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A cross-over controlled trial has been conducted among 32 adult patients with mite-sensitive asthma. The bedclothes and pillows of each subject were laundered and vacuum-cleaned and a plastic cover applied to the mattress for six weeks in an attempt to reduce exposure to mites. No improvement in daily peak-flow reading or drug usage was found in comparison with a control period.
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Ovine IgG was detected in homogenates of repeatedly washed Psoroptes ovis. Some of the immunoglobulin in the homogenates was fragmented although the host IgG present in mite washings was largely intact. The host immunoglobulin was immuno-localised to the surface or cytoplasm of the gut cells of feeding stages of freshly harvested P. ovis examined by cryosectioning. A similar distribution of rabbit IgG was detected in P. cuniculi. The IgG demonstrated in the mite gut represented partially digested as well as intact immunoglobulin. The presence of intact host immunoglobulin suggests that P. ovis may be susceptible to vaccination by the gut antigen approach, a method used successfully for blood-feeding ectoparasites like Boophilus microplus.
In vitro trials were carried out to evaluate the potential of fungal pathogens as biological control agents of parasitic mites, Psoroptes ovis (Hering) (Acari: Psoroptidae) from rabbit hosts (synonym: Psoroptes cuniculi). The fungus Hirsutella thompsonii Fisher showed no pathogenicity. Metarhizium anisopoliae (Metschinkoff), however, showed a high level of pathogenicity; 3 days after exposure to fungal conidia all mites were dead and 6 days after exposure 60% of the dead adult females, 10% of the dead adult males and 30% of the dead female nymphs had fungal hyphae protruding from their cuticular surface. There was a significant effect of conidial concentration on the number of mite cadavers that displayed fungal infection. Exposure to between 1x10(4) and 1x10(6) conidiaml(-1) resulted in 2-25% of the mites being infected. Mean infection levels were highest, 71%, when the mites were exposed to 1x10(7) conidiaml(-1). Similarly, there was a significant effect of conidial concentration on the time taken for the mites to reach 50% levels of mortality (LT(50)) The mean LT(50) value was approximately 2.7 days, when the mites were exposed to a solution of 1x10(7) and 1x10(8) conidiaml(-1) which was significantly shorter than controls exposed to 0.03% Tween-80 solution only. There was no significant effect of passaging the fungus, either once or twice, through the host on the subsequent infectivity of M. anisopliae. The potential for use of entornopathogenic fungi for the control of parasitic mites, particularly in relation to sheep, is discussed.
Antibodies to the canine nasal mite, Pneumonyssoides caninum, were demonstrated by ELISA in sera from four experimentally and 77 naturally infected dogs employing a crude P. caninum antigen. In sera from the four experimentally infected dogs, antibodies to P. caninum were first detected on day 11 post-inoculation (p.i.). Optical density (OD) values remained high throughout the observation period of 14 weeks. Two major protein bands with apparent molecular weights of 83 and 74kDa were visible by western blot (WB) from day 11 p.i. On day 14 p.i., another three major protein bands at 44, 37, and 34kDa were visible. The protein pattern then remained essentially constant until the end of the experiment except for some weak bands between 250 and 30kDa which were sometimes visible. In sera obtained from a non-inoculated control dog, no P. caninum antibodies were detected, neither by the ELISA nor by the WB. With sera from 77 naturally infected dogs with a verified diagnosis of P. caninum infection, the OD values varied between 0.24 and 0.95. When sera from four of these dogs were analysed by WB, the protein pattern observed was equivalent with that seen with sera from the experimentally infected dogs on day 25 p.i. Sera from four experimental Beagles, in which no P. caninum mites were found at necropsy, were also analysed by the P. caninum ELISA, the OD values demonstrated never exceeded 0.15. In addition, 48 sera obtained from dogs infected with or allergic to other arthropods were used for studies of possible cross-reactivity. With 10 sera, elevated OD values were found by the ELISA. Eight of them showed a similar banding pattern by the WB as did the experimentally infected dogs on day 25 p.i. This was, therefore, interpreted as an effect of a concurrent P. caninum infection.
The occurrence of bovine external otitis in tropical regions is predominantly assigned to parasitic infections by rhabditiform nematodes and infestations by mites of the genus Raillietia. This research had the purpose of investigating the prevalence of parasitic otitis in the dry and rainy seasons of Minas Gerais and correlating it with variables age, breed and the presence of horns. The secretion or cerumen of 981 cattle was collected with sterile swabs, placed in test tubes and exposed to sunlight for the identification of clinical infections caused by rhabditiform nematodes. The ear canals of 109 animals were flushed to study the occurrence of mites of the genus Raillietia. Clinical otitis caused by rhabditiform nematodes was observed only in animals of the Gyr breed, affecting 169 (60.1%) of the total (278) of these cattle. The prevalence of otitis in this breed was significantly higher for mature adult cows (P<0.001) and in cows with horns (P<0.001). In a total of nine animals suspected of raillietiosis, the examinations revealed the presence of Raillietia spp. in two Dutch cows. These results demonstrate that treatment must be focused on adult Gyr cattle with horns. This and future studies with an emphasis on epidemiological aspects may contribute to development of alternative approaches to reduce disease.
