- Open Access
A controlled study on gastrointestinal nematodes from two Swedish cattle farms showing field evidence of ivermectin resistance
© Areskog et al.; licensee BioMed Central Ltd. 2014
- Received: 13 September 2013
- Accepted: 19 December 2013
- Published: 8 January 2014
Anthelmintic resistance (AR) is an increasing problem for the ruminant livestock sector worldwide. However, the extent of the problem is still relatively unknown, especially for parasitic nematodes of cattle. The effect of ivermectin (IVM) (Ivomec inj.®, Merial) was investigated in Swedish isolates of gastrointestinal nematode (GIN) populations showing signs of AR in the field to further characterise the AR status by a range of in vivo and in vitro methods.
Three groups, each of 11 calves, were infected with an equal mixture of third stage larvae (L3) of Cooperia oncophora and Ostertagia ostertagi. Group A was inoculated with an IVM-susceptible laboratory isolate and groups B and C with isolates originating from ‘resistant’ cattle farms. Faecal egg counts (FEC) were monitored from 0 to 45 days post infection (d.p.i.), and L3 were harvested continuously for larval migration inhibition testing (LMIT) and species-specific PCR (ITS2). At 31 d.p.i., one calf from each group was necropsied and adult worms were recovered pre-treatment. At 35 d.p.i., calves from all groups were injected with IVM at the recommended dose (0.2 mg/kg bodyweight). At 45 d.p.i., another two animals from each group were sacrificed and established gastrointestinal worms were collected and counted.
A few animals in all three groups were still excreting eggs (50-150 per g faeces) 10 days post IVM injection. However, there was no significant difference in the FEC reductions in groups A (95%; 95% CI 81-99), B (98%; 92-100) and C (99%; 97-100) between 35 and 44 d.p.i. Furthermore, LMIT showed no significant difference between the three groups. Approximately 100 adult O. ostertagi were found in the abomasum of one calf (group B), whereas low to moderate numbers (400-12 200) of C. oncophora remained in the small intestine of the calves in all three groups at 45 d.p.i. PCR on L3 harvested from faecal samples up to 10 days post treatment showed a ratio of 100% C. oncophora in the calves inoculated with isolates A and B, whereas C also had 8% O. ostertagi.
Overall, this experiment showed that the animals were successfully treated according to the Faecal egg count reduction test (FECRT) standard (≥ 95% reduction). However, several adult worms of the dose-limiting species C. oncophora demonstrably survived the IVM treatment.
- Gastrointestinal nematodes
- Macrocyclic lactones
- Ostertagia ostertagi
- Cooperia oncophora
- Anthelmintic resistance
- Controlled efficacy test
Gastrointestinal nematode (GIN) infections in livestock are common world-wide and assessments have repeatedly shown that they can cause considerable live weight gain losses during the first grazing season of calves in Sweden [1–3]. It has also recently been demonstrated that there is a negative interaction between exposure to GIN and individual daily milk yields in Swedish dairy herds, even when the overall exposure is relatively low . In temperate regions of the world such as Sweden, the most important GINs include Cooperia oncophora and the more pathogenic Ostertagia ostertagi, which are usually present as mixed infections in pasture-based cattle production .
The use of modern broad spectrum anthelmintics since their introduction in the 1960s has been a convenient and often efficient method to control parasite infections in grazing livestock. However, recent reports have shown that extensive use of anthelmintics has led to a worldwide spread of anthelmintic resistance (AR) in the cattle industry [6, 7]. In Europe, AR to macrocyclic lactones (ML), the market-dominating anthelmintic family, has been reported for cattle nematodes in both the UK [8–13] and Belgium . Widespread resistance was also reported in a multinational European survey including German, Belgian and Swedish farms . In a recently performed two-year Swedish faecal egg count reduction test (FECRT) in cattle, the results indicated that the efficacy of topical ML under Swedish field conditions is insufficient, and that C. oncophora is the predominant species surviving deworming .
