Seroprevalence of Leptospira spp serovar hardjo among Cattle Slaughtered at Katsina Central Abattoir, Katsina State, Nigeria

Authors

  • Saulawa, M. A. Department of Veterinary Public Health and Preventive Medicine, Faculty of Veterinary Medicine, Bayero University Kano, Nigeria https://orcid.org/0000-0003-4685-0388
  • Ayuba, K. Department of Veterinary Public Health and Preventive Medicine, Faculty of Veterinary Medicine, University of Abuja, Abuja, Nigeria
  • Fouad, M. ECOWAS Regional Animal Health Center, Parc de Sotuba, BP: E2165, Bamako, Mali

DOI:

https://doi.org/10.47430/ujmr.25103.004

Keywords:

Abattoir, Cattle, ELISA, Katsina State, Leptospira hardjo, Sero-survey, Slaughter

Abstract

Study’s Excerpt:

  • Leptospira hardjo infection was detected in 16.2% of slaughtered cattle in Katsina abattoir.
  • Bulls had a higher seroprevalence (20%) than cows (14.3%), though not statistically significant.
  • Younger cattle showed higher exposure, but age differences lacked statistical significance.
  • White Fulani cattle showed the highest breed-specific prevalence at 20.8%.
  • Findings highlight occupational and public health risks of leptospirosis in abattoir settings.

Full Abstract:

Leptospirosis is a globally distributed zoonotic disease caused by the bacterium Leptospira spp. serovar hardjo, posing a significant threat to livestock industries and public health. This study investigated the seroprevalence of Leptospira hardjo infection among cattle slaughtered at Katsina Central abattoir. A total of 179 blood samples were aseptically collected from the jugular veins of various cattle breeds using anticoagulant-free vacutainers. The samples were centrifuged to separate sera, followed by analysis using an indirect Enzyme-Linked Immunosorbent Assay (ELISA) based on the manufacturer’s protocol (ELISA Bovicheck® Lepto HP, Bioveta, Canada). The overall prevalence of Leptospira spp. serovar hardjo was 16.2%. Bulls exhibited a higher prevalence (20%) compared to cows (14.3%), although no significant difference was observed between sexes (p > 0.05). Age-specific prevalence indicated that younger cattle were more exposed; however, statistical associations were not significant (p > 0.05). Breed-specific prevalence revealed higher rates in White Fulani cattle (20.8%) and lower in Red Bororo (12.9%), with no statistically significant association between breed and infection (p > 0.05). This study indicates a high prevalence of Leptospira spp. infection among cattle in Katsina Central abattoir. The occurrence of leptospirosis in these cattle poses occupational risks for abattoir workers, endangers livestock productivity, and raises significant public health concerns due to its potential to spread from animals to humans.

Downloads

Download data is not yet available.

References

Agunloye, C. A., Alabi, F. O., Odemuyiwa, S. O., & Olaleye, O. D. (2002). Leptospirosis in Nigeria: A seroepidemiological survey. Indian Veterinary Journal, 78(5), 371-375.

Assenga, J. A., Matemba, L. E., Muller, S. K., Mhamphi, G. G., & Kazwala, R. R. (2015). Predominant leptospiral serogroups circulating among humans, livestock and wildlife in Katavi-Rukwa ecosystem, Tanzania. PLoS Neglected Tropical Diseases, 9(4), e0003607. https://doi.org/10.1371/journal.pntd.0003607

Behera, B., Rama, C., Anubhav, P., Anant, M., Lalit, D., Martha, M. P., Ekta, G., Shobha, B., & Parveen, A. (2010). Co-infection due to leptospira, dengue and hepatitis E: A diagnostic challenge. Journal of Infectious Diseases in Developing Countries, 4(1), 48-50.

