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ospA

OspA (Outer Surface Protein A) is a major surface-expressed lipoprotein of the spirochete Borrelia burgdorferi, the causative agent of Lyme disease. The ospA gene encodes a 27 kDa protein that anchors to the bacterial outer membrane via a covalently attached lipid moiety at its N‑terminal cysteine residue. Structurally, OspA consists of a series of alpha‑helical segments that form a dimeric assembly, presenting antigenic loops accessible to host antibodies.

In the tick midgut, OspA expression is highly up‑regulated during larval feeding, facilitating bacterial adhesion to

The immunogenicity of OspA has been exploited for vaccine development. One of the first licensed Lyme disease

Detection of OspA or anti‑OspA antibodies is also employed in diagnostic assays to infer recent exposure to

epithelial
cells
and
preventing
premature
transmission
to
a
mammalian
host.
When
the
tick
molts
and
the
spirochete
is
transferred
to
a
vertebrate,
ospA
expression
is
sharply
down‑regulated
while
other
outer
surface
proteins
such
as
OspC
are
induced,
promoting
colonization
of
host
tissues.
This
phase‑variable
regulation
is
controlled
by
a
stringent
response
system
and
epigenetic
mechanisms.
vaccines,
LYMErix,
consisted
of
recombinant
OspA
conjugated
to
a
carrier
protein
and
linked
to
alum
adjuvant.
The
vaccine
elicited
high
titers
of
anti‑OspA
IgG,
which
could
neutralize
spirochetes
in
the
tick
midgut,
thereby
reducing
transmission.
However,
concerns
about
autoimmune
cross‑reactivity,
low
efficacy
in
high‑endemic
areas,
and
declines
in
public
acceptance
led
to
its
withdrawal
in
the
United
States.
Novel
subunit
and
adjuvant
formulations
are
currently
under
investigation
to
improve
safety
and
robustness
of
the
immune
response.
tick‑borne
B.
burgdorferi.
In
murine
models,
the
presence
of
OspA
mRNA
in
infected
tissues
correlates
with
early
infection,
whereas
persistent
expression
has
been
noted
during
chronic
phases
in
some
hosts.
Overall,
OspA
remains
a
key
molecular
marker
for
both
the
biology
of
Lyme
disease
transmission
and
the
development
of
targeted
interventions.