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Biomedical subjects

D M West

Publications and source records attributed to D M West.

At least 73 records · Page 4Linked to original sources

Comparison of a complement fixation test, a gel diffusion test and two absorbed and unabsorbed ELISAs for the diagnosis of paratuberculosis in sheep.

A complement fixation test for paratuberculosis, a gel diffusion test and two enzyme-linked immunosorbent assays (ELISA) were evaluated using sera from Mycobacterium paratuberculosis infected and non-infected sheep. Gross pathology and histopathology were used as parameters of infection. The two ELISAs, one of which is commercially available for testing cattle, were used before and after sera had been absorbed with a soluble sonicate of Mycobacterium phlei. Differences between the various tests and between ELISAs before and after absorption were non-significant (P > 0.05) in non-infected sheep or in animals with gross or histopathological lesions. The specificity of all the tests was at least 97%. Sensitivity in histopathologically positive sheep was at least 98%. Sheep from infected flocks but without histopathological lesions showed serological results which were poorly correlated between the various tests.

Animals↗

Nematode worm egg output by ewes.

The results from routine monitoring of parasite burdens in ewe flocks from 1980 to 1991 by the Massey University Veterinary Clinic were analysed. Faecal strongylate nematode egg counts from 401 flock samples were analysed according to ewe age (two-tooth, 16-23 month-old vs mixed-age, greater than 2-year-old ewes) and month of the year. Each flock sample contained faeces from ten ewes and nematode egg counts were carried out on each faecal sample. ln the mixed-age ewes, the overall mean faecal egg count per gram of faeces (epg) was lowest during January (82 epg) and rose to a peak during October (539 epg). The overall mean faecal egg count in two-tooth ewes remained constant from January (240 epg) to June (294 epg) and dropped during July (156 epg). Overall, 8% of the mixed-age ewes and 12% of the two-tooth ewe submissions had a mean egg count equal to or greater than 500 epg. It is possible that these data over-estimate the pasture contamination by ewes as farmers are more likely to submit faecal samples and to seek veterinary assistance when parasitism is thought to be a problem. The role of ewes as a source of pasture contamination should be considered when developing parasite control regimes on farms.

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The effect of repeated doses of toltrazuril on coccidial oocyst output and weight gain in suckling lambs.

Coccidial oocyst output and liveweight were monitored in 43 pairs of lamb twins over a 10-week period during September-November 1992. One of each set of twins was treated orally with toltrazuril (20 mg/kg) weekly while the other was an untreated control. The oocyst output was significantly lower (P < 0.01) and the weight gain over the trial period was significantly greater (P < 0.05) in the treated group than in the control group.

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Observations on three outbreaks of Leptospira interrogans serovar pomona infection in lambs.

Sickness and deaths associated with leptospirosis were reported in three lamb flocks in the Manawatu region. The clinical, pathological and serological features of Leptospiru interrogans serovar pomona infection are described. The mucous membranes of affected animals were pale and jaundiced. Haemoglobinuria, haemoglobinaemia and centrilobular hepatocellular necrosis were also consistent findings. All clinically sick lambs had very high titres in the microscopic agglutination test for L. pomona. Circumstantial evidence of pigs being the source of infection was found in one of the three cases.

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Serological and necropsy findings for rams infected with Brucella ovis which were not identified by the complement fixation test.

The eradication of Brucella ovis from a commercial flock of 36 Romney rams was complicated by four infected rams remaining undetected despite four successive flock examinations using the complement fixation test. These four rams were subsequently tested using an enzyme-linked immunosorbent assay and a gel diffusion test and shown to be infected by semen culture. All four rams could have been identified as infected at the initial test if the enzyme-linked immunosorbent assay had been used in addition to the complement fixation test. Although gross evidence of epididymitis was found in only one ram at necropsy, three had histological lesions of epididymitis and all four had a seminal vesiculitis.

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Observations on the eradication of Brucella ovis infection from a ram flock.

