Analyze Diet
Frontiers in veterinary science2025; 12; 1663577; doi: 10.3389/fvets.2025.1663577

Progress in serology and molecular biology of equine parasite diagnosis: sustainable control strategies.

Abstract: Internal parasitic infections are a persistent challenge for horse owners, in the absence of effective vaccines and the growing challenge of drug resistance, leading many researchers to view current control strategies as unsustainable. Despite slow progress over the past two decades, effective parasitic diagnosis remains crucial for controlling infections and preventing the growing issue of drug resistance. This review examines the research progress in serological and molecular biological diagnostic methods for major equine parasites. Currently, most diagnostic techniques are based on genes such as ITS1, ITS2, COI, and IGS, which have been applied to equine strongylids, including spp., spp., and spp. These methods are particularly suitable for large-scale epidemiological studies and rapid species identification. Although many diagnostic methods have been developed, most remain confined to laboratory research and have seldom been used for real-time field diagnostics. Future research should prioritize precise diagnostic methods and clinically applicable alternatives. Additionally, whole genome sequencing has been widely used in eukaryotes for population genetics and the development of diagnostic markers. However, comprehensive genomic data on parasitic species infecting equines is still limited. With the decrease in sequencing costs in the post-genomic era, a growing number of genome assemblies are expected to be released soon. These genome maps will offer comprehensive genomic data to identify specific genetic markers and variations associated with parasitic infections, enabling more accurate and reliable diagnostic techniques. High-throughput sequencing technologies will significantly accelerate progress in equine parasitology research and the development of diagnostic tools like enzyme-linked immunosorbent assay (ELISA) and TaqMan quantitative PCR (qPCR). At the same time, this paper also provides some insights into the research direction of sustainable control programs and equine parasite diagnostic methods.
Publication Date: 2025-09-04 PubMed ID: 40979365PubMed Central: PMC12443559DOI: 10.3389/fvets.2025.1663577Google 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
  • Review

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.

Overview

  • This article reviews the advances in serological and molecular biological techniques for diagnosing parasitic infections in horses.
  • It highlights the importance of accurate diagnosis for sustainable parasite control, considering current challenges such as drug resistance and the lack of effective vaccines.

Introduction to the Problem

  • Internal parasitic infections in horses are a significant and ongoing problem for horse owners worldwide.
  • The absence of effective vaccines makes prevention difficult.
  • Increasing resistance to antiparasitic drugs complicates treatment and control efforts.
  • Traditional control strategies are considered unsustainable in the long term.
  • Hence, precise and effective diagnostic methods are essential to manage infections and limit drug resistance.

Current Diagnostic Methods

  • Diagnostic techniques predominantly rely on molecular markers from parasite DNA sequences.
  • Commonly used genetic loci include:
    • ITS1 (Internal Transcribed Spacer 1)
    • ITS2 (Internal Transcribed Spacer 2)
    • COI (Cytochrome Oxidase I)
    • IGS (Intergenic Spacer)
  • These markers have been applied extensively for identifying equine strongylids, which include several important species causing infection.
  • Molecular methods enable:
    • Rapid and accurate species identification.
    • Large-scale epidemiological surveillance.
  • Serological methods like ELISA are also under development or use, providing immunological detection of parasitic infections.
  • Despite the development of these tools, many remain restricted to laboratory settings and are not yet widely adapted for real-time or field use.

Challenges and Limitations

  • Limited translation of sophisticated diagnostic methods into practical field applications.
  • Incomplete genomic data for many parasitic species infecting horses restricts the discovery of novel markers.
  • Slow progress over two decades in improving control due to technical, economic, and logistical barriers.

Future Directions and Opportunities

  • Advancements in whole genome sequencing (WGS) technologies are opening new opportunities:
    • WGS can be used for detailed population genetics studies of parasites.
    • Provides comprehensive data for identifying unique genetic markers associated with infection or resistance traits.
    • WGS aids the development of novel diagnostic tools with high sensitivity and specificity.
  • Cost reductions in sequencing are accelerating genome assembly projects, which will increase available data on equine parasites.
  • High-throughput sequencing platforms enable:
    • Faster pathogen detection.
    • Quantitative assays such as TaqMan qPCR for precise parasite load measurement.
    • Immunoassays like ELISA for serological diagnosis.
  • Integration of molecular diagnostics with sustainable parasite control strategies is a priority:
    • Early and accurate detection facilitates targeted treatment.
    • Helps reduce indiscriminate drug use and delays resistance.
    • Supports design of better control programs adapted to field conditions.

Conclusion

  • Effective and sustainable control of equine parasitic infections hinges on advanced, reliable diagnostic methods.
  • Current molecular markers and serological tools have improved identification but need adaptation for field use.
  • The coming surge in genomic data and high-throughput techniques is expected to revolutionize diagnostics and enhance sustainable parasite management.
  • The review emphasizes ongoing research efforts and encourages future focus on clinically applicable diagnostics and sustainable control solutions in equine parasitology.

Cite This Article

APA
Wang T, Chen X, Yan X, Su Y, Gao W, Liu C, Wang W. (2025). Progress in serology and molecular biology of equine parasite diagnosis: sustainable control strategies. Front Vet Sci, 12, 1663577. https://doi.org/10.3389/fvets.2025.1663577

Publication

ISSN: 2297-1769
NlmUniqueID: 101666658
Country: Switzerland
Language: English
Volume: 12
Pages: 1663577
PII: 1663577

Researcher Affiliations

Wang, Tengyu
  • Key Laboratory of Animal Disease Clinical Diagnosis and Treatment Technology, College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot, China.
Chen, Xindi
  • Key Laboratory of Animal Disease Clinical Diagnosis and Treatment Technology, College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot, China.
Yan, Xu
  • National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Su, Ya
  • Department of Husbandry and Veterinary, Ulanqab Vocational College, Ulanqab, China.
Gao, Wa
  • Inner Mongolia Key Laboratory of Tick-Borne Zoonotic Infectious Disease, Department of Medicine, Hetao College, Bavan Nur, China.
Liu, Chunxia
  • Key Laboratory of Animal Disease Clinical Diagnosis and Treatment Technology, College of Life Science, Inner Mongolia Agricultural University, Hohhot, China.
Wang, Wenlong
  • Key Laboratory of Animal Disease Clinical Diagnosis and Treatment Technology, College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot, China.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

