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Efficacy of a new long-acting formulation of ivermectin and other injectable avermectins against induced Psoroptes ovis infestations in cattle.

Two studies describe the therapeutic and protective efficacy of commercially available, injectable avermectins against Psoroptes ovis infestations. In each study, six untreated calves were compared to groups of six calves each treated with ivermectin long-acting injectable (LAI) 3.15% w/v solution, generic long-acting (LA) ivermectin 1% w/v solution or 1% w/v doramectin solution. Treatments were carried out according to the manufacturer's instructions at 1 ml/50 kg body weight. Live mites in skin scrapings were counted prior to treatment and at weekly intervals for 8 weeks thereafter in the therapeutic study, or at 15, 21 and 28 days after P. ovis challenge which occurred 28 days post-treatment in the study to compare protective efficacy. P. ovis infested calves treated with ivermectin LAI had significantly ( P<0.05) fewer mites than did the untreated controls from 1 week after treatment. They also had significantly fewer mites at 7 and 8 weeks after treatment than did the calves treated with generic LA ivermectin and at 8 weeks after treatment than the calves treated with doramectin. No mites were counted on the animals treated with ivermectin LAI from 4 weeks after treatment through to the end of the study; however, five of the six calves from each of the groups treated with generic LA ivermectin or doramectin were infested with P. ovis at 8 weeks after treatment. No P. ovis mites were recorded on the calves treated prophylactically with ivermectin LAI. In contrast, five or all of the six calves treated prophylactically with generic LA ivermectin or doramectin, respectively, were positive for P. ovis mites at the end of the study. Calves treated prophylactically with ivermectin LAI gained significantly more weight than the untreated controls.

Animals↗

Immunocytochemistry of Psoroptes cuniculi stained by sera from naive and infested rabbits: preliminary results.

Immunocytochemistry was used to identify possible target antigens in the digestive system of Psoroptes cuniculi. Sera from three recently acutely infested rabbits, from rabbits with a mild long lasting infestation, and from a rabbit with repeated mite infestations and no longer able to maintain a population of P. cuniculi were used to determine any antibody specificity to the mite digestive system. The reactivity of these sera was compared with sera from three un-infested animals. The different pool of sera targeted different mite antigens; in particular, sera from the resistant rabbit and the chronically infested rabbits reacted with gut cells, faecal material and cuticle, while sera from the recently infested rabbits reacted with gut contents, faecal material and cuticle of the parasites but not with gut cells. Finally, sera from un-infested rabbits did not demonstrate any specificity to P. cuniculi antigens reacting only with mite gut contents in a weak manner. These preliminary data suggest the presence of antibodies induced in the host blood by infection, which act against the parasite by binding to antigen at the surface of its gut.

Animal Diseases↗

Efficacy of some pyrethroids against a strain of the rabbit ear mite (Psoroptes cuniculi): an unusual cross-resistance pattern.

An in vitro immersion bioassay was used to compare the efficacy of selected pyrethroids against a deltamethrin-resistant strain of rabbit ear mite (Psoroptes cuniculi). A lack of cross-resistance between bromo (deltamethrin) and chloro analogues (cypermethrin) of alpha-cyano-3-phenoxybenzyl-dihalovinyl-dimethylcyclopropane carboxylate was detected. Whereas deltamethrin proved to be inactive (48-h mortality 21.9% at 1000 mg/kg), each cypermethrin isomer mixture tested, including alpha-cypermethrin [IR(cis) alpha S + 1 S (cis) alpha R] and theta-cypermethrin [1R(trans) alpha S + 1 S (trans) alpha R] and their mixture at a ratio of 4/6, beta-cypermethrin, showed high efficiency (48-h mortality > or = 95% at 1000 mg/kg).

Analysis of Variance↗

Therapeutic and prophylactic efficacy of the Ivomec SR Bolus against nematodes and Psoroptes ovis in cattle weighing more than 300 kg at the time of treatment.

