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Anthelmintic activity of European fern extracts against Haemonchus contortus


Most drugs used in the treatment of helminthiasis in humans and animals have lost their efficacy due to the development of drug-resistance in helminths. Moreover, since anthelmintics, like many pharmaceuticals, are now recognized as hazardous contaminants of the environment, returning to medicinal plants and their products represents an environmentally friendly way to treat helminthiasis. The goal of the present study was to test the anthelminthic activity of methanol extracts of eight selected European ferns from the genera Dryopteris, Athyrium and Blechnum against the nematode Haemonchus contortus, a widespread parasite of small ruminants. Eggs and adults of H. contortus drug-susceptible strain ISE and drug-resistant strain WR were isolated from experimentally infected sheep. The efficacy of fern extracts was assayed using egg hatch test and adults viability test based on ATP-level measurement. Among the ferns tested, only Dryopteris aemula extract (0.2 mg/mL) inhibited eggs hatching by 25% in comparison to control. Athyrium distentifolium, Dryopteris aemula and Dryopteris cambrensis were effective against H. contortus adults. In concentration 0.1 mg/mL, A. distentifolium, D. aemula, D. cambrensis significantly decreased the viability of females from ISE and WR strains to 36.2%, 51.9%, 32.9% and to 35.3%, 27.0%, 23.3%, respectively in comparison to untreated controls. None of the extracts exhibited toxicity in precise cut slices from ovine liver. Polyphenol’s analysis identified quercetin, kaempferol, luteolin, 3-hydroxybenzoic acid, caffeic acid, coumaric acid and protocatechuic acid as the major components of these anthelmintically active ferns.


Parasitic nematodes cause serious livestock diseases worldwide, afflicting hundreds of millions of food-producing animals. The anthelmintics; benzimidazoles, imidazothiazoles, tetrahydropyrimidines and macrocyclic lactones used for decades in the prevention and treatment of helminths’ infections have lost their effectiveness due to the development of resistance. Such resistance has been reported on all continents except Antarctica [1]. Due to the socio-economic impact of nematode infections of livestock and human populations as well as the worldwide spread of anthelmintic resistance, there is an urgent need to discover and develop new drugs for the sustained and effective control of nematodes [2].

New anthelmintics development, involves four different approaches, each of them with certain advantages and disadvantages [3]. The first, classical approach is the synthesis of new chemical entities active against parasitic nematodes [4]. The synthesis of derivatives of known drugs with an approved usage represents another approach [5]. The third approach of drug repurposing is based on finding new anthelmintically active substances among drugs approved for other diseases [6]. These three approaches have in common the fact that they use pharmaceuticals that are now considered to be hazardous environmental contaminants. In particular, the use of these substances in large quantities in the treatment of livestock puts a heavy burden on the environment and poses high risks to ecosystems [1, 7,8,9,10]. On the other hand, returning to medicinal plants and their products, which is the fourth alternative approach to control helminthiasis, represents an environmentally friendly way.

Despite the efficacy of medicinal plants in the treatment of parasitic diseases which has been known and used for centuries, the use of plant-based prophylaxis and therapies to treat parasitosis has been stifled by the expansion and availability of synthetic drugs [11]. Nevertheless, plants remain a major source for the development and discovery of new therapeutics, with countless diverse active compounds with anthelmintic activities identified from plant sources [12]. Moreover, increasing public and professional interest in the ecological impact of pharmaceuticals has stimulated a revival in the search for and use of medicinal plants in helminthiasis treatment [13,14,15]. In addition to other higher plants, ferns (Pteridophytes) have emerged as an interesting group of vascular plants which have attracted attention in terms of their potential use in medicine [16,17,18]. Accordingly, the purpose of our project is to identify a fern that shows anthelmintic effects and could be added (in a proper form) to livestock feed to replace (at least partly) or supplement synthetic anthelmintics.