This article includes 240 references
  1. Dissanayake S, Rajapakse RPVJ, Rajakaruna RS. Gastrointestinal parasites of domesticated and Feral Horses () in Sri Lanka. Ceylon J Sci (2017) 46:17.
    doi: 10.4038/cjs.v46i1.7414google scholar: lookup
  2. Owen J, Slocombe D. Pathogenesis of helminths in equines. Vet Parasitol (1985) 18:139–53.
    doi: 10.1016/0304-4017(85)90063-9pubmed: 2930935google scholar: lookup
  3. Wolf D, Hermosilla C, Taubert A, Fox MT, Uche UE, Vaillant C. Effects of and omeprazole treatment on feed intake and gastrin-related responses in the calf. Vet Parasitol (2002) 105:285–301.
    doi: 10.1016/S0304-4017(02)00026-2pubmed: 11983304google scholar: lookup
  4. Coop RL, Holmes PH. Nutrition and parasite interaction. Int J Parasitol (1996) 26:951–62.
    doi: 10.1016/S0020-7519(96)80070-1pubmed: 8923142google scholar: lookup
  5. Sims TA, Hay J, Talbot IC. An electron microscope and immunohistochemical study of the intracellular location of Toxoplasma tissue cysts within the brains of mice with congenital toxoplasmosis. Br J Exp Pathol (1989) 70:317–25.
    pmc: PMC2040570pubmed: 2504268
  6. Ferguson DJP, Hutchison WM, Pettersen E. Tissue cyst rupture in mice chronically infected with .. Parasitol Res (1989) 75:599–603.
    doi: 10.1007/BF00930955pubmed: 2771928google scholar: lookup
  7. Chappuis F, Rijal S, Soto A, Menten J, Boelaert M. A meta-analysis of the diagnostic performance of the direct agglutination test and rK39 dipstick for visceral leishmaniasis. BMJ (2006) 333:723.
    doi: 10.1136/bmj.38917.503056.7Cpmc: PMC1592383pubmed: 16882683google scholar: lookup
  8. Ozensoy S, Ozbel Y, Turgay N, Alkan MZ, Gul K, Gilman-Sachs A. Serodiagnosis and epidemiology of visceral leishmaniasis in Turkey. Am J Trop Med Hyg (1998) 59:363–9.
    doi: 10.4269/ajtmh.1998.59.363pubmed: 9749626google scholar: lookup
  9. Healy GR, Ruebush TK. Morphology of in human blood smears. Am J Clin Pathol (1980) 73:107–9.
    doi: 10.1093/ajcp/73.1.107pubmed: 7188717google scholar: lookup
  10. Torres-Guerrero E, Quintanilla-Cedillo MR, Ruiz-Esmenjaud J, Arenas R. Leishmaniasis: a review. F1000Res (2017) 6:750.
  11. Duffy P, Fried M. Malaria: new diagnostics for an old problem. Am J Trop Med Hyg (2005) 73:482–3.
    doi: 10.4269/ajtmh.2005.73.482pubmed: 16172466google scholar: lookup
  12. Croft AM, Kitson MM, Jackson CJ, Minton EJ, Friend HM. African Trypanosomiasis in a British Soldier. Mil Med (2007) 172:765–9.
    doi: 10.7205/MILMED.172.7.765pubmed: 17691692google scholar: lookup
  13. Scott I, Bishop R, Pomroy W. Anthelmintic resistance in equine helminth parasites – a growing issue for horse owners and veterinarians in New Zealand?. N Z Vet J (2015) 63:188–98.
    doi: 10.1080/00480169.2014.987840pubmed: 25608588google scholar: lookup
  14. Peregrine AS, Molento MB, Kaplan RM, Nielsen MK. Anthelmintic resistance in important parasites of horses: does it really matter?. Vet Parasitol (2014) 201:1–8.
    doi: 10.1016/j.vetpar.2014.01.004pubmed: 24485565google scholar: lookup
  15. Jabbar A, Iqbal Z, Kerboeuf D, Muhammad G, Khan MN, Afaq M. Anthelmintic resistance: the state of play revisited. Life Sci (2006) 79:2413–31.
    doi: 10.1016/j.lfs.2006.08.010pubmed: 16979192google scholar: lookup
  16. Köhler P. The biochemical basis of anthelmintic action and resistance.. Int J Parasitol (2001) 31:336–45.
    doi: 10.1016/S0020-7519(01)00131-Xpubmed: 11400692google scholar: lookup
  17. Lifschitz A, Suarez VH, Sallovitz J, Cristel SL, Imperiale F, Ahoussou S. Cattle nematodes resistant to macrocyclic lactones: comparative effects of P-glycoprotein modulation on the efficacy and disposition kinetics of ivermectin and moxidectin.. Exp Parasitol (2010) 125:172–8.
    doi: 10.1016/j.exppara.2010.01.009pubmed: 20109455google scholar: lookup
  18. Geurden T, Chartier C, Fanke J, di Regalbono AF, Traversa D, von Samson-Himmelstjerna G. Anthelmintic resistance to ivermectin and moxidectin in gastrointestinal nematodes of cattle in Europe.. Int J Parasitol Drugs Drug Resist (2015) 5:163–71.
  19. Coles GC. Anthelmintic resistance – looking to the future: a UK perspective.. Res Vet Sci (2005) 78:99–108.
    doi: 10.1016/j.rvsc.2004.09.001pubmed: 15563915google scholar: lookup
  20. Domke AVM, Chartier C, Gjerde B, Höglund J, Leine N, Vatn S. Prevalence of anthelmintic resistance in gastrointestinal nematodes of sheep and goats in Norway.. Parasitol Res (2012) 111:185–93.
    doi: 10.1007/s00436-012-2817-xpmc: PMC3378835pubmed: 22290446google scholar: lookup
  21. Geurden T, Betsch J-M, Maillard K, Vanimisetti B, D'Espois M, Besognet B. Determination of anthelmintic efficacy against equine cyathostomins and in France.. Equine Vet Educ (2013) 25:304–7.
  22. Wolf D, Hermosilla C, Taubert A. Oxyuris equi: lack of efficacy in treatment with macrocyclic lactones.. Vet Parasitol (2014) 201:163–8.
    doi: 10.1016/j.vetpar.2013.12.009pubmed: 24472770google scholar: lookup
  23. Saes IL, Vera JHS, Fachiolli DF, Yamada PH, Dellaqua JVT, de Lima Saes R. Time required by different anthelmintics to reach expected efficacy levels in horses infected by strongyles.. Vet Parasitol (2016) 229:90–2.
    doi: 10.1016/j.vetpar.2016.10.002pubmed: 27809986google scholar: lookup
  24. Abbas G, Ghafar A, McConnell E, Beasley A, Bauquier J, Wilkes EJA. A national survey of anthelmintic resistance in ascarid and strongylid nematodes in Australian thoroughbred horses.. Int J Parasitol Drugs Drug Resist (2024) 24:100517.
  25. Ashrafzadeh-Shiraz M, Tavassoli M, Dalir-Naghadeh B, Sazmand A. Impaired efficacy of fenbendazole and ivermectin against intestinal nematodes in adult horses in Iran.. Res Vet Sci (2024) 166:105078.
    doi: 10.1016/j.rvsc.2023.105078pubmed: 37952299google scholar: lookup
  26. Canever RJ, Braga PRC, Boeckh A, Grycajuck M, Bier D, Molento MB. Lack of Cyathostomin sp. reduction after anthelmintic treatment in horses in Brazil.. Vet Parasitol (2013) 194:35–9.
    doi: 10.1016/j.vetpar.2012.12.020pubmed: 23318166google scholar: lookup
  27. Coles GC, Jackson F, Pomroy WE, Prichard RK, von Samson-Himmelstjerna G, Silvestre A. The detection of anthelmintic resistance in nematodes of veterinary importance.. Vet Parasitol (2006) 136:167–85.
    doi: 10.1016/j.vetpar.2005.11.019pubmed: 16427201google scholar: lookup
  28. Taylor MA, Hunt KR, Goodyear KL. Anthelmintic resistance detection methods.. Vet Parasitol (2002) 103:183–94.
    doi: 10.1016/S0304-4017(01)00604-5pubmed: 11750111google scholar: lookup
  29. Vainionpää R, Waris M, Leinikki P. Diagnostic techniques: serological and molecular approaches.. Ref Mod Biomed Sci (2015) 6:B978-0-12-801238-3.02558-7.
  30. Baboo ASA, Naeem M, Behan AA, Rajput N. Serum cortisol concentration is a reliable tool to assess stress level among stereotypic and non-stereotypic thoroughbred horses.. PVJ (2024) 44:155–61.
    doi: 10.29261/pakvetj/2023.115google scholar: lookup
  31. Apsari IAP, Swacita IBN, Dharmawan NS, Winaya IBO, Praing UYA, Agustina KK. Investigation into infection in horses in East Sumba-Indonesia.. Int J Vet Sci (2024) 13:794–8.
  32. Verma R, Das G, Manjunathachar HV, Muwel N. Advances in diagnostics of parasitic diseases: current trends and future prospects.. Int J Curr Microbiol App Sci (2018) 7:3261–77.
  33. Dalton JP, Robinson MW, Mulcahy G, O'Neill SM, Donnelly S. Immunomodulatory molecules of : candidates for both vaccine and immunotherapeutic development.. Vet Parasitol (2013) 195:272–85.
    doi: 10.1016/j.vetpar.2013.04.008pubmed: 23623183google scholar: lookup
  34. Johnston MJG, MacDonald JA, McKay DM. Parasitic helminths: a pharmacopeia of anti-inflammatory molecules.. Parasitology (2009) 136:125–47.
    doi: 10.1017/S0031182008005210pubmed: 19079844google scholar: lookup
  35. Mezo M, González-Warleta M, Ubeira FM. Optimized serodiagnosis of sheep fascioliasis by fast-D protein liquid chromatography fractionation of . excretory–secretory antigens.. J Parasitol (2003) 89:843–9.
    doi: 10.1645/GE-74RI.1pubmed: 14533701google scholar: lookup
  36. Marzok M, Gattan HS, Albokhadaim I, Alruhaili MH, Salem M, Selim A. Seroprevalence and risk factors associated with infection in horses in Egypt.. Kafkas Univ Vet Fak Derg (2024) 30:787–92.
    doi: 10.9775/kvfd.2024.32527google scholar: lookup
  37. Kuerpick B, Schnieder T, Strube C. Evaluation of a recombinant cathepsin L1 ELISA and comparison with the Pourquier and ES ELISA for the detection of antibodies against .. Vet Parasitol (2013) 193:206–13.
    doi: 10.1016/j.vetpar.2012.11.021pubmed: 23246075google scholar: lookup
  38. Sánchez-Andrade R, Paz-Silva A, Suárez JL, Panadero R, Pedreira J, Díez-Baños P. Effect of fasciolicides on the antigenaemia in sheep naturally infected with .. Parasitol Res (2001) 87:609–14.
    doi: 10.1007/s004360100425pubmed: 11510995google scholar: lookup
