Skip to main content
Log in

Comparison of Light Microscopy and Polymerase Chain Reaction for the Detection of Haemoparasites in Cattle in Nigeria

  • Original Paper
  • Published:
Acta Parasitologica Aims and scope Submit manuscript

Abstract

Purpose

Haemoparasitic diseases are among the important factors that threaten cattle health and productivity especially in the sub-Saharan region. In Nigeria, their detection using sensitive molecular techniques is scanty. This study was designed to investigate and to reevaluate the repertoire of haemoparasites of cattle in Ibadan, Nigeria with a comparative evaluation of light microscopy (LM) and polymerase chain reaction (PCR) methods.

Methods

Blood samples from 100 cattle slaughtered at Ibadan abattoirs were examined using LM and PCR techniques for haemoparasite detection. The PCR reactions using three primer sets targeting the 16S rRNA genes for Hemoplasma spp. and Anaplasma/Ehrlichia spp. and 18S rRNA genes of Babesia/Theleiria spp. were done. A few randomly selected amplicons from each set were sequenced and analysed.

Results

A total infection rate of 34% by LM including Hemoplasma spp. (17%), Anaplasma spp. (16%), microfilaria (5%) and Trypanosoma spp. (12%) was recorded. While, 86% positivity was recorded with PCR amplification as follows: Hemoplasma spp. (64%), Babesia/Theleiria spp. (46%) and Anaplasma/Ehrlichia spp. (5%). Comparison of LM and PCR findings showed that no LM Anaplasma spp.-positive samples and 7 out of the 17 LM hemoplasma-positive cattle were confirmed by PCR. In addition, LM led to misdiagnosis of 46 Babesia/Theleiria spp.-positive samples. Amplicon sequencing and phylogenetic analysis of Babesia/Theileria spp.-positive samples revealed Theileria velifera and Theileria annulata. In the Anaplasma/Ehrlichia spp.-positive samples, only Anaplasma marginale was characterized. Mycoplasma wenyonii, “Candidatus Mycoplasma haemobos” and Pseudomonas fluorescens like were characterized among the hemoplasma-infected cattle.

Conclusions

The first report of “Candidatus Mycoplasma haemobos” and Pseudomonas fluorescens like in Nigerian cattle is herewith documented. The alarming LM misdiagnosis of haemoparasites during this study confirms its limitations as it fails to identify many parasites and emphasizes the need for inclusion of molecular techniques to improve their detection. The study also shows for the first time the high prevalence of haemotropic mycoplasma in Nigerian cattle via molecular diagnostic methods, thus indicating a strong need for the investigation of their zoonotic implications.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Bock R, Jackson L, De Vos A, Jorgensen W (2004) Babesiosis of cattle. Parasitol 129:S247–S269

    Article  Google Scholar 

  2. EFSA (European Food Safety Authority) (2010) Scientific opinion on geographic distribution of tick-borne infections and their Vectors in Europe and the other Regions of the Mediterranean Basin. EFSA J 8(9):1723

    Article  Google Scholar 

  3. Ellis JT, Morrison DA, Reichel MP (2003) Genomics and its impact on parasitology and the potential for development of new parasite control methods. DNA Cell Biol 32:395–403

    Article  CAS  Google Scholar 

  4. CFSPH (2008) Bovine babesiosis. The Centre for Food Security and Public Health, Tick Fever, Cattle Fever, Texas Fever, Piroplasmosis, Redwater. Iowa State University, Ames, Iowa 50011. http://www.cfsph.iastate.edu/Factsheets/pdfs/bovine_babesiosis.pdf

  5. Akande FA, Takeet MI, Makanju OA (2010) Haemoparasites of cattle in Abeokuta, South West Nigeria. Sci World J 5:19–21

    Google Scholar 

  6. Kamani J, Sannusi A, Egwu OK, Dogo GI, Tanko TJ, Kemza S, Tafarki AE, Gbise DS (2010) Prevalence and significance of haemoparasitic infections of cattle in North-Central, Nigeria. Vet World 3(10):445–448

    Article  Google Scholar 

  7. Okorafor UP, Nzeako SO (2014) Prevalence of haemoparasites of cattle from three abattoirs in Ibadan Metropolis, Nigeria. Int J Sci Res Environ Sci 2(7):244–249

