Mycoplasma synoviae surface protein MSPB as a recombinant antigen in an indirect ELISA

• Published in: Microbiology (Society for General Microbiology) Vol. 145; no. 8; pp. 2087 - 2094
• Main Authors: Noormohammadi, A.H, Markham, P.F, Markham, J.F, Whithear, K.G, Browning, G.F
• Format: Journal Article
• Language: English
• Published: Reading Soc General Microbiol 01.08.1999; Society for General Microbiology
• Subjects: Animal bacterial diseases; Animals; Antibodies, Bacterial - blood; Antigens, Bacterial - genetics; Antigens, Bacterial - immunology; Antigens, Surface - genetics; Antigens, Surface - immunology; Bacterial diseases; Biological and medical sciences; Chickens; Cloning, Molecular; Electrophoresis, Polyacrylamide Gel; Enzyme-Linked Immunosorbent Assay - methods; genbank/af035624; Genes, Bacterial - genetics; Immunoblotting; immunology; Infectious diseases; Medical sciences; Molecular Sequence Data; Mycoplasma - immunology; Mycoplasma - isolation & purification; Mycoplasma Infections - diagnosis; Mycoplasma Infections - immunology; Mycoplasma Infections - veterinary; Mycoplasma synoviae; Polymerase Chain Reaction; Poultry Diseases - diagnosis; Poultry Diseases - immunology; Recombinant Proteins - immunology; surface antigens; Species specificity; Enzyme immunoassay; Mycoplasma synoviae; Mycoplasmataceae; Infection; Mollicutes; Antigen; Mycoplasmatales; Vertebrata; Animal; Bacteriosis; Bacteria; Chicken; Diagnosis; Recombinant protein; Aves; Veterinary; Mycoplasmal infection; ELISA assay
• ISSN: 1350-0872; 1465-2080
• DOI: 10.1099/13500872-145-8-2087

Mycoplasma synoviae is a poultry pathogen causing respiratory disease and synovitis. A number of serological assays have been developed for diagnosis of M. synoviae infection; however, they lack sensitivity and/or are prone to false-positive reactions. Using a combination of PCR and expression cloning, four overlapping regions (regions 1-4) of the surface antigen MSPB of M. synoviae WVU-1853 were expressed in a bacterial expression system. Immunostaining of the resultant polypeptides with chicken sera raised against different M. synoviae strains, or Mycoplasma gallisepticum S6, suggested that region 4 contained a highly antigenic and species-specific domain (amino acids 178-213) of MSPB. A fusion protein of region 4 was expressed in the pMAL expression system and purified from cold-osmotic-shock fluids of Escherichia coli cells for use in an indirect ELISA. The potential of the purified antigen for detection of M. synoviae antibodies was assessed with sera obtained from chickens experimentally infected with different strains of M. synoviae or M. gallisepticum, or from uninoculated chickens. All the sera from M. synoviae-inoculated chickens provided higher absorbance values than those from M. gallisepticum-inoculated or uninoculated chickens. Chickens inoculated with M. synoviae 86079/7NS had detectable increases of serum anti-MSPB immunoglobulins at day 7 after inoculation. These studies have identified the most antigenic region of one of the major species-specific surface proteins of M. synoviae, and shown the potential of this protein as a serodiagnostic reagent.