Opsonic requirements for phagocytosis of Borrelia hermsii by human polymorphonuclear leukocytes.

Opsonic requirements for phagocytosis by human polymorphonuclear leukocytes (PMNLs) of a laboratory strain of Borrelia hermsii were examined. Intracellular localization of spirochetes was confirmed by electron microscopy and cinephotomicroscopy. Phagocytosis of 3H-labeled spirochetes was increased with higher concentrations of pooled human serum or greater ratios of spirochetes to PMNLs and was unaffected by diminished classical complement pathway activity. Immune rabbit serum markedly increased phagocytosis of spirochetes beyond levels observed with preimmune rabbit serum. Immune rabbit serum also demonstrated direct activity against B. hermsii, which decreased the motility and viability and increased agglutination of the spirochetes independently of complement. Both the direct activity against B. hermsii and the opsonic activity of immune rabbit serum were eliminated by immunoabsorption of immunoglobulins. These observations suggest a role for the alternative complement pathway and for immunoglobulins in the opsonization of spirochetes for phagocytosis by PMNLs. Immunoglobulins may also play a role in the direct clearance of spirochetes.

[1]  T. Butler,et al.  Phagocytosis of Borrelia recurrentis by blood polymorphonuclear leukocytes is enhanced by antibiotic treatment , 1980, Infection and immunity.

[2]  T. Butler,et al.  Infection with Borrelia recurrentis: pathogenesis of fever and petechiae. , 1979, The Journal of infectious diseases.

[3]  N. Schiller,et al.  The role of natural IgG and complement in the phagocytosis of type 4 Neisseria gonorrhoeae by human polymorphonuclear leukocytes. , 1979, The Journal of infectious diseases.

[4]  J. Verhoef,et al.  Complement-mediated phagocytosis of Pseudomonas aeruginosa. , 1978, The Journal of laboratory and clinical medicine.

[5]  G. Weissmann,et al.  Thromboxane generation by human peripheral blood polymorphonuclear leukocytes , 1978, The Journal of experimental medicine.

[6]  C. Jenkin,et al.  Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A-sepharose. , 1978, Immunochemistry.

[7]  D. Fine Comparison of ethyleneglycoltetraacetic acid and its magnesium salt as reagents for studying alternative complement pathway function , 1977, Infection and immunity.

[8]  J. Verhoef,et al.  Kinetics of staphylococcal opsonization, attachment, ingestion and killing by human polymorphonuclear leukocytes: a quantitative assay using [3H]thymidine labeled bacteria. , 1977, Journal of immunological methods.

[9]  J. Verhoef,et al.  Extracellular and bacterial factors influencing staphylococcal phagocytosis and killing by human polymorphonuclear leukocytes , 1976, Infection and immunity.

[10]  L. S. Young,et al.  Neutrophil function in gram-negative rod bacteremia. The interaction between phagocytic cells, infecting organisms, and humoral factors. , 1976, The Journal of clinical investigation.

[11]  R. Root,et al.  Abnormal bactericidal, metabolic, and lysosomal functions of Chediak-Higashi Syndrome leukocytes. , 1972, The Journal of clinical investigation.

[12]  J. Plorde,et al.  Penicillin vs. tetracycline in the treatment of louse-borne relapsing fever. A preliminary report. , 1972, Ethiopian medical journal.

[13]  R. Kelly Cultivation of Borrelia hermsi , 1971, Science.

[14]  W. Wood,et al.  Heat labile opsonins to pneumococcus. II. Involvement of C3 and C5. , 1969 .

[15]  A. Shahar,et al.  PHAGOCYTOSIS AND ITS SIGNIFICANCE IN LEPTOSPIRAL INFECTION. , 1964, The Australian journal of experimental biology and medical science.

[16]  R. Dieterle METHOD FOR DEMONSTRATION OF SPIROCHAETA PALLIDA IN SINