Genetic structure of Oestrus ovis populations in sheep and goats.

A genetic analysis using RAPD markers was performed on 12 natural populations of Oestrus ovis (Linné, 1761). Three-hundred and six O. ovis larvae (first, second and third instars) were randomly recovered in nasal cavities of sheep and goats naturally infected in Algeria, Ethiopia, France, Mauritania, Rumania and Tunisia and were analysed by 56 RAPD fragments. The results showed a high diversity within all samples. A significant genetic divergence was showed by discriminant analyses among the 12 populations sampled (p<0.0001). Moreover, discriminant analyses showed significant differentiation (p<0.0001) between O. ovis larva populations of sheep and goats and also among samples collected in the same region.     

Overberg research projects. X. Faecal egg counts in the interpretation of nematode worm burdens in sheep

Worm egg counts were compared with nematode worm burdens from data collected from greater than 400 sheep killed in experiments on the epidemiology of nematode parasites in the Overberg, in the winter rainfall area of the southern Cape Province. Data were analysed in several ways but no method could be found to accurately estimate the number of nematodes present from the faecal egg count in respect of individual sheep. However, the mean natural log egg count (epg) can roughly predict the mean natural log nematode count in groups of sheep.     

Oestrus ovis in sheep: relative third-instar populations, risks of infection and parasitic control.

Oestrus ovis (L.) (Diptera: Oestridae), the nasal bot fly, has a relatively short free-living life cycle outside of the host, and therefore it is necessary to know when the parasitic period occurs in order to prevent the clinical signs and economic losses caused by this parasite. The length of this parasitic portion of the life cycle is quite variable: a few weeks to several months depending on the season and climatic conditions. Surveys of Oestrus ovis larval populations in sheep show different results on the number of generations according to the local climate. Mean monthly larval profiles of L1 and L3 burdens of sheep from West African Sahelian countries, Mediterranean countries (Morocco, Tunisia and Sicily) and Southwest France were compared. Valuable information on the suspected extension of the fly season is obtained showing the period of infection in each area. This knowledge will be a valuable tool to help in choosing the right treatment at the right period.     

Epidemiology of Oestrus ovis infection of sheep in the highveld of Zimbabwe

During a period of 13 months, 507 heads of sheep, obtained from an abattoir near Harare, were examined for infection with Oestrus ovis larvae. The prevalence of infection varied from 6 to 52%, the highest being in November and the lowest in April. The mean annual larval burden was 1.12. The maximum number of larvae recovered from a single head was 57 in the month of November. Two larval peaks were observed, the first and highest in November and the second in August/September. Some flies are present throughout the year, except in May. There are at least 3 generations of flies per year. The wet summer period from January to May seems to be unfavourable, as very few flies are present. There is no overwintering of first instar larvae in the heads of sheep.     

Parasites of domestic and wild animals in South Africa. I. Oestrus ovis in sheep

Separate groups of 3 oestrid-free lambs were exposed to infestation on irrigated pasture for periods of approximalely 33 days each over30 months, and on dry-land pasture for approxomately 42 days over a period of 18 months. With some exceptions, the lambs slaughtered from October-June were found to be infested with Oestrus ovis while, with one exception, those slaughtered from July-September were free. A minimum of 4 sheeps' heads, obtained weekly over 24 months from the Pretoria Municipal Abattoir, was examined for infestation. Of a total of 542 heads examined, 73,4% were infested, having a mean burden of 15,2 larvae. Mean larval burdens were slightly greater in hornless than in horned sheep in Dorper-type than in Merino-type sheep, and in lambs than in sheep with 2 or more permanent incisors. The largest larval burdens were recovered from sheep slaughtered during May and June and the smallest during September and October. The greatest number of 1st instar larvae were recovered during May and June and the smallest during September, but those recovered during the latter month were the largest. With one exception, mature larvae which pupated after 21 March or before 16 August failed to hatch as viable flies. Those which pupated after 16 August hatched as flies after a pupal stage of approximately 50 days and the first flies to hatch were invariably recovered during the first 2 weeks of October. The pupal stage decreased to approximately 25 days during December and January and increased again to approximately 50 days for flies hatching during May. No flies hatched between 18 May and 1 Cctober. The following life cycle ofr Oestrus ovis is suggested: sheep are repeatedly infested from October-June; thereafter infestation survives in the sheeps' heads until August, mainly as 1st instar larvae, then as pupae and larvae until fresh infestation takes place during October.     

Evaluation of a direct ELISA for the serodiagnosis of Oestrus ovis infections in sheep.

Oestrosis is a parasitic disease of sheep and goats caused by the nasal bot fly Oestrus ovis. In the United Kingdom the economic losses as a result of infestation can be considered negligible, but the differentiation of O ovis cases from more serious diseases such as listeriosis, gid and sheep scab is of considerable importance. Currently, diagnosis of oestrosis relies on the subjective observation of clinical signs or the demonstration of larvae postmortem. This paper assesses the effectiveness of a direct enzyme-linked immunosorbent assay (ELISA) using a crude somatic antigen from first-stage larvae (L1) in the serodiagnosis of oestrosis. The system has been validated with sera from both endemic and non-endemic areas and the results correlated with the clinical data found postmortem. The sensitivity and specificity of the assay were 97.4 per cent and 97.6 per cent, respectively, using a cut-off point based on 35 per cent binding of a reference positive control serum.     

Age and seasonal variations in the prevalence of Oestrus ovis larvae among sheep in northern Jordan

During the period March 1996-July 1997, 417 heads of Awassi sheep slaughtered at the Irbid Abattoir (northern Jordan) were examined for the three larval instars (L1, L2 and L3) of Oestrus ovis. Of the 417 heads, 242 (58%) were infested with O. ovis larvae. Larval numbers were highly aggregated. The lowest number of larvae and the lower quartile were both zero, whilst the median was two and the upper quartile was 12. The highest number of larvae recovered from one head was 151. All three larval instars were observed in each month of the year. July and October had the highest proportions of L1, 75 and 78%, respectively, among infected animals (adjusted for age). The number of larvae increased with age. Infestation with live larvae was associated with inflammatory responses in the upper respiratory tract and with catarrhal or purulent discharge. The percentage of infested sheep and the mean monthly total number of larvae/sheep peaked in the warmer part of the year. Most larvae were L1 except during the spring when L2 and L3 predominated. Distribution analysis demonstrates that the numbers of larvae recovered in the sheep population followed a negative-binomial distribution. Furthermore, the negative-binomial constant k for each month correlated with the monthly prevalence.     

Comparison of infection rates of Oestrus ovis between sheep and goats kept in mixed flocks

Oestrosis is a nasal myiasis of sheep and goats caused by larvae of the fly Oestrus ovis and can lead to severe clinical signs, which together with the disturbance caused by the adult fly may result into serious economic losses. Infection rates and larval burdens are always higher in sheep than in goats after either natural or artificial infestation. The aim of this study was to compare the host preference of the adult fly O. ovis between sheep and goats in mixed flocks, where they are kept together under the same husbandry conditions and hence, are very similarly exposed to the fly preference. Blood sera samples were collected from a total of 397 sheep and 335 goats, from 43 mixed flocks located at different regions of Greece. Antibodies specific to O. ovis IgG were measured by ELISA. A flock was considered positive when at least one individual was positive, i.e. showed a seropositivity of >or=20% in relation to positive control sera. A total of 193 (48.6%) sheep and 58 (17.9%) goats were found to be seropositive against O. ovis. Thirty-eight (88.4%) out of 43 flocks had at least one seropositive animal. The mean seroconversion against O. ovis in animals from the different flocks was 38.6% and 13.6% for sheep and goats, respectively, whereas the variance of infection within each flock was 0-100%. The mean seropositivity between sheep that were found to be positive or negative was 60.6% and 5.4%, respectively, whereas the corresponding values between goats were 35.2% and 5.2%, respectively. No significant difference in the seroconversion values was noted between flocks from the different areas (P=0.817), whereas a very significant difference was observed between animal species (P=0.001). However, there was no significant difference when seroconversion comparisons were made within samples of the same animals species, sheep or goats from different flocks of all the regions included in the study (P=0.695). The results of this study clearly demonstrate that O. ovis has a widespread distribution in Greece, and the seroprevalence is significantly higher in sheep than goats (P=0.001).     

