The use of immunochemically purified anti-brucella antibody in a direct fluorescent antibody test for Brucella abortus

Antibodies specific for Brucella abortus were purified from the serum of hyperimmunized sheep using immunochemical procedures. They were conjugated to fluorescein isothiocyanate and used in a fluorescent antibody (FA) test for B. abortus. The conjugate did not stain any heterologous bacterial or fungal species tested and background fluorescence associated with its use on smears and sections of abortion materials was particularly low. Of 239 cases of abortion examined fluorescent microscopy demonstrated B. abortus in all 12 cases in which the organism was isolated. A few areas of fluorescence typical of B. abortus were also seen in 3 cases from which the organism was not cultured. B. abortus was demonstrated in lymph nodes from 6 of 36 Brucella reactor cows by culture and 7 by the FA test. However, only very low numbers of B. abortus were isolated or seen and sampling errors would have been significant. Use of the FA test allows diagnosis of Brucellosis to be made in 2 hours, compared to 6 days by the usual cultural procedures.     

The correlation between Salmonella serology and isolation of Salmonella in Danish pigs at slaughter

In Denmark, a serological Salmonella surveillance programme in finishing pig herds has been in place since 1995. The programme was founded on data from experimental studies, which demonstrated a strong association between Salmonella serology and the prevalence of these bacteria. The current study was carried out in three Danish abattoirs to evaluate the correlation under field conditions. A total of 160 Danish finishing pig herds were included. Seven out of these were examined twice, yielding a total of 167 observations. The herds were selected according to their herd serology based on data from the national surveillance. From each herd, samples were taken from 10 finishers at slaughter. The prevalence of Salmonella bacteria was measured at four sites: (1) caecal-content; (2) carcass surface; (3) pharynx; and (4) caecal lymph nodes. A logistic regression model was constructed for each sampling site. Abattoir, sanitary slaughter and herd seroprevalence were used as explanatory variables. The results demonstrated that there was a strong association between herd serology and the prevalence of Salmonella bacteria measured at three of the sampling sites: caecal-content, pharynx, and carcass surface. For these sites, the odds for being culture-positive for Salmonella varied from 1.3 to 1.5 for each increase of 10% in herd serology (P < 0.0001). For caecal lymph nodes, however, no linear association was found.     

Canine nasal aspergillosis: serology and treatment with ketoconazole

Seven cases of nasal aspergillosis in dogs were diagnosed using radiography, endoscopy, culture and serology. Treatment with oral ketoconazole (an imidazole derivative) at 40 mg/kg b. wt, alone or in combination with surgery resulted in three cures, while in four dogs this therapy was not successful. In all cases inappetance and hypoal-buminaemia were noted and rises in levels of serum alkaline phosphatase (SAP) and alanine aminotransferase (ALT) were recorded in six of the seven cases. Serological monitoring was conducted during the period of therapy and in cases that recovered a fall in titre was noted.     

Heartwater serology: some problems with the interpretation of results

Antibodies in the sera of domestic ruminants that have been infected with Ehrlichia bovis and other ehrlichial agents cross-react with the Kümm strain of Cowdria ruminantium used in the indirect fluorescent antibody test as antigen. These cross-reactions are also shown by the Elisa test in which the Ball 3 strain of the heartwater agent is used as antigen.     

Diagnosis of brucellosis by serology

Serological diagnosis of brucellosis began more than 100 years ago with a simple agglutination test. It was realized that this type of test was susceptible to false positive reactions resulting from, for instance, exposure to cross reacting microorganisms. It was also realized that this test format was inexpensive, simple and could be rapid, although results were subjectively scored. Therefore, a number of modifications were developed along with other types of tests. This served two purposes: one was to establish a rapid screening test with high sensitivity and perhaps less specificity and a confirmatory test, usually more complicated but also more specific, to be used on sera that reacted positively in screening tests. This led to another problem: if a panel of tests were performed and they did not all agree, which interpretation was correct? This problem was further compounded by the extensive use of a vaccine which gave rise to an antibody response similar to that resulting from field infection. This led to the development of an assay that could distinguish vaccinal antibody, starting with precipitin tests. These tests did not perform well, giving rise to the development of primary binding assays. These assays, including the competitive enzyme immunoassay and the fluorescence polarization assay are at the apex of current development, providing high sensitivity and specificity as well as speed and mobility in the case of the fluorescence polarization assay.     

