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1.
Fifty Havanna, Small Chinchilla and crossbred rabbits were each infected at 3 to 4 months of age with a single dose of 5-20 thousand third-stage larvae of the trichostrongyle. After infection with 10 thousand larvae, third-stage larvae were present on the 1st and 2nd days, fourth-stage on the 4th-6th days, fifth-stage on the 7th and 8th days and sexually mature trichostrongyles on the 8th-10th days. Only a small proportion of third-stage and fourth-stage larvae failed to develop into sexually mature neamtodes. Prepatent period of infection was 9-10 days; patency lasted from a few weeks to 2-3 months. Single infection with 5000-7000 invasive larvae produced no clinical signs. A dose of 10 thousand larvae produced diarrhoea even during the prepatent period, and this was accompanied by expulsion of a considerable part of the parasite population. Infection with 20 thousand larvae produced a loss of weight in the experimental rabbits.  相似文献   

2.
Pigs fed Ascarissuum eggs attenuated by short wave ultraviolet-radiation developed resistance to challenge infection. Per os inoculation of pigs on three successive weeks with 10,000 eggs irradiated to total exposures of 150,100 and 75 μW-min/cm2, respectively, resulted in an 88% reduction in the number of larvae recovered from the lungs 7 days after challenge with 10,000 infective eggs. Peripheral blood lymphocytes (PBL) from vaccinated pigs were specifically stimulated in vitro to incorporate tritiated thymidine by egg hatching fluid (Ea) and by excretory-secretory products obtained from cultures in defined-media of second-stage larvae (L2) developing to third-stage (L2–3) and from cultures of third-stage larvae developing to fourth-stage (L3–4). PBL were also specifically stimulated by living L2. Ea and L2 stimulated pig PBL significantly at 7 days after the first inoculation; responses to L2–3 and L3–4 developed 7 days after a second inoculation. The antigen-responsive cells in the PBL population were non-immunoglobulin-bearing lymphocytes. Antibodies to Ea and L2–3 were not detected in the serum of vaccinated pigs, and only 3 of 7 pigs had low concentrations of serum antibodies to L3–4.  相似文献   

3.
Ascaris suum third-stage larvae (L3) were converted from infected rabbits and cultured in a stationary multi-well plate system. Several different culture media including Mediuim 199, NCTC-135, Minimum Essential Medium-Eagle, Dulbecco's Modified Eagle's Medium, RPMI 1640, McCoy's 5A and Neuman-Tytell mdium were tested to determine which was best for overall larval survival, development and growth. Larvae developed from L3 to fourth-stage (L4) in all media tested, but larval survival and the yield and growth of L. were superior in RPMI 1640. Pyruvate is an important medium component because its addition to RPMI 1640 enhanced the yield and growth of L4 while its removal from DMEM reduced larval survival and the yield and growth of L4. Cholesterol markedly enhanced larval survival and the yield and growth of L4 when added to RPMI 1640 as either a soluble supplement in Tween 80 or to a lesser degree, as a component of liposomes. The multi-well culture plate system is a convenient method for determining the effects of different media and changes in media composition on larvae in vitro.  相似文献   

4.
After infection of pigs by the larvae of Oesophagostomum dentatum, granulomas are formed around the third-stage larvae in the submucosa of the gut which contain a considerable number of neutrophils. This has no obvious impact on the larvae, which develop to fourth-stage larvae within these granulomas. We therefore asked, whether the products of O. dentatum larvae modulate the functional capacity of porcine neutrophils. The antibody-independent cellular cytotoxicity (AICC) was chosen as a model system. This assay was developed for the pig and quantified using flow cytometry. Bovine lymphoblastoid cells (cell line Anna TA1) served as targets. The measurement of cytotoxicity was based on the determination of absolute numbers of vital target cells. This procedure proved to be reliable and required no additional labelling of target and/or effector cells. Porcine neutrophils, when stimulated with phorbol 12-myristate 13-acetate (PMA; > or = 10 nmol/l), killed target cells at effector: target ratios between 1:1 and 9:1. AICC was not demonstrable after 4 h but could be observed between 16 h and 20 h after in vitro co-culture. Killing of targets required close physical contact between effector and targets, since supernatants of PMA-stimulated polymorphonuclear cells were not able to lyse the target cells. Homogenates of third- and fourth-stage larvae of O. dentatum did not affect the vitality of porcine granulocytes or target cells in vitro, nor did they modulate the AICC capacity of porcine granulocytes.  相似文献   