In presented study, the anthelminthic activity of methanol extracts from eight selected European ferns from the genera Dryopteris, Athyrium and Blechnum was tested. The nematode Haemonchus contortus, was used as a model species. H. contortus is a hematophagous gastrointestinal parasite of small ruminants which is extremely detrimental to animal health and productivity on a global scale. Moreover, H. contortus is able to effectively defend itself against anthelmintic drugs, with field populations of this species now showing resistance to all major anthelmintic drug classes [19]. Therefore, new therapy against H. contortus is extremely needed. The effect of the fern extracts was tested in H. contortus eggs and adults of both drug-sensitive (ISE, Inbred-Susceptible-Edinburgh, MHco3) and drug-resistant strain (WR, White River, MHco4) of the nematode. In addition, the potential toxicity of these extracts was assayed in ovine liver, as sheep represent a common host of H. contortus. In the three fern species determined as active, the content of the main polyphenols was analyzed.

Materials and methods

Chemicals and reagents

The Pierce BCA Protein Assay Kit and Williams’ Medium E-GlutaMAX (32551) was purchased from Thermo Fisher Scientific (Prague, Czech Republic). The standards of polyphenols and all other chemicals were purchased from Sigma-Aldrich (Prague, Czech Republic).

Ferns and their extraction

Eight European fern species (Athyrium distentifolium, Athyrium filix-femina, Blechnum spicant, Dryopteris aemula, Dryopteris borreri, Dryopteris cambrensis, Dryopteris dilatata, Dryopteris remota) were used in this study. Plant material was collected in 2019 and 2020 from the Garden center of Jakub Krulich, Prague, Czech Republic, Garden center Franc, Kamenné Žehrovice, Czech Republic, or the private fern collection of RNDr. Libor Ekrt, Ph.D. (University of South Bohemia) in Telč, Czech Republic (Table 1). Each sample represented approximately 50 g fresh weight of mature leaves of one fern species collected out of three individual plants at minimum. Plant material collection and extraction methods have been described in Langhansova et al. [20]. Briefly, the fern leaves were freeze-dried, homogenized using a mortar, pestle, and liquid nitrogen. The tissue was extracted overnight in a ratio of 1 g of dry mass and 20 mL of MeOH p.a. The extract was separated from the plant tissue by centrifugation at 1730 × g, 15 min (Centrifuge Hettich Universal 32R, Tuttlingen, Germany) at room temperature, with the supernatant filtered through a 30 mm PVDF 0, 45 µm membrane filter (ProFill, Fisher Scientific, Pardubice, Czech Republic). The extracts were reduced in a vacuum in a rotary evaporator and dried completely under a nitrogen flow. The obtained dry extracts were redissolved in dimethyl sulfoxide (DMSO) at a concentration of 100 mg/mL, with the DMSO aliquots maintained at −80 °C until use. The extract yield was on average 27% of the dry mass.

Table 1 List of tested fern species.

Infecting sheep

In one experiment, two lambs were infected with ISE strain and two lambs with WR strain. Three independent experiments were performed. All experimental procedures were approved by the Ethics Committee of the Ministry of Education, Youth and Sports (Protocol MSMT-25908/2019) and performed in accordance with Czech Act No 246/1992 Coll. on the Protection of Animals against Cruelty.

Six-month-old lambs were firstly dewormed by albendazole (5 mg/kg), after which the feces were microscopically examined for the absence of parasites. Three weeks later, when the lambs were free of parasites, they were orally infected with L3 larvae of Haemonchus contortus ISE and WR strain. Prior to infection, the stock L3 were incubated overnight (25 °C) in sieve with pore diameter 20–25 µM to remove dead larvae. Only the living L3 could pass through the sieve, and those were used for infection. The infection dose was dependent on the weight of the animal and ranged between 6000 and 8000 L3.

