The
genomic
repertoire
of
vibrios
has
been
extensively
studied,
particularly
regarding
their
metabolic
plasticity,
symbiotic
interactions,
and
resistance
mechanisms
to
environmental
stressors.
However,
little
is
known
about
the
diversity
adaptations
inhabiting
deep-sea
marine
sediments.
In
this
study,
we
investigated
isolated
from
core
sediments
collected
using
a
manned
submersible
off
Japan.
A
total
50
vibrio
isolates
were
obtained
characterized
phenotypically,
by
genome
sequencing.
From
total,
disclosed
22
novel
species
examining
genome-to-genome
distance,
average
amino
acid
identity,
phenotypes
(Alivibrio:
1;
Enterovibrio:
Photobacterium:
8;
Vibrio:
12).
have
fallen
within
clades
(e.g.,
Fisheri,
Enterovibrio,
Profundum,
Splendidus)
(JAMM0721,
JAMM0388,
JAMM0395).
28
remainder
identified
as
species:
Aliivibrio
sifiae
(2),
A.
salmonicida
(1),
Enterovibrio
baiacu
E.
norvegicus
Photobacterium
profundum
(3),
P.
angustum
chitiniliticum
frigidiphilum
indicum
sanguinicancri
(1).
swingsii
Vibrio
alginolyticus
V.
anguillarum
campbellii
fluvialis
gigantis
lentus
splendidus
(4),
tasmaniensis
Genomic
analyses
revealed
that
all
harbored
genes
associated
with
high-pressure
adaptation,
including
sensor
kinases,
chaperones,
autoinducer-2
(AI-2)
signaling,
oxidative
damage
repair,
polyunsaturated
fatty
biosynthesis,
stress
response
related
periplasmic
outer
membrane
protein
misfolding
under
heat
shock
osmotic
stress.
Additionally,
alternative
sigma
factors,
trimethylamine
oxide
(TMAO)
respiration,
osmoprotectant
acquisition
pathways
identified,
further
supporting
ability
thrive
in
environments.
Notably,
genomes
exhibited
high
prevalence
antibiotic
genes,
efflux
pumps
being
most
abundant
group.
ugd
gene
expanded
number
some
(Photobacterium
satsumensis
sp.
nov.
JAMM1754:
4
copies;
makurazakiensis
JAMM1826:
3
copies).
This
may
confer
(polymyxin)
these
vibrios.
Nature Communications,
Год журнала:
2023,
Номер
14(1)
Опубликована: Фев. 9, 2023
Acinetobacter
baumannii
and
Klebsiella
pneumoniae
are
opportunistic
pathogens
frequently
co-isolated
from
polymicrobial
infections.
The
infections
where
these
co-exist
can
be
more
severe
recalcitrant
to
therapy
than
caused
by
either
species
alone,
however
there
is
a
lack
of
knowledge
on
their
potential
synergistic
interactions.
In
this
study
we
characterise
the
genomes
A.
K.
strains
single
human
lung
infection.
We
examine
various
aspects
interactions
through
transcriptomic,
phenomic
phenotypic
assays
that
form
basis
for
understanding
effects
antimicrobial
resistance
virulence
during
co-infection.
Using
co-culturing
analyses
secreted
metabolites,
discover
ability
cross-feed
by-products
sugar
fermentation.
Minimum
inhibitory
concentration
testing
mono-
co-cultures
reveals
cross-protect
against
cephalosporin,
cefotaxime.
Our
demonstrates
distinct
syntrophic
occur
between
pneumoniae,
helping
elucidate
co-existence
in
Proceedings of the National Academy of Sciences,
Год журнала:
2025,
Номер
122(2)
Опубликована: Янв. 9, 2025
The
bacterial
type
6
secretion
system
(T6SS)
is
a
toxin-injecting
nanoweapon
that
mediates
competition
in
plant-
and
animal-associated
microbial
communities.
Bacteria
can
evolve
de
novo
resistance
against
T6SS
attacks,
but
far
from
universal
natural
communities,
suggesting
key
features
of
weaponry
may
act
to
limit
its
evolution.
Here,
we
combine
ecoevolutionary
modeling
experimental
evolution
examine
how
toxin
multiplicity
Acinetobacter
baylyi
attackers
shape
susceptible
Escherichia
coli
competitors.
In
both
our
models
experiments,
find
combinations
multiple
distinct
toxins
by
creating
genetic
bottlenecks,
driving
resistant
lineages
extinct
before
they
reach
high
frequency.
We
also
show
that,
paradoxically,
single-toxin
drive
the
cross-resistance,
protecting
bacteria
unfamiliar
combinations,
even
though
such
evolutionary
pathways
were
inaccessible
multitoxin
attackers.
Our
findings
indicate
comparable
antimicrobial
anticancer
combination
therapies,
arsenals
function
competing
microbes.
This
helps
us
understand
why
T6SSs
remain
widespread
effective
weapons
many
T6SS-armed
encode
functionally
diverse
anticompetitor
toxins.
The
life
of
bacteria
is
challenging,
to
endure
employ
a
range
mechanisms
optimize
their
environment,
including
deploying
the
type
VI
secretion
system
(T6SS).
Acting
as
bacterial
crossbow,
this
delivers
effectors
responsible
for
subverting
host
cells,
killing
competitors
and
facilitating
general
access
common
goods.
Due
its
importance,
lethal
machine
has
been
evolutionarily
maintained,
disseminated
specialized
fulfil
these
vital
functions.
In
fact,
T6SS
structural
clusters
are
present
in
over
25
%
Gram-negative
bacteria,
varying
number
from
one
six
different
genetic
per
organism.
Since
discovery
2006,
research
on
rapidly
progressed,
yielding
remarkable
breakthroughs.
identification
characterization
novel
components
T6SS,
combined
with
biochemical
studies,
have
revealed
fascinating
governing
assembly,
loading,
firing
disassembly
processes.