Detection of AR is usually based on the FECRT and resistance in ruminant parasitic nematodes is declared when the reduction after ML treatment is ≤95% and with a lower confidence interval (CI) of <90% . AR in trichostrongyloid cattle nematodes detected by FECRT has been reported against all major anthelmintic classes, i.e. against ML and to a lesser extent also the well-investigated benzimidazoles (BZ) . Multiple or cross resistance to both compounds has also been reported in several cases world-wide (for a review, see ). In addition to FECRT, a range of in vitro bioassays have recently been developed and validated for detection of AR in cattle nematodes, such as the egg hatch test (EHT), the larval development test (LDT), and the larval migration inhibition test (LMIT) [18, 19]. Furthermore, there have been attempts to develop molecular-based tests to identify ML resistance, by investigating nematode-specific P-glycoprotein (Pgp) gene expression [20–23] and altered avr-14B gene transcription patterns , although no standardised test for routine screening of AR is available as yet.
The survey by Demeler et al.  on the efficacy of ML (Ivomec inj.®) included five cattle herds in central Sweden. The evaluation was made among first season grazing (FSG) cattle some weeks after turnout, and was conducted using the FECRT. It showed unsatisfactory efficacy results, with only one farm achieving acceptable reductions in egg output in 2006. In 2007, the reduction was insufficient on all farms where animals were treated with IVM. Isolates from two of these Swedish farms were collected and maintained for further testing. The aim of the present study was to investigate suspected resistance in these O. ostertagi and C. oncophora isolates after IVM treatment, by performing a controlled efficacy test but also by using a range of available in vivo and in vitro methods for further characterisation of the AR and species composition status.
Three different worm isolates with mixed O. ostertagi and C. oncophora L3 were used in this study. Isolate A was obtained from Tierärztliche Hochschule, Hannover (TiHo), but was originally identified at the Central Veterinary Laboratory in Weybridge, UK, in 1997. It is a well-investigated laboratory strain that has been repeatedly passaged in calves and with no history of being refractory to treatment with any anthelmintics. Isolates B and C were obtained from two Swedish farms and showed poor reductions to IVM according to FECRT, with 84% (95% CI: 67-95) and 85% (62-99) reductions, respectively, at day 7 . The two Swedish isolates were obtained by collection of faecal samples from FSG at the two farms, mixing them with vermiculite and then incubating them under moist conditions for 2 weeks at 25°C. L3 were harvested by the inverted cover glass technique, and larval cultures were identified according to the morphological key in Borgsteede and Hendriks . After harvest, L3 were passaged once and propagated at SLU’s research department Götala, in naïve dairy cattle that never had access to pasture and were checked for egg shedding prior to experimental infection.
Housing and animals
The infection trial was performed during seven weeks in February to April 2009 at SLU’s research department Kungsängen, with dairy cattle born and bred on the farm. A total of 33 calves were randomly allocated based on weight and sex to three groups, each with three male calves and eight heifers of the Swedish Red and White breed. All animals were between 3 and 7 months old, weaned but with no experience of grazing, and were checked for GIN egg shedding prior to experimental infection. All calves were weighed prior to the start, then at 21, 35, 51 days post infection (d.p.i.) and when euthanized. Weight varied from 81 to 234 kg, with an average weight at 127 kg at the start of the trial. The calves were allocated to different indoor pens, with 8-9 animals in each. The pens had automatic cleaning systems, with a slowly moving rubber mat removing manure. No changes were made to the diet when the calves were participating in the experiment.
Experimental infection and anthelmintic treatments
On day 1, each calf was infected with ~40,000 L3 of O. ostertagi (50%) and C. oncophora (50%) in a small volume of water. Isolates A, B and C were administered to calves in groups A, B and C, respectively. At 35 d.p.i., animals with patent infections were treated with IVM (Ivomec® vet.) as subcutaneous (s.c.) injections. Dosage was according to standard recommendations, 1 mL per 50 kg body weight or 0.2 mg IVM per kg. Animals were treated and the trial was performed according to formal institutional ethical approval (C276/8).
