Immune and parasitological response in horses infected with gastrointestinal nematodes in the humid tropic of Mexico

Authors

  • Roberto González-Garduño Universidad Autónoma Chapingo, Unidad Regional Universitaria Sursureste
  • Ema Maldonado-Simán Universidad Autónoma Chapingo, Pos- grado de Zootecnia., km 38.5 Carretera México-Texcoco. Texcoco, Estado de México, México.
  • Glafiro Torres-Hernández Colegio de Postgraduados-Campus Montecillo
  • José Luis Ponce Covarrubias Universidad Autónoma de Guerrero, Escuela Superior de Medicina Veterinaria y Zootecnia No. 3
  • Jorge Oliva-Hernández Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias, Campo Experimental Huimanguillo, Huimanguillo, Tabasco, México.
  • Pedro Mendoza-de Gives Centro Nacional de Investigación Disciplinaria en Salud Animal e Inocuidad, INIFAP. Boulevard Paseo Cuaunháhuac No. 8534, Col. Progreso, Jiutepec, Mor. México. CP 62550. http://orcid.org/0000-0001-9595-3573

DOI:

https://doi.org/10.19136/era.a8n1.2687

Keywords:

Cyathostomins, equines, immunoglobulins, parasites, Strongylus.

Abstract

The objective of the study was to determine the parasitological and immune response in horses naturally re-infected with gastrointestinal nematodes (GIN) after an- thelmintic treatment in the humid tropic of Mexico. The study was conducted in Tenosique, Tabasco, Mexico. A total of 30 horses were sampled monthly for nine months. Fecal samples were obtained to determine the number of nematode eggs per gram (EPG) of feces. Stool cultures were performed to obtain and identify infective larvae (L3) genera. Blood samples were also obtained to determine the packed cell volume (PCV), the total plasma protein (TPP), and the differential leukocyte count (DLC). Serum enzyme-linked immunosorbent assays (ELISA) were performed to determine IgA levels against adult cyathostomins and Strongylus nematode antigen. The analyses considered the age and gender of the horses, and the season (Cold, rainy and dry). The number of EPG and TPP were higher in females (1224 ± 1269 and 7.6 ± 0.6 gdL−1, respectively) than males (623 ± 671 and 7.4 ± 0.5 gdL−1, respectively), and no differences were observed with animal age (p > 0.05). The number of EPG increased in the rainy season. The main nematodes involved were of the subfamily Cyathostominae (97.4%) and to a lesser degree of species Strongylus equinus, S. edentatus, S. vulgaris, and Oxyuris equii. The season affected the leukocytes, neutrophils, and lymphocytes counts but not eosinophils. Variables such as gender, animal age, and environmental conditions are important elements for a diagnosis of GIN and the application of treatments for its control.

Downloads

Download data is not yet available.

Author Biography

  • Pedro Mendoza-de Gives, Centro Nacional de Investigación Disciplinaria en Salud Animal e Inocuidad, INIFAP. Boulevard Paseo Cuaunháhuac No. 8534, Col. Progreso, Jiutepec, Mor. México. CP 62550.

    Head of Department

    Department of Helminthology

References

Abo-aziza FAM, Hendawy SHM, Namaky AHE, Ashry HM (2017) Th1 / Th2 balance and humoral immune response to potential antigens as early diagnostic method of equine Strongylus nematode infection. Veterinary World 10: 679-687.

Andersen UV, Howe DK, Olsen SN, Nielsen MK (2013) Recent advances in diagnosing pathogenic equine gastrointestinal helminths : The challenge of prepatent detection. Veterinary Parasitology 192: 1-9.

Bowman DD (2011) Georgis Parasitología para Veterinarios. 9a Edition. Elsevier. Barcelona, España. 453 p.

Bradford MM (1976) A Rapid and sensitive method for the quantitation microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72: 248-254.

Burden FA, Du Toit N, Hernandez-Gil M, Prado-Ortiz O, Trawford AF (2010) Selected health and management issues facing working donkeys presented for veterinary treatment in rural Mexico : some possible risk factors and potential intervention strategies. Tropical Animal Health and Production 42: 597-605.

CONAGUA (2020) Servicio Meteorológico Nacional. Normales climatológicas. https://smn.conagua.gob.mx/es/informacion-climatologica-por-estado?estado=tab. Fecha de consulta 21 de julio de 2020.

Dobson RJ, Hosking BC, Jacobson CL, Cotter JL, Besier RB, Stein PA, Reid SA (2012) Preserving new anthelmintics : A simple method for estimating faecal egg count reduction test (FECRT) confidence limits when efficacy and / or nematode aggregation is high. Veterinary Parasitology 186: 79-92.

Domínguez-Sánchez C, Cervantes P, Pérez-Rico A, Delgado J, Jiménez L, Aguirre L, Brandariz C, Nuñez L, Cortés O, Farman S, Costa MR, Kelly L, Vega-Pla JL (2015). Estructura genética del caballo local de Veracruz, México, usando microsatélites. Actas Iberoamericanas de Conservación Animal 6: 192-200.

Francisco I, Arias M, Cortiñas FJ, Francisco R, Mochales E, Dacal V, Suárez JL, Uriarte L, Morrondo P, Sánchez-Andrade R, Díez-Baños P, Paz-Silva A (2009) Intrinsic factors influencing the infection by helminth parasites in horses under an oceanic climate area ( NW Spain ). Journal of Parasitology Research 2009: 5.

