Abundance and survival of infective larvae of the cattle nematodes Cooperia punctata, Haemonchus placei and Oesophagostomum radiatum from faecal pats in a wet tropical climate

Observations were made on the abundance and survival of Haemonchus placei, Cooperia punctata and Oesophagostomum radiatum infective larvae from cattle faecal pats exposed at various times of the year in north Queensland wet tropics. Pats exposed in the hot, wet season yielded abundant larvae on herbage. In the dry season, although low numbers of infective larvae were usual, considerable numbers were produced under conditions of heavy dews on dense herbage. Irrespective of season of deposition of pats, the resulting larvae persisted generally for not longer than 10 to 12 weeks, and in large numbers for only 2 to 6 weeks. The findings suggest that prevention of contamination in the wet season, and in the dry season when light rainfalls are accompanied by heavy dews on dense herbage, will result in low levels of larval infestation on herbage. Rotational grazing in the area is suggested as a means of worm control.     

Observations on the free-living stages of cattle gastrointestinal nematodes

A 4-year study on the free-living stages of cattle gastrointestinal nematodes was conducted to determine (a) the development time from egg to infective larvae (L3) inside the faecal pats, (b) the pasture infectivity levels over time, and (c) the survival of L3 on pasture. Naturally infected calves were allowed to contaminate 16 plots on monthly basis. Weekly monitoring of eggs per gram of faeces (epg) values and faecal cultures from these animals provided data for the contamination patterns and the relative nematode population composition. At the same time, faecal pats were shaped and deposited monthly onto herbage and sampled weekly to determine the development time from egg to L3. Herbage samples were collected fortnightly over a 16-month period after deposition to evaluate the pasture larval infectivity and survival of L3 over time. The development time from egg to L3 was 1-2 weeks in summer, 3-5 weeks in autumn, 4-6 weeks in winter, and 1-4 weeks in spring. The levels of contamination and pasture infectivity showed a clear seasonality during autumn-winter and spring, whilst a high mortality of larvae on pasture occurred in summer. Ostertagia spp., Cooperia spp. and Trichostrongylus spp. were predominant and a survival of L3 on pasture over a 1-year period was recorded in this study.     

Survival of infective Ostertagia ostertagi larvae on pasture plots under different simulated grazing conditions

This study was carried out to examine the survival of infective Ostertagia ostertagi larvae (L(3)) on pasture under different simulated conditions of grazing, i.e. mixed grazing of cattle and nose-ringed sows, or grazing by cattle alone. Standardised pats of cattle faeces containing O. ostertagi eggs were deposited on three types of herbage plots, which were divided into zone 1: faecal pat; zone 2: a circle extending 25cm from the edge of the faecal pat; zone 3: a circle extending 25cm from the edge of zone 2. For "tall herbage" (TH) plots, the herbage in zone 2 was allowed to grow naturally, while the herbage in zone 3 was cut down to 5-7cm fortnightly, imitating a cattle-only pasture. For "short herbage" (SH) plots, the herbage in both zones 2 and 3 were cut down to 5-7cm fortnightly, imitating mixed grazing of cattle and sows. The grass in the "short herbage and scattered faeces" (SH/SF) plots were cut as for SH plots, and the faeces were broken down 3 weeks after deposition and scattered within zone 2, imitating the rooting behaviour of co-grazing sows. Five faecal pats from each plot group were collected on monthly basis, along with the herbage from zones 2 and 3 cut down to the ground. Infective larvae were then recovered from both faeces and herbage. The numbers of L(3) recovered from zone 1 were higher in the TH plots than in the other two groups and, furthermore, the larval counts from SH plots were always higher than from SH/SF plots. The three groups followed a similar pattern during the season regarding numbers of L(3) in zone 2, and no clear patterns between plot types were obtained. The presence of L(3) in zone 3 was almost negligible. Important differences were seen throughout the study from the biological point of view; more L(3) were able to survive in faeces on the TH plots, presumably reflecting a better protection from heat and desiccation compared to those in the other plots. The overall results support the idea that mixed grazing of cattle and pigs favour the reduction of O. ostertagi larval levels in pasture. This reduction is mainly due to the grazing behaviour of pigs, which by grazing up to the very edge of the cattle faeces, will either expose the larvae in faeces to adverse environmental summer conditions or ingest cattle parasite larvae, or both.     

The efficacy of two isolates of the nematode-trapping fungus Duddingtonia flagrans against Dictyocaulus viviparus larvae in faeces.

A series of experiments was carried out to examine the effects of two different isolates of the nematode-trapping fungus Duddingtonia flagrans to reduce the number of free-living larvae of the bovine lungworm, Dictyocaulus viviparus. A laboratory dose-titration assay showed that isolates CI3 and Troll A of D. flagrans significantly reduced (P < 0.05 to P < 0.001) the number of infective D. viviparus larvae in cultures at dose-levels of 6250 and 12,500 chlamydospores/g of faeces. The larval reduction capacity was significantly higher for Troll A compared to CI3 when lungworm larvae were mixed in faecal cultures with eggs of Cooperia oncophora or Ostertagia ostertagi and treated with 6250 chlamydospores/g of faeces. Both fungal isolates showed a stronger effect on gastrointestinal larvae than on lungworm larvae. Two plot trials conducted in 1996 and 1997 involved deposition of artificial faecal pats containing free-living stages of D. viviparus and C. oncophora on grass plots. Herbage around the pats was collected at regular intervals and infective larvae recovered, counted and identified. These experiments showed that both D. flagrans isolates reduced the number of gastrointestinal as well as lungworm larvae in faecal pats. During both plot trials, the transmission of C. oncophora larvae, but not D. viviparus, from faecal pats to the surrounding herbage was clearly affected by climatic conditions. After collection of faecal pats from the grass plots one month after deposition, the wet and dry weight of pats as well as organic matter content were determined. No differences were found between the fungus-treated and non-treated control pats. This indicated that the rate of degradation of faeces was not affected by the addition of the fungus.     

Seasonal translation of infective larvae of gastrointestinal nematodes of cattle and the effect of Duddingtonia flagrans: a 3-year pilot study

A study was conducted over 3 years (1998-2000) to investigate larval availability of gastrointestinal nematodes from faeces of cattle reared under different parasite control schemes. These cattle were part of a parallel, but separate grazing trial, and were used as donor animals for the faecal material used in this experiment. At monthly intervals, faeces were collected and pooled from three groups of first-season grazing cattle. These groups were either untreated, ivermectin bolus treated or fed the nematophagous fungus Duddingtonia flagrans. The untreated and fungus treated animals were infected with gastrointestinal nematodes and the number of eggs per gram (epg) pooled faeces ranged between 50 and 700 in the untreated group and between 25 and 525 epg in the fungus treated group. Each year between June and September, artificial 1 kg dung pats were prepared and deposited on pasture and protected from birds. The same treatments, deposition times and locations were repeated throughout the study. Larval recovery from herbage of an entire circular area surrounding the dung pats was made in a sequential fashion. This was achieved by clipping samples in replicate 1/4 sectors around the dung pats 4, 6, 8 and 10 weeks after deposition. In addition, coinciding with the usual time of livestock turn-out in early May of the following year, grass samples were taken from a circular area centred where the dung pats had been located to estimate the number of overwintered larvae, which had not been harvested during the intensive grass sampling the previous year. It was found that recovery and number of infective larvae varied considerably within and between seasons. Although the faecal egg counts in 1999 never exceeded 300 epg of the faecal pats derived from the untreated animals, the abnormally dry conditions of this year generated the highest level of overwintered larvae found on herbage in early May 2000, for the 3 years of the study. Overall, biological control with D. flagrans significantly reduced larval availability on herbage, both during and between the grazing seasons, when compared with the untreated control. However, the fungus did not significantly reduce overwintered larvae derived from early season depositions (June and July), particularly when dung pats disappeared within 2 weeks after deposition. Very low number of larvae (<3 per kg dry herbage) were sporadically recovered from grass samples surrounding the ivermectin bolus faecal pats.     

Direct measurement of dispersal of Dictyocaulus viviparus in sporangia of Pilobolus species

Dispersal of Dictyocaulus viviparus larvae by Pilobolus sporangia was studied on 29 faecal pats deposited between the end of June and late October 1988. Faecal pats were covered daily from day 3 to 4 after deposition with a large petri dish to measure the numbers of sporangia released and the numbers of larvae carried. The yield of both was variable. Dispersal of lungworm larvae was lowest on over-grazed pasture or when Pilobolus growth was very poor. When faecal pats were sheltered by a long sward, 17 per cent or more of larvae present at deposition were transported in this manner. In July and August, peak dispersal of lungworm larvae was on day 5, in September on day 6 and in October on day 7, the increasing time intervals being probably associated with decreasing temperature.     

