Bulletin of the National Research Centre/Bulletin of the National Research Center,
Journal Year:
2024,
Volume and Issue:
48(1)
Published: July 24, 2024
Abstract
Background
Antimicrobial
resistance
affects
the
treatment
of
several
bacterial
infections,
including
pneumonia.
This
subsequently
increased
morbidity
and
mortality
rates
patients
with
pneumonia,
especially
in
resource-limited
settings.
In
this
study,
we
aimed
to
determine
patterns
multidrug-resistant
(MDR)
bacteria
isolated
from
sputum
samples
pneumonia
attending
a
tertiary
hospital
Tanzania.
Methodology
A
retrospective
cross-sectional
study
was
conducted.
It
involved
reviewing
laboratory
data
information
system
at
Muhimbili
National
Hospital
The
were
previously
processed
using
standard
methods
(culture,
Gram
staining,
biochemical
tests)
isolate
identify
bacteria.
At
same
time,
antibiogram
profiles
determined
antimicrobial
susceptibility
tests.
Bacterial
isolates
that
expressed
MDR
identified.
Demographic
collected
patients'
medical
records.
We
used
chi-square
test
factors
associated
MDR.
p-value
<
0.05
considered
significant.
Results
retrieved
analysed
169
records
provisional
clinical
diagnosis
confirmed
microbiology
laboratory.
Nearly
98%
adult
patients.
patients’
mean
age
48.3
years
17.3
deviations.
About
84%
Gram-negative;
most
predominant
Klebsiella
pneumoniae
(59/142;
41.5%).
Gram-positive
Staphylococcus
aureus
(25/27;
92.6%).
Furthermore,
80
out
(47.3%)
MDR;
(32.5%)
predominant.
addition,
50%
methicillin
resistance.
highly
observed
admitted
Intensive
Care
Unit
(p
0.05).
Conclusions
Although
our
limited
by
variations
number
subjected
antibiotic
drugs
lack
on
risk
such
as
occupation,
smoking
history,
marital
status,
high
proportion
is
caused
Gram-negative
local
setting.
These
results
inform
need
improve
infection
prevention
control
measures
hospitals
reduce
burden
settings
other
similar
Future Microbiology,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 13
Published: March 26, 2025
Multidrug-resistant
hypervirulent
Klebsiella
pneumoniae
(MDR-hvKP)
combines
high
pathogenicity
with
multidrug
resistance
to
become
a
new
superbug.
MDR-hvKP
reports
continue
emerge,
shattering
the
perception
that
K.
(hvKP)
strains
are
antibiotic
sensitive.
Patients
infected
have
been
reported
in
Asia,
particularly
China.
Although
hvKP
can
acquire
drug
genes,
seems
be
more
easily
transformed
from
classical
(cKP),
which
has
strong
gene
uptake
ability.
To
better
understand
biology
of
MDR-hvKP,
this
review
discusses
virulence
factors,
mechanisms,
formation
pathways,
and
identification
MDR-hvKP.
Given
their
destructive
transmissible
potential,
continued
surveillance
these
organisms
enhanced
control
measures
should
prioritized.
Antibiot Khimioter = Antibiotics and Chemotherapy,
Journal Year:
2025,
Volume and Issue:
69(11-12), P. 59 - 66
Published: April 19, 2025
Background
.
Superinfection
caused
by
Klebsiella
pneumoniae
occupies
a
leading
position
in
the
structure
of
bacterial
complications
COVID-19
patients.
The
intensive
circulation
specialised
hospitals
has
contributed
to
consolidation
most
clinically
and
epidemiologically
important
strains
this
pathogen,
particular,
representatives
hypervirulent
carbapenem-resistant
clonal
lines,
which
have
not
lost
their
relevance
even
post-pandemic
period.
use
bacteriophages
as
therapeutic
anti-epidemic
agents
seems
justified
given
widespread
multidrugresistant
K.
pneumoniae.
Aim
study
To
evaluate
susceptibility
associated
with
nosocomial
infections
patients
polyvalent
bacteriophage
medications.