  39. Gonzales Santana B, Dalton JP, Vasquez Camargo F, Parkinson M, Ndao M. The diagnosis of human fascioliasis by enzyme-linked immunosorbent assay (ELISA) using recombinant Cathepsin L protease.. PLoS Negl Trop Dis (2013) 7:e2414.
  40. Kang J-M, Bahk Y-Y, Cho P-Y, Hong S-J, Kim T-S, Sohn W-M. Family of cathepsin F cysteine proteases of is the major secreted proteins that are expressed in the intestine of the parasite.. Mol Biochem Parasitol (2010) 170:7–16.
  41. Norbury LJ, Beckham S, Pike RN, Grams R, Spithill TW, Fecondo JV. Adult and juvenile Fasciola cathepsin L proteases: different enzymes for different roles.. Biochimie (2011) 93:604–11.
    doi: 10.1016/j.biochi.2010.12.004pubmed: 21167899google scholar: lookup
  42. Meemon K, Sobhon P. Juvenile-specific cathepsin proteases in spp: their characteristics and vaccine efficacies.. Parasitol Res (2015) 114:2807–13.
    doi: 10.1007/s00436-015-4589-6pubmed: 26099239google scholar: lookup
  43. Boulard C, Villejoubert C. Use of pooled serum or milk samples for the epidemiological surveillance of bovine hypodermosis.. Vet Parasitol (1991) 39:171–83.
    doi: 10.1016/0304-4017(91)90072-4pubmed: 1897116google scholar: lookup
  44. Boulard C. Degradation of bovine C3 by serine proteases from parasites Hypoderma lineatum (Diptera, Oestridae).. Vet Immunol Immunopathol (1989) 20:387–98.
    doi: 10.1016/0165-2427(89)90083-4pubmed: 2718374google scholar: lookup
  45. Atelge M, Inci A, Yildirim A, Sozdutmaz I, Adler PH. First molecular characterization of hypodermin genes of and serodiagnosis of bovine hypodermosis with recombinant hypodermin C antigen and a synthetic peptide containing its linear B-cell epitope.. Vet Parasitol (2021) 292:109394.
    doi: 10.1016/j.vetpar.2021.109394pubmed: 33689962google scholar: lookup
  46. Reyburn H, Mbatia R, Drakeley C, Carneiro I, Mwakasungula E, Mwerinde O. Overdiagnosis of malaria in patients with severe febrile illness in Tanzania: a prospective study.. BMJ (2004) 329:1212.
    doi: 10.1136/bmj.38251.658229.55pmc: PMC529364pubmed: 15542534google scholar: lookup
  47. Andersen UV, Howe DK, Olsen SN, Nielsen MK. Recent advances in diagnosing pathogenic equine gastrointestinal helminths: the challenge of prepatent detection.. Vet Parasitol (2013) 192:1–9.
    doi: 10.1016/j.vetpar.2012.11.003pubmed: 23199789google scholar: lookup
  48. Bastos RG, Sears KP, Dinkel KD, Kappmeyer L, Ueti MW, Knowles DP. Development of an indirect ELISA to detect equine antibodies to .. Pathogens (2021) 10:270.
    doi: 10.3390/pathogens10030270pmc: PMC7997436pubmed: 33673478google scholar: lookup
  49. Tjitra E, Suprianto S, Dyer M, Currie BJ, Anstey NM. Field evaluation of the ICT malaria Pf/Pv immunochromatographic test for detection of and in patients with a presumptive clinical diagnosis of malaria in Eastern Indonesia.. J Clin Microbiol (1999) 37:2412–7.
  50. Mayxay M, Pukrittayakamee S, Chotivanich K, Looareesuwan S, White NJ. Persistence of HRP-2 in successfully treated acute falciparum malaria.. Trans R Soc Trop Med Hyg (2001) 95:179–82.
    doi: 10.1016/S0035-9203(01)90156-7pubmed: 11355555google scholar: lookup
  51. Moody A. Rapid diagnostic tests for malaria parasites.. Clin Microbiol Rev (2002) 15:66–78.
    doi: 10.1128/CMR.15.1.66-78.2002pmc: PMC118060pubmed: 11781267google scholar: lookup
  52. Zarlenga DS, Higgins J. PCR as a diagnostic and quantitative technique in veterinary parasitology.. Vet Parasitol (2001) 101:215–30.
    doi: 10.1016/S0304-4017(01)00568-4pubmed: 11707298google scholar: lookup
  53. Gorman T, Aballay J, Fredes F, Silva M, Aguillón JC, Alcaíno HA. Fasciolosis in horses: a neglected, re-emerging disease.. Equine Vet Educ (2017) 29:202–4.
    doi: 10.1111/eve.12521google scholar: lookup
  54. Mens P, Spieker N, Omar S, Heijnen M, Schallig H, Kager PA. Is molecular biology the best alternative for diagnosis of malaria to microscopy? A comparison between microscopy, antigen detection and molecular tests in rural Kenya and urban Tanzania.. Tropical Med Int Health (2007) 12:238–44.
  55. Wang L, Lv Q, He Y, Gu R, Zhou B, Chen J. Integrated qPCR and staining methods for detection and quantification of Enterocytozoon hepatopenaei in Shrimp .. Microorganisms (2020) 8:1366.
  56. de Paiva-Cavalcanti M, de Morais RCS, Pessoa-E-Silva R, Trajano-Silva LAM, Gonçalves-de-Albuquerque SC, Tavares DHC. Leishmaniases diagnosis: an update on the use of immunological and molecular tools.. Cell Biosci (2015) 5:31.
    doi: 10.1186/s13578-015-0021-2pmc: PMC4474361pubmed: 26097678google scholar: lookup
  57. Duncan R. Advancing molecular diagnostics for Trypanosomatid parasites.. J Mol Diagn (2014) 16:379–81.
    doi: 10.1016/j.jmoldx.2014.04.001pubmed: 24815378google scholar: lookup
  58. Guo S-Q, Fu Y-W, Hou T-L, Huang S-L, Zhang Q-Z. Establishment and application of TaqMan probe-based quantitative real-time PCR for rapid detection and quantification of in farming environments and fish tissues.. Vet Parasitol (2025) 334:110381.
    doi: 10.1016/j.vetpar.2024.110381pubmed: 39742554google scholar: lookup
  59. Souza AP, Soto M, Costa JML, Boaventura VS, de Oliveira CI, Cristal JR. Towards a more precise serological diagnosis of human Tegumentary Leishmaniasis using Leishmania recombinant proteins.. PLoS One (2013) 8:e66110.
  60. da Silveira JF, Umezawa ES, Luquetti AO. Chagas disease: recombinant antigens for serological diagnosis.. Trends Parasitol (2001) 17:286–91.
    doi: 10.1016/S1471-4922(01)01897-9pubmed: 11378036google scholar: lookup
  61. Alruhaili MH, Marzok M, Gattan HS, Salem M, Abd El-Lateef HM, Selim A. Seroprevalence and assessment of risk factors associated to infection in Egyptian horses.. Kafkas Univ Vet Fak Derg (2024) 30:349–54.
    doi: 10.9775/kvfd.2023.31264google scholar: lookup
  62. 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) 174:77–84.
    doi: 10.1016/j.vetpar.2010.08.007pubmed: 20850927google scholar: lookup
  63. Dowdall SMJ, Matthews JB, Mair T, Murphy D, Love S, Proudman CJ. Antigen-specific IgG(T) responses in natural and experimental cyathostominae infection in horses.. Vet Parasitol (2002) 106:225–42.
    doi: 10.1016/S0304-4017(02)00085-7pubmed: 12062511google scholar: lookup
  64. Dowdall SMJ, Proudman CJ, Klei TR, Mair T, Matthews JB. Characterisation of IgG(T) serum antibody responses to two larval antigen complexes in horses naturally- or experimentally-infected with cyathostomins.. Int J Parasitol (2004) 34:101–8.
    doi: 10.1016/j.ijpara.2003.09.008pubmed: 14711595google scholar: lookup
  65. Dowdall SMJ, Proudman CJ, Love S, Klei TR, Matthews JB. Purification and analyses of the specificity of two putative diagnostic antigens for larval cyathostomin infection in horses.. Res Vet Sci (2003) 75:223–9.
    doi: 10.1016/S0034-5288(03)00116-4pubmed: 13129671google scholar: lookup
  66. McWilliam HEG, Nisbet AJ, Dowdall SMJ, Hodgkinson JE, Matthews JB. Identification and characterisation of an immunodiagnostic marker for cyathostomin developing stage larvae.. Int J Parasitol (2010) 40:265–75.
    doi: 10.1016/j.ijpara.2009.08.004pubmed: 19703459google scholar: lookup
  67. Tzelos T, Geyer KK, Mitchell MC, McWilliam HEG, Kharchenko VO, Burgess STG. Characterisation of serum IgG(T) responses to potential diagnostic antigens for equine cyathostominosis.. Int J Parasitol (2020) 50:289–98.
    doi: 10.1016/j.ijpara.2020.01.004pubmed: 32171845google scholar: lookup
  68. Höglund J, Ljungström B-L, 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
  69. Proudman CJ, Trees AJ. Use of excretory/secretory antigens for the serodiagnosis of cestodosis.. Vet Parasitol (1996) 61:239–47.
    doi: 10.1016/0304-4017(95)00837-3pubmed: 8720562google scholar: lookup
  70. PROUDMAN CJ, TREES AJ. Correlation of antigen specific IgG and IgG(T) responses with infection intensity in the horse.. Parasite Immunol (1996) 18:499–506.
  71. Anderson RM, May RM. Infectious Diseases of Humans: Dynamics and Control.. Oxford, UK: Oxford University Press; (1991).
  72. Bohórquez A, Meana A, Pato NF, Luzón M. Coprologically diagnosing in the presence of A. magna.. Vet Parasitol (2014) 204:396–401.
    doi: 10.1016/j.vetpar.2014.04.023pubmed: 24877786google scholar: lookup
  73. Lightbody KL, Davis PJ, Austin CJ. Validation of a novel saliva-based ELISA test for diagnosing tapeworm burden in horses.. Vet Clin Pathol (2016) 45:335–46.
    doi: 10.1111/vcp.12364pubmed: 27218436google scholar: lookup
  74. Jin D. Indirect ELISA Procedures of Horse Gastric myiasis and Study on the Discharge Dynamics of Gasterophilus spp. Larvae after Administration of Ivermectin.. Beijing Forestry University (2017).
  75. Lyons ET, Drudge JH, Tolliver SC. Studies on the development and chemotherapy of larvae of (Nematoda: Ascaridoidea) in experimentally and naturally infected foals.. J Parasitol (1976) 62:453.
    doi: 10.2307/3279157pubmed: 945338google scholar: lookup
