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Concurrent infections with vector-borne pathogens associated with fatal anaemia in cattle: haematology and blood chemistry

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Abstract

An outbreak of a fatal haemolytic anaemia in a dairy herd of cattle in Switzerland was shown to be associated with infections with five vector-borne pathogens, namely Anaplasma marginale, A. phagocytophilum, Babesia bigemina, a Theileria spp belonging to the buffeli/sergenti/orientalis complex and haemotrophic Mycoplasma spp. The latter three had not been documented before this outbreak in Switzerland. To characterise the haematological and blood chemical changes in these unique cows, packed cell volume was determined in all 286 blood samples, blood smears, and complete haematology were performed from 285 and 173 blood samples, respectively, and biochemical parameters were assayed in 105 serum samples. Regenerative anaemia was the key sign of illness. Red blood cells of anaemic cattle were hypochromic and macrocytic. Anaemic animals had reduced platelet cell counts and increased total white cell counts. In addition, increased serum bilirubin, blood aspartate aminotransferase, gamma glutamyltransferase, glutamic dehydrogenase and blood urea nitrogen and decreased magnesium, calcium and albumin levels were found in anaemic cattle when compared to animals with normal packed cell volume. Most changes could not be attributed to a single infection. A. marginale seemed to be important in causing the outbreak, but co-infections may have aggravated the disease development and clinical signs. Thus, when encountering cattle with haemolytic anaemia, all of the mentioned pathogens should be included as differential diagnosis.

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References

  • Ajayi SA, Wilson AJ, Campbell RS (1978) Experimental bovine anaplasmosis: clinico-pathological and nutritional studies. Res Vet Sci 1:76–81

    Google Scholar 

  • Allbritton AR, Seger CL (1962) The transport and excretion of bile pigments in anaplasmosis. Am J Vet Res 23:101–108

    PubMed  CAS  Google Scholar 

  • Allen PC, Kuttler KL (1981) Effect of Anaplasma marginale infection upon blood gases and electrolytes in splenectomized calves. J Parasitol 6:954–956

    Article  Google Scholar 

  • Brulisauer F, Thoma R, Cagienard A et al (2004) [Anaplasmosis in a Swiss dairy farm: an epidemiological outbreak investigation]. Schweiz Arch Tierheilkd 10:451–459

    Article  Google Scholar 

  • Cagnasso A, Abate O, Guglielmino R et al (1983) [Occurrence of eperythrozoonosis in calves]. Schweiz Arch Tierheilkd 6:353–357

    Google Scholar 

  • Campbell JR, Watts C (1970) Blood urea in the bovine animal. Vet Rec 5:127–132

    Article  Google Scholar 

  • Cossio-Bayugar R, Pillars R, Schlater J et al (2002) Theileria buffeli infection of a Michigan cow confirmed by small subunit ribosomal RNA gene analysis. Vet Parasitol 2:105–110

    Article  Google Scholar 

  • De Vico G, Macri B, Sammartino C et al (1999) Bovine babesiosis in Sicily: preliminary study on pathology. Parassitologia 41:37–38

    PubMed  Google Scholar 

  • Donnelly J, Crossman PJ, McKendrick MD (1970) An outbreak of redwater on a farm in Sussex. Vet Rec 23:729

    Article  Google Scholar 

  • Feldmann BF , Zinkl JG, Jain NC (2000) Schalm’s veterinary hematology. Lippincott Williams and Wilkins, Philadelphia, PA

    Google Scholar 

  • Hilpertshauser H, Deplazes P, Meli ML et al (2007) Genotyping of Babesia bigemina from cattle from a non-endemic area (Switzerland). Vet Parasitol 154:59–64

    Article  CAS  Google Scholar 

  • Hofmann-Lehmann R, Meli ML, Dreher UM et al (2004) Concurrent infections with vector-borne pathogens associated with fatal hemolytic anemia in a cattle herd in Switzerland. J Clin Microbiol 8:3775–3780

