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K W Angus

Publications and source records attributed to K W Angus.

At least 37 records · Page 2Linked to original sources

Effect of concurrent infection with Ostertagia circumcincta and Trichostrongylus vitrinus on the performance of lambs.

The interaction between Ostertagia circumcincta and Trichostrongylus vitrinus was investigated in lambs continuously infected over 12 weeks. Four groups of seven lambs were given either zero, 1000 T vitrinus larvae per day, 2500 O circumcincta larvae per day or infected concurrently. Overall liveweight gain was reduced by 17, 20 and 30 per cent in T vitrinus, O circumcincta and concurrent infection, respectively. T vitrinus infection significantly lowered serum phosphorus concentrations by week 4. In the concurrent infection the decline in phosphorus concentration was more gradual and only differed significantly from the controls during the final four weeks of the trial. There were no significant differences between the total numbers of T vitrinus or O circumcincta recovered from single or combined infections. The lack of an additive effect on performance may be due to a delayed establishment of T vitrinus in the presence of O circumcincta.

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Infectivity of a strain of Cryptosporidium found in the guinea-pig (Cavia porcellus) for guinea-pigs, mice and lambs.

Cryptosporidiosis was diagnosed in guinea-pigs bred by a commercial laboratory supplier on histological examination of the intestine. Oral transmission to laboratory guinea-pigs aged up to 16 weeks and to infant mice, with gut contents containing oocysts, was successful, but the organism failed to infect adult mice. From day 5 post-inoculation (pi) in guinea-pigs, infection of the ileum was associated with villous stunting and fusion, and with infiltrates of macrophages and other mononuclear cells, and eosinophils. Some guinea-pigs died; others were depressed and anorectic, with diarrhoea or watery caecal contents. Mouse infections were subclinical and caused no significant pathological changes. By contrast, a bovine Cryptosporidium isolate infected infant mice but failed to infect young guinea-pigs. Guinea-pigs and infant mice excreted oocysts in faeces after a prepatent period of 3 to 4 days. Some guinea-pigs excreted oocysts for up to 2 weeks, but excretion in mice lasted only about 4 days. Infection of guinea-pigs by contact with a contaminated environment occurred, with excretion of oocysts between 17 and 27 days after exposure. An indirect fluorescent antibody test (IFA) showed that antibody was present by day 17 pi with infected bowel contents, but none was detected in the guinea-pigs exposed to the contaminated environment. The IFA test demonstrated a serological relationship between the guinea-pig isolate and a bovine strain used to infect gnotobiotic lambs. Transmission electron microscopy of intestine from infected guinea-pigs and mice showed that more than one schizont generation occurred. The first consisted of 8 merozoite packets attached to enterocytes, but many packets of 2 or 4 merozoites of the second or subsequent generations were apparently released into the gut lumen. Fixed microgametocytes contained lipid vacuoles and had microneme-like structures in their cytoplasm. Oocysts and sporocysts were also identified, with sporulation occurring within the parasitiphorous vacuole. A sparse infection was established in 1 of 2 12-day-old specific pathogen-free lambs by day 3 pi, but no oocysts were detected in its caecal contents or those of a second lamb killed 4 days later.

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Effect of experimental Ostertagia circumcincta infection on the performance of grazing lambs.

Groups of 10 three-and-a-half-month-old Suffolkcross lambs were infected daily, five times a week, for 12 weeks with either zero, 500, 1500, 3000 or 5000 larvae of Ostertagia circumcincta and grazed together on a series of 'clean' paddocks. All the lambs were moved at seven to 10 day intervals to a fresh paddock to prevent autoinfection and were killed after 14 weeks. Another group was killed at the outset as a control for carcase analysis. Mean O circumcincta populations were 34 (grazing control) and 1224, 473, 1092 and 4331 for the groups receiving 500, 1500, 3000 and 5000 larvae per day respectively. The percentage of fourth stage larvae increased with increasing larval intake. Extensive abomasal damage with mucosal hypertrophy and depletion of parietal cells occurred in the lambs receiving 3000 and 5000 O circumcincta larvae per day. Intakes of 1500 larvae per day and above depressed growth rate by 24 to 37 per cent, reduced the deposition of protein in the carcase by 34 to 52 per cent and lowered calcium/phosphorus deposition by 23 to 48 per cent. Plasma pepsinogen concentrations were consistently elevated in lambs receiving 3000 or 5000 larvae per day and may be a useful aid to recognising abomasal damage sufficient to affect productivity.

Abomasum↗

Effect of Ostertagia ostertagi on lamb performance and cross resistance to O circumcincta.

