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Horses grazing with cattle have reduced strongyle egg count due to the dilution effect and increased reliance on macrocyclic lactones in mixed farms

Published online by Cambridge University Press:  04 November 2019

L. Forteau
Affiliation:
Université Clermont Auvergne, INRA, VetAgro Sup, UMR Herbivores, Saint-Genès-Champanelle, France Institut Français du Cheval et de l’Equitation (IFCE), Pôle développement innovation et recherche, Exmes, France
B. Dumont*
Affiliation:
Université Clermont Auvergne, INRA, VetAgro Sup, UMR Herbivores, Saint-Genès-Champanelle, France
G. Sallé
Affiliation:
Institut National de la Recherche Agronomique (INRA), Université François Rabelais Tours, UMR Infectiologie et Santé Publique, Nouzilly, France
G. Bigot
Affiliation:
Université Clermont Auvergne, AgroParisTech, INRA, Institut national de Recherche en Sciences et Technologies pour l’Environnement et l’Agriculture (Irstea), VetAgro Sup, UMR Territoires, Clermont Ferrand, France
G. Fleurance
Affiliation:
Université Clermont Auvergne, INRA, VetAgro Sup, UMR Herbivores, Saint-Genès-Champanelle, France Institut Français du Cheval et de l’Equitation (IFCE), Pôle développement innovation et recherche, Exmes, France

Abstract

Strongyle infection is an important issue in horse breeding. It impairs horse health and performance, with young horses being the most sensitive. Strongyle control has long relied on the systematic use of chemical treatments. However, expanding anthelmintic resistance among strongyles calls for alternative options. Mixed grazing is assumed to reduce strongyle load on the pasture as the result of a dilution effect. This has been shown in small ruminants grazing with cattle, but the putative benefits of co-grazing between horses and cattle have not yet been evaluated. Here, we conducted field surveys and face-to-face interviews on 44 farms from two contrasted saddle-horse production areas, Normandy and northern Massif Central, to compare equine strongyle management practices between specialized systems and mixed horse-cattle systems. Our goals were (i) to quantify breeders’ awareness of the putative benefits associated with the co-grazing of horses and cattle, (ii) to establish whether mixed farming was associated with different strongyle management strategies and (iii) to test whether strongyle egg excretion was reduced in horses grazed with beef cattle. Every breeder relied on systematic calendar treatments, and only 8 out of the 23 mixed breeders were aware that co-grazing of horses with cattle could be used as part of their strongyle control strategy. Management practices were similar across both systems in Normandy. In Massif Central, mixed breeders formed a distinct cluster from their specialized counterparts: deworming was less frequent and stocking density was higher in mixed farms, while specialized breeders seemed more willing to integrate herd and plot management into control strategies. Faecal egg counts measured in horses from Massif Central were significantly reduced when horses were grazed with cattle. This was the result of an increased reliance on macrocyclic lactones in mixed farms (P < 0.01) and a significant dilution effect (P < 0.01). When considering a subsample of horses treated with macrocyclic lactones only, young horses grazed with cattle had 50% fewer strongyle eggs excreted in their faeces than horses grazed in equine-only pastures (P < 0.01). This is the first evidence of the benefits of mixed grazing with cattle as an alternative to control strongyle infection in horses, although this promising alternative remains largely unknown by horse breeders.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s) 2019

Implications

Horse breeders are increasingly challenged by drug resistance when controlling strongyle infection. Although largely unknown by mixed breeders, alternate grazing or co-grazing with horses and cattle is assumed to reduce strongyle load in pastures as the result of a dilution effect. Here, we reveal a decrease in strongyle egg excretion in young saddle horses grazing with beef cattle. This dilution effect is likely to decrease treatment frequency and thus veterinary costs and environmental side-effects of drug metabolites on dung beetle assemblages.

Introduction

Parasitic infection by strongyle nematodes (mostly cyathostomins) is common in grazing horses. High levels of infection affect horse welfare and performance and can eventually lead to death (Giles et al., Reference Giles, Urquhart and Longstaffe1985). Cyathostomin infection is indeed associated with enteropathy, leading to protein losses and potentially to horse death when a large number of encysted larvae are released from the mucosa of the large intestine, a phenomenon called ‘larval cyathostomosis’ (Love et al., Reference Love, Murphy and Mellor1999). Young horses between 1 and 4 years are the most sensitive to strongyles, as they are still developing immunity (Love and Duncan, Reference Love and Duncan1992; Lind et al., Reference Lind, Höglund, Ljungström, Nilsson and Uggla1999; Kornaś et al., Reference Kornaś, Cabaret, Skalska and Nowosad2010).