The origin and overwintering survival of the free living stages of cattle parasites in Sweden

During the 1997 Swedish grazing season, faeces were collected every 3 weeks on 7 occasions from young grazing cattle with moderate nematode parasite infections. From this source 12, 400 g dung pats were set up on each sampling occasion on a specially designated area of pasture. Half of these pats were placed on pasture where it was aimed to prevent snow cover during the subsequent winter. During the grazing season, herbage growth was kept at reasonably uniform height by clipping and the dung pats were protected from destruction by animals and birds. At the time of animal turn-out the following year (7th April 1998), it was observed that all dung pats had disappeared. Assessments of the survival of infective larvae, both on pasture and in soil, were made in a circular area encompassing the location of each pat. These sampling procedures were completed within a 3 week period. All faecal deposits yielded infective larvae at turn-out the following year, with proportionally greater numbers developing from nematode eggs deposited in cattle dung during the mid third of the previous grazing season. The surface layer of soil was found to be an important reservoir for infective larvae, with numbers recovered being approximately half those found in the overlying pasture samples. No significant differences were found between the normal pasture and snow excluded pasture in the number of infective larvae recovered from both pasture and soil samples. The epidemiological consequences of these findings are discussed.     

Survival of infective larvae of nematode parasites of cattle during drought

In a study originally designed to determine the seasonal origin of the high levels of availability of nematode larvae to cattle in winter and spring, plots were serially contaminated with eggs of Ostertagia ostertagi and Cooperia oncophora by naturally-infected calves at monthly intervals from February 1980 to September 1980. The availability of infective larvae was monitored by monthly pasture sampling and larval recovery. Because of the intervention of a 15 month drought, recoveries of larvae from the pastures were very low until March 1981 (autumn in Australia) when large numbers of larvae appeared on pastures contaminated in the preceding spring. Examination of dry dung pats at that time showed that significant numbers of larvae were present in pats deposited up to a year previously, and particularly in pats deposited in May, August and September. Following the resumption of normal rainfall in May 1981, larval numbers in pats rapidly declined and concentrations of larvae on the pastures increased to extremely high levels. It is suggested that survival of infective larvae in dry dung pats was enhanced by the drought, with implications for control of nematode infections of cattle, particularly in winter rainfall environments.     

Spread of infective Dictyocaulus viviparus larvae in pasture and to grazing cattle: Experimental evidence of the role of Pilobolus fungi

Four calves experimentally infected with Dictyocaulus viviparus were made Pilobolus-free by hygienic measures and by feeding them irradiation sterilized feed. Two of the calves were orally administered laboratory cultured Pilobolus sporangia daily. As a result, the faeces from one air contained D. viviparus larvae and Pilobolus spores, and the faeces from the other pair contained D. viviparus larvae, but no Pilobolus spores.

Two identical plots were used for deposition of the two kinds of faeces, and one of them remained free of Pilobolus fructification. Herbage sampling and the use of tracer calves revealed that on this plot the larval contamination and the infectivity of the pasture were greatly reduced. A mean larval count of 1321 near the faecal pats (0–5 cm) in the plot where Pilobolus was observed was reduced to 69 per kg of herbage on the Pilobolus-free plot. At a distance of 100 cm from the pats, a reduction from 99 to 3 larvae per kg herbage was found.

Each plot was grazed by four parasite-free tracer calves for 3 days. During the subsequent stabling period of these calves, the lungworm larval excretion of those from the Pilobolus-free plot was reduced by 90% and the clinical symptoms were milder than those which grazed the plot which contained the fungus. The mean post mortem worm counts after 4 weeks of stabling showed a reduction from 167 to 25 worms.

A more marked effect of Pilobolus fungi on the transmission of D. viviparus infection is to be expected under field conditions where calves are grazing more selectively than in the present study.     

Dispersal of Dictyocaulus viviparus larvae from bovine faeces in Ireland

An involvement of Pilobolus species fungus in the dispersal of Dictyocaulus viviparus third stage larvae from dung to surrounding herbage under Irish conditions was investigated. The presence of Pilobolus kleinii on artificial dung pats containing first stage larvae of D viviparus was associated with a 19-fold increase (P less than 0.05) in numbers of third stage larvae recovered from the surrounding herbage. A subjective examination of natural dung pats showed that the presence of Pilobolus species was significantly correlated with hours of bright sunshine (r = -0.5, P less than 0.01), total rainfall (r = 0.41, P less than 0.05) and the height of herbage surrounding the pats (r = 0.31, P less than 0.001). A multiple regression analysis showed that meteorological parameters and the height of surrounding herbage accounted for 38 per cent of the variation in growth of Pilobolus species on dung pats. The incidence of extensive damage to natural dung pats within five days of deposition, caused by biotic factors, another possible cause of D viviparus third stage larvae dispersal, varied from 0 to 92 per cent of the pats depending on their degree of dryness.     

