bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 9, 2024
Abstract
The
presence
of
extended-spectrum
β-lactamase
(ESBL)
encoding
plasmids
in
bacteria
contributes
towards
rising
resistance
rates,
mortality
and
healthcare
costs
clinical
settings.
An
EBSL-encoding
plasmid,
pESBL-PH
was
identified
during
a
nosocomial
outbreak
Klebsiella
pneumoniae
ST628
at
United
Kingdom
general
district
hospital
2018.
A
plasmid
from
the
earliest
2018
K.
strain
discovered
assembled
using
both
Oxford
nanopore
long
reads
illumina
short
reads,
yielding
fully
closed
pESBL-PH-2018.
pESBL-PH-2018
queried
against
complete
NCBI
RefSeq
Plasmid
Database,
comprising
93,823
plasmids,
downloaded
on
July
16,
2024.
To
identify
structurally
similar
strict
thresholds
were
applied:
shared
hash
ratio
>
0.9
mash
similarity
≥
0.98.
This
returned
61
belonging
to
13
unique
sequence
types
(STs)
hosts.
detected
countries,
dating
2012-2023,
associated
with
range
infections
including
bacteremia.
Low
numbers
single
nucleotide
polymorphisms
(SNPs)
between
query
further
confirming
their
relatedness.
AMR
region
varied;
interestingly
IS
26
mediated-tandem
amplification
genes,
ESBL
bla
CTX-M-15
two
independent
strains
raising
copy
number
three.
Furthermore,
genomic
background
carrying
pESBL-PH-2018-like
analyzed,
revealing
truncation
chromosomal
ompK36
porin
gene
carbapenemase
carriage
accessory
17.85%
26.78%
chromosome
available.
analysis
reveals
widespread
dissemination
an
ESBL-encoding
resistance-encoding
strains,
requiring
active
surveillance.
Microbial Genomics,
Journal Year:
2024,
Volume and Issue:
10(5)
Published: May 8, 2024
Improvements
in
the
accuracy
and
availability
of
long-read
sequencing
mean
that
complete
bacterial
genomes
are
now
routinely
reconstructed
using
hybrid
(i.e.
short-
long-reads)
assembly
approaches.
Complete
allow
a
deeper
understanding
evolution
genomic
variation
beyond
single
nucleotide
variants.
They
also
crucial
for
identifying
plasmids,
which
often
carry
medically
significant
antimicrobial
resistance
genes.
However,
small
plasmids
missed
or
misassembled
by
algorithms.
Here,
we
present
Hybracter
allows
fast,
automatic
scalable
recovery
near-perfect
first
approach.
can
be
run
either
as
assembler
only
assembler.
We
compared
to
existing
automated
tools
diverse
panel
samples
varying
levels
with
manually
curated
ground
truth
reference
genomes.
demonstrate
is
more
accurate
faster
than
gold
standard
Unicycler.
show
long-reads
most
comparable
methods
accurately
recovering
plasmids.
Emerging infectious diseases,
Journal Year:
2025,
Volume and Issue:
31(3)
Published: Feb. 21, 2025
Two
unvaccinated
infants
residing
in
the
same
borough
of
New
York,
USA,
had
Haemophilus
influenzae
type
b
meningitis
develop
1
year
apart.
Whole-genome
sequencing
and
phylogenetic
analysis
revealed
isolates
shared
a
previously
undescribed
multilocus
sequence
were
more
closely
related
to
each
other
than
sequenced
strains.
Variant
calling
is
fundamental
in
bacterial
genomics,
underpinning
the
identification
of
disease
transmission
clusters,
construction
phylogenetic
trees,
and
antimicrobial
resistance
detection.
This
study
presents
a
comprehensive
benchmarking
variant
accuracy
genomes
using
Oxford
Nanopore
Technologies
(ONT)
sequencing
data.
We
evaluated
three
ONT
basecalling
models
both
simplex
(single-strand)
duplex
(dual-strand)
read
types
across
14
diverse
species.
Our
findings
reveal
that
deep
learning-based
callers,
particularly
Clair3
DeepVariant,
significantly
outperform
traditional
methods
even
exceed
Illumina
sequencing,
especially
when
applied
to
ONT’s
super-high
model.
superior
performance
attributed
its
ability
overcome
Illumina’s
errors,
which
often
arise
from
difficulties
aligning
reads
repetitive
variant-dense
genomic
regions.
Moreover,
use
high-performing
callers
with
data
mitigates
errors
homopolymers.
also
investigated
impact
depth
on
calling,
demonstrating
10×
super-accuracy
can
achieve
precision
recall
comparable
to,
or
better
than,
full-depth
sequencing.
These
results
underscore
potential
combined
advanced
algorithms,
replace
short-read
resource-limited
settings.
Variant
calling
is
fundamental
in
bacterial
genomics,
underpinning
the
identification
of
disease
transmission
clusters,
construction
phylogenetic
trees,
and
antimicrobial
resistance
detection.
This
study
presents
a
comprehensive
benchmarking
variant
accuracy
genomes
using
Oxford
Nanopore
Technologies
(ONT)
sequencing
data.
We
evaluated
three
ONT
basecalling
models
both
simplex
(single-strand)
duplex
(dual-strand)
read
types
across
14
diverse
species.
Our
findings
reveal
that
deep
learning-based
callers,
particularly
Clair3
DeepVariant,
significantly
outperform
traditional
methods
even
exceed
Illumina
sequencing,
especially
when
applied
to
ONT’s
super-high
model.
superior
performance
attributed
its
ability
overcome
Illumina’s
errors,
which
often
arise
from
difficulties
aligning
reads
repetitive
variant-dense
genomic
regions.