Fifteen worm-free lambs (two-and-a-half to three months or four to four-and-a-half months old) were infected with 3500 or 4000 Ostertagia ostertagi larvae on five days each week for six weeks, and their performance compared to that of controls. Eleven lambs were killed after eight weeks and four were challenged with O circumcincta to determine whether any cross resistance had developed. A feature of the O ostertagi infection was the considerable variation in response. Overall liveweight gain was lowered by 24 per cent in the two-and-a-half to three-month-old infected lambs, mainly due to reductions of 27 to 40 per cent in four of the seven lambs. There was no consistent effect in the older lambs. The worm populations consisted mainly of early fourth stage larvae and developing worms, but a small percentage reached sexual maturity and these produced a low faecal egg count (1 to 63 eggs per gram). Numerous intraluminal refractive crystals were present in the gut of both adult worms and developing stages, possibly reflecting degenerative changes. Hypertrophy of the abomasal mucosa with patchy loss of differentiation was a feature of the infection, and in four lambs serum pepsinogen concentrations were elevated. Exposure to O ostertagi did confer some protection against challenge with O circumcincta in that worm counts were reduced to about 60 per cent of those in controls, although no increase was observed in the numbers of arrested larvae. The successful passage of O ostertagi through young lambs could be important in mixed or alternate grazing systems by providing a reservoir of infection for the alternate host.

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Infection of specific-pathogen free lambs with a herpesvirus isolated from pulmonary adenomatosis.

In two experiments, 18 specific-pathogen free (SPF) lambs were inoculated by several routes with the Scottish strain of caprine herpesvirus 1 (CHV 1). Seventeen of the lambs developed interstitial changes in the lungs ranging from focal cellular infiltration to a widespread proliferative pneumonia. Five weeks after the initial inoculation 3 lambs were given a course of corticosteroid by intravenous injection. Subsequently virus was reisolated from all 3 lambs. Virus was also recovered from one of these lambs on one occasion prior to steroid treatment. It has therefore been established that CHV 1 can cause pneumonia and can be reisolated from infected sheep for at least 6 weeks after infection. It is suggested that CHV 1 might cause a latent infection in sheep which is reactivated following the development of pulmonary adenomatosis.

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Experimental cryptosporidiosis in germfree lambs.

Contaminating bacteria were removed from an isolate of calf Cryptosporidium by 3 sequential passages of the parasite in gnotobiotic lambs, together with antibiotic treatment of the lambs. This preparation, which contained no detectable bacteria or viruses, was given by mouth to 8 2-day-old gnotobiotic lambs, 3 of which were dosed at the same time with bacterial flora from a healthy calf. Lambs were killed at intervals from 12 to 288 h post-inoculation and the sequential development of the parasite, of enteric lesions, and of clinical illness was observed. Lesions were characterized by severe villus stunting and fusion. Clinically the most consistent sign was anorexia, with some lambs developing also a severe watery diarrhoea. Lesions and clinical signs were similar in lambs with and without intestinal bacteria. This demonstration of the enteropathogenicity of Cryptosporidium in germfree lambs suggests that it is a pathogen of significance.

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Chronic infections with Trichostrongylus colubriformis in lambs: influence of anthelmintic treatment on intestinal morphology and mucosal cell populations.

Intestinal mucosal morphology, topography and populations of crypt intraepithelial globule leucocytes (IGLs), goblet cells and mucosal mast cells were compared in 4 groups of 3-month-old lambs which had been reared worm-free from birth. Groups 1 and 2 were infected daily on 5 days per week with 2500 Trichostrongylus colubriformis larvae for 18 weeks. Group 2 lambs were treated with fenbendazole (5 mg per kg) at week 10 and week 15. Group 3 lambs were infected as above with T. colubriformis for 10 weeks, dosed with fenbendazole and given no further larvae. A fourth group of 4 lambs (Group 4) was maintained worm-free throughout the experiment as controls. All lambs were killed at week 20. Worm populations (range 410 to 30460) and mucosal damage varied considerably between individuals in the untreated Group 1 lambs, but damage was severe, with total villous atrophy, in lambs with large worm burdens. In 3 lambs with moderate worm burdens, worms were seen only in circumscribed flat "finger-print" lesions in the jejunal mucosa. There was no correlation between IGL numbers, mast cell numbers and final worm burdens in Group 1 lambs, though there was a trend towards an association between high worm populations and low IGL numbers. Only trivial pathological changes were detected in the re-infected Group 2 lambs. Low worm egg counts were found in this group 4 weeks after the first anthelmintic treatment, and virtually no eggs were present after the second treatment. Mucosal morphology in Group 3 lambs, which were not re-infected, resembled the controls at the end of the experiment. IGL numbers were greater in both treated groups than in controls, and numbers in the re-infected Group 2 lambs were greater than those in Group 3 lambs. Mucosal mast cell numbers did not differ significantly between groups, but crypt goblet cell numbers were increased in all 3 infected groups, compared with controls.

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Effect of anthelmintic treatment on the productivity of lambs infected with the intestinal nematode, Trichostrongylus colubriformis.

