- Open Access
Anti-parasitic activity of pelleted sainfoin (Onobrychis viciifolia) against Ostertagia ostertagi and Cooperia oncophora in calves
© The Author(s). 2016
- Received: 14 January 2016
- Accepted: 1 June 2016
- Published: 10 June 2016
Increasing anthelmintic-resistance in nematodes of ruminants emphasises the need for sustainable parasite control. Condensed tannin-containing legume forages such as sainfoin (Onobrychis viciifolia) have shown promising anthelmintic properties in small ruminants but this has never been explored in cattle. Therefore, our aim was to examine the efficacy of sainfoin against cattle nematodes in vivo.
Fifteen Jersey male calves (2–4 month-old) were allocated into two groups and fed isoproteic and isoenergetic diets mainly composed of sainfoin pellets (Group SF; n = 9, three pens) or concentrate and grass-clover hay (Group CO; n = 6, two pens). After 16 days of adaptation, all animals were experimentally infected with 10,000 and 66,000 third-stage larvae of Ostertagia ostertagi and Cooperia oncophora, respectively. Egg excretion, blood parameters and bodyweights were recorded throughout the study. Worms were harvested by sieving for quantification and scanning electron microscopy (SEM) 42 days post-infection (dpi) when the calves were necropsied.
The number of O. ostertagi adults in the abomasum was reduced by 50 % in Group SF compared with Group CO (P < 0.05). This was further reflected in higher albumin (P < 0.1) and lower pepsinogen levels (P < 0.05) in Group SF at 21 dpi, and structural damage of the worm cuticle could be visualised by SEM. Yet, the nematode egg excretion in Group SF was not significantly different from that of the controls (P > 0.05). Likewise, no statistical difference in total worm burdens of C. oncophora was found between the groups. Weight gains were lower for Group SF (P < 0.05), which may reflect lower digestibility and phosphorus levels in the SF diet, despite similar feed intake at pen-level.
Overall, the effect of sainfoin on abomasal nematodes corroborates results from studies with small ruminants and encourages further investigations of the use of this crop for control of cattle nematodes.
- Condensed tannins
- Ostertagia ostertagi
- Cooperia oncophora
Gastrointestinal nematode (GIN) infections in grazing ruminant livestock remain an important problem, which affect health and welfare of the animals and cause serious economic losses. While anthelmintic (AH) drugs are still considered a keystone for GIN control in ruminants, the awareness of the impact of drug resistance among nematode populations  urges farmers and researchers worldwide to explore new strategies, including feeding of bioactive forages containing plant secondary metabolites (PSM) with AH properties. While PSM can be administered on a short term as herbal remedies, we opted for a “nutraceutical” approach, which also consider bioactive plants for their nutritive value and require long term consumption to obtain substantial health benefits, including AH effects . Plants with condensed tannins (CT; syn. proanthocyanidins) have been thoroughly investigated in small ruminants, particularly the use of CT-rich temperate/subtropical leguminous forages: sulla (Hedysarum coronarium), lotus species (Lotus corniculatus and L. pedunculatus), sericea lespedeza (Lespedeza cuneata) and sainfoin (Onobrychis viciifolia). Due to their nitrogen fixating capacity, legumes have an essential role to play for the sustainability and competitiveness of grassland-livestock systems in Europe .
CT are polyphenolic PSMs found throughout the plant kingdom resulting from the polymerisation of flavan-3-ols units; using either epi-/catechin, known as procyanidins (PC), or epi-/gallocatechin, known as prodelphinidins (PD). Both PC and PD have the ability to reversibly bind proteins and other macromolecules. They have shown beneficial effects on animal health through lower GIN parasitism and bloat prevention, on animal nutrition due to better use of dietary protein and by reducing the environmental impact of livestock by mitigating emissions of greenhouse gases . However, the bioactivity of CT in vivo against GIN of small ruminants is known to be highly variable depending on the plant source, the parasite and the host . Plants have different concentration and composition of CT according to species, cultivar, season and general growth conditions. Also, it seems that a CT concentration of 3–4 % of dry matter (DM) in plant material is a lower threshold for AH effects , albeit different methods were used to estimate CT and may give variable results. Moreover, CT with a higher proportion of PD units have been associated with a higher efficacy both in vivo and in vitro [6–10]. Forage preservation processes, e.g. ensiling  or pelleting, releasing CT from the plant cells, have been shown to alter the status of CT from “free” to “bound”, notably to proteins, but may also positively influence the AH activity. Moreover, parasite species and stages have different susceptibilities to CT [12–14]. In addition, different host species are differently adapted to CT and/or various gut environments ensuring the formation or release of CT-protein complexes . This has been illustrated, e.g. in sheep and goats using wattle tannin . Although most in vitro assays and short-term CT feeding trials have demonstrated a direct AH effect of CT , the high nutritive value of some temperate legumes and the protection of protein by CT from microbial degradation in the rumen (rumen by-pass protein) can improve the immune response and be indirectly detrimental to the parasites [16, 17].