Strongyle control in saddle horses is classically based on a calendar treatment with anthelmintics, but this practice is currently challenged. First, drug resistance has accumulated in many countries (Relf et al., Reference Relf, Lester, Morgan, Hodgkinson and Matthews2014; Sallé et al., Reference Sallé, Cortet, Bois, Dubès, Guyot-Sionest, Larrieu, Landrin, Majorel, Wittreck, Woringer, Couroucé, Guillot, Jacquiet, Guégnard, Blanchard and Leblond2017; Nielsen et al., Reference Nielsen, Branan, Wiedenheft, Digianantonio, Garber, Kopral, Philippi-Taylor and Traub-Dargatz2018). Second, the metabolites of some of these drugs exert detrimental side-effects on dung beetle assemblages (Sands and Wall, Reference Sands and Wall2018). Therefore, alleviating drug selection pressure on equine strongylid communities should reduce environmental side-effects and decrease associated economic costs (Lester et al., Reference Lester, Bartley, Morgan, Hodgkinson, Stratford and Matthews2013; Sallé et al., Reference Sallé, Cortet, Koch, Reigner and Cabaret2015).

An alternative strategy could be to limit the risk of horse infection by co-grazing with another species in order to disrupt parasites’ life cycles by reducing contact between hosts and infective larvae (Waller, Reference Waller2006; Hoste and Torres-Acosta, Reference Hoste and Torres-Acosta2011). Gastrointestinal parasites indeed exhibit high specificity for their hosts, apart from liver flukes and the nematode species Trichostrongylus axei, which infects both horses and cattle. Because of the relative host specificity of parasitic helminths, each grazing species is assumed to act as a dead-end for the parasites infecting members of the other species. The so-called ‘dilution effect’ has been successfully implemented with cattle and sheep, whereby lamb parasite burden was significantly reduced (Marley et al., Reference Marley, Fraser, Davies, Rees, Vale and Forbes2006; Brito et al., Reference Brito, Dallago, Louvandini, dos Santos, Torres, Gomes, do Amarante, de Melo and McManus2013), and with cattle and goats; strongyle egg excretion by Creole kids grazed on irrigated pastures was significantly reduced by sequential grazing with heifers (Mahieu, Reference Mahieu2013).

To our knowledge, the putative benefits associated with co-grazing of horses with another species have never been studied. The sole observations available were obtained from an alternate grazing system in the Netherlands. In that case, ponies were either moved to a pasture previously grazed by sheep or stayed on the pasture they had been grazing throughout spring (Eysker et al., Reference Eysker, Jansen and Mirck1986). The study found a significant reduction of cyathostomin load in ponies grazing after sheep, which was, however, associated with an increased prevalence of Trichostrongylus axei (Eysker et al., Reference Eysker, Jansen and Mirck1986). Because the alternative pasture was mostly grazed by sheep (with occasional but unquantified grazing by ponies) in the previous year, this trial could not soundly evaluate the benefits of species alternation for parasite control in ponies, but rather accounted for the action of moving ponies to a pasture with limited cyathostomin contamination.

In an attempt to evaluate the putative benefits associated with the co-grazing of horses and cattle, we undertook a survey across 46 French farms located in two contrasted French saddle-horse production areas, that is, Normandy and the lowlands of northern Massif Central. Our objectives were (i) to establish if horse breeders integrate herd and grassland management as part of their strongyle control strategy, (ii) to analyse if horse deworming and grazing management differ between mixed horse-cattle and specialized horse farms, and (iii) to quantify strongyle egg excretion in both types of system to determine putative benefits of co-grazing horses with beef cattle.

Material and methods

Surveys of management practices at the farm level

The study was conducted on 44 farms producing saddle horses with or without beef cattle that were selected according to three additional criteria: at least three mares were kept on a farm, farms were located in lowlands (i.e., lower than 600 m above sea level) and grasslands represented more than 80% of the agricultural area. Normandy and northern Massif Central were considered as two contrasted case studies: in Normandy, high-level sport horses are bred and grazed on productive grasslands, while in Massif Central, horses are mainly bred for leisure and grazed on less productive grasslands.

Face-to-face interviews were carried out on 23 farms from Normandy (12 mixed and 11 specialized farms) and 21 farms from northern Massif Central (11 mixed and 10 specialized farms). Interviews (1 to 2.5-h long according to farm size and the complexity of pasture management) focused on farmer beliefs and practices related to grazing, plot cleaning and animal health management.

Grassland management variables

Using collected data, three variables were constructed:

  1. (i) The annual mean stocking rate at the farm level (the sum of the mean annual stocking rate per plot multiplied by plot area, divided by the sum of the grazed and mixed plot areas). To obtain three balanced classes for statistical analyses, annual mean stocking rate was considered low between 0.2 and 0.6 livestock unit (LU) per hectare, intermediate between 0.6 and 1.0 LU/ha and high between 1.0 and 1.4 LU/ha (see Table 1 for LU definition). Reducing stocking rate is indeed likely to reduce the risks of strongyle infection by horses (Martins et al., Reference Martins, Verocai, Correia, Melo, Pereira, Scott and Grisi2009).