Sampling and laboratory procedures
Individual faecal samples were collected rectally on 23 occasions between 0 and 45 d.p.i., with more frequent sampling after the third week. A modified McMaster method  was used to determine the number of O. ostertagi and C. oncophora eggs in 3 g of faeces, giving a diagnostic sensitivity of 50 eggs per gram faeces (epg). In addition, the FLOTAC© method  with a sensitivity of 2 epg, based on 10 g faeces and 90 mL saturated NaCl, was used at 35 and 44 d.p.i. for comparison. The anthelmintic efficacy of the drug was interpreted through the FECRT, by comparing the results of two different formulae . The first one was based on each group’s arithmetic mean reduction: FECR3 = 100 × (1 - [T2/T1]), using arithmetic means and with no control group , where T is treated hosts and the faecal samples were taken pre-treatment or at the moment of treatment (1) and X days post-treatment (2). Individually based FECR formulae were also calculated using before and after treatment individual evaluations in treated hosts: iFECR3 = (1/n) ∑ (100 × (1 - [T i2 /T i1 ])), where T i2 is post-treatment and T i1 is pre-treatment epg in host i from a total of n hosts. Each host served as its own control. The FECR data were compared (repeated measures MANOVA) using SAS JMP software (version 10.0.2) and the Minitab statistics programme (version 15) and considered significantly different at p < 0.05.
L3 were also cultured by pooling and mixing 10-20 g of each faecal sample with vermiculite and incubating for 2 weeks at 26-27°C. The number of L3 was then counted and identified according to the morphological key in Borgsteede and Hendriks .
Total worm counts
At 31 d.p.i., four days before IVM treatment, one animal per group (A, B and C) was euthanized intravenously with pentobarbital (ex tempore 300 mg/mL, 60 mL/calf). Another two animals per group were euthanized at 45 d.p.i., 10 days post IVM treatment. The abomasum and approximately 7 m of the proximal small intestine (duodenum, jejunum) were separated, truncated, and their contents emptied into individual beakers. The mucosal surfaces were carefully washed with tap water, and the total volume of each calf’s bowel contents was adjusted to 4 L. For each calf, four 20-mL subsamples were then collected under constant stirring from every vessel with bowel or abomasum contents giving a detection level of >200 worms in the original sample . The abomasal mucosa was scraped off into a separate bucket and digested for 6 h at 40°C in a solution with 17 mL HCl (37%) and 10 g pepsin in 1 L H2O. The total volume was adjusted to 2 L after digestion and subsampling as above, giving a diagnostic sensitivity of >100 worms. Sub-samples were stored at -20°C, stained with Lugols iodine and examined to count and differentiate worms. Results were compared via one-way ANOVA and boxplots of worm counts (Minitab® 22.214.171.124. software) and considered significantly different at p < 0.05.
Larval migration inhibition test
Larvae from faecal cultures (21-32 d.p.i.) from each group were obtained via the inverted cover glass technique to ensure that only viable L3 were used. Larval suspension was adjusted to approximately 100 L3 per 20 μL. IVM (MW 871) was purchased from Sigma (I8898). A stock dilution of IVM 10-2 M (8.71 mg/mL) was made in dimethyl sulphoxide (DMSO, 100%) and a further dilution into 10 different concentrations of IVM ranging between 10-5 and 5 × 10-10 M.
The LMIT was carried out with sheathed larvae following the method of Demeler et al. . L3 were incubated in the gradually increasing concentrations of IVM at 28°C in a 24-well plate (incubation plate). After 24 h, the whole contents of each well (liquid + L3) were transferred onto sieves (mesh size 28 μm) suspended on rows 1 and 3 of a 24-well Bacto agar (1.5%) coated plate (migration plate), and allowed to migrate for a further 24 h at 28°C. For every incubation plate, two migration plates were used. After 24 h, migrated L3 in the wells of rows 1 and 3 and non-migrated L3, flushed into corresponding wells of rows 2 and 4, were counted under a stereo microscope. Each isolate was tested over a range of 10 drug concentrations in duplicate (two migration plates per isolate), and negative (water, no drug) and positive (stock solution) controls were run in duplicate on each plate. The percentage of non-migrated L3 in the total amount of L3 was calculated for the controls and every IVM concentration tested. The data were analysed according to Demeler et al.  using a logistic regression model to determine LC50/LC99 with GraphPad Prism® software (version 5.02). The EC50 values, the 95% confidence intervals and R2 values were calculated, and the three groups compared accordingly. Differences were considered significant at p < 0.05.
