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The in vitro lethal activity of two Bacillus thuringiensis strains (IB-16 and IB-61) against Haemonchus contortus histotropic fourth stage larvae (L(4)) was evaluated. Each B. thuringiensis strain was used as soluble proteins at different concentrations. In addition, the in vitro lethal dose (LD(50)) of each strain was determined against H. contortus L(4) at different times. Data were analyzed by ANOVA and Tukey tests. Less than 50% mortality was observed at 50 and 100 microg/mL during all bioassays. More than 50% mortality was observed at 200 microg/mL at 3 and 5 days after interaction with IB-16 and IB-61, respectively. A 100% mortality was observed with IB-16 on day 5. The LD(50) with IB-16 was 248 microg/mL on day 3, and IB-61 showed an LD(50) at 227 microg/mL on the day 5. Both toxins may have potential as biocontrol agents.

This research evaluated the use of multinutritional pellets (MP) containing Duddingtonia flagrans chlamydospores as vehicles for oral administration in sheep against Haemonchus contortus. Pellets containing urea, wheat coat, soy meal, molasses, and D. flagrans chlamydospores were offered for 10 days to six nematode-free sheep (group 1, treated). Group 2 (control), also six nematode-free sheep, was supplied for the same period with nonfungi pellets. Feces were collected daily from each animal and deposited on water agar plates containing 500 H. contortus infective larvae. Three plates were used as three replicates per treatment, and all plates were incubated for 7 days. Microscopic observations revealed trap formation and the captured larvae. Washes from the plate content were passed through a Baermann funnel to collect noncaptured larvae and to quantify nematode reduction by fungal action. A larval reduction of 82% was found in fungal culture plates. The use of MP containing D. flagrans chlamydospores could be considered as a viable alternative control tool against sheep haemonchosis.

This investigation was aimed to evaluate the use of an oral bio-preparation containing Duddingtonia flagrans chlamydospores for the control of sheep gastrointestinal parasitic nematodes under the Mexican cold high plateau conditions. Two groups of gastrointestinal parasitic nematode naturally infected sheep, were randomly selected and located into two free-gastrointestinal nematode larvae paddocks. Group 1 received once a week a supplement containing D. flagrans chlamydospores mixed with oats and molasses. Group 2 received a similar supplement without any fungal material. After 5 months grazing animals were discarded from the experiment and two groups of free-nematode "tracer" sheep were located into the same paddocks to collect larvae from the contaminated pastures. Animals were slaughtered and necropsied and the nematodes were obtained and counted. A screening of the number of gastrointestinal nematode larvae present on the grass was performed and compared between the two grazing areas. The results showed 56% reduction in the Ostertagia (Teladorsagia) circumcincta and 94% reduction in the Nematodirus sp. population of the "tracer" sheep who grazed on the D. flagrans-treated sheep area, compared to the nematode population in animals grazed on the non-treated area. The results of the number of larvae on the grazing pastures showed a 51.1% reduction for H. contortus, and 100% for Cooperia sp. in the area with fungi. In the case of Trichostrongylus sp. no reduction was observed, when compared to the control group.

One trial was carried out to evaluate the nematophagous capacity of two Duddingtonia flagrans cultures, one maintained during one year at laboratory temperature and the other one was a recent culture, twelve Petri dishes with flour-corn-agar media were seeded with the 1YC another 12 Petri dishes were inoculated with the RC. Both were added with 150 larvae/dish of the free living nematode Panagrellus redivivus and 12 fluor-corn-agar dishes only with the free living nematode were used as a control. The results showed that the nematophagous capacity of both cultures were similar but it was statistically different (p < 0.05) with respect to the control group. It was concluded that the nematophagous capacity of D. flagrans was not affected in spite of being kept one year at laboratory temperature.

The aim of this study was to evaluate the predacious capacity in vitro of eight isolates of nematophagous fungi: four of Arthrobotrys sp., one of Arthrobotrys oligospora, one of Duddingtonia flagrans, one of Dactylaria sp. and one Monacrosporium eudermatum. Nine groups of Petri dishes with 13 repetitions each were set up. The fungi were seeded in fluor-corn-agar media, following this each Petri dish was added with 150 larvae of the free living nematode Panagrellus redivivus. Five days after larval addition these were collected by Baermannization and were quantified. A significant difference (p < 0.05) between all treated group was observed respect with the control. Isolates FTHO-8 D. flagrans, R6 M. eudermatum, DAC Dactylaria sp. as well as FTHO-4 and FTHO-6 Arthrobotrys sp., showed an excellent predatory activity (> 90%) and they could be considered as potential bio-control agents in future field trials.

