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Veterinary parasitology2012; 194(1); 35-39; doi: 10.1016/j.vetpar.2012.12.020

Lack of Cyathostomin sp. reduction after anthelmintic treatment in horses in Brazil.

Abstract: The increase of anthelmintic resistance in the last years in the nematode population of veterinary importance has become a major concern. The objective of the present study was to evaluate the efficacy of the main anthelmintic drugs available in the market against small strongyles of horses in Brazil. A total of 498 horses from 11 horse farms, located in the states of Paraná, São Paulo, Rio de Janeiro and Minas Gerais, in Brazil, were treated with ivermectin, moxidectin, pyrantel and fenbendazole, orally at their recommended doses. The fecal egg count reduction test (FECRT) was used to determine the product's efficacy and fecal culture was used to determine the parasite genus. Reduction on anthelmintic efficacy was found for fenbendazole in all horse farms (11/11), pyrantel in five yards (5/11) and ivermectin had low efficacy in one of the yards studied (1/11). Multidrug resistance of up to 3 drugs classes was found in one of the tested farms (1/11). Cyathostomin were the most prevalent parasite. The results showed that resistance to fenbendazole is widespread; the efficacy of pyrantel is in a critical situation. Although the macrocyclic lactones compounds still showed high efficacy on most farms, suspected resistance to macrocyclic lactones is of great concern.
Publication Date: 2012-12-20 PubMed ID: 23318166DOI: 10.1016/j.vetpar.2012.12.020Google Scholar: Lookup
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  • Journal Article
  • Randomized Controlled Trial
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The study focuses on assessing anthelmintic drug effectiveness against small strongyles, a type of parasitic nematode, in horses across various farms in Brazil. It found that resistance to these drugs is growing, with fenbendazole proving ineffective across all tested horse farms and multidrug resistance observed in one.

Study Objective and Methodology

  • The aim of this research was to evaluate the performance of widely-used anthelmintic drugs against small strongyles in horses in Brazil. Small strongyles are a nematode species of considerable importance in veterinary medicine.
  • The authors tested the drugs on a total of 498 horses, sourced from 11 farms located in different states across Brazil. The drugs tested include common anthelmintics like ivermectin, moxidectin, pyrantel and fenbendazole, all administered orally at recommended doses.
  • The research utilized the fecal egg count reduction test (FECRT) to assess the effectiveness of the drugs. Alongside this, fecal cultures were analyzed to determine the parasitic genus present.

Key Findings

  • Results demonstrated a decrease in anthelmintic efficacy across the board. Fenbendazole showed no efficacy on any of the studied horse farms (11/11). Pyrantel seemed ineffective in five of the farms (5/11) and ivermectin had low performance in one of the studied yards (1/11).
  • Alarmingly, the study also discovered multidrug resistance – to a maximum of three drug classes – in one of the tested farms (1/11). This indicates that some horses were resistant to multiple anthelmintic drugs.
  • The most prevalent parasite found was Cyathostomin, suggesting this species is the most resistant to the tested anthelmintic drugs.

Conclusions and Implications

  • The study concludes that resistance to the drug fenbendazole is widely spread amongst the horse farms in Brazil. The efficacy of pyrantel is also reaching a critical level.
  • Despite the majority of farms still showing high efficacy to macrocyclic lactones like ivermectin and moxidectin, the suspected resistance to these is a growing concern. If these drugs also lose their efficacy, it could pose significant treatment challenges for parasitic infection in horses.
  • The prevalence of multidrug resistance in one farm is particularly concerning, necessitating further research and new treatment strategies to counter this escalating issue.

Cite This Article

APA
Canever RJ, Braga PR, Boeckh A, Grycajuck M, Bier D, Molento MB. (2012). Lack of Cyathostomin sp. reduction after anthelmintic treatment in horses in Brazil. Vet Parasitol, 194(1), 35-39. https://doi.org/10.1016/j.vetpar.2012.12.020

Publication

ISSN: 1873-2550
NlmUniqueID: 7602745
Country: Netherlands
Language: English
Volume: 194
Issue: 1
Pages: 35-39
PII: S0304-4017(12)00668-1

Researcher Affiliations

Canever, Ricardo J
  • Laboratory of Parasitic Diseases, Department of Veterinary Medicine, Federal University of Paraná, Curitiba, PR, Brazil.
Braga, Pollyana R C
    Boeckh, Albert
      Grycajuck, Marcelly
        Bier, Daniele
          Molento, Marcelo B

            MeSH Terms

            • Animals
            • Antinematodal Agents / pharmacology
            • Antinematodal Agents / therapeutic use
            • Brazil
            • Drug Resistance
            • Drug Resistance, Multiple
            • Feces / parasitology
            • Female
            • Fenbendazole / pharmacology
            • Fenbendazole / therapeutic use
            • Horses
            • Macrolides / pharmacology
            • Macrolides / therapeutic use
            • Male
            • Parasite Egg Count / veterinary
            • Prevalence
            • Pyrantel / pharmacology
            • Pyrantel / therapeutic use
            • Strongyle Infections, Equine / drug therapy
            • Strongyle Infections, Equine / parasitology
            • Strongyloidea / drug effects
            • Strongyloidea / physiology