Species-specific single larvae PCR (ITS2)
Genomic DNA from L3 of unknown species (C. oncophora or O. ostertagi) was isolated from single L3 for traditional PCR. This was carried out via a crude method using proteinase K and 10 mM Tris pH 7.6 in the wells of PCR plates, with minor modifications, according to Zarlenga et al. . In brief, the temperature and incubation time were reduced to 52°C and 1 h, instead of 65°C and 3 h, and 800 μg mL-1 proteinase K was used instead of 10 μg mL-1. For each plate, ~ 50 single individual L3 were tested to determine whether they belonged to C. oncophora or O. ostertagi, using species-specific primers targeting the ITS-2 ribosomal DNA gene, as described by Schnieder et al.  and Höglund et al. . The primer sequences used were Cooperia ITS2 Forward 5’ TAA TGG CAT TTG TCT ACA TCT 3’, Cooperia ITS2 Reverse 5’ ATG ATA ACG AAT ACT ACT ATC T 3’, Ostertagia ITS2 Forward 5’ GTC GAA TGG TAT TTA TTA CT 3’ and Ostertagia ITS2 Reverse 5’ TTA GTT TCT TTT CCT CCG CT 3’. The reaction mixtures contained 25 μL volume with 2.5 μL 10 × Buffer (10 mM Tris-HCl pH 8.3, 50 mM KCl, 1.5 mM MgCl2 ), 0.5 μL Forward primer (10 pmol), 0.5 μL Reverse primer (10 pmol), 0.5 μL dNTP (0.2 mM), 0.1 μL Polymerase AmpliTaq (0.5 U), 19.9 μL H2O, and 1 μL genomic DNA. Samples were run in an Applied Biosystems 2720 Thermal Cycler. Cycling conditions were denaturation at 94°C for 2 min followed by 30 cycles of 94°C for 30 s, 55°C for 30 s and 72°C for 1 minute, followed by 3 min at 72°C. A 6 μL portion of the PCR product was separated on 1% agarose gel (GelRed, Biotium) to check the PCR reactions. Bands were documented using UV illumination and digital imaging system (Biorad). PCR products were then purified and amplicons sequenced with BigDye Chemistry (Applied Biosystems) before analysis on an ABI PRISM 3100 Genetic Analyzer (Applied Biosystems).
Faecal egg count reduction test
Adult worm recoveries
Calf epg data and recovered worms before and after IVM treatment
Larval migration inhibition test
Larval migration inhibition test
Species-specific single larvae PCR (ITS2)
Species-specific single larvae PCR (ITS2)
7-10 days post IVM
% O. ostertagi
% O. ostertagi
In this study, we performed a controlled efficacy test with additional available in vivo (e.g. FECRT) and in vitro methods (LMIT and species identification of surviving larvae by PCR), in order to further investigate previously detected anthelmintic resistance (AR) against Ivomec inj.® (IVM) in two nematode isolates from two Swedish dairy farms. This is the first extended investigation of ML resistance in Sweden under experimental conditions, and the results are somewhat ambiguous.
As in a Belgian survey by El-Abdellati et al. , we failed to confirm suspected AR (<95% FECR), regardless of the diagnostic sensitivity of the egg counting method used. Only C. oncophora were found in the coprocultures morphologically investigated post treatment, whereas PCR identification of L3 showed that group C calves also shed O. ostertagi (8%) post treatment. The adult worm recoveries increased our understanding of the current worm burden, showing considerable quantities of surviving C. oncophora but only modest amounts of O. ostertagi. Lifschitz et al.  have shown that the concentration of IVM is lower in the intestinal mucosa than in the abomasal mucosa, which are the predilection sites of C. oncophora and O. ostertagi, respectively. The pharmacokinetic properties of IVM may to some extent explain why C. oncophora has a higher resilience to the drug than O. ostertagi, and why it is the dose-limiting species. Our results from the LMIT showed approximately 10-fold higher EC50 values than obtained previously by Demeler et al. [18, 19], but in contrast to those studies we tested material with mixed species larvae, which made comparisons difficult.