  76. de Savigny DH, Voller A, Woodruff AW. Toxocariasis: serological diagnosis by enzyme immunoassay.. J Clin Pathol (1979) 32:284–8.
    doi: 10.1136/jcp.32.3.284pmc: PMC1145636pubmed: 372253google scholar: lookup
  77. Chatterjee BP, Santra A, Karmakar PR, Mazumder DNG. Evaluation of IgG4 response in ascariasis by ELISA for serodiagnosis.. Tropical Med Int Health (1996) 1:633–9.
  78. Lind P, Eriksen L, Nansen P, Nilsson O, Roepstorff A. Response to repeated inoculations with eggs in pigs during the fattening period.. Parasitol Res (1993) 79:240–4.
    doi: 10.1007/BF00931899pubmed: 8493248google scholar: lookup
  79. Burk SV, Dangoudoubiyam S, Brewster-Barnes T, Bryant UK, Howe DK, Carter CN. culture of larvae and initial investigation of parasite excretory-secretory products.. Parasitol Res (2014) 113:4217–24.
    doi: 10.1007/s00436-014-4097-0pubmed: 25209615google scholar: lookup
  80. Gasser RB, Jenkins DJ, Heath DD, Lawrence SB. Use of worm antigens for immunodiagnosis of infection in dogs.. Vet Parasitol (1992) 45:89–100.
    doi: 10.1016/0304-4017(92)90030-Dpubmed: 1485424google scholar: lookup
  81. Abbott JB, Mellor DJ, Barrett EJ, Proudman CJ, Love S. Serological changes observed in horses infected with after treatment with praziquantel and natural reinfection.. Vet Rec (2008) 162:50–3.
    doi: 10.1136/vr.162.2.50pubmed: 18192657google scholar: lookup
  82. Proudman CJ, Holdstock NB. Investigation of an outbreak of tapeworm-associated colic in a training yard.. Equine Vet J Suppl (2000) 32:37–41.
  83. Voller A, De Savigny D. Diagnostic serology of tropical parasitic diseases.. J Immunol Methods (1981) 46:1–29.
    doi: 10.1016/0022-1759(81)90328-8pubmed: 6793664google scholar: lookup
  84. Bohórquez A, Meana A, Luzón M. Differential diagnosis of equine cestodosis based on E/S and somatic and antigens.. Vet Parasitol (2012) 190:87–94.
    doi: 10.1016/j.vetpar.2012.06.001pubmed: 22763349google scholar: lookup
  85. Rinaldi L, Krücken J, Martinez-Valladares M, Pepe P, Maurelli MP, de Queiroz C. Advances in diagnosis of gastrointestinal nematodes in livestock and companion animals.. Adv Parasitol (2022) 118:85–176.
    doi: 10.1016/bs.apar.2022.07.002pubmed: 36088084google scholar: lookup
  86. Mu X, Guo J, Wang H, Li Y, Yuan K, Xu H. Establishment and preliminary application of PCR-RFLP genotyping method for in goats.. BMC Vet Res (2024) 20:527.
    doi: 10.1186/s12917-024-04386-0pmc: PMC11590275pubmed: 39593122google scholar: lookup
  87. Campbell AJD, Gasser RB, Chilton NB. Differences in a ribosomal DNA sequence of strongylus species allows identification of single eggs.. Int J Parasitol (1995) 25:359–65.
    doi: 10.1016/0020-7519(94)00116-6pubmed: 7601594google scholar: lookup
  88. Gasser RB, Stevenson LA, Chilton NB, Nansen P, Bucknell DG, Beveridge I. Species markers for equine strongyles detected in intergenic rDNA by PCR-RFLP.. Mol Cell Probes (1996) 10:371–8.
    doi: 10.1006/mcpr.1996.0050pubmed: 8910892google scholar: lookup
  89. Gasser RB, Monti JR. Identification of parasitic nematodes by PCR-SSCP of ITS-2 rDNA.. Mol Cell Probes (1997) 11:201–9.
    doi: 10.1006/mcpr.1997.0106pubmed: 9232619google scholar: lookup
  90. Siles-Lucas M, Felleisen R, Cuesta-Bandera C, Gottstein B, Eckert J. Comparative genetic analysis of Swiss and Spanish isolates of by southern hybridization and random amplified polymorphic DNA technique.. Appl Parasitol (1994) 35:107–17.
    pubmed: 8087150
  91. Humbert JF, Cabaret J. Use of random amplified polymorphic DNA for identification of ruminant trichostrongylid nematodes.. Parasitol Res (1995) 81:1–5.
    doi: 10.1007/BF00932409pubmed: 7724508google scholar: lookup
  92. Courtot É, Boisseau M, Dhorne-Pollet S, Serreau D, Gesbert A, Reigner F. Comparison of two molecular barcodes for the study of equine strongylid communities with amplicon sequencing.. PeerJ (2023) 11:e15124.
    doi: 10.7717/peerj.15124pmc: PMC10105562pubmed: 37070089google scholar: lookup
  93. Hodgkinson JE, Love S, Lichtenfels JR, Palfreman S, Ramsey YH, Matthews JB. Evaluation of the specificity of five oligoprobes for identification of cyathostomin species from horses.. Int J Parasitol (2001) 31:197–204.
    doi: 10.1016/S0020-7519(00)00161-2pubmed: 11239940google scholar: lookup
  94. Hodgkinson JE, Lichtenfels JR, Mair TS, Cripps P, Freeman KL, Ramsey YH. PCR–ELISA for the identification of cyathostomin fourth-stage larvae from clinical cases of larval cyathostominosis.. Int J Parasitol (2003) 33:1427–35.
    doi: 10.1016/S0020-7519(03)00140-1pubmed: 14527525google scholar: lookup
  95. Hodgkinson JE, Freeman KL, Lichtenfels JR, Palfreman S, Love S, Matthews JB. Identification of strongyle eggs from anthelmintic-treated horses using a PCR-ELISA based on intergenic DNA sequences.. Parasitol Res (2005) 95:287–92.
    doi: 10.1007/s00436-004-1289-zpubmed: 15682337google scholar: lookup
  96. Hung G-C, Gasser RB, Beveridge I, Chilton NB. Species-specific amplification by PCR of ribosomal DNA from some equine strongyles.. Parasitology (1999) 119:69–80.
    doi: 10.1017/S0031182099004497pubmed: 10446706google scholar: lookup
  97. Cwiklinski K, Kooyman FNJ, van Doorn DCK, Matthews JB, Hodgkinson JE. New insights into sequence variation in the IGS region of 21 cyathostomin species and the implication for molecular identification.. Parasitology (2012) 139:1063–73.
    doi: 10.1017/S0031182012000467pubmed: 22717256google scholar: lookup
  98. Traversa D, Milillo P, Barnes H, von Samson-Himmelstjerna G, Schurmann S, Demeler J. Distribution and species-specific occurrence of cyathostomins (Nematoda, Strongylida) in naturally infected horses from Italy, United Kingdom and Germany.. Vet Parasitol (2010) 168:84–92.
    doi: 10.1016/j.vetpar.2009.10.006pubmed: 19906489google scholar: lookup
  99. van Doorn DCK, Ploeger HW, Eysker M, Geurden T, Wagenaar JA, Kooyman FNJ. Cylicocyclus species predominate during shortened egg reappearance period in horses after treatment with ivermectin and moxidectin.. Vet Parasitol (2014) 206:246–52.
    doi: 10.1016/j.vetpar.2014.10.004pubmed: 25458565google scholar: lookup
  100. 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) 11:61.
    doi: 10.1186/s13071-018-2638-6pmc: PMC5785887pubmed: 29370872google scholar: lookup
  101. Martins AV, Corrêa LL, Ribeiro MS, de Lima Coelho A, Lobão LF, Palmer JPS. Identification of third stage larvae of strongyles and molecular diagnosis of in the feces of Thoroughbred horses kept in training centers in Rio de Janeiro, Brazil.. Vet Parasitol (2024) 50:101019.
    doi: 10.1016/j.vprsr.2024.101019pubmed: 38644042google scholar: lookup
  102. Alhassan A, Thekisoe OMM, Yokoyama N, Inoue N, Motloang MY, Mbati PA. Development of loop-mediated isothermal amplification (LAMP) method for diagnosis of equine piroplasmosis.. Vet Parasitol (2007) 143:155–60.
    doi: 10.1016/j.vetpar.2006.08.014pubmed: 16973284google scholar: lookup
  103. Moghaddassani H, Mirhendi H, Hosseini M, Rokni M, Mowlavi G, Kia E. Molecular diagnosis of infection by PCR detection of specific DNA in human stool samples.. Iran J Parasitol (2011) 6:23–30.
    pmc: PMC3279873pubmed: 22347284
  104. Levenhagen MA, Costa-Cruz JM. Update on immunologic and molecular diagnosis of human strongyloidiasis.. Acta Trop (2014) 135:33–43.
  105. Zhang H, Thekisoe OMM, Aboge GO, Kyan H, Yamagishi J, Inoue N. Toxoplasma gondii: sensitive and rapid detection of infection by loop-mediated isothermal amplification (LAMP) method.. Exp Parasitol (2009) 122:47–50.
    doi: 10.1016/j.exppara.2009.01.012pubmed: 19545521google scholar: lookup
  106. Ding L, Razavi Bazaz S, Hall T, Vesey G, Ebrahimi Warkiani M. Giardia purification from fecal samples using rigid spiral inertial microfluidics.. Biomicrofluidics (2022) 16:014105.
    doi: 10.1063/5.0069406pmc: PMC12313327pubmed: 40746946google scholar: lookup
  107. Melville L, Kenyon F, Javed S, McElarney I, Demeler J, Skuce P. Development of a loop-mediated isothermal amplification (LAMP) assay for the sensitive detection of eggs in ovine faecal samples.. Vet Parasitol (2014) 206:308–12.
    doi: 10.1016/j.vetpar.2014.10.022pubmed: 25468028google scholar: lookup
  108. Chen Y-X, Lou Y-R, Duan L-J, Zhou Q-J, Xu Z-J, Chen F-J. Parallel detection of multiple zoonotic parasites using a real-time fluorogenic loop-mediated isothermal amplification-based quadruple-sample microfluidic chip.. Front Microbiol (2023) 14:1238376.
    doi: 10.3389/fmicb.2023.1238376pmc: PMC10562543pubmed: 37822745google scholar: lookup
  109. Pattanayak P, Singh SK, Gulati M, Vishwas S, Kapoor B, Chellappan DK. Microfluidic chips: recent advances, critical strategies in design, applications and future perspectives.. Microfluid Nanofluid (2021) 25:99.
    doi: 10.1007/s10404-021-02502-2pmc: PMC8547131pubmed: 34720789google scholar: lookup