    Google Scholar 

  8. Maria R, Jeffrey AG (1996) Babesiosis. Clin Infect Dis 22:611–615

    Article  Google Scholar 

  9. Sasaki M, Omobowale O, Tozuka M, Ohta K, Matsuu A, Nottidge HO, Hirata H, Ikadai H, Oyamada T (2007) Molecular survey of Babesia canis in dogs in Nigeria. J Vet Med Sci 69(11):1191–1193

    Article  CAS  PubMed  Google Scholar 

  10. Kamani J, Baneth G, Mumcuoglu KY, Waziri NE, Eyal O, Guthmann Y, Harrus S (2013) Molecular detection and characterization of tick-borne pathogens in dogs and ticks from Nigeria. PLoS Negl Trop Dis 7(3):2108

    Article  Google Scholar 

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

    Article  Google Scholar 

  12. Happi AN, Toepp AJ, Ugwu CA, Petersen CA, Sykes JE (2018) Detection and identification of blood-borne infections in dogs in Nigeria using light microscopy and the polymerase chain reaction. Vet Parasitol Reg Stud Rep 11:55–60

    Google Scholar 

  13. Swallow BM (2000) Impacts of trypanosomosis on African agriculture. PAAT technical and Scientific Series, vol 2. FAO, Rome

    Google Scholar 

  14. Leeflang P, Ilemobade AA (1977) Tick-borne diseases of domestic animals in Northern Nigeria. Trop Anim Health Pro 9(4):211–218

    Article  CAS  Google Scholar 

  15. Obi TU, Anosa VO (1980) Haematological studies on domestic animals in Nigeria: IV. Clinico-haematological features of bovine trypanosomiasis, theileriosis, anaplasmosis, eperythrozoonosis and helminthiasis. J Vet Med 27(9–10):789–797

    CAS  Google Scholar 

  16. Lorusso V, Wijnveld M, Majekodunmi AO, Dongkum C, Fajinmi A, Dogo AG, Thrusfield M, Mugenyi A, Vaumourin E, Igweh AC, Jongejan F (2016) Tick-borne pathogens of zoonotic and veterinary importance in Nigerian cattle. Parasit Vect 9(1):217

    Article  CAS  Google Scholar 

  17. Maggi RG, Compton SM, Trull CL, Mascarelli PE, Mozayeni BR, Breitschwerdt EB (2013) Infection with hemotropic Mycoplasma species in patients with or without extensive arthropod or animal contact. J Clin Microbiol 51(10):3237–3241

    Article  PubMed  PubMed Central  Google Scholar 

  18. McAuliffe L, Lawes J, Bell S, Barlow A, Aylin R, Nicholas R (2006) The detection of mycoplasma (formerly Eperythrozoon) wenyonii by 16S rDNA PCR and denaturing gradient gel electrophoresis. Vet Microbiol 117:292–296

    Article  CAS  PubMed  Google Scholar 

  19. Tagawa M, Matsumoto K, Inokuma H (2008) Molecular detection of Mycoplasma wenyonii and ‘Candidatus Mycoplasma haemobos in cattle in Hokkaido, Japan. Vet Microbiol 132:177–180

    Article  CAS  PubMed  Google Scholar 

  20. Meli ML, Willi B, Dreher UM, Cattori V, Knubben-Schweizer G, Nuss K, Braun U, Lutz H, Hofmann-Lehmann R (2010) Identification, molecular characterization, and occurrence of two bovine Hemoplasma spp. in Swiss cattle and development of real-time TaqMan quantitative PCR assays for diagnosis of bovine hemoplasma infections. J Clin Microbiol 48(10):3563–3568

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Uilenberg G (2009) Candidatus Mycoplasma haemobos. Vet Microbiol 138(1–2):200–201

    Article  PubMed  Google Scholar 

  22. Girotto A, Zangirólamo AF, Bogado ALG, Souza ASL, da Silva GCF, Garcia JL, Boas AAV, Biondo AW, Vidotto O (2012) Molecular detection and occurrence of ‘Candidatus Mycoplasma haemobos’ in dairy cattle of Southern Brazil. Rev Bras Parasitol Vet 21(3):342–344