To the best of our knowledge no data are available on potential AH effects of CT against cattle nematodes in vivo. However, sainfoin seems to be a good candidate based on in vitro studies [8, 18]. It is a crop known for its appealing features such as high palatability, high protein levels and importance in biodiversity preservation. In GIN infected small ruminants intake of sainfoin has been consistently associated with a reduction in faecal egg counts (FEC), except when CT levels were lower than 2 % of DM intake [19–23]. Several studies have indicated reduction in worm burdens at CT dietary concentrations of 5.1 % and 8 %, without negative effects on animal performance [21, 22].
Our main objective was to assess whether feeding sainfoin has an effect on pathophysiological and parasitological measurements in calves experimentally infected with the most pathogenic and prevalent GIN of cattle in temperate regions: Ostertagia ostertagi and Cooperia oncophora.
Fifteen Jersey male calves with no grazing history (2.5−4.5 month-old, 91.4 ± 24.0 kg [mean ± standard deviation, SD]) were acquired from a commercial farm. Upon arrival they were orally treated with fenbendazole (Panacur®Vet 10 %, MSD Animal Health, 5 mg/kg bodyweight [BW]) to ensure helminth-free condition (later confirmed with negative FEC one week post treatment). During the whole study period the calves were reared indoor in solid concrete floored pens with straw bedding and external feeders. All animals were allowed an acclimatisation period of 16 days and were clinically assessed on a daily basis throughout the study.
Feed constituents and nutritional analysis
Sainfoin (O. viciifolia) pellets were provided by Multifolia/MG2MIX (Viâpres-le-Petit, France) Ltd., and consisted of a pure-stand 3rd cut (cultivar: Perly) harvested in 2012 and processed to obtain dehydrated pellets. The other feed sources included grass-clover hay and a commercial concentrate (Danish Ragna Grønmix©, Danish Agro Ltd., Karise, DK). The level of DM, crude protein (CP), neutral detergent fibre (NDF) and ash was analysed in all feed components by an accredited, authorised laboratory (Eurofins Steins Laboratorium Ltd., Holstebro, DK). Digestible organic matter (DOM) was calculated considering OM content in feeds and OM digestibility (OMD) of hay, sainfoin and concentrate that was analysed by near-infrared (NIR) spectroscopy, an in vitro method  and in vitro enzymatic method (EFOS ), respectively. The values for OMD of sainfoin and concentrate were corrected to in vivo OMD (OMD %) using the following regression functions: OMD %sainfoin = 4.1 + (0.959 × in vitro digestibilityTilley & Terry %) (used for most forages) and OMD %concentrate = 22.0 + (0.752 × in vitro digestibilityEFOS %) . Metabolisable energy levels, expressed in MJ/kg of DM, were calculated from the net energy lactation values, which were provided by manufacturers or laboratory, and divided by 0.65 . Mineral composition values were obtained from suppliers. Feeds were analysed for CT content by the acetone-butanol-HCl assay  with pure fraction of CT from dried sainfoin as standard. In addition, CT in sainfoin pellets were characterised after in situ thiolysis  and LC-MS analysis . This gives information on the content and composition of CT: their mean degree of polymerisation (mDP)-values (i.e. size), percentages of PC versus PD type tannins, and cis versus trans flavan-3-ol subunits.