  2. (ii) The proportion of total grassland area in both cut and grazed management (i.e., mixed as opposed to grazed-only grasslands) was partitioned into three categories: lower than 30%, intermediate (between 30% and 45%) or higher than 45% of grassland area. Grazing horses on mixed grasslands can strongly decrease numbers of infective larvae in pastures (Martin-Rosset, Reference Martin-Rosset2015).

  3. (iii) The integration of herd and grassland management practices as part of the strongyle control strategy: none when strongyle control only relied on a systematic calendar treatment; yes_livestock when additional practices were based on herd management, for example, reducing stocking rate (Waller, Reference Waller2006); yes_cleaning when additional practices were based on pasture management, for example, pasture grinding or mowing before animals grazed pastures to decrease larval density in the sward (Cabaret, Reference Cabaret2017) and yes_livestock_and_cleaning when both types of practices were combined.

Table 1 Livestock unit values used for the different categories of horses and beef cattle. We used values recently actualized to account for liveweight evolution in beef cattle (Inosys Réseaux d’élevage, 2018) and saddle horses (Martin-Rosset, Reference Martin-Rosset2015)

Variables related to deworming strategy

The implemented deworming strategy was also addressed during the interviews. Four variables were covered: (i) the number of anthelmintic treatments administered to young horses (0 to 4 years; considered low between 4 and 9 treatments per horse over 4 years, intermediate between 10 and 13, and high between 14 and 20), or mares (low: 1 to 2 treatments per year; high: 3 to 4); (ii) the strategy used for deworming (systematic, systematic with additional treatments (based on indicators such as diarrhoea, poor coat or body condition), or systematic plus additional treatments based on faecal egg counts (FECs)); (iii) the person in charge of parasite control (the breeder, the veterinarian or both) and (iv) the anthelmintic class given to young horses and mares.

The egg reappearance period (ERP) indeed varies across anthelmintic classes (Gokbulut et al., Reference Gokbulut, Nolan and Mckellar2001; Relf et al., Reference Relf, Lester, Morgan, Hodgkinson and Matthews2014). To account for egg reappearance in a synthetic way, we considered the proportion of macrocyclic lactones (moxidectin and ivermectin) used for young horses (low: less than 40%; intermediate: 40% to 60%; high: 60% to 90%; almost exclusive: more than 90%) and mares (low: less than 50%; high: 50% to 90%; exclusive: 100%), as macrocyclic lactones have the longest ERPs.

Finally, as the strategy of parasitism control may vary according to the genetic merit of horses, farms were classified into three groups based on French genetic indices of mares currently on the farm in the different equestrian disciplines (jumping, dressage, eventing and endurance). A farm was considered of excellent genetic merit when at least one of the mares was registered with a score higher than +9 for one of the genetic indices. A farm was considered of high genetic merit when at least one of the mares was registered with a positive score for one index. All other farms were considered to produce horses for leisure.

Strongyle faecal egg counts in horses from mixed and specialized farms

To test whether FEC was reduced in horses from mixed systems, faeces were sampled in autumn in horses at greater risk of infection (18 to 42 months old). For logistical reasons and according to breeders’ willingness to participate, the sampling took place on Massif Central farms only.

Sampled horses were either grazed with cattle (n = 23 horses, 6 farms) or alone in a specialized farm (n = 23 horses, 5 farms). Fresh individual faeces were collected on the ground and kept at 4°C for less than 48 h; eggs were counted (test sensitivity: 15 eggs/g) at the official local veterinary services (DDCSPP du Puy de Dôme), based on sedimentation and concentration by a flotation technique (Raynaud, Reference Raynaud1970).

Sampled horses had been treated with anthelmintic treatments having different ERPs, which induced extra-variance in measured FEC. Recent reports suggest these ERPs have become shorter over the years (Tzelos et al., Reference Tzelos, Barbeito, Nielsen, Morgan, Hodgkinson and Matthews2017; Molena et al., Reference Molena, Peachey, Di Cesare, Traversa and Cantacessi2018), but current ERPs are unknown in France. In a conservative approach, we chose to correct measured FEC by the last anthelmintic class used according to their original ERPs; that is, 90 and 60 days for moxidectin and ivermectin, respectively; 28 days for pyrantel and 0 days for fenbendazole.

Statistical analyses

Statistical analyses were performed with R software (The R Core Team, 2019, 3.4.4 version). As variables were all transformed into qualitative variables, a multiple correspondence analysis was conducted followed by hierarchical classification with the FactoMineR package (Lê et al., Reference Lê, Josse and Husson2008).

To establish whether FEC was significantly associated with the farming system, a linear regression was performed. We built a full model regressing FEC (n = 46) on farming system (two classes), the number of treatments (three classes), the proportion of time each horse spent on mixed grasslands, grassland stocking rate and time since the end of the ERP. A variable selection procedure was implemented with the stepAIC() function of the MASS package that retained the farming system, the time since the end of ERP and stocking rate.