  110. Siavash Moakhar R, Mahimkar R, Khorrami Jahromi A, Mahshid SS, del Real Mata C, Lu Y. Aptamer-based electrochemical microfluidic biosensor for the detection of .. ACS Sens (2023) 8:2149–58.
    doi: 10.1021/acssensors.2c01349pubmed: 37207303google scholar: lookup
  111. Mitchell CJ, O'Sullivan CM, Pinloche E, Wilkinson T, Morphew RM, Mcewan NR. Using next-generation sequencing to determine diversity of horse intestinal worms: identifying the equine ‘nemabiome'.. JES (2019) 30:1–5.
    doi: 10.1294/jes.30.1pmc: PMC6445754pubmed: 30944540google scholar: lookup
  112. Abbas G, Ghafar A, Bauquier J, Beasley A, Ling E, Gauci CG. Prevalence and diversity of ascarid and strongylid nematodes in Australian Thoroughbred horses using next-generation sequencing and bioinformatic tools.. Vet Parasitol (2023) 323:110048.
    doi: 10.1016/j.vetpar.2023.110048pubmed: 37844388google scholar: lookup
  113. Hamad MH, Islam SI, Jitsamai W, Chinkangsadarn T, Naraporn D, Ouisuwan S. Metabarcoding study to reveal the structural community of strongylid nematodes in domesticated horses in Thailand.. BMC Vet Res (2024) 20:70.
    doi: 10.1186/s12917-024-03934-ypmc: PMC10893705pubmed: 38395874google scholar: lookup
  114. Wang D, Zeng J, Ma H, Fouad D, Su Z. Comparative analysis of the gut microbiota between two horse species.. PVJ (2024) 44:449–57.
    doi: 10.29261/pakvetj/2024.151google scholar: lookup
  115. Синяков MП, Ятусевич AИ, Стогначева ГA. Antiparasitic drugs for the treatment and prevention of horse diseases.. Vestnik APK Verhnevolzh‘ia (2021) 1:28–32.
  116. Panova OA, Arkhipov IA, Baranova MV, Khrustalev AV. The problem of anthelminthic resistance in horse breeding.. Russ J Parasitol (2022) 16:230–42.
  117. Beg ZA, Roohi N, Iqbal Z, Iqbal MA, Zulfiqar A. Role of herbs as anthelmintic in the control of parascariasis in equines.. J Anim Plant Sci (2023) 33:235–40.
    doi: 10.36899/JAPS.2023.1.0615google scholar: lookup
  118. Payne SE, Kotze AC, Durmic Z, Vercoe PE. Australian plants show anthelmintic activity toward equine cyathostomins .. Vet Parasitol (2013) 196:153–60.
    doi: 10.1016/j.vetpar.2013.01.012pubmed: 23394801google scholar: lookup
  119. Payne SE, Flematti GR, Reeder A, Kotze AC, Durmic Z, Vercoe PE. Procyanidin A2 in the Australian plant has anthelmintic activity against equine cyathostomins .. Vet Parasitol (2018) 249:63–9.
    doi: 10.1016/j.vetpar.2017.11.008pubmed: 29279088google scholar: lookup
  120. Sneha A, Preet S. Impact of sublethal conventional and biorational larvicidal stress on fitness status in nutritionally challenged larvae.. Int J Mosq Res (2016) 3:39–46.
  121. Klongsiriwet C, Quijada J, Williams AR, Mueller-Harvey I, Williamson EM, Hoste H. Synergistic inhibition of exsheathment by flavonoid monomers and condensed tannins.. Int J Parasitol Drugs Drug Resist (2015) 5:127–34.
  122. Chicaiza-Tisalema E, Barros-Rodríguez M, Zurita-Vásquez H, Mera-Andrade R, Velástegui-Espín G, Muñoz-Espinoza M. Efecto Antihelmíntico del Extracto de Albizia Lophantha sobre Nematodos Gastrointestinales de Caballos (Spanish).. Rev Investig Vet Perú (2016) 27:556.
  123. Leone A, Spada A, Battezzati A, Schiraldi A, Aristil J, Bertoli S. Cultivation, genetic, ethnopharmacology, phytochemistry and pharmacology of leaves: an overview.. Int J Mol Sci (2015) 16:12791–835.
    doi: 10.3390/ijms160612791pmc: PMC4490473pubmed: 26057747google scholar: lookup
  124. Vergara-Jimenez M, Almatrafi MM, Fernandez ML. Bioactive components in leaves protect against chronic disease.. Antioxidants (2017) 6:91.
    doi: 10.3390/antiox6040091pmc: PMC5745501pubmed: 29144438google scholar: lookup
  125. Ferreira PMP, Farias DF, Oliveira JTA, Carvalho AFU. Moringa oleifera: bioactive compounds and nutritional potential.. Rev Nutr (2008) 21:431–7.
  126. Tayo GM, Poné JW, Komtangi MC, Yondo J, Ngangout AM, Mbida M. Anthelminthic activity of leaf extracts evaluated on four developmental stages of from goats.. AJPS (2014) 05:1702–10.
    doi: 10.4236/ajps.2014.511185google scholar: lookup
  127. Elghandour MMMY, Maggiolino A, Vázquez-Mendoza P, Alvarado-Ramírez ER, Cedillo-Monroy J, De Palo P. Moringa oleifera as a natural alternative for the control of gastrointestinal parasites in equines: a review.. Plants (2023) 12:1921.
    doi: 10.3390/plants12091921pmc: PMC10181162pubmed: 37176979google scholar: lookup
  128. Buono F, Pacifico L, Piantedosi D, Sgroi G, Neola B, Roncoroni C. Preliminary observations of the effect of garlic on egg shedding in horses naturally infected by intestinal strongyles.. J Equine Vet Sci (2019) 72:79–83.
    doi: 10.1016/j.jevs.2018.10.025pubmed: 30929787google scholar: lookup
  129. Salama AA, AbouLaila M, Terkawi MA, Mousa A, El-Sify A, Allaam M. Inhibitory effect of allicin on the growth of and parasites.. Parasitol Res (2014) 113:275–83.
    doi: 10.1007/s00436-013-3654-2pubmed: 24173810google scholar: lookup
  130. Bhatwalkar SB, Mondal R, Krishna SBN, Adam JK, Govender P, Anupam R. Antibacterial properties of organosulfur compounds of garlic ().. Front Microbiol (2021) 12:613077.
    doi: 10.3389/fmicb.2021.613077pmc: PMC8362743pubmed: 34394014google scholar: lookup
  131. Peachey LE, Pinchbeck GL, Matthews JB, Burden FA, Mulugeta G, Scantlebury CE. An evidence-based approach to the evaluation of ethnoveterinary medicines against strongyle nematodes of equids. Vet Parasitol (2015) 210:40–52.
    doi: 10.1016/j.vetpar.2015.03.009pubmed: 25868847google scholar: lookup
  132. Alves do Carmo T, Oliveira Mena M, de Almeida Cipriano I, Mascoli de Favare G, Jabismar Guelpa G, da Costa Pinto S. Biological control of gastrointestinal nematodes in horses fed with grass in association with nematophagus fungi and. Biol Control (2023) 182:105219.
  133. Larsen M. Prospects for controlling animal parasitic nematodes by predacious micro fungi. Parasitology (2000) 120:121–31.
    doi: 10.1017/S0031182099005739pubmed: 10874715google scholar: lookup
  134. Araújo JV, Braga FR, Mendoza-de-Gives P, Paz-Silva A, Vilela VLR. Recent advances in the control of helminths of domestic animals by helminthophagous fungi. Parasitologia (2021) 1:168–76.
  135. 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
  136. Duddington CL. Fungi that attack microscopic animals. Bot Rev (1955) 21:377–439.
    doi: 10.1007/BF02872434google scholar: lookup
  137. Buzatti A, Santos CP, Fernandes MAM, Yoshitani UY, Sprenger LK, Molento MB. Duddingtonia flagrans no controle de nematoides gastrintestinais de equinos em fases de vida livre. Arq Bras Med Vet Zootec (2017) 69:364–70.
    doi: 10.1590/1678-4162-9028google scholar: lookup
  138. Bampidis V, Azimonti G, de Lourdes Bastos M, Christensen H, Dusemund B, Kos Durjava M. Safety and efficacy of BioWorma ( NCIMB 30336) as a feed additive for all grazing animals. EFS2 (2020) 18:e06208.
    doi: 10.2903/j.efsa.2020.6208pmc: PMC7376537pubmed: 32714465google scholar: lookup
  139. Clark A, Sallé G, Ballan V, Reigner F, Meynadier A, Cortet J. Strongyle infection and gut microbiota: profiling of resistant and susceptible horses over a grazing season. Front Physiol (2018) 9:272.
    doi: 10.3389/fphys.2018.00272pmc: PMC5871743pubmed: 29618989google scholar: lookup
  140. Peachey LE, Molena RA, Jenkins TP, Di Cesare A, Traversa D, Hodgkinson JE. The relationships between faecal egg counts and gut microbial composition in UK Thoroughbreds infected by cyathostomins. Int J Parasitol (2018) 48:403–12.
  141. Markowiak P, Sliżewska K. The role of probiotics, prebiotics and synbiotics in animal nutrition. Gut Pathog (2018) 10:21.
    doi: 10.1186/s13099-018-0250-0pmc: PMC5989473pubmed: 29930711google scholar: lookup
  142. Gavina K, Franco LC, Khan H, Lavik J-P, Relich RF. Molecular point-of-care devices for the diagnosis of infectious diseases in resource-limited settings – a review of the current landscape, technical challenges, and clinical impact. J Clin Virol (2023) 169:105613.
    doi: 10.1016/j.jcv.2023.105613pubmed: 37866094google scholar: lookup
  143. Escobedo P, Erenas MM, Martinez Olmos A, Carvajal MA, Tabraue Chavez M, Luque Gonzalez MA. Smartphone-based diagnosis of parasitic infections with colorimetric assays in centrifuge tubes. IEEE Access (2019) 7:185677–86.
  144. Dacal E, Bermejo-Peláez D, Lin L, Álamo E, Cuadrado D, Martínez Á. Mobile microscopy and telemedicine platform assisted by deep learning for the quantification of infection. PLoS Negl Trop Dis (2021) 15:e0009677.
  145. Bucki M, Dhufaigh KN, O'Brien C, Weatherley A, Walshe N, McElligott T. Comparison of ovine faecal Strongyle egg counts from an accredited laboratory and a rapid, on-site parasite diagnostic system utilising a smartphone app and machine learning. Vet Parasitol (2023) 320:109976.
    doi: 10.1016/j.vetpar.2023.109976pubmed: 37385104google scholar: lookup
