Abstract: Over the past 25 years, significant progress has been made in understanding and managing equine gastrointestinal parasites in the Asia-Pacific region, particularly in Australia and New Zealand. This review synthesises current knowledge of the epidemiology, diagnostic methods, anthelmintic resistance (AR), and control strategies for major equine intestinal parasites, including cyathostomins, Parascaris spp., Anoplocephala perfoliata, and Strongyloides westeri. Recent studies highlight substantial regional variation in parasite prevalence, egg shedding and cyathostomin population composition, shaped by diverse climatic conditions. Of increasing concern is the emergence of resistance to commonly used anthelmintics which is now evident in both Parascaris and cyathostomins, although data for S. westeri and A. perfoliata remain limited. High-throughput molecular diagnostics, such as next-generation sequencing, have advanced species-level characterisation in Australia and Thailand. ELISA-based tests for A. perfoliata and encysted cyathostomins are promising but remain unvalidated and underutilised regionally. The routine use of combination anthelmintics, including benzimidazoles, praziquantel, pyrimidines, and macrocyclic lactones, may accelerate resistance across nematode and cestode populations, emphasising the need for regular efficacy monitoring and improved antiparasitic stewardship. Findings from recent research on horse parasites in Australia have informed the development of country's first national equine parasite control guidelines which recommend targeted or selective treatment strategies. However, the effectiveness of these strategies requires ongoing evaluation, particularly in year-round grazing systems in tropical and subtropical regions. Sustainable parasite control will depend on the integration of non-chemical strategies along with the use of anthelmintics and the establishment of a national parasite surveillance database. This review highlights the need for climate-specific treatment protocols, strengthened collaborative research infrastructure, and continued investment in innovative diagnostic and control methods to preserve equine health and anthelmintic efficacy across the region.
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.
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.
Overview
This research article reviews the latest progress and challenges in understanding, diagnosing, and controlling intestinal helminth parasites in horses within the Asia-Pacific region over the past 25 years.
It focuses on key parasites affecting horses, the issue of drug resistance, advances in diagnostics, and future directions for sustainable parasite management.
Background and Regional Context
The Asia-Pacific region, especially Australia and New Zealand, has seen significant strides in research on equine gastrointestinal parasites.
There is notable variability in parasite presence and behavior across this region, largely due to diverse climates ranging from tropical to temperate zones.
The major equine intestinal parasites discussed include:
Cyathostomins (small strongyles)
Parascaris species (roundworms)
Anoplocephala perfoliata (tapeworm)
Strongyloides westeri (threadworm)
Epidemiology and Parasite Population Dynamics
Parasite prevalence and egg shedding rates vary considerably within the region depending on local environmental conditions.
The composition of cyathostomin populations shows regional differences, influenced by climate and grazing practices.
Such ecological variation impacts parasite transmission cycles, infection intensities, and treatment outcomes.
Emergence of Anthelmintic Resistance (AR)
A growing concern is the detection of resistance to primary classes of anthelmintics used to treat these parasites.
Resistance is now documented in both Parascaris spp. and cyathostomins, complicating control efforts.
Limited data currently exist on resistance patterns in Strongyloides westeri and Anoplocephala perfoliata.
The widespread and routine use of combination anthelmintics (including benzimidazoles, praziquantel, pyrimidines, macrocyclic lactones) may further drive resistance development.
Advances in Diagnostic Methods
High-throughput molecular diagnostics like next-generation sequencing have enabled precise species-level parasite identification, notably in studies from Australia and Thailand.
Enzyme-linked immunosorbent assays (ELISA) targeting A. perfoliata and encysted cyathostomin stages show promise for improved detection but remain largely unvalidated and underused in the region.
Improved diagnostics are critical for guiding targeted treatment and reducing unnecessary anthelmintic application.
Control Strategies and Guidelines
Australia has developed the first national equine parasite control guidelines informed by recent research findings.
These guidelines emphasize targeted or selective treatment strategies rather than blanket deworming to slow resistance emergence.
Effectiveness of such strategies requires ongoing validation, especially considering year-round grazing in tropical and subtropical climates where parasite exposure is continuous.
Sustainable control involves integrating non-chemical interventions along with strategic anthelmintic use.
Future Directions and Recommendations
Establish a national parasite surveillance database to track infection trends and resistance development.
