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The Importance of Parasite Control and Targeted Treatment

The Importance of Parasite Control and Targeted Treatment

Anouk Frieling, Senior Nutritionist

 

Horses turned out on grass are likely to have issues with parasites throughout their life (Nielsen, Pfister & Von Samson-Himmelstjerna, 2014). Serious health issues caused by parasite infections are better prevented than cured, which makes it important to test and treat horses, which are identified as high egg shedders, during the winter period for parasite infections. This reduces outbreaks of parasites during spring when they become more active again and will control the parasite population by preventing them from increasing in number.

All horses have parasites to some degree, the important factor is the level of infection as parasite infections can affect the health and welfare of the horse (Stratford et al., 2014). Infections can cause health issues such as weightloss, colic or diarrhoea (Matthews et al., 2019). Therefore for horse owners parasite control is an important part of managing the health and welfare of their horse(s) (Wilkes et al., 2020). The most common parasites in adult horses are small strongyles (cyathostomins), large strongyles (strongylus vulgaris) and tapeworms (Anoplocephala perfoliate) (Matthews, 2011).

 

Figure 1: It is most likely that grazing horses will be infected with parasites throughout their life, therefore management and control of parasites is important.

TREATMENT STRATEGY

Through recent years control strategies and treating parasite infections have been revised and have changed (Robert et al., 2015). Previously parasite infections were controlled through frequent use of anthelmintic treatments (Robert et al., 2015). This has led to certain parasite species developing resistance against these anthelmintic treatments (Nielsen, 2015). It is suggested that instead of frequently administering anthelmintic treatments, parasites are controlled with use of targeted treatment (Sallé and Cabaret, 2015). Targeted treatment can be achieved by monitoring the faecal egg count (FEC) and only selecting horses for treatment with a high number of eggs as these horses are classed as high shedders, meaning that they excrete a high number of parasite eggs which in turn supports continued parasite infections and poses a risk to other horses (Matthews et al., 2019). A high egg count is considered when there are between 200 and 500 eggs per gram (epg) of faeces (Matthews & Lester, 2015). It is then suggested to treat the horse with the proper deworming treatment (Matthews & Lester, 2015). Horses with egg counts lower than 200 EPG will not be treated (Matthews & Lester, 2015). Analysis has shown that the use of targeted treatment reduces the use of dewormers by about 82%, which also reduces the costs of parasite treatment on a yearly basis (Matthews et al., 2019). Faecal egg counts have also been used to detect the resistance of certain parasite species against anthelmintic treatments (Raza et al., 2019). The eggs in the faeces of a horse are counted, enabling the risk to other horses to be assessed by determining if the horse has a low, medium or high egg count. The egg count does not determine the horses own parasite burden as there is no correlation between the amount of eggs in the faeces and the number of parasites within the host horse, however FEC do enable horses that shed lots of eggs to be identified and treated with the appropriate anthelmintic treatment. This reduces the risk to other horses and helps to control the parasite levels in the population of horses. After horses have been treated with anthelmintics further FEC should be performed so the number of eggs can be assessed and the impact of the anthelmintic to be determined (Raza et al., 2019). Determining the anthelmintic resistance this way is one of the most reliable and suitable tests that can be used for resistance in horses (Raza et al., 2019). Another strategy accompanying the targeting treatment to reduce parasite infections is managing the pasture. This is accomplished by for instance removing faeces from the pastures at least every 3 days (preferably every day), rotating the horses on different parts of the pasture or letting the horses graze with other ruminants (Rendle et al., 2019).

Figure 2: With use of a targeted treatment plan, use of anthelmintic treatments will decrease. This prevents the resistance of certain parasite species to these treatments.

 

PARASITE TESTING KITS

Testing kits have been developed to identify the specific parasite and the burden of the infection of the parasite in the horse. Two separate tests have been developed, one that is able to identify small red worms with use of blood samples and the other one is able to detect and estimate the burden of tapeworm in a horse using saliva samples.

The small strongyles (cyathostomins), also known as small red worms, are the most common parasites in horses (Lester et al., 2013). Red worm infections do not always cause health issues but serious infections by these parasites can cause cyathostominosis which is colic caused by the red worm larvae emerging in large numbers from their cysts within the large intestine wall. These parasites can also cause rapid weight loss or diarrhoea (Lester et al., 2013). In the worst case these health issues can be fatal to the horse (Lester et al., 2013). Due to overuse of anthelmintics to treat infections of red worms, they have become resistant to these treatments (Santos, Madeira de Carvalho and Molento, 2018), therefore it is of importance to use targeted treatment to properly treat small redworm infections in horses (Rose Vineer et al., 2017). Small red worms have shown resistance against the anthelmintics benzimidazoles and tetrahydropyrimidines (Matthews, 2014). Recently the use of Ivermectin and moxidectin for small red worm infections seemed to be less effective due to reappearance of small red worm eggs shortly after administration of the anthelmintic and is reported as an early sign of anthelmintic resistance (Nielsen et al., 2014). Even though there are signs of reduced efficiency of moxidectin and ivermectin treatments, these anthelmintics are currently the most effective treatments against small red worms (Traversa et al., 2012). A commercial blood test has been developed to detect antibodies which are related to an red worm infection (Austin Davis Biologics Ltd, 2020). This test is able to detect the small redworm during all stages of the lifecycle (Austin Davis Biologics Ltd, 2020). It is advised to consider testing after monitoring the FEC of the horse to identify horses with a high egg count (200 or more eggs per gram of faecal sample) which indicates active red worms in the horse (Austin Davis Biologics Ltd, 2020). The distributer of this test recommends to perform the test during autumn or early winter due to the fact that guidelines advise to treat for encysted red worms at this time of year (Austin Davis Biologics Ltd, 2020). After testing, the results of these tests and the probabilities of the infection burden in the horse will be shared with the veterinarian (Austin Davis Biologics Ltd, 2020). In consultation with the veterinarian a treatment plan can be made for the specific infection in the horse.

Another parasite which is very common in grazing horses is tapeworm. The tapeworm Anoplocephala perfoliate is an especially common tapeworm species in horses in the UK (Austin Davis Biologics Ltd, 2018). This tapeworm is also associated with clinical signs such as colic and rapid weight loss (Lightbody et al., 2018). Through FEC it sometimes is not possible to estimate the actual tapeworm burden in the horse, therefore using a testing kit can determine the burden of the infection of the tapeworm in the horse (Austin Davis Biologics Ltd, 2018). The testing kit is able to identify tapeworm through antibodies in the saliva of the horse (Austin Davis Biologics Ltd, 2018). If the saliva score indicates a moderate or high burden of tapeworms, it is suggested that the horse is treated with the appropriate anthelminitic (Lightbody et al., 2018). Tapeworm infections are treated with the anthelmintics pyrantel pamoate and praziquantel (Nielsen, 2016). Currently anthelmintic resistance of tapeworms has not been documented yet (Lightbody et al., 2018), and using this test can help to prevent the over usage of treatment against tapeworms and therefore prevent the resistance of tapeworm against anthelmint treatment (Lightbody et al., 2018).

 

Figure 3: Blood and saliva tests are developed to identify the parasite infection, enabling the right treatment plan to be followed.

 

 

In summary, it is important to control and manage parasite infections in the horse to manage their health and welfare. It is advised to avoid frequent use of anthelmintic treatments to prevent or worsen anthelmintic resistance of parasites. Targeted treatment is used to control parasite infections and treat horses that support the parasites life cycle by using FEC monitoring and diagnostic tests to identify high risk horses.

 

REFERENCES

Austin Davis Biologics Ltd (2020) ‘Guidelines for Use: Small Redworm Blood Test’, https://cdn.website-editor.net/88f85cd9154141f880badb10905b7906/files/uploaded/Austin%2520Davis%2520Small%2520Redworm%2520Guidelines%2520Final.pdf. Available at: https://www.austindavis.co.uk/small-redworm-blood-test.

Austin Davis Biologics Ltd (no date) ‘EquiSal – Tapeworm burden diagnosis straight from the horse ’ s mouth !’

Lester, H. E., Spanton, J., Stratford, C. H., Bartley, D. J., Morgan, E. R., Hodgkinson, J. E., Coumbe, K., Mair, T., Swan, B., Lemon, G., Cookson, R. and Matthews, J. B. (2013) ‘Anthelmintic efficacy against cyathostomins in horses in Southern England’, Veterinary Parasitology. doi: 10.1016/j.vetpar.2013.06.009.

Lightbody, K. L., Matthews, J. B., Kemp-Symonds, J. G., Lambert, P. A. and Austin, C. J. (2018) ‘Use of a saliva-based diagnostic test to identify tapeworm infection in horses in the UK’, Equine Veterinary Journal, 50(2). doi: 10.1111/evj.12742.

Matthews, J. B. (2011) ‘Facing the threat of equine parasitic disease’, Equine Veterinary Journal. doi: 10.1111/j.2042-3306.2010.00356.x.

Matthews, J. B. (2014) ‘Anthelmintic resistance in equine nematodes’, International Journal for Parasitology: Drugs and Drug Resistance. Australian Society for Parasitology, 4(3), pp. 310–315. doi: 10.1016/j.ijpddr.2014.10.003.

Matthews, J. and Lester, H. (2015) ‘Control of equine nematodes: Making the most of faecal egg counts’, In Practice, 37(10). doi: 10.1136/inp.h6139.

Matthews, J., Tzelos, T. and Lester, H. (no date) ‘Guidelines for the control of worms in equines’.

Nielsen, M. K. (2015) ‘Universal challenges for parasite control: A perspective from equine parasitology’, Trends in Parasitology. doi: 10.1016/j.pt.2015.04.013.

Nielsen, M. K. (2016) ‘Equine tapeworm infections: Disease, diagnosis and control’, Equine Veterinary Education. doi: 10.1111/eve.12394.

Nielsen, M. K., Pfister, K. and Von Samson-Himmelstjerna, G. (2014) ‘Selective therapy in equine parasite control-Application and limitations’, Veterinary Parasitology. doi: 10.1016/j.vetpar.2014.03.020.

Nielsen, M. K., Reinemeyer, C. R., Donecker, J. M., Leathwick, D. M., Marchiondo, A. A. and Kaplan, R. M. (2014) ‘Anthelmintic resistance in equine parasites-Current evidence and knowledge gaps’, Veterinary Parasitology, 204(1–2). doi: 10.1016/j.vetpar.2013.11.030.

Raza, A., Qamar, A. G., Hayat, K., Ashraf, S. and Williams, A. R. (2019) ‘Anthelmintic resistance and novel control options in equine gastrointestinal nematodes’, Parasitology. doi: 10.1017/S0031182018001786.

Rendle, D., Austin, C., Bowen, M., Cameron, I., Furtado, T., Hodgkinson, J., McGorum, B. and Matthews, J. (2019) ‘Equine de-worming: a consensus on current best practice’, UK-Vet Equine, 3(Sup1). doi: 10.12968/ukve.2019.3.s.3.

Robert, M., Hu, W., Nielsen, M. K. and Stowe, C. J. (2015) ‘Attitudes towards implementation of surveillance-based parasite control on Kentucky Thoroughbred farms - Current strategies, awareness and willingness-to-pay’, Equine Veterinary Journal, 47(6). doi: 10.1111/evj.12344.

Rose Vineer, H., Vande Velde, F., Bull, K., Claerebout, E. and Morgan, E. R. (2017) ‘Attitudes towards worm egg counts and targeted selective treatment against equine cyathostomins’, Preventive Veterinary Medicine, 144. doi: 10.1016/j.prevetmed.2017.05.002.

Sallé, G. and Cabaret, J. (2015) ‘A survey on parasite management by equine veterinarians highlights the need for a regulation change’, Veterinary Record Open, 2(2). doi: 10.1136/vetreco-2014-000104.

Santos, D. W., Madeira de Carvalho, L. M. and Molento, M. B. (2018) ‘Identification of third stage larval types of cyathostomins of equids: An improved perspective’, Veterinary Parasitology, 260. doi: 10.1016/j.vetpar.2018.08.007.

Stratford, C. H., Lester, H. E., Morgan, E. R., Pickles, K. J., Relf, V., Mcgorum, B. C. and Matthews, J. B. (2014) ‘A questionnaire study of equine gastrointestinal parasite control in Scotland’, Equine Veterinary Journal, 46(1). doi: 10.1111/evj.12101.

Traversa, D., Castagna, G., von Samson-Himmelstjerna, G., Meloni, S., Bartolini, R., Geurden, T., Pearce, M. C., Woringer, E., Besognet, B., Milillo, P. and D’Espois, M. (2012) ‘Efficacy of major anthelmintics against horse cyathostomins in France’, Veterinary Parasitology, 188(3–4). doi: 10.1016/j.vetpar.2012.03.048.

Wilkes, E. J. A., Heller, J., Raidal, S. L., Woodgate, R. G. and Hughes, K. J. (2020) ‘A questionnaire study of parasite control in Thoroughbred and Standardbred horses in Australia’, Equine Veterinary Journal, 52(4). doi: 10.1111/evj.13207.