Isolation of H. contortus eggs

The eggs were isolated from ovine feces 4 weeks after infection. Around the anus of each lamb, plastic bags were fastened to the hair using clips, into which feces were continuously excreted. When some bag was full, the new bag was used. The feces were collected within 1 day and one night. As the temperature in sheep stable was approx. 10 °C, the hatching of eggs during feces collecting was limited and the amounts of larvae was negligible. The feces in cooled boxes were transported in laboratory, then pooled together and mashed. The fecal mass was passed through 3 sieves with a decreasing pore diameter (250, 100, and 25 µm) to remove coarse particles. The eggs were captured in the last sieve together with the mud and transferred to the 50 µL falcon tubes and centrifuged for 3 min (481 × g). The supernatant was then replaced by sucrose flotation solution (FS, saturated sucrose solution with density 1.27 g/cm3), mixed and centrifuged for 3 min (188 × g). The eggs floating on the top were collected into new 15 mL falcons with FS and centrifugation was repeated. The eggs were then cleaned by repeated centrifugation in tap water (481 × g). Freshly isolated eggs were used immediately for the egg hatch test.

Egg hatch test

Firstly, the eggs of H. contortus were diluted to concentration 25 eggs/100 µL. The stock solutions of fern extracts (or albendazole as a positive control) were diluted with DMSO, and 1 µL of these solutions (or 1 µL of DMSO for the negative control) of each concentration were pipetted into one well of 96-well plates in 8 biological replicates. Then 199 µL of egg suspension was added to each well, and the eggs were incubated at 27 °C for 48 h. The final tested concentrations of fern extracts were 12.5; 25; 50; 100 and 200 µg/mL; final concentration of DMSO in all samples and controls was 0.5% and each well contained approximately 50 eggs. The incubation was halted by adding 5 µL of concentrated Lugol’s iodine solution. The proportion of unhatched eggs and larvae was counted under the microscope and compared to the control. Two independent experiments in eight biological replicates were performed.

Isolation of H. contortus adults

The adults of H. contortus were isolated by the agar method as described previously [21]. In brief, the sheep were euthanized 6 weeks post infection, and their abomasa were removed. The adult nematodes were released together with the abomasa content into a beaker filled with physiological solution (PHS, 0.9% NaCl, 37 °C). When the nematodes sedimented to the bottom of the beaker, the extra PHS was sucked out, and the remaining fluid containing adult nematodes was mixed with agar in a proportion of 1:1. This agar mixture was then poured in a thin layer over gauzes. Once the mixture solidified, the gauzes were placed into aquariums filled with temperate PHS and incubated (37 °C) until the alive adults extracted themselves out of the agar and sedimented to the bottom of the beaker. The adults were then collected and cleaned, then manually separated according to gender and used immediately for the experiments.

Viability assay on H. contortus adults

The viability testing was based on the measurement of remaining ATP in the adult worms after 48 h of incubation with increasing concentrations of the respective fern extract being tested. Levamisole (as a positive control) was used to check the correctness of the test performance.

The fern extracts and levamisole were pre-dissolved in DMSO, then dissolved in supplemented RMPI-1640 medium. The medium was supplemented according to [21] with glucose (0.8%), amphotericin B (0.25 µg/mL), penicillin (10 U/mL), streptomycin (10 µg/mL) and HEPES (10 mM; (N-[2-hydroxyethyl] piperazine-N′-[4-butanesulfonic acid] buffer, pH 6.8). The assay was performed according to [22, 23] with the following adjustments: Firstly, 8 male or 4 female adults were placed into one well of 24-well plate with 1 mL RMPI-1640 media containing 1.0; 10; 50; and 100 µg/mL fern extract (or only 0.1% DMSO for the control samples) and incubated in a humid atmosphere at 37 °C for 48 h. After incubation, the worms from each well were washed in PBS and placed into a 2 mL plastic tube containing 100 µL of SONOP (sonification solution, 70% ethanol with 2 mM EDTA (ethylenediaminetetraacetic acid); pH 10.9) and immediately frozen in dry ice. The samples were stored at −80 °C until measurement.