Infective third-stage larvae (L3) for inoculations were isolated from donor calves experimentally infected with O. ostertagi and C. oncophora following standard larval culture procedures (14 days at 21 °C). The larvae were stored at 13 °C for 3 months until evaluation of ensheathment and viability 1–3 days prior to inoculation. Hundred baermannised L3 were then morphologically differentiated , and a batch comprising 13 % O. ostertagi and 87 % C. oncophora was used. All calves (n = 15) were orally inoculated with a total dose of 10,000 L3 of O. ostertagi and 66,000 L3 of C. oncophora per calf, given as three sub-doses for three consecutive days.
Experimental design, diets and sample collection
Sixteen days prior to the experimental infection the calves were randomly allocated into two groups after stratification by BW. The Sainfoin group (SF) (n = 9; 90.9 ± 28.1 kg) was allocated to three pens, each containing three animals with almost similar BWs in order to allow a better estimation of the feed consumption and to avoid bullying (i.e. a pen for the smaller, intermediate and larger calves). The Control group (CO) (n = 6; 92.1 ± 18.5 kg) was allocated to two pens of three calves. All calves were weighed weekly except for the last time point.
In Group SF sainfoin pellets were gradually offered in addition to hay until becoming the main feed component (> 90 %) after a period of 12 days. Calves from Group CO received commercial concentrate (ranging from 55 to 65 % of the diet) and hay of ryegrass-clover. The intakes of sainfoin pellets, hay and commercial pellets were calculated every day for each pen (feed offered - feed refusals). Four days prior to infection, the diets were formulated in order to fulfil requirements of CP and energy and to obtain similar levels adjusted for BW in both groups. Diet in Group SF was offered close to ad libitum and the diet in Group CO was adjusted with concentrate every second day to match the diet of Group SF, with a maximum of 2 and 3 kg of DM for small and larger animals, respectively. All animals had free access to water. Straw bedding consumption was observed in both groups but could not be recorded. Individual faecal samples were rectally collected once weekly during the pre-patency period and every 2–3 days from 14 days post-infection (dpi) onwards. Faecal egg counts (FEC) and larval cultures were prepared as described in the next section. Individual blood samples were collected by jugular venipuncture at weekly intervals, and the recovered serum was stored at -20 °C until use. At 40−42 dpi all calves were euthanized with captive bolt pistol followed by exsanguination.
Serum and faecal samples analysis
Serum samples obtained from week 0 to 6 were analysed for pepsinogen as previously described  and for total protein (TP), albumin (ALB) and inorganic phosphate (IP) using an ADVIA1800 analyzer (Siemens). A more detailed biochemical profile analysis was performed at necropsy: alkaline phosphatase, alanine aminotransferase, total bilirubin, cholesterol, creatinine, creatinine kinase, iron, aspartate aminotransferase, urea, gamma-glutamyl transpeptidase, calcium, magnesium, sodium and potassium.
FEC were determined using a modified McMaster technique with a sensitivity of 5 eggs per gram faeces . Faecal DM from each animal was determined during the patency period from 3 g subsample dried at 60 °C for 24 hours, and FEC were expressed as the number of eggs per gram of dried faeces (FECDM). Species-specific FECDM was estimated from larval cultures that were prepared at selected time points from pooled faecal samples (10 g of faeces per animal) for each pen, which were mixed with vermiculite and incubated for 13 days at 20–22 °C.
Recovery and analyses of adult nematodes
Immediately after euthanasia, the abomasum and the whole small intestine from each animal were opened separately and washed with 5 and 10 l of 38 °C warm saline (0.9 % NaCl), respectively. For each organ, one subsample of 500 ml of washed digesta content (i.e. representing 10 % of the abomasum and 5 % of the small intestine contents) was passed through a 38 μm metallic sieve and retained material was stored in 70 % ethanol. Worm counts and sex determination were performed. Sex ratio was reported as the percentage of male worms in the total worm burden. Changes in sex ratio are a good indicator of worm expulsion for C. oncophora because expulsion initially includes male worms . Worm fecundity was assessed by counting the number of eggs from 16 female worms of both nematode species per calf. These worms were recovered from individual animals and lysed in 200 μl of a 20 % household bleach solution. Eggs were enumerated 10 min after lysis for O. ostertagi and after 30 min for C. oncophora female worms. Finally, the cleaned mucosa of the abomasum from one animal in each group was scraped and digested in pepsin/hydrochloric acid for 2–3 hours . Each digested mucosa was passed over a 38 μm sieve, and the retained material was examined for inhibited fourth-stage larvae.
