Parasites of domestic and wild animals in South Africa. III. Oestrus spp. and Gedoelstia h?ssleri in the blesbok

Four blesbok culled in the Rietvlei Nature Reserve, Pretoria, District during May 1972 were found to harbour large burdens of 1st instar Oestrus spp. larvae and from 16-37 3rd instar larvae of Oestrus macdonaldi. They were also infested with large numbers of 1st instar Gedoelstia h?ssleri larvae but only 2 harboured 3rd stage larvae of this species. During an 18-month period 34 blesbok were culled in pairs in the Percy Fyfe Nature Reserve, Potgietersrus District. These antelope harboured peak numbers of 1st instar Oestrus spp. larvae during February, July and December but few if any during early October. Third instar Oestrus variolosus larvae were generally recovered from July-February and those of O. macdonaldi during July 1972 and from May-September 1973. Some 1st instar larvae of these flies appeared to undergo a pulmonary migration before returning to the naso-pharyngeal area to mature. The pupal period of O. variolosus varied from 67 days during the spring to 35 days during the summer. G. h?ssleri larvae reached peak numbers from October 1972-January 1973 and during May and June 1973. The lowest numbers were recovered from August-October 1973. Recovery and measurement of 1st instar larvae indicated that they either undergo an ocular-cranial or ocular-vascular-pulmonary migration before reaching the naso-pharyngeal area. Pupal periods varied from 46 days for flies hatching during October to 22 days for those hatching during December.     

THE EPIDEMIOLOGY OF EQUINE STRONGYLOSIS IN SOUTHERN QUEENSLAND 1. The Bionomics of the Free-Living Stages in Faeces and on Pasture

SUMMARY Development of the free-living stages of strongylid nematodes of the horse to the infective stage occurred in faeces in all months of the year in southern Queensland, at a rate which depended on the season. Most rapid development to the infective stage occurred in the warmer months, with the hatching of strongyle eggs being completed in 2 days in summer. During the winter, egg hatching continued for over 2 weeks. Larval moults proceeded at a faster rate in summer—all larvae were infective in 7 days during the hottest months, but it was as long as 5 weeks before all were infective in winter. However, even though development was rapid in summer, survival rates varied from 1 to 10%, in contrast to the spring and autumn, when over 80% reached the infective stage. One percent of larvae in faeces survived for up to 20 weeks in autumn and winter, but for only 4 weeks in summer. These results highlight the inadequacy of short-term pasture spelling for all but the hottest months. Infective larvae were found on herbage in all months of the year, but greatest numbers were recovered in spring and early summer, and in autumn and early winter. The relationship of pasture infestation to migration of larvae from Paecal reservoirs in response to rain was clearly shown. Most infective larvae were found within 30 cm of faecal masses, and in fact 89% of all larvae isolated from herbage in this study were found within 15 cm of faeces. Migration of larvae from faeces to herbage occurred with falls of rain as small as 25 mm. Horse faecal masses dried out completely in 6–8 days in summer and in 14–16 days in winter. Strongyle larvae developed to the infective stage in faeces in the absence of rain, although many remained in the pre-infective stage and completed their development when rain fell. This study shows that massive contamination of pastures with the eggs of strongylid nematodes must be prevented in spring and autumn if susceptible young horses are not to be at serious risk.     

Diagnosis of Elaphostrongylus cervi infection in New Zealand red deer (Cervus elaphus) quarantined in Canada, and experimental determination of a new extended prepatent period.

A modified Baermann assay was used to recover dorsal-spined, first stage larvae of Elaphostrongylus cervi from feces and lungs of red deer (Cervus elaphus elaphus) from three of four herds imported from New Zealand into Canadian quarantine facilities. Tests done on a series of fecal collections showed that larval output from infected red deer was low and sporadic, casting doubt on the efficacy of the Baermann assay to detect all infected individuals in the herds. The animals had passed repeated preembarkation Baermann tests for E. cervi in New Zealand. Seven larvae recovered from these red deer were used to establish a patent infection in a naive red deer. The prepatent period was 206 days and larval shedding was intermittent. Elaphostrongylus cervi is a foreign animal parasite in continental North America, which could become irrevocably established if it were introduced. The data reported indicates that there is currently no reliable method for the detection of E. cervi infection.     