To measure ATP level, the samples were firstly homogenized in 700 µL of cooled Tris/EDTA buffer (100 mM Tris–HCl; 2 mM EDTA; pH 7.8) in FastPrep-24 5G homogenizer (MP Biomedicals, Irvine, CA, USA) for 20 s, following which 700 µL of fresh Tris/EDTA buffer was added and homogenization was repeated. The samples were centrifuged (Eppendorf, 12 000 × g, 10 min, 4 °C) and ATP was measured in 5 µL of supernatant pipetted from each sample onto one well of a 96-well black plate. The volume of each well was topped up to 50 µL with Tris/EDTA buffer. 50 µL of Luciferase was added right before the measurement, and the value of luminescence was measured within 5 min (Spark Control Tecan, v. 2.2). The amount of ATP was calculated from a calibration curve and normalized to the µg of total protein measured in the supernatant according to the manufacturer’s protocol (Pierce™ BCA Protein Assay Kit). The values of ATP in the control samples were considered as 100% viability. Reagents from ATP Bioluminescence assay kit CLS II (Roche, Mannheim, Germany) were used for the experiment.

Hepatotoxicity testing

The liver lobes removed immediately after the sheep were euthanized were placed into Euro-Collins’ solution and transported to the laboratory within 20 min. Precision-cut liver slices (PCLS) were used to determine the potential hepatotoxic effect of each of the selected fern extracts to ovine liver. The PCLS preparation and the measurement of ATP level (as a viability marker) were performed according to [24]. In brief, 8 mm wide and 150–170 µm thick liver slices were preincubated for 1 h in 1 mL of Williams’ E Medium (with L-glutamine, Invitrogen, Paisley, UK) supplemented with glucose (final concentration 36 mM) and 50 μg/mL gentamycin at 37 °C in an atmosphere of 85% O2 and 5% CO2. Then PCLS were placed into 1.3 mL of fresh media (temperature 37 °C) containing fern extracts at the concentration 100 µg/mL (or 10% DMSO, which kills all PCLS, as a positive control and 0.1% DMSO as a negative control) and incubated for 24 h in the same conditions. After incubation the PCLS were collected separately, washed in PBS, and placed into 150 µL of SONOP and immediately frozen on dry ice and stored at −80 °C until measurement.

Prior to ATP measurement, the samples were homogenized in 1 mL of SONOP (FastPrep-24 5G homogenizer) and centrifuged (centrifuge Eppendorf, 12 000 × g, 5 min, 4 °C). ATP was determined in 5 µL of supernatant as described above (paragraph 2.7.). The total protein content used for correction was measured by BCA assay (Pierce BCA Protein Assay Kit) in the remaining sample pellet after SONOP evaporation. The pellet was then dissolved in 200 µL of 5 M NaOH (60 min, 37 °C), and diluted with redistilled water to 1 mL. The calibration plot was also prepared in 1 M NaOH.

Analysis of polyphenol content in fern extracts

The extracts were dissolved in 100% MeOH and maintained for 24 h at −18 °C to precipitate protein, centrifuged (15 000 rpm for 10 min at 4 °C), with the supernatant collected into vials. The purified extracts were then analyzed using an UHPLC/MS-HRAM system consisting of high-resolution accurate-mass (HRAM) Q-TOF spectrometer Impact II (Bruker Daltonik, Germany) coupled with Ultimate 3000 chromatograph (Thermo Fisher Scientific, USA). Chromatographic separation was performed using an Acclaim RSLC 120 C18 column (2.2 µm, 2.1 × 100 mm, Thermo Fisher Scientific, USA) and gradient elution with mobile phases 0.2% formic acid (A) and 100% methanol (B). The gradient started at 2% B (0–2 min), and then was ramped from 2 to 100% B (2–15 min), maintained at 100% B (15–20 min), returned to starting conditions 2% B (20–21 min) and equilibrated at 2% B (21–26 min). The flow rate was 250 µL/min, and column temperature was maintained at 40 °C. Detection was performed in positive mode using an ESI ion source with mass resolution 60 000. Injection volume was 5 µL. The measured compounds were identified through a comparison of their exact mass and retention time with commercial standards (Sigma-Aldrich, Czech Republic). MS data were acquired using oTof Control 4.0 and HyStar 3.2 software, with qualitative and quantitative analysis carried out by DataAnalysis 4.3 and TASQ 4 software, respectively (all Bruker Daltonics, Germany).

