Characteristics of parasitic egg shedding over a 1-year period in foals and their dams in 2 farms in central Saskatchewan.
Abstract: The goals of this study were to report the seasonal shedding patterns of strongyle and spp. eggs in repeated fecal samples for mares ( = 38) and foals ( = 39), and to evaluate the efficacy of ivermectin treatment in mares from 2 selected horse breeding farms in central Saskatchewan. Median strongyle fecal egg counts (FEC) peaked in July and August in adult horses. The farms differed significantly ( = 0.0005) in regard to strongyle shedding categories ( 500 eggs/g) over time, but for each individual horse (both farms combined) these categories did not differ over time ( = 0.13) on samples collected in grazing season. When evaluating 3 samples collected fall, summer and fall in 2 consecutive grazing seasons, 94% of horses that shed < 200 eggs/g on 2 initial samples, remained in the same category on the third sample. Mares on each farm didn't differ statistically in shedding categories when comparing September samples from 2 consecutive years (Farm A: = 0.56, Farm B: = 0.06). Peak strongyle shedding occurred late fall in the first year of life for foals on Farm A, and in July in the second year of life for foals on Farm B. spp. FEC were greatest in foals ≤ 6 months of age, with peak observed when foals were 5 to 6 months old. Ivermectin was 100% effective at reducing strongyle FEC 2 weeks after treatment in adult horses. Horses in Saskatchewan had relatively high strongyle shedding levels, which were significantly different between the farms, and high prevalence of Strongyle shedding consistency was observed for FECs collected from mares in grazing season (July to September). . Cette étude avait pour but de dresser un rapport sur les tendances d’excrétion saisonnière des oeufs des strongyles et de spp. dans des prélèvements fécaux répétés pour les juments ( = 38) et les poulains ( = 39) et d’évaluer l’efficacité du traitement à l’ivermectine chez deux juments provenant de deux fermes d’élevage de chevaux dans le centre de la Saskatchewan. Les comptes médians d’oeufs fécaux des strongyles ont culminé en juillet et en août chez les chevaux adultes. Les fermes présentaient des différences significatives ( = 0,0005) à l’égard des catégories d’excrétion des strongyles ( 500 oeufs/g) dans le temps, mais, pour chaque cheval individuel (les deux fermes combinées), ces catégories ne présentaient pas de différences à la longue ( = 0,13) pour les échantillons prélevés durant la saison de pâturage. Lors de l’évaluation des reois échantillons prélevés à l’automne, à l’été et à l’automne pendant deux saisons de pâturage consécutives, 94 % des chevaux qui avaient excrété < 200 oeufs/g pour deux prélèvements initiaux, sont demeurés dans la même catégorie pour le troisième échantillon. Les juments de chaque ferme ne présentaient pas de différences statistiques pour les catégories d’excrétion lorsque l’on comparait les échantillons de septembre provenant de deux années consécutives (Ferme A : = 0,56, Ferme B : = 0,06). L’excrétion des strongyles a culminé à la fin de l’automne pendant la première année de vie pour les poulains de la Ferme A et en juillet de la deuxième année de vie pour les poulains de la Ferme B. Les comptes d’oeufs fécaux de spp. étaient les plus importants chez les poulains âgés de ≤ 6 mois et le point culminant était observé lorsque les poulains étaient âgés de 5 ou 6 mois. L’ivermectine était efficace à 100 % pour réduire les comptes d’oeufs fécaux 2 semaines après le traitement chez les chevaux adultes. Les chevaux de la Saskatchewan ont présenté des taux d’excrétion relativement élevés de strongyles, qui étaient significativement différents entre les fermes, et une forte prévalence d’ La constance de l’excrétion des strongyles a été observée pour les comptes d’oeufs fécaux obtenus auprès des juments pendant la saison de pâturage (de juillet à septembre).(Traduit par Isabelle Vallières).
Publication Date: 2018-03-31 PubMed ID: 29599559PubMed Central: PMC5819021
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- Journal Article
- Multicenter Study
Summary
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The research focuses on studying the patterns of parasitic egg shedding in foals and mares over a year at two horse breeding farms in Central Saskatchewan. It also evaluates the effectiveness of ivermectin treatment in controlling the shedding.