In a second analysis, we considered a subsample of 28 horses treated with macrocyclic lactones only. A two-sample t test was used to test for equality of FEC means between horses from specialized (n = 9) and mixed systems (n = 19). For all statistical analyses, effects were considered significant when the P-value was lower than 0.05.

Results

The putative benefits associated with the co-grazing of horses and cattle were largely overlooked

Face-to-face interviews were also undertaken to evaluate the general beliefs and awareness regarding parasite control management in both mixed and specialized systems. Strongyle control relied on a systematic calendar treatment in all 44 farms surveyed. The most commonly used anthelmintics were fenbendazole (in 36 farms) and macrocyclic lactones (ivermectin, n = 33 farms; moxidectin n = 22 farms). Additional herd and grassland management practices were implemented and considered as part of breeders’ strongyle control strategy in a total of 18 farms, 11 from Massif Central and 7 from Normandy.

Plot-cleaning practices were the most common (n = 14 farms) and included pasture liming (n = 5), use of rotary slashers (n = 5) or dung-spreading harrows (n = 4), avoiding rapidly returning herds to the same pasture (n = 3) and removing dung from pastures (n = 1). The sum is higher than 14, as some breeders used 2 of these grassland management practices.

Herd management strategies were reported in nine farms, and only eight mixed horse-cattle breeders surveyed were aware that mixed grazing could be used to control strongyle infection in saddle horses. The remaining 15 breeders of that group did not know or believe in any benefit of mixed grazing to decrease horse parasite burden. Reducing stocking rate was reported three times. Two breeders maintained stable group composition, and another used rotational grazing for parasite control.

Implementation of mixed grazing discriminates between farms in Massif Central but not in Normandy

Following the analysis of breeders’ awareness, we attempted to summarize their strategies in order to establish whether mixed farming systems were associated with particular practices. Multiple correspondence analysis applied to management practice data revealed three clusters separated along two axes explaining 13.0% and 10.6% of total variance, respectively. The first cluster, named Nor, included 22 farms, mainly in Normandy (n = 18), two-thirds of which were mixed cattle-horse farms and one-third specialized horse farms. Remaining clusters, named MC-mix and MC-spe, were mostly composed of mixed (70%) or specialized (83%) farms from northern Massif Central, respectively. This suggests that practices were different between mixed and specialized systems in Massif Central, whereas practices were much more similar across systems in Normandy.

Despite variable reliance on macrocyclic lactones in both the MC-mix and MC-spe systems (Table 2), parasite control strategies accounted for significant portions of their discrepancies. Indeed, drug usage was lighter in farms belonging to the mixed cluster (Table 2), while breeders from the specialized cluster were more reliant on veterinarians to decide upon treatment (in 42% of these farms deworming decisions were only made by veterinarians, Table 2). Specialized breeders were also more willing to integrate herd and plot management into control strategy (Table 3), and they mostly decided upon deworming according to certain indicators or FEC (Table 2). These discrepancies may be underpinned by the higher genetic merit of the mares reared in the specialized farms (excellent or high) relative to that from the MC-mix cluster that was more variable (excellent in 40% of the farms but low in the remaining 60%).

Table 2 Deworming practices in mixed horse-cattle and specialized horse farms grouped in the three clusters obtained from multiple correspondence analysis and hierarchical clustering on principal components

FEC = faecal egg counts.

Clust-1 Nor is mostly composed of Normandy farms; Clust-2 MC-mix is mostly composed of mixed farms from northern Massif Central; Clust-3 MC-spe is mostly composed of specialized horse farms from northern Massif Central.

Table 3 Grazing management practices in mixed horse-cattle and specialized horse farms grouped in the three clusters obtained from multiple correspondence analysis and hierarchical clustering on principal components

LU = livestock unit.

Clust-1 Nor is mostly composed of Normandy farms; Clust-2 MC-mix is mostly composed of mixed farms from northern Massif Central; Clust-3 MC-spe is mostly composed of specialized horse farms from northern Massif Central.

The two Massif Central clusters were also contrasted for grassland management. Annual stocking rate was higher in mixed farms. Half of the farms from the MC-mix cluster indeed had annual stocking rates higher than 1 LU/ha, while the proportion of grasslands under both cut and grazed management usually fell in the intermediate class (Table 3). Conversely, nearly 60% of the farms from the MC-spe cluster had an annual stocking rate lower than 0.6 LU per ha, while the proportion of grasslands under both cut and grazed management was the highest of all three clusters (Table 3).

Horse faecal egg counts is lower in mixed farms

FEC was conducted on 46 horses from mixed and specialized farms to establish whether farming system was impacting horse excretion and what variables underpinned this variation. Our regression model found that time since the end of ERP was significantly driving observed variation in FEC (F 1,42 = 11.74, P < 0.01) but not stocking rate (F 1,42 = 2.61, P = 0.11). Farming system was also associated with a significant difference in FEC (F 1,42 = 10, P < 0.01), with horses from the mixed farming systems excreting half as many eggs than their counterparts from specialized farms.

