Prevalence and Risk Factors of Gastrointestinal Parasites in Sheep in Kajiado North Sub-County, Kenya.
Authors
Department of Land Resources Management and Agricultural Technology, Faculty of Agriculture, University of Nairobi (Kenya)
Department of Land Resources Management and Agricultural Technology, Faculty of Agriculture, University of Nairobi (Kenya)
Faculty of Health Sciences, Outspan Global University, Nyeri (Kenya)
Department of Clinical Studies, Faculty of Veterinary Medicine, University of Nairobi (Kenya)
Department of Clinical Studies, Faculty of Veterinary Medicine, University of Nairobi (Kenya)
Article Information
DOI: 10.51584/IJRIAS.2025.10100000134
Subject Category: Health Science
Volume/Issue: 10/10 | Page No: 1483-1496
Publication Timeline
Submitted: 2025-10-20
Accepted: 2025-10-26
Published: 2025-11-14
Abstract
The gastrointestinal parasite (G.I.P.) species of Public Health, Agricultural and Veterinary concern, which affect the health of sheep and goat, belong to several Genera in the Phylum Protozoa (Unicellular Organisms), Phylum Nematohelminthes (Round Worms), and Phylum Platyhelminthes (Flatworms). The species of clinical significance in the Phylum Protozoa belong to the Genera: Eimeria, Isospora, Cryptosporidium, Cyclospora, Toxoplasma, and Giardia. Roundworm species belong to the Class Nematoda, with several Genera. These are Trichostrongylus, Strongylus, Cyanthostomin, Strongyloides, Haemonchus, Cooperia, Nematodirus, Trichuris, Toxocara, Ostertagia, Oesophagostomum, Cherpertia, Bunostomum (Hookworms), and Gongylonema. Flatworm species belong to two classes: Trematoda (Flukes) and Cestoda (Tapeworms). Trematodes of clinical concern belong to the Genera: Fasciola, Dicroelium, and Paramphistomum. The cestode species of clinical concern belong to the Genera: Moniezia, Avitellina and Echinococcus. The Unicellular parasites belong to Phylum: Protozoa, Sub-phylum: Sporozoa, Class Telosporidea and Sub-class Coccidea. The Coccidian parasite species of clinical concern belong to several Genera, namely: Eimeria, Isospora, Cyclospora, Toxoplasma, Cryptosporidium, and Sarcocystis. Gastrointestinal parasites (G.I.P.) of sheep are a threat to sheep industry worldwide. A cross-sectional study was conducted to determine the prevalence and risk factors associated with GIP in sheep under an extensive grazing system from 16 farms in Kajiado North Sub-County.
Faecal samples equal to 640 were collected from randomly selected Red Maasai and Red Maasai x Dorper crossbred sheep in both dry and wet seasons. Faecal samples were subjected to the McMaster technique, sedimentation, larval cultures. Coccidia species identification of eggs and oocysts was based on morphology.
Overall parasites prevalence was 91.3%, with many sheep showing one or more G.I.P (Gastro-Intestinal Parasites). The study revealed Strongylus species nematode eggs (80%), Eimeria species. oocysts at (60.8%) and Cestode eggs (5.2%). The highest prevalence of gastro-intestinal parasites was recorded in the wet season than in the dry season (p<0.05). Haemonchus, Trichostrongylus, Cooperia and Oesophagostomum were parasites identified using Baerman’s technique. Haemonchus species was the commonest and Oesophagostomum was the least common. Cestodes (Moniezia species) were present, but there were no Trematode species seen. E. parva, E. ovinoidalis, E. crandallis, E. bakuensis, E. faurei, E. ahsata, E. pallida. The following Eimeria species were identified: E. intricata, E. marsica, and E. granulosa, after sporulation using 2.5% potassium dichromate. The majority of sheep were also severely infested with gastrointestinal nematodes (Strongylus species). Multiple correlation analysis revealed elevation, deworming, Body Condition Scores (B.C.S.), and age of the sheep as factors of Gastro-intestinal Parasite (G.I.P.) infection. The study area was highly infested with gastro- intestinal parasites requiring an effective and strategic deworming of all sheep before the rainy season, especially considering the lambs. Further studies should also be taken on Gastrointestinal Nematode (G.I.N.) anthelmintic resistance and their economic losses for effective management practices to minimise the associated mortality and morbidity of sheep.