The initial infection process of nematode-trapping fungi is based on an interaction between the trapping structure of the fungus and the surface of the nematode cuticle. A bioassay was designed to investigate the predatory response of several isolates of nematode-trapping fungi against 3 mutants of Caenorhabditis elegans (AT6, AT10 and CL261), which have been reported to differ in the reaction of their cuticle to antibodies and lectins. The bioassay was also applied to infective larvae of animal (Haemonchus contortus, Teladorsagia (Ostertagia) circumcincta and Trichostrongylus axei) and plant (Meloidogyne spp.) parasitic nematodes. Differences in trapping ability were most marked in the first 24 h, and were density dependent. Although the isolate of Arthrobotrys responded very rapidly in the first 24 h, Duddingtonia flagrans was generally the most effective isolate and Monacrosporium responded relatively poorly throughout all experiments. All the fungi tested trapped the srf mutants of C. elegans more efficiently than the wild type, and there were differences between the different srf mutants of C. elegans. Differences in trapping ability were also observed between different isolates of D. flagrans; similarly, differences in trapping behaviour were observed not only amongst the different species of plant-parasitic nematodes, but also between the sheathed and exsheathed larvae of the animal-parasitic nematodes.

Populations of Pasteuria penetrans isolated from root-knot nematodes (Meloidogyne spp.) and cyst nematodes (Heterodera spp.) were tested for their ability to adhere to a limited selection of sheathed and ex-sheathed animal parasitic nematodes, free living nematodes, including Caenorhabditis elegans wild type and several srf mutants, and plant parasitic nematodes. The attachment of spores of Pasteuria was restricted and no spores were observed adhering to any of the animal parasitic nematodes either with or without their sheath or to any of the free living nematodes including C. elegans and the srf mutants. All spore attachment was restricted to plant parasitic nematodes; however, spores isolated from cyst nematodes showed the ability to adhere to other genera of plant parasitic nematodes which was not the case with spores isolated from root-knot nematodes. The results are discussed in relationship to cuticular heterogeneity.

In an in vitro trial, the trapping ability of Arthrobotrys robusta and Monacrosporium gephyropagum against Strongyloides papillosus infective larvae on corn meal agar plates, was evaluated after seven days of interaction at 25 degrees C. Monacrosporium gephyropagum trapped 93.1% of the larvae whereas A. robusta trapped only 32.3%. Variability in the capture of S. papillosus infective larvae by both trapping fungi is discussed.

Three freeze protectants were evaluated to preserve H. contortus infective larvae. Freezing solutions used: A) saline solution phosphate buffer pH 7.2 (PBS); B) 10% DMSO (dimethyl sulphoxide); C) 10% glycerol. Fifty thousand infective larvae were put into each of 10 vials per freeze protectant and then stored into liquid nitrogen. Results were based on the motility of the larvae under a light microscope at 30, 90, 180, and 360 days of freezing. Ten vials of each freeze protectant were removed from the liquid nitrogen at these times and immediately were put on water at 37 C during a minute. Motility percentages obtained were as follows: PBS: 36%, 20%, 7% and 39%; DMSO,: 87%, 69%, 46% and 85%; glycerol: 67%, 62%, 29% and 55%; at 30, 90, 180 and 360 days respectively. Inoculation of infectiva larvae from DMSO and glycerol to calves was successful after 28 days. DMSO was a better freeze preserver for H. contortus.

The reduction of Haemonchus contortus (L3) infective larvae in sheep faecal cultures caused by the action of three nematophagous fungi conidia was evaluated in vitro. Addition of 20,000 conidia of Monacrosporium eudermatum, Arthrobotrys oligospora and Arthrobotrys robusta per gram of faeces caused a reduction of 95.7%, 98.3% and 10.1%, respectively, compared with the control group. A 97.4% reduction was observed when combined conidia of the three fungi were used. Total reduction of the larval population was observed by addition of the three fungi at 100,000 conidia per gram of faeces.

In an in vitro trial, the effect of the nematode-destroying fungus Arthrobotrys robusta on Haemonchus contortus infective larvae was evaluated in petri dishes containing corn meal agar. After seven days incubation at 25 degrees C, 92.33% (+/- 4.1) predation was recorded.

Anthelmintic efficacy of ivermectin against Mecistocirrus digitatus was evaluated in 10 naturally infected zebu calves. Group 1 (n = 5) was not treated, and group 2 (n = 5) was treated SC with 200 micrograms of ivermectin/kg of body weight. Calves were euthanatized 14 or 15 days after treatment. There was 100% overall reduction of M digitatus in treated calves, which was significant (P = 0.0079) compared with reduction in controls. Cooperia punctata, Haemonchus similis, and Trichostrongylus axei were found in controls. Efficacy against these parasites in treated calves was 100%.