5.
The efficacy of ivermectin against later fourth-stage Strongylus vulgaris larvae was studied in pony foals at 14 and 35 days after treatment. These foals had been reared parasite-free, inoculated with 500 infective larvae and 56 days later given either ivermectin at 200 micrograms/kg or a placebo intramuscularly. At necropsy, foals were examined for lesions and larvae grossly and histologically. Ivermectin was found to be highly effective (98.6%) against later fourth-stage larvae in five foals which were examined at 35 days after treatment, but not in five others examined at 14 days (72.5%). In some foals larvae were found in the tunica media of the ileocolic arteries. The conformation of these larvae appeared normal, but there were degenerative changes which suggested that they were dying or dead. Questions as to how the larvae attained that site and the consequences of their presence there were raised.  相似文献   

6.
Rats which were immunized with increasing doses of Trichinella spiralis muscle larvae per os and inoculated with 2 000 Nippostrongylus brasiliensis third-stage larvae 11 day after the last immunizing dose harbored significantly fewer N. brasiliensis adults at necropsy than did unimmunized controls. Immunized rats were solidly immune to homologous infection with T. spiralis. Some N. brasiliensis infective larvae incubated in vitro at 37°C in T. spiralis antiserum developed mild oral precipitates. They developed strong oral, excretory pore and occasionally anal precipitates in homologous antiglobulins, and none in normal rat sera or globulins. T. spiralis larvae developed strong oral precipitates in homologous antisera, but none in N. brasiliensis antiglobulins or normal rat sera or globulins. Inflammation, altered intestinal conditions and delayed hypersensitivity following T. spiralis infection may be contributing to the cross-resistance observed.  相似文献   

7.
The ELISA technique was found to be very useful for the detection and monitoring of anti-Cooperia and anti-Ostertagia antibodies in calves. Six differens antigens were used; saline extracts from third- and fourth-stage larvae and from adult worms of both genera.Some degree of genus specificity was found when using L4 or adult antigens but not when L3 antigens were used. Stage-specificity could be observed for Cooperia L4 antigen for a limited period after primary single infection. These findings were supported by the results of immuno-electrophoresis.  相似文献   

8.
In order to establish the mammalian parasitic cycle of the nematode Neostrongylus linearis 18 lambs were infected with 5000 third-stage larvae obtained from the snail Cernuella (Xeromagna) cespitum arigonis. In the subsequent days, larvae were found in the walls of the caecum and colon, in the liver and the lungs, suggesting that the bloodstream is the main migratory route. The presence of low numbers of migrating larvae in the mesenteric lymph nodes indicates that this route is probably secondary. The first still sexually undifferentiated, fourth-stage larvae were found in the lungs on the 8th day post-infection (p.i.) and the first sexually differentiated fifth-stage larvae, on the 10th day. Also described are the macroscopic changes of the parasitized organs.  相似文献   

9.
The efficacy of eprinomectin in an extended-release injection (ERI) formulation was determined in cattle harboring naturally acquired infestations of first- or second- and third-stage larvae of Hypoderma spp. in three studies conducted according to the same protocol in the USA (two studies) and Germany (one study). Thirty cattle sourced from herds with a history of Hypoderma infestation were included in each study. Cattle were formed into replicates of three animals each on the basis of pre-treatment anti-Hypoderma antibody titers. Within replicates each animal was randomly allocated to one of the following treatments: ERI vehicle (control) at 1 mL/50 kg bodyweight, administered once on Day 0; Eprinomectin 5% ERI at 1 mL/50 kg bodyweight (1.0 mg eprinomectin/kg), administered once on Day 0 (when larvae were expected to be first instars); or Eprinomectin 5% ERI at 1 mL/50 kg bodyweight (1.0 mg eprinomectin/kg), administered once when larvae were second or third instars (study dependent, Day 73, 119, or 140). Treatments were administered by subcutaneous injection in front of the shoulder. In all studies, emerging and/or expressed Hypoderma larvae were recovered, speciated, and counted and viability was determined. Eprinomectin LAI treatment was 100% (p < 0.05) efficacious against first- and second- or third-stage larvae of Hypoderma bovis (two studies) and Hypoderma lineatum (one study). All animals accepted the treatment well. No adverse reaction to treatments was observed in any animal in any study.  相似文献   