    Article  PubMed  Google Scholar 

  23. Picozzi K, Tilley A, Fèvre EM, Coleman PG, Magona JW, Odiit M, Eisler MC, Welburn SC (2002) The diagnosis of trypanosome infections: applications of novel technology for reducing disease risk. Afr J Biotechnol 1(2):39–45

    Article  CAS  Google Scholar 

  24. Latimer KS (2011) Duncan and Prasse’s veterinary laboratory medicine: clinical pathology, 5th edn. Wiley-Blackwell, Oxford

    Google Scholar 

  25. Schouls LM, Van De Pol I, Rijpkema SGT, Schot CS (1999) Detection and identification of Ehrlichia, Borrelia burgdorferi sensu lato, and Bartonella spp. in Dutch Ixodes ricinus ticks. J Clin Microbiol 37:2215–2222

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Bekker CPJ, de Vos S, Taoufik A, Sparagano OAE, Jongejan F (2002) Simultaneous detection of Anaplasma and Ehrlichia spp. in ruminants and detection of Ehrlichia ruminantium in Amblyomma variegatum ticks by reverse line blot hybridisation. Vet Microbiol 89:223–238

    Article  CAS  PubMed  Google Scholar 

  27. Georges K, Loria GR, Riili S, Greco A, Caracappa S, Jongejan F, Sparagano O (2001) Detection of haemoparasites in cattle by reverse line blot hybridisation with a note on the distribution of ticks in Sicily. Vet Parasitol 99:273–286

    Article  CAS  PubMed  Google Scholar 

  28. Fujihara Y, Sasaoka F, Suzuki J, Watanabe Y, Fujihara M, Ooshita K, Ano H, Harasawa R (2011) Prevalence of hemoplasma infection among cattle in the western part of Japan. J Vet Med Sci 73(12):1653–1655

    Article  CAS  PubMed  Google Scholar 

  29. Nishizawa I, Sato M, Fujihara M, Sato S, Harasawa R (2010) Differential detection of hemotropic Mycoplasma spp. in cattle by melting curve analysis of PCR products. J Vet Med Sci 72(1):77–79

    Article  CAS  PubMed  Google Scholar 

  30. Su QL, Song HQ, Lin RQ, Yuan ZG, Yang JF, Zhao GH, Huang WY, Zhu XQ (2010) The detection of “Candidatus Mycoplasma haemobos” in cattle and buffalo in China. Trop Anim Health Pro 42(8):1805–1808

    Article  CAS  Google Scholar 

  31. Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, Valentin F, Wallace IM, Wilm A, Lopez R, Thompson JD (2007) Clustal W and Clustal X version 2.0. Bioinformatics 23(21):2947–2948

    Article  CAS  PubMed  Google Scholar 

  32. Kearse M, Moir R, Wilson A, Stones-Havas S, Cheung M, Sturrock S, Buxton S, Cooper A, Markowitz S, Duran C, Thierer T, Ashton B, Meintjes P, Drummond A (2012) Geneious basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics 28(12):1647–1649

    Article  PubMed  PubMed Central  Google Scholar 

  33. Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4(4):406–425

    CAS  PubMed  Google Scholar 

  34. Tamura K, Nei M (1993) Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol Biol Evol 10(3):512–526

    CAS  PubMed  Google Scholar 

  35. Carelli G, Decaro N, Lorusso A, Elia G, Lorusso E, Mari V, Ceci L, Buonavoglia C (2007) Detection and quantification of Anaplasma marginale DNA in blood samples of cattle by real-time PCR. Vet Microbiol 124(1–2):107–114

    Article  CAS  PubMed  Google Scholar 

  36. Hoelzle LE (2008) Haemotrophic mycoplasmas: recent advances in Mycoplasma suis. Vet Microbiol 130:215–226

    Article  CAS  PubMed  Google Scholar 

  37. Aylin RD, Bisgaard-Frantzen S, Adler A, Blowey RW, Barlow AM, Millar MF, van der Burgt GM (2012) Detection of ‘Candidatus Mycoplasma haemobos, Mycoplasma wenyonii and Anaplasma phagocytophilum from cattle in England. Vet Rec 170(21):543a

