Potential of exocellular carbohydrate antigens of Staphylococcus epidermidis in the serodiagnosis of orthopaedic prosthetic infection.

The potential of exocellular carbohydrate antigens of Staphylococcus epidermidis as markers of infection in bone was investigated by immunoblotting and enzyme-linked immunosorbent assay (ELISA). Exocellular antigens were prepared by gel filtration chromatography of concentrated brain heart infusion culture supernates. The antigenic material appeared as diffuse bands between 24 and 32 kDa on the immunoblots and was not susceptible to digestion with trypsin, indicating that the response in the patients was to non-protein (polysaccharide or teichoic acid, or both) exocellular material. Significant differences were detected between the immunoblot antigen profiles for serum IgG from patients with S. epidermidis bone infection and those with an uninfected prosthetic joint. Thirteen of 16 patients with S. epidermidis prosthetic joint infection showed an elevated serum IgG level by ELISA compared with controls with uninfected joints. However, the antigen was not specific for S. epidermidis bone infection; high levels of IgG were also detected in patients with other serious staphylococcal and streptococcal infections. The ELISA test may be valuable in distinguishing between staphylococcal infection of joints and aseptic loosening by excluding cases of infection.

[1]  J. Heesemann,et al.  Characterization of transposon mutants of biofilm-producing Staphylococcus epidermidis impaired in the accumulative phase of biofilm production: genetic identification of a hexosamine-containing polysaccharide intercellular adhesin , 1994, Infection and immunity.

[2]  I. Hancock,et al.  The capsular turnover product of Staphylococcus aureus strain Smith. , 1994, FEMS microbiology letters.

[3]  P. Lambert,et al.  Enzyme-linked immunosorbent assay for the detection of antibodies to exocellular proteins of Staphylococcus aureus in bone infection. , 1992, FEMS microbiology letters.

[4]  P. White,et al.  Comparison of cell-wall teichoic acid with high-molecular-weight extracellular slime material from Staphylococcus epidermidis. , 1992, Journal of medical microbiology.

[5]  P. Lambert,et al.  Extracellular proteins as a potential marker of active Staphylococcus aureus infection in bone. , 1992, Journal of medical microbiology.

[6]  L. Baddour,et al.  Identification of an antigenic marker of slime production for Staphylococcus epidermidis , 1990, Infection and immunity.

[7]  J. Kalbfleisch,et al.  Pathogenicity of Staphylococcus lugdunensis, Staphylococcus schleiferi, and three other coagulase-negative staphylococci in a mouse model and possible virulence factors. , 1990, Canadian journal of microbiology.

[8]  B. Jansen,et al.  New aspects in the pathogenesis and prevention of polymer-associated foreign-body infections caused by coagulase-negative staphylococci. , 1989, Journal of investigative surgery : the official journal of the Academy of Surgical Research.

[9]  D. Goldmann,et al.  Isolation and characterization of a capsular polysaccharide adhesin from Staphylococcus epidermidis. , 1988, The Journal of infectious diseases.

[10]  E. Beachey,et al.  Bacterial adherence: the attachment of group A streptococci to mucosal surfaces. , 1987, Reviews of infectious diseases.

[11]  T. Pennington,et al.  Western blot analysis of staphylococcal antibodies present in human sera during health and disease. , 1987, Journal of medical microbiology.

[12]  I. Poxton,et al.  Analysis of the membrane lipocarbohydrate antigen of Clostridium difficile by polyacrylamide gel electrophoresis and immunoblotting , 1986 .

[13]  T. Pennington,et al.  Typing of strains of Staphylococcus aureus by Western Blot analysis of culture supernates. , 1986, Journal of medical microbiology.

[14]  G. Peters,et al.  Adherence and growth of coagulase-negative staphylococci on surfaces of intravenous catheters. , 1982, The Journal of infectious diseases.

[15]  B. Lugtenberg,et al.  Electrophoretic resolution of the ‘major outer membrane protein’ of Escherichia coli K12 into four bands , 1975, FEBS letters.

[16]  Amstutz Hc Complications of total hip replacement. , 1970, Clinical orthopaedics and related research.