Develop climate-specific treatment protocols tailored to local parasite epidemiology and transmission dynamics.
Strengthen collaborative research infrastructure across Asia-Pacific to facilitate data sharing and coordinated studies.
Invest in novel diagnostic tools and alternative control methods to lessen reliance on chemical treatments.
Promote judicious anthelmintic stewardship to preserve drug efficacy and protect equine health.
Significance
This review consolidates comprehensive region-specific knowledge on equine intestinal parasites.
It highlights the urgent need to adapt strategies to changing parasite drug resistance landscapes and environmental factors.
By emphasizing integrated, evidence-based approaches and monitoring, it guides veterinarians and horse owners towards more sustainable parasite management.
Ensuring effective parasite control is vital for maintaining horse health, performance, and welfare in the Asia-Pacific region.
Cite This Article
APA
Abbas G, Nielsen MK, E-Hage C, Ghafar A, Beveridge I, Bauquier J, Beasley A, Wilkes EJA, Carrigan P, Cudmore L, Jacobson C, Hughes KJ, Jabbar A.
(2025).
Recent advances in intestinal helminth parasites of horses in the Asia-Pacific region: Current trends, challenges and future directions.
Int J Parasitol Drugs Drug Resist, 29, 100622.
https://doi.org/10.1016/j.ijpddr.2025.100622
Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Werribee, Victoria, Australia.
Nielsen, Martin K
Department of Animal and Veterinary Sciences, Aarhus University, Tjele, Denmark.
E-Hage, Charles
Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Werribee, Victoria, Australia.
Ghafar, Abdul
Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Werribee, Victoria, Australia.
Beveridge, Ian
Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Werribee, Victoria, Australia.
Bauquier, Jenni
Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Werribee, Victoria, Australia.
Beasley, Anne
School of Agriculture and Food Sustainability, The University of Queensland, Gatton, Queensland, Australia.
Wilkes, Edwina J A
Racing Victoria, Flemington, Victoria, 3031, Australia.
Carrigan, Peter
Scone Equine Hospital, Scone, New South Wales, 2337, Australia.
Cudmore, Lucy
Scone Equine Hospital, Scone, New South Wales, 2337, Australia.
Jacobson, Caroline
Centre for Animal Production and Health, Murdoch University, Murdoch, Western Australia, 6150, Australia.
Hughes, Kristopher J
School of Agricultural, Environmental and Veterinary Sciences, Charles Sturt University, Wagga Wagga, New South Wales, Australia.
Jabbar, Abdul
Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Werribee, Victoria, Australia. Electronic address: jabbara@unimelb.edu.au.
MeSH Terms
Animals
Horses
Anthelmintics / therapeutic use
Anthelmintics / pharmacology
Helminthiasis, Animal / epidemiology
Helminthiasis, Animal / drug therapy
Helminthiasis, Animal / diagnosis
Helminthiasis, Animal / parasitology
Horse Diseases / epidemiology
Horse Diseases / parasitology
Horse Diseases / drug therapy
Horse Diseases / diagnosis
Intestinal Diseases, Parasitic / veterinary
Intestinal Diseases, Parasitic / epidemiology
Intestinal Diseases, Parasitic / drug therapy
Intestinal Diseases, Parasitic / diagnosis
Intestinal Diseases, Parasitic / parasitology
Australia / epidemiology
Helminths / drug effects
Helminths / isolation & purification
Drug Resistance
Asia / epidemiology
New Zealand / epidemiology
Prevalence
Conflict of Interest Statement
Declaration of competing interests The authors of this manuscript are members of the Australian Equine Parasitology Advisory Panel (AEPAP), including Abdul Jabbar, Ghazanfar Abbas, Jenni Bauquier, Charles El-Hage, Abdul Ghafar and Ian Beveridge (The University of Melbourne), Anne Beasley (University of Queensland), Kristopher Hughes (Charles Sturt University), Caroline Jacobson (Murdoch University), Edwina Wilkes (Racing Victoria), and Peter Carrigan and Lucy Cudmore (Scone Equine Hospital). Boehringer Ingelheim supported the panel. The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work or views reported in this paper.
