The pathogenesis of quail bronchitis.

To determine the fate of virus and characterize the development of lesions, 1-week-old bobwhite quails (Colinus virginianus) were inoculated intratracheally with 10(6) mean tissue-culture-infective doses of quail bronchitis virus. Quails were killed and necropsied sequentially at 2, 4, 8, 16, and 24 hours postinoculation (PI) and on days 2-10 PI. Virus was first isolated from the lung as early as 2 hours PI, from cecal tonsils and bursa of Fabricius 4 hours PI, and from spleen and liver 8 hours PI.

Immune function in pheasants experimentally infected with marble spleen disease virus.

Two experiments were conducted to evaluate the effect of marble spleen disease virus (MSDV) infection on the immune response of pheasants. In the first, 15 ring-necked pheasants were inoculated orally with cell-culture-propagated MSDV and 15 received saline (controls). On days 7, 21, and 35 postinoculation (PI), all birds received sheep erythrocytes intravenously.

Detection of type II avian adenoviral antigen in tissue sections using immunohistochemical staining.

An immunohistochemical staining technique for the detection of marble spleen disease (MSD) viral antigens and other type II avian adenoviral antigens was developed using a mixture of monoclonal antibodies produced against hemorrhagic enteritis (HE) virus and a commercial streptavidin-biotin peroxidase indicator system. This technique was applied to both frozen and formalin-fixed paraffin-embedded tissue sections. The immunohistochemical staining technique was used on tissues from pheasants with experimental MSD, on tissues from a pheasant with natural MSD, and on tissues from turkeys with natural HE.

The influence of age on the response of ring-necked pheasants to infection with marble spleen disease virus.

Ring-necked pheasants that were negative for maternal antibody against type II avian adenoviruses were orally inoculated with 5.0 x 10(2) tissues-culture-infective doses of marble spleen disease (MSD) virus at 1-week intervals through 6 weeks of age, and at 9 and 13 weeks of age. Groups of four virus-inoculated birds and two control birds were necropsied at 4, 6, 8, and 10 days postinoculation, and the spleens were evaluated for gross and microscopic lesions.

Identification of Pneumocystis carinii in immunodeficient mice.

Various procedures were utilized to determine the most sensitive, cost and labor effective techniques for detection of Pneumocystis carinii in immunologically compromised mice. Immunoperoxidase staining techniques that utilized polyclonal antibodies directed against purified rat or mouse P. carinii were more sensitive and specific than staining with Gomori's methenamine silver.