Fritzen B, Rohn K, Schnieder T, von Samson-Himmelstjerna G (2010) Endoparasite control management on horse farms – lessons from worm prevalence and questionnaire data. Equine Veterinary Journal 42: 79-83.

González-Garduño R, López Arellano ME, Mendoza De Gives P, Arece García J, Marie-Magdeleine C, Torres Hernández G, Oliva Hernández J, Hinojosa-Cuéllar JA (2017) Comparative response of IgA and IgG activity and hematological parameters among four main beef-cattle breeds infected with gastrointestinal nematodes in the warm humid tropic of Mexico. Annals of Animal Science 17:819-833.

González-Garduño R, Nuncio-Ochoa MGJ, Navarro-Martínez F, Balán FA, Arias Vázquez MS, Paz-Silva A (2015). Intensity of infection with strongylids nematodes in horses from Southeast Mexico. Chilean Journal of Agricultural and Animal Sciences 31: 127-136.

Gras LM, Usai F, Stancampiano L (2011). Strongylosis in horses slaughtered in Italy for meat production: Epidemiology, influence of the horse origin and evidence of parasite self-regulation. Veterinary Parasitology 179: 167-174.

Hinney B, Wirtherle NC, Kyule M, Miethe N, Zessin KH, Clausen PH (2011). Prevalence of helminths in horses in the state of Brandenburg, Germany. Parasitology Research 108: 1083.

Hubert JD, Seahorn TL, Klei TR, Hosgood G, Horohov DW, Moore RM (2004) Clinical signs and hematologic, cytokine, and plasma nitric oxide alterations in response to Strongylus vulgaris infection in helminth-naïve ponies. The Canadian Journal of Veterinary Research 68: 193-200.

Ibrahim N, Berhanu T, Deressa B, Tolosa T (2011). Survey of prevalence of helminth parasites of donkeys in and around Hawassa town, Southern Ethiopia. Global Veterinaria 6: 223-227.

Khan MA, Roohi N, Rana MAA (2015). Strongylosis in equines: a review. The Journal of Animal and Plant Science 25: 1-9.

Lumsden JH, Rowe R, Mullen K (1980). Hematology and biochemistry reference values for the light horse. Canadian Journal of Comparative Medicine 42: 32-42.

Matthews JB (2014) Anthelmintic resistance in equine nematodes. International Journal for Parasitology: Drugs and Drug Resistance 4: 310-315.

Moreau E, Chauvin A (2010) Immunity against Helminths: Interactions with the host and the intercurrent infections. Journal of Biomedicine and Biotchnology 2010: 1-9.

Musa MT, Abdel Wahab MB, Adam ME (2016). Internal and external parasitic infections of equines in South Darfur state, Western Sudan. University of Khartoum Journal of Veterinary Medicine and Animal Production 7: 1-9.

Navarro dos Santos C, Soares de Souza L, de Freitas Vieira V, Pinheiro J, de Azevedo Rodrigues M (2012) Cyathostomin larvae : presence on Brachiaria humidicola grass during the rainy and dry seasons of Brazil. Revista Brasileira de Parasitologia Veterinaria 2961: 28-31.

Nielsen MK, Baptiste KE, Tolliver SC, Collins SS, Lyons ET (2010) 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. Veterinary Parasitology 174: 77-84.

Perkins GA, Wagner B (2015). The development of equine immunity : Current knowledge on immunology in the young horse. Equine Veterinary Journal 47: 267-274.

SAS (2017) SAS/STAT User´s Guide. Release 6. Inst., S. (ed.),. Cary, NC, USA.

Schneider S, Pfister K, Becher AM, Scheuerle MC (2014) Strongyle infections and parasitic control strategies in German horses - a risk assessment. BMC Veterinary Research 10: 1-9.

Seyoum Z, Tesfaye M, Derso S (2015) Prevalence, intensity and risk factors of infestation with major gastrointestinal nematodes in equines in and around Shashemane, Southern Ethiopia. Tropical Animal Health and Production 47: 1515-1521.

Tavassoli M, Dalir-Naghadeh B, Esmaeili-Sani S (2010). Prevalence of gastrointestinal parasites in working horses. Polish Journal of Veterinary Scicences 13: 319-324.

Thienpont D, Rochette F, Vanparijs OFJ (2003). Diagnosing helminthiasis by coprological examination. 3th Edition. Janssen Research Foundation. Beerse, Belgium. 215 p.

Valdéz-cruz MP, Hernández-Gil M, Galindo-Rodríguez L, Alonso-Díaz MÁ (2013). Gastrointestinal nematode burden in working equids from humid tropical areas of central Veracruz, Mexico, and its relationship with body condition and haematological values. Tropical Animal Health and Production 45: 603-607.

Downloads

Published

2021-04-17

Issue

Section

SCIENTIFIC ARTICLE

How to Cite

González-Garduño R. ., Maldonado-Simán E., Torres-Hernández, G. ., Ponce Covarrubias, J. L., Oliva-Hernández, J., & Mendoza-de Gives, P. (2021). Immune and parasitological response in horses infected with gastrointestinal nematodes in the humid tropic of Mexico. Ecosistemas Y Recursos Agropecuarios, 8(1). https://doi.org/10.19136/era.a8n1.2687

Similar Articles

You may also start an advanced similarity search for this article.

Most read articles by the same author(s)