  146. Ochwo S, Perez AM, Pérez Aguirreburualde MS. Beyond accuracy: leveraging ASSURED criteria for field evaluation of point-of-care tests for food animal diseases. Front Vet Sci (2023) 10:.
    doi: 10.3389/fvets.2023.1239111pmc: PMC10500061pubmed: 37720479google scholar: lookup
  147. Kaplan RM, Denwood MJ, Nielsen MK, Thamsborg SM, Torgerson PR, Gilleard JS. World Association for the Advancement of Veterinary Parasitology (WAAVP) guideline for diagnosing anthelmintic resistance using the faecal egg count reduction test in ruminants, horses and swine. Vet Parasitol (2023) 318:109936.
    doi: 10.1016/j.vetpar.2023.109936pubmed: 37121092google scholar: lookup
  148. Nielsen MK. Anthelmintic resistance in equine nematodes: current status and emerging trends. Int J Parasitol Drugs Drug Resist (2022) 20:76–88.
  149. Coles GC, Bauer C, Borgsteede FHM, Geerts S, Klei TR, Taylor MA, Waller PJ. World Association for the Advancement of Veterinary Parasitology (WAAVP) methods for the detection of anthelmintic resistance in nematodes of veterinary importance. Vet Parasitol (1992) 44:35–44.
    doi: 10.1016/0304-4017(92)90141-Upubmed: 1441190google scholar: lookup
  150. Königová A, Várady M, Corba J. Comparison of methods and faecal egg count reduction test for the detection of benzimidazole resistance in small strongyles of horses. Vet Res Commun (2003) 27:281–8.
    doi: 10.1023/A:1024079907895pubmed: 12872828google scholar: lookup
  151. Königová A, Craven J, Bjørn H, Barnes EH, Henriksen SA, Nansen P. comparison of tests and a faecal egg count reduction test in detecting anthelmintic resistance in horse strongyles. Vet Parasitol (1999) 85:49–59.
    doi: 10.1016/S0304-4017(99)00113-2pubmed: 10447192google scholar: lookup
  152. Whittaker JH, Carlson SA, Jones DE, Brewer MT. Molecular mechanisms for anthelmintic resistance in strongyle nematode parasites of veterinary importance. Vet Pharm & Therapeutics (2017) 40:105–15.
    doi: 10.1111/jvp.12330pubmed: 27302747google scholar: lookup
  153. Fissiha W, Kinde MZ. Anthelmintic resistance and its mechanism: a review. Infect Drug Resist (2021) 14:5403–10.
    doi: 10.2147/IDR.S332378pmc: PMC8687516pubmed: 34938088google scholar: lookup
  154. Chen X, Shi Y, Wang T, Liu C, Wang W, Wang Y. Study on the effect of GCY-12 gene on albendazole sensitivity of by RNA interference. Front Vet Sci (2025) 12:1567869.
    doi: 10.3389/fvets.2025.1567869pmc: PMC12104661pubmed: 40420951google scholar: lookup
  155. von Samson-Himmelstjerna G, Thompson RA, Krücken J, Grant W, Bowman DD, Schnyder M. Spread of anthelmintic resistance in intestinal helminths of dogs and cats is currently less pronounced than in ruminants and horses – Yet it is of major concern. Int J Parasitol (2021) 17:36–45.
  156. Mpofu TJ, Nephawe KA, Mtileni B. Prevalence and resistance to gastrointestinal parasites in goats: a review. Vet World (2022) 15:2442–52.
  157. Wit J, Dilks CM, Andersen EC. Complementary approaches with free-living and parasitic nematodes to understanding anthelmintic resistance. Trends Parasitol (2021) 37:240–50.
    doi: 10.1016/j.pt.2020.11.008pmc: PMC7878357pubmed: 33317926google scholar: lookup
  158. Papaiakovou M, Waeschenbach A, Ajibola O, Ajjampur SS, Anderson RM, Bailey R. Global diversity of soil-transmitted helminths reveals population-biased genetic variation that impacts diagnostic targets. Nat Commun (2025) 16:6374.
    doi: 10.1038/s41467-025-61687-0pmc: PMC12246136pubmed: 40640199google scholar: lookup
  159. Chen X, Wang T, Guo W, Yan X, Kou H, Yu Y. Transcriptome reveals the roles and potential mechanisms of lncRNAs in the regulation of albendazole resistance in . BMC Genomics (2024) 25:188.
    doi: 10.1186/s12864-024-10096-6pmc: PMC10873934pubmed: 38368335google scholar: lookup
  160. Dabrowska J, Sroka J, Cencek T. Investigating spp. using genomic, proteomic and transcriptomic techniques: current progress and future directions. IJMS (2023) 24:12867.
    doi: 10.3390/ijms241612867pmc: PMC10454211pubmed: 37629046google scholar: lookup
  161. Antonopoulos A, Gilleard JS, Charlier J. Next-generation sequencing technologies for helminth diagnostics and surveillance in ruminants: shifting diagnostic barriers. Trends Parasitol (2024) 40:511–26.
    doi: 10.1016/j.pt.2024.04.013pubmed: 38760257google scholar: lookup
  162. Quansah E, Chen Y, Yang S, Wang J, Sun D, Zhao Y. CRISPR-Cas13 in malaria parasite: diagnosis and prospective gene function identification. Front Microbiol (2023) 14:1076947.
    doi: 10.3389/fmicb.2023.1076947pmc: PMC9905151pubmed: 36760507google scholar: lookup
  163. Lobanov VA, Peckle M, Massard CL, Brad Scandrett W, Gajadhar AA. Development and validation of a duplex real-time PCR assay for the diagnosis of equine piroplasmosis. Parasit Vectors (2018) 11:125.
    doi: 10.1186/s13071-018-2751-6pmc: PMC5834856pubmed: 29499748google scholar: lookup
  164. Piesz J, Scro A, Corbett R, Markey Lundgren K, Smolowitz R, Gomez-Chiarri M. Development of a multiplex qPCR for the quantification of three protozoan parasites of the eastern oyster . Dis Aquat Org (2022) 151:111–21.
    doi: 10.3354/dao03694pubmed: 36300764google scholar: lookup
  165. Robert-Gangneux F, Duval X, Cazala C, Belaz S, Dupuis A, Guegan H. Improvement of the diagnosis of intestinal protozoa using a multiplex qPCR strategy compared to classical microscopy: a prospective study on 3,500 stool samples over 3 years. J Clin Microbiol (2025) 63:e0161024.
    doi: 10.1128/jcm.01610-24pmc: PMC12077082pubmed: 40162804google scholar: lookup
  166. Kotze AC, Gilleard JS, Doyle SR, Prichard RK. Challenges and opportunities for the adoption of molecular diagnostics for anthelmintic resistance. Int J Parasitol Drugs Drug Resist (2020) 14:264–73.
  167. Mbong Ngwese M, Prince Manouana G, Nguema Moure PA, Ramharter M, Esen M, Adégnika AA. Diagnostic techniques of soil-transmitted helminths: impact on control measures. TropicalMed (2020) 5:93.
    doi: 10.3390/tropicalmed5020093pmc: PMC7344795pubmed: 32516900google scholar: lookup
  168. Li X, Dang Z, Tang W, Zhang H, Shao J, Jiang R. Detection of parasites in the field: the ever-innovating CRISPR/Cas12a. Biosensors (2024) 14:14 5.
    doi: 10.3390/bios14030145pmc: PMC10968006pubmed: 38534252google scholar: lookup
  169. Feddema JJ, Fernald KDS, Keijser BJF, Kieboom J, van de Burgwal LHM. Commercial opportunity or addressing unmet needs—loop-mediated isothermal amplification (LAMP) as the future of rapid diagnostic testing?. Diagnostics (2024) 14:1845.
  170. Bari T, Al Mamun MdA, Toet H, Rathinasamy V, Larkins J-A, Beddoe T, Spithill TW, Piedrafita D, Greenhill AR. Evaluation of LAMP for detection from faecal samples of experimentally and naturally infected cattle. Vet Parasitol (2024) 327:110132.
    doi: 10.1016/j.vetpar.2024.110132pubmed: 38280252google scholar: lookup
  171. Doyle SR, Sankaranarayanan G, Allan F, Berger D, Jimenez Castro PD, Collins JB. Evaluation of DNA extraction methods on individual helminth egg and larval stages for whole-genome sequencing. Front Genet (2019) 10:826.
    doi: 10.3389/fgene.2019.00826pmc: PMC6764475pubmed: 31616465google scholar: lookup
  172. Li Y, Zheng R, Wu Y, Chu K, Xu Q, Sun M. Low-cost, automated parasite diagnostic system via a portable, robotic microscope and deep learning. J Biophotonics (2019) 12:e201800410.
    doi: 10.1002/jbio.201800410pubmed: 31081258google scholar: lookup
  173. Saha B, Tchiotsop D, Tchinda R, Wolf D, Noubom M. Automatic recognition of human parasite cysts on microscopic stools images using principal component analysis and probabilistic neural network. IJARAI (2015) 4:26–33.
  174. Widmer KW, Oshima KH, Pillai SD. Identification of oocysts by an artificial neural network approach. Appl Environ Microbiol (2002) 68:1115–21.
  175. Widmer KW, Srikumar D, Pillai SD. Use of artificial neural networks to accurately identify cryptosporidium oocyst and giardia cyst Images. Appl Environ Microbiol (2005) 71:80–4.
    doi: 10.1128/AEM.71.1.80-84.2005pmc: PMC544245pubmed: 15640173google scholar: lookup
  176. . Optimization of Resistance to Gastrointestinal Nematodes in Santa Inês sheep: A Genomic Selection, Machine Learning and Image Analysis Approach. .
  177. Yilmaz Adkinson A, Abouhawwash M, VandeHaar MJ, Parker Gaddis KL, Burchard J, Peñagaricano F. Assessing different cross-validation schemes for predicting novel traits using sensor data: an application to dry matter intake and residual feed intake using milk spectral data. J Dairy Sci (2024) 107:8084–99.
    doi: 10.3168/jds.2024-24701pubmed: 38876215google scholar: lookup
  178. Mota LFM, Giannuzzi D, Pegolo S, Toledo-Alvarado H, Schiavon S, Gallo L. Combining genetic markers, on-farm information and infrared data for the in-line prediction of blood biomarkers of metabolic disorders in Holstein cattle. J Animal Sci Biotechnol (2024) 15:83.