Statistical analysis

For the statistical analyses GraphPad Prism 9.1.2. software was used. Two-way ANOVA with Dunnett’s multiple comparisons test was used to process the data.


Effect of fern extracts on eggs hatching

In the ISE strain, only the F4 extract and only at the highest concentration tested (200 µg/mL) decreased eggs hatching significantly by approximately 25%. In lower concentrations, none of the tested fern extracts showed a significant effect on H. contortus ISE eggs hatching. The results are expressed as a percentage of hatched eggs compared to control and summarized in Table 2. In the WR strain, no effect of any fern extract on eggs hatching was observed (data not shown). The IC50 for positive control albendazole was 1.9 and 4.4 µM in ISE and WR strain, respectively.

Table 2 The effect of the fern extracts on hatching of H. contortus eggs (ISE strain).

Effects of fern extracts on the ATP level in H. contortus adults

Eight fern extracts (in concentration 100 µg/mL) were tested in adults of H. contortus ISE strain. Only extracts of F1, F4, and F6 significantly diminished the level of ATP in H. contortus adults, F1 and F6 in males and F1, F4, and F6 in females (Figure 1).

Figure 1
figure 1

The effect of 100 µg/mL fern extracts on viability of H. contortus ISE strain adults. The results are presented as means ± SEM. The data were obtained from one experiment in eight biological replicates. For statistical analysis, two-way ANOVA with Dunnett’s multiple comparisons test was used, * p < 0.05.

Based on these results, ferns F1, F4, and F6 were selected for further testing at various concentrations (1, 10, 50, and 100 µg/mL) with adults of both ISE and WR strains. The results are presented in Table 3 (ISE strain) and Table 4 (WR strain). In concentration 100 µg/mL, F1, F4 and F6 significantly decreased the ATP level in females from ISE strain to 36.2%, 51.9%, 32.9% in comparison to untreated controls. In the males of ISE strain, the effect of F4 and F6 was less pronounced than in the females. On the other hand, F1 was more active in the males of ISE, decreasing ATP level to 17.1%. In the females of WR strain, F1, F4 and F6 (in concentration 100 µg/mL) significantly decreased the ATP level to 35.3%, 27.0%, 23.3%, respectively, in comparison to untreated controls. Moreover, F4 was effective also in concentration 50 µg/mL decreasing the ATP level to 28.8%. In the males of WR strain, the F1 and F4 (in concentration 100 µg/mL) significantly decreased ATP level to 63.8 and 49.0% in comparison to control. The comparison of the ferns effect in adults of ISE and WR strains is presented in Figure 2. The IC50 for positive control levamisole was 6.3 µM and 36.5 µM in males of ISE and WR strain, respectively.

Table 3 ATP content of H. contortus adults of ISE strain after 48 h incubation of males and females with ferns extract of Athyrium distentifolium, Dryopteris aemula and Dryopteris cambrensis.
Table 4 ATP content of H. contortus adults of WR strain after 48 h incubation of males and females with ferns extract of Athyrium distentifolium, Dryopteris aemula and Dryopteris cambrensis.
Figure 2
figure 2

Comparison of the effect of selected fern extracts on the viability of H. contortus adults in the ISE and WR strain. The viability of H. contortus adults in cultivation medium without fern extracts (zero concentration) represent the controls. The data were obtained from three independent experiments, each in 4–6 biological replicates. The results are presented as means ± SEM. For statistical analysis, two-way ANOVA with Dunnett’s multiple comparisons test was used, * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

The test of potential hepatotoxicity

The three anthelmintically active ferns F1, F4, and F6 were tested for potential hepatotoxic effects in the ovine liver. The viability of precision-cut liver slices (PCLS) after 24 h incubation with the tested fern extracts in concentration 100 µg/mL was assayed. The amount of ATP per mg of protein in PCLS exposed to the fern extracts and in the control PCLS was measured and compared. The ATP level (expressed as percentage of control) of PCLS exposed to F1, F4, and F6 extracts was 107.8 ± 3.58%; 132.6 ± 40.86%; and 125.3 ± 8.3%, respectively. Therefore, none of the ferns tested (in concentration 100 µg/mL) showed a significant hepatotoxic effect on ovine liver.

