Yf. Chang et al., RECOMBINANT OSPA PROTECTS DOGS AGAINST INFECTION AND DISEASE CAUSED BY BORRELIA-BURGDORFERI, Infection and immunity, 63(9), 1995, pp. 3543-3549
Twenty-two Specific-pathogen free beagles were vaccinated with recombi
nant OspA (ospA gene derived from Borrelia burgdorferi B31) alone or w
ith adjuvant (QuilA, Montanide ISA25, or aluminum hydroxide) at 6 week
s of age. Thirteen dogs were used as nonvaccinated controls with or wi
thout adjuvant. Three dogs were kept as contact controls and received
neither vaccine nor challenge. Six weeks or 6 months after the first v
accination, the vaccinated (20 of 22) anti nonvaccinated dogs (13) wer
e challenged by exposure to adult ticks (Ixodes scapularis) naturally
that were infected with B. burgdorferi (tick infection rate, greater t
han or equal to 60%) and that were collected from Westchester County,
N.Y. Protection from infection was evaluated by culture for B. burgdor
feri from skin biopsies taken near the sites of tick bites. Skin biops
ies were taken at monthly intervals for 3 months. B. burgdorferi was n
ot isolated from any of the vaccinated dogs. In contrast, 12 of 13 con
trol dogs challenged by exposure to the Licks were culture positive. T
he histopathology of the joint capsules 3 months after the challenge w
as used to evaluate protection from arthritis. Eight of 13 control dog
s showed synovitis in single or multiple joints, while only 1 of the 2
2 vaccinated dogs had a single focus of mild inflammation in a single
joint; At the time of the challenge, the vaccinated dogs had antibody
to B. burgdorferi, which was demonstrable by kinetic enzyme-linked imm
unosorbent assay, Western blotting (immunoblotting), and a serum growt
h inhibition assay. The vaccinal antibody declined gradually after the
challenge, especially in dogs vaccinated with OspA without adjuvants.
Antibodies in the challenge control dogs were only detectable by 4 to
6 weeks after the challenge and remained at high levels until the ter
mination of the study. Contact control dogs showed no antibody respons
es or histopathologic lesions and were culture negative. By Western bl
ot analysis, antibodies to OspA first appeared in the sera of vaccinat
ed dogs 3 weeks after the first vaccination. The absence of additional
bands after the challenge suggests that infection in vaccinated dogs
was blocked. Results from this study show that vaccination with recomb
inant OspA protected dogs against infection and disease after an exper
imental challenge with B. burgdorferi by exposure to ticks.