Factors affecting the survival and migration of the free-living stages of gastrointestinal nematode parasites of cattle in central queensland

Faecal pats containing parasitic nematode eggs were deposited monthly on worm-free pasture, from mid-1975 to early in 1979, near Rockhampton in central Queensland. Pasture samples were collected monthly from beside these pats and the number of infective larvae on the samples was counted.

Cooperia spp. were the most numerous larvae on pasture all year round and Haemonchus placei were commonly present in low numbers. Small numbers of Oesophagostonum radiatum larvae were found, mostly during summer.

Dung beetle activity and rainfall influenced larval populations on pasture, but temperature did not. Beetles were not active in winter, and pats deposited in spring, summer and autumn when beetles were active yielded only 42, 44 and 26%, respectively, as many larvae per 1000 eggs deposited as winter pats. Pats in which beetle activity was minimal (feeding only), moderate and intense (complete destruction), yielded 43, 10 and 6%, respectively, as many larvae per 1000 eggs as intact pats.

Larval densities on pasture were highest after the first saturating rains during the spring-summer period and most of these larvae migrated from unattacked pats deposited in winter. Beetle numbers and activity increased with the summer rains and so few larvae were available to migrate onto pasture during late summer and autumn when the highest falls of rain were recorded. The regression of larval recovery on rainfall was positive and statistically significant when data collected soon after these very heavy rainfall periods were omitted from the analysis.

In 1977, drought-breaking rains increased the normal larval density on pasture 10-fold because larvae in pats deposited in the last 4 months of the drought migrated onto pasture immediately after the rains.

This work suggests that in summer rainfall areas where dung beetles are active, helminth control may be achieved by reducing the worm egg output from cattle during the winter.     

Pilobolus species and rapid translation of Dictyocaulus viviparus from cattle faeces

In a series of five laboratory experiments observations were made on the role of Pilobolus in the translation of infective lungworm larvae from faeces of cattle. The results indicated that a substantial proportion of the lungworm larvae present in the faeces may be translated from the faeces by this fungus within eight days at a temperature of 15 degrees C. No clear relationship was observed between the numbers of Pilobolus and the translation of lungworm larvae. Further a longitudinal study on the occurrence of Pilobolus on faecal pats of grazing calves showed that between the beginning of July and the middle of September peak emergence of sporangia generally occurred within one week and most sporangia emerged within three weeks. From faecal pats which had been deposited at the end of September and the middle of October emergence of sporangia was lower and mainly occurred after two to four weeks.     

Effect of different times of administration of the nematophagous fungus Duddingtonia flagrans on the transmission of ovine parasitic nematodes on pasture--a plot study

Investigations were made into the timing of administration of Duddingtonia flagrans as a biological control agent against ovine parasitic nematodes including stongylid and Nematodirus spp. Faeces from 3-4 months old male lambs were deposited onto pasture plots that had never been grazed by sheep. The trial was conducted over two consecutive years (1998 and 1999). For both years, the following three plot types were involved: Sim plots had faeces containing nematode eggs and Duddingtonia flagrans spores deposited simultaneously; Post plots had faeces containing nematode eggs followed 2 weeks later by faeces containing D. flagrans spores alone; Control plots had faeces containing only nematode eggs; Prior plots (included in 1999) had faeces containing D. flagrans spores alone followed 2 weeks later by faeces containing nematode eggs. In each year, two deposition periods were involved: July and August in 1998 and June and July in 1999. During the first year pasture samples were collected at 2, 4, 6, 8 and 12 weeks after initial deposition. In 1999, additional samples were collected at 10, 16 and 20 weeks. Larvae were extracted from the pasture samples and counts performed to estimate the number and species of infective third-stage (L(3), larvae) present. The number of third-stage strongylid larvae on pasture was significantly lower on Sim plots compared to the remaining plot types for both years at all deposition times (P<0.001). This was also the case for the number of Nematodirus infective larvae in August deposition plots in 1998 (P<0. 02). There was no significant difference between treatments in both deposition times in 1999 and July deposition plots in 1998 for the Nematodirus data. These results suggest that D. flagrans, if deposited at the same time as parasite eggs prevents transmission of third-stage larvae from the faecal deposit onto pasture, including occasionally Nematodirus species, but does not have an effect on third-stage parasitic nematode larvae in the surrounding soil.     