The polyphenols in fern extracts

The content of polyphenols in the extracts of F1, F4, and F6 was analyzed, with the major components quantified using commercially available standards. The results showed significant differences (both qualitative and quantitative) in polyphenols content among ferns tested. Only quercetin was present in a relatively high amount in all the extracts. Taxifolin was abundant in F4, although in F1 it was detected in a much lower amount, and not present at all in F6. On the other hand, luteolin, a major component of F6, was detected only in traces in F4, and it was not found in F1. Coumaric acid and caffeic acid were detected only in F4, vitexin only in F1. A much greater amount of 3-hydroxybenzoic acid was present in F6 than in F1 and F4. The results are presented in Table 5 and the content of particular polyphenols is expressed in µg per gram of dry extract.

Table 5 The quantification of polyphenols in fern methanolic extracts.


In previous study, some European fern species from genus Dryopteris, Athyrium and Blechnum were shown to exhibit antioxidative, anti-inflammatory and anticancer activity [20]. In our present study, the anthelmintic activity of these ferns was tested against parasitic nematodes, with Haemonchus contortus (family Trichostrongylidae), a hematophagous gastrointestinal parasite of small ruminants, chosen as the model for this purpose. The drug- resistance in H. contortus is widespread in field populations showing resistance to all available anthelmintics [25]. When excrements of sheep and goats from 34 farms in mid-Atlantic U.S. regions were analyzed, H. contortus was the most common parasite found in feces, resistant to benzimidazoles almost in 100% of farms [26]. For these reasons, there is a great need to find and determine new active compounds which will be also effective against resistant strains of H. contortus.

Among eight fern extracts tested, the extracts of Athyrium distentifolium (F1), Dryopteris aemula (F4), and Dryopteris cambrensis (F6) were effective against H. contortus adults in the concentration 100 µg/mL. Higher concentrations could not be tested due to limited solubility and the risk of undesired interference with bioluminescent detection, thus IC50 values could not be calculated. Interestingly, in some cases lower concentrations of fern extract increased the ATP level. This might mean that lower concentrations of extracts did not kill the nematodes but evoked stress, which is manifested by increased ATP production. Nevertheless, it must be emphasized that extracts of A. distentifolium and D. cambrensis were effective not only in the drug-susceptible strain ISE, but also in the drug-resistant strain WR. In addition, the results are valuable also because adults of H. contortus were used for testing and not more easily obtainable larvae. Adults represent the parasitic developmental stage that a potential drug should target. If the tested substance is effective on adults ex vivo, there is a greater chance that it could also be effective in vivo. The measurement of ATP level as a viability marker has been optimized for use in H. contortus recently and represent the relatively simple biochemical method for anthelmintic efficacy testing [23].

D. aemula (at the highest concentration tested) diminished the hatching of eggs. This indicates that this extract might prevent the larval development of H. contortus in the feces of treated animals, which could partially reduce the risk of reinfection. The inhibitory effect on eggs’ development is an advantage of this extract which many widely-used anthelmintics (ivermectin, levamisole, monepantel) do not show. In addition, none of the three extracts exhibited toxicity in ovine liver. This fact is very important for approval of planned in vivo study.

The anthelmintic effect of some ferns has been reported previously. Blechnum orientale extract (5 mg/mL) showed mild anthelmintic activity against isolated Gastrothylax crumenifer adult trematodes [17]. D. filix-mas (2 mg/mL) extract had in vitro moderate nematocidal activity against the infective third-stage larvae of Trichostrongylus colubriformis [27] Comparing these data with our results, the extracts from A. distentifolium, D. aemula and D. cambrensis seem to be promising, as they were effective in much lower concentrations (0.1 mg/mL).