10.
Rabbits of the New Zealand White and Small Chinchilla breeds were each infected at 3-4 months of age with 4-10 thousand invasive trichostrongyle larvae. Prepatent period of the infection was 22-32 days. Third-stage larvae were present up to the 6th day of infection, fourth-stage from the 8th day, fifth-stage from the 14th day and sexually mature trichostrongyles on the 18th day. The period of patency of the infection lasted for over a year, but only small numbers of eggs were passed in faeces, and food intake was not affected. Between 14 and 44% of the third-stage larvae developed into sexually mature nematodes, regardless of infection dose or duration of infection.  相似文献   

11.
Sixteen controlled laboratory studies, involving 420 kittens and cats, were conducted to evaluate the efficacy and safety of topically applied formulations of imidacloprid and moxidectin for the prevention of feline heartworm disease, treatment of flea infestations and treatment and control of intestinal nematodes. Unit-dose applicators and the dosing schedule used in these studies were designed to provide a minimum of 10mg imidacloprid and 1mg moxidectin/kg. Treatments were applied topically by parting the hair at the base of the skull and applying the solution on the skin. Imidacloprid treatment alone did not display activity against Dirofilaria immitis or intestinal nematodes and moxidectin treatment alone provided little or no activity against adult Ctenocephalides felis infestations. The formulation containing 10% imidacloprid and 1% moxidectin was 100% efficacious against the development of adult D. immitis infections when cats were treated 30 days after inoculation with third-stage larvae. A single treatment with this formulation also provided 88.4-100% control of adult C. felis for 35 days. Imidacloprid/moxidectin was 100% efficacious against adult Toxocara cati and 91.0-98.3% efficacious against immature adults and fourth-stage T. cati larvae. The formulation provided 98.8-100% efficacy against adult Ancylostoma and immature adults and third-stage A. tubaeforme larvae. Monthly topical application with 10% imidacloprid/1% moxidectin is convenient, efficacious and safe for the prevention of feline heartworm disease, treatment of flea infestation and for the treatment and control of intestinal nematode infections of cats.  相似文献   

12.
Single doses of Ostertagia ostertagi, followed in 42 days by multiple increasing doses in calves, were monitored by fecal egg counts and plasma pepsinogen. The level of plasma pepsinogen increase was related to the increase in graded levels of inoculation and to the fecal egg counts. Plasma pepsinogen in uninfected controls remained below 1 IU/L. Plasma pepsinogen in all calves reached levels greater than 5 IU/L at 48 days of the extended inoculation period, although fecal egg counts remained low in the previously inoculated calves. The previously infected calves had a higher proportion of early fourth-stage larvae, while larger adult worm burdens were found in the previously uninfected calves. Early fourth-stage larvae were observed in extra-glandular sites, notably between the glandular epithelium and basement membrane or within the lamina propria. An immunological response of the host was suggested by the lymphoid cell infiltration in the mucosa. This host immune response may account for the greater larval inhibition exhibited by the previously infected calves.  相似文献   

13.

Background

This study investigated seasonal changes in naturally acquired gastrointestinal nematode (GIN) infections on two Lithuanian goat farms with different parasite control practices.

Findings

On both farms, nematode faecal egg counts (FEC) and larval cultures were obtained from 15 adult and 10 young goats at bi-weekly intervals from April 2012 to April 2013. Goats on farm A were dewormed with ivermectin (0.3 mg/kg body weight) in October/November 2012, whereas the animals on farm B were left untreated. Thirteen young goats were slaughtered in August/November 2012 and April 2013 and worm burdens in the gastrointestinal tract were enumerated. In goats from both farms, Teladorsagia, Trichostrongylus, Oesophagostomum, Chabertia and Haemonchus were the dominant GIN genera. Herbage contamination with infective third-stage larvae (L3) peaked in July/August and resulted in high FEC in September/October. Parasitological examination at slaughter showed that Teladorsagia spp. and Haemonchus contortus survived the winter, both in the abomasal mucosa as adults and as early fourth-stage larvae (EL4). Deworming on farm A significantly reduced FEC, especially of H. contortus, at the start of the grazing period compared with the untreated farm B (P < 0.05).