Materials
methods
included
96
non-repeating
isolated
from
clinical
material
admitted
major
hospital
St.
Petersburg
severe
moderate
forms
May
2020
January
2021.
was
assessed
using
spot
test
analysis.
Commercially
available
preparations
used
for
testing
following:
purified
pyobacteriophage,
sextaphage,
pyobacteriophage.
In
order
identify
probable
mechanisms
resistance
pneumoniae,
nucleotide
sequences
genomes
6
pathogen
belonging
dominant
genetic
lines
ST3,
ST39,
ST307,
ST395,
ST874
were
studied.
Results.
Negative
results
tests
observed
32.29%
(95%
CI=23.8–42.2)
cases;
general,
proportion
eligible
treatment
phage
therapy
49%
CI=39.2–58.8).
Loci
class
1
subtypes
IV-A3
I-E,
potentially
CRISPR-Cas,
identified
genome
studied
strains,
well
number
prophage
bacteriophages.
Conclusion
demonstrated
low
activity
medications
against
causing
COVID-19.
Increasing
diversity
active
relevant
clones
can
expand
possibilities
infections.
rational
containing
these
is
possible
within
paradigm
personalised
therapy.
Antibiotics,
Journal Year:
2024,
Volume and Issue:
13(6), P. 561 - 561
Published: June 15, 2024
Klebsiella
pneumoniae
strains
that
are
resistant
to
multiple
drugs
(KPMDRs),
which
often
acquired
in
hospital
settings
and
lead
healthcare-associated
infections,
pose
a
serious
public
health
threat,
as
does
hypervirulent
K.
(hvKp),
can
also
cause
infections
otherwise
healthy
individuals.
The
widespread
unnecessary
use
of
antibiotics
seen
during
the
recent
COVID-19
pandemic
has
exacerbated
challenges
posed
by
antibiotic
resistance
clinical
settings.
There
is
growing
concern
(hvKp)
may
acquire
genes
confer
antimicrobial
resistance,
thus
combining
an
MDR
profile
with
their
increased
ability
spread
body
sites,
causing
difficult-to-treat
infections.
This
study
aimed
compare
virulence
profiles
KPC-3-producing
isolates
collected
over
four
years
(2020–2023).
A
genome-based
surveillance
all
CRE-K.
was
used
identify
genetic
differences
characterize
profiles.
Our
results
provide
picture
evolution
contribute
avoiding
possible
characteristics
multi-drug
virulence,
thought
be
one
main
global
health,
within
our
hospital.
Microorganisms,
Journal Year:
2024,
Volume and Issue:
12(11), P. 2224 - 2224
Published: Nov. 2, 2024
harbors
various
antibiotic
resistance
determinants
like
extended-spectrum
and
plasmid-mediated
AmpC
β-lactamases
carbapenemases.
In
the
last
three
years,
in
period
of
intense
population
aging,
migrations
climate
changes
Europe
Croatia
as
well,
we
observed
patters
carbapenem-resistant
Antimicrobial Agents and Chemotherapy,
Journal Year:
2024,
Volume and Issue:
68(11)
Published: Oct. 4, 2024
ABSTRACT
Carbapenemase-producing
Klebsiella
pneumoniae
(CP-Kp)
isolates
are
a
public
health
concern
as
they
can
cause
severe
hospital-acquired
infections
that
difficult
to
treat.
It
has
recently
been
shown
CP-Kp
take
up
virulence
factors
from
hypervirulent
K.
lineages.
In
this
study,
109
clinical
the
University
Hospital
Cologne
were
examined
for
presence
of
acquired
using
whole-genome
sequencing
and
phenotypic
tests,
results
linked
data.
The
factor
iuc
was
present
in
18/109
isolates.
Other
factors,
such
ybt
,
cbt
iro
rmpA/rmpA2
peg-344
hypervirulence-associated
capsule
types
detected
various
combinations
among
these
-positive
produced
OXA-232
(
n
=
7),
OXA-48
6),
OXA-48+NDM
3),
NDM,
KPC
(each
1),
7/18
resistant
ceftazidime-avibactam,
colistin,
and/or
cefiderocol.
