Haemobiochemical Alterations Associated with Haemoparasitic Infections in Dogs in Jos North, Nigeria

Main Article Content

Deborah Maigawu Buba
Samuel Chukwudi Eze
Charibu Hurdison Dishon
George Yilzem Gurumyen

Abstract

Introduction: Dogs in Nigeria are commonly affected by haemoparasitic infections. These infections are mainly transmitted by ticks and cause significant illness. The present study aimed to investigate the impact of blood parasites on the haemobiochemical parameters in dogs in Jos North, Plateau State, Nigeria.
Materials and methods: Forty dogs from three different veterinary clinics in Jos North, Plateau State, Nigeria, were examined. Dogs were grouped by sex (male and female), age (puppies under 6 months, young dogs 6-24 months, adults over 24 months), and breed, such as Nigerian indigenous breeds (NIBD) and exotic breeds. The study lasted for 10 months. Blood samples from all dogs were collected for haematological and serum biochemical analyses. Giemsa-stained smears were examined under a light microscope to identify haemoparasites. Haematological parameters and serum biochemical markers, including urea, creatinine, liver enzymes (alkaline phosphatase, alanine aminotransferase, and aspartate aminotransferase), bilirubin, and electrolytes, were assessed. Haemobiochemical evaluations were conducted on the same day as sample collection.
Results: The present study found a high prevalence of haemoparasites (77.5%) among the 40 dogs examined in Jos North, with Babesia spp. being the most prevalent (52.5%), followed by Anaplasma platys (20%), Mycoplasma haemocanis (20%), and Hepatozoon canis (5%). Infected dogs with these parasites demonstrated significant haematological alterations, including anaemia, thrombocytopenia, and lymphopenia, with puppies (12.5%) and NIBD (20%) most severely affected. Inflammatory changes such as neutrophilia and leukocytosis were common and varied among breeds. Biochemical changes included elevated urea, creatinine, liver enzymes, and bilirubin in puppies and NIBD. The mineral alterations, specifically Na, Cl, Ca, HCO3, and phosphorus, exhibited significant variation based on age (puppies) and breed (NIBD), but demonstrated no significant difference concerning sex.
Conclusion: The current results provided essential baseline data to improve the diagnosis, management, and control of haemoparasitic infections, ultimately supporting stronger canine health and welfare in Jos North, Plateau State, Nigeria. Biochemical abnormalities, such as elevated urea, creatinine, liver enzymes, and bilirubin levels, indicated hepatic and renal involvement, as well as significant electrolyte disturbances associated with haemoparasite infection.


 

Article Details

How to Cite
Buba, D. M., Eze, S. C., Dishon, C. H., & Gurumyen, G. Y. (2026). Haemobiochemical Alterations Associated with Haemoparasitic Infections in Dogs in Jos North, Nigeria. Journal of Veterinary Physiology and Pathology, 5(1), 8–20. https://doi.org/10.58803/jvpp.v5i1.81
Section
Original Articles

References

Kwaghe AV, Okomah D, Okoli I, Kachalla MG, Aligana M, Alabi O, et al. Estimation of dog population in Nasarawa state, Nigeria: A pilot study. Pan Afr Med J. 2019; 34(1): 1-12. DOI: 10.11604/pamj.2019.34.25.16755

Ogbu KI, Olaolu OS, Ochai SO, and Tion MT. A review of some tick-borne pathogens of dogs. J Anim Sci Vet Med. 2018; 3(5): 140-153. DOI: 10.31248/JASVM2018.10

Schoeman JP. Canine babesiosis. Onderstepoort J Vet Res. 2009; 76(1): 59-66. DOI: 10.4102/ojvr.v76i1.66

Sainz Á, Roura X, Miró G, Estrada-Peña A, Kohn B, Harrus S, et al. Guideline for veterinary practitioners on canine ehrlichiosis and anaplasmosis in Europe. Parasites Vectors. 2015; 8(1): 75. DOI: 10.1186/s13071-015-0649-0

Ybañez RH, Ybañez AP, Arnado LL, Belarmino LM, Malingin KG, Cabilete PB, et al. Detection of Ehrlichia, Anaplasma, and Babesia spp. in dogs of Cebu, Philippines. Vet World. 2018; 11(1): 14-19. DOI: 10.14202/vetworld.2018.14-19

Ola-Fadunsin S, Ademola IO, Adejinmi JO, and Okediran BS. Haemoparasites and the haematobiochemical profiles associated with Anaplasma marginale infections of cattle in Ilorin, Nigeria. Veterinaria. 2021; 70(3): 335-349. DOI: 10.51607/22331360.2021.70.3.335