Keywords
Risk Factors, Sheep, Eimeria,
Downloads
References
1. Jeffrey, H.C. and Leach, R.M. (1988). Atlas of Medical Helminthology and2. Protozoology, 2nd Edition, Churchill Livingstone, Edinburgh, U.K. [Google Scholar] [Crossref]
2. Chiodini, P. L., Moody, A. H. and Manser, D.W. (2001). Atlas of Medical Helminthology and Protozoology, Churchill Livingstone, 4th Edition, Edinburgh, U.K. [Google Scholar] [Crossref]
3. FAO. (2022). World Food and Agriculture – Statistical Yearbook 2022. In World Food and Agriculture – Statistical Yearbook 2022. https://doi.org/10.4060/cc2211en. [Google Scholar] [Crossref]
4. MALFI. (2019). Agricultural Sector Transformation and Growth Strategy: Towards Sustainable Agricultural Transformation and Food Security in Kenya. Abridged 9. version. Ministry of Agriculture, Livestock, Fisheries and Irrigation (MALFI). 1–215. [Google Scholar] [Crossref]
5. Ministry of Agriculture and Livestock Development. (2023). EXPRESSION OF INTEREST (By the consulting firm in response to the REOI issued by the procuring 12. entity) For Consulting services to develop, configure and commission a system with e- extension module and e-marketing module. May. [Google Scholar] [Crossref]
6. FAO (2019). The future of livestock in Kenya. Food and Agriculture Opportunities and challenges in the face of uncertainty. Rome, pp. 56. [Google Scholar] [Crossref]
7. Ministry of Agriculture, Livestock, Fisheries, and, C. (2020). State Department for Livestock the Livestock Policy 2020 Printed by the Government Printer, Nairobi. 3. [Google Scholar] [Crossref]
8. IFAD. (2018). International Fund for Agricultural Development Republic of Kenya Country Strategy and Programme Evaluation (Issue November). [Google Scholar] [Crossref]
9. Silva, S., Birrento, L. S., Almeida, M. Ribeiro, D. M. et al (2022). Extensive sheep and 21. Goat Production: The Role of Novel Technologies towards sustainability and Animal 22. welfare. Animals, 12 (7): 885.D01: 10.3390/ani 12070885. [Google Scholar] [Crossref]
10. Mbong, E., Payne, V. K., Cedric, Y., Nadia, N. et al (2021). Prevalence of Gastro- 24. intestinal Parasites of Sheep and Goats of Bui and Donga-Mantung Divisions of the 25. North West Region of Cameroon. Asian Journal of Animal and Veterinary Advances, 7 (4):1-15. [Google Scholar] [Crossref]
11. Molla, W., Moliso, M. M., Gizaw, S., Nane, T., Arke, A. Ayele, F and Knight Jones, T. 28. (2023). Ovine gastro-intestinal parasite burden and the impact of strategic anthelmintic treatment in community-based breeding sites in Ethiopia. Front. Vet. Sa., 10. [Google Scholar] [Crossref]
12. Rufino-Moya, P. J., Leva, R. Z., Reis, L. G., Garcia, I. A., Di Genova, D. R., Gomex, A. S., Garcia, F. G and Martinez-Moreno, F. J. (2024). Prevalence of Gastro-intestinal Parasites in small ruminant Farms in Southern Spain. Animals, 14 (11): 1668. [Google Scholar] [Crossref]
13. Faran, N., Khatoon, S., Kumar, V., Meena A. and Jangid, S. K. (2024). Prevalence of 33. helminth infection in sheep in Udaipur district (Rajashan). International Journal of Veterinary Sciences and Animal Husbandry SP-9 (1): 95-99. [Google Scholar] [Crossref]
14. Semakula, J., Corner-Thomas, R. A., Morris, S. T., and Blair, Hugh (2021). Predicting 36. everybody condition score using adjusted live weight, height at withers and previous 37. body condition score record. Translational Animal Science, 5 (3): D01:10.1093/tas/txab.130. [Google Scholar] [Crossref]
