Canine herpesvirus 47 kD and mutated 41 kD glycoproteins are responsible for hemagglutination

Monoclonal antibodies (MoAbs) were used to identify the hemagglutinin of canine herpesvirus (CHV). The inhibition of viral hemagglutination (HA) activity was observed with MoAbs against 41 kD glycoprotein, while no hemagglutination-inhibition (HI) activity was observed with those against 145/112 kD and 80 kD glycoproteins, suggesting that the 41 kD glycoprotein is the hemagglutinin of plaque-selected virus of CHV YP11 strain used as immunogen for MoAb production. All of the HI MoAbs also showed HI activities against HA antigens which were prepared from cells infected with other CHV strains, namely, F-205 V and Glasgow CHV2 reference strains, eight Japanese isolates, and the original YP11 strain. However, on immunoblotting analysis, a 47 kD protein band was detected in these strains by the HI MoAbs. These data suggest that the 47 kD glycoprotein is the common molecule of the hemagglutinin among CHV strains and the plaque-selected virus of YP11 strain appears to be a mutant whose molecular weight of the hemagglutinin changed into 41 kD.     

Hemagglutination-inhibition test applied to the study of akabane virus infection in domestic animals

Some factors affecting the hemagglutination-inhibition (HI) reaction with Akabane virus were investigated and an HI test developed. The test was proven to be useful in studies of antibody responses in cattle and other domestic animals infected with Akabane virus. HI antibody titers of individual animals were shown to be closely correlated with their neutralizing antibody titers and to remain undiminished for a relatively long time. In some early sera from domestic animals infected with Akabane virus, HI antibody sensitive to 2-mercaptoethanol was demonstrated.     

Serodiagnosis of canine herpesvirus infection--development of an enzyme-linked immunosorbent assay and its comparison with two improved methods of serum neutralization test

An enzyme-linked immunosorbent assay (ELISA) for the diagnosis of canine herpesvirus (CHV) infection using antigen prepared by solubilizing infected cells was developed. The ELISA and two improved methods of serum neutralization test, the microplate serum neutralization test (MSNT) with complement and the 50% plaque reduction (PR) assay with complement, were compared for the results of antibody detection from a total of 557 field canine sera. Of 529 sample sera that were negative in the MSNT with complement, 119 were ELISA positive, and this result together with time course of serum antibody detection in a dog experimentally infected with CHV strongly suggested that the MSNT with complement is less sensitive for the detection of antibody in CHV infected dogs, especially those in early stages of infection. A correlation was found between the titers measured by the ELISA and 50% PR assay with complement, however, for field use, the ELISA is recommended as a highly sensitive test method of serodiagnosis of CHV infection adequate for dealing with a large number of samples with less demand on time and effort.     

Reproduction of acute bracken poisoning in a calf with ptaquiloside, a bracken constituent

Acute bracken fern toxicity in a calf was reproduced with ptaquiloside, a norsesquiterpene glucoside, isolated from the boiling water extract of bracken fern. Ptaquiloside was dissolved in 500 ml of saline and administered by drench at increasing dosages for six days out of every seven for the following periods: 400 mg/day for 24 days, 800 mg/day for 14 days and 1600 mg/day for four days. Neutrophilic granulocytes began to decrease markedly around 50 days after the start of the experiment, and granulocytopenia continued for a further 35 days until the autopsy, despite the discontinuance of ptaquiloside administration. Thrombocytes showed a relatively slow depression and reached 1 X 10(5)/mm3 at the lowest level. The calf was autopsied 86 days after the start of administration of ptaquiloside. Sternal bone marrow was found to be mostly replaced with fat marrow and only small foci of erythropoietic cells and a small number of megakaryocytes remained.     

Turnover of Dominant Follicles prior to First Ovulation and Subsequent Fertility in Postpartum Dairy Cows

Contents: The ovaries of 64 multiparous Holstein cows were scanned twice weekly by ultrasonographyfrom Day 6 postpartum until 60 days or return to normal estrous cycle, and turnover of dominant follicles in relation to subsequent fertility were determined. The mean (SD) number of days from parturition to detection of the first postpartum dominant follicle (10 mm) was 9.0 0.5, which was predominantly located in the ovary contralateral to previous pregnancy in 54/64 cows. The first postpartum dominant follicle ovulated in 34 cows, failed to ovulate in 18, became cystic in 10, and only 2 were diagnosed as ovarian quiescent which delayed the detection of dominant follicles until days 25 and 30 postpartum. Number of dominant follicles in cows with anovulated first dominant follicle was 2.8. 1.1 prior to first ovulation (range 2–5). Growth and regression of cystic follicles were observed 24 times in 6110 cows, and a total of 20 cystic follicles persisted 32.7 9.0 days (range 18–58 days) except one which persisted for 124 days. Conception rate was 89.5% and postpartum interval to conception within 180 d after calving was 96.7 days in cows detected with less than 3 dominant follicles before first ovulation compared with those of 42.9% and 141 days in cows detected with more than 4 dominant follicles. It is concluded that the number of dominant follicles detected prior to first ovulation varied from I to 5, which positively correlated with ovulation intervals, while only those cows which first ovulated less than 3 dominant follicles resulted in reasonable reproductive performance.