Four
carried
hybrid
plasmids
harbored
alongside
carbapenemase
genes
bla
NDM-1/5
or
.
15/18
patients,
isolated
clinically
manifest
infection
site.
Among
these,
four
patients
had
osteomyelitis,
died
pneumonia
with
OXA-232-producing
ST231
isolates,
three
them
part
an
outbreak.
conclusion,
frequently
carbapenemase-producing
Germany,
warranting
continuous
monitoring
caused
by
strains.
Jundishapur Journal of Microbiology,
Journal Year:
2024,
Volume and Issue:
16(12)
Published: Feb. 6, 2024
Background:
Carbapenem-resistant
Klebsiella
pneumoniae
(Cr-KPN)
poses
a
significant
global
public
health
challenge.
Objectives:
This
study
aimed
to
investigate
the
prevalence
and
expression
levels
of
carbapenemase-encoding
genes
in
Cr-KPN
isolated
from
patients
admitted
teaching
hospitals
Shiraz,
Iran.
Methods:
A
total
671
distinct
clinical
samples
were
collected
two
Shiraz.
Initial
identification
final
confirmation
K.
isolates
carried
out
using
conventional
biochemical
tests
PCR
assays,
respectively.
The
detection
carbapenemase-producing
pneumoniae,
both
phenotypically
genotypically,
was
performed
through
modified
carbapenem
inactivation
methods
(mCIM)
multiplex
assays.
Real-time
utilized
assess
genes.
Results:
overall
frequency
strains
14.9%
(n
=
100/671).
mCIM
indicated
that
26%
exhibited
carbapenemase
production.
Furthermore,
24%
17%
demonstrated
resistance
imipenem
meropenem,
blaIMI/IMP
gene
detected
91%
isolates.
Among
imipenem-resistant
isolates,
62.5%
tested
positive
for
blaOXA-48
gene.
Additionally,
29.4%,
76.5%,
11.8%
meropenem-resistant
blaKPC,
blaOXA-48,
blaNDM
genes,
analysis
revealed
increased
blaKPC
(1.66-fold),
(7.30-fold),
(4.22-fold),
blaIMI/NMC
(2.39-fold)
resistant
when
exposed
imipenem.
Conclusions:
These
findings
underscore
significance
establishing
active
surveillance
networks
monitor
track
dissemination
which
presents
threat.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(19), P. 14754 - 14754
Published: Sept. 29, 2023
The
emergence
of
hyper-virulent
and
multidrug-resistant
(MDR)
strains
Klebsiella
pneumoniae
isolated
from
patients
with
hospital-
community-acquired
infections
is
a
serious
health
problem
that
increases
mortality.
molecular
analysis
virulome
expression
related
to
antimicrobial-resistant
genotype
infection
type
in
K.
has
been
poorly
studied.
In
this
study,
we
analyzed
the
overall
virulence
associated
antimicrobial
resistance
pulse
field
gel
electrophoresis
(PFGE)
(PFtype)
pneumoniae.
We
studied
25
who
developed
bacteremia
pneumonia
during
their
hospital
stay
125
outpatients
acquired
infections.
Susceptibility
12
antimicrobials
was
determined
by
Kirby–Bauer.
identification
antibiotic-resistance
genes
performed
using
polymerase
chain
reaction
(PCR).
To
promote
pneumoniae,
an
vitro
model
used
human
epithelial
cell
lines
A549
A431.