Conclusions

Goats were heavily infected with several GIN throughout the year. Strategic anthelmintic treatment during housing significantly reduced nematode egg output, in particular by H. contortus, at the start of the grazing season.  相似文献   

14.
Gongylonema pulchrum is an important parasite of captive primates. Twelve rabbits were infected with 30 third-stage larvae of G. pulchrum. At 4–7 months post-infection, animals were administered levamisole at a single dose of 12 mg/kg, levamisole at 8 mg/kg three times at 2-day intervals, levamisole at a single dose of 8 mg/kg after administration of mebendazole at 70 mg/kg for 3 days or 8 ml of distilled water for 3 days (control). Necropsy at 14 days after treatment revealed that single and multiple dosages of levamisole reduced nematode burdens by 68.4% and 89.5%, respectively. The combined regimen of mebendazole and levamisole exhibited high efficacy for treating G. pulchrum located widely within the upper digestive tract, with a reduction of 98.2%. These results suggest that this combined chemotherapy treatment may be effective against G. pulchrum infection, including buccal and lingual gongylonemiasis in primates.  相似文献   

15.
Necropsy at various intervals of three week old pigs following experimental infection with larvae of Strongyloides ransomi showed distribution of the larvae through the body during the first 24 hours. Quiescent larvae at the 24 hour necropsy, as indicated by higher recovery before and after this period may be an indication of physiological changes preceding a moult. Whether or not a moult occurs in the lung prior to migration of the larvae to the intestine has not been determined. At the 72 hour necropsy, larvae were largely confined to the lung and juvenile worms were beginning to appear in the small intestine. Migration to the small intestine was completed by the 96 hour necropsy. Lesions were observed in the skin and lungs up to the 96 hour necropsy, and lymphocytic accumulations were observed in the skin and lungs to this point and lymphocytic accumulations were observed in the liver to the 72 hour necropsy. At 28 days post-application lung lesions were still evident and the duodenum and jejunum were heavily parasitized.

Egg passage began on the sixth day post-application and peaked on the 12th day.

  相似文献   

16.
Twenty-five known anthelmintic compounds were evaluated in vitro against the highly motile exsheathed non-feeding third-stage of Haemonchus contortus larvae. Activity was based on lack of motility or death of larvae after 24 h of chemical exposure. Six compounds (avermectins, closantel, levamisole, morantel, phenylhydrazone and ticarbodine) were active at a concentration of 100 μg cm?3 or less. The most active compounds were avermectins and levamisole. When higher in vitro concentrations were used, ten compounds (bephenium, coumaphos, dichlorovos, disophenol, hygromycin b, methyridine, parbendazole, phenothiazine, pyrantel and thiabendazole) exhibited activity. Nine compounds were found to be inactive; among these were the new benzimidazoles, i.e., albendazole, fenbendazole, mebendazole and oxibendazole. Because of the inactivity of the new benzimidazoles, this in vitro system is unsuitable as a routine screening tool. Also, the system appears to favor drugs that act quickly through percuticular entry. In an initial group of 5280 untested compounds, 254 (4.8%) exhibited in vitro activity at 100 μg cm?3 against the non-feeding larvae stage. The exogenous and in vitro cultivation techniques required for collecting, cleaning and exsheating the larvae are described.  相似文献   

