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A simple and efficient method for purifying and quantifying schizonts fromTheileria parva-infected cells

Abstract

An improved method for the purification ofTheileria parva schizonts from infected bovine cells is described. The technique is simpler and more rapid than previously described methods and gives rise to greater yields of schizonts with negligible contamination by host-cell components. In addition, a fluorescent staining technique was developed whereby live schizonts purified from infected cells can be enumerated and sorted using the flow cytometer. An assessment of the quality of schizonts prepared according to our method as a source of RNA for the construction of parasite cDNA libraries suggests that RNA derived from these preparations is free of host nucleic acids.

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References

  • Chomczynski P, Sacchi N (1987) Single-step method RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction. Anal Biochem 162:156–159

    Google Scholar 

  • Gerhards J, Gill AC, Ehrfeld AYB, Dobbelaere DAE, Williams RO (1989) Isolation and characterization of RNA from the intracellular parasiteTheileria parva. Mol Biochem Parasitol 34:15–24

    Google Scholar 

  • Hulliger L, Wilde JKH, Brown CGD, Turner L (1964) Mode of multiplication ofTheileria in cultures of bovine lymphocytic cells. Nature 203:728–730

    Google Scholar 

  • Kemp SJ (1988) Automation of the lymphocytotoxicity test for the detection of anti-class II antibodies. Anim Genet 19 [Suppl 1]:13–15

    Google Scholar 

  • Morrison WI, Goddeeris BM, Teale AJ, Groocock CM, Kemp SJ, Stagg DA (1987) Cytotoxic T cells elicited in cattle challenged withTheileria parva (Muguga): evidence for restriction by class I MHC determinants and parasite strain specificity. Parasite Immunol 9:563–578

    Google Scholar 

  • Nene V, Iams K, Musoke AJ, Nkonge C, Minja S, Gobright E (1988) Characterisation of the gene that codes for the 67 kDa surface antigen ofTheileria parva sporozoites. In: ILRAD Annual Scientific Report. ILRAD, Nairobi, pp 11–12

    Google Scholar 

  • Radley DE, Brown CGD, Cunningham MP, Kimber CD, Musisi FL, Payne RC, Purnell RE, Stagg SM, Young AS (1975) East Coast fever: 3. Chemoprophylactic immunization of cattle using oxytetracycline and a combination of theilerial strains. Vet Parasitol 1:51–60

    Google Scholar 

  • Stagg DA, Chasey D, Young AS, Morzaria SP, Dolan TT (1980) Synchronisation of the division ofTheileria macroschizonts and their mammalian host cells. Ann Trop Med Parasitol 74:263–265

    Google Scholar 

  • Sugimoto C, Conrad PA, Ito S, Brown WC, Grab DJ (1988) Isolation ofTheileria parva schizonts from infected lymphoblastoid cells. Acta Trop (Basel) 45:203–216

    Google Scholar 

  • Teale AJ, Williams J, Young J (1988) Cloning of bovine class I MHC genes. In: ILRAD Annual Scientific Report. ILRAD, Nairobi, pp 19–20

    Google Scholar 

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Goddeeris, B.M., Dunlap, S., Innes, E.A. et al. A simple and efficient method for purifying and quantifying schizonts fromTheileria parva-infected cells. Parasitol Res 77, 482–484 (1991). https://doi.org/10.1007/BF00928414

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  • DOI: https://doi.org/10.1007/BF00928414

Keywords

  • Nucleic Acid
  • Infected Cell
  • cDNA Library
  • Efficient Method
  • Flow Cytometer