A second analysis was performed on a subsample of 28 horses last treated with macrocyclic lactones. It confirmed that young horses grazed with cattle had 50% fewer strongyle eggs excreted in their faeces than horses grazed in equine-only pastures (P < 0.01; Figure 1).

Figure 1 Box and whisker plot of FEC in horses from specialized farms (n = 9, mean = 400 epg, median = 340 epg) or grazing with cattle in mixed farms (n = 19, mean = 230 epg, median = 150 epg) (t test, P < 0.01). FEC = faecal egg counts.

Discussion

The purpose of our study was to compare specialized saddle horse farms with mixed horse-cattle farms and to establish whether any difference in parasite control could be found. The limited awareness of the putative beneficial effects associated with the co-grazing strategy was striking, especially because mixed grazing is a key pillar of integrated parasite management in agroecological grassland-based systems (Dumont et al., Reference Dumont, González-García, Thomas, Fortun-Lamothe, Ducrot, Dourmad and Tichit2014). These results are consistent with other surveys. In Sweden, mixed grazing was found in 10% of horse farms (Lind et al., Reference Lind, Rautalinko, Uggla, Waller, Morrison and Höglund2007), while 39% of horse breeders sampled in Rio de Janeiro state (Brazil) indicated they used mixed grazing with ruminants as an alternative to control strongyles and for better pasture management (Martins et al., Reference Martins, Verocai, Correia, Melo, Pereira, Scott and Grisi2009). These results strongly contrast with what has been observed in Irish equine farms, where 71% of respondents were aware of the health benefits of mixed grazing and utilized it effectively to lower strongyle pasture contamination (O’Meara and Mulcahy, Reference O’Meara and Mulcahy2002). Some of the mixed breeders we surveyed reported grazing horses and cattle on separate pastures because they want to keep mares close to farm buildings but accept grazing suckler cows that require less day-to-day surveillance on more distant pastures. One breeder was also concerned about agonistic interactions between the horses and cattle. Beyond this, a majority of mixed breeders surveyed (15 out of 23) were not aware of the benefits of mixed grazing for parasite management. This stresses the need to pursue the transfer effort of research outputs so that these become available to horse breeders.

This lack of awareness regarding mixed grazing was also associated with the widespread use of fenbendazole, despite high prevalence of resistant strongyle populations in France (Traversa et al., Reference Traversa, Castagna, von Samson-Himmelstjerna, Meloni, Bartolini, Geurden, Pearce, Woringer, Besognet, Milillo and D’Espois2012; Sallé et al., Reference Sallé, Cortet, Bois, Dubès, Guyot-Sionest, Larrieu, Landrin, Majorel, Wittreck, Woringer, Couroucé, Guillot, Jacquiet, Guégnard, Blanchard and Leblond2017). All breeders also used systematic horse chemical treatment, which confirms previous surveys in Irish (O’Meara and Mulcahy, Reference O’Meara and Mulcahy2002) and Swedish (Lind et al., Reference Lind, Rautalinko, Uggla, Waller, Morrison and Höglund2007) horse structures. However, additional preventive strategies like plot-cleaning practices were also implemented in a third of surveyed farms, corroborating findings gathered in Ireland (O’Meara and Mulcahy, Reference O’Meara and Mulcahy2002) and Sweden (Lind et al. Reference Lind, Rautalinko, Uggla, Waller, Morrison and Höglund2007). Some of these practices, however, do not provide efficient control of strongyles. This is, for example, seen in the case of pasture liming, reported by five farmers from our survey, which does not provide strongyle control when the annual spreading is applied in March, and in the case of the temporary exclusion of horses from some pastures for decreasing parasite load (reported by three farmers), as it is usually too short to be efficient (Martin-Rosset, Reference Martin-Rosset2015).

A key finding from our surveys is that specialized horse breeders from Massif Central seemed more willing than the mixed breeders to integrate herd and plot management into their control strategies. In these farms, the proportion of grasslands under both cut and grazed management was also the highest, and early cuts under mixed management are known to strongly decrease the number of infective larvae in pastures (Martin-Rosset, Reference Martin-Rosset2015). Nearly 60% of these farms had an annual stocking rate lower than 0.6 LU/ha, which is likely to reduce the risks of strongyle infection by horses (Martins et al., Reference Martins, Verocai, Correia, Melo, Pereira, Scott and Grisi2009). There was also a high frequency of deworming treatments in these specialized farms, where breeders partly based deworming decisions on indicators. In Sweden, many specialized horse breeders also made additional anthelmintic treatments based on indicators such as the body condition or the presence of worms in faeces (Lind et al., Reference Lind, Rautalinko, Uggla, Waller, Morrison and Höglund2007). Overall, specialized horse breeders developed more elaborate strategies for controlling strongyle infection in their animals. Their concern may partly result from the higher genetic merit of their mares compared to those in mixed cattle-horse farms in the Massif Central case study. In addition, our observations suggest that deworming practices were much more similar across systems in Normandy, where mare genetic merit was the highest (it was excellent in 77% of the farms and high in the remaining 23%). Normandy breeders strongly relied on macrocyclic lactones and used additional treatments based on indicators such as diarrhoea, poor coat or body condition, or faecal egg counts. A first hypothesis for this discrepancy between the two case studies is that the high genetic merit of their mares may have led Normandy breeders to adopt a risk-adverse strategy that homogenized strongyle management practices.