Seasonal variations in the larval burden distribution of Oestrus ovis in sheep in the southwest of Spain

A chronobiological study of oestrosis was conducted for larval instars of Oestrus ovis from November 2000 to September 2002 with the examination of 477 adult sheep of the southwest region of Spain. Skulls from slaughtered sheep were examined and the different O. ovis larval stages (L1, L2, L3) were recovered from the nasal-sinus cavities. O. ovis larvae were detected in 339 sheep, reaching a prevalence of 71.1%. Only one farm was free of infested sheep indicating a prevalence of the 97.91% among studied flocks. The mean larval burden was 18.54 larvae per infested head during the coldest months in the southwest of Spain when the larval burden reached its highest levels, especially of the first larval stage (L1). However, the maximum percentage of L1 coincided with the minimum percentage of the second larval stage (L2). The third larval stage (L3) was observed in relatively low levels during the entered study period, but two peaks occurred in April-May and in September-October. During the 2 years of sampling, all the different larval stages were simultaneously recovered throughout the year, indicating the existence of a long favourable period for the evolution and development of the larval instars, which would start between February and March and finishing in November.     

Some observations on the biology and control of the sheep scab mite Psoroptes ovis (Hering) in Britain

Sheep scab was eradicated from Britain in 1952 but reappeared in 1973. The host specificity of the sheep scab mite is discussed; sheep are the only reservoir of the disease in Britain. Control is by single dipping in the approved acaricides, HCH, diazinon or propetamphos. Acaricides are approved only if the minimum use rate (Maintenance level) will give at least 4 weeks' protection. The method of testing is described. Traditionally, compulsory dipping has been in the winter when the disease is most active. Although the mites were originally thought to enter a latent phase during the summer, new observations indicate that there is little difference between their summer and winter behaviour. In Britain, dipping is now compulsory in both the summer and winter.     

Detection of Oestrus ovis and associated risk factors in sheep from the central region of Yucatan, Mexico

A cross-sectional epidemiologic study was conducted in order to detect the presence of and to estimate the seroprevalence of Oestrus ovis L. infection in flocks of sheep from the central region of the state of Yucatan, Mexico. The risk factors associated with disease were also identified. A sample size of 10 animals per farm was used to detect seropositive animals, considering a 30% prevalence and 95% confidence level. Blood samples of 689 sheep from 88 flocks were collected and a questionnaire with questions about the flock and the host was applied. The thin layer immune assay test was used. The risk factors were screened using logistic regression procedures. 77% of the flocks had at least one-positive animal with antibodies against O. ovis. The overall seroprevalence and standard error was 30.6 +/- 3.5%. Only flock size and sheep nose color showed association (P < 0.05) with the disease. The odds ratios for flocks with less than 11 and with 11 to 25 sheep, as related to herds with 25 or more sheep, were 0.74 and 1.73, respectively. Sheep with dark noses had a higher risk (OR = 1.46) compared with sheep having light noses (P < 0.05).     

Efficacy of eprinomectin pour-on against gastrointestinal nematodes and the nasal bot fly (Oestrus ovis) in sheep

The efficacy of the pour-on formulation of eprinomectin, at a dose rate of 0.5 mg/kg bodyweight, was assessed in sheep against three main species of gastrointestinal nematodes and against the nasal bot fly, Oestrus ovis, and some pharmacokinetic parameters were determined for 21 days after the treatment. By comparison with untreated control sheep, infected experimentally with Haemonchus contortus, Teladorsagia circumcincta and Trichostrongylus colubriformis, eprinomectin was 100 per cent effective against the two abomasal species and 99.5 per cent effective against T. colubriformis. In ewes naturally infected with the nasal bot fly, the efficacy of the drug against O. ovis was 97.7 per cent. The mean (se) systemic area under the curve (AUC) was 56.0 (26.2) ng/day/ml and the mean residence time was 5.3 (1.0) days, but there were wide variations between individual sheep.     