    Article  Google Scholar 

  • Jensen WA, Lappin MR, Kamkar S et al (2001) Use of a polymerase chain reaction assay to detect and differentiate two strains of Haemobartonella felis in naturally infected cats. Am J Vet Res 4:604–608

    Article  Google Scholar 

  • Kuttler KL (1984) Anaplasma infections in wild and domestic ruminants: a review. J Wildl Dis 1:12–20

    Google Scholar 

  • Lotze JC (1947) Variables and constants in experimental bovine anaplasmosis and their relationship to chemotherapy. Am J Vet Res 8:267–274

    CAS  PubMed  Google Scholar 

  • Meuten DJ, Chew DJ, Capen CC et al (1982) Relationship of serum total calcium to albumin and total protein in dogs. J Am Vet Med Assoc 1:63–67

    Google Scholar 

  • Persing DH, Mathiesen D, Marshall WF et al (1992) Detection of Babesia microti by polymerase chain reaction. J Clin Microbiol 8:2097–2103

    Google Scholar 

  • Pusterla N, Huder JB, Leutenegger CM et al (1999) Quantitative real-time PCR for detection of members of the Ehrlichia phagocytophila genogroup in host animals and Ixodes ricinus ticks. J Clin Microbiol 5:1329–1331

    Google Scholar 

  • Sandhu GS, Grewal AS, Singh A et al (1998) Haematological and biochemical studies on experimental Theileria annulata infection in crossbred calves. Vet Res Commun 5:347–354

    Article  Google Scholar 

  • Siegel SC, Castellan NJ Jr (1988) Non-parametric statistics for the behavioral sciences. McGraw-Hill, New York

    Google Scholar 

  • Smith RD, Molinar E, Larios F et al (1980) Bovine babesiosis: pathogenicity and heterologous species immunity of tick-borne Babesia bovis and B. bigemina infections. Am J Vet Res 12:1957–1965

    Google Scholar 

  • Thrall MA (2004) Veterinary hematology and clinical chemistry. DB Troy Baltimore, Philadelphia

    Google Scholar 

  • Tieze NW (1995) Clinical guide to laboratory tests. WB Saunders, Philadelphia

  • Torioni de Echaide S, Knowles DP, McGuire TC et al (1998) Detection of cattle naturally infected with Anaplasma marginale in a region of endemicity by nested PCR and a competitive enzyme-linked immunosorbent assay using recombinant major surface protein 5. J Clin Microbiol 3:777–782

    Google Scholar 

  • Yadav CL, Sharma NN (1986) Changes in blood chemical components during experimentally induced Theileria annulata infections in cattle. Vet Parasitol 2:91–98

    Article  Google Scholar 

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Acknowledgements

The authors are indebted to E. Rogg, E. Schuler, Y. Bosshart, Ch. Brönnimann, U. Egger, B. Glaus, E. Grässli, M. Huder, B. Lange, T. Meili Prodan, M. Nussbaumer, J. Wälchli, B. Weibel, C. Wolfensberger and B. Wenger for excellent technical assistance. The authors also thank Drs. R. Perl and G. Regi (Gemeinschaftspraxis Perl, Regi und Iselin), and M. Mehli, Chur, Switzerland, for their efficient corporation. Laboratory work was performed using the logistics of the Center for Clinical Studies at the Vetsuisse Faculty of the University of Zurich. This work was supported in part by the Swiss Federal Veterinary Office, Bern, Switzerland and the Schweizerische Vereinigung für Wiederkäuermedizin (SVW), Switzerland. R.H.-L. is the recipient of a professorship by the Swiss National Science Foundation (PP00B-102866).

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Correspondence to Regina Hofmann-Lehmann.

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Riond, B., Meli, M.L., Braun, U. et al. Concurrent infections with vector-borne pathogens associated with fatal anaemia in cattle: haematology and blood chemistry. Comp Clin Pathol 17, 171–177 (2008). https://doi.org/10.1007/s00580-007-0713-z

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  • DOI: https://doi.org/10.1007/s00580-007-0713-z

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