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BMC veterinary research2025; 22(1); 30; doi: 10.1186/s12917-025-05226-5

Potassium carbonate as an alternative solution for detecting Anoplocephalid eggs in horse faecal samples.

Abstract: Anoplocephalid species are responsible for causing tapeworm infection in horses. The disease may cause serious health issues, including discomfort, colic, and even intestinal perforation and death. A study was carried out to compare the detection rates of tapeworm eggs in naturally infected horses using two different examination solutions. For this purpose, faecal samples of 241 horses were examined with a combined sedimentation + centrifugation + flotation technique using saturated sugar solution (specific gravity (SG) = 1.30) as the basis and potassium carbonate (KCO) solution (SG = 1.45). Tapeworm eggs were detected in 43 samples in saturated sugar solution and 59 samples in potassium carbonate solution ( < 0.05), whereas 42 samples were detected egg-positive in either. The potassium carbonate solution detected significantly more positive samples than the saturated sugar solution ( < 0.05). According to the results, potassium carbonate, as a non-toxic and high-density solution, can be a feasible alternative for detecting tapeworm eggs in horses.
Publication Date: 2025-12-22 PubMed ID: 41430231PubMed Central: PMC12817757DOI: 10.1186/s12917-025-05226-5Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study evaluates the use of potassium carbonate solution to detect tapeworm eggs in horse feces and compares its efficacy to that of a traditional saturated sugar solution.
  • The results suggest that potassium carbonate is more effective for detecting infections caused by Anoplocephalid tapeworms in horses.

Background

  • Anoplocephalid species are tapeworms that infect horses, causing health problems like discomfort, colic, intestinal perforation, and even death.
  • Detecting the presence of tapeworm eggs in horse feces is important for diagnosing tapeworm infections.
  • Traditional methods use solutions like saturated sugar for egg flotation during microscopic examination of fecal samples.

Objective of the Study

  • To compare the effectiveness of potassium carbonate (KCO) solution versus saturated sugar solution in detecting Anoplocephalid eggs in horse feces.
  • Both solutions were used in a combined sedimentation, centrifugation, and flotation protocol.

Methodology

  • Samples: Fecal samples were collected from 241 naturally infected horses.
  • Solutions tested:
    • Saturated sugar solution with a specific gravity (SG) of 1.30 (traditional method).
    • Potassium carbonate solution with a higher specific gravity (SG) of 1.45 (alternative method).
  • Procedure: Both solutions were used with a combined sedimentation, centrifugation, and flotation technique to concentrate and detect tapeworm eggs under the microscope.

Results

  • Detection in saturated sugar solution: 43 positive samples.
  • Detection in potassium carbonate solution: 59 positive samples.
  • Both solutions detected eggs in 42 of the same samples.
  • Significant difference in detection rates (p-value < 0.05), indicating potassium carbonate detected more positive samples.

Interpretation of Results

  • The higher specific gravity of potassium carbonate solution likely helps in better flotation and recovery of tapeworm eggs.
  • Potassium carbonate solution’s non-toxic nature makes it a safer alternative compared to many other flotation solutions.
  • Increased detection rates may improve diagnostic accuracy and subsequently better treatment planning for horses infected with tapeworms.

Conclusions

  • Potassium carbonate solution is a viable alternative to saturated sugar solution for the detection of Anoplocephalid eggs in horse feces.
  • Its higher density and safety profile contribute to improved detection rates.
  • This method can potentially lead to better management and control of tapeworm infections in horses.

Cite This Article

APA
Girisgin O, Gülegen E, Girisgin AO, Cirak VY. (2025). Potassium carbonate as an alternative solution for detecting Anoplocephalid eggs in horse faecal samples. BMC Vet Res, 22(1), 30. https://doi.org/10.1186/s12917-025-05226-5

Publication

ISSN: 1746-6148
NlmUniqueID: 101249759
Country: England
Language: English
Volume: 22
Issue: 1
Pages: 30
PII: 30

Researcher Affiliations

Girisgin, Oya
  • Karacabey Vocational School, Bursa Uludag University, Bursa, Türkiye.
Gülegen, Ender
  • Faculty of Veterinary Medicine, Department of Parasitology, Bursa Uludag University, Bursa, Türkiye.
Girisgin, Ahmet Onur
  • Faculty of Veterinary Medicine, Department of Parasitology, Bursa Uludag University, Bursa, Türkiye. aogirisgin@uludag.edu.tr.
Cirak, Veli Yilgor
  • Faculty of Veterinary Medicine, Department of Parasitology, Bursa Uludag University, Bursa, Türkiye.