    doi: 10.1186/s40104-024-01042-3pmc: PMC11162571pubmed: 38851729google scholar: lookup
  179. Aboshady HM, Stear MJ, Johansson A, Jonas E, Bambou JC. Immunoglobulins as biomarkers for gastrointestinal nematodes resistance in small ruminants: a systematic review. Sci Rep (2020) 10:7765.
    doi: 10.1038/s41598-020-64775-xpmc: PMC7210940pubmed: 32385321google scholar: lookup
  180. Santana TEZ, Silva JCF, da Silva LOC, Alvarenga AB, Menezes GRO, Torres RAA. Genome-enabled classification of stayability in Nellore cattle under a machine learning framework. Livest Sci (2022) 260:104935.
  181. Kjetså MV, Gjuvsland AB, Nordbø Ø, Grindflek E, Meuwissen T. Accuracy of genomic prediction of maternal traits in pigs using Bayesian variable selection methods. J Animal Breeding Genetics (2022) 139:654–65.
    doi: 10.1111/jbg.12729pmc: PMC9796620pubmed: 35758628google scholar: lookup
  182. Quinn JA, Nakasi R, Mugagga PKB, Byanyima P, Lubega W, Andama A. Deep convolutional neural networks for microscopy-based point of care diagnostics. PMLR (2016) 56:271–81.
  183. Li S, Du Z, Meng X, Zhang Y. Multi-stage malaria parasite recognition by deep learning. GigaScience (2021) 10:giab040.
    doi: 10.1093/gigascience/giab040pmc: PMC8210472pubmed: 34137821google scholar: lookup
  184. Li S, Li A, Molina Lara DA, Gómez Marín JE, Juhas M, Zhang Y. Transfer learning for recognition. mSystems (2020) 5:e00445-19.
    doi: 10.1128/msystems.00445-19pmc: PMC6989130pubmed: 31992631google scholar: lookup
  185. Palasuwan D, Naruenatthanaset K, Kobchaisawat T, Chalidabhongse TH, Nunthanasup N, Boonpeng K. Parasitic egg detection and classification in microscopic images. IEEE Dataport (2022).
  186. Hiremath PS, Bannigidad P. Identification and classification of cocci bacterial cells in digital microscopic images. IJCBDD (2011) 4:262.
    doi: 10.1504/IJCBDD.2011.041414pubmed: 21778559google scholar: lookup
  187. El-Sayed SAE-S, Rizk MA, Baghdadi HB, Ringo AE, Sambuu G, Nugraha AB. Development of a promising antigenic cocktail for the global detection of in horse by ELISA. PLoS ONE (2023) 18:e0284535.
  188. Mitchell MC, Tzelos T, Handel I, McWilliam HEG, Hodgkinson JE, Nisbet AJ. Development of a recombinant protein-based ELISA for diagnosis of larval cyathostomin infection. Parasitology (2016) 143:1055–66.
    doi: 10.1017/S0031182016000627pubmed: 27174468google scholar: lookup
  189. Camoin M, Kocher A, Chalermwong P, Yangtarra S, Kamyingkird K, Jittapalapong S. The indirect ELISA in equids: optimisation and application to a serological survey including racing horses, in Thailand. Biomed Res Int (2019) 2019:1–12.
    doi: 10.1155/2019/2964639pmc: PMC6915159pubmed: 31886196google scholar: lookup
  190. Moore JN, Steiss J, Nicholson WE, Orth DN, Moore JN, Steiss J. A case of pituitary adrenocorticotropin-dependent cushing's syndrome in the horse. Endocrinology (1979) 104:576–82.
    doi: 10.1210/endo-104-3-576pubmed: 220013google scholar: lookup
  191. Caporale V, Biancifiori F, Frescura F, Dimatteo A, Nannini D, Urbani G. Comparison of various tests for the serological diagnosis of infection in the horse. Comp Immunol Microbiol Infect Dis (1981) 4:243–6.
    doi: 10.1016/0147-9571(81)90009-6pubmed: 7037279google scholar: lookup
  192. Mercer JG, Munn AE, Rees HH. Echinococcus granulosus: occurrence of ecdysteroids in protoscoleces and hydatid cyst fluid. Mol Biochem Parasitol (1987) 24:203–14.
    doi: 10.1016/0166-6851(87)90107-1pubmed: 3627169google scholar: lookup
  193. Rüegg SR, Torgerson P, Deplazes P, Mathis A. Age-dependent dynamics of and infections in southwest Mongolia based on IFAT and/or PCR prevalence data from domestic horses and ticks. Parasitology (2007) 134:939–47.
    doi: 10.1017/S0031182007002405pubmed: 17306055google scholar: lookup
  194. Jongejan F, Du C, Papadopoulos E, Blanda V, Di Bella S, Cannella V. Diagnostic performance of a rapid immunochromatographic test for the simultaneous detection of antibodies to and in horses and donkeys. Parasit Vectors (2021) 17:160.
    doi: 10.1186/s13071-024-06253-1pmc: PMC10979598pubmed: 38549117google scholar: lookup
  195. Borges-Silva W, de Jesus RF, Ferreira R, Gondim LFP. Reactivity of horse sera to antigens derived from Sarcocystis falcatula–Like and Sarcocystis neurona. Front Vet Sci (2020) 7:573016.
    doi: 10.3389/fvets.2020.573016pmc: PMC7667019pubmed: 33240954google scholar: lookup
  196. Tirosh-Levy S, Mazuz M, Savitsky I, Pinkas D, Gottlieb Y, Steinman A. Serological and molecular prevalence of in apparently healthy horses in Israel. Pathogens (2021) 10:445.
    doi: 10.3390/pathogens10040445pmc: PMC8068206pubmed: 33917822google scholar: lookup
  197. Onyiche TE, Sivakumar T, Tuvshintulga B, Nugraha AB, Ahedor B, Mofokeng L. Serosurvey for equine piroplasms in horses and donkeys from North-Western Nigeria using IFAT and ELISA. J Immunoassay Immunochem (2021) 42:648–61.
    doi: 10.1080/15321819.2021.1935274pubmed: 34097577google scholar: lookup
  198. Claes F, Ilgekbayeva GD, Verloo D, Saidouldin TS, Geerts S, Buscher P. Comparison of serological tests for equine trypanosomosis in naturally infected horses from Kazakhstan. Vet Parasitol (2005) 131:221–5.
    doi: 10.1016/j.vetpar.2005.05.001pubmed: 15951112google scholar: lookup
  199. Hébert L, Froger D, Madeline A, Lecouturier F, Lemans C, Zientara S. European inter-laboratory proficiency test for dourine antibody detection using the complement fixation test. Vet Sci (2005) 10:592.
    doi: 10.3390/vetsci10100592pmc: PMC10610798pubmed: 37888544google scholar: lookup
  200. Baldani CD, Machado RZ, Raso TF, Pinto AA. Serodiagnosis of in horses submitted to exercise stress. Pesq Vet Bras (2007) 27:179–83.
  201. Weiland G. Species-specific serodiagnosis of equine piroplasma infections by means of complement fixation test (CFT), immunofluorescence (IIF), and enzyme-linked immunosorbent assay (ELISA). Vet Parasitol (1986) 20:43–8.
    doi: 10.1016/0304-4017(86)90091-9pubmed: 3518216google scholar: lookup
  202. Kaspar A, Pfister K, Nielsen MK, Silaghi C, Fink H, Scheuerle MC. Detection of in equine faecal samples by real-time PCR and larval culture – method comparison and occurrence assessment. BMC Vet Res (2016) 13:19.
    doi: 10.1186/s12917-016-0918-ypmc: PMC5225560pubmed: 28077153google scholar: lookup
  203. Tirosh-Levy S, Steinman A, Levy H, Katz Y, Shtilman M, Gottlieb Y. Parasite load and genotype are associated with clinical outcome of piroplasm-infected equines in Israel. Parasit Vectors (2020) 13:267.
    doi: 10.1186/s13071-020-04133-ypmc: PMC7240905pubmed: 32434550google scholar: lookup
  204. Elsawy BSM, Nassar AM, Alzan HF, Bhoora RV, Ozubek S, Mahmoud MS. Rapid detection of equine piroplasms using multiplex PCR and first genetic characterization of in Egypt. Pathogens (2021) 10:1414.
    doi: 10.3390/pathogens10111414pmc: PMC8620363pubmed: 34832570google scholar: lookup
  205. Diekmann I, Blazejak K, Krücken J, Strube C, von Samson-Himmelstjerna G, Diekmann I. Comparison of morphological and molecular Strongylus spp. identification in equine larval cultures and first report of a patent infection in a horse. Equine Vet J (2025) 57:522–9.
    doi: 10.1111/evj.14134pmc: PMC11807925pubmed: 39012065google scholar: lookup
  206. Stout AE, Hofmar-Glennon HG, André NM, Goodman LB, Anderson RR, Mitchell PK. Infectious disease surveillance of apparently healthy horses at a multi-day show using a novel nanoscale real-time PCR panel. J VET Diagn Invest (2021) 33:80–6.
    doi: 10.1177/1040638720972096pmc: PMC7758683pubmed: 33179576google scholar: lookup
  207. Chen K, Hu Z, Yang G, Guo W, Qi T, Liu D. Development of a duplex real-time PCR assay for simultaneous detection and differentiation of and . Transbound Emerg Dis (2022) 69:e1338–49.
    doi: 10.1111/tbed.14464pubmed: 35089645google scholar: lookup
  208. Gummery L, Jallow S, Raftery AG, Bennet E, Rodgers J, Sutton DGM. Comparison of loop-mediated isothermal amplification (LAMP) and PCR for the diagnosis of infection with ssp. in equids in The Gambia. PLoS ONE (2020) 15:e0237187.
  209. Ahmed ME, Eldigail MH, Elamin FM, Ali IA, Grobusch MP, Aradaib IE. Development and evaluation of real-time loop-mediated isothermal amplification assay for rapid detection of cystic echinococcosis. BMC Vet Res (2016) 12:202.
    doi: 10.1186/s12917-016-0809-2pmc: PMC5020552pubmed: 27619674google scholar: lookup
  210. Salim B, Hayashida K, Mossaad E, Nakao R, Yamagishi J, Sugimoto C. Development and validation of direct dry loop mediated isothermal amplification for diagnosis of . Vet Parasitol (2018) 260:53–7.
    doi: 10.1016/j.vetpar.2018.08.009pubmed: 30197015google scholar: lookup
  211. Hifumi T, Akioka K, Tanaka T, Miyoshi N. Development of a loop-mediated isothermal amplification (LAMP) assay targeting the mitochondrial cytochrome b gene for the rapid detection of alveolar echinococcosis in hepatic nodules of horses. Vet Parasitol (2021) 299:109573.