Moreover,
use
high-performing
callers
with
data
mitigates
errors
homopolymers.
also
investigated
impact
depth
on
calling,
demonstrating
10×
super-accuracy
can
achieve
precision
recall
comparable
to,
or
better
than,
full-depth
sequencing.
These
results
underscore
potential
combined
advanced
algorithms,
replace
short-read
resource-limited
settings.
Microbiology Resource Announcements,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 8, 2025
ABSTRACT
Bovine
tuberculosis
is
an
important
zoonotic
infectious
disease
that
presents
a
risk
to
human
health,
livestock,
and
wildlife.
We
report
the
complete
genome
sequence
of
new
Mycobacterium
bovis
strain
caused
bovine
outbreak
on
cattle
farm
in
Saskatchewan,
Canada,
2023.
Microbiology Spectrum,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 19, 2025
ABSTRACT
We
investigated
emerging
multidrug-resistant
(MDR)
Salmonella
enterica
serovar
Agona
in
Taiwan.
These
MDR
strains
commonly
harbored
the
efflux
pump
activator
gene
ramAp
and
up
to
15
resistance
genes,
including
aac
(3)-IId
,
aadA22
aph(3')-Ia
aph
(6)-Id
arr-2
bla
CTX-M-55
LAP-2
TEM-1
dfrA14
floR
lnu(F
),
qnrS13
sul2
sul3
tet(A
within
IncHI2-IncHI2A
plasmids
or
diverse
chromosomal
genomic
islands
(RGIs).
newly
comprised
44.9%
74.4%
of
S
.
isolates
collected
2023
2024,
respectively.
Through
analysis
insertion
sites,
we
identified
11
distinct
RGIs.
Strains
containing
RGI_SA11
became
predominant,
comprising
59.2%
2024.
IMPORTANCE
The
emergence
clonal
expansion
represent
a
growing
public
health
concern.
This
study
identifies
significant
shift
mechanisms,
driven
by
chromosomally
integrated
(RGIs),
which
likely
originated
from
IncHI2–IncHI2A
plasmids.
integration
antimicrobial
genes
enhances
evolutionary
fitness
these
strains,
facilitating
their
persistence
dissemination
both
human
animal
populations.
findings
underscore
urgent
need
for
enhanced
surveillance,
targeted
interventions,
global
stewardship
curb
spread
pathogens
safeguard
health.
Microbial Genomics,
Journal Year:
2025,
Volume and Issue:
11(3)
Published: March 21, 2025
Nanopore
sequencing
is
a
third-generation
technology
known
for
its
portability,
real-time
analysis
and
ability
to
generate
long
reads.
It
has
great
potential
use
in
clinical
diagnostics,
but
thorough
validation
required
address
accuracy
concerns
ensure
reliable
reproducible
results.
In
this
study,
we
automated
an
open-source
workflow
(freely
available
at
https://gitlab.com/FLI_Bioinfo/nanobacta
)
the
assembly
of
Oxford
data
used
it
investigate
reproducibility
results
under
consistent
conditions.
We
benchmark
dataset
five
bacterial
reference
strains
generated
eight
technical
replicates
same
DNA
using
Ligation
Rapid
Barcoding
kits
together
with
Flongle
MinION
flow
cells.
assessed
by
measuring
discrepancies
such
as
substitution
insertion/deletion
errors,
analysing
plasmid
recovery
examining
genetic
markers
clustering
information.
compared
genome
assemblies
without
short-read
polishing.
Our
show
average
99.999955%
nanopore-only
99.999996%
when
short
reads
were
The
genomic
highly
read
following
areas:
identification
antimicrobial
resistance
virulence,
classical
MLST,
taxonomic
classification,
completeness
contamination
analysis.
Interestingly,
information
from
core
SNP
MLST
analyses
also
assemblies,
pairwise
differences
up
two
allele
SNPs
across
replicates.
After
polishing
reads,
cgMLST
0
cgSNP
0–1
These
highlight
advances
nanopore
Microbiology Resource Announcements,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 28, 2025
ABSTRACT
Burkholderia
pseudomallei
is
the
causative
agent
of
melioidosis.
Here,
we
present
complete
genome
sequence
strain
22-10884_313#20
,
isolated
from
a
soil
sample
in
Guadeloupe
(French
West
Indies).
Microbiology Resource Announcements,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 7, 2025
ABSTRACT
The
human
gut
microbiota
is
dominated
by
obligately
anaerobic
bacteria.
A
method
based
on
species-targeted
sorting
using
flow
cytometry
under
conditions
has
been
performed
to
analyze
the
microbiome.
This
report
describes
complete
genome
sequences
of
two
Hominenteromicrobium
mulieris
strains
CIP
112194
and
112527
that
were
isolated
from
feces
a
healthy
adult
France.
volunteer
young
having
vegetarian
diet.
Microbiology Resource Announcements,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 7, 2025
ABSTRACT
Piscinibacterium
candidicorallinum
LMG
29480
is
a
motile
gram-stain-negative
bacterium
able
to
reduce
nitrate
and
accumulate
poly-β-hydroxybutyrate
storage
granules.
Here,
we
report
the
complete
genome
sequence
(3,829,664
bp,
65.16
mol%
G+C
content),
which
may
prove
useful
in
future
taxonomic
comparisons
efforts
assess
role
of
nutrient
cycling.