17.
The efficacy of eprinomectin in an extended-release injection (ERI) formulation in the treatment of cattle harboring naturally acquired nematode populations (including inhibited nematodes) was evaluated. Five studies were conducted under a similar protocol in the USA, the UK, and in Germany. All study animals were infected by grazing naturally contaminated pastures. The adequacy of pasture infectivity was confirmed by examining tracer calves prior to allocation and treatment of the study animals. The cattle were of various breeds or crosses, weighing 79–491 kg, and aged approximately 6–15 months. In each study, 20 animals were infected by grazing, and then removed from pasture and housed in a manner to preclude further nematode infections for 8–16 days until treatment. Animals were blocked based on descending pre-treatment body weight and randomly allocated to one of two treatments: ERI vehicle (control) at 1 mL/50 kg body weight or eprinomectin 5% (w/v) ERI at 1 mL/50 kg body weight (1.0 mg eprinomectin/kg). Treatments were administered once on Day 0 by subcutaneous injection in front of the shoulder. For parasite recovery and count, all study animals were humanely euthanized 14/15 days after treatment. Cattle treated with eprinomectin ERI had significantly (p < 0.05) fewer of the following nematodes than the controls with overall reduction of parasite counts of ≥94%: adult Dictyocaulus viviparus, Capillaria spp., Cooperia oncophora, Cooperia pectinata, Cooperia punctata, Cooperia surnabada, Haemonchus placei, Nematodirus helvetianus, Oesophagostomum radiatum, Ostertagia lyrata, Ostertagia ostertagi, Trichostrongylus axei, Trichostrongylus colubriformis, Trichuris discolor, Trichuris skrjabini, and Trichuris spp.; developing fourth-stage larvae of Ostertagia spp. and Trichostrongylus spp.; and inhibited fourth-stage larvae of Cooperia spp., Haemonchus spp., Nematodirus spp., Oesophagostomum spp., Ostertagia spp., and Trichostrongylus spp.  相似文献   

18.
The resistance of cotton rats, Sigmodon hispidus to Nippostrongylus brasiliensis infection was examined and compared the response to that of the susceptible Indian soft-furred rat, Millardia meltada. After a primary infection with infective third-stage N. brasiliensis larvae (L3), the number of eggs in feces and adult worm recovery rates from the small intestine of cotton rats were significantly lower than in the controls. To determine whether cotton rat resistance was observed during the migratory phase or the intestinal phase, cotton rats and control animals were challenged subcutaneously with L3 or intraduodenally with adult worms, and larval recovery from lungs and adult worm burden were evaluated. The recovery rate of larvae from the lungs of cotton rats was about five-fold lower than from controls. Adult worm recovery from the small intestine of cotton rats was also lower than that from the controls, but the difference (two-fold lower) was smaller than that observed for lung recovery. Carbon treatment at a dose of 250-500 mg/kg effectively increased larval worm recovery from the lungs of cotton rats. However, this treatment had no effect on worm recovery from the intestine after intraduodenal implantation of adult N. brasiliensis. These results suggest that macrophage function have important role in the expression of strong resistance during the migratory phase of N. brasiliensis infection in cotton rats.  相似文献   

19.
Treatment of Goats Infected with the Lungworm Muellerius capillaris   总被引：1，自引：1，他引：0       下载免费PDF全文
Goats naturally infected with Muellerius capillaris were treated with ivermectin subcutaneously once or twice at the rate of 200 or 300 μg/kg body wt or with fenbendazole per os twice at 15 μg/kg body wt. Goats ceased passing larvae 11 to 20 days after treatment, and except for one doe, larvae reappeared in feces 34 to 59 days after treatment. In sections of lung of ivermectin-treated goats, adult Muellerius had swollen body walls and disrupted intestinal tracts. Granulomas, some mineralized, were present. It is suggested that immature Muellerius were not destroyed by either anthelmintic and that following destruction of the adults, immature Muellerius resumed development to the adult stage and produced more first-stage larvae. Treatment of Muellerius may be more effective if repeated after approximately a 35-day interval.  相似文献   

20.
Pairs of sheep infected with 120 000 larvae of Trichostrongylus rugatus were killed at intervals from 2 to 56 days after infection (DAI). Worms were located in tunnels in the epithelium of villi or upper intestinal crypts at all stages of development. Villus atrophy developed progressively until 16 DAI, when surface microtopography, characterised by subtotal villus atrophy, stabilised. Most severe lesions were in the first 3 m of small intestine where the density of nematodes was highest. Discontinuities in the epithelium and effusion of inflammatory cells and tissue fluids into the lumen were rare. No effects of infection on body-weight gain, appetite or serum total protein and albumin were evident in the first 20 days of infection. However, it was concluded that T. rugatus fundamentally resembled T. colubriformis and T. vitrinus in the response it elicited in the intestine of sheep, and must be considered potentially pathogenic.  相似文献   

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