Conflict of Interest Statement

Declarations. Ethics approval and consent to participate: The study involved non-invasive faecal sampling from horses. According to Regulation on the Working Procedures and Principles of the Animal Experiments Ethics Committees of the Animal Protection Law No. 5199-Article 8/K of the Turkish Ministry of Agriculture and Forestry, ethics committee approval was not required for this type of research. Permission to collect samples was obtained from the farm owners prior to sampling. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.

References

This article includes 33 references
  1. Nielsen MK. Equine tapeworm infections: Disease, diagnosis and control.. Equine Vet Educ 2016;28:388–95.
    doi: 10.1111/eve.12394google scholar: lookup
  2. Ryu SH, Bak UB, Kim JG, Yoon HJ, Seo HS, Kim JT. Cecal rupture by infection in a thoroughbred horse in Seoul race Park, South Korea.. J Vet Sci 2001;2(3):189–93.
    doi: 10.4142/jvs.2001.2.3.189pubmed: 12441687google scholar: lookup
  3. Pavone S, Veronesi F, Genchi C, Fioretti DP, Brianti E, Mandaraa MT. Pathological changes caused by in the mucosa/submucosa and in the enteric nervous system of equine ileocecal junction.. Vet Parasitol 2011;176:43–52.
    doi: 10.1016/j.vetpar.2010.10.041pubmed: 21075534google scholar: lookup
  4. Back H, Nyman A, Osterman LE. The association between and colic in Swedish horses-a case control study.. Vet Parasitol 2013;197(3–4):580–5.
    doi: 10.1016/j.vetpar.2013.07.020pubmed: 23993633google scholar: lookup
  5. Proudman CJ, Edwards GB. Validation of centrifugation/flotation technique for the diagnosis of equine cestodiasis.. Vet Rec 1992;131:71–2.
    doi: 10.1136/vr.131.4.71pubmed: 1529504google scholar: lookup
  6. Rehbein S, Lindner T, Visser M, Winter R. Evaluation of a double centrifugation technique for the detection of eggs in horse faeces.. J Helminthol 2011;85:409–14.
    doi: 10.1017/S0022149X10000751pubmed: 21138608google scholar: lookup
  7. Tomczuk K, Kostro K, Szczepaniak KO, Grzybek M, Studzińska M, Demkowska-Kutrzepa M, Roczeń-Karczmarz M. Comparison of the sensitivity of coprological methods in detecting invasions.. Parasitol Res 2014;113(6):2401–6.
    doi: 10.1007/s00436-014-3919-4pmc: PMC4031382pubmed: 24777342google scholar: lookup
  8. Höglund J, Ljungström BL, Nilsson O, Uggla A. Enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies to in horse Sera.. Vet Parasitol 1995;59:97–106.
    doi: 10.1016/0304-4017(94)00755-2pubmed: 7483241google scholar: lookup
  9. Kania SA, Reinemeyer CR. Coproantigen detection: a preliminary study.. Vet Parasitol 2005;127:115–9.
    doi: 10.1016/j.vetpar.2004.10.003pubmed: 15631904google scholar: lookup
  10. Bohórquez GA, Luzón M, Martín-Hernández R, Meana A. New multiplex PCR method for the simultaneous diagnosis of the three known species of equine tapeworm.. Vet Parasitol 2015;207(1–2):56–63.
    doi: 10.1016/j.vetpar.2014.11.002pubmed: 25498328google scholar: lookup
  11. Lightbody KL, Matthews JB, Kemp-Symonds JG, Lambert PA, Austin CJ. Use of a saliva-based diagnostic test to identify tapeworm infection in horses in the UK.. Equine Vet J 2018;50(2):213–9.
    doi: 10.1111/evj.12742pubmed: 28805265google scholar: lookup
  12. Matthews JB, Peczak N, Lightbody KL. The use of innovative diagnostics to inform sustainable control of equine helminth infections.. Pathogens 2023;12(10):1233.
    doi: 10.3390/pathogens12101233pmc: PMC10610145pubmed: 37887749google scholar: lookup
  13. Beroza GA, Marcus LC, Williams R, Bauer SM. Laboratory diagnosis of infection in horses.. Proc Am Assoc Equine Pract 1986;32:435–9.
  14. Meana A, Luzon M, Corchero J, Bautista MG. Reliability of coprological diagnosis of infection.. Vet Parasitol 1998;74:79–83.
    doi: 10.1016/S0304-4017(97)00145-3pubmed: 9493312google scholar: lookup