Three trials using 50 European breed cattle were conducted to evaluate the therapeutic and prophylactic efficacy of the Ivomec SR Bolus against nematodes (2 trials) and Psoroptes ovis (1 trial) in cattle weighing more than 300 kg at the time of treatment. The Ivomec SR Bolus proved to be highly effective against economically important gastrointestinal and pulmonary nematodes (Ostertagia ostertagi, Trichostrongylus axei, Cooperia punctata, Oesophagostomum radiatum, Dictyocaulus viviparus) and improved the rate of weight gain significantly. P. ovis was eliminated from cattle treated with an Ivomec SR Bolus. The treatment also provided prophylaxis against an infestation of P. ovis and increased the weight gain of cattle infested with P. ovis.

Animals↗

Relationship between Psoroptes cuniculi and the internal bacterium Serratia marcescens.

The bacterium Serratia marcescens isolated from surface-sterilised Psoroptes cuniculi was found sensitive to the antibiotic Amikacin. Mites placed in this antibiotic for 48-72 h and then washed by centrifugation were found to be alive and S. marcescens-free. Two experimental infestations were undertaken in order to verify the ability of the S. marcescens-free mites to infect and to give ear skin lesions in healthy rabbits and to evaluate the differential ability of the S. marcescens-free and S. marcescens-infected mites to give ear skin lesions. All rabbits were found to be infested, but only rabbits infested with S. marcescens-free mites presented crusts in their ears, whereas mites and/or eggs were only detected in the ear cerumen of all rabbits infested with S. marcescens-infected mites. S. marcescens was isolated only from P. cuniculi mites taken from these latter rabbits. Results indicate that P. cuniculi mites do not need S. marcescens to live and to be able to infest a healthy rabbit. In addition, S. marcescens was not isolated from eggs and newly born larvae of S. marcescens-infected P. cuniculi, demonstrating that in a population of P. cuniculi this bacterium is not transmitted transovarially.

Amikacin↗

Ultrastructural morphology of the male and female genital tracts of Psoroptes spp. (Acari: Astigmata: Psoroptidae).

The structure of the male and female genital systems of the astigmatid mite Psoroptes ovis (Hering) is described. The male genital system is composed of a paired testis, fused at its proximal part, two vasa deferentia, an ejaculatory duct, into which a single accessory gland opens, and a copulatory organ. The testis is characterized by a peripheric syncytial cell surrounding spermatogonia, spermatocytes, spermatids and spermatozoa which are distributed regularly in the gonad according to the sequence of spermatogenesis. The female genital system consists of a copulatory pore (the bursa copulatrix), a seminal receptacle, paired ovaries and oviducts, a glandular uterus and an ovipositor which leads to the oviporus. Ovaries are composed of somatic cells, germ cells and a central cell, with a multilobular nucleus, connected to oocytes by a stalk. Similarities with other astigmatic mites belonging to Psoroptidia and Acaridia are also discussed.

Animals↗

Stimulation of the in vitro migration of ovine eosinophils by factors derived from the sheep scab mite, Psoroptes ovis.

The ectoparasitic astigmatid mite Psoroptes ovis causes sheep scab, a highly contagious, severe allergic dermatitis associated with damage to the fleece and hide, loss of condition and occasional mortality. The scab lesion is characterized by a massive infiltration of eosinophils that begins very rapidly after infection. This paper reports the finding that mite-derived factors directly enhance the migration of ovine eosinophils in vitro. Significant (p < 0.01) and dose-dependent (r = 0.972 +/- 0.018 (SD)) activity was initially identified in whole mite extracts, by comparison with medium controls in an assay based on modified Boyden chambers and ovine bone marrow target cells. Similar pro-migratory activity (p < 0.005; r = 0.928 +/- 0.069 (SD)) was detected in washes containing mite excretory/secretory material. By direct comparison with migration ratios (n = 3) for defined chemotactic (rmeotaxin = 3.430 +/- 0.360 (SD)) and chemokinetic (rminterleukin-5 = 0.982 +/- 0.112 (SD)) stimuli it was determined that the activity in both mite extracts (0.992 +/- 0.038 (SD)) and mite washes (0.969 +/- 0.071 (SD)) was chemokinetic. Subsequent experiments (n = 3) in which live mites were incorporated directly into the in vitro assay system indicated that they produced factors that significantly (p < 0.001) enhanced eosinophil migration to a degree directly related to mite numbers (r = 0.993 +/- 0.005 (SD)). The identity of the factor(s) responsible is uncertain, but their presence suggests that mites may be capable of directly activating eosinophils in vivo, and raises the possibility that mites could directly influence, perhaps even initiate, the rapid early tissue eosinophilic response observed in experimental sheep scab infections.