Benacer, D., Zain, S. N. M., Sim, S. Z., Khalid, N. K. N. M., Galloway, R. L., Souris, M., & Thong, K. L. (2016). Determination of Leptospira borgpetersenii serovar Javanica and Leptospira interrogans serovar Bataviae as the persistent Leptospira serovars circulating in the urban rat populations in Peninsular Malaysia. Parasites & Vectors, 9(1), 1-11. https://doi.org/10.1186/s13071-016-1400-1

Bradley, E. A., & Lockaby, G. (2023). Leptospirosis and the environment: A review and future directions. Pathogens, 12(9), 1167. https://doi.org/10.3390/pathogens12091167

Costa, F., Hagan, J. E., Calcagno, J., Kane, M., Torgerson, P., et al. (2015). Global morbidity and mortality of leptospirosis: A systematic review. PLoS Neglected Tropical Diseases, 9(9), e0003898. https://doi.org/10.1371/journal.pntd.0003898

Dereje, T. R., Ararsa, B., Beksisa, U., & Melkam, A. (2024). Seroprevalence of Coxiella burnetii, Leptospira interrogans serovar hardjo, and Brucella species and associated reproductive disorders in cattle in southwest Ethiopia. Heliyon, 10(3), e25558. https://doi.org/10.1016/j.heliyon.2024.e25558

Ellis, W. A. (1986). The present state of leptospirosis diagnosis and control. In W. A. Ellis & T. W. A. Little (Eds.), The diagnosis of leptospirosis in farm animals (pp. 13-31). Martinus Nijhoff Publishers.

Fraga, T. R., Carvalho, E., Isaac, L., & Barbosa, A. S. (2024). Leptospira and leptospirosis. In Molecular medical microbiology (pp. 1849-1871). Academic Press. https://doi.org/10.1016/B978-0-12-818619-0.00159-3

Garba, B., Faleke, O. O., Salihu, M. D., Garba, H. S., Suleiman, N., Bashir, S., & Aliyu, M. (2013). Seroprevalence of leptospires in sheep slaughtered at Sokoto metropolitan abattoir. Scientific Journal of Veterinary Advances, 2(3), 26-29.

Karpagam, K. B., & Ganesh, B. (2020). Leptospirosis: A neglected tropical zoonotic infection of public health importance - An updated review. European Journal of Clinical Microbiology & Infectious Diseases, 39(5), 835-846. https://doi.org/10.1007/s10096-019-03797-4

Kumar, S. S. (2013). Indian guidelines for the diagnosis and management of human leptospirosis. Medical Update, 1, 24-29.

López-Robles, G., Córdova-Robles, F. N., Sandoval-Petris, E., & Montalvo-Corral, M. (2021). Leptospirosis at human-animal-environment interfaces in Latin-America: Drivers, prevention, and control measures. Biotecnia, 23(3), 89-100. https://doi.org/10.18633/biotecnia.v23i3.1442

Mgode, G. F., Mhamphi, G. G., Massawe, A. W., & Machang'u, R. S. (2021). Leptospira seropositivity in humans, livestock and wild animals in a semi-arid area of Tanzania. Pathogens, 10(6), 696. https://doi.org/10.3390/pathogens10060696

Msemwa, B., Mirambo, M. M., Silago, V., Samson, J. M., Majid, K. S., Mhamphi, G., Genchwere, J., Mwakabumbe, S. S., Mngumi, E. B., Mgode, G., & Mshana, S. E. (2021). Existence of similar Leptospira serovars among dog keepers and their respective dogs in Mwanza, Tanzania, the need for a one health approach to control measures. Pathogens, 10(5), 609. https://doi.org/10.3390/pathogens10050609

Ngbede, E. O., Raji, M. A., Kwanashie, C. N., Okolocha, E. C., Momoh, A. H., & Adole, E. B. (2012). Risk practices and awareness of leptospirosis in an abattoir in North-western Nigeria. Scientific Journal of Veterinary Advances, 1(2), 65-69. https://doi.org/10.1016/S2222-1808(12)60080-2

Ngbede, E. O., Raji, M. A., Kwanashie, C. N., Okolocha, C., Maurice, N. A., Akange, E. N., & Odeh, L. E. (2012a). Leptospirosis among zebu cattle in farms in Kaduna State, Nigeria. Asian Pacific Journal of Tropical Disease, 2(5), 367-369. https://doi.org/10.1016/S2222-1808(12)60080-2

Ngbede, E. O., Raji, M. A., & Kwanashie, C. N. (2013). Serosurvey of Leptospira spp serovar Hardjo in cattle from Zaria, Nigeria. Revista de Medicina Veterinaria, 164(2), 85-89.