Research Objectives and Methodology
- The study aims to document the seasonal shedding patterns of strongyle and spp. eggs in the feces of mares and foals. The sample consisted of 38 mares and 39 foals from two selected horse breeding farms in central Saskatchewan.
- The study monitored the fecal egg counts (FEC) of strongyles, which peaked in July and August for adult horses. It evaluated differences in strongyle shedding categories (less than 200; 200 to 500; and more than 500 eggs per gram) over time.
- The study also aimed to evaluate the efficacy of ivermectin treatment, a commonly used antiparasitic medication in horses, by observing if it reduced FEC two weeks after its administration.
Research Findings
- The study findings revealed significant differences in strongyle shedding categories between the two farms. However, the shedding categories for each individual horse across both farms did not display significant alterations over time during the grazing season.
- Out of the horses that shed less than 200 eggs per gram in the first two samples, 94% stayed within the same category in the third sample.
- Comparisons of September samples from two consecutive years did not show a statistical difference in the shedding categories amongst mares in each farm.
- The study noted peak strongyle shedding occurred in the late fall during the first year for foals on one farm, and in July during the second year of life for foals on the other farm.
- Foals aged 6 months or less had the highest FEC of spp., peaking when the foals were 5 to 6 months old.
- The ivermectin treatment was found to be 100% effective at reducing strongyle FEC in adult horses two weeks after treatment.
Implications of the Study
- Horses in Saskatchewan demonstrated relatively high strongyle shedding levels which were notably different across the two farms and showed a high prevalence of spp. However, there was a consistent pattern of strongyle shedding for FECs collected from mares during the grazing season (July to September), suggesting a predictable pattern to their shedding.
- This study plays a fundamental role in understanding the parasitic behavior in foals and adult horses. Such information can aid in developing efficient treatment protocols and preventative parasitic management on farms.
Cite This Article
APA
Misuno E, Clark CR, Anderson SL, Jenkins E, Wagner B, Dembek K, Petrie L.
(2018).
Characteristics of parasitic egg shedding over a 1-year period in foals and their dams in 2 farms in central Saskatchewan.
Can Vet J, 59(3), 284-292.
Publication
Researcher Affiliations
- Department of Large Animal Clinical Sciences (Misuno, Clark, Petrie), Department of Veterinary Microbiology (Jenkins, Wagner), University of Saskatchewan, Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4; Lincoln Memorial University, College of Veterinary Medicine, 6965 Cumberland Gap Parkway, Harrogate, Tennessee 37752, USA (Anderson); Iowa State University, College of Veterinary Medicine, 2503 Vet Med, 1600 S 16th Street, Ames, Iowa 50011, USA (Dembek).
- Department of Large Animal Clinical Sciences (Misuno, Clark, Petrie), Department of Veterinary Microbiology (Jenkins, Wagner), University of Saskatchewan, Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4; Lincoln Memorial University, College of Veterinary Medicine, 6965 Cumberland Gap Parkway, Harrogate, Tennessee 37752, USA (Anderson); Iowa State University, College of Veterinary Medicine, 2503 Vet Med, 1600 S 16th Street, Ames, Iowa 50011, USA (Dembek).
- Department of Large Animal Clinical Sciences (Misuno, Clark, Petrie), Department of Veterinary Microbiology (Jenkins, Wagner), University of Saskatchewan, Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4; Lincoln Memorial University, College of Veterinary Medicine, 6965 Cumberland Gap Parkway, Harrogate, Tennessee 37752, USA (Anderson); Iowa State University, College of Veterinary Medicine, 2503 Vet Med, 1600 S 16th Street, Ames, Iowa 50011, USA (Dembek).
- Department of Large Animal Clinical Sciences (Misuno, Clark, Petrie), Department of Veterinary Microbiology (Jenkins, Wagner), University of Saskatchewan, Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4; Lincoln Memorial University, College of Veterinary Medicine, 6965 Cumberland Gap Parkway, Harrogate, Tennessee 37752, USA (Anderson); Iowa State University, College of Veterinary Medicine, 2503 Vet Med, 1600 S 16th Street, Ames, Iowa 50011, USA (Dembek).