15. Salehi, A., Razavi, M. and Nouri, N. V. (2022). Seasonal Prevalence of Helminthic 40. Infections in the Gastro-intestinal Tract of sheep in Mazandaran Province, Northern Iran. Journal of Parasite res., 2022: 7392801.doi:10.1155/2022/7392801. [Google Scholar] [Crossref]
16. Terfa, W., Kumsa, B., Ayana, D., Bekele, H., Maurizio, A., Tessarin, C. and Cassini, R. (2023). Epidemiology of Gastro-intestinal Parasites of Sheep in Three Agro-ecological 44. Zones in West Shewa Zone, Oromia State, Central Ethiopia. Journal of Veterinary Medicine and Research 12379-948x. [Google Scholar] [Crossref]
17. Rerkyusuke, S., Lerk-u-suke, S., Mektrirate, R., Wratsudakul, A., Kanjanupa P., et al (2024). Prevalence and Associated Risk Factors of Gastro-intestinal Parasite Infections among Meat Goats in Khonkaen, Thailand. Veterinary Medicine International, 2024 (1): 3267028. [Google Scholar] [Crossref]
18. Chen, J., Gong, Y., Chen, P., Li, S. and Zhou, Y. (2024). Global Burden of Soil- 51. Transmitted helminth infections, 1990-2021 Infectious Diseases of Poverty, 13: 77. [Google Scholar] [Crossref]
19. Palomino-Guerrera, W., Huaman, M. R. et al (2024). Gatsro-intestinal parasites in free 53. grazing goats from Ayacucho, Peru: Prevalence and risk factors associated with 54. infection in herds. Tropical Animal Health and Production, 56: 365. [Google Scholar] [Crossref]
20. Ballesteros, C., Mwasi, A., Mungai, E. Ibrahim, A., Thuranira-McKeever, C., Aboge, G.O., Onono J. O. and Alarcon, P. (2021). Developing and validating a rapid assessment tool for small ruminant reproduction and production in pastoralist flocks in Kajiado, Kenya. Veterinary and Animal Science, 13:100186. [Google Scholar] [Crossref]
21. Kruchynemko, O. (2024). Three different faecal egg counting techniques in ruminants (2024). Regulatory Mechanisms in Biosystems, 15 (4): 776-781. [Google Scholar] [Crossref]
22. Bosco, A., Ciuca, L., Maurelli, M.P., Viliello, P., Cringoli, G., Prada, J.M. and Rinaddi, A. L. (2023). Comparison of Mini-Flotac, Fluke Finder and Sedimentation techniques for etection and Qualification of Fasciola hepatica and Calicophoron daubneui eggs using spiked and naturally infected florine faecal samples. Parasite vectors, 16: 260.doi: 10:1186/5/3071. [Google Scholar] [Crossref]
23. Bathmanaban, P., Chandrawathani, P., Omar, J. Pricilla, Jackie and Josephine (2015). McMaster Method of worm egg count from faecal samples of goats: A comparison of66. single and double chamber enumeration of worm eggs, Malaysian Journal of Veterinary Research, 6 (1): 81-87. [Google Scholar] [Crossref]
24. Lozano, J., Anaya, A.M.D., Rinaldi, L., Cringoli, G. Gomes, L. et al (2021). Diagnosis 69. of Coccidiosis by Eimeria species in free-range chickens using Mini-FLOTAC and McMaster techniques preliminary results. Sci. Parasitol, 22 (1):13-18. [Google Scholar] [Crossref]
25. Sabatini, G. A., Borges, F. de. A., Claerebout, E. Gianechini, S. et al (2023). Practical guide to the diagnostics of ruminant gastro-intestinal nematodes, liver flukes and 73. lungworm infection: interpretation and usability of results. Parasite vectors, 16: 58. Doi:10-1186/s 13071. [Google Scholar] [Crossref]
26. Gelaye, W., Williams, N.A., Kepha, S., Junior, A.M. et al (2021). Performance A. evaluation of Baermann’s techniques: The guest for developing a microscopy B. reference standard for the diagnosis of Strongyloides stercoralis. PLoS Negl Trop. C. Dis., 15 (2): e0009076.doi:10.1371/journal. Pntd. [Google Scholar] [Crossref]
