Abstract
A rabbit model was used to study the effect of allogeneic demineralized bone powder (DBP) implants on the persistence of Staphylococcus aureus osteomyelitis. Thirty-one rabbits with chronic osteomyelitis of the tibia established by day 21, were started on systemic antibiotics followed by either no additional treatment or debridement plus either DBP (with or without supplemental antibiotics) or supplemental antibiotics only. On day 21, cultures showed a mean of 2 x 10(4) CFU/mg of debrided osseous material. By day 70, the treatment most effective in clearing infection was found in animals treated with supplemental antibiotics only (mean of 142 +/- 116 CFU/mg). In contrast, infection persisted at a 7- to 10-fold-higher level in animals receiving DBP with and without supplemental antibiotics; these results suggest that DBP contributed to persistence of infection. Longitudinal sera were tested again staphylococcal sonic extracts by immunoblot. Detection of numerous probe-positive bands indicated complex but remarkably similar antibody responses among infected animals. Antibodies attached directly to the cell surfaces of staphylococci as shown by immunogold and blocked the binding of organisms to HEp-2 and human fetal lung cells in a radioadherence assay. Antibodies could be absorbed out by intact organisms and were unreactive by immunoblot against antigens derived from cells pretreated with pronase, proteinase K, or lysostaphin. These results indicate that the major response was directed against staphylococcal cell surface proteins. Surprisingly, only one major band (molecular weight, approximately 12,000) was detected when a homologous in vivo antigen preparation was studied by immunoblot. Antibody reactive against this peptide did not appear to react with staphylococci grown in vitro.
Full text
PDF








Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bell J. A., Pennington T. H., Petrie D. T. Western blot analysis of staphylococcal antibodies present in human sera during health and disease. J Med Microbiol. 1987 Mar;23(2):95–99. doi: 10.1099/00222615-23-2-95. [DOI] [PubMed] [Google Scholar]
- Brown M. R., Williams P. The influence of environment on envelope properties affecting survival of bacteria in infections. Annu Rev Microbiol. 1985;39:527–556. doi: 10.1146/annurev.mi.39.100185.002523. [DOI] [PubMed] [Google Scholar]
- CLAMP J. R., HOUGH L. THE PERIODATE OXIDATION OF AMINO ACIDS WITH REFERENCE TO STUDIES ON GLYCOPROTEINS. Biochem J. 1965 Jan;94:17–24. doi: 10.1042/bj0940017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cheung A. L., Fischetti V. A. Variation in the expression of cell wall proteins of Staphylococcus aureus grown on solid and liquid media. Infect Immun. 1988 May;56(5):1061–1065. doi: 10.1128/iai.56.5.1061-1065.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cohen M. L., Falkow S. Protein antigens from Staphylococcus aureus strains associated with toxic-shock syndrome. Science. 1981 Feb 20;211(4484):842–844. doi: 10.1126/science.7466361. [DOI] [PubMed] [Google Scholar]
- Daugharty H., Warfield D. T., Davis M. L. Solid-phase radioimmunoassay of total and influenza-specific immunoglobulin G. Appl Microbiol. 1972 Feb;23(2):360–367. doi: 10.1128/am.23.2.360-367.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ebeling W., Hennrich N., Klockow M., Metz H., Orth H. D., Lang H. Proteinase K from Tritirachium album Limber. Eur J Biochem. 1974 Aug 15;47(1):91–97. doi: 10.1111/j.1432-1033.1974.tb03671.x. [DOI] [PubMed] [Google Scholar]
- Espersen F., Clemmensen I., Barkholt V. Isolation of Staphylococcus aureus clumping factor. Infect Immun. 1985 Sep;49(3):700–708. doi: 10.1128/iai.49.3.700-708.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Espersen F., Hedström S. A. Precipitating antibodies against Staphylococcus aureus in experimental rabbit osteomyelitis, investigated by means of quantitative immunoelectrophoretic methods. Acta Pathol Microbiol Immunol Scand B. 1982 Jun;90(3):211–216. doi: 10.1111/j.1699-0463.1982.tb00107.x. [DOI] [PubMed] [Google Scholar]
- Espersen F., Hedström S. A. Precipitating antibodies against Staphylococcus aureus in serum from patients with staphylococcal osteomyelitis, investigated by means of quantitative immunoelectrophoretic methods. Acta Pathol Microbiol Immunol Scand B. 1982 Jun;90(3):205–210. doi: 10.1111/j.1699-0463.1982.tb00106.x. [DOI] [PubMed] [Google Scholar]
- Glowacki J., Altobelli D., Mulliken J. B. Fate of mineralized and demineralized osseous implants in cranial defects. Calcif Tissue Int. 1981;33(1):71–76. doi: 10.1007/BF02409414. [DOI] [PubMed] [Google Scholar]
- Green S. A., Dlabal T. A. The open bone graft for septic nonunion. Clin Orthop Relat Res. 1983 Nov;(180):117–124. [PubMed] [Google Scholar]
- Gristina A. G. Biomaterial-centered infection: microbial adhesion versus tissue integration. Science. 1987 Sep 25;237(4822):1588–1595. doi: 10.1126/science.3629258. [DOI] [PubMed] [Google Scholar]
- Gristina A. G., Costerton J. W. Bacterial adherence and the glycocalyx and their role in musculoskeletal infection. Orthop Clin North Am. 1984 Jul;15(3):517–535. [PubMed] [Google Scholar]
- Gristina A. G., Oga M., Webb L. X., Hobgood C. D. Adherent bacterial colonization in the pathogenesis of osteomyelitis. Science. 1985 May 24;228(4702):990–993. doi: 10.1126/science.4001933. [DOI] [PubMed] [Google Scholar]
- Iversen O. J., Grov A. Studies on lysostaphin. Separation and characterization of three enzymes. Eur J Biochem. 1973 Oct 5;38(2):293–300. doi: 10.1111/j.1432-1033.1973.tb03061.x. [DOI] [PubMed] [Google Scholar]
- Kaban L. B., Glowacki J. Induced osteogenesis in the repair of experimental mandibular defects in rats. J Dent Res. 1981 Jul;60(7):1356–1364. doi: 10.1177/00220345810600071201. [DOI] [PubMed] [Google Scholar]
- Kaban L. B., Mulliken J. B., Glowacki J. Treatment of jaw defects with demineralized bone implants. J Oral Maxillofac Surg. 1982 Oct;40(10):623–626. doi: 10.1016/0278-2391(82)90109-4. [DOI] [PubMed] [Google Scholar]
- Karakawa W. W., Young D. A. Immunochemical study of diverse surface antigens of a Staphylococcus aureus isolate from an osteomyelitis patient and their role in in vitro phagocytosis. J Clin Microbiol. 1979 Mar;9(3):399–408. doi: 10.1128/jcm.9.3.399-408.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Lifeso R. M., Al-Saati F. The treatment of infected and uninfected non-union. J Bone Joint Surg Br. 1984 Aug;66(4):573–579. doi: 10.1302/0301-620X.66B4.6378916. [DOI] [PubMed] [Google Scholar]
- Mayberry-Carson K. J., Tober-Meyer B., Smith J. K., Lambe D. W., Jr, Costerton J. W. Bacterial adherence and glycocalyx formation in osteomyelitis experimentally induced with Staphylococcus aureus. Infect Immun. 1984 Mar;43(3):825–833. doi: 10.1128/iai.43.3.825-833.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mulliken J. B., Glowacki J., Kaban L. B., Folkman J., Murray J. E. Use of demineralized allogeneic bone implants for the correction of maxillocraniofacial deformities. Ann Surg. 1981 Sep;194(3):366–372. doi: 10.1097/00000658-198109000-00015. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Norden C. W. Experimental osteomyelitis. I. A description of the model. J Infect Dis. 1970 Nov;122(5):410–418. doi: 10.1093/infdis/122.5.410. [DOI] [PubMed] [Google Scholar]
- Park J. T., Shaw D. R., Chatterjee A. N., Mirelman D., Wu T. Mutants of staphylococci with altered cell walls. Ann N Y Acad Sci. 1974 Jul 31;236(0):54–62. doi: 10.1111/j.1749-6632.1974.tb41481.x. [DOI] [PubMed] [Google Scholar]
- Reddi A. H., Huggins C. Biochemical sequences in the transformation of normal fibroblasts in adolescent rats. Proc Natl Acad Sci U S A. 1972 Jun;69(6):1601–1605. doi: 10.1073/pnas.69.6.1601. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rodeheaver G. T., Rukstalis D., Bono M., Bellamy W. A new model of bone infection used to evaluate the efficacy of antibiotic-impregnated polymethylmethacrylate cement. Clin Orthop Relat Res. 1983 Sep;(178):303–311. [PubMed] [Google Scholar]
- Sanford B. A., Davison V. E., Ramsay M. A. Staphylococcus aureus adherence to influenza A virus-infected and control cell cultures: evidence for multiple adhesins. Proc Soc Exp Biol Med. 1986 Jan;181(1):104–111. doi: 10.3181/00379727-181-42230. [DOI] [PubMed] [Google Scholar]
- Sanford B. A., Thomas V. L., Ramsay M. A., Jones T. O. Characterization of clinical strains of Staphylococcus aureus associated with pneumonia. J Clin Microbiol. 1986 Jul;24(1):131–136. doi: 10.1128/jcm.24.1.131-136.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sonis S. T., Kaban L. B., Glowacki J. Clinical trial of demineralized bone powder in the treatment of periodontal defects. J Oral Med. 1983 Jul-Sep;38(3):117–122. [PubMed] [Google Scholar]
- Speers D. J., Nade S. M. Ultrastructural studies of adherence of Staphylococcus aureus in experimental acute hematogenous osteomyelitis. Infect Immun. 1985 Aug;49(2):443–446. doi: 10.1128/iai.49.2.443-446.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Watson D. L., Prideaux J. A. Comparisons of Staphylococcus aureus grown in vitro or in vivo. Microbiol Immunol. 1979;23(6):543–547. doi: 10.1111/j.1348-0421.1979.tb00493.x. [DOI] [PubMed] [Google Scholar]
- Watson D. L. Virulence of Staphylococcus aureus grown in vitro or in vivo. Res Vet Sci. 1982 May;32(3):311–315. [PubMed] [Google Scholar]
- Wheat L. J., White A. C., Norden C. Serological diagnosis of Staphylococcus aureus osteomyelitis. J Clin Microbiol. 1985 May;21(5):764–767. doi: 10.1128/jcm.21.5.764-767.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]