The measures taken to eradicate Brucella ovis infection from a naturally infected flock of 64 rams are described. Lesions of epididymitis were detected in 18 rams, all of which gave either positive or suspicious reactions in the complement fixation test. A further 20 rams gave serological reactions in the complement fixation test. Subsequently, semen was collected from 14 of these 20 rams and B. ovis was cultured from the semen of all 14 rams. Serum samples from two rams failed to react in the complement fixation test. However, they were identified as infected with the aid of an enzyme-linked immunosorbent assay and the subsequent culture of semen samples. It is suggested that, when eradicating B. ovis infection from ram flocks, the enzyme-linked immunosorbent assay be used in addition to both the complement fixation test and the physical examination. Using a combination of tests as described can increase the likehood of an earlier eradication of B. ovis infection.

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Multigeneric resistance to benzimidazole anthelmintics in four sheep flocks.

Clinical parasitism associated with multigeneric resistance to benzimidazole anthelmintics was investigated in four sheep flocks during February and March 1989. The genera considered resistant were Haemonchus and Nematodirus spp. on all four farms and Trichostrongylus and Ostertagia spp. on three of the four farms. It is suggested that when investigating cases of suspected drench resistance, post-drenching worm counts are useful to help identify the resistant worm species present.

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Local tissue reaction to the administration of an inactivated Brucella ovis saline-in-oil vaccine by the intraperitoneal route.

An inactivated Brucella ovis saline-in-oil vaccine was administered to 14 adult ewes using both the intraperitoneal route and the subcutaneous route. Pairs of animals were necropsied at intervals between 24 hours and ten weeks after injection. The nature of the local inflammatory reaction to the administration of the vaccine was similar at all sites. The lesion consisted of granulomatous inflammation arranged around droplets of oily vaccine. Diffuse peritonitis was seen at necropsy in 12 of the 14 animals. A local extraperitoneal inflammatory response at the injection site was present in four animals despite careful attempts to deposit the vaccine within the abdominal cavity. A second study of 30 rams vaccinated by the intraperitoneal technique confirmed that extraperitoneal deposition of vaccine commonly occurred and that approximately 20% of animals vaccinated by the intraperitoneal method still had peritonitis six months later.

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The response of vaccinated rams to experimental challenge using Brucella ovis.

One hundred and thirty eight rams were allocated to four experimental groups. An inactivated Br. ovis vaccine was administered either once by the intraperitoneal route (1 i/p), twice by the intraperitoneal route (2 i/p), or twice by the subcutaneous route (2 s/c), and the last group was left unvaccinated. They were then challenged by the intravenous inoculation of between 123 and 1.23 x 108 live Br. ovis bacteria. The number of rams that succumbed to infection within the four groups was 4135 (11%) for the 2 s/c, 7133 (21%) for the 2 i/p, 9135 (26%) for the 1 i/p and 18135 (51%) for the unvaccinated rams. Vaccination reduced the number of rams that succumbed to experimental challenge and although there were differences between the vaccinated groups, these were not statistically significant. Following challenge, unvaccinated rams were the first to excrete Br. ovis in their semen three weeks following inoculation. Next, those vaccinated by either one or two doses by the intraperitoneal technique began to excrete the organism (five weeks) and then finally those rams vaccinated twice by the subcutaneous route (seven weeks).

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The serological response of rams to four methods of vaccination against Brucella ovis infection.

A comparative study was made of the serological response of rams to an inactivated Brucella ovis saline in-oil vaccine administered either once or twice by either the subcutaneous or the intraperitoneal route. The serological response of rams to two spaced doses of vaccine was more consistent and more persistent than when a single dose of vaccine was used. The rise in titre was more rapid and the final titre of greater magnitude when the subcutaneous route of administration was used in comparison with the intraperitoneal route. On a serological basis, the most satisfactory vaccination technique investigated consisted of two subcutaneous injections of vaccine administered ten weeks apart. The least satisfactory technique was a single intraperitoneal injection.

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