Wolfensohn S, and Lloyd M, editors. Handbook of laboratory animal management and welfare. 4th ed. Wiley-Blackwell; 2013. p. 89-108. DOI: 10.1002/9780470751077

Doig K, and Thompson LA. A methodical approach to interpreting the white blood cell parameters of the complete blood count. Am Soci Clin Lab Sci. 2017; 30(3): 186-193. DOI: 10.29074/ascls.30.3.186

Thrall MA, Weiser G, Allison RW, and Campbell TW, editors. Veterinary haematology and clinical chemistry. 2nd ed. John Wiley & Sons; 2012. Available at: https://scholar.google.com/scholar?q=Thrall+MA,+Weiser+G,+Allison+RW,+Campbell+TW,+editors.+Veterinary+hematology+and+clinical+chemistry.+John+Wiley+%26+Sons%3B+2012+Jul+2&hl=en&as_sdt=0,5

Audu Y, Mustapha M, Ezema KU, Mairig IA, Bukar-kolo YM, and Mamman MM. Prevalence of haemoparasites and associated haematological changes in dogs in Potiskum local government area, Yobe State, Nigeria. Savannah Vet J. 2022; 5(1): 33. DOI: 10.36759/svj.2021.157

Happi AN, Toepp AJ, Ugwu CA, Petersen CA, and Sykes JE. Detection and identification of blood-borne infections in dogs in Nigeria using light microscopy and the polymerase chain reaction. Vet Parasitol Reg Stud Reports. 2018; 11: 55-60. DOI: 10.1016/j.vprsr.2017.12.002

Vonkur GC, Dogo AG, Bukar BAM, Karaye GP, Ogbein KE, and Odey MJ. Prevalence of haemoprotozoan parasites of dogs presented at the Veterinary Teaching Hospital, University of Jos, Nigeria. Appl Vet Res. 2022; 2(1): 2023002. DOI: 10.31893/avr.2023002

Irwin PJ, and Hutchinson GW. Clinical and pathological findings of Babesia infection in dogs. Aust Vet J. 1991; 68(6): 204-209. DOI: 10.1111/j.1751-0813.1991.tb03194.x

Kamani J, Baneth G, Mumcuoglu KY, Waziri NE, Eyal O, Guthmann Y, et al. Molecular detection and characterisation of tick-borne pathogens in dogs and ticks from Nigeria. PLoS Negl Trop Dis. 2013; 7(3): e2108. DOI: 10.1371/journal.pntd.0002108

Kolo A. Anaplasma species in Africa - A century of discovery: A Review on molecular epidemiology, genetic diversity, and control. Pathogens. 2023; 12(5): 702. DOI: 10.3390/pathogens12050702

Hasani SJ, Rakhshanpour A, Enferadi A, Sarani S, Samiei A, and Esmaeilnejad B. A review of Hepatozoonosis caused by Hepatozoon canis in dogs. J Parasit Dis. 2024; 48(3): 424-438. DOI: 10.1007/s12639-024-01682-2

Turna H, Vichova B, Miterpakova M, Szarkova A, Baneth G, and Svoboda M. Clinical and haematologic findings in Babesia canis infection in Eastern Slovakia. Acta Parasit. 2022; 67(3): 1329-1334. DOI: 10.1007/s11686-022-00584-8

Mshelbwala FM, Ajayi OL, Adebiyi AA, Olaniyi MO, Oladipo TM, Okpe EF, et al. Clinical, cytological, hematological and biochemical findings in dogs with cholangiocarcinoma in Abeokuta, Nigeria. Vet World. 2024; 17(9): 2053-2061. DOI: 10.14202/vetworld.2024.2053-2061

Adamu M, Dzever S, and Ikurior S. Haemoparasites of dogs in Makurdi and associated risk factors. Niger J Parasitol. 2017; 38(2): 253-257. DOI: 10.4314/njpar.v38i2.22

Zygner W, Gójska-Zygner O, and Wędrychowicz H. Strong monovalent electrolyte imbalances in the serum of dogs infected with Babesia canis. Ticks Tick-Borne Dis. 2012; 3(2): 107-113. DOI: 10.1016/j.ttbdis.2012.02.002

Adamu M, Troskie M, Oshadu DO, Malatji DP, Penzhorn BL, and Matjila PT. Occurrence of tick-transmitted pathogens in dogs in Jos, Plateau State, Nigeria. Parasit Vectors. 2014; 7(1): 119.

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