Evaluation of a PCR test for the diagnosis of Brucella ovis infection in semen samples from rams

The sensitivity and specificity of a PCR assay with primers derived from the insertion sequence IS6501 was compared with that of bacteriological culture and serological tests for the diagnosis of Brucella ovis infection in rams. No amplifications were detected with DNAs from the strains phylogenetically related to Brucella and from the seven bacterial species considered as the main etiologic agents of epididymitis in rams. In addition, the specificity of the PCR was 100% when testing semen samples from Brucella-free rams. The comparison of the semen culture and PCR results from 192 semen samples tested, showed a proportion of agreement of 0.91 between both tests. The PCR-based test described has sensitivity similar to that of semen culture and could be used as a complementary test for the direct diagnosis of Brucella ovis in semen samples of rams.     

Evaluation of an enzyme linked-immunosorbent assay for the diagnosis of Brucella ovis infection in rams

A simple enzyme linked immunosorbent assay (ELISA) was developed for the serological diagnosis of Brucella ovis infections in rams. Serums from brucellosis accredited-free flocks and flocks known to be infected with B. ovis were tested and the results correlated with warm complement fixation (CF) test and bacteriological examination of semen. Both the ELISA and the CF test detected 0.5% false positive reactions in rams from clinically negative flocks. However the ELISA detected significantly more positive reactors in infected flocks and the CF test failed to detect some rams excreting B. ovis. The ELISA proved to be a valuable test in eradicating brucellosis from infected flocks.     

Evaluation of a technique for measurement of gamma-glutamyltranspeptidase in equine urine

gamma-Glutamyltranspeptidase (GGT) activity in equine urine was measured, using an assay developed for use with serum and was found to be reproducible. The GGT activity was measured in samples prepared by serial dilution of exogenous GGT with equine urine, and the activity was determined to be linear between 21 IU/L and 407 IU/L. The behavior of exogenously added GGT was compared in equine serum and urine. The enzyme behaved similarly in both fluids. The GGT activity was measured in serum and urine samples after storage at -20, 4, and 25 C for 24 and/or 72 hours. Enzyme activity decreased after storage at all temperatures and times, but the decrease was greatest and most variable at -20 C. The urine GGT: urine creatinine ratio was calculated on serial urine samples collected over 24 hours. Although the urine GGT activity and creatinine concentration had significant variation, the ratio remained constant. The urine GGT: urine creatinine ratio was calculated from random urine samples collected from 27 clinically healthy adult horses and was found to be 10.52 +/- 4.78 (mean +/- SD).     

Intraperitoneal vaccination of rams

Extract

Sir, —A recent issue of the Animal Health Division's excellent publication Surveillance (1978 No.5 Spring), reported that the Palmerston North Animal Health Laboratory had encountered a case involving 40 two-year-old rams, the majority of which had intramuscular perirenal abscesses. It was reported that these abscesses were due to vaccination with a single dose of Br. ovis vaccine, administered by the intraperitoneal route.     

Evaluation of a minimally invasive arthrodesis technique for the carpometacarpal joint in horses

Objective: To evaluate a minimally invasive technique for arthrodesis of the carpometacarpal (CMC) joint in horses. Study Design: Experimental study. Animals: Healthy horses (n=6). Methods: A 5.5 mm, 3‐drill tract arthrodesis technique was evaluated in 1 randomly selected CMC joint in each of 6 normal horses. Peak vertical ground reaction force (GRF) values were recorded before surgery and at 6, 8, and 12 months thereafter. Radiographic and clinical lameness scores were assigned at regular intervals until 12 months after surgery when the horses were euthanatized. Gross and histologic examinations were performed on the treated CMC joints. Results: After surgery, all horses were lame. Clinical resolution of lameness occurred in 2 by 12 months. Mean peak vertical GRF values significantly differed between treated and nontreated limbs at all recorded time points after surgery. Radiographic scores significantly differed from day 0 at all times after surgery, but did not change significantly after 4 months. Intraarticular bony ankylosis only occurred in 2 horses, based on gross, histologic, and microradiographic examination of sagittal sections of the operated CMC joints. Conclusion: The 5.5 mm, 3‐drill tract arthrodesis technique was considered successful in only 2 of 6 normal CMC joints treated. Greater articular damage may be necessary to achieve arthrodesis in normal horses. Better results may be achieved by technique modification or in horses affected by CMC osteoarthritis.     

Chemotherapy of brucellosis in rams

Abstract

Extract

Recognition that one infective agent could cause ram epididymitis and ewe abortion in New Zealand was due to McFarlane et al. (1952 McFarlane, D., Jebson, J. L., Hartley, W. J., Salisbury, R. M., McClure, T. J. and Osborne, H. G. 1952. Aust. vet. J., 28: 226–226. [Crossref] , [Google Scholar]). The organism was not identified at that time, but Buddie and Boyes (1953 Buddle, M. B. and Boyes, B. W. 1953. Aust. vet. J., 29: 145–153. [Crossref] , [Google Scholar]) classified it in the genus Brucella—possibly a variant of Br. melitensis. This finding provided a basis for research on control and treatment of the disease. The present paper describes studies on one aspect of this problem, the chemotherapy of affected rams.     