The survival in sheep and infectivity to dogs of Taenia hydatigena and T. ovis in sheep

Lambs were reared from birth to 3 months of age on pasture contaminated with the eggs of either Taenia hydatigena or Taenia ovis. They were necropsied at 3, 6, 9 or 12 months. Almost all larvae that were viable at 3 months continued to survive throughout the experiment. Larvae of T. hydatigena were infective to dogs at 3 months, whereas those of T. ovis required more than 3 months to reach the infective stage.     

Nutrition of intensive pastures in the summer rainfall areas of southern Africa

Consideration is given to the current state of knowledge regarding the nutrition of cultivated pastures in the summer rainfall areas of southern Africa. Research efforts over the years have concentrated on the nitrogen (N) requirements of pastures, with relatively little significant work being undertaken on phosphorus (P), potassium (K) and lime. The numerous N response curves derived in cutting trials provide a useful basis for predicting N requirements under cutting‐and‐removal type utilization, but are of little value in predicting N requirements under grazing. The critical roles of P, K and lime in pasture productivity and persistence have been demonstrated in field trials undertaken in the Natal Midlands and south‐eastern Transvaal. Soil test calibrations, established for several important pasture species on Natal soils, have been found to provide a sound basis for predicting P, K and lime requirements of pastures. In considering the direction of future research, it is suggested that considerable potential exists for more efficient fertilizer and lime usage; research efforts should therefore be channelled in that direction.     

Parasites of comestic and wild animals in South Africa. II. Oestrus ovis in goats

During a period of 13 months, 130 goats' heads, obtained form the Johannesburg Municipal Abattoir, were examined for infestation with Oestrus ovis. Investation was present in 73,8% of the heads and the mean burden comprised 4,4 larvae. Such a small nuber of larvae were present that no clear seasonal incidence pattern could be determined. Pupal periods could be as long as approximately 60 days for flies hatching during October and May and as short as approximately 24 days for those hatching from December-February. The findings are compared with those obtained from surveys in sheep in south africa.     

The effect of corticosteroids on the cysticerci of Taenia ovis in sheep.

The effect of two synthetic corticosteroids on the cysticerci of Taenia ovis in sheep has been investigated. Dexamethasone given from four days before infection had no effect on the number of cysticerci recovered but did enhance their survival. When betamethasone was used there was an increase in the number of cysts compared with controls. Corticosteroids given for 12 days after infection did not increase the number of viable cysticerci recovered at autopsy three months later but when treatment was continued until the time of autopsy, a very high proportion of cysticerci were viable.     

Detection of antibodies to Brucella ovis in sheep milk using B. ovis and B. canis antigen

The diagnostic techniques most widely used for detecting brucellosis caused by Brucella ovis are serological tests such as complement fixation (CFT), agar gel immunodiffusion (AGID), and ELISAs. However, to our knowledge, milk tests, with the advantage that samples may be taken in a non invasive manner, have not been investigated as diagnostic tools. We studied 144 samples of milk and sera from lactating ewes, comparing bacteriological studies, serological and milk tests using Brucella canis and B. ovis antigens. A group of 75 ewes in an uninfected flock were serologically negative to rapid slide agglutination test (RSAT), indirect ELISA (IELISA)-B. canis, AGID and IELISA-B. ovis. The milk of these ewes had an IELISA-B. canis mean (%P) value of 16.18 (S.D. 5.63), while the IELISA-B. ovis had a mean (%P) value of 12.52 (S.D. 4.94). A cut-off value of (%P) 27.44 (+2 S.D.) or (%P) 33 (+3 S.D.) was determined by milk-ELISA-B. canis and (%P) 22.4 (+2 S.D.) and (%P) 27.34 (+3 S.D.) by milk-IELISA-B. ovis. These cut-off values were adjusted by receiver-operator characteristics (ROC) analysis using 23 positive samples from infected ewes, which indicated a milk-IELISA-B. canis cut-off value of (%P) 33 and milk-IELISA-B. ovis of (%P) 26 with 100% sensitivity and specificity. Based on our results, we propose that, following a study of a larger number of samples, the milk-IELISA-B. canis could be considered a suitable test for the diagnosis of B. ovis brucellosis in lactating ewes.