27. Parlovic, I., Bojkorski, J., Caro- Petrovk, V., Tasic, A., Pavlovic, M., Zidravkovic, N. A. and Mederle, N. (2023). Control of Coccidiosis of Farm-Breeding Sheep. Scientific B. Papers Journal Veterinary Series, 66 (1): 77-80. [Google Scholar] [Crossref]
28. Khan, M. N., Iqbal, Z., & Sajid Bhutta, M. (2011). Prevalence and associated risk A. factors of Eimeria in sheep of Punjab, Pakistan Tissue culture of medicinal/horticultural plants View project. https://www.researchgate.net/publication/281925702. [Google Scholar] [Crossref]
29. Challaton, K. P., Akouedegni, C. G., Boko, K. C., Alowanou, G. G., Houndonougbo, P. V., Kifouly, A. H., & Hounzangbé-Adoté, M. S. (2023). Evaluation of the Gastrointestinal Parasite Burden of Goats in Traditional Breeding in Benin. Journal of Animal Health and Production, 11(2), 144–154. https://doi.org/10.17582/journal.jahp/2023/11.2.144.154. [Google Scholar] [Crossref]
30. Dafur, B. S., Mbap, S. T., Tok, C. C., & Okoh, J. J. (2020). Breed and environmental 86. factors influencing the prevalence of helminths in sheep. Nigerian Journal of Animal Production, 47(5), 13–28. https://doi.org/10.51791/njap.v47i5.1269. [Google Scholar] [Crossref]
31. Ruhoollah, Khan, W., Al-Jabr, O. A., Khan, T., Khan, A., El-Ghareeb, W. R., Aguilar- Marcelino, L., Hussein, E. O. S., Alhimaidi, A. R., & Swelum, A. A. (2023). Prevalence of gastrointestinal parasite in small ruminants of District Dir Upper Khyber Pakhtunkhwa Province of Pakistan. Brazilian Journal of Biology, 83, 1–5. https://doi.org/10.1590/1519-6984.248978. [Google Scholar] [Crossref]
32. Rizwan, H. M., Sajid, M. S., Iqba, Z., Nadeem, R., Ahmad, M., Sultan, M., Saqib, M., Abbas, H., Shamim, A., Qudoos, A., & Haenlein, G. F. W. (2021). Correlation of the 95. Gastrointestinal Parasitism with the Phyto minerals in the Grazing Sheep (Ovis aries). International Journal of Agriculture and Biology, 26(1), 60–68. https://doi.org/10.17957/IJAB/15.1809. [Google Scholar] [Crossref]
33. Mohamed, H. I., Arafa, W. M., & El-Dakhly, K. M. (2023). Prevalence and associated risk factors of gastrointestinal helminths and coccidian infections in domestic goats, 100. Capra hircus, in Minya, Egypt. Beni-Suef University Journal of Basic and Applied 101. Sciences, 12(1). https://doi.org/10.1186/s43088-023-00369-6. [Google Scholar] [Crossref]
34. Ngetich, E. C., Ngeiywa, M., Ng’wena, G. M., & Chemwolo, L. (2019). Haematological Parameters by Age and Sex of Asymptomatic Indigenous Cattle and 104. Sheep Infected with Gastrointestinal Parasites in Kerio Valley, Kenya. American 105. Journal of Biomedical Research, 7(2), 44–50. https://doi.org/10.12691/ajbr-7-2-4. 106. [Google Scholar] [Crossref]
35. Ahmed, N., Ramadan, M., El-Maadawy, R., & Al-Assas, M. (2023). Prevalence of A. gastrointestinal helminths infesting sheep in Qalyubia governorate, Egypt. [Google Scholar] [Crossref]
36. Sebro, E., Kebamo, M., & Abebe, A. (2022). Prevalence of Gastrointestinal Parasites A. of Sheep and Goats in An- Lemo, Hadiya Zone Southern Ethiopia. Indian Journal of B. Science and Technology, 15(22), 1084–1090. https://doi.org/10.17485/IJST/v15i22.1384. [Google Scholar] [Crossref]
37. Baihaqi, Z. A., Widiyono, I., & Nurcahyo, W. (2019). Prevalence of gastrointestinal 110. worms in Wonosobo and thin-tailed sheep on the slope of Mount Sumbing, Central 111. Java, Indonesia. Veterinary World, 2(11), 1866–1871. https://doi.org/10.14202/vetworld.2019.1866-1871. [Google Scholar] [Crossref]