Pace, J. E., & Wakeman, D. L. (2003). Determining the age of cattle by their teeth. University of Florida, IFAS Extension.

Rebecca, H., Laurent, C., Jonas, E., Karine, G., Mathias, G., Audrey, C., Camille, E., Gualbert, H., Thibaut, L., Julien, C., Gauthier, D., & Florence, A. (2024). Seroprevalence and renal carriage of pathogenic Leptospira in livestock in Cotonou, Benin. Veterinary Medicine and Science. https://doi.org/10.1002/vms3.1430

Robi, D. T., Bogale, A., Urge, B., Melkam, A., & Shiferaw, T. (2023). Neglected zoonotic bacteria causes and associated risk factors of cattle abortion in different agro-ecological zones of southwest Ethiopia. Veterinary Immunology and Immunopathology. https://doi.org/10.1016/j.vetimm.2023.110592

Sandra, G. G. (2024). Leptospirosis. https://emedicine.medscape.com/article/220563-overview?form=fpf

Saulawa, M. A., Ukashatu, S., Garba, M. G., Magaji, A. A., Bello, M. B., & Magaji, A. S. (2012). Prevalence of indigestible substances in the rumen and reticulum of small ruminants slaughtered at Katsina Central Abattoir, Katsina State, Northwestern Nigeria. Scientific Journal of Pure and Applied Sciences, 2(1), 17-21.

Sharma, S., Vijayachari, P., Sugunan, A. P., & Kalimuthusamy, N. (2014). Sero-prevalence and carrier status for leptospirosis in cattle and goats in Andaman Island, India. Journal of Veterinary Science and Technology, 5(5), 1-4.

Solomon, D., Gift, M., Lisa, M., Keith, D., & Davis, M. P. (2012). Seroprevalence of leptospirosis in dogs in urban Harare and selected rural communities in Zimbabwe. Onderstepoort Journal of Veterinary Research, 79(1), 1-6. https://doi.org/10.4102/ojvr.v79i1.447

Sykes, J. E., Haake, D. A., Gamage, C. D., Mills, W. Z., & Nally, J. E. (2022). A global One Health perspective on leptospirosis in humans and animals. Journal of the American Veterinary Medical Association, 260(13), 1589-1596. https://doi.org/10.2460/javma.22.06.0258

Tilahun, Z., Reta, D., & Simenew, K. (2013). Global epidemiological overview of leptospirosis. International Journal of Microbiology Research, 4(1), 9-15.

Udechukwu, C. C., Kudi, A. C., Abdu, P. A., Pilau, N. N., Jolayemi, K. O., Okoronkwo, M. O., & Kuyet, G. Z. (2024). Leptospirosis: A review of the silent threat in West Africa. Journal of Veterinary Science Research. https://doi.org/10.23880/oajvsr-16000275

World Health Organization. (1982). Guidelines for the control of leptospirosis (Offset Publication No. 67).

World Organization for Animal Health. (2008). Manual for standards and diagnostic test and vaccine (Chapter 2.1.9). OIE.

Published

30-06-2025

How to Cite

Saulawa, M. A., Ayuba, K., & Fouad, M. (2025). Seroprevalence of Leptospira spp serovar hardjo among Cattle Slaughtered at Katsina Central Abattoir, Katsina State, Nigeria. UMYU Journal of Microbiology Research (UJMR), 10(3), 28–34. https://doi.org/10.47430/ujmr.25103.004