Foot-and-mouth disease typing and serology in Zimbabwe

A small foot-and-mouth disease diagnostic unit was established in Zimbabwe. Twenty-six out of 27 field specimens were successfully typed using the complement fixation technique. The antibody response in cattle to the SAT II vaccine was determined using a microtitre neutralisation method. Techniques are described which should be within the capacity of laboratories in developing countries.     

The bacteriology and serology of ewes inoculated with viable Brucella ovis organisms

A series of 10 farm trials was conducted in which the lambing performance of ewes immunised against polyandroalbumin was compared with that of untreated ewes in the same flock. The trials show that polyandroalbumin treatment is a reliable method of increasing lambing and tailing percentages in New Zealand flocks. An average of 39 extra lambs born per 100 ewes tupped was achieved on farms where ewes were given two treatments about four weeks apart and rams were introduced 18–26 days after the second dose. On farms where rams were introduced less than 12 days after this booster injection an average of 19 extra lambs born per 100 ewes tupped resulted.

On farms where rams were introduced at 18–26 days post booster injection an average of 35 extra lambs were tailed for every 100 ewes tupped.

The response for immunization increased in direct relation to the liveweight of the ewes at tupping.     

ELISA for the serology of FIP virus

Summary

An enzyme linked immunosorbent assay (ELISA) for feline infectious peritonitis (FIP) virus serology is described. The assay is analogous to a previously developed indirect heterologous immunofluorescence test (IFT) in which transmissible gastroenteritis (TGE) viral antigen was used. Comparative testing of selected feline sera in both assays resulted in corresponding titers, which justifies the conclusion that the ELISA is a reliable test for the serology of FIP virus.     

Listeria abortions in cattle--bacteriology, serology and epizootiology

Listeria abortions were established in foetuses of cattle in 1.2% of the cases investigated in the Erfurt region and 1.8% in the Cottbus region from 1984 to 1989. The isolated strains have been found biochemically to be L. monocytogenes. The serological discrimination revealed a majority of serovar O I, II. Typing by phages of a part of isolated strains showed a clear predominance of code number 000 124 by the 1/2 a isolate (corresponds to O I, II). This type of phages seems to have a epizootiological importance. Listeria abortions were found in (a lot of 63) flocks in the Erfurt region. Nevertheless there were almost no accumulations of listeria abortions and listeria encephalitis at the same time in the analysed flocks.     

ELISA for the serology of FIP virus

Summary An enzyme linked immunosorbent assay (ELISA) for feline infectious peritonitis (FIP) virus serology is described. The assay is analogous to a previously developed indirect heterologous immunofluorescence test (IFT) in which transmissible gastroenteritis (TGE) viral antigen was used. Comparative testing of selected feline sera in both assays resulted in corresponding titers, which justifies the conclusion that the ELISA is a reliable test for the serology of FIP virus.     

Reovirus serology in broiler parents and their progeny and its correlation with performance.

An intensive vertically integrated monitoring program for broiler breeders and their offspring was set up in a Belgian poultry integration between 1993 and 1997. Serology for anti-reovirus antibodies was performed by enzyme-linked immunosorbent assay on blood samples taken from the broiler parents throughout rearing and production and also on blood samples taken at day-old and at slaughter from the broilers. Furthermore, production parameters of the birds were registered. All data were used two by two in a simple correlation study to calculate the degree to which these variables were linearly correlated. The reovirus antibody pattern indicated frequent field infections breaking through vaccinal immunity in the broiler parents. Under the epidemiologic conditions of this study, high antibody titers in the parents or in the broilers at day-old were significantly correlated with poor feed conversion, increased mortality, increased slaughterhouse condemnation, and low production score in the broilers. These correlations strongly support the view that reovirus infections can be economically important under European conditions of broiler production. Improvement of reovirus vaccines or the vaccination scheme in broiler parents or both may lead to better production results in the broiler offspring.     

Prevalence and serology of hydatidosis in large ruminants of Pakistan

Hydatidosis was seen in 38.90% of cattle, 33.06% of buffaloes and 58.9% of camels slaughtered at a local abattoir. No statistically significant seasonal difference in prevalence was observed. Most cysts (63.14%) were infertile. Protein and carbohydrate contents of fluid from fertile and infertile cysts did not differ significantly. Sensitivity, specificity and efficiency of indirect haemagglutination test and enzyme-linked immunosorbent assay were low.