The effect of permethrin impregnated plastic strips (Die No Mite Strips) was evaluated on Dermanyssus gallinae populations in aviary systems for layers in Sweden. Two application strategies of the strips were tested: (A) attached in the housing system, allowing the birds to rub against the strips and thereby get the acaricide released onto their plumage, and (B) attached out of reach of the hens, at two different sites (perches and egg-belt lids) of the inner surfaces of the system, where the mites sheltered during the day. On two farms with 2030 (A) and 3384 (B) hens, and existing mite populations, strips were mounted for 20 and 10 weeks, respectively, and mite numbers were monitored by traps. With application A an overall mite reduction of 53% was observed, while with B the mean mite numbers decreased by 39% at the perches and 92% at the egg-belt lid. The strips were originally designed for caged hens afflicted by ectoparasites that stay on the host for most of their life cycle. However, since D. gallinae spends most of its time off the host, it was not possible to control the parasite with application A. Resistance tests performed on mites from both treated and control compartments where application A was used showed no indication of resistance to permethrin, while 95% of the mites survived a 48 h exposure to the compound where application B was performed. Thus, permethrin resistant mites appeared to be the main reason for the failure to control D. gallinae with application B.
The mite Psoroptes ovis causes sheep scab disease in flocks throughout much of the world. A serious impediment to the development of novel control measures for this mite is our inability to produce in vitro colonies of the mite. Here, we describe the alimentary canal of the mite with the particular aim of determining what it feeds on, as part of a longer term goal, to develop in vitro culture techniques for P. ovis. The alimentary canal of P. ovis consists of a cuticle-lined foregut and hindgut separated by a microvilli-lined midgut. The foregut is divided into a pre-oral cavity and a muscular pharynx and oesophagus. The midgut consists of three ultrastructurally discrete areas: a stomach with bi-lobed ventriculi, a colon and a post-colon. The stomach is composed of two cell types. The most common cells (Type 1) are either cuboidal or squamous depending on the degree of gut distension and possess short microvilli, a single basally located nucleus, extensive rough endoplasmic reticulum and other components suggesting active secretion. The less common cells (Type 2), possess an extensive apical network of tubules and basally food vacuoles suggesting intracellular digestion. These cells extend into the gut lumen, become free-floating and degenerate. The colon and post-colon are composed of cells similar to Type 1 stomach cells but the post-colon epithelium possesses significantly longer microvilli. Cells from these areas have not been observed to leave the surrounding epithelium and enter the gut lumen, but it is suggested that significant absorption occurs in these two areas. Faecal pellets, often containing a significant number of bacteria, leave the digestive system through the cuticle-lined anal atrium.
In Sweden, the poultry red mite, Dermanyssus gallinae, is the only haematophagous mite of poultry. After obtaining a blood meal the parasite spends most of its life off the host aggregated in cracks and crevices where mating and reproduction occur. Cardboard traps (1000 mm x 40 mm x 3 mm; 160 mm x 140 mm x 3 mm and 100 mm x 70 mm x 3 mm) containing 2% metriphonate were placed where mites gathered, out of reach of the hens, in two different types of multi-tiered floor systems for layers. In two separate trials, treated traps were replaced every second day for 2 weeks and every week for 8 weeks. In the 2-week trial the whole floor system was treated while in the 8-week trial six of 12 existing compartments studied were treated. The untreated compartments were used as controls. Throughout the study, the parasite populations were monitored by collections of mites with untreated cardboard traps (100 mm x 70 mm x 3 mm). A 95% reduction of mites was recorded in the 8-week trial whereas a 99% reduction of mites was recorded in the 2-week trial. The placement of treated traps near mite aggregation sites was essential for satisfactory control.
The efficacy of formic acid in a gel matrix was evaluated in two groups of honeybee colonies. In Group 1, a dispenser with 120 g of formic acid (70%) in gel was placed on the brood combs and another dispenser with the same dose was located on the hive bottom (total dose, 240 g). Group 2 received two doses of 240 g of formic acid (70%) in gel and each application was applied in two dispensers containing 120 g of the formic acid solution each and they were located over the brood chamber (total dose, 480 g). In Group 2, the period between both applications was 15 days, and the efficacies after the first and both applications were calculated. Significant differences were registered for final efficacy between both groups. When final efficacy of Group 1 was compared with efficacy after first application of Group 2, significant differences were found (P=0.0005). Same doses in different positions within the hive have different final efficacy. The higher efficacy was registered when the dispensers were placed over brood combs and on the hive bottom. It is suggested that efficacy is related to dispenser position within the hive.
This is the first report describing the finding of the canine nasal mite, Pneumonyssoides caninum, in a silver fox (Vulpes vulpes). It is also the first time P. caninum has been found in a species other than the dog (Canis familiaris). A severely debilitated 10-month-old, male silver fox was euthanised due to suspected renal failure. During autopsy, a female mite matching the description of P. caninum was found in the nasal cavity of the fox. The finding of P. caninum in the fox suggests the existence of a new host, or at the very least a transient host. The fox's role in maintaining and/or propagating canine nasal mite infection needs to be explored.
In a prospective study, the skulls of 250 dogs submitted for necropsy during 1993 at the Norwegian College of Veterinary Medicine were examined for the presence of parasites. All skulls were cleaved sagitally, and the frontal sinuses and nasal cavities were visually inspected. Eighteen dogs (7%) had Pneumonyssoides caninum infection at necropsy. No other parasites were observed. Sixteen dogs had heavy or moderate infection scores and 60% of these had concurrent sinusitis. The infected dogs belonged to 14 different breeds, 10 were male and eight were female and they varied in age from four months to 10 years old. Breed distribution, sex and age of the infected dogs did not differ significantly from the total study population. This study indicates that nasal mite infection occurs commonly in Norwegian dogs.