A deviating finding was that the adult O. ostertagi recovered at necropsy came from group B calves, whereas the larvae from shed eggs post treatment came from group C calves. In theory, the lack of shed O. ostertagi eggs in group B could be explained by the fact that the nematode uterine muscle is one of the most susceptible target organs for ML . This could mean that the drug may temporarily suppress nematode egg laying, even though adult worms survive treatment. Although we failed to recover adult O. ostertagi from the two slaughtered calves in group C at necropsy, L3 in faecal cultures from the same group were observed post treatment according to the species-specific single larva PCR. The most likely explanation is that these fecund females were harboured by another calf in group C that was not slaughtered.
According to the FECRT standard [17, 36], all three isolates investigated in this pen trial were successfully treated, with reductions ≥95%. However, the criterion for suspected resistance, i.e. <90 lower limit of the 95% CI, was fulfilled for isolate A (95%, 81-99), which was included as the “susceptible” control isolate, when calculated on group-based means. It was also equal to 90% in isolate A when means were calculated on individual reductions using the McMaster method, and in isolate B when means were calculated on individual reductions using the FLOTAC method.
The reason for the discrepancy between our results and those from the previous field trial remains unknown and needs to be further investigated. In both trials, we used injectable IVM at the same dose rate. The only difference was that in the field trial , animal weight was estimated using girth tape, while the animals in the present pen trial were weighed on scales. The remaining differentiating factor is that the calves described by Demeler et al.  were dewormed following turn-out. IVM is a very lipophilic substance with an extensive distribution binding to fatty tissues, including sites of parasite location [34, 37–39]. Its long persistence after subcutaneous administration to cattle is also based on the deposition of active drug in fatty tissues , which could theoretically affect pharmacokinetic patterns under field conditions, since FSG calves in Sweden are well known to suffer from extensive weight loss during the first month after the transition to feeding on pasture [41, 42]. In contrast, the animals in this study did not suffer from weight loss or changes in diet, whereas reduced live weight is frequently observed up to four weeks post turn-out in Sweden .
It has previously also been shown that factors affecting the pharmacokinetics of IVM clearly affect the efficacy of the drug , but the theory of altered pharmacokinetics as a cause of reduced anthelmintic efficacy is still speculative and few investigations have been carried out. Accordingly, further trials under field conditions are needed to test whether the physiological changes FSG undergo during turnout alter the pharamacokinetics of the drug, and how this reduces the efficacy of treatment. Blood samples from field studies where lack of efficacy in ML treatment has been shown  would have been a helpful tool in distinguishing between the effect of deviating pharmacokinetics in the host and the effect of AR in the parasitic nematodes, but unfortunately no such samples were available.
This study showed that calves experimentally infected with two different GIN isolates defined as resistant according to FECRT were successfully treated, although considerable numbers of C. oncophora and also small numbers of O. ostertagi survived IVM treatment. Genetic AR may be one of several confounding factors leading to anthelmintic failure, but others, such as differences in the pharmacokinetic profile in the field versus compared with in pen trials, cannot yet be excluded.
The authors thank the participating Swedish farmers in “Gråmunkehöga” and “Kolsta” who contributed sample material, and Frida Dahlström, Jonas Dahl and David Johansson at Götala research farm in Skara, Sweden, for assistance in housing calves and collecting samples. We also thank Märta Blomqvist and the staff at Kungsängen research farm in Uppsala, for assistance in the trial. The study was funded by EU-project KBBE 2011.1.3-04 – Management and control of increased livestock helminth parasite infection risks due to global change (GLOWORM) and Coping with Anthelmintic Resistance in ruminants (CARES). The authors also thank Dr. David Morrison and Dr. Jürgen Krücken for advice on statistical analysis.
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