Analyze Diet
Veterinary parasitology2017; 240; 75-81; doi: 10.1016/j.vetpar.2017.03.026

Managing anthelmintic resistance in Parascaris spp.: A modelling exercise.

Abstract: A previously described model for the dynamics of the parasitic stages of Parascaris spp. was modified to include eggs outside the host and the genetics of anthelmintic resistance before being used to address questions regarding the development of resistance. Three broad questions were addressed; i) How sustainable is the current common practice of treating foals monthly for their first year of life (i.e. 12 treatments/year)? ii) Does the timing of treatments have an effect on resistance development? (i.e. do certain treatments select for resistance more strongly than others?), and iii) How sustainable is the currently recommended strategy of targeting ascarid infections in foals with two treatments applied during the first five months of life? A range of variations within these broad questions were considered, such as the value in rotational deworming, whether larvicidal treatments are more selective for resistance, and whether combination anthelmintics should be introduced. Twelve anthelmintic treatments at monthly intervals resulted in the development of resistance to all the anthelmintics used, regardless of how they were used, indicating that such intensive treatment frequency is unlikely to be sustainable. The timing of a single annual treatment influenced resistance development with treatments at 3 and 4 months of age being more selective than treatments at other times. Treatments administered to foals older than 6 months of age did not select for resistance within the timeframe of these simulations. Treatments with activity against migrating third stage larvae (ivermectin and a programme of 5 daily treatments with fenbendazole) were more selective for resistance than those which only killed worms in the intestine. Restricting the number of treatments to young foals to two, administered at 2 and 5 months of age slowed the development of resistance by allowing a small contribution from susceptible genotype worms to subsequent generations. If the interval between treatments was reduced, resistance developed more rapidly demonstrating the importance of allowing some susceptible worms to reach patency before the second treatment is administered. Under a reduced treatment schedule with a clearly defined 'refugium' of susceptibility, the use of effective actives in combination appears to offer advantages for delaying resistance development. The model offers insights into more sustainable drug use strategies and has identified some priority questions for future research.
Publication Date: 2017-03-30 PubMed ID: 28433409DOI: 10.1016/j.vetpar.2017.03.026Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

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 research article presents a study on how managing the rate of anthelmintic resistance in the parasitic species Parascaris can be achieved through adjustments in treatment strategies.

Objective of the Research

  • The main aim of the study was to modify a previously described model for the dynamics of the parasitic stages of Parascaris spp. This model now included details about eggs outside the host and the genetics of anthelmintic resistance. The model was then used to address three major questions concerning the development of resistance in the parasite.

Questions Addressed

  • The first question probed the sustainability of the common practice of treating foals monthly during their first year of life. It asked if a year-round (12 treatments/year) treatment strategy is an effective or sustainable approach to managing the parasitic infection.
  • The second question asked whether the timing of treatments could affect the development of resistance. In other words, it investigated if some treatments enhance resistance more strongly than others. This sought to understand if different time points in the parasite’s lifecycle might be more vulnerable to treatments.
  • The last question sought to understand the effectiveness of the current recommended strategy of specifically targeting ascarid infections in young foals with two treatments in the first five months.

Findings and Conclusion

  • The research findings revealed that 12 treatments at monthly intervals led to the development of resistance to all types of anthelmintics used, suggesting that a high frequency of treatment may not be sustainable.
  • The study also determined that the timing of treatments can influence the development of resistance, with treatments at three and four months being more selective than treatments at other times.
  • The study suggested that treatments active against migrating third stage larvae were more selective for resistance than those killing only intestinal worms.
  • The results indicated that reducing the number of treatments to two, given at 2 and 5 months, slows down the development of resistance. This is because it allows a slight contribution from susceptible genotype worms to future generations.
  • Resistance developed more rapidly if the interval between treatments was shortened. This shows the importance of allowing some susceptible worms to reach patency before administering the second treatment.
  • Under a reduced treatment regimen with a designated ‘refugium’ of susceptible individuals, the use of effective actives in combination appears to delay the development of resistance.
  • The study concluded that the model provides insights for developing more sustainable drug use strategies. It has also highlighted critical questions that need to be addressed in future research.

Cite This Article

APA
Leathwick DM, Sauermann CW, Geurden T, Nielsen MK. (2017). Managing anthelmintic resistance in Parascaris spp.: A modelling exercise. Vet Parasitol, 240, 75-81. https://doi.org/10.1016/j.vetpar.2017.03.026

Publication

ISSN: 1873-2550
NlmUniqueID: 7602745
Country: Netherlands
Language: English
Volume: 240
Pages: 75-81

Researcher Affiliations

Leathwick, Dave M
  • AgResearch Grasslands, Private Bag 11008, Palmerston North, 4442, New Zealand. Electronic address: dave.leathwick@agresearch.co.nz.
Sauermann, Christian W
  • AgResearch Grasslands, Private Bag 11008, Palmerston North, 4442, New Zealand.
Geurden, Thomas
  • Zoetis, Mercuriuslaan 20, 1930 Zaventem, Belgium.
Nielsen, Martin K
  • M.H. Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, KY, USA.

MeSH Terms

  • Animals
  • Anthelmintics / pharmacology
  • Anthelmintics / therapeutic use
  • Ascaridida Infections / drug therapy
  • Ascaridida Infections / parasitology
  • Ascaridida Infections / veterinary
  • Ascaridoidea / drug effects
  • Drug Resistance
  • Horse Diseases / drug therapy
  • Horse Diseases / parasitology
  • Horses
  • Models, Biological
  • Ovum / drug effects

Citations

This article has been cited 4 times.
  1. Lu Y, Deng L, Peng Z, Zhou M, Wang C, Han L, Huang S, Wei M, Wei R, Tian L, Li D, Hou Z. Investigation of the Efficacy of Pyrantel Pamoate, Mebendazole, Albendazole, and Ivermectin against Baylisascaris schroederi in Captive Giant Pandas. Animals (Basel) 2022 Dec 29;13(1).
    doi: 10.3390/ani13010142pubmed: 36611749google scholar: lookup
  2. Studzińska MB, Sallé G, Roczeń-Karczmarz M, Szczepaniak K, Demkowska-Kutrzepa M, Tomczuk K. A survey of ivermectin resistance in Parascaris species infected foals in south-eastern Poland. Acta Vet Scand 2020 Jun 5;62(1):28.
    doi: 10.1186/s13028-020-00526-2pubmed: 32503589google scholar: lookup
  3. Hu Y, Miller M, Zhang B, Nguyen TT, Nielsen MK, Aroian RV. In vivo and in vitro studies of Cry5B and nicotinic acetylcholine receptor agonist anthelmintics reveal a powerful and unique combination therapy against intestinal nematode parasites. PLoS Negl Trop Dis 2018 May;12(5):e0006506.
    doi: 10.1371/journal.pntd.0006506pubmed: 29775454google scholar: lookup
  4. Muñoz J, Ballester MR, Antonijoan RM, Gich I, Rodríguez M, Colli E, Gold S, Krolewiecki AJ. Safety and pharmacokinetic profile of fixed-dose ivermectin with an innovative 18mg tablet in healthy adult volunteers. PLoS Negl Trop Dis 2018 Jan;12(1):e0006020.
    doi: 10.1371/journal.pntd.0006020pubmed: 29346388google scholar: lookup