Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Comparative Genomics Reveal That Host-Innate Immune Responses Influence the Clinical Prevalence of Legionella pneumophila Serogroups.
[legionellosis]
Legionella
pneumophila
is
the
primary
etiologic
agent
of
legionellosis
,
a
potentially
fatal
respiratory
illness
.
Amongst
the
sixteen
described
L
.
pneumophila
serogroups
,
a
majority
of
the
clinical
infections
diagnosed
using
standard
methods
are
serogroup
1
(
Sg
1
)
.
This
high
clinical
prevalence
of
Sg
1
is
hypothesized
to
be
linked
to
environmental
specific
advantages
and
/
or
to
increased
virulence
of
strains
belonging
to
Sg
1
.
The
genetic
determinants
for
this
prevalence
remain
unknown
primarily
due
to
the
limited
genomic
information
available
for
non-
Sg
1
clinical
strains
.
Through
a
systematic
attempt
to
culture
Legionella
from
patient
respiratory
samples
,
we
have
previously
reported
that
34
%
of
all
culture
confirmed
legionellosis
cases
in
Ontario
(
n
 
=
 
351
)
are
caused
by
non-
Sg
1
Legionella
.
Phylogenetic
analysis
combining
multiple
-locus
variable
number
tandem
repeat
analysis
and
sequence
based
typing
profiles
of
all
non-
Sg
1
identified
that
L
.
pneumophila
clinical
strains
(
n
 
=
 
73
)
belonging
to
the
two
most
prevalent
molecular
types
were
Sg
6
.
We
conducted
whole
genome
sequencing
of
two
strains
representative
of
these
sequence
types
and
one
distant
neighbour
.
Comparative
genomics
of
the
three
L
.
pneumophila
Sg
6
genomes
reported
here
with
published
L
.
pneumophila
serogroup
1
genomes
identified
genetic
differences
in
the
O-
antigen
biosynthetic
cluster
.
Comparative
optical
mapping
analysis
between
Sg
6
and
Sg
1
further
corroborated
this
finding
.
We
confirmed
an
altered
O-
antigen
profile
of
Sg
6
,
and
tested
its
possible
effects
on
growth
and
replication
in
in
vitro
biological
models
and
experimental
murine
infections
.
Our
data
indicates
that
while
clinical
Sg
1
might
not
be
better
suited
than
Sg
6
in
colonizing
environmental
niches
,
increased
bloodstream
dissemination
through
resistance
to
the
alternative
pathway
of
complement
mediated
killing
in
the
human
host
may
explain
its
higher
prevalence
.