Scanning electron microscopy (SEM)
Adult O. ostertagi were examined by SEM. The worms were collected from randomly selected animals (CO: n = 2; SF: n = 4) after washing with tap water, and fixed in PBS with 2 % glutaraldehyde. They were merged per Group and post-fixed in 1 % OsO4 and 0.05 M K3FeCN6 in 0.12 M cacodylate buffer for 2 hours at room temperature and stirred. Then, the samples were rinsed with 0.15 M cacodylate buffer and distilled water, followed by dehydration in a gradient of ethanol concentrations in a critical point dryer. The worms were coated with 4 nm gold with a coating instrument (Leica EM ACE200) and loaded in a scanning electron microscope (Phillips XL 30 FEG) for visual analysis using Scandium software.
The effects of feeding sainfoin were assessed by linear mixed-effects models fitted with maximum likelihood. BW, faecal DM and biochemical markers were analysed as repeated measures as described by . These models included Pen as random effect and the fixed effects were Group and Time, and the interaction between Group and Time if significant. Baseline measurements were used as covariates for biochemical markers (week 0 value) and BW (initial BW). Pepsinogen data were log-transformed prior statistical analysis but presented as back-transformed means. The variance homogeneity between observations of the models was also tested. The residual plots were used to validate the final models. Likewise, statistical differences between groups in relation to: worm counts (for O. ostertagi), sex ratio, fecundity of female worms (i.e. number of eggs in utero), and additional blood parameters (42 dpi) were analysed by mixed effects models including post-hoc comparison of means by Tukey’s test, with Group as fixed effect and Pen as random effect. Counts data for adult worms of C. oncophora and FECDM were over-dispersed therefore we used generalised linear mixed-effects models for the negative binomial family with Group as fixed effect and Pen as random effect. Statistical analyses were carried out with R (version 3.2.0).
Feed composition and diets
Nutrient contents of experimental feeds and daily dietary intake
Daily dietary intake (mean across all weeks) (kg/100 kg BW)
Hay of grass/clover
3.28 ± 0.33
3.36 ± 0.29
Ash (% of DM)
CP (% of DM)
0.54 ± 0.04
0.52 ± 0.06
NDF (% of DM)
0.92 ± 0.14
1.36 ± 0.10
DOM (% of DM)
1.92 ± 0.19
2.31 ± 0.22
ME (MJ/kg DM)
31.0 ± 2.74
30.5 ± 2.92
P (% of DM)
Ca (% of DM)
CT (% of DM)
Health and bodyweights
Overall, the general condition of the animals was good during the study period although the youngest animals in Group CO had soft faeces to mild diarrhoea for most of the study period. The faecal DM was significantly higher in Group SF (F (1,3) = 17.48, P = 0.025) across the patency period (pooled means [± SD] in Groups SF and CO, respectively: 18.2 ± 0.8 % and 15.2 ± 1.1 %). Although the effect of Time was not significant (P > 0.05), a gradual decrease in faecal DM was observed in Group CO from 14 to 28 dpi (16.0 ± 2.8 % and 12.8 ± 4.3 %, respectively) and then increased until 42 dpi (16.9 ± 3.1 %), which was not seen in Group SF.
Faecal egg counts
Parasitological data from worms recovered 42 days post-infection
2,715 ± 894
44 ± 6
41 ± 09
1,331 ± 947a
42 ± 7
43 ± 12
22,447 ± 17,639
34 ± 15
53 ± 45
19,664 ± 22,496
29 ± 23
40 ± 36
For C. oncophora, no significant differences between Group SF and CO (P > 0.05) were found regarding total worm burden, sex ratio and female fecundity. However, these results showed a strong variation within each group (Table 2). In Group SF, three animals (one in each pen) had close to none adult C. oncophora 42 dpi (≤ 100), and were therefore not included in the analysis of sex ratio and female fecundity.