While our results are thus likely influenced by regional context, they also provide the first indication that the co-grazing of horses and cattle has beneficial effect for equine strongyle control. Our results are consistent with previous observations in ruminant farming, showing that simultaneous grazing by cattle and sheep (Southcott and Barger, Reference Southcott and Barger1975; Giudici et al., Reference Giudici, Aumont, Mahieu, Saulai and Cabaret1999; Marley et al., Reference Marley, Fraser, Davies, Rees, Vale and Forbes2006; Brito et al., Reference Brito, Dallago, Louvandini, dos Santos, Torres, Gomes, do Amarante, de Melo and McManus2013), alternate grazing with cattle and sheep (Rocha et al., Reference Rocha, Bresciani, Barros, Fernandes, Silva and Amarante2008) or mixed grazing by cattle and goats (Mahieu, Reference Mahieu2013) reduce parasitic infection in lambs and goat kids. Because our survey was designed to characterize both types of farming systems with a number of similar characteristics between farms, it was not possible to sample the whole range of equine-to-cattle ratio. Further research is now needed to investigate how the ratio between the two species may influence the contamination of horses by strongyles. Additionally, integrated health management usually combines different practices to control parasitic infection in grassland-based systems (O’Meara and Mulcahy, Reference O’Meara and Mulcahy2002; Waller, Reference Waller2006; Dumont et al., Reference Dumont, González-García, Thomas, Fortun-Lamothe, Ducrot, Dourmad and Tichit2014). Mixed grazing by cattle and horses could, for instance, be combined with the short-term use of tannin-rich plants in the horse diet, as this practice has been shown to impair strongyle egg development into infective larvae (Collas et al., Reference Collas, Sallé, Dumont, Cabaret, Cortet, Martin-Rosset, Wimel and Fleurance2018). Finally, both specialized and mixed horse breeders were shown to use various herd management and plot-cleaning practices. Further research is needed to provide evidence of their effectiveness in the control of horse strongyles (Martin-Rosset, Reference Martin-Rosset2015).

Conclusion

We provide the first evidence of a decrease in the parasite burdens of young saddle horses grazing the same pastures as cattle in mixed farms, compared with horses grazing alone in specialized systems. This opens a promising alternative for controlling horse parasitic infection that remains largely unknown by horse breeders. Association between horses and cattle at pasture is facilitated through the use of the same type of fencing for the two species, with possible limitations due to injury risks which could be solved through alternate grazing. This suggests a diversity of more sustainable agroecological parasite management strategies in horse farms as alternatives to repeated chemical treatment, which raises serious resistance issues.

Acknowledgements

This research was supported by grants from IFCE and INRA-Phase Division. Additional funding was obtained through the PSDR4 project new-DEAL co-funded by INRA, Irstea and the Auvergne-Rhône-Alpes region. We are grateful to the farmers who agreed to answer our questions and let us collect dung samples in their fields. We also thank Margot Mouilleau, Cécile Cochetel and Julien Soulat for their contributions to the farm surveys and statistical analyses.

B. Dumont 0000-0001-8376-4417

Declaration of interest

The authors declare no competing interests regarding this publication.

Ethics statement

Section is irrelevant for this article based on farm surveys and collection of dung samples in pastures.

Software and data repository resources

No new software or databases were generated as outcomes of this research.