The use of irradiated embryos of Chrysomya bezziana for the detection of the Old World screw-worm fly

Irradiation of Chrysomya bezziana embryos 1 h before hatching with doses less than or equal to 7 kilorad (kr) had a significant effect on percentage egg hatch, weights and survival of larvae. Doses greater than or equal to 1 kr allowed larval development to the end of the 3rd instar stage in vitro, but prevented normal pupal development. Cattle with wounds infested with 1st instar larvae derived from irradiated embryos had 3rd instar larvae present after 3 d but these failed to pupate. Thus it would be feasible to use such larvae for wound infestation for the enhanced detection of screw-worm fly in areas where the release of fertile flies is undesirable.     

Experimental Elaphostrongylus cervi infection in moose (Alces alces)

An 8-week-old male moose calf was inoculated with 360 infective third-stage larvae (L3) of E. cervi. The calf started to expel first-stage larvae (L1) of E. cervi in faeces 63 days after inoculation. The highest faecal larval count of 1,920 L1 per gram faeces was recorded 133 days post inoculation. Clinically, intermittent lameness, mild ataxia and general stiffness were observed over a 3 months’ period from day 75 after inoculation. The symptoms were moderate, faded gradually and were not seen during the last three weeks of the observation period. The calf had a good appetite and the bodyweight increased continuously throughout the experiment. On day 202 after inoculation the calf was euthanized and autopsied. Adult E. cervi were found in the epidural space of the central nervous system (CNS) and in skeletal muscles. Oedema, haemorrhages, discolouration and extensive inflammatory reactions were observed in the fat and loose connective tissue of the epidural space between the 5 th cervical vertebra and cauda equina. Nematodes or lesions indicating nematode infestation could not be demonstrated in the leptomeninges or in the neural parenchyma of the CNS. Numerous eggs and larvae of E. cervi associated with moderate pathological changes were observed in the lungs.     

Larvae of Elaphostrongylus cervi in the deer of Scotland

Protostrongylid larvae were recovered from the faeces or lungs of red deer (Cervus elaphus), roe deer (Capreolus capreolus) and reindeer (Rangifer tarandus) in Scotland during 1981. Typical protostrongylid first-stage larvae were also recovered from possible intermediate hosts, the grey field slug (Agriolimax reticulata) and the white-soled slug (Arion fasciatus). All these protostrongylid larvae were microscopically identical to those of the nematode Elaphostrongylus cervi. Despite careful search, adult E cervi were not found, but it is concluded that infection with E cervi is widespread in Scottish deer.     

苦楝提取物对捻转血矛线虫卵和幼虫活性的影响

为初步探讨苦楝对捻转血矛线虫的作用,本试验通过观察苦楝提取物对虫卵和幼虫活性及形态变化的影响,评估其对捻转血矛线虫的驱虫活性,以期为家畜捻转血矛线虫病的防控及植物驱虫药物的研发奠定基础。试验对苦楝水提取物和乙醇提取物设置5个浓度（25、12.5、6.25、3.125、1.562 mg/mL）进行虫卵孵化试验和幼虫活性试验,对不同浓度药物处理的虫卵及幼虫进行计数,并观察药物作用后虫卵和幼虫的孵化状态及形态变化。结果显示,正常孵育的虫卵和幼虫活力良好,苦楝提取物作用48 h后,虫卵呈未孵化、半孵化状态,发育至桑葚期、蝌蚪期及幼虫期死亡,并且各浓度苦楝水提物和醇提物对虫卵均具有抑制作用,其中苦楝皮醇提物对虫卵孵化的抑制效果最佳,在浓度25 mg/mL时,对虫卵孵化的抑制率高达98.2%,在12.5 mg/mL时,苦楝子醇提物对虫卵的抑制率极显著高于苦楝皮醇提取物（P<0.01）。苦楝子提取物对感染性三期幼虫的致死效果较差,在50 mg/mL时对幼虫有较高致死率（82.6%）。苦楝皮水提取物在浓度为50 mg/mL时对幼虫的致死效果尤为突出,幼虫死亡率为97.0%,死亡的幼虫呈"直线型"或"弓型"。经方差分析,在12.5~50 mg/mL浓度范围内,相同浓度苦楝水提取物之间的致死率存在显著或极显著差异（P<0.05;P<0.01）,同浓度苦楝醇提取物对幼虫的致死率存在极显著性差异（P<0.01）。综上所述,苦楝提取物对体外的捻转血矛线虫卵和感染性三期幼虫的活性均有抑制作用,其中25 mg/mL苦楝皮醇提物对虫卵孵化的抑制效果最佳,50 mg/mL苦楝皮水提物对感染性三期幼虫的致死作用最好。     