This study showed that calves fed pelleted sainfoin as the sole, continuous diet had a significant reduction by 51 % in the worm burden of O. ostertagi 42 days after experimental inoculation, as compared with animals fed a control diet. Our results confirm AH effects of sainfoin observed in earlier studies of abomasal nematodes in sheep. In one study, sainfoin (6.1 % CT of dietary DM) consumption for 16 days significantly reduced the number of worms in an already established population of adult H. contortus . Similar results have been reported for Teladorsagia spp. in naturally infected animals fed sainfoin containing 8.3 % CT for 13 days . Moreover, the pelleting of sainfoin may have influenced the AH activity as shown by Terrill et al. . These researchers found that consumption of the pelleted form of sericea lespedeza was even more potent as compared with hay of the same bioactive forage (both containing 6.4 % total CT) in reducing the worm burden of H. contortus. This was, however, not the case for T. colubriformis. Further, it has been highlighted that the molecular structure (e.g. PD/PC ratio) of CT may have a greater importance than the ratio of bound/unbound forms of CT in the diet . This hypothesis was substantiated by our results. In fact, although bound CT were not determined directly in our study, the lower CT % obtained with thiolysis compared with acetone-butanol-HCl may indicate that CT have a low accessibility in the pellets. However, CT in sainfoin is mainly of the PD type and especially in our case (PD % > 80) that is known to greatly influence the AH activity of CT in vitro [8, 10].
Although the majority of feeding trials with sainfoin have been associated with a significant reduction in FEC, the non-significant egg count reduction in our study was presumably due to the apparent lack of effect on C. oncophora which was the dominant species in the inoculum and responsible for the majority of the egg output throughout the trial. A few studies found that a lower female worm fecundity, rather than a lower worm burden, was responsible for FEC reduction in goats and sheep [20, 23]. Other studies have reported reduced numbers of adult H. contortus in lambs without any accompanying significant effect on worm fecundity after feeding sainfoin for 16 or 70 days [21, 38].
We expect that the effect of sainfoin against O. ostertagi is mainly related to direct effects of CT rather than an immunologically induced expulsion, since it is known that the acquisition of protective immunity against O. ostertagi needs a continuous larval exposure for longer than the first grazing season to arise . Moreover, it has been shown that the loss of adult worms was very limited even 50 dpi after a single infection with 10,000 L3 of O. ostertagi . Our study was not designed to pinpoint which stage of infection was affected by sainfoin. The levels of serum-pepsinogen indicated a low infection level  and the albumin values were in all cases within the range of healthy calves , although significant differences were found between groups. However, the lower pepsinogen in Group SF at 21 dpi, when O. ostertagi young adults had emerged from the gastric glands, could indicate an effect of sainfoin at this stage of infection, or perhaps even on establishment. In fact, Brunet et al.  found that the larval exsheathment of O. ostertagi was reduced in vitro in the presence of sainfoin extracts. Furthermore, sainfoin has been shown to reduce the larval exsheathment process of H. contortus in the rumen of cannulated sheep fed with fresh sainfoin , and to inhibit the following penetration into the abomasal mucosa after in vitro incubation with sainfoin extracts . The authors linked these effects with structural alterations of the infective larvae at both external and internal levels, depending on the presence of the sheath . Moreover, we also found local cuticular damage by SEM on adult O. ostertagi of sainfoin-fed calves (Fig. 4). Previously, structural damage of worms at intestinal and muscular levels have been visualised by transmission electron microscopy of adult female H. contortus from goats fed sainfoin . The external surfaces of worms from goats was also damaged when animals were fed sainfoin, tzalam (Lysiloma latisiliquum)  and more recently sericea lespedeza . Interestingly, the latter study concluded that the degree of cuticle damage was influenced by the length of exposure to CT; all worms were affected after 77 treatment days whereas only a smaller proportion was affected after 28 days. In our case, adult worms were in contact with CT for approximately 25 days which may explain the inconsistencies between worms. In addition, adult worms were pooled per group and calves may have had different CT concentrations in the digestive tract considering the variation in straw consumption.
