The effects of condensed tannins (CTs) extracted from pine bark on egg hatching, larval development and the viability of infective L3 larvae of Trichostrongylus colubriformis (Giles, 1892) and Teladorsagia circumcincta (Stadelmann, 1894) (syn. Ostertagia circumcincta) were evaluated using in vitro bioassays. Significant inhibitory effects of CTs were obtained on the viability of the infective larvae, egg hatching and larval development of both nematodes. In all bioassays, the larval stages of Te. circumcincta were significantly (P < 0.05) more susceptible to the inhibitory effects of CT than those of Tr. colubriformis. At 1 000 µg/ml, CTs from pine bark inhibited 48% and 69% of the infective larvae of Tr. colubriformis and Te. circumcincta, respectively, from passing through the sieve relative to the control incubations (no CT added; P < 0.0001). At the same concentration, CTs were able to inhibit 36% and 47% of the eggs of the two parasites, respectively, from hatching relative to the control incubations without CTs. Moreover, at 150 µg/ml, the CTs were able to inhibit 88% and 95% (P < 0.0001 relative to control incubation) of L1 larvae of the two nematodes, respectively, from attaining the full development to L3 larvae in comparison with the control incubations without CTs. At 200 µg/ml, CTs were able to inhibit completely the larval development in both nematodes. Addition of 2 µg polyethylene glycol (PEG; tannin inhibitor) per µg CT eliminated up to 87% of the CT activity (P < 0.0001) compared to incubations without PEG. In conclusion, this study shows that CTs are able to disrupt the life cycle of nematodes and their effects varied according to the parasite species and stage.
The effects of condensed tannins (CT) extracted from seven forages on the motility of the economically important nematode, Trichostrongylus colubriformis (Giles, 1892), were evaluated by using a larval migration inhibition (I.MI) assay. The assay involved incubation of third stage (L3) exsheathed T. colubriformis larvae with CT extracted from Lotus pedunculatus, Lotus corniculatus, sulla (Hedysarum coronorium), sainfoin (Onobrychis viciifolia), Dorycnium rectum, Dorycnium pentaphyllum and dock (Rumex abtusifolius) and measurement of larval migration through nylon mesh with a 20pm pore size. At 100 pg ml'1, CT from L. pedunculatus, L. corniculatus, sulla, sainfoin, D. rectum, D. pentaphyllum and dock inhibited 20%, 10%, 15%, 25%, 28%, 32% and 27% of the larvae, respectively from passing through the sieves compared to controls (no CT added). At 1000 pg CT ml'1, CT purified from D. pentaphyllum had the highest inhibitory activity (63%) against 1-month old larvae followed by sainfoin (59%), L. pedunculatus (57%), D. rectum (53%), dock (50%), sulla (40%) and L. corniculatus (37%). Seven-month old larvae were more sensitive to the action of CT than 1-month old larvae (P < 0.001). Addition of 2 pg polyethylene glycol ([PHG] per pg CT; to remove the effect of'CT) eliminated 81-93% of the CT activity (P < 0.001) compared to incubations without PEG. The impact of CT on larval migration suggests a possible role for these plants in ruminant diets as a means to reduce dependence upon proprietary anthelmintics.
The effects of condensed tannins (CTs) extracted from five species of plants on egg hatching and larval development of Teladorsagia circumcincta (Stadelmann, 1894) (syn. Ostertagia circumcincta) were evaluated using in vitro bioassays. The extracts of CTs were obtained from Lotus pedunculatus (LP), Lotus corniculatus (LC), Dorycnium pentaphyllum (DP), Dorycnium rectum (DR) and Rumex obtusifolius (RO). The results of egg hatching assay showed that about 53%, 68%, 51%, 60% and 46% of the eggs hatched when in vitro incubations contained 900 mg/ml of CTs from LP, LC, DP, DR and RO, respectively (P< 0.001 relative to control incubation), while in control incubations (no CT added) 87% of the eggs hatched. In the larval development assay, development was allowed to proceed for 7 days, by which time 89% of the hatched larvae in control wells (no CTs) had reached the infective third stage (L3). In incubations containing 200 mg CT from LP, LC, DP, DR and RO/ml, about 8%, 15%, 14%, 8% and 4% of the eggs attained full development to L3 larvae, respectively (P< 0.001 relative to control incubation). Only 1% of the eggs were able to develop to L3 larvae in incubations containing 400 mg CT extracted from LC/ml, whilst in the incubations containing the same concentration of other CTs the eggs were not able to develop to L3 larvae. It seems that CTs are not only slowing down the larval development but also kill the undeveloped larvae. At 400 mg/ml, for example, CT from LP, LC, DP, DR and RO killed 67%, 48%, 68%, 93% and 91% of first-stage (L1) and second-stage (L2) larvae, respectively. This study shows that CTs are able to disrupt the life cycle of nematodes.