Recent
findings
also
demonstrated
efficacy
against
fungal
Gram-positive
expanding
scope.
Ongoing
continues
uncover
an
extensive
repertoire
effectors,
genuine
mediators
function.
These
studies
shedding
light
new
aspects
biology
prokaryotic
eukaryotic
organisms.
This
review
provides
comprehensive
overview
highlighting
recent
discoveries
structure
diversity
effectors.
Additionally,
it
injects
personal
perspective
avenues
future
research,
aiming
deepen
our
understanding
combative
system.
Molecular Systems Biology,
Год журнала:
2024,
Номер
20(6), С. 702 - 718
Опубликована: Апрель 24, 2024
Abstract
The
type
VI
secretion
system
(T6SS)
is
an
important
mediator
of
microbe–microbe
and
microbe–host
interactions.
Gram-negative
bacteria
use
the
T6SS
to
inject
effectors
(T6Es),
which
are
usually
proteins
with
toxic
activity,
into
neighboring
cells.
Antibacterial
have
cognate
immunity
that
neutralize
self-intoxication.
Here,
we
applied
novel
structural
bioinformatic
tools
perform
systematic
discovery
functional
annotation
T6Es
their
from
a
dataset
17,920
T6SS-encoding
bacterial
genomes.
Using
clustering,
identified
517
putative
T6E
families,
outperforming
sequence-based
clustering.
We
developed
logistic
regression
model
reliably
quantify
protein–protein
interaction
new
T6E-immunity
pairs,
yielding
candidate
for
231
out
families.
used
sensitive
structure-based
yielded
annotations
51%
again
annotation.
Next,
validated
four
pairs
using
basic
experiments
in
E.
coli
.
In
particular,
showed
Pfam
domain
DUF3289
homolog
Colicin
M
DUF943
acts
as
its
protein.
Furthermore,
discovered
SleB,
lytic
transglycosylase,
specific
glutamate
catalytic
residue.
Overall,
this
study
applies
pair
discovery,
provides
extensive
database
annotated
pairs.
Proceedings of the National Academy of Sciences,
Год журнала:
2025,
Номер
122(3)
Опубликована: Янв. 15, 2025
Bacterial–fungal
interaction
(BFI)
has
significant
implications
for
the
health
of
host
plants.
While
diffusible
antibiotic
metabolite-mediated
competition
in
BFI
been
extensively
characterized,
impact
intercellular
contact
remains
largely
elusive.
Here,
we
demonstrate
that
is
a
prevalent
mode
between
beneficial
soil
bacteria
and
pathogenic
filamentous
fungi.
By
generating
antibiotics-deficient
mutants
two
common
bacteria,
Lysobacter
enzymogenes
Pseudomonas
fluorescens
,
show
antibiotics-independent
effectively
inhibits
Furthermore,
transcriptional
genetic
evidence
revealed
this
relies
on
mediated
by
type
VI
secretion
system
(T6SS),
which
may
facilitate
translocation
bacterial
toxic
effectors
into
fungal
cells.
Finally,
using
“conidia
enrichment”
platform,
found
T6SS-mediated
inhibition
resulting
from
naturally
occurs
within
microbiome,
particularly
represented
fulva
.
Overall,
these
results
microbiome
can
protect
plants
infection
through
contacts,
thus
revealing
occurring
ecologically
important
agricultural
contexts.
Microbial Genomics,
Год журнала:
2025,
Номер
11(2)
Опубликована: Фев. 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.
Abstract
The
type
VI
secretion
system
(T6SS)
is
a
double‐tubular
nanomachine
widely
found
in
gram‐negative
bacteria.
Its
spear‐like
Hcp
tube
capable
of
penetrating
neighboring
cell
for
cytosol‐to‐cytosol
protein
delivery.
However,
gram‐positive
bacteria
have
been
considered
impenetrable
to
such
T6SS
action.
Here
we
report
that
the
plant
pathogen,
Acidovorax
citrulli
(AC),
could
deliver
an
Rhs‐family
nuclease
effector
RhsB
kill
not
only
but
also
Using
bioinformatic,
biochemical,
and
genetic
assays,
systematically
identified
T6SS‐secreted
effectors
determined
crucial
antibacterial
effector.
contains
N‐terminal
PAAR
domain,
middle
Rhs
unknown
C‐terminal
domain.
subject
self‐cleavage
at
both
its
N‐
domains
requires
upstream‐encoded
chaperone
EagT2
VgrG3.
toxic
C‐terminus
exhibits
DNase
activities
toxicity
neutralized
by
either
two
downstream
immunity
proteins,
RimB1
RimB2.
Deletion
rhsB
significantly
impairs
ability
killing
Bacillus
subtilis
while
ectopic
expression
proteins
or
RimB2
confers
protection.
We
demonstrate
AC
can
effectively
outcompete
Escherichia
coli
B.
planta
highly
potent
other
bacterial
fungal
species.
Collectively,
these
findings
highlight
greatly
expanded
capabilities
modulating
microbiome
compositions
complex
environments.
The
type
VI
secretion
system
(T6SS)
is
a
molecular
puncturing
device
that
enables
Gram-negative
bacteria
to
kill
competitors,
manipulate
host
cells
and
take
up
nutrients.
Who
would
want
miss
such
superpowers?
Indeed,
many
studies
show
how
widespread
the
apparatus
among
microbes.
However,
it
becoming
evident
that,
on
multiple
taxonomic
levels,
from
phyla
species
strains,
some
lack
T6SS.
Here,
we
review
who
does
not
have
speculate
dynamic
process
of
gaining
losing
better
understand
its
spread
distribution
across
microbial
world.