Data-driven risk assessment of gastrointestinal parasitism in zero-grazed goats: Influence of age, gender, and body weight

Gastrointestinal parasites in goats

Authors

  • Md Safiul Alam Bhuiyan Faculty of Sustainable Agriculture, Universiti Malaysia Sabah, 90000 Sandakan, Sabah, Malaysia.
  • Rayhan Firdaus Rusly Faculty of Sustainable Agriculture, Universiti Malaysia Sabah, 90000 Sandakan, Sabah, Malaysia.
  • Fatin Naazira Along Faculty of Sustainable Agriculture, Universiti Malaysia Sabah, 90000 Sandakan, Sabah, Malaysia.
  • Su Chui Len Candyrine Faculty of Sustainable Agriculture, Universiti Malaysia Sabah, 90000 Sandakan, Sabah, Malaysia.
  • Mohamad Asrol Kalam Faculty of Sustainable Agriculture, Universiti Malaysia Sabah, 90000 Sandakan, Sabah, Malaysia.
  • Rohaida Abdul Rasid Faculty of Sustainable Agriculture, Universiti Malaysia Sabah, 90000 Sandakan, Sabah, Malaysia.
  • Rovina Kobun Faculty of Sustainable Agriculture, Universiti Malaysia Sabah, 90000 Sandakan, Sabah, Malaysia.
  • Mohammad Mijanur Rahman Faculty of Sustainable Agriculture, Universiti Malaysia Sabah, 90000 Sandakan, Sabah, Malaysia.
  • Norafizah Abdul Rahman Faculty of Sustainable Agriculture, Universiti Malaysia Sabah, 90000 Sandakan, Sabah, Malaysia.

DOI:

https://doi.org/10.51200/jsffs.v2i1.7351

Keywords:

data-driven risk assessment, faecal egg count, gastrointestinal parasite, goat host demographic, katjang goats

Abstract

Gastrointestinal parasite (GIP) infections are a primary constraint on health and productivity in intensive caprine production, yet their impact in zero-grazing systems is frequently underestimated. This study aimed to quantify the prevalence and intensity of GIP infections in a research herd and to identify host-specific demographic drivers of parasite shedding. A cross-sectional study was conducted on 50 Katjang goats at the Livestock Research Unit, Universiti Malaysia Sabah. Faecal egg counts (EPG) were quantified using standardised methods, and the resulting data were analysed using Negative Binomial (NB) regression to account for high overdispersion. Results revealed an exceptionally high herd prevalence of 98%. Parasite intensity was highly aggregated, characterised by a small percentage of "super-shedders," including one extreme outlier exceeding 26,000 EPG. The NB model (α = 0.656, P < 0.001) identified age and gender as the most significant predictors of infection intensity. Younger goats (<1 year) exhibited the highest mean EPG (2,640), suggesting increased susceptibility due to physiological immaturity. Furthermore, gender was a primary driver of variation (P = 0.034), with males exhibiting significantly higher mean EPG and greater shedding variance than females. While body weight showed high variability among mid-weight individuals, lower body weight often coincided with peak shedding in younger cohorts. These findings indicated that in confined, zero-grazing systems, infection intensity is heavily influenced by host-specific factors rather than environmental exposure alone. The study highlights the inadequacy of traditional, herd-wide deworming protocols. Instead, a data-driven risk assessment approach utilising Targeted Selective Treatment (TST) is recommended. By focusing monitoring and treatment on high-risk demographics—specifically young kids and breeding males—producers can effectively reduce environmental contamination, improve animal welfare, and enhance overall food security in intensive goat farming operations.

References

Arthur, T. M., Brichta-Harhay, D. M., Bosilevac, J. M., Kalchayanand, N., Shackelford, S. D., Wheeler, T. L., & Koohmaraie, M. (2010). Super shedding of Escherichia coli O157 by cattle and the impact on beef carcass contamination. Meat Science, 86(1), 32–37. https://doi.org/10.1016/j.meatsci.2010.04.019

Basripuzi, H. B., Sani, R. A., Ariff, O. M., & Chandrawathani, P. (2013). Presence of parasite larvae in goat manure for use as fertiliser. Pertanika Journal of Tropical Agricultural Science, 36(3), 211–216.

