Whole
genome
sequencing
used
to
identify
that
cause
Transmission
electron
microscopy,
antimicrobial
susceptibility
tests,
growth
assays,
biofilm
formation,
membrane
permeability
RNA-seq
analysis
investigate
specific
different
Compared
parental
mcsw
morphotype,
ntrd
morphotype
resulted
mutation
genes
involved
capsular
polysaccharide
biosynthesis
(wza,
wzc,
wbaP),
result
validated
by
gene
knockout
experiments.
This
showed
capsule
deficiency
lower
potential,
but
higher
production.
By
contrast,
msdw
displayed
competition
increased
chlorhexidine
polymyxin
B.
Further
analyses
indicated
these
caused
interruption
sigma
factor
rpoN
insertion
deletion
gene,
which
attenuated
integrity
presumably
downregulating
phage
shock
protein
operon.
These
data
expand
current
understanding
genetic,
virulence,
resistance