- Department of Large Animal Clinical Sciences (Misuno, Clark, Petrie), Department of Veterinary Microbiology (Jenkins, Wagner), University of Saskatchewan, Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4; Lincoln Memorial University, College of Veterinary Medicine, 6965 Cumberland Gap Parkway, Harrogate, Tennessee 37752, USA (Anderson); Iowa State University, College of Veterinary Medicine, 2503 Vet Med, 1600 S 16th Street, Ames, Iowa 50011, USA (Dembek).
- Department of Large Animal Clinical Sciences (Misuno, Clark, Petrie), Department of Veterinary Microbiology (Jenkins, Wagner), University of Saskatchewan, Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4; Lincoln Memorial University, College of Veterinary Medicine, 6965 Cumberland Gap Parkway, Harrogate, Tennessee 37752, USA (Anderson); Iowa State University, College of Veterinary Medicine, 2503 Vet Med, 1600 S 16th Street, Ames, Iowa 50011, USA (Dembek).
- Department of Large Animal Clinical Sciences (Misuno, Clark, Petrie), Department of Veterinary Microbiology (Jenkins, Wagner), University of Saskatchewan, Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4; Lincoln Memorial University, College of Veterinary Medicine, 6965 Cumberland Gap Parkway, Harrogate, Tennessee 37752, USA (Anderson); Iowa State University, College of Veterinary Medicine, 2503 Vet Med, 1600 S 16th Street, Ames, Iowa 50011, USA (Dembek).
MeSH Terms
- Animal Husbandry
- Animals
- Animals, Newborn
- Anthelmintics / administration & dosage
- Anthelmintics / therapeutic use
- Antiparasitic Agents / therapeutic use
- Ascaridida Infections / drug therapy
- Ascaridida Infections / veterinary
- Ascaridoidea / isolation & purification
- Ascaridoidea / pathogenicity
- Farms
- Feces / parasitology
- Female
- Horse Diseases / drug therapy
- Horse Diseases / parasitology
- Horses
- Ivermectin / therapeutic use
- Male
- Parasite Egg Count / veterinary
- Saskatchewan
- Seasons
References
This article includes 37 references
- American Association of Equine Practitioners [ www.aaep.org] c2016. Available from: http://www.aaep.org/custdocs/AAEPParasiteControlGuidelines.pdf.
- Kaplan RM. Anthelmintic resistance in nematodes of horses.. Vet Res 2002 Sep-Oct;33(5):491-507.
- Molento MB, Nielsen MK, Kaplan RM. Resistance to avermectin/milbemycin anthelmintics in equine cyathostomins - current situation.. Vet Parasitol 2012 Apr 19;185(1):16-24.
- Lyons ET, Tolliver SC, Ionita M, Lewellen A, Collins SS. Field studies indicating reduced activity of ivermectin on small strongyles in horses on a farm in Central Kentucky.. Parasitol Res 2008 Jun;103(1):209-15.
- Kaplan RM, Klei TR, Lyons ET, Lester G, Courtney CH, French DD, Tolliver SC, Vidyashankar AN, Zhao Y. Prevalence of anthelmintic resistant cyathostomes on horse farms.. J Am Vet Med Assoc 2004 Sep 15;225(6):903-10.
- Slocombe JO, de Gannes RV. Cyathostomes in horses in Canada resistant to pyrantel salts and effectively removed by moxidectin.. Vet Parasitol 2006 Aug 31;140(1-2):181-4.
- Slocombe JO, Coté JF, de Gannes RV. The persistence of benzimidazole-resistant cyathostomes on horse farms in Ontario over 10 years and the effectiveness of ivermectin and moxidectin against these resistant strains.. Can Vet J 2008 Jan;49(1):56-60.
- Molento MB, Antunes J, Bentes RN, Coles GC. Anthelmintic resistant nematodes in Brazilian horses.. Vet Rec 2008 Mar 22;162(12):384-5.
