The Mycoplasma gallisepticum α-enolase is cell surface-exposed and mediates adherence by binding to chicken plasminogen

Microb Pathog. 2011 Oct;51(4):285-90. doi: 10.1016/j.micpath.2011.03.012. Epub 2011 Jun 1.

Abstract

The α-enolase protein is reported to be an adhesin in several pathogenic bacterial species, but its role in Mycoplasma gallisepticum is unknown. In this study, the M. gallisepticum α-enolase gene was adapted to heterologous expression in Escherichia coli by performing overlapping polymerase chain reaction with site-directed mutagenesis to introduce A960G and A1158G mutations in the nucleotide sequence. The full-length mutated gene was cloned into a pGEM-T Easy vector and subcloned into the expression vector pET32a(+) to construct the pET-rMGEno plasmid. The expression of rMGEno in E. coli strain DE3 was confirmed by sodium dodecyl sulfate polyacrylamide gel electrophoresis with Coomassie blue staining. Purified rMGEno exhibited α-enolase catalytic activity that it could reflect the conversion of NADH to NAD(+). Mouse antiserum to α-enolase was generated by immunization with rMGEno. Immunoblotting and immunofluorescence assay with the antiserum identified α-enolase on the surface of M. gallisepticum cells. Enzyme-linked immunosorbent assay characterized rMGEno as a chicken plasminogen binding protein. An adherence inhibition assay on immortalized chicken fibroblasts (DF-1) demonstrated more than 77% inhibition of adhesion in the presence of mouse antiserum, suggesting that α-enolase of M. gallisepticum participates in bacterial adhesion to DF-1 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adhesins, Bacterial / genetics
  • Adhesins, Bacterial / metabolism*
  • Animals
  • Antibodies, Bacterial
  • Bacterial Adhesion*
  • Cells, Cultured
  • Chickens
  • Enzyme-Linked Immunosorbent Assay
  • Escherichia coli / genetics
  • Fibroblasts / microbiology
  • Fluorescent Antibody Technique
  • Gene Expression
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Mutagenesis, Site-Directed
  • Mutant Proteins / genetics
  • Mutant Proteins / metabolism
  • Mycoplasma gallisepticum / enzymology*
  • Mycoplasma gallisepticum / pathogenicity*
  • NAD / metabolism
  • Phosphopyruvate Hydratase / genetics
  • Phosphopyruvate Hydratase / metabolism*
  • Plasminogen / metabolism*
  • Point Mutation
  • Protein Binding
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism

Substances

  • Adhesins, Bacterial
  • Antibodies, Bacterial
  • Membrane Proteins
  • Mutant Proteins
  • Recombinant Proteins
  • NAD
  • Plasminogen
  • Phosphopyruvate Hydratase