Animals↗

Effect of ivermectin on the ear mange mite, Psoroptes cuniculi, of rabbits.

Rabbits, naturally infected with ear mange mite, Psoroptes cuniculi, were injected subcutaneously with a single dose of ivermectin at 200 micrograms or 400 micrograms/kg of body weight. The effect of the drug was evaluated clinically and parasitologically over 4 weeks. The animals in both groups became negative for mites 6 days after treatment and remained so until the end of trial. The ear lesions disappeared in both groups. However, the regression of lesions was faster in rabbits administered 400 micrograms/kg of ivermectin.

Animals↗

Cross-reacting antibodies to Sarcoptes suis, Chorioptes bovis and Notoedres cati and anti-P. ovis IgE in sera from sheep infested naturally with Psoroptes ovis.

For the development of immunodiagnostic tests to detect mange mite infections in man and animals, it is necessary to know about antigen structure and cross-reactivity between different mite species and other arthropods in contact with the host. Sera from sheep infected with Psoroptes ovis (sheep anti-P. ovis sera) showed positive reactions in dot blots to P. ovis antigen and cross-reactivity to crude antigen extracts from Sarcoptes suis, Notoedres cati and Chorioptes bovis. Using sheep Specific Pathogen Free (SPF) sera in dot blots, weak reactions were seen to all but the Ch. bovis antigen. In SDS PAGE-separated P. ovis antigens at least 35 different proteins could be distinguished. In western blots, at least 24 out of these 35 were recognized as antigens by sheep anti-P. ovis immunoglobulins. At least 13 were recognized by sheep anti-P. ovis IgE. One of these, at 19 kDa, was recognized only with sheep anti-P. ovis IgE, the other 12 also with anti-P. ovis immunoglobulins. Cross-reactive antigens were recognized by sheep anti-P. ovis immunoglobulins in SDS PAGE-separated, and nitrocellulose transferred mite extracts in western blots as follows: 13 antigens in S. suis extracts, 9 in N. cati and 8 in Ch. bovis. Sheep SPF sera recognized an antigen at 67 kDa in each of these 4 mite species. Rabbit anti-sheep immunoglobulins in the P. ovis antigen control bound to a protein at 28 kDa which may be sheep IgG light chain taken up by P. ovis feeding on sheep. Despite the antigenic similarities between mange mites, sufficient differences were apparent to make immunodiagnostic tests for mange feasible.

Animals↗

Effects of Psoroptes ovis (Acarina:Psoroptidae) on certain biochemical constituents of cattle serum.

Sera from Psoroptes ovis-infested calves were examined for 17 selected biochemical constituents to determine if P. ovis caused changes in any of these constituents. In order to recognize a scabies effect, there had to be a statistically significant (P less than or equal to 0.10) scabies exposure X time interaction and the changes in the biochemical constituents should have been correlated with the changes in the mite infestation. Five serum biochemical constituents fulfilled these criteria. Total protein, alpha-, beta-, and gamma-globulin were increased and total cholesterol was decreased at the peak of the scabies infestation. Precipitating antibodies to a P. ovis antigen were detected by immunodiffusion in some of the stored sera of the infested calves just after the peak of the infestation. Total protein, beta-, and gamma-globulin values were probably increased as a result of antibody production; alpha-globulin values were probably increased as a result of inflammation. As the scabies infestation declined, the mean values of all the above constituents from the infested calves, except cholesterol, began declining. Decreases in total cholesterol occurred, but they could not be entirely attributed to scabies. Examination of the serum biochemical constituents from a heavily infested calf that died during the test suggested that, in addition to antibody production and inflammation, kidney and liver damage may have occurred.