Epidemiology of Nematodirus species infections of sheep in a subarctic climate: development and persistence of larvae on herbage

As part of a study on the epidemiology of Nematodirus species of sheep in subarctic Greenland, the development and persistence of eggs and larvae were investigated by experimentally contaminating plots of pasture with infected faeces and by placing tubes containing a suspension of eggs on to or into the soil. Despite low ambient temperatures, infective larvae appeared within a month during the summer. The greatest numbers of larvae were recovered from herbage in August and September. Eggs did not develop synchronously as development beyond the morula stage could be delayed for up to two years. Larvae were found on herbage for up to 37 months after faecal deposition. In the sheep rearing area of Greenland, therefore, Nematodirus species larvae can be present on herbage throughout the whole summer but peak numbers occur late in the grazing season.     

The origin of winter populations of infective larvae of nematode parasites of cattle in a Mediterranean-type climatic environment

An experiment to determine the origin of populations of infective larvae of cattle nematode parasites on pasture during winter was conducted in south-west Western Australia. Six pasture plots were contaminated with worm eggs by grazing worm-infected cattle for periods of a month during summer and autumn. Each plot was contaminated at a different time from the rest. The levels of infective larvae were determined by counting the worm burdens of tracer calves which test-grazed the plots the following winter.Tracer calves which grazed the plots contaminated during summer acquired few worms, whereas those that grazed the plots contaminated during autumn acquired many worms. It was concluded that the hot, dry conditions prevailing during summer and early autumn prevented the development of eggs or survival of larvae in dung pats or free on pasture. In this environment, a programme of worm control which relied on administration of anthelmintic to grazing cattle to prevent autumn contamination of pasture would be most likely to succeed if the first treatment was given in early autumn.     

Effect of the nematophagous fungus,Duddingtonia flagrans,on the larval development of goat parasitic nematodes: a plot study

Effective alternatives to anthelmintic treatment against nematode parasites of goats are required because of the high prevalence of benzimidazole resistance. Towards this objective, the nematophagous fungus, Duddingtonia flagrans (Df), was used in a plot study against two main parasitic nematode species of goats, Teladorsagia circumcincta (Tcir) and Trichostrongylus colubriformis (Tcol). Worm-free, culled goats were experimentally infected with strains of Tcir and Tcol to constitute donors. Half of the animals were periodically given Df chlamydospores at a daily dose of 2.5 x 10(5) spores/kg BW while the remaining animals were kept as controls. At 5 time periods i.e. March, May, July, September and November 2001, corresponding to the main grazing season in France for goats, faeces were collected from the 6th day of fungus administration for the following 2 days to obtain approximately 1 kg of faeces from each group of animals: Tcir/Control, Tcol/Control, Tcir/Fungus, Tcol/Fungus. For each period and each group, the faeces were deposited on a 1 m2 grass plot and the grass was cut (3 replicates) on weeks 2, 4, 6, 8,12 after deposition, for infective larval recovery. Larvae were counted and the results were expressed as a ratio of larvae/eggs deposited. On the plots with the control faeces deposited in March, July and September, the grass infectivity due to Tcir and Tcol was similar and the maximum number occurred between 2 and 4 weeks post deposition. In May, the maximum numbers of larvae were not recorded until 8 weeks after deposition, due to high daily temperatures and dryness. In November, larval development took place only for Tcir. On the plots with the fungus treated faeces, a significant reduction in grass infectivity occurred for both nematodes and ranged from 50-60% in May, July and November deposits to 80-90% in the September deposit. On the contrary to these findings, no difference was recorded between the fungus and control plots for the March deposit. In conclusion, D. flagrans is suitable for reducing the number of infective larvae in the herbage during the main part of the grazing period for the most important digestive nematodes of goats.     