38. Khatlak, I., Akhtar, A. Shams, S., Usman, T., Haider, J. Noreen, N., Khan, A. and A. Said, M.B. (2023). Diversity Prevalence and risk factors associated to gastro-intestinal B. tract parasites in wild and domestic animals from Pakistan, Parasitology C. International, 97: 102777. [Google Scholar] [Crossref]
39. Musa, K. Y., Jima, C. N. and Asoffa, M. S. (2024); Prevalence of gastro-intestinal tract parasites in small ruminants in and around Jaja town, Melka Belo Woreda of East haraghe Zone Oromia, Ethiopia. Journal of Research in Veterinary Sciences, 2 (2): 51- 116. 66. [Google Scholar] [Crossref]
40. Khan, A., Jamil, M., Ullah, S., Ramzan, F., Khan, H., Ali, M., Rehman, A.U., Jabeen, 118. N. and Amber, R. (2023). The Prevalence of Gastro-intestinal Nematodes in Livestock 119. and their Health Hazards: A review-, World’s Veterinary Journal, 13 (1): 57-64. [Google Scholar] [Crossref]
41. Cai, W., Cheng, C., Feug, R., Ma, Y., Hua, E., Jiang, S., Hou, Z., Liu, D., Yang A., Cheng, D., Xu, and Tao, J. (2023). Prevalence and rsk factors associated with gastro- 122. intestinal parasites in goats (Capra hircus) and sheep (Ovis aries) from three provinces A. of China. Frontiers in Microbiology, 14:1287835. Doi.10.3389/. [Google Scholar] [Crossref]
42. Catsgna, F., Bava, R., Gagliardi, M., Russo, S., Poerio, G., Ruga, S. et al (2024). A. Prevalence of Helminths in Small Ruminant Farms and Evaluation of Control B. Practices Used to Counter Anthelmintic Resistance in Southern Italy. Pathogens, 13 124. (6): 493.doi:10.3390/pathogens. [Google Scholar] [Crossref]
43. Tachack, E. B., Oviedo-Socarrás, T., Pastrana, M. O., Pérez-Cogollo, L. C., Benavides, Y. H., Pinto, C. R., & Garay, O. V. (2022). Status of gastrointestinal nematode 127. infections and associated epidemiological factors in sheep from Córdoba, Colombia. Tropical Animal Health and Production, 54(3), 1–9. https://doi.org/10.1007/s11250- 022-03170-2. [Google Scholar] [Crossref]
44. Arsenopoulos, K. V., Fthenakis, G. C., Katsarou, E. I., & Papadopoulos, E. (2021). Haemonchosis: A challenging parasitic infection of sheep and goats. Animals, 11(2), 132. 1–29. https://doi.org/10.3390/ani11020363 [Google Scholar] [Crossref]
45. Zulu, G., Stelzle, D., Mwape, K.E. et al (2023). The epidemiology of human Taenia solium infections: A systematic review of the distribution in Eastern and Southern Africa. PloS Negl Trop. Dis., 17 (3): E0011042.doi: 10.1371/journal. pntd. [Google Scholar] [Crossref]
46. Rashid, A., Khattak, M. N. K., Khan, M. F., Ayaz, S., & Rehman, A. U. (2016a). 136. Gastrointestinal Helminthoses: Prevalence and Associated Risk Factors In Small A. Ruminants Of District Kohat, Pakistan. In The J. Anim. Plant Sci (Vol. 26, Issue 4). [Google Scholar] [Crossref]
47. Taylor, Coop, & Wall. (2016). No 4th Edition Title VETERINARY PARASITOLOGY. In Wiley Blackwell (Vol. 6, Issue August). [Google Scholar] [Crossref]
48. Kanyari, P. W. N. (1993). The relationship between coccidial and helminth infections in sheep and goats in Kenya. Veterinary Parasitology, 51(1–2), 137–141. https://doi.org/10.1016/0304-4017(93)90204-Z. [Google Scholar] [Crossref]
49. Kaya, G. (2004). Prevalence of Eimeria species in lambs in Antakya province. Turkish 143. Journal of Veterinary and Animal Sciences, 28(4), 687–692. [Google Scholar] [Crossref]
