Molecular Characterization of Babesia species infecting Dogs (Canis familiaris) in the Federal Capital Territory, Abuja, Nigeria

https://dx.doi.org/10.4314/njpar.v43i2.5

Authors

  • S. S. Obeta Department of Parasitology and Entomology, Faculty of Veterinary Medicine, University of Abuja, P.M.B 117, Abuja, Nigeria.
  • A. I. Lawal Department of Parasitology and Entomology, Faculty of Veterinary Medicine, Ahmadu Bello University, Zaria 2222, Nigeria.
  • A. J. Natala Department of Parasitology and Entomology, Faculty of Veterinary Medicine, Ahmadu Bello University, Zaria 2222, Nigeria.
  • N. I. Ogo Parasitology Division, National Veterinary Research Institute, PMB 01, Vom, Plateau State, Nigeria.
  • M. N Opara Department of Parasitology and Entomology, Faculty of Veterinary Medicine, University of Abuja, P.M.B 117, Abuja, Nigeria.
  • O. C. Jegede Department of Parasitology and Entomology, Faculty of Veterinary Medicine, University of Abuja, P.M.B 117, Abuja, Nigeria.
  • E. O. Balogun Department of Biochemistry, Faculty of Life Science, Ahmadu Bello University, Zaria 2222, Nigeria.

Keywords:

FCT, Dogs, Molecular characterisation, Prevalence, Babesia species

Abstract

Babesiosis is a tick-borne disease caused by an intra-erythrocytic protozoan of the genus Babesia. The genus contains a large number of species capable of infecting a variety of mammalian hosts, including humans. Misdiagnosis of the infection is a major setback in disease management, monitoring, and control. Therefore, timely and precise identification of infecting Babesia species is critical. This     study aimed at detecting and characterizing the Babesia species infecting dogs in the Federal Capital Territory (FCT) Abuja. Blood samples were collected from apparently healthy dogs (n=480), thin smears were prepared, Giemsa-stained, and examined under a microscope. DNA was extracted from positive blood samples (n=15), and PCR amplification of the 18S rRNA gene was performed using generic primers. PCR products were purified, electrophoresed on 1.5% agarose gels and thereafter, sequenced bidirectionally. The prevalence of Babesia species in thin smear was 3.1%. The prevalence in the six Area Councils was 5.0%, 3.75%, 2.5%, 2.5%, 2.5% and 2.5% for Gwagwalada, Municipal, Bwari, Kuje, Kwali and Abaji respectively. The prevalence in relation to age was 3.87% in dogs >1year old and 1.76% in dogs ≤ 1 year old. Prevalence by breed, was 4.38% in exotic dogs, 3.23% in local and 2.35% in crossbred. The
prevalence in relation to sex was 3.96% in males and 2.37% in females. The BLAST search was carried out in the NCBI database, and a phylogenetic tree was constructed using nucleotide sequences in GenBank. Electrophoresed PCR products revealed a band size of about 612bp. Blast in NCBI demonstrated 100% similarity with Babesia canis vogeli nucleotide sequences. This study reaffirmed the molecular identification of B. c. vogeli in apparently healthy dogs in Nigeria and it may be of clinical importance to veterinary clinicians in the management and control of the disease.

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References

Solano-Gallego, L. and Baneth, G. (2011). Babesiosis in dogs and cats expanding parasitological and clinical spectra. Veterinary Parasitology 181: 48- 60

Beck, A., Huber, D., Polkinghorne, A., Gudan Kurilj, A., Benko, V., Mrljak, V., Reljić, S., Kusak, J., Reil, I. and Beck, R. (2017). The prevalence and impact of Babesia canis and Theileria sp. in freeranging grey wolf (Canis lupus) populations in Croatia. Parasites & Vectors 10: 168.

Bilić, P., Kuleš, J., Barić, R. R., and MRLJAK, V. (2018). Canine babesiosis: where do we stand? Acta VeterinariaBeograd 68 (2): 127-160.

Zygner, W., Gojska, O., Rapacka, G., Jaros, D. and Wedrychowicz, H. (2007). Hematological changes during the course of canine babesiosis caused by large Babesia in domestic dogs in Warsaw (Poland). Veterinary Parasitology 145: 46 -151.

Abalaka, S. E., Ubah, S. A., Umeakuana, P. U., Idoko, I. S., Sani, N. A., Obeta, S. S., Hikosaka, K., Inaoka, D. K., Kita, K., Watanabe, Y. I. and Balogun, E. O. (2018).Pathological and Molecular diagnosis of canine babesiosis in Nigeria: A case report. Veterinary Parasitology Regional Studies and Reports 14: 150-154.

Ajoke, E. A., Abdullahi, S. U., Ayo, J. O., Okubanjo, O. O., and Balogun, E. O. (2019). Ameliorative effects of alpha-lipoic acid and imidocarb dipropionate on clinichaematological changes induced by experimental Babesia canis vogeli infection in dogs. Comparative Clinical Pathology 28,1119–1135.

Solano-Gallego, L., Sainz, A., Roura, X.,Estrada-Peña, A. and Miró, G. (2016). Areview of canine babesiosis: the European perspective. Parasites & Vectors. 9: 336.

Kuttler, K. L. (1988). World-wide impact of babesiosis. In: Ristic, M. (Ed.), Babesiosis of Domestic Animals and Man. CRC Press,

Boca Raton, FL, pp. 122.

Passos, L. M. F., Geiger, S. M., Ribeiro, M.F. B., Pfister, K. and ZahlerRinder, M.(2005). First molecular detection of Babesia vogeli in dogs from Brazil. Veterinary Parasitology 127: 81–85.