Recovery of Mycobacterium avium subsp. paratuberculosis from nematode larvae cultured from the faeces of sheep with Johne's disease

A study was conducted to determine whether trichostrongylid nematode larvae become contaminated with Mycobacterium avium subsp. paratuberculosis when they develop in the faeces of sheep with Johne's disease. Nematode larvae were hatched from ova in the faecal samples of affected sheep. Larval sheaths were removed and these as well as exsheathed larvae were subjected to radiometric culture for M. paratuberculosis. The organism was recovered from washing water used to prepare the larvae, third stage larvae and larval sheaths, but not from exsheathed larvae. The recovery of M. paratuberculosis from larvae was associated with the severity of the histological lesions in affected sheep and with the results of culture of the organism from intestinal tissues and faeces. Nematode parasites of sheep might be able to act as mechanical vectors for M. paratuberculosis as the organism associates with infective third stage larvae when these develop in the faeces of sheep with Johne's disease.     

Neuro-angiostrongylosis in wild Black and Grey-headed flying foxes (Pteropus spp)

OBJECTIVE: To identify nematodes seen in histological sections of brains of flying foxes (fruit bats) and describe the associated clinical disease and pathology. PROCEDURES: Gross and histological examination of brains from 86 free-living flying foxes with neurological disease was done as part of an ongoing surveillance program for Australian bat lyssavirus. Worms were recovered, or if seen in histological sections, extracted by maceration of half the brain and identified by microscopic examination. Histological archives were also reviewed. RESULTS: There was histological evidence of angiostrongylosis in 16 of 86 recently submitted flying foxes with neurological disease and in one archival case from 1992. In 10 flying foxes, worms were definitively identified as Angiostrongylus cantonensis fifth-stage larvae. A worm fragment and third stage larvae were identified as Angiostrongylus sp, presumably A cantonensis, in a further three cases. The clinical picture was dominated by paresis, particularly of the hindlimbs, and depression, with flying foxes surviving up to 22 days in the care of wildlife volunteers. Brains containing fifth-stage larvae showed a moderate to severe eosinophilic and granulomatous meningoencephalitis (n = 14), whereas there was virtually no inflammation of the brains of bats which died when infected with only smaller, third-stage larvae (n = 3). There was no histological evidence of pulmonary involvement. CONCLUSION: This is the first report of the recovery and identification of A cantonensis from free-living Australian wildlife. While angiostrongylosis is a common cause of paresis in flying foxes, the initial clinical course cannot be differentiated from Australian bat lyssavirus infection, and wildlife carers should be urged not to attempt to rehabilitate flying foxes with neurological disease.     

Effects of the chitin synthesis inhibitor diflubenzuron on development of Ascaris suum and Haemonchus contortus

The potential of the chitin synthesis inhibitor diflubenzuron (DFB) to alter the development of the parasitic nematodes (Ascaris suum and Haemonchus contortus was investigated. DFB given orally (10 mg kg-1 per day for 30 days) to sheep inoculated with H. contortus infective larvae did not prevent the establishment of adults or affect fecal egg output. However, there was a significant (greater than 90%) decrease in the number of infective larvae recovered from fecal cultures derived from lambs harboring H. contortus adults that were treated with DFB. DFB did not affect egg hatching. Oral administration (10 mg kg-1 per day for 20 days) of DFB to swine harboring adult A. suum adults had no effect on the adult worm burden or on egg morphology, but eggs removed from worms obtained from DFB-treated swine contained less chitin than eggs removed from untreated control swine. DFB also inhibited chitin synthesis in vitro in the isolated reproductive tract of A. suum adults. These results indicate that DFB at high doses can inhibit the subsequent development of H. contortus larvae in the feces. Since H. contortus larvae lack chitin, DFB may act on these larvae by a mechanism independent of a direct effect on chitin synthesis.     