With aim to know the composition of these anthelmintically active extracts, the content of polyphenols was analyzed. The results showed significant qualitative and quantitative inter-species differences. The major components were quercetin, 3-hydroxybenzoic acid, kaempferol, and protocatechuic acid (detected in all three extracts), luteolin and taxifolin (detected in two extracts), caffeic acid and p-coumaric acid (detected only in D. aemula) and vitexin (only in A. distentifolium). In the present study, the anthelmintic effect of pure individual polyphenols was not tested, as several previous studies have already addressed this. When many polyphenols were tested in larvae of H. contortus, taxifolin proved to be ineffective, whereas quercetin and luteolin were highly effective [28]. Kaempferol and quercetin were the major component of extracts from Pithecellobium dulce (Robx.) with ovicidal activity against H. contortus [29]. The relatively high level of 3- hydroxybenzoic acid was found in the fruit of the Surinam cherry (Eugenia uniflora L.), which exhibits anthelmintic effects in the free-living nematode Caenorhabditis elegans [30]. The activity of caffeic acid against H. contortus as well as other nematodes has been reported [31, 32].

Although several polyphenols exhibit anthelmintic activity, they could act synergistically or antagonistically in helminths when used together as a complex mixture of compounds (as whole plant or plant extracts). From practical point of view, the effect of these “natural mixtures” is important because for farmers it would be cheaper to add fresh or dry plants (e.g., ferns) into fodder for livestock than to use an anthelmintic drug (even one based on pure polyphenols). Similarly, the anthelmintic activity of many medicinal plants and natural products has been tested in vivo, and in some cases has been proven effective [33, 34]. Based on our ex vivo results, the ferns of A. distentifolium, D. aemula, and D. cambrensis species would also merit testing in vivo. Only in vivo study in sheep infected with H. contortus could show the anthelmintic efficacy of these ferns. For these experiments, we might make following estimation: since the extracts were effective beginning at concentration 0.1 mg/mL, 1 g of fresh fern leaves prepared for the preparation of 67 mg of extract, the volume of ovine plasma is 3–4 L, and the bioavailability of polyphenols is low (below 1–10%), one sheep should be fed with at least 100 g of fresh fern leaves (or 25 g of dry fern leaves) to achieve the anthelmintic effect in sheep infected with H. contortus.

The extract from European ferns Athyrium distentifolium, Dryopteris aemula, and Dryopteris cambrensis exhibited significant anthelmintic activity in concentrations 0.1 mg/mL against the adults of parasitic nematodes H. contortus ex vivo.


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We would like to thank Prof. Marián Várady of the Institute of Parasitology, Slovak Academy of Sciences for providing H. contortus larvae as well as MVDr. Tomáš Kaňka for assisting with the sheep infection. Our gratitude is also expressed to Daniel Sampey, MDA for the English revision.


The study was funded by Charles University, “Grant Schemes at CU” (reg. no. CZ.02.2.69/0.0/0.0/19_073/0016935). Michaela Šadibolová and Gabriela Svobodová were supported by Charles University Specific research program (SVV260664), Univerzita Karlova v Praze. Lenka Langhansová was supported by the Czech Ministry of Education, Youth, and Sports under the Inter-COST program [Grant Number LTC17035], Ministerstvo Školství, Mládeže a Tělovýchovy.

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LS designed the project, and LS and PM controlled the project. LL collected the ferns. AP and LL prepared the extracts. BS and PM infected the animals, isolated and cultivated the helminths. AP and MZ performed and evaluated all experiments in helminths. MŠ and GS prepared PCLS, performed and evaluated the hepatotoxicity tests. PM analyzed the polyphenols in the extracts. AP wrote the manuscript, PM, BS and LS revised the manuscript. All authors read and approved the final manuscript.

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Correspondence to Lenka Skálová.

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All experiments with animals were performed according to the protocols evaluated and approved by the Ethics Committee of the Ministry of Education, Youth and Sports of the Czech Republic (Protocol MSMT-25908/2019).

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Pavičić, A., Zajíčková, M., Šadibolová, M. et al. Anthelmintic activity of European fern extracts against Haemonchus contortus. Vet Res 54, 59 (2023).

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