Abbas G, Ghafar A, Bauquier J, Beasley A, Ling E, Gauci CG, El-Hage C, Wilkes EJA, McConnell E, Carrigan P, Cudmore L, Hurley J, Beveridge I, Nielsen MK, Stevenson MA, Jacobson C, Hughes KJ, Jabbar A. Prevalence and diversity of ascarid and strongylid nematodes in Australian thoroughbred horses using next-generation sequencing and bioinformatics tools.. Vet. Parasitol. 2023;323.
Abbas G, Ghafar A, McConnell E, Beasley A, Bauquier J, Wilkes EJA, El-Hage C, Carrigan P, Cudmore L, Hurley J, Gauci CG, Beveridge I, Ling E, Jacobson C, Stevenson M, Nielsen MK, Hughes K, Jabbar A. A national survey of anthelmintic resistance in ascarid and strongylid nematodes in Australian thoroughbred horses.. Int. J. Parasitol. Drugs Drug Resist. 2024;24.
Beasley AM, Kotze AC, Barnes TS, Coleman GT. Equine helminth prevalence and management practices on Australian properties as shown by coprological survey and written questionnaire.. Anim. Prod. Sci. 2020;60:2131–2144.
Drogemüller M., Beelitz P., Pfister K., Schieder T., Samson-Himmelstjerna G.v.. Amplification of ribosomal DNA of Anoplocephalidae: Anoplocephala perfoliata diagnosis by PCR as a possible alternative to coprological methods. Vet. Parasitol. 2005;124:205–215.
Duan H., Gao J.F., Su X., Fu X., Yue D.M., Gao Y., Qiu J.H., Wang C.R.. Genetic variation between and within Triodontophorus brevicauda and Triodontophorus nipponicus revealed by analyses of mtDNA and rDNA gene. Mitochondrial DNA PART A, DNA Mapp Seq Anal. 2017;28:570–574.
Elghryani N., Crispell J., Ebrahimi R., Krivoruchko M., Lobaskin V., McOwan T., O'Connor W., Power E., Voisin B., Scholtz D., De Waal T.. Preliminary evaluation of a novel, fully automated, telenostic device for rapid field-diagnosis of cattle parasites. Parasitology 2020;147:1249–1253.
English A.W.. Effects of dung beetles (Coleoptera Scarabaeinae) on the free-living stages of strongylid nematodes of the horse. Aust. Vet. J. 1979;55:315–321.
Finnerty C.A., Bonometti S., Ripley N.E., Smith M.A., Nielsen M.K.. Evidence of tapeworm treatment failure in a Central Kentucky Thoroughbred farm. Equine Vet. Educ. 2024;36:579–585.
Forbes A.B., Scholtz C.H.. The impact of dung beetles on the free-living stages of ruminant parasites in faeces and their role as biological control agents in grazing livestock. Vet. Parasitol. 2024;331.
Gao Y, Qiu J-H, Zhang B-B, Su X, Fu X, Yue D-M, Wang C-R. Complete mitochondrial genome of parasitic nematode Cylicocyclus nassatus and comparative analyses with Cylicocyclus insigne.. Exp. Parasitol. 2017;172:18–22.
Gao Y, Qiu Y-Y, Meng X-Q, Yang X, Zhang Z-H, Diao Z-Y, Wang S, Wang C-R, Song M-X. Comparative analysis of mitochondrial DNA datasets indicates that Cylicostephanus minutus represents a species complex.. Infect. Genet. Evol. 2020;84.
Gao Y, Wang X-X, Ma X-X, Zhang Z-H, Lan Z, Qiu Y-Y, Wang S, Song M-X, Wang C-R. Characterization of the complete mitochondrial genomes of Coronocyclus labiatus and Cylicodontophorus bicoronatus: comparison with Strongylidae species and phylogenetic implication.. Vet. Parasitol. 2021;290.
Ghafar A, Abbas G, King J, Jacobson C, Hughes K.J, El-Hage C, Beasley A, Bauquier J, Wilkes E, Hurley J, Cudmore L, Carrigan P, Tennent-Brown B, Nielsen M.K, Gauci C.G, Beveridge I, Jabbar A. Comparative studies on faecal egg counting techniques used for the diagnosis of gastrointestinal parasites of equines: a systematic review.. Curr. Res. Parasitol. Vector-Borne Dis. 2021;1.