50. Minnat, T. R. (2014). Detection of gastrointestinal parasite infection of sheep and goats in Diyala Province-IraqoaJournal of Vet. Med. Sci, 13(2). [Google Scholar] [Crossref]
51. Tadalech, K., Dimshasha, T., & Abaje, A. (2020). Prevalence and the associated risk factors of gastrointestinal parasites of shoats in Tiyo District, Arsi zone, Oromia, South 148. West Ethiopia. International Journal of Agricultural Science and Food Technology, 149. 6(1), 075–078. https://doi.org/10.17352/2455-815x.000058. [Google Scholar] [Crossref]
52. Gunathilaka, N., Niroshana, D., Amarasinghe, D., & Udayanga, L. (2018a). Prevalence of Gastrointestinal Parasitic Infections and Assessment of Deworming 152. Program among Cattle and Buffaloes in Gampaha District, Sri Lanka. BioMed 153. Research International, 2018. https://doi.org/10.1155/2018/3048373. [Google Scholar] [Crossref]
53. Martins, N. S., dos Santos, C. C., da Motta, S. P., da Silva Moreira, A., da Rosa Farias,N. A., & Ruas, J. L. (2022). Gastrointestinal Parasites in Sheep from the Brazilian 156. Pampa Biome: Prevalence and Associated Factors. Revista Brasileira de Medicina 157. Veterinaria, 44. https://doi.org/10.29374/2527-2179.bjvm001522. [Google Scholar] [Crossref]
54. Desalean, C.& Berhanu, G. (2023). Assessment of the Epidemiology of the Gastro A. intestinal Tract Nematode Parasites in sheep in Toke Kutaye, West Shoa Zone, B. Ethiopia, Veterinary Medicine: Research and Reports, 14:177-183! 159. 56. Dabasa, G., Shanko, T., Zewdei, W., Jilo, K., Gurmesa, G., & Abdela, N. (2017). [Google Scholar] [Crossref]
55. Journal of Parasitology and Vector Biology Prevalence of small ruminant gastrointestinal parasites infections and associated risk factors in selected districts of C. Bale zone, south-eastern Ethiopia. 9 (6): 81–88. https://doi.org/10.5897/JPVB2017.0286. [Google Scholar] [Crossref]
56. Regassa, F., Sori, T., Dhuguma, R., & Kiros, Y. (2006). Epidemiology of 161. gastrointestinal parasites of ruminants in Western Oromia, Ethiopia. International 162. Journal of Applied Research in Veterinary Medicine, 4 (1), 51–57. http://www.jarvm.com. [Google Scholar] [Crossref]
57. Odoi, A., Gathuma, J. M., Gachuiri, C. K., & Omore, A. (2007). Risk factors of 165. gastrointestinal nematode parasite infections in small ruminants kept in smallholder 166. mixed farms in Kenya. BMC Veterinary Research, 3.https://doi.org/10.1186/1746- 6148-3-6. [Google Scholar] [Crossref]
58. Namutosi, W.Hifeny, J. Kizito, E. & Omodo, M. (2020). Prevalence and risk factors of 169. gastro-intestinal Parasite infection in goats in Soronko District, Eastern, Uganda. International Journal & Veterinary Science and Animal Husbandry, 5 (3): 27-35. [Google Scholar] [Crossref]
Metrics
Views & Downloads
Similar Articles
- Measuring Waste of Patient Time in Health Care at Non-Digitized Hospital: An Observational Study in Bangabandhu Sheikh Mujib Medical University, Bangladesh
- Reaffirming Clinical Confidence in Atorvastatin Therapy: A Digital Outreach Case Study from Tamil Nadu, India
- Clinical Manifestations and Therapeutic Response in a Patient with Hypothyroidism: A Case Report
- Eranda (Ricinus Communis) In Gridhrasi (Sciatica): Classical Rationale, Pharmacology and Clinical Evidence- A Narrative Literature Review
- Magnetotherapy in Pain Management: Mechanisms, Clinical Applications, and Future Perspectives – A Review