Jt. Meehan et al., INFECTED CELL-TYPES IN OVINE LUNG FOLLOWING EXPOSURE TO BOVINE RESPIRATORY SYNCYTIAL VIRUS, Veterinary pathology, 31(2), 1994, pp. 229-236
Sixteen adult sheep (ten females, six males obtained from a dosed floc
k at National Animal Disease Center, Ames, IA) were experimentally inf
ected with bovine respiratory syncytial virus strain 375 (BRSV), and l
ung tissues were stained for viral antigen. Two infected sheep were eu
thanatized at each of the following post-inoculation times: 12, 24, 36
, 48, 72, 96, 144, and 192 hours. Lung, nasal turbinates, trachea, rig
ht cranial bronchial and mediastinal lymph nodes, liver, and spleen we
re collected for histologic evaluation. An indirect immunoperoxidase t
echnique was performed on routine paraffin-embedded sections of lung t
issue, trachea, turbinates, and bronchial and mediastinal lymph nodes
to determine the location of the BRSV antigen. For lung tissue from ea
ch sheep 400 light microscopic fields at 160x magnification were exami
ned for staining for BRSV antigen. Lung tissue was also collected for
virus and bacterial isolation. Daily serum samples were taken for dete
rmination of anti-BRSV titers. Severe respiratory disease was not prod
uced in any sheep. Bovine respiratory syncytial virus was isolated fro
m lung tissue collected from all sheep up through 144 hours postinocul
ation At 12 hours post-inoculation (case No. 2) respiratory syncytial
virus antigen was detected in bronchiolar epithelium and a mononuclear
cell within an alveolar space. Lung tissue from the sheep necropsied
between 24 and 144 hours post-inoculation (case Nos. 3-14) contained B
RSV antigen in bronchiolar epithelium, type I pneumocytes, type II pne
umocytes, alveolar macrophages, and mononuclear cells within alveolar
spaces. Macrophages staining for viral antigen were rare. Bronchiolar
and type I epithelial cells comprised the majority of infected cells.
In a separate experiment, lung slices inoculated in vitro with either
BRSV or ovine adenovirus did not stain for the respective antigens. Sl
ices inoculated with parainfluenzavirus-3 did stain for that viral ant
igen.