    Article  Google Scholar 

  38. McFadden AMJ, Ha HJ, Donald JJ, Bueno IM, van Andel M, Thompson JC, Tisdall JC, Pulford DJ (2016) Investigation of bovine hemoplasmas and their association with anaemia in New Zealand cattle. N Z Vet J 64:65–68

    Article  PubMed  Google Scholar 

  39. Olabode HOK, Jegede OC, Ajagbonna OP, Adah BMJ, Obafemi FA (2014) Evaluation of haemoparasites in trade cattle slaughtered in Jos Abattoir, Plateau State-Nigeria. Int J Livest Res 4(1):113–120

    Article  Google Scholar 

  40. Birkenheuer AJ, Breitschwerdt EB, Alleman AR, Pitulle C (2002) Differentiation of Haemobartonella canis and Mycoplasma haemofelis on the basis of comparative analysis of gene sequence. Am J Vet Res 63(10):1385–1388

    Article  CAS  PubMed  Google Scholar 

  41. Criado-Fornelio A, Martinez-Marcos A, Buling-Saraña A, Barba-Carretero JC (2003) Presence of Mycoplasma haemofelis, Mycoplasma haemominutum and piroplasmids in cats from southern Europe: a molecular study. Vet Microbiol 93(4):307–317

    Article  CAS  PubMed  Google Scholar 

  42. Willi B, Filoni C, Catão-Dias JL, Cattori V, Meli ML, Vargas A, Martínez F, Roelke ME, Ryser-Degiorgis MP, Leutenegger CM, Lutz H, Hofmann-Lehmann R (2007) Worldwide occurrence of feline hemoplasma infections in wild felid species. J Clin Microbiol 45:1159–1166

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Bauer N, Balzer HJ, Thüre S, Moritz A (2008) Prevalence of feline haemotropic mycoplasmas in convenience samples of cats in Germany. J Feline Med Surg 10:252–258

    Article  PubMed  Google Scholar 

  44. Maggi RG, Mascarelli PE, Havenga LN, Naidoo V, Breitschwerdt EB (2013) Co-infection with Anaplasma platys, Bartonella henselae and Candidatus Mycoplasma haematoparvum in a veterinarian. Parasit Vect 6(1):103

    Article  Google Scholar 

  45. Yuan CL, Liang AB, Yao CB, Yang ZB, Zhu JG, Cui L, Yu F, Zhu NY, Yang XW, Hua XG (2009) Prevalence of Mycoplasma suis (Eperythrozoon suis) infection in swine and swine-farm workers in Shanghai, China. Am J Vet Res 70:890–894

    Article  CAS  PubMed  Google Scholar 

  46. Sykes JE, Lindsay LL, Maggi RG, Breitschwerdt EB (2010) Human coinfection with Bartonella henselae and two hemotropic mycoplasma variants resembling Mycoplasma ovis. J Clin Microbiol 48:3782–3785

    Article  PubMed  PubMed Central  Google Scholar 

  47. Steer JA, Tasker S, Barker EN, Jensen J, Mitchell J, Stocki T, Chalker VJ, Hamon M (2011) A novel hemotropic Mycoplasma (hemoplasma) in a patient with hemolytic anemia and pyrexia. Clin Infect Dis 53:e147–e151

    Article  PubMed  PubMed Central  Google Scholar 

  48. Bihonegn W, Haimanot D, Tadele K, Tilahun Z, Girma K (2015) Study on the prevalence of bovine babesiosis and its associated risk factors in and around Assosa Woreda, Benishangul Gumuz Regional State, Western Ethiopia. Researcher 7(8):33–39

    Google Scholar 

  49. Saad F, Khan K, Ali S, ul Akbar N (2015) Zoonotic significance and prophylactic measure against babesiosis. Int J Curr Microbiol App Sci 4(7):938–953

    CAS  Google Scholar 

  50. Ademola IO, Onyechi TE (2013) Haemoparasites and haematological parameters of slaughtered ruminants and pigs at Bodija Abattoir, Ibadan, Nigeria. Afr J Biomed Res 16:101–105