Our study showed no influence of sainfoin-feeding on the worm counts of C. oncophora in the small intestine. This is in accordance with a previous study of established populations of C. curticei in experimentally infected sheep fed sainfoin (6.1 % CT in DM) . The same study reported a significant reduction of abomasal species. In addition, they found a significantly lower fecundity of C. curticei, although no data in utero were presented . However, a reduction in numbers of adult C. curticei has been reported in naturally infected lambs fed sulla (Hedysarum coronarium) which had a high CT content (12 % CT of DM in the leaves) . Despite these examples, there seems to be an apparent lack of bioactivity of CT in sainfoin against nematodes in the small intestine. This may be due to a lower availability or binding capacity in the small intestine where the local conditions are different from the abomasum . Accordingly, the majority of studies in sheep have reported a greater effect of sainfoin against abomasal versus small intestinal nematodes [21, 38, 50], but similar AH effect of sainfoin in the two gut compartments has also been reported . The opposite case: a better effect against small intestinal nematodes, was only reported in studies of sheep fed with quebracho as a source of CT that contains profisetinidins, another type of flavanol basic units . Controlled in vivo and in vitro studies with tannins against cattle nematodes at species level are very limited. Recently, it has been reported that O. ostertagi was more susceptible to CT than C. oncophora in vitro , although such difference was not found in other studies [8, 18]. In vivo studies may yield a different result. The low number of adult C. oncophora recovered from some calves in both groups, 42 dpi, was likely related to the expulsion of worms in those animals. In fact, a primary infection with C. oncophora has been shown to elicit a Th2-biased immune response against adult worms in high responder type animals, which confers a rapid protective immunity . Moreover, in the same study the worm sex ratio proved to be a good indicator of the worm expulsion as males were first expelled, which was also observed in our case.
In general, calves appeared healthy and showed no signs of clinical disease. Group SF and had less soft faeces compared with Group CO. Although we found higher levels of iron and gamma-glutamyl transpeptidase in serum of calves of Group CO compared with Group SF 42 dpi, only one value of serum iron in Group SF was slightly lower than the reference range for calves [42, 52]. Therefore we did not consider this biologically significant. However, the mean levels of inorganic phosphorus in Group SF were ≤ 1.3 mmol/l from 21 dpi which is at the lower marginal threshold for calves . This emphasizes the need for possible supplementation with phosphorus. In previous studies, infected small ruminants fed sainfoin hay had similar or improved weight gain with CT concentrations up to 8 % [21–23]. Yet, the relatively low number and variable size of animals in our study preclude firm conclusions on performance. Moreover, it was challenging to maintain similar levels of CP and energy in the diets of CO and SF groups with the low replication of feed intake. Therefore the feed intake adjustments and nutritional differences in favour of the concentrate-rich diet in Group CO including higher digestible OM, NDF, and phosphorus need to be considered as explanatory factors of the relatively large difference in animal performance observed in this study.
Pelleted sainfoin as a sole feed significantly reduced the population of O. ostertagi in young calves. Our promising results confirm the potential value of sainfoin and perhaps other tannin-rich forages with a high percentage of prodelphinidins in integrated control of bovine ostertagiosis. Although O. ostertagi is the main species responsible for reduced productivity in grazing calves, the apparent lack of effect against C. oncophora is a drawback and may hamper the practical use of sainfoin as a “broad-spectrum” anthelmintic forage. More research is needed to address the background of the lacking effect against C. oncophora.
AH, Anthelmintic; ALB, Albumin; CP, Crude protein; CT, Condensed tannins; DM, Dry matter; FEC, Faecal egg counts; GIN, Gastrointestinal nematodes; IP, Inorganic phosphate; OMD, Organic matter digestibility; PC, Procyanidins; PD, Prodelphinidins; PEP, Pepsinogen; SEM, Scanning electron microscopy
The authors gratefully acknowledge P. Lund and all animal caretakers (Tåstrup, Denmark) as well as colleagues from our groups for their great assistance with sampling on the last day, A.R. Williams for his help with electron microscopy and the Core Facility for Integrated Microscopy, University of Copenhagen. Sainfoin pellets were kindly provided by Multifolia/MG2MIX Ltd., FR.
This research was supported by the EU Marie Curie Initial Training Network (‘LegumePlus’; PITN-GA-2011-289377).
Availability of data and materials
OD, MPE, HLE and SMT conceived and designed the study. OD, MPE and TVAH performed the sampling and recordings throughout the study. OD counted the samples and analysed the data. OD wrote the paper. All the authors contributed to improve the manuscript and approved the final version.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The experiment was approved by the Animal Experiments Inspectorate of the Ministry of Food, Agriculture and Fisheries of Denmark (j. No. 2013-15-2934-00763).
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