Han L, Lan T, Lu Y, Zhou M, Li H, Lu H, Wang Q, Li X, Du S, Guan C, Zhang Y, Sahu S.K., Qian P, Zhang S, Zhou H, Guo W, Chai H, Wang S, Liu Q, Liu H, Hou Z. Equus roundworms (Parascaris univalens) are undergoing rapid divergence while genes involved in metabolic as well as anthelmintic resistance are under positive selection.. BMC Genom. 2022;23:489.
Hansen E.P., Fromm B, Andersen S.D., Marcilla A, Andersen K.L., Borup A, Williams A.R., Jex A.R., Gasser R.B., Young N.D.. Exploration of extracellular vesicles from Ascaris suum provides evidence of parasite–host cross talk.. J. Extracell. Vesicles. 2019;8.
Lyons E, Tolliver S. Strongyloides westeri and Parascaris equorum: observations in field studies in Thoroughbred foals on some farms in Central Kentucky, USA.. Helminthologia. 2014;51:7–12.
Martin F, Halvarsson P, Delhomme N, Höglund J, Tydén E. Exploring the β-tubulin gene family in a benzimidazole-resistant Parascaris univalens population.. Int. J. Parasitol. Drugs Drug Resist. 2021;17:84–91.
McEvoy A, O'Boyle P, Ellis S, Dalton J.P., Parkinson M, Keane O.M., Machin C. Comparison of traditional copromicroscopy with image analysis devices for detection of gastrointestinal nematode infection in sheep.. Vet. Parasitol. 2024;329.
Mfitilodze M.W., Hutchinson G.W.. Development of free-living stages of equine strongyles in feces on pasture in a tropical environment.. Vet. Parasitol. 1988;26:285–296.
Mohanty M.C., Sahoo P.K., Satapathy A.K., Ravindra B. Setaria digitata infections in cattle: parasite load, microfilaraemia status and relationship to immune response.. J. Helminthol. 2000;74:343–347.
Nagamori Y, Sedlak R.H., DeRosa A, Pullins A, Cree T, Loenser M, Larson B.S., Smith R.B., Goldstein R. Evaluation of the VETSCAN IMAGYST: an in-clinic canine and feline fecal parasite detection system integrated with a deep learning algorithm.. Parasites Vectors. 2020;13:346.
Nielsen M.K., Wang J., Davis R., Bellaw J.L., Lyons E.T., Lear T.L., Goday C. Parascaris univalens – a victim of large-scale misidentification?. Parasitol. Res. 2014;113:4485–4490.
Nielsen M.K., Kaplan R.M., Abbas G., Jabbar A.. Biological implications of long-term anthelmintic treatment: what else besides resistance are we selecting for?. Trends Parasitol. 2023;39:945–953.
Northcote H.M., Wititkornkul B., Cutress D.J., Allen N.R., Brophy P.M., Wonfor R.E., Morphew R.M.. A dominance of Mu class glutathione transferases within the equine tapeworm Anoplocephala perfoliata.. Parasitology 2024;151:282–294.
Qiu Y.Y., Zeng M.H., Diao P.W., Wang X.X., Li Q., Li Y., Gao Y., Wang C.R.. Comparative analyses of the complete mitochondrial genomes of Cyathostomum pateratum and Cyathostomum catinatum provide new molecular data for the evolution of Cyathostominae nematodes.. J. Helminthol. 2018;93:643–647.
Tydén E., Enemark H.L., Franko M.A., Höglund J., Osterman-Lind E.. Prevalence of Strongylus vulgaris in horses after ten years of prescription usage of anthelmintics in Sweden.. Vet. Parasitol. 2019;X 2.
Xu W.-W., Qiu J.-H., Liu G.-H., Zhang Y., Liu Z.-X., Duan H., Yue D.-M.-, Chang Q.-C., Wang C.-R., Zhao X.-C.. The complete mitochondrial genome of Strongylus equinus (Chromadorea: strongylidae): Comparison with other closely related species and phylogenetic analyses.. Exp. Parasitol. 2015;159:94–99.
Zakeri A., Whitehead B.J., Stensballe A., de Korne C., Williams A.R., Everts B., Nejsum P.. Parasite worm antigens instruct macrophages to release immunoregulatory extracellular vesicles.. J. Extracell. Vesicles. 2021;10.