    Google Scholar 

  51. Tagawa M, Ybañez AP, Matsumoto K, Yokoyama N, Inokuma H (2012) Prevalence and risk factor analysis of bovine hemoplasma infection by direct PCR in eastern Hokkaido, Japan. J Vet Med Sci 74:1171–1176

    Article  CAS  PubMed  Google Scholar 

  52. Adejinmi JO, Sadiq NA, Fashanu SO, Lasisi OT, Ekundayo S (2004) Study on the blood parasite of sheep in Ibadan, Nigeria. Afr J Biomed Res 7:42–43

    Google Scholar 

  53. Tagawa M, Matsumoto K, Yokoyama N, Inokuma H (2010) Comparison of the effect of two Hemoplasma spp. on hematological parameters in cattle. J Vet Med Sci 72(1):113–115

    Article  PubMed  Google Scholar 

  54. Salih DA, El Hussein AM, Hayat M, Taha KM (2003) Survey of Theileria lestoquardi antibodies among Sudanese sheep. Vet Parasitol 111(4):361–367

    Article  CAS  PubMed  Google Scholar 

  55. Al-Hamidhi S, Weir W, Kinnaird J, Tageledin M, Beja-Pereira A, Morrison I, Thompson J, Tait A, Shiels B, Babiker HA, Babiker HA (2016) Theileria lestoquardi displays reduced genetic diversity relative to sympatric Theileria annulata in Oman. Infect Genet Evol 43:297–306

    Article  PubMed  Google Scholar 

  56. Ali AM, Salih DA, Njahira MN, Hassan SK, El Hussein AM, Liu Z, Yin H, Pelle R, Skilton RA (2017) Genotyping of Theileria lestoquardi from sheep and goats in Sudan to support control of Malignant Ovine Theileriosis. Vet Parasitol 239:7–14

    Article  CAS  PubMed  Google Scholar 

  57. Awad H, Al-Hamidhi S, El Hussein ARM, Yousif YM, Taha KM, Salih DA, Weir W, Babiker HA (2018) Theileria lestoquardi in Sudan is highly diverse and genetically distinct from that in Oman. Infect Genet Evol 62:46–52

    Article  PubMed  Google Scholar 

  58. Leemans I, Brown D, Hooshmand-Rad P, Kirvar E, Uggla A (1999) Infectivity and cross-immunity studies of Theileria lestoquardi and Theileria annulata in sheep and cattle: in vivo responses. Vet Parasitol 82(3):179–192

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Peters IR, Helps CR, McAuliffe L, Neimark H, Lappin MR, Gruffydd-Jones TJ, Day MJ, Hoelzle LE, Willi B, Meli M, Hofmann-Lehmann R (2008) RNase P RNA gene (rnpB) phylogeny of Hemoplasmas and other Mycoplasma spp. J Clin Microbiol 46(5):1873–1877

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Watanabe Y, Fujihara M, Obara H, Matsubara K, Yamauchi K, Harasawa R (2010) Novel hemoplasma spp detected in free-ranging sika deer (Cervus nippon). J Vet Med Sci 72(11):1527–1530

    Article  CAS  PubMed  Google Scholar 

  61. Ade J, Niethammer F, Schade B, Schilling T, Hoelzle K, Hoelzle LE (2018) Quantitative analysis of Mycoplasma wenyonii and “Candidatus Mycoplasma haemobos” infections in cattle using novel gapN-based realtime PCR assays. Vet Microbiol 220:1–6

    Article  CAS  PubMed  Google Scholar 

  62. Hoelzle K et al (2011) Detection of ‘Candidatus Mycoplasma haemobos’ in cattle with anaemia. Vet J 187:408–410

    Article  PubMed  Google Scholar 

  63. Kwon SW, Kim JS, Park IC, Yoon SH, Park DH, Lim CK, Go SJ (2003) Pseudomonas koreensis sp. nov., Pseudomonas umsongensis sp. nov. and Pseudomonas jinjuensis sp. nov., novel spp from farm soils in Korea. Int J Syst Evol Microbiol 53(1):21–27