Alpha-Globulins↗

Development of serum antibody activity as determined by enzyme-linked immunosorbent assay to Psoroptes ovis (Acarina:Psoroptidae) antigens in cattle infested with P. ovis.

Calves infested with Psoroptes ovis (Hering, 1838) for the first time (naive) or previously infested calves were examined for serum antibody activity to P. ovis (obtained from rabbits) antigens by enzyme-linked immunosorbent assay (ELISA) to determine the temporal appearance of specific serum antibody activity. The development of the serum antibody activity to P. ovis antigens was then correlated with the development of lesions (% scab) and with changes in the number of P. ovis. The serum antibody activity [ELISA OD414 value (EODV) greater than 0.290] to P. ovis antigens in naive calves, in most cases, is first detected at the same time or slightly after the detection of mites and mite-caused lesions; and the development of specific serum antibody activity paralleled the increase in the P. ovis population and the percentage scab until 7 weeks post-infestation (PI). In previously infested calves, if serum antibody activity to P. ovis antigens was not already present from the previous infestation, specific serum antibody activity was detected at the same time and developed in a similar manner as in the naive calves. The serum antibody activity to P. ovis antigens could be detected after calves were relieved of their P. ovis burdens by pesticide treatment or after the P. ovis population began to decline when the calves were allowed to groom themselves. Serum antibody activity to P. ovis antigens was not detected in any of the control calves during the test period.

Animals↗

The prevalence and pathogenicity of Chorioptes bovis (Hering, 1845) and Psoroptes cuniculi (Delafond, 1859) (Acari: Psoroptidae) infestations in feral goats in New Zealand.

Between October 1976 and January 1980 a total of 368 feral goats was examined in New Zealand for the presence of Chorioptes bovis and 434 for the presence of Psoroptes cuniculi. The seasonal pattern of C. bovis infestation in feral goats was similar to that seen in sheep and cattle. The prevalence of infestation reached 100% in July and August (winter) and declined to 27% in February and March (summer). Fewer goats were infested with P. cuniculi and prevalence of infestation reached a maximum of 41% in July. No goats were found infested in the December and January samples. Chorioptes bovis infestation was independent of the age and sex of hosts. Infestation with P. cuniculi was independent of the sex of the hosts, but older goats were more frequently infested (16%) than younger goats (8.6%). Unilateral infestation with P. cuniculi was more common (74.5%) than bilateral infestation. No severe lesions were associated with C. bovis, but 21.3% of goats with P. cuniculi had the external auditory meatus blocked by waxy material and 12.8% had scabby encrustations on the ears. The importance of goats as a possible source of infestation to domestic animals is discussed.

Age Factors↗

In vitro feeding of Psoroptes ovis (Acari:Psoroptidae).

An in vitro feeding test is described for Psoroptes ovis. The criterion for feeding response was established on the basis of coloration of mites by a red dye or by red blood cells. Feeding response was about 85% for female mites held off host cattle for 1 day. Mites preferred water plasma or serum and low-salt diets over whole blood. Feeding response was detected within 5 min of exposure to the diet, and maximum response was observed within 30 min of contact. Mites ingested an average 0.29 microliter of diet/100 mites in a single feeding. At temperatures between 10 degrees and 42 degrees C, feeding response was not significantly different.

Animal Feed↗

Humoral and cellular immunoresponsiveness of stanchioned cattle infested with Psoroptes ovis.

Bovine scabies in a clinical problem during the cool autumn and cold winter months. In south Texas it is necessary to stanchion animals in order to elicit patent infestation during summer months. Environmental factors and grooming have been purported to account for summer resistance to infestation. However, stanchioned animals exhibit varied levels of susceptibility to infestation, suggesting that the noted variability may be influenced by the host immune response. In this study, animals were infested with Psoroptes ovis while in stanchions. The development of anti-P. ovis antibody activity was measured by the enzyme-linked immunosorbent assay and cellular immune function was monitored with mitogens and P. ovis antigens. A correlation was noted between the development of anti-P. ovis antibody activity and the increase in mite numbers and dermatitis. Coincident with the developing infestation was a suppression of T-cell function that appeared to be stress-related as a result of stanchioning. A working hypothesis is presented that attempts to correlate the developing humoral response and the depressed T-cell response with both an increasing dermatitis and mite population.