Brucella ovis vaccination of rams

Abstract

Extract

An infectious epididymitis of rams caused by Brucella ovis (Buddie, 1956 Buddle, M. B. 1956. J. Hygiene, 54: 351–351.  [Google Scholar]) infection, first described in Australia (Simmons and Boyes, 1953 Simmons, C. G. and Hall, W. J. K. 1953. Aust.vet.J., 29: 33–33. [Crossref] , [Google Scholar]) and New Zealand (Buddie and Boyes, 1953 Buddle, M. B. and Boyes, B. W. 1953. Aust.vet. J., 29: 145–145. [Crossref] , [Google Scholar]) was recognized subsequently in Czechoslovakia (Gdovin et al, 1955 Gdovin, T., Hrudka, F., Chladecky, E. and Koppel, Z. 1955. Shorn, ces. Akad. zemedelsk Ved., 28: 617–617.  [Google Scholar]), the United States (McGowan and Shultz, 1956 McGowan, B. and Shultz, G. 1956. Cornel Vet., 46: 277–277.  [Google Scholar]), South Africa (Van Rensburg et al, 1958 Van Rensburg, S. W. J., Van Heerden, K. M., Le Roux, D. J. and Snyders, A. J. 1958. J.S.Afr. vet. med. Ass., 29: 223–223.  [Google Scholar]), Rumania (Tudoriu, et al, 1958 Tudoriu, C. D., Andrei, M., Draghici, D. and Moldoveanu, P. 1958. Anu. Inst. Pat.Igien. anim. Bucaresti, 8: 5–5.  [Google Scholar]), and South America (Dr Justo Zomara B, 1961, pers. comm.). As the infection can affect ram fertility and, further, can be responsible for abortion in ewes and perinatal mortality in lambs, attention has been directed to the development, evaluation, and application of control measures in a number of important sheep-raising countries.     

Evaluation of a standardised radiographic technique of the equine hoof

Radiography of the equine hoof is often used to obtain a diagnosis. Quantitative interpretation, especially for research purposes requires high quality and accuracy of radiographs. The purpose of this study was to describe and evaluate a radiographic technique for the lateromedial (LM) and the dorsopalmar (DP) view of the equine hoof. Ten radiographs for each view from one cadaver limb and from both front feet in a standing horse were taken in order to assess repeatability of the radiographic technique. The method requires easy to use adjustable and portable equipment and strictly defined external radio opaque markers on the hoof capsule. The digitalised radiographs were processed and analysed with the software package Metron PX, measuring 13 parameters in the LM view and 10 parameters in the DP view, respectively. Results show that with few exceptions measurements of these parameters revealed a coefficient of variation that was smaller than 0.05. It was concluded that this easy to use standardised radiographic technique ensures excellent accuracy and repeatability for both the LM and DP view. Hence, this method provides an adequate tool for quantitative assessment of the equine hoof, inter- and intraindividually.     

A specific suppurative epididymitis of rams

On the basis of worm counts in naturally infected Angora-X goats, albendazole at either 3.8mg/kg repeated after 24 hours or as a single dose at 7.6mg/kg, was >99% effective in removing adult Ostertagia and Trichostrongylus spp. Small numbers of adult Haemonchus contortus, Cooperia sp. and Chabertia ovina were present in control but not treated animals. The single dose of 7.6mg/kg removed > 99% of adult Oesophagostomum venulosum whereas the repeated dose of 3.8mg/kg removed only 96%.     

Evaluation of surface components of Brucella ovis as antigens for the detection of precipitin antibody in serums from artificially exposed rams

Surface components of Brucella ovis obtained by gentle physical shearing were tested as a potentially useful source of reagent for selective serological diagnosis. These antigens were used in a radial immunodiffusion (RID) test against serum from rams which had been inoculated with infective semen containing B. ovis by one of 4 routes namely mating rams with ewes previously inoculated intravaginally with infective semen, or by direct inoculation in the prepuce, rectum or nasal passage. Loosely attached surface antigens in the RID test formed precipitin bands with serums collected from rams 2 and 10 weeks after inoculation. In contrast, a detergent extracted membrane antigen B developed precipitin bands only with serum collected 10 weeks after inoculation from rams confirmed bacteriologically to be infected with B. ovis in the genital tract. The route by which the rams were artificially exposed did not affect the outcome of the RID test using the membrane B antigen. However, all experimentally exposed rams had demonstrable CF titres when a heat extracted antigen was used.