Journal of Immunology and Immunopathology
  • Year: 2017
  • Volume: 19
  • Issue: 2

Cloning, Expression and Immunogenic Analysis of P33 Protein of Mycoplasma bovigenitalium

  • Author:
  • Sabarinath Thankappan1, Rajneesh Rana1,*, Arun Thachappully Remesh1, Viswas Konasagara Nagaleekar1, Bhavani Puvvala1, Rekha Valsala1
  • Total Page Count: 5
  • Published Online: Jun 1, 2017
  • Page Number: 92 to 96

1Division of Bacteriology and mycology, Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh, India

*Corresponding author email id: rajneeshrana01@yahoo.com

Abstract

Mycoplasma bovigenitalium is a bovine mycoplasma which has been a severe blight for dairy industry, as it is implicated in reproductive failure in both breeding bulls and dairy cattle. Recombinant protein-based serological tests which show high sensitivity and specificity have got distinct advantage over conventional whole-cell antigen-based tests owing to high concentration of immunoreactive antigens and lack non-specific moieties associated with whole-cell antigen-based preparations. Material and Methods: Small Ubiquitin-like Modifier SUMO-tagged recombinant P33 antigen expression was attempted in the present study in Escherichia cloni 10G cells and its immunogenicity was assessed by both dot blot and western blot analyses. Results: The expressed recombinant protein was found to be immunogenic against hyperimmune sera raised against whole-cell sonicated antigen of M. bovigenitalium. Discussion and Conclusion: Recombinant p33 antigen holds promise to be used in immunodiagnostics such as Enzyme Linked Immuno Sorbant Assay ELISA for serodiagnosis of M. bovigenitalium infection.

Keywords

Cloning, Expression, P33 protein, Western blot, Dot blot