Animal Husbandry↗

Control of psoroptic scabies of cattle with fenvalerate.

Fenvalerate [Cyano(3-phenoxyphenyl)methyl-4-chloro-alpha-(1-methylethyl) benzene acetate] was evaluated as a one- or two-dip treatment at two different concentrations against cattle infested with Psoroptes ovis (Hering). One or two dips at 0.025% or one dip at 0.05% failed to eliminate P. ovis; two dips in fenvalerate at 0.05% provided complete elimination of all mites. Fenvalerate was equally effective against male, female, and immature mites, but did not exhibit ovicidal properties.

Animals↗

Influence of Psoroptes ovis on the energy metabolism of heifer calves.

To determine the effect of Psoroptes ovis on the energy metabolism of heifers, 32 calves were randomly assigned to four treatments in a 2 X 2 factorial arrangement. Calves were fed the same diet at two intake levels, high or low, and were either infested or were not infested with P. ovis mites. Calves were housed in antigrooming stanchions. Body composition was determined by urea dilution on Days 0 and 63. Ration digestibility was determined on fecal grab samples using acid-insoluble ash as a marker. Infested calves had developed a severe P. ovis infestation 7 weeks following exposure and had significantly lower daily gain, gain:feed, and energy retention and higher serum glutamic-oxaloacetic transaminase than control calves. P. ovis infestation increased the maintenance energy requirement of calves by greater than 50% (79 vs. 123 kcal of net energy kg-1 body wt.75). For each 10% increase in the body surface affected by P. ovis, maintenance energy requirement increased 0.5 mcal day-1.

Animal Feed↗

Comparison of cryofixation methods for skin biopsies from sheep infested with Psoroptes ovis (Acari: Psoroptidae).

Two methods of cryofixing skin samples from sheep infested with Psoroptes ovis were compared. In one method the skin biopsy was placed in a capped vial before immersion, while the other allowed direct contact with liquid nitrogen. No statistically significant differences were found between the cryofixation methods with regard to location of P. ovis sections or engaged mouthparts. Direct contact with liquid nitrogen is recommended as the preferred method for cryofixing epidermal feeding ectoparasites on skin samples.

Animals↗

Lipid ingestion from sheep epidermis by Psoroptes ovis (Acari: Psoroptidae).

Skin biopsies from three groups of sheep infested with Psoroptes ovis were cryofixed in liquid nitrogen to preserve outer epidermis with its lipid. From one group of five sheep (Group A), biopsies were taken from relatively healthy skin near the edge of scab lesions where mites had congregated. Frozen vertical sections from these biopsies were stained with Oil Red O and haematoxylin before mounting. Red lipid globules were plentiful within the body cavity of sectioned mites, but ingested lipid could not be distinguished from endogenous mite body stores by this technique. In a second group of five sheep (Group B), enclosed lumbar skin areas were coloured red with the lipophilic stains Oil Red O or Sudan IV. These enclosed coloured skin areas were inoculated with P. ovis and sampled by skin biopsy 1 or 4 days later. Cryofixed biopsies were cut into vertical frozen sections and mounted without staining for examination. Red-coloured lipid within mites, matching red-coloured lipid on outer epidermis, was evidence for the epidermal origin of P. ovis ingesta in the early stages of an infestation. From two other sheep (Group C), cryofixed biopsies were examined by scanning electron microscope and mites were seen with mouthparts embedded in abraded outer epidermis, but the precise depth of epidermal penetration was not determined. A light microscope survey of 3198 frozen vertical skin sections from the first 10 sheep (Groups A and B) showed that inner stratum corneum of the epidermis was the deepest penetration recorded for gnathosomes of P. ovis cryofixed in situ by liquid nitrogen. No structure of P. ovis was identified in dermal tissues.

Animals↗