Cryopreservation of the infective larvae of the common nematodes of ruminants

Exsheathed infective larvae (L 3) of 19 species of nematodes were tested for infectivity in either sheep or cattle after they had been frozen in 0,9% NaCl solution, stored for a relatively short time in the gas phase of liquid nitrogen and subsequently thawed. In addition, 13 of these species were tested after similar storage for up to 18 months. In sheep, Haemonchus contortus, Ostertagia circumcincta, Trichostrongylus axei, Trichostrongylus colubriformis, Nematodirus spathiger and Oesophagostomum columbianum were viable after 2 years of cryopreservation, a mean of greater than 90% of the L 3 being alive when thawed after this period. Similar results were obtained with Chabertia ovina L 3 after 18 months and with Marshallagia marshalli, Trichostrongylus falculatus and Dictyocaulus filaria, after a short period of freezing. On the other hand, Gaigeria pachyscelis and Strongyloides papillosus survived freezing for up to 7 months but neither was viable at the end of this period, nor was exsheathed G. pachyscelis viable without freezing. Most of these infestations were established by inoculating the infective larvae into the abomasum and/or duodenum. M. marshalli, T. falculatus and C. ovina also proved infective after oral dosing. D. filaria, the only other species tested by this route, was not infective when dosed per os after thawing. The infective larvae of the bovine nematodes, Haemonchus placei, Ostertagia ostertagi, Nematodirus helvetianus, Oesophagostomum radiatum, Cooperia pectinata and Cooperia punctata survived freezing for a mean of 26 months, greater than 90% being alive on thawing, but infectivity was generally lower than with the same genera in sheep. Even when not frozen, exsheathed Bunostomum phlebotomum was non-infective. When Cooperia spp. after thawing were tested for infectivity by the oral route, more worms developed in one calf infested orally than in another infested by inoculation into the duodenum. Ova of H. contortus, M. marshalli, O. circumcincta, T. colubriformis, T. falculatus, N. spathiger, C. ovina, H. placei, O. ostertagi, Cooperia spp. and N. helvetianus were recovered from the faeces of animals infested with cryopreserved L 3. No ova of O. columbianum or O. radiatum were recovered from faeces, because differential larval counts were performed before they were patent. Nevertheless, gravid females were obtained post-mortem. Frozen L 3 of N. helvetianus were used to re-establish a pure strain in calves, 2,3 million ova being recovered from infestations with 10 670 L 3 frozen for 26 months. The infectivity of the progeny of frozen L 3 was tested with M. marshalli and C. ovina. In both instances infectivity was high and the worms which developed also produced ova, thus completing the cycle. This appears to be the first report of infective larvae of parasitic nematodes retaining their infectivity after being frozen in liquid nitrogen (gas phase) for longer than 2 years. This is also apparently the first time that M. marshalli T. colubriformis, T. falculatus, T. axei, N. spathiger, C...     

Effect of condensed tannins on egg hatching and larval development of Trichostrongylus colubriformis in vitro

The effects of condensed tannins extracted from seven forages on the viability of the eggs and first stage (L1) larvae of the sheep nematode Trichostrongylus colubriformis were evaluated in in vitro assays. The extracts of condensed tannins were obtained from Lotus pedunculatus (LP), Lotus corniculatus (LC), sulla (Hedysarum coronarium), sainfoin (Onobrychus viciifolia), Dorycnium pentaphylum (DP), Dorycnium rectum (DR) and dock (Rumex obtusifolius). Extracts containing 200 to 500 microg/ml reduced the proportion of eggs that hatched. The larval development assay was used to evaluate the effect of the extracts on the development of either eggs or L1 larvae to L3 infective larvae. Development was allowed to proceed for seven days by which time the larvae in control incubations had reached the infective L3 stage. Extracts containing 200 microg/ml from LP, DP, DR or dock prevented egg development, and only 11, 8 and 2 per cent of the eggs developed to L3 larvae with extracts from LC, sulla and sainfoin, respectively. When the concentration was 400 microg/ml no eggs developed to L3 larvae. The addition of the extracts after hatching also inhibited the development of L1 to L3 larvae; 200 microg/ml extracted from LP, LC, sulla, sainfoin, DP, DR and dock resulted in only 14, 18, 17, 15, 14, 16 and 4 per cent of L1 larvae developing to the L3 stage compared with 85 per cent for controls, and 400 microg/ml further reduced the development of L1 larvae. Statistical analyses showed that when the extracts were added before hatching they were significantly (P<0.001) more effective at inhibiting the larval development than when they were added after hatching. The condensed tannins from dock had the greatest inhibitory effect on egg development followed by the tannins from DR, sainfoin, DP, LP, sulla and LC.     