References

Brito, DL, Dallago, BSL, Louvandini, H, dos Santos, VRV, Torres, SEFD, Gomes, EF, do Amarante, AFT, de Melo, CB and McManus, CM 2013. Effect of alternate and simultaneous grazing on endoparasite infection in sheep and cattle. Revista Brasileira de Parasitologia Veterinária 22, 485494.CrossRefGoogle ScholarPubMed
Cabaret, J 2017. Parasitisme interne des ruminants (strongles) et utilisation du pâturage : comment faire durablement bon ménage? Fourrages 229, 3745.Google Scholar
Collas, C, Sallé, G, Dumont, B, Cabaret, J, Cortet, J, Martin-Rosset, W, Wimel, L and Fleurance, G 2018. Are sainfoin or protein supplements alternatives to control small strongyle infection in horses? Animal 12, 359365.CrossRefGoogle ScholarPubMed
Dumont, B, González-García, E, Thomas, M, Fortun-Lamothe, L, Ducrot, C, Dourmad, JY and Tichit, M 2014. Forty research issues for the redesign of animal production systems in the 21st century. Animal 8, 13821393.CrossRefGoogle ScholarPubMed
Eysker, M, Jansen, J and Mirck, MH 1986. Control of strongylosis in horses by alternate grazing of horses and sheep and some other aspects of the epidemiology of strongylidae infections. Veterinary Parasitology 19, 103115.CrossRefGoogle ScholarPubMed
Giles, CJ, Urquhart, KA and Longstaffe, JA 1985. Larval cyathostomiasis (immature trichonema-induced enteropathy): a report of 15 clinical cases. Equine Veterinary Journal 17, 196201.CrossRefGoogle ScholarPubMed
Giudici, C, Aumont, G, Mahieu, M, Saulai, M and Cabaret, J 1999. Changes in gastro-intestinal helminth species diversity in lambs under mixed grazing on irrigated pastures in the tropics (French West Indies). Veterinary Research 30, 573581.Google Scholar
Gokbulut, C, Nolan, AM and Mckellar, QA 2001. Plasma pharmacokinetics and faecal excretion of ivermectin, doramectin and moxidectin following oral administration in horses. Equine Veterinary Journal 33, 494498.CrossRefGoogle ScholarPubMed
Hoste, H and Torres-Acosta, JFJ 2011. Non chemical control of helminths in ruminants: adapting solutions for changing worms in a changing world. Veterinary Parasitology 180, 144154.CrossRefGoogle Scholar
Inosys Réseaux d’élevage 2018. Référentiel élevage 2018 bovins lait et bovins viande – Auvergne-Aveyron-Lozère. Conjoncture 2017. Retrieved on 19 July 2019 from https://extranet-cantal.chambres-agriculture.fr/fileadmin/user_upload/Auvergne-Rhone-Alpes/117_Extr-Cantal_img/Actus-agendas/2018/Service_References/Fiches_bovins_lait.pdfGoogle Scholar
Kornaś, S, Cabaret, J, Skalska, M and Nowosad, B 2010. Horse infection with intestinal helminths in relation to age, sex, access to grass and farm system. Veterinary Parasitology 174, 285291.CrossRefGoogle ScholarPubMed
, S, Josse, J and Husson, F 2008. FactoMineR: an R Package for Multivariate Analysis. Journal of Statistical Software 25, https://doi.org/10.18637/jss.v025.i01, Published on 18 March 2008.CrossRefGoogle Scholar
Lester, HE, Bartley, DJ, Morgan, ER, Hodgkinson, JE, Stratford, CH and Matthews, JB 2013. A cost comparison of faecal egg count-directed anthelmintic delivery versus interval programme treatments in horses. Veterinary Record 173, 371.CrossRefGoogle ScholarPubMed
Lind, EO, Höglund, J, Ljungström, BL, Nilsson, O and Uggla, A 1999. A field survey on the distribution of strongyle infections of horses in Sweden and factors affecting faecal egg counts. Equine Veterinary Journal 31, 6872.CrossRefGoogle Scholar
Lind, EO, Rautalinko, E, Uggla, A, Waller, PJ, Morrison, DA and Höglund, J 2007. Parasite control practices on Swedish horse farms. Acta Veterinaria Scandinavia 49, 25.CrossRefGoogle ScholarPubMed
Love, S and Duncan, JL 1992. The development of naturally acquired cyathostome infection in ponies. Veterinary Parasitology 44, 127142.CrossRefGoogle ScholarPubMed
Love, S, Murphy, D and Mellor, D 1999. Pathogenicity of cyathostome infection. Veterinary Parasitology 85, 113122.CrossRefGoogle ScholarPubMed
Mahieu, M 2013. Effects of stocking rates on gastrointestinal nematode infection levels in a goat/cattle rotational stocking system. Veterinary Parasitology 198, 136144.CrossRefGoogle Scholar
Marley, CL, Fraser, MD, Davies, DA, Rees, ME, Vale, JE and Forbes, AB 2006. The effect of mixed or sequential grazing of cattle and sheep on the faecal egg counts and growth rates of weaned lambs when treated with anthelmintics. Veterinary Parasitology 142, 134141.CrossRefGoogle ScholarPubMed
Martin-Rosset, W 2015. Equine nutrition. INRA nutrient requirements, recommended allowances and feed tables. Wageningen Academic Publishers, Wageningen, NL.CrossRefGoogle Scholar