Uilenberg, G. (2006). Babesia a historical overview. Veterinary Parasitology 138: 3 - 10.

Ogo, N. I., Lawal, A. I., Okubanjo, O. O., Kamani, J. and Ajayi, O. O. (2011). Current status of canine babesiosis and the situation in Nigeria: a review. Nigerian Veterinary Journal 32: 69–78.

Hambolu, S. E., Dzikwi, A. A., Kwaga, J. K. P., Kazeem, H. M., Umoh, J. U. and Hambolu, D. A. (2014). Dog ecology and population studies in Lagos State, Nigeria. Global Journal of Health Science 6(2): 209- 220.

Ubah, A. S., Abalaka, S. E., Idoko S. I., Obeta, S. S., Ejiofor, C. E., Mshelbwala, P. P., Omeje, J. N. and Ajayi, I. E. (2019). Canine babesiosis in a male Boerboel: Hematobiochemical and anatomic pathological changes in the cardiorespiratory and reproductive organs. Veterinary and Animal Science 7: 1-6

Opara, M., Adewumi, N., Mohammed, B. R., Obeta, S. S., Simon, M. K. Jegede, O. C. and Agbede, R. I. S. (2017). Investigations on the Haemoprotozoan parasites of Nigerian Local Breed of Dogs in Gwagwalada Federal Capital Territory (FCT), Nigeria. Journal of Parasitology

Research 10: 1- 7.

Obeta, S. S., Ibrahim, B., Lawal, I. A., Natala,A. J., Ogo, N. I. and Balogun, E. O. (2020). Prevalence of canine babesiosis and their risk factors among asymptomatic dogs in the Federal Capital Territory, Abuja, Nigeria. Parasite Epidemiology and Control 511: e00186

Balogun, O. (2001). The Federal Capital Territory of Nigeria: Geography of its Development. University of Ibadan Press Limited, Ibadan, Nigeria 6-7.

Duarte, S. C., Linhares, G. F. C., Romanowsky, T. N., Neto, O. J. S. and Borges, L. M. F. (2008). Assessment of primers designed for the subspecies-specific discrimination among Babesia canis canis, Babesia canis vogeli and Babesia canis rossi by PCR assay. Veterinary Parasitology 152(1-2): 16–20.

Altschul, S. F., Gish, W., Miller, W., Meyers, E. W., and Lipman, D. J. (1990). Basic local alignment search tool. Journal of Molecular Biology 215: 403–410.

Kumar, S., Stecher G. and Tamura, K. (2016). MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Molecular Biology and Evolution 33 (7): 1870-1874.

Tamura, K., Stecher, G., Peterson, D., Filipski, A. and Kumar, S. (2013). MEGA 6: Molecular Evolutionary Genetics Analysis version 6.0. Molecular Biology and Evolution, 30:9- 2725. Tool. Journal of Molecular Biology 215: 403–410

Saitou, N., and Nei, M. (1987). The Neighbour-Joining method: a new method for reconstructing phylogenetic trees. Molecular Biology and Evolution 4: 406–425.

Ogden, N. H., Radojevic, M., Wu, X., Duvvuri, V. R., Leighton, P. A. and Wu, J. (2014). Estimated effects of projected climate change on the basic reproductive number of the Lyme disease vector Ixodes scapularis. Environmental Health Perspective 122: 631–638.

Ogden, N. H., Beard, C. B., Ginsberg, H. S, Tsao, J. I. (2021). Possible Effects of Climate Change on Ixodid Ticks and the Pathogens They Transmit: Predictions and Observations, Journal of Medical Entomology, 58(4) 1536–1545

Sasaki, M., Omobowale, O., Tozuka, M., Ohta, K., Matsuu, A., Nottidge, H.O., Hirata, H., Ikadai, H., and Oyamada, T. (2007). Molecular survey of Babesia canis in dogs in Nigeria. Journal of Veterinary Medicine and Science 69: 1191- 1193.

Kamani, J., Sannusi, A., Dogo, A.G., Tanko, J. T., Egwu, K. O., Tafarki, A. E., Ogo, I. N., Kemza, S., Onovoh, E., Shamaki, D., Lombin, L. H., Catto, V., and Birkenheuer, A. J. (2010). Babesia canis and Babesia rossi coinfection in an untraveled Nigerian dog. Veterinary Parasitology 173, 334- ¬335.

Adamu, M., Troskie, M., Oshadu, D. O., Malatji, D. P., Penzhorn, B. L., and Matjila, P. T. (2014). Occurrence of ticktransmitted pathogens in dogs in Jos, Plateau State, Nigeria. Parasites & Vectors 7: 119.

Jegede, O. C., Obeta, S. S., and Faisal, B. (2014). Infection of dogs with Babesia canis in Gwagwalada area of Federal Capital Territory, Abuja, Nigeria. Sokoto Journal of Veterinary Sciences 12(3): 37-41.

Penzhorn, B. L. (2011). Why is Southern African canine babesiosis so virulent? An evolutionary perspective. Parasites & Vectors 4: 51.

Schoeman, J. P. (2009). Canine babesiosis. Onderstepoort Journal of Veterinary Research 76(1): 59

Published

2022-09-01

How to Cite

Obeta, S. S., Lawal, A. I., Natala, A. J., Ogo, N. I., Opara, M. N., Jegede, O. C., & Balogun, E. O. (2022). Molecular Characterization of Babesia species infecting Dogs (Canis familiaris) in the Federal Capital Territory, Abuja, Nigeria: https://dx.doi.org/10.4314/njpar.v43i2.5. Nigerian Journal of Parasitology, 43(2), 237–243. Retrieved from https://njpar.com.ng/index.php/home/article/view/226

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