Bautista-Garfias, C. R., Castañeda-Ramírez, G. S., Estrada-Reyes, Z. M., Soares, F. E. d. F., Ventura-Cordero, J., González-Pech, P. G., Morgan, E. R., Soria-Ruiz, J., López-Guillén, G., & Aguilar-Marcelino, L. (2022). A review of the impact of climate change on the epidemiology of gastrointestinal nematode infections in small ruminants and wildlife in tropical conditions. Pathogens, 11(2), 148. https://doi.org/10.3390/pathogens11020148

Besier, R. B. (2012). Refugia-based strategies for sustainable worm control: Factors affecting the acceptability to sheep and goat owners. Veterinary Parasitology, 186(1–2), 2–9. https://doi.org/10.1016/j.vetpar.2011.11.057

Besier, R. B., Love, R. A., Lyon, J., & van Burgel, A. J. (2010). A targeted selective treatment approach for effective and sustainable sheep worm management: Investigations in Western Australia. Animal Production Science, 50(12), 1034–1042. https://doi.org/10.1071/AN10123

Boareki, M. N., Schenkel, F. S., Willoughby, O., Suarez-Vega, A., Kennedy, D., & Cánovas, A. (2021). Comparison between methods for measuring fecal egg count and estimating genetic parameters for gastrointestinal parasite resistance traits in sheep. Journal of Animal Science, 99(12), skab341. https://doi.org/10.1093/jas/skab341

Carson, A., Reichel, R., Bell, S., Collins, R., Smith, J., & Bartley, D. (2023). Haemonchus contortus: An overview. Veterinary Record, 192(1), 26–28. https://doi.org/10.1002/vetr.2613

Cooper, L., Kang, S. Y., Bisanzio, D., Maxwell, K., Rodriguez-Barraquer, I., Greenhouse, B., Drakeley, C., Arinaitwe, E., Staedke, S. G., Gething, P. W., Eckhoff, P., Reiner, R. C., Hay, S. I., Dorsey, G., Kamya, M. R., Lindsay, S. W., Grenfell, B. T., & Smith, D. L. (2019). Pareto rules for malaria super-spreaders and super-spreading. Nature Communications, 10(1), 3939. https://doi.org/10.1038/s41467-019-11861-y

Davison, C., Michie, C., Tachtatzis, C., Andonovic, I., Bowen, J., & Duthie, C.-A. (2023). Feed conversion ratio (FCR) and performance group estimation based on predicted feed intake for the optimisation of beef production. Sensors, 23(10), 4621. https://doi.org/10.3390/s23104621

Food and Agriculture Organization (FAO). (2024). FAOSTAT statistical database. Retrieved June 30, 2026, from https://www.fao.org/statistics/en

Grear, D. A., Perkins, S. E., & Hudson, P. J. (2009). Does elevated testosterone result in increased exposure and transmission of parasites? Ecology Letters, 12(6), 528–537. https://doi.org/10.1111/j.1461-0248.2009.01306.x

Hassanen, E. A. A., Gouda, A. A. H., & Anter, R. G. A. (2020). Prevalence and associated risk factors of gastrointestinal parasitic infection in goats in Sharkia Governorate, Egypt. Journal of Experimental Biology and Agricultural Sciences, 8(4), 524–530. https://doi.org/10.18006/2020.8(4).524.530

Hellard, E., Fouchet, D., Rey, B., Mouchet, A., Poulet, H., & Pontier, D. (2013). Differential association between circulating testosterone and infection risk by several viruses in natural cat populations: A behavioural-mediated effect. Parasitology, 140(4), 521–529. https://doi.org/10.1017/S0031182012001862

Lim, W. C., Mohd Nadzir, M. N. H., Hiew, M. W. H., Mamat, M. S., & Shohaimi, S. (2022). Feed intake, growth performance and digestibility of nutrients of goats fed with outdoor-grown hydroponic maize sprouts. Pertanika Journal of Tropical Agricultural Science, 45(1), 321–336. https://doi.org/10.47836/pjtas.45.1.19