Liveweight gain, food intake, wool growth and concentration of serum constituents were measured in four groups of three-month-old lambs. Groups 1 and 2 were infected on five days each week with 2500 Trichostrongylus colubriformis larvae for 18 weeks. Group 2 lambs were treated with fenbendazole (5 mg kg-1) at week 10 and week 15. Group 3 lambs were similarly infected for 10 weeks, treated with fenbendazole, but given no further larvae. A fourth control group remained uninfected throughout the trial. All lambs were killed at week 20. Mean worm populations were 16,130, 430 and zero for groups 1, 2 and 3 respectively. Over the first 10 weeks of infection, liveweight gain was reduced by 52, 43 and 51 per cent and wool growth by 33, 28 and 27 per cent respectively, in groups 1, 2 and 3. Serum hypophosphataemia and hypoalbuminaemia occurred in all three infected groups. Between weeks 10 and 20 overall weight gain and wool growth in group 1 lambs were 44 and 46 per cent lower than the controls, whereas weight gains of group 2 and group 3 lambs were similar to or slightly higher than in the controls. However, wool growth in these two groups after treatment was only 73 to 74 per cent of control values. Serum phosphorus concentrations increased to control levels within one week of anthelmintic treatment and serum albumin concentrations by two to four weeks. The ability of group 2 lambs to improve their performance after anthelmintic treatment, in the face of continued challenge, was attributed to development of resistance to reinfection.

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Experimental cryptosporidiosis in calves: clinical manifestations and pathological findings.

Twenty-two calves between one and 20 days old were infected orally or by contact with cryptosporidia. Calves were maintained as either specific pathogen free, colostrum fed or sucking and were inoculated with either a bacteria free or a contaminated cryptosporidium preparation. Enteritis was characterised by depression, anorexia and diarrhoea and cryptosporidium oocysts were excreted during the clinical course of the illness. In the initial stages of the disease, cryptosporidium infestation was found throughout the small intestine; in the later stage the large intestine was also affected. Villous atrophy and fusion was present at small intestinal sites infected with cryptosporidia and lactase levels were depressed. No lesions were seen in infected large intestinal mucosa. Although the incubation period was longest (five to seven days) in calves infected by contact, there were few differences in the clinical course of disease or the pathological findings between any of the infected calves.

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Rapid transmission of sheep pulmonary adenomatosis (jaagsiekte) in young lambs. Brief report.

Jaagsiekte, a contagious lung tumour of sheep, was induced within 3-6 weeks in day-old lambs by intratracheal inoculation of SPA lung fluids concentrated by centrifugation. Electronmicroscopic examination of the tumour revealed retrovirus particles whose morphogenesis and morphology support biophysical and immunological findings that suggest a relationship with type B and type D retroviruses.

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Ultrastructural features of lung lesions in sheep dipped in a carbolic dip.

Ultrastructural changes in the lungs of 3 young sheep which became acutely ill with respiratory distress and severe pulmonary lesions 4 to 5 days after dipping in a proprietary carbolic sheep dip consisted of extensive alveolar damage associated with regenerative changes. Damage to alveolar epithelium was associated with accumulations of plasma fluid and cell debris in alveolar spaces, which also contained neutrophils and macrophages. Concurrently, damage to capillary endothelium resulted in liberation of plasma fluid and erythrocytes into the tissues and alveoli. Interstitial oedema was also present. Regeneration took the form of hyperplasia of type II alveolar epithelial cells, many of which were in mitosis, and which often lined alveolar spaces completely. Many of these cells were undergoing early metaplasia into type I pneumocytes, as shown by the development of elongated cytoplasmic extensions which increased the thickness of the blood-air barrier. Interstitial fibrosis was not a prominent feature. It is presumed that these effects resulted from skin absorption of an unknown toxic substance in the dip.

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Further evidence for a retrovirus as the aetiological agent of sheep pulmonary adenomatosis (jaagsiekte).

The infective agent of jaagsiekte was shown to be present in the fluid which accumulates in the respiratory tract of sheep during the terminal stages of the disease. The fluid also contained reverse transcriptase (RT) activity which showed a clear preference for a ribonucleic acid synthetic template over the corresponding deoxyribonucleic acid template and which utilised the RT specific template/primer poly (2'-0-methylcytidylate) oligodeoxyguanylate. This enzyme activity was associated with a particle which had typical retroviral buoyant densities in a range of gradient media.

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Development of morphological changes in the small intestine of lambs continuously infected with Trichostrongylus vitrinus.

Groups of three-month-old worm-free Suffolk cross lambs were given 2500 Trichostrongylus vitrinus larvae on five days each week for four, six, eight and 13 weeks and killed one week later. Severe villous atrophy, epithelial erosion and cellular infiltration were common features in the duodenum and the following 2 to 3 m of intestine of lambs killed at weeks 5 and 7. There was evidence of intestinal recovery in the lambs killed at weeks 9 and 14; five of the seven lambs had large areas of intestine which appeared relatively normal and worm activity appeared to be confined largely within focal areas ("fingerprint lesions'). There was no change in the linear distribution of the worms in the intestine over the course of the experiment. The highest percentage of the larval challenge was recovered from lambs killed at week 5 and worm burdens were not cumulative. Lambs killed at week 14 were resistant to larval reinfection.

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