Bacterial
RNA
extracted
QIAcube
robotic
workstation,
reverse
transcription
cDNA
Reverse
Transcription
QuantiTect
kit
(Qiagen).
determination
real-time
PCR.
addition,
57.3%
(n
=
86)
were
(MDR),
mainly
beta-lactam
antibiotics
(CB,
AM,
CFX,
CF),
aminoglycosides
(GE),
quinolones
(CPF
NOF),
nitrofurantoin
(NF),
sulfamethoxazole/trimethoprim
(SXT).
most
frequently
expressed
among
adhesion-type,
ycfm
(80%),
mrkD
(51.3%),
fimH
(30.7%);
iron
uptake,
irp2
(84%),
fyuA
(68.7%),
entB
(64.7%),
irp1
(56.7%);
protectins,
rpmA
(26%),
which
genes,
blaTEM
(96%),
blaSHV
(64%),
blaCITM
(52.6%),
blaCTXM-1
(44.7%),
tetA
(74%),
sul1
(57.3%),
aac(3)-IV
(40.7%),
aadA1
(36%).
results
showed
existence
different
patterns
PFtypes
cause
These
findings
are
important
may
contribute
improving
medical
treatment
strategies
against
caused
Infection and Drug Resistance,
Journal Year:
2023,
Volume and Issue:
Volume 16, P. 7597 - 7611
Published: Dec. 1, 2023
In
clinical
settings,
CG23
Klebsiella
pneumoniae
(Kp)
is
the
most
virulent
clonal
group
of
Kp.
Continuous
fusions
hypervirulent
(Hv)
and
highly
resistant
strains
have
been
reported;
however,
few
studies
analysed
molecular
epidemiology
characteristics
strains,
especially
MDR-sequence
type
ST23
strains.
this
study,
we
investigated
Kp
infections
in
a
large
teaching
hospital
third
class
China.ST23
isolates
were
screened
using
whole-genome
sequencing
data
from
single
centre.
We
compared
isolated
community-acquired
(CAI)
acquired
infection
(HAI).
addition,
MDR
poor-prognosis
investigated.
genetic
further
evolutionary
relationship
based
on
single-nucleotide
polymorphism
phylogenetic
trees.We
detected
184
between
2013
July
2018.
There
no
significant
differences
isolation
rates
pulmonary,
bloodstream,
urinary
tract,
cutaneous
soft
tissue
community
hospitals,
except
for
abscess
infections.
primarily
cause
pulmonary
abscesses;
with
poor
prognosis
are
typically
bloodstream
Fourteen
producing
extended-spectrum
or
C
beta-lactamases,
resulting
resistance
to
third-generation
cephalosporins.
3.8%
clb
locus
was
absent.
The
tree
revealed
that
divided
into
three
clades,
data,
it
inferred
transmission
events
occurred,
mainly
ICU
causing
lung
infection.This
study
demonstrates
virulence
drug-resistance
fusion
occur
gradually,
clones
facilitate
widespread
dissemination
CAI
HAI,
particularly
pulmonary.
Monitoring
genomics
developing
antivirulence
strategies
essential.
Antibiotics,
Journal Year:
2023,
Volume and Issue:
12(6), P. 959 - 959
Published: May 25, 2023
The
acquisition
of
hypervirulence-associated
genes
by
carbapenemase-producing
Klebsiella
pneumoniae
is
being
increasingly
observed,
and
easy-to-use
diagnostic
tests
are
needed
for
the
surveillance
hypervirulent
K.
(hvKp).
In
this
pilot
study,
87
isolates
from
invasive
infections
collected
in
2022
2023
were
analysed
using
LAMP-based
eazyplex®
Superbug
CRE
hvKp
assays
simultaneous
identification
carbapenemases
virulence
(rmpA/A2,
iuC,
iroC,
ybt,
clb).
Nine
showed
a
Kleborate
score
4
or
5
(10.3%).
time
results
ranged
6.5
to
13
min,
total
turnaround
time,
including
sample
preparation,
was
less
than
30
min.
Five
isolates,
three
which
produced
New
Delhi
metallo-beta
lactamase
(NDM),
subjected
whole-genome
sequencing
(WGS)
analysis
further
characterisation.
test
beta-lactamase
confirmed.
hvKp,
currently
only
available
as
Research
Use
Only
assay,
may
be
useful
tool
rapid
without
significant
additional
workload
when
combined
with
assay
detection
carbapenemases.