    doi: 10.1016/j.vetpar.2021.109573pubmed: 34521042google scholar: lookup
  212. Choi B, Vu HT, Vu HT, Radwanska M, Magez S, Choi B. Advances in the immunology of the host–parasite interactions in African Trypanosomosis, including single-cell transcriptomics. Pathogens (2024) 13:188.
    doi: 10.3390/pathogens13030188pmc: PMC10975194pubmed: 38535532google scholar: lookup
  213. Adamu L, Turaki U, BukarKolo Y, Husainy A, Dauda I, Wakil Y. Current updates on diagnostic methodologies for tick-borne hemoparasitic diseases in equids: a review. J Adv Vet Anim Res (2016) 3:84.
    doi: 10.5455/javar.2016.c148google scholar: lookup
  214. Gavriliuc ST. Development of Non-Invasive Genomic Tools for Feral Horses. (Master's thesis, University of Calgary, Calgary, Canada) (2023).
    doi: 10.11575/PRISM/40699google scholar: lookup
  215. Sabir N, Chaudhry ZI, Aslam A, Muhammad K, Shahid M, Hussain A. A study on prevalence and molecular characterization of trypanosomal species infecting equines in Lahore region, Pakistan. J Parasit Dis (2018) 42:96–101.
    doi: 10.1007/s12639-017-0972-9pmc: PMC5825374pubmed: 29491567google scholar: lookup
  216. Zuccherato LW, Furtado LF, Medeiros CS, Pinheiro CS, Rabelo ÉM. PCR-RFLP screening of polymorphisms associated with benzimidazole resistance in and from different geographical regions in Brazil. PLoS Negl Trop Dis (2018) 12:e0006766.
  217. Song J, Song R, Wang P, Zhang Y, Yan Y, Zhou J. Preparation of monoclonal antibody against Ema-1 and development of rapid serological detection method for infection, Xinjiang, China. J Parasitol (2020) 106:283.
    doi: 10.1645/19-98pubmed: 32296849google scholar: lookup
  218. Furtado LFV, Magalhães JGS, Rabelo ÉML, Furtado LFV, Magalhães JGS, Rabelo ÉML. Standardization and application of a modified RFLP-PCR methodology for analysis of polymorphisms linked to treatment resistance in . Parasit Vectors (2018) 11:540.
    doi: 10.1186/s13071-018-3125-9pmc: PMC6178248pubmed: 30301454google scholar: lookup
  219. Davaasuren B, Amgalanbaatar T, Musinguzi SP, Suganuma K, Otgonsuren D, Mossaad E. The evaluation of GM6-based ELISA and ICT as diagnostic methods on a Mongolian farm with an outbreak of non-tsetse transmitted horse trypanosomosis. Vet Parasitol (2017) 244:123–8.
    doi: 10.1016/j.vetpar.2017.07.036pubmed: 28917303google scholar: lookup
  220. Maharana BR, Tewari AK, Saravanan BC, Sudhakar NR, Maharana BR, Tewari AK. Important hemoprotozoan diseases of livestock: challenges in current diagnostics and therapeutics: an update. Vet World (2016) 9:487–95.
  221. Gehlen H, Wulke N, Ertelt A, Nielsen MK, Morelli S, Traversa D. Comparative analysis of intestinal helminth infections in colic and non-colic control equine patients. Animals (2020) 10:1916.
    doi: 10.3390/ani10101916pmc: PMC7603170pubmed: 33086590google scholar: lookup
  222. Kooyman FNJ, van Doorn DCK, Geurden T, Wagenaar JA, Kooyman FNJ, van Doorn DCK. Semi-quantitative differentiation of cyathostomin larval cultures by reverse line blot. Vet Parasitol (2016) 216:59–65.
    doi: 10.1016/j.vetpar.2015.12.009pubmed: 26801596google scholar: lookup
  223. Johnson ACB, Biddle AS. the use of molecular profiling to track equine reinfection rates of cyathostomin species following anthelmintic administration. Animals (2021) 11:1345.
    doi: 10.3390/ani11051345pmc: PMC8150961pubmed: 34065099google scholar: lookup
  224. Alzan HF, Mahmoud MS, Suarez CE. Current vaccines, experimental immunization trials, and new perspectives to control selected vector borne blood parasites of veterinary importance. Front Vet Sci (2024) 11:1484787.
    doi: 10.3389/fvets.2024.1484787pmc: PMC11602000pubmed: 39606652google scholar: lookup
  225. Drescher G, dos Santos HG, Pinto MMG, Morello LG, Figueiredo FB. Diagnosis of fasciolosis antibodies in Brazilian cattle through ELISA employing both native and recombinant antigens. Microbiol Spectr (2024) 12:e0009524.
    doi: 10.1128/spectrum.00095-24pmc: PMC11064638pubmed: 38534120google scholar: lookup
  226. de Albergaria IS, Elsheikha H. Diagnostic challenges and alternatives for difficult-to-detect equine gastrointestinal parasites. UK-Vet Equine (2025) 9:138–47.
    doi: 10.12968/ukve.2024.0028google scholar: lookup
  227. Baghdadi HBA, Abdelsalam M, Attia MM. Diagnostic innovations in equine parasitology: a nanogold-ELISA for sensitive serodiagnosis of migratory larvae infections. BMC Vet Res (2024) 20:579.
    doi: 10.1186/s12917-024-04389-xpmc: PMC11674170pubmed: 39731087google scholar: lookup
  228. Hongsrichan N, Donthaisong P, Chaisongkram C, Eamudomkarn C, Pitaksakulrat O, Ponsrila K. Epidemiological surveillance of intestinal parasites and serological analysis of in captive felids from Thailand zoos. Vet Med Int (2025) 2025:1596677.
    doi: 10.1155/vmi/1596677pmc: PMC12259328pubmed: 40662085google scholar: lookup
  229. Attia MM, Omar HM. Gastric equine myiasis: prevalence, pathogenesis, molecular and serological implications. J Parasit Dis (2025) 1–9.
    doi: 10.1007/s12639-025-01782-7pmc: PMC12399486pubmed: 40901419google scholar: lookup
  230. Gondim LFP, Mineo JR, Schares G. Importance of serological cross-reactivity among , Hammondia spp, Neospora spp, Sarcocystis spp and . Parasitology (2017) 144:851–68.
    doi: 10.1017/S0031182017000063pmc: PMC5471829pubmed: 28241894google scholar: lookup
  231. Davenport K, Liu J, Sarquis J, Beall M, Montoya A, Drexel J. Performance of a point-of-care test for the detection of anti- antibodies is associated with immunofluorescent antibody titer and clinical stage of leishmaniosis in dogs from endemic regions.. Vet Parasitol Reg Stud Reports (2024) 53:101061.
    doi: 10.1016/j.vprsr.2024.101061pubmed: 39025539google scholar: lookup
  232. Toaleb NI, Shaapan RM, Elaadli H, Abdel Megeed KN, Aboelsoued D. Sarcocystis species: molecular identification and seroprevalence in water buffaloes (). BMC Vet Res (2025) 21:482.
    doi: 10.1186/s12917-025-04933-3pmc: PMC12281994pubmed: 40696429google scholar: lookup
  233. Gharban H, Sray A, Essa I. Serological prevalence of anti- antibodies in sheep.. J Vet Sci (2024) 55:1583–90.
  234. Hobbs EC, Colling A, Gurung RB, Allen J. The potential of diagnostic point-of-care tests (POCTs) for infectious and zoonotic animal diseases in developing countries: technical, regulatory and sociocultural considerations.. Transbound Emerg Dis (2021) 68:1835–49.
    doi: 10.1111/tbed.13880pmc: PMC8359337pubmed: 33058533google scholar: lookup
  235. Domrazek K, Jurka P. Application of next-generation sequencing (NGS) techniques for selected companion animals.. Animals (2024) 14:1578.
    doi: 10.3390/ani14111578pmc: PMC11171117pubmed: 38891625google scholar: lookup
  236. Leutenegger CM, Lozoya CE, Tereski J, Andrews J, Mitchell KD, Meeks C. Comparative study of a broad qPCR panel and centrifugal flotation for detection of gastrointestinal parasites in fecal samples from dogs and cats in the United States.. Parasit Vectors (2023) 16:288.
    doi: 10.1186/s13071-023-05904-zpmc: PMC10433665pubmed: 37587483google scholar: lookup
  237. Baltrušis P Höglund J. Digital PCR: modern solution to parasite diagnostics and population trait genetics.. Parasit Vectors (2023) 16:143.
    doi: 10.1186/s13071-023-05756-7pmc: PMC10131454pubmed: 37098569google scholar: lookup
  238. Musa Abdullahi A, Mallam Hamisu T, Muhammed Chafe U, Ibrahim Daneji A, Olayinka, Alayande M. Molecular identification of isolated from Camels () in Sokoto and its environs, Nigeria.. SAJOLS (2025) 3:298–303.
  239. Peña-Espinoza M, Em D, Shahi-Barogh B, Berer D, Duscher GG, van der Vloedt L. Molecular pathogen screening of louse flies (Diptera: Hippoboscidae) from domestic and wild ruminants in Austria.. Parasit Vectors (2023) 16:179.
    doi: 10.1186/s13071-023-05810-4pmc: PMC10236838pubmed: 37269018google scholar: lookup
  240. Rojas A, Germitsch N, Oren S, Sazmand A, Deak G. Wildlife parasitology: sample collection and processing, diagnostic constraints, and methodological challenges in terrestrial carnivores.. Parasit Vectors (2024) 17:127.
    doi: 10.1186/s13071-024-06226-4pmc: PMC10938792pubmed: 38481271google scholar: lookup

Citations

This article has been cited 2 times.
  1. Gentilini F, Ogundipe TG, Turba ME, Romagnoli N, Lambertini C, Pollera C, Cremonesi P, Stancampiano L. Beyond the host: Unveiling the independent microbiome of equine gastrointestinal nematodes. PLoS One 2026;21(2):e0339596.
    doi: 10.1371/journal.pone.0339596pubmed: 41666179google scholar: lookup
  2. Ullah A, Geng M, Chen W, Zhu Q, Shi L, Zhang X, Akhtar MF, Wang C, Khan MZ. Effect of Parasitic Infections on Hematological Profile, Reproductive and Productive Performance in Equines. Animals (Basel) 2025 Nov 14;15(22).
    doi: 10.3390/ani15223294pubmed: 41302002google scholar: lookup