Effect of condensed tannins extracted from four forages on the viability of the larvae of deer lungworms and gastrointestinal nematodes

The inhibitory activity of condensed tannins extracted from four forage legume plants were evaluated by using a larval migration inhibition assay. The first (L1) and third (L3) stages of deer lungworm (Dictyocaulus viviparus), and the third stage (L3) of deer gastrointestinal nematodes were incubated with tannins extracted from Lotus pedunculatus, Lotus corniculatus, sulla (Hedysarum coronarium) and sainfoin (Onobrychus viciifolia). The tannins extracted from all the forages had inhibitory activity as measured by their ability to paralyse the larvae and inhibit them from passing through sieves. At the highest concentration used (1200 microg/ml) the tannins extracted from sainfoin had the highest activity against ensheathed L1 lungworm larvae (58 per cent), followed by L. pedunculatus (45 per cent), sulla (42 per cent) and L. comiculatus (35 per cent) when the larvae were incubated at 37 degrees C. The same trend, but with lower activities, was observed when the larvae were incubated at 22 degrees C. Anthelmintic activity against L3 lungworm larvae was evaluated by measuring the death rate of ensheathed L3 larvae after incubation with condensed tannins for two, 24 and 48 hours at room temperature (22 degrees C). The death rate was significantly higher (P<0.001) after 48 hours incubation than after two hours or 24 hours, and significantly higher (P<0.001) after 24 hours than after two hours incubation. Condensed tannins from sainfoin had the highest inhibitory activity followed by L. pedunculatus, sulla and L. comiculatus. The tannins from sainfoin also had the highest activity against L3 larvae of gastrointestinal nematodes, followed by L. pedunculatus, sulla and L. comiculatus. Exsheathed larvae of gastrointestinal nematodes were significantly more susceptible to the action of the tannins than ensheathed larvae.     

Small strongyles. Recent advances

The recent increased interest in cyathostomes can be traced to simplification of their taxonomy, improved knowledge of pathogenicity, and failures of practical control due to anthelmintic resistance. Cyathostome ova develop to infective third-stage larvae (L3) at a rate that is directly proportional to environmental temperature. Equine feces serve as a reservoir for L3, which are liberated by moderate amounts of rainfall. Third-stage larvae persist for longer periods at low temperatures, easily surviving over-winter on pastures to provide a source of infection during the following grazing season. Third-stage larvae exsheath within the host and enter the mucosa and submucosa of the cecum and large colon. Larvae develop within mucosal cysts, molt to the fourth stage, and may persist within the tissues for up to 2 1/2 years. Larvae ultimately emerge from the mucosa to become adults in the lumen. Adult populations are replenished by recently ingested larvae and by immature worms newly emerged from arrested development. The magnitude of larval and adult populations within the host displays seasonal variations, with peak numbers occurring in early spring and autumn in the United States. In typical natural infections, a small number of species comprise the majority of the cyathostome populations. Cyathostome infection may result in anorexia, weight loss, diarrhea, colic, and death. Cyathostome ova are easily detected in feces, but ova may not be present during larval cyathostomiasis. Increased concentrations of beta-globulins, hypoalbuminemia, anemia, and leukocytosis occur inconsistently. Two major problems in the treatment of cyathostome infections are anthelmintic resistance and the insusceptibility of encysted larvae to recommended dosages of most anthelmintics. The major goal of cyathostome control is prevention of environmental contamination with nematode ova. Host resistance appears to protect against cyathostome disease rather than cyathostome infection, and one manifestation of this resistance appears to be prolongation of the prepatent period.     