  15. Öge S. Quantitative comparison of various methods and solutions for detecting eggs of in horse faeces.. Ankara Univ Vet Fak Derg 2003;50:119–22.
    doi: 10.1501/Vetfak_0000002239google scholar: lookup
  16. Joye IJ. Acids and bases in food. Encyclopedia of Food Chemistry Holland: Elsevier; page: 2019. pp. 1–9.
  17. FokE, Takats C, Smidova B, Kecskemethy S, Karakas M. Prevalence of intestinal helminthoses in dogs and cats. Parasitol Hung 1988;21:53–69.
  18. Rehbein S, Kokott S, Lindner T. Evaluation of techniques for the enumeration of dicrocoelium eggs in sheep faeces. J Vet Med A 1999;46(3):133–40.
  19. Gohla J, Bračun S, Gretschel G, Koblmüller S, Wagner M, Pacher C. Potassium carbonate (K2CO3)-A cheap, non-toxic and high-density floating solution for microplastic isolation from beach sediments. Mar Pollut Bull 2021;170:112618.
  20. Minitab Inc. Statistical Software. Minitab 15 State College, PA, USA, 2007.
  21. Tınar R, Coşkun ŞZ, Aydın L, Çırak VY, Demirel M. Parasites obtained from horses of bursa. Uludag Univ Vet Fak Derg 1994;13:11–6.
  22. Çırak VY, Güleğen E, Girişgin O, Bakırcı S, Kütükoğlu F. Occurrence of (Abildgaard, 1789) in two horses. T Parazitol Derg 2004;28(2):94–5.
  23. Ghafar A, Abbas G, Beasley A, Bauquier J, Wilkes EJA, Jacobson C. Molecular diagnostics for Gastrointestinal helminths in equids: Past, present and future. Vet Parasitol 2023;313:109851.
    doi: 10.1016/j.vetpar.2022.109851pubmed: 36521296google scholar: lookup
  24. Buono F, Castaldo E, Veneziano V, Veronesi F, Roncoroni C, Scarcelli S, Sgroi G, Matthews JB, Piantedosi D. Equine tapeworm infections in italy: A nationwide coprological survey. Res Vet Sci 2025;188:105616.
    doi: 10.1016/j.rvsc.2025.105616pubmed: 40120390google scholar: lookup
  25. Hreinsdóttir I, Hreinsdóttir A, Eydal M, Tysnes KR, Robertson LJ. infection in horses in iceland: investigation of associations between intensity of infection and lesions. J Parasitol 2019;105:379–86.
    doi: 10.1645/18-159pubmed: 31038388google scholar: lookup
  26. Slocombe JOD. A modified critical test for the efficacy of pyrantel pamoate for in equids. Can J Vet Res 2004;68:112–7.
    pmc: PMC1142154pubmed: 15188955
  27. Anderson HC, Warner SF, Ripley NE, Nielsen MK. Performance of three techniques for diagnosing equine tapeworm infection. Vet Parasitol 2024.
    doi: 10.1016/j.vetpar.2024.110152pubmed: 38430622google scholar: lookup
  28. OʼGrady MR, Slocombe JO. An investigation of variables in a fecal flotation technique. Can J Comp Med 1980;44:148–57.
    pmc: PMC1320050pubmed: 7190861
  29. Norris JK, Steuer AE, Gravatte HS, Slusarewicz P, Bellaw JL, Scare JA, Nielsen MK. Determination of the specific gravity of eggs of equine strongylids, spp., and .. Vet Parasitol 2018;260:45–8.
    doi: 10.1016/j.vetpar.2018.08.004pubmed: 30197012google scholar: lookup
  30. Norris JK, Slusarewicz P, Nielsen MK. Pixel by pixel: real-time observation and quantification of passive flotation speeds of three common equine endoparasite egg types. Int J Parasitol 2019;49(11):885–92.
    doi: 10.1016/j.ijpara.2019.06.004pubmed: 31545964google scholar: lookup
  31. David ED, Lindquist WD. Determination of the specific gravity of certain helminth eggs using sucrose density gradient centrifugation. J Parasitol 1982;68(5):916–9.
    doi: 10.2307/3281005pubmed: 6890102google scholar: lookup
  32. Nielsen MK. Apparent treatment failure of praziquantel and pyrantel pamoate against anoplocephalid tapeworms. Int J Parasitol Drugs Drug Resist 2023;22:96–101.
  33. Finnerty CA, Bonometti S, Ripley NE, Smith MA, Nielsen MK. Evidence of tapeworm treatment failure on a central Kentucky thoroughbred farm. Equine Vet Educ 2024;36:579–85.
    doi: 10.1111/eve.139google scholar: lookup

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