    Article  CAS  PubMed  Google Scholar 

  64. Ganeshan G, Kumar AM (2005) Pseudomonas fluorescens, a potential bacterial antagonist to control plant diseases. J Plant Interact 1(3):123–134

    Article  CAS  Google Scholar 

  65. Lin H, Hu S, Liu R, Chen P, Ge C, Zhu B, Guo L (2016) Genome sequence of Pseudomonas koreensis CRS05-R5, an antagonistic bacterium isolated from rice paddy field. Front Microbiol 7:1756

    PubMed  PubMed Central  Google Scholar 

  66. Chiesa F, Lomonaco S, Nucera D, Garoglio D, Dalmasso A, Civera T (2014) Distribution of Pseudomonas spp. in a dairy plant affected by occasional blue discoloration. Int J Food Saf 3:245–248

    Google Scholar 

  67. Cho ST, Chang HH, Egamberdieva D, Kamilova F, Lugtenberg B, Kuo CH (2015) Genome analysis of Pseudomonas fluorescens PCL1751: a rhizobacterium that controls root diseases and alleviates salt stress for its plant host. PLoS One 10(14):231

    Google Scholar 

  68. Rafikova GF, Korshunova TY, Minnebaev LF, Chetverikov SP, Loginov ON (2016) A new bacterial strain, Pseudomonas koreensis IB-4, as a promising agent for plant pathogen biological control. Microbiol 85(3):333–341

    Article  CAS  Google Scholar 

  69. Schlusselhuber M, Godard J, Sebban M, Bernay B, Garon D, Seguin V, Oulyadi H, Desmasures N (2018) Characterization of Milkisin, a novel lipopeptide with antimicrobial properties produced by Pseudomonas sp. UCMA 17988 isolated from bovine raw milk. Front Microbiol 9:1030

    Article  PubMed  PubMed Central  Google Scholar 

  70. Ming L, Yi L, Hasi S, He J, Hai L, Wang Z, Gu F, Qiao X (2017) Comparative analysis of fecal microbial communities in cattle and Bactrian camels. PLoS One 12(3):e0173062

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  71. Scaccabarozzi L, Leoni L, Ballarini A, Barberio A, Locatelli C, Casula A, Bronzo V, Pisoni G, Jousson O, Morandi S, Rapetti L (2015) Pseudomonas aeruginosa in dairy goats: genotypic and phenotypic comparison of intramammary and environmental isolates. PLoS One 10(11):e0142973

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  72. Serrano I, De Vos D, Santos JP, Bilocq F, Leitão A, Tavares L, Pirnay JP, Oliveira M (2016) Antimicrobial resistance and genomic rep-PCR fingerprints of Pseudomonas aeruginosa strains from animals on the background of the global population structure. BMC Vet Res 13(1):58

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors are gratefully indebted to Professor Christian Happi for his unceasing support and for allowing us to use his laboratory facilities at the African Center of Excellence for Genomics of Infectious Diseases (ACEGID), Redeemer’s University, Ede, Nigeria, for the molecular analyses carried out in this study. Our unreserved thanks and gratitude goes particularly to Mrs. Philonema Eromon and Mr. Adeyemi T Kayode for their technical assistance in the molecular laboratory at the ACEGID. We immensely appreciate Mrs Ademakinwa Josephine and Mrs Ayomikun Adeyeyi for their support in the haematology work at the Clinical Pathology Laboratory, Department of Veterinary Pathology, University of Ibadan, Nigeria.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Anise N. Happi.

Ethics declarations

Conflict of Interest

The authors declare that they have no competing interests.

Statement of animal rights

The present study was carried out by collecting blood from cattle at the slaughtering point during bleeding. This was done with the consent of the owners of the respective cattle at the local municipal abattoir in Ibadan, Nigeria. Therefore as we were not on our own handling the animals, we thought there was no need for ethical approval.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Happi, A.N., Osifade, O., Oluniyi, P.E. et al. Comparison of Light Microscopy and Polymerase Chain Reaction for the Detection of Haemoparasites in Cattle in Nigeria. Acta Parasit. 65, 44–56 (2020). https://doi.org/10.2478/s11686-019-00123-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.2478/s11686-019-00123-y

Keywords

Navigation