Lu, C. D. (2023). The role of goats in the world: Society, science, and sustainability. Small Ruminant Research, 227, Article 107056. https://doi.org/10.1016/j.smallrumres.2023.107056

Maurizio, A., Perrucci, S., Tamponi, C., Scala, A., Cassini, R., Rinaldi, L., & Bosco, A. (2023). Control of gastrointestinal helminths in small ruminants to prevent anthelmintic resistance: The Italian experience. Parasitology, 150(12), 1105–1118. https://doi.org/10.1017/S0031182023000343

Mpofu, T. J., Nephawe, K. A., & Mtileni, B. (2022). Prevalence and resistance to gastrointestinal parasites in goats: A review. Veterinary World, 15(10), 2442–2452. https://doi.org/10.14202/vetworld.2022.2442-2452

Notter, D. R. (2013). Selection for parasite resistance. In Proceedings of the XL Reunión de la Asociación Mexicana para la Producción Animal y la Seguridad Alimentaria and IX Seminario Internacional de Producción de Ovinos en el Trópico (pp. 3–12). Universidad Juárez Autónoma de Tabasco.

Ojo, A. O., Mulim, H. A., Campos, G. S., Junqueira, V. S., Lemenager, R. P., Schoonmaker, J. P., & Oliveira, H. R. (2024). Exploring feed efficiency in beef cattle: From data collection to genetic and nutritional modeling. Animals, 14(24), Article 3633. https://doi.org/10.3390/ani14243633

Playford, M. C., & Besier, R. B. (2025). Gastrointestinal nematode parasites of grazing ruminants: A comprehensive literature review of diagnostic methods for quantifying parasitism, larval differentiation and measuring anthelmintic resistance. New Zealand Veterinary Journal, 73(3), 149–164. https://doi.org/10.1080/00480169.2024.2415029

Ripoll, G., Alcalde, M. J., Argüello, A., Córdoba, M. d. G., & Panea, B. (2020). Effect of rearing system on the straight and branched fatty acids of goat milk and meat of suckling kids. Foods, 9(4), Article 471. https://doi.org/10.3390/foods9040471

Saha, S., Gupta, M., Saha, R., Saqib, M., Korotkova, E. I., & Kar, P. K. (2026). Climatic and host-related drivers of gastrointestinal parasite dynamics in domestic ruminants of North Bengal, India. Animals, 16(2), Article 338. https://doi.org/10.3390/ani16020338

Sellau, J., Hansen, C. S., Gálvez, R. I., Linnemann, L., Honecker, B., & Lotter, H. (2024). Immunological clues to sex differences in parasitic diseases. Trends in Parasitology, 40(11), 1029–1041. https://doi.org/10.1016/j.pt.2024.09.006

Sontigun, N., Sansamur, C., Klong-Klaew, T., Kaewthamasorn, M., Fungwithaya, P., & Mektrirat, R. (2025). Seasonal infective dynamics and risk factors associated with prevalence of zoonotic gastrointestinal parasites from meat goats in Southern Thailand. Animals, 15(14), Article 2040. https://doi.org/10.3390/ani15142040

Tan, T. K., Chandrawathani, P., Low, V. L., Premaalatha, B., Lee, S. C., Chua, K. H., Sharma, R. S. K., Romano, N., Tay, S. T., Quaza, N. H. N., & Lim, Y. A. L. (2017). Occurrence of gastro-intestinal parasites among small ruminants in Malaysia: Highlighting Dicrocoelium infection in goats. Tropical Biomedicine, 34(4), 963–969.

Whitlock, H. V. (2009). A technique for counting trematode eggs in sheep faeces. Journal of Helminthology, 24(1–2), 47–52. https://doi.org/10.1017/S0022149X00019106

Downloads

Published

2026-06-30

Issue

Section

Research Articles
Total Views: 0 | Total Downloads: 0