The experimental infection of guinea pigs with the tissue worm of deer - Elaphostrongylus cervi

Infection of six guinea pigs with up to 100 third-stage larvae of Elaphostrongylus cervi produced clinical signs of severe weight loss and ataxia or death in five. These signs occurred approximately eighty days after the larvae had been given per os. Single female E. cervi sub-adults were recovered from four affected animals and both a male and female E. cervi from one animal. Individual worms were found at the base of the brain against the internal surface of the dura mater. Histological and haematological parameters differed significantly between infected and control animals.     

Spread of equine lungworm (Dictyocaulus arnfieldi) larvae from faeces by Pilobolus fungi

Between 10 and 25% of the Dictyocaulus arnfieldi larvae excreted in faeces from a naturally infected donkey were harvested as infective stages from faecal cultures by means of Pilobolus fungi. The faeces were collected between 24 and 56 hours after drenching the donor animal with Pilobolus spores and kept at 16 +/- 2 degrees C. Most larvae were collected between the 5th and the 8th day of culturing during which period fructification and sporangium discharge also peaked. The sporangia and the adhering larvae were collected in Petri dishes inserted between the faecal mass and a light source. All recovered larvae were viable. A mean larval length of 368 microns (range 312-440 microns) and width of 14.6 microns (range 12-20 microns) was recorded for the infective stage. The method was found suitable for the recovery of infective stages for experimental purposes. The authors suggest that the Pilobolus mechanism play an important part in the spread of equine lungworm infection under field conditions similar to the situation in bovine lungworm (Dictyocaulus viviparus) infection.     

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.     

Effects of grazing undrenched weaner deer on chicory or perennial ryegrass/white clover pasture on the viability of gastrointestinal nematodes and lungworms

This study determined the in vitro effects on the viability of internal parasites of grazing undrenched weaner deer on either chicory (Cichorium intybus) or perennial ryegrass (Lolium perenne)/white clover (Trifolium repens) pasture. One experiment investigated the hatching and development of gastrointestinal nematode eggs and larvae, and the development and motility of L1 lungworm (Dictyocaulus eckerti) larvae, and a second experiment used larval migration inhibition assays to test the viability of L1 lungworm larvae extracted from the faeces of weaner deer grazed on either chicory or pasture when they were incubated with rumen and abomasal fluids from fistulated deer also grazing on chicory or pasture. The incubations were undertaken with and without added condensed tannins purified from chicory and with or without polyethylene glycol (PEG) to bind the tannins. Chicory had no effect on the hatching and development of gastrointestinal nematode eggs and larvae. Grazing chicory reduced the number of lungworm larvae developing to the L3 stage, and L1 lungworm larvae from the faeces of chicory-grazed deer were less viable in rumen and abomasal fluid than larvae from pasture-grazed animals. Abomasal fluid was significantly (P < 0.001) less inhibitory to the migration of L1 lungworms than rumen fluid. When the larvae were incubated in rumen and abomasal fluids from chicory-grazed deer, their passage through sieves was significantly (P < 0.001) reduced in comparison with when they were incubated in the fluids from pasture-grazed deer Adding condensed tannins to rumen fluid increased the inhibition of the migration of L1 lungworm larvae but PEG removed this inhibition; this effect was not observed with abomasal fluid.     

Inactivation of eggs and larvae of the cattle nematodes Ostertagia ostertagi and Cooperia oncophora after passage in pigs

The study investigated the effect of gastrointestinal passage in pigs on free-living stages of bovine nematodes. Two Landrace x Yorkshire pigs, A and B, were fed fresh eggs of Ostertagia ostertagi and Cooperia oncophora while two other pigs, C and D, were fed third stage larvae (L3) of the same parasites. Faeces from the pigs were collected for 48 h after ingestion. In pigs A and B, 15 and 66% of the eggs were recovered after passage, respectively. However, only 0.003 and 0.002% of the ingested eggs developed into third stage larvae (L3) after subsequent culturing. In pigs C and D, 0.01 and 0.02% of the L3 survived the passage of the gastrointestinal tract. Fresh O. ostertagi and C. oncophora eggs were cultured in parasite free porcine and bovine faeces. Only 0.05% L3 developed in porcine faeces, whereas 21% of the eggs developed into L3 in the bovine culture. Our results demonstrate an extremely poor rate of development and survival of both bovine nematode eggs and infective larvae after passage in pigs. It may imply that pigs can play an important role in reducing transmission of cattle nematodes if the two species are grazed together or alternately.