Martins, IVF, Verocai, GG, Correia, TR, Melo, RMPS, Pereira, MJS, Scott, FB and Grisi, L 2009. Survey on control and management practices of equine helminthes infection. Pesquisa Veterinária Brasileira 29, 253257.CrossRefGoogle Scholar
Molena, RA, Peachey, LE, Di Cesare, A, Traversa, D and Cantacessi, C 2018. Cyathostomine egg reappearance period following ivermectin treatment in a cohort of UK Thoroughbreds. Parasites & Vectors 11, 61.CrossRefGoogle Scholar
Nielsen, MK, Branan, MA, Wiedenheft, AM, Digianantonio, R, Garber, LP, Kopral, CA, Philippi-Taylor, AM and Traub-Dargatz, JL 2018. Parasite control strategies used by equine owners in the United States: a national survey. Veterinary Parasitology 250, 4551.CrossRefGoogle ScholarPubMed
O’Meara, B and Mulcahy, G 2002. A survey of helminth control practices in equine establishments in Ireland. Veterinary Parasitology 109, 101110.CrossRefGoogle ScholarPubMed
Raynaud, JP 1970. Etude de l’efficacité d’une technique de coproscopie quantitative pour le diagnotic de routine et le contrôle des infestations parasitaires des bovins, ovins, équins et porcins. Annales de Pathologie Humaine et Comparée 45, 321342.CrossRefGoogle Scholar
Relf, VE, Lester, HE, Morgan, ER, Hodgkinson, JE and Matthews, JB 2014. Anthelmintic efficacy on UK Thoroughbred stud farms. International Journal of Parasitology 44, 507514.CrossRefGoogle ScholarPubMed
Rocha, RA, Bresciani, KDS, Barros, TFM, Fernandes, LH, Silva, MB and Amarante, AFT 2008. Sheep and cattle grazing alternately: nematode parasitism and pasture decontamination. Small Ruminant Research 75, 135143.CrossRefGoogle Scholar
Sallé, G, Cortet, J, Bois, I, Dubès, C, Guyot-Sionest, Q, Larrieu, C, Landrin, V, Majorel, G, Wittreck, S, Woringer, E, Couroucé, A, Guillot, J, Jacquiet, P, Guégnard, F, Blanchard, A and Leblond, A 2017. Risk factor analysis of equine strongyle resistance to anthelmintics. International Journal for Parasitology-Drugs and Drug Resistance 7, 407415.CrossRefGoogle ScholarPubMed
Sallé, G, Cortet, J, Koch, C, Reigner, F and Cabaret, J 2015. Economic assessment of FEC-based targeted selective drenching in horses. Veterinary Parasitology 214, 159166.CrossRefGoogle ScholarPubMed
Sands, B and Wall, R 2018. Sustained parasiticide use in cattle farming affects dung beetle functional assemblages. Agriculture, Ecosystems and Environment 265, 226235.CrossRefGoogle Scholar
Southcott, WH and Barger, IA 1975. Control of nematode parasites by grazing management—II. Decontamination of sheep and cattle pastures by varying periods of grazing with the alternate host. International Journal of Parasitology 5, 4548.CrossRefGoogle ScholarPubMed
The R Core Team 2019. R: a Language and Environment for Statistical Computing. Version 3.6.1. Retrieved on 30 September 2019 from https://cran.r-project.org/doc/manuals/r-release/fullrefman.pdfGoogle Scholar
Traversa, D, Castagna, G, von Samson-Himmelstjerna, G, Meloni, S, Bartolini, R, Geurden, T, Pearce, MC, Woringer, E, Besognet, B, Milillo, P and D’Espois, M 2012. Efficacy of major anthelmintics against horse cyathostomins in France. Veterinary Parasitology 188, 294300.CrossRefGoogle ScholarPubMed
Tzelos, T, Barbeito, JSG, Nielsen, MK, Morgan, ER, Hodgkinson, JE and Matthews, JB 2017. Strongyle egg reappearance period after moxidectin treatment and its relationship with management factors in UK equine populations. Veterinary Parasitology 237, 7076.CrossRefGoogle ScholarPubMed
Waller, PJ 2006. Sustainable nematode parasite control strategies for ruminant livestock by grazing management and biological control. Animal Feed Science and Technology 126, 277289.CrossRefGoogle Scholar
Figure 0

Table 1 Livestock unit values used for the different categories of horses and beef cattle. We used values recently actualized to account for liveweight evolution in beef cattle (Inosys Réseaux d’élevage, 2018) and saddle horses (Martin-Rosset, 2015)

Figure 1

Table 2 Deworming practices in mixed horse-cattle and specialized horse farms grouped in the three clusters obtained from multiple correspondence analysis and hierarchical clustering on principal components

Figure 2

Table 3 Grazing management practices in mixed horse-cattle and specialized horse farms grouped in the three clusters obtained from multiple correspondence analysis and hierarchical clustering on principal components

Figure 3

Figure 1 Box and whisker plot of FEC in horses from specialized farms (n = 9, mean = 400 epg, median = 340 epg) or grazing with cattle in mixed farms (n = 19, mean = 230 epg, median = 150 epg) (t test, P < 0.01). FEC = faecal egg counts.