            Citations

            This article has been cited 18 times.
            1. Martins AV, Coelho AL, Corrêa LL, Ribeiro MS, Lobão LF, Palmer JPS, Moura LC, Molento MB, Barbosa ADS. First microscopic and molecular parasitological survey of Strongylus vulgaris in Brazilian ponies.. Rev Bras Parasitol Vet 2023;32(3):e006323.
              doi: 10.1590/S1984-29612023036pubmed: 37377279google scholar: lookup
            2. Dauparaitė E, Kupčinskas T, Varady M, Petkevičius S. Anthelmintic resistance of horse strongyle nematodes to fenbendazole in Lithuania.. Acta Vet Scand 2022 Sep 15;64(1):26.
              doi: 10.1186/s13028-022-00645-ypubmed: 36109767google scholar: lookup
            3. Nápravníková J, Várady M, Vadlejch J. Total Failure of Fenbendazole to Control Strongylid Infections in Czech Horse Operations.. Front Vet Sci 2022;9:833204.
              doi: 10.3389/fvets.2022.833204pubmed: 35265696google scholar: lookup
            4. Abbas G, Ghafar A, Hurley J, Bauquier J, Beasley A, Wilkes EJA, Jacobson C, El-Hage C, Cudmore L, Carrigan P, Tennent-Brown B, Gauci CG, Nielsen MK, Hughes KJ, Beveridge I, Jabbar A. Cyathostomin resistance to moxidectin and combinations of anthelmintics in Australian horses.. Parasit Vectors 2021 Dec 4;14(1):597.
              doi: 10.1186/s13071-021-05103-8pubmed: 34863271google scholar: lookup
            5. Johnson ACB, Biddle AS. The Use of Molecular Profiling to Track Equine Reinfection Rates of Cyathostomin Species Following Anthelmintic Administration.. Animals (Basel) 2021 May 9;11(5).
              doi: 10.3390/ani11051345pubmed: 34065099google scholar: lookup
            6. de Oliveira LDSSCB, Dias FGS, Melo ALT, de Carvalho LM, Silva EN, Araújo JV. Bioverm(®) in the Control of Nematodes in Beef Cattle Raised in the Central-West Region of Brazil.. Pathogens 2021 May 1;10(5).
              doi: 10.3390/pathogens10050548pubmed: 34062798google scholar: lookup
            7. Maestrini M, Molento MB, Mancini S, Martini M, Angeletti FGS, Perrucci S. Intestinal Strongyle Genera in Different Typology of Donkey Farms in Tuscany, Central Italy.. Vet Sci 2020 Dec 2;7(4).
              doi: 10.3390/vetsci7040195pubmed: 33276602google scholar: lookup
            8. Flota-Burgos GJ, Rosado-Aguilar JA, Rodríguez-Vivas RI, Borges-Argáez R, Martínez-Ortiz-de-Montellano C, Gamboa-Angulo M. Anthelmintic Activity of Extracts and Active Compounds From Diospyros anisandra on Ancylostoma caninum, Haemonchus placei and Cyathostomins.. Front Vet Sci 2020;7:565103.
              doi: 10.3389/fvets.2020.565103pubmed: 33173794google scholar: lookup
            9. Nielsen MK, Banahan M, Kaplan RM. Importation of macrocyclic lactone resistant cyathostomins on a US thoroughbred farm.. Int J Parasitol Drugs Drug Resist 2020 Dec;14:99-104.
              doi: 10.1016/j.ijpddr.2020.09.004pubmed: 33022574google scholar: lookup
            10. Papini RA, Orsetti C, Sgorbini M. A Controlled Study on Efficacy and Egg Reappearance Period of Ivermectin in Donkeys Naturally Infected with Small Strongyles.. Helminthologia 2020 Jun 1;57(2):163-170.
              doi: 10.2478/helm-2020-0017pubmed: 32518493google scholar: lookup
            11. Sallé G, Kornaś S, Basiaga M. Equine strongyle communities are constrained by horse sex and species dipersal-fecundity trade-off.. Parasit Vectors 2018 May 2;11(1):279.
              doi: 10.1186/s13071-018-2858-9pubmed: 29716644google scholar: lookup
            12. Molena RA, Peachey LE, Di Cesare A, Traversa D, Cantacessi C. Cyathostomine egg reappearance period following ivermectin treatment in a cohort of UK Thoroughbreds.. Parasit Vectors 2018 Jan 25;11(1):61.
              doi: 10.1186/s13071-018-2638-6pubmed: 29370872google scholar: lookup
            13. 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, Leblond A. Risk factor analysis of equine strongyle resistance to anthelmintics.. Int J Parasitol Drugs Drug Resist 2017 Dec;7(3):407-415.
              doi: 10.1016/j.ijpddr.2017.10.007pubmed: 29149701google scholar: lookup
            14. Peachey LE, Pinchbeck GL, Matthews JB, Burden FA, Lespine A, von Samson-Himmelstjerna G, Krücken J, Hodgkinson JE. P-glycoproteins play a role in ivermectin resistance in cyathostomins.. Int J Parasitol Drugs Drug Resist 2017 Dec;7(3):388-398.
              doi: 10.1016/j.ijpddr.2017.10.006pubmed: 29121562google scholar: lookup
            15. Zak A, Siwinska N, Slowikowska M, Borowicz H, Kubiak K, Hildebrand J, Popiolek M, Niedzwiedz A. Searching for ivermectin resistance in a Strongylidae population of horses stabled in Poland.. BMC Vet Res 2017 Jul 3;13(1):210.
              doi: 10.1186/s12917-017-1133-1pubmed: 28673347google scholar: lookup
            16. Matthews JB. Anthelmintic resistance in equine nematodes.. Int J Parasitol Drugs Drug Resist 2014 Dec;4(3):310-5.
              doi: 10.1016/j.ijpddr.2014.10.003pubmed: 25516842google scholar: lookup
            17. Storey B, Marcellino C, Miller M, Maclean M, Mostafa E, Howell S, Sakanari J, Wolstenholme A, Kaplan R. Utilization of computer processed high definition video imaging for measuring motility of microscopic nematode stages on a quantitative scale: "The Worminator".. Int J Parasitol Drugs Drug Resist 2014 Dec;4(3):233-43.
              doi: 10.1016/j.ijpddr.2014.08.003pubmed: 25516834google scholar: lookup
            18. Schneider S, Pfister K, Becher AM, Scheuerle MC. Strongyle infections and parasitic control strategies in German horses - a risk assessment.. BMC Vet Res 2014 Nov 12;10:262.
              doi: 10.1186/s12917-014-0262-zpubmed: 25387542google scholar: lookup