Background and Purpose: Mycoplasma pulmonis is a natural pathogen of the re
spiratory and genital tracts of rats. Differential susceptibility and sever
ity of the respiratory form of the disease, known as murine respiratory myc
oplasmosis (MRM), exist between rat strains. We now report that specific ra
t strains vary in susceptibility to genital tract infection and pregnancy o
utcome.
Methods: Specific-pathogen-free (SPF) female F344, LEW, Wister (WIS) and Sp
rague Dawley (SD) rats were intravaginally inoculated with 3 x 10(7) colony
-forming units (CFU) of M. pulmonis strain X1048 or sterile diluent, and al
lowed to breed at 10 days after inoculation. Pregnant darns and pups were n
ecropsied within 24 hours of parturition. At necropsy, culture for M. pulmo
nis was performed on dam and pups, and adverse effects on pregnancy outcome
were assessed by determination of the incidence of infertility, fetal reso
rption, stillbirths, changes in litter size, and pup birth weight. Blood fr
om darns was collected prior to inoculation and at time of necropsy for mea
surement of IgM and IgG antibodies to M. pulmonis.
Results: At time of necropsy, WIS (50%) and SD (60%) dams had a higher freq
uency of M. pulmonis culture positivity in the genital tract than did LEW (
22.2%) and F344 (17.6%) dams. Dams that were still infected with M. pulmoni
s at time of necropsy had various complications. The SD rats had the greate
st degree of adverse effects on pregnancy outcome, which were: infertility,
decreased litter size (P less than or equal to 0.01), decreased pup birth
weight (P less than or equal to 0.01), increased frequency of resorptions,
stillbirths (P less than or equal to 0.05), and the highest rate of pup pul
monary infection (23.1%) (P less than or equal to 0.001). Despite a 50% col
onization rate, WIS dams were the least adversely affected. The WIS pups bo
rn from M. pulmonis-infected dams had slight decrease in birth weight, and
only 6% had pulmonary infections. The LEW infected dams developed infertili
ty and lower numbers of liveborn pups without evidence of vertical transmis
sion. The F344 infected darns had lower numbers of liveborn pups that were
smaller than their control counterparts, and none had pulmonary infections.
None of the animals had detectable IgM and IgG antibodies to M. pulmonis b
efore inoculation. At time of necropsy, all animals inoculated with M. pulm
onis developed significantly (P less than or equal to 0.001) higher amounts
of M. pulmonis IgG and IgM antibodies, with SD rats developing the highest
amounts (P less than or equal to 0.005),
Conclusions: Both F344 and LEW rats are more resistant to vaginal inoculati
on with M. pulmonis than are WIS and SD rats. However, only SD darns suffer
ed severe adverse effects on pregnancy outcome. The SD dame also had the gr
eatest IgM and IgG antibody response to M. pulmonis. Our studies clearly in
dicate differences among rat strains in their susceptibility to vaginal ino
culation with M. pulmonis and in secondary complications associated with in
fection. This system may be a useful model for determining host-specific fa
ctors that influence the outcome of natural mycoplasmal infections of the g
enital tract.