Development of free-living stages of equine strongyles in faeces on pasture in a tropical environment

The development of the free-living stages and yields of infective third stage strongyle larvae in faeces from a horse with a mixed natural infection deposited on pasture plots were studied over a 2-year period in a coastal area in tropical north Queensland. Two sets of faecal masses (one exposed to, and the other protected from the action of a natural population of dung beetles) were deposited monthly and after 7 days faecal samples were taken for larval recovery and counts. Hatching and development of the free-living stages occurred in faeces on pasture throughout the year. Development was rapid as infective stages were reached within a week of faecal deposition in all months. Yields of infective larvae were affected by the season and the action of dung beetles on the faecal masses. Highest yields were obtained from both beetle-exposed and protected faeces during winter (June to August) and lowest yields were in spring (September to November). High temperatures in spring and summer resulted in low yields of larvae, however, the dry conditions in spring made this season the most unfavourable period. In autumn and winter the temperatures were never low enough to stop or markedly slow down the rate of development, and allowed the development of large numbers of infective larvae. Dung beetle activity was observed throughout the year, and exposed faeces were usually completely dispersed within 24 h of deposition. This resulted in lower yields of infective larvae from these than from protected faeces. Though larval yields were lower, the actual numbers were still substantial so as to cast doubt on the usefulness of these beetles as biological control agents for equine strongylosis in the dry tropics.     

Disintegration of dung pats from cattle treated with the ivermectin anthelmintic bolus, or the biocontrol agent Duddingtonia flagrans

An experiment was performed during the grazing seasons of 1998, 1999 and 2000 to study the influence of the antiparasitic drug ivermectin and the nematophagous fungus Duddingtonia flagrans on cattle dung disintegration. The faeces originated from groups of animals that were part of a separate grazing experiment where different control strategies for nematode parasite infections were investigated. Each group consisted of 10 first-season grazing cattle that were either untreated, treated with the ivermectin sustained-release bolus, or fed chlamydospores of D. flagrans. Faeces were collected monthly on 4 occasions and out of pooled faeces from each group, 4 artificial 1 kg dung pats were prepared and deposited on nylon mesh on an enclosed pasture and protected from birds. The position of the new set of pats was repeated throughout the 3 years of the study. Each year, the dung pats were weighed 4, 6, 8 and 10 weeks after deposition and immediately afterwards replaced to their initial positions. Results showed that there was no difference in faecal pat disintegration between groups. However, the time-lag between deposition and complete disintegration of the faeces varied significantly between deposition occasions. Dung pats disappeared within 2 weeks (visual observation) when subjected to heavy rainfall early after deposition, whereas an extended dry period coincided with faeces still remaining 12 months after deposition.     

Feasibility of herbage sampling in large extensive pastures and availability of cattle nematode infective larvae in mountain pastures

Herbage sampling has been used to ascertain the contamination and epidemiology of cattle nematode infective in large extensive pastures situated in the centre of France, where heifers graze for four months on a total area of one ha/heifer in mountains at 1200 or 1400 m above sea level. The sampling was done for each paddock in four virtual “hectares”, tufts of grass being picked both close to faecal pats or “refusals”, and far from these pats.Ostertagia was the predominant parasite and the occurrence of Dictyocaulus resulted from silent-carrier heifers. Just after the thawing of the snow, when the heifers arrived in the mountains, the contamination was very high: 8000–9000 L3 and 45.00 to 63.00 L3 kg^?1 dry herbage, respectively, far from and close to faecal pats, but this contamination decreases regularly during the season.The sampling of four areas (four “hectares”) in each paddock was found to be a very valuable method. The variation of the mean was low and found mainly when the number of larvae was high (6–19% only for the spring sampling).This technique could have some merit in parallel or concurrently with tracer calves which are always difficult and expensive to use.     

Soil Nematode Populations Beneath Faecal Pats from Grazing Cattle Treated with the Ivermectin Sustained-release Bolus or Fed the Nematophagous Fungus Duddingtonia flagrans to Control Nematode Parasites

The size and composition of the nematode assemblage in soil under faecal pats derived from young cattle treated or untreated with either ivermectin sustained-release boluses, or the nematophagous fungus Duddingtonia flagrans, were studied in each of three years. Soil samples taken 4, 6, 8 and 10 weeks after four deposition dates in 1998 showed significant temporal effects in many taxa and treatment effects in a few genera. In 2000, soil samples taken 10 weeks after deposition in July, August and September showed treatment effects in the plant-associated Tylenchus and Cephalenchus, and the bacterial-feeding Cephalobus 1 and Cephalobus 2 taxa. However, overall it was found that the nematode assemblages were similar below all three types of pat, and the assemblages varied with the season of deposition. D. flagrans, the novel biological control agent being tested against the free-living stages of nematode parasites of cattle, had no detectable impact on the size or the structure of the soil nematode communities under the faecal pats.