- Lyons ET, Tolliver SC, Ionita M, Collins SS. Evaluation of parasiticidal activity of fenbendazole, ivermectin, oxibendazole, and pyrantel pamoate in horse foals with emphasis on ascarids (Parascaris equorum) in field studies on five farms in Central Kentucky in 2007.. Parasitol Res 2008 Jul;103(2):287-91.
- Larsen ML, Ritz C, Petersen SL, Nielsen MK. Determination of ivermectin efficacy against cyathostomins and Parascaris equorum on horse farms using selective therapy.. Vet J 2011 Apr;188(1):44-7.
- von Samson-Himmelstjerna G, Fritzen B, Demeler J, Schürmann S, Rohn K, Schnieder T, Epe C. Cases of reduced cyathostomin egg-reappearance period and failure of Parascaris equorum egg count reduction following ivermectin treatment as well as survey on pyrantel efficacy on German horse farms.. Vet Parasitol 2007 Mar 15;144(1-2):74-80.
- Reinemeyer CR. Diagnosis and control of anthelmintic-resistant Parascaris equorum.. Parasit Vectors 2009 Sep 25;2 Suppl 2(Suppl 2):S8.
- Nielsen MK, Fritzen B, Duncan JL, Guillot J, Eysker M, Dorchies P, Laugier C, Beugnet F, Meana A, Lussot-Kervern I, von Samson-Himmelstjerna G. Practical aspects of equine parasite control: a review based upon a workshop discussion consensus.. Equine Vet J 2010 Jul;42(5):460-8.
- Nielsen MK, Reist M, Kaplan RM, Pfister K, van Doorn DC, Becher A. Equine parasite control under prescription-only conditions in Denmark--awareness, knowledge, perception, and strategies applied.. Vet Parasitol 2014 Jul 30;204(1-2):64-72.
- von Samson-Himmelstjerna G, Traversa D, Demeler J, Rohn K, Milillo P, Schurmann S, Lia R, Perrucci S, di Regalbono AF, Beraldo P, Barnes H, Cobb R, Boeckh A. Effects of worm control practices examined by a combined faecal egg count and questionnaire survey on horse farms in Germany, Italy and the UK.. Parasit Vectors 2009 Sep 25;2 Suppl 2(Suppl 2):S3.
- Nielsen MK, Baptiste KE, Tolliver SC, Collins SS, Lyons ET. Analysis of multiyear studies in horses in Kentucky to ascertain whether counts of eggs and larvae per gram of feces are reliable indicators of numbers of strongyles and ascarids present.. Vet Parasitol 2010 Nov 24;174(1-2):77-84.
- Swiderski C, French DD. Paradigms for parasite control in adult horse populations: A review. Proc American Association of Equine Practitioners San Diego, California. December 6–10, 2008; pp. 316–321.
- Dobson RJ, Hosking BC, Jacobson CL, Cotter JL, Besier RB, Stein PA, Reid SA. Preserving new anthelmintics: a simple method for estimating faecal egg count reduction test (FECRT) confidence limits when efficacy and/or nematode aggregation is high.. Vet Parasitol 2012 May 4;186(1-2):79-92.
- Waghorn TS, Leathwick DM, Miller CM, Atkinson DS. Brave or gullible: testing the concept that leaving susceptible parasites in refugia will slow the development of anthelmintic resistance.. N Z Vet J 2008 Aug;56(4):158-63.
- Kaplan RM, Nielsen MK. An evidence-based approach to equine parasite control: It ain’t the 60s anymore. Equine Vet Educ 2010;22:306–316.
- Döpfer D, Kerssens CM, Meijer YG, Boersema JH, Eysker M. Shedding consistency of strongyle-type eggs in Dutch boarding horses.. Vet Parasitol 2004 Oct 5;124(3-4):249-58.
- Nielsen MK, Haaning N, Olsen SN. Strongyle egg shedding consistency in horses on farms using selective therapy in Denmark.. Vet Parasitol 2006 Feb 18;135(3-4):333-5.
- Becher AM, Mahling M, Nielsen MK, Pfister K. Selective anthelmintic therapy of horses in the Federal states of Bavaria (Germany) and Salzburg (Austria): an investigation into strongyle egg shedding consistency.. Vet Parasitol 2010 Jul 15;171(1-2):116-22.
- Scheuerle MC, Stear MJ, Honeder A, Becher AM, Pfister K. Repeatability of strongyle egg counts in naturally infected horses.. Vet Parasitol 2016 Sep 15;228:103-107.
- Polley L. Strongylid parasites of horses: experimental ecology of the free-living stages on the Canadian prairie.. Am J Vet Res 1986 Aug;47(8):1686-93.
- Nielsen MK, Kaplan RM, Thamsborg SM, Monrad J, Olsen SN. Climatic influences on development and survival of free-living stages of equine strongyles: implications for worm control strategies and managing anthelmintic resistance.. Vet J 2007 Jul;174(1):23-32.
- COX DD, TODD AC. Survey of gastrointestinal parasitism in Wisconsin dairy cattle.. J Am Vet Med Assoc 1962 Sep 15;141:706-9.
- Kyvsgaard NC, Lindbom J, Andreasen LL, Luna-Olivares LA, Nielsen MK, Monrad J. Prevalence of strongyles and efficacy of fenbendazole and ivermectin in working horses in El Sauce, Nicaragua.. Vet Parasitol 2011 Sep 27;181(2-4):248-54.
- Larsen MM, Lendal S, Chriél M, Olsen SN, Bjørn H. Risk factors for high endoparasitic burden and the efficiency of a single anthelmintic treatment of Danish horses.. Acta Vet Scand 2002;43(2):99-106.
- Klei TR, Chapman MR. Immunity in equine cyathostome infections.. Vet Parasitol 1999 Aug 31;85(2-3):123-33; discussion 133-6, 215-25.
- Vidyashankar AN, Hanlon BM, Kaplan RM. Statistical and biological considerations in evaluating drug efficacy in equine strongyle parasites using fecal egg count data.. Vet Parasitol 2012 Apr 19;185(1):45-56.
- Corbett CJ, Love S, Moore A, Burden FA, Matthews JB, Denwood MJ. The effectiveness of faecal removal methods of pasture management to control the cyathostomin burden of donkeys.. Parasit Vectors 2014 Jan 24;7:48.
- Reavell DG. Measuring and estimating the weight of horses with tapes, formulae and by visual assessment. Equine Vet Educ 1999;11:314–317.
- Wagner EL, Tyler PJ. A comparison of weight estimation methods in adult horses. J Equine Vet Sc 2011;31:706–710.
- Nielsen MK, Wang J, Davis R, Bellaw JL, Lyons ET, Lear TL, Goday C. Parascaris univalens--a victim of large-scale misidentification?. Parasitol Res 2014 Dec;113(12):4485-90.
- Reinemeyer CR, Nielsen MK. Review of the biology and control of Oxyuris equi. Equine Vet Educ 2014;26:584–591.
- Elsener J, Villeneuve A. Does examination of fecal samples 24 hours after cestocide treatment increase the sensitivity of Anoplocephala spp. detection in naturally infected horses?. Can Vet J 2011 Feb;52(2):158-61.
Citations
This article has been cited 3 times.- Özben M, von Samson-Himmelstjerna G, Freiin von Streit MKB, Wilkes EJA, Hughes KJ, Krücken J. Absence of Polymorphisms in Codons 167, 198 and 200 of All Seven β-Tubulin Isotypes of Benzimidazole Susceptible and Resistant Parascaris spp. Specimens from Australia.. Pathogens 2022 Apr 20;11(5).
- Jenkins E, Backwell AL, Bellaw J, Colpitts J, Liboiron A, McRuer D, Medill S, Parker S, Shury T, Smith M, Tschritter C, Wagner B, Poissant J, McLoughlin P. Not playing by the rules: Unusual patterns in the epidemiology of parasites in a natural population of feral horses (Equus caballus) on Sable Island, Canada.. Int J Parasitol Parasites Wildl 2020 Apr;11:183-190.
- Harvey AM, Meggiolaro MN, Hall E, Watts ET, Ramp D, Šlapeta J. Wild horse populations in south-east Australia have a high prevalence of Strongylus vulgaris and may act as a reservoir of infection for domestic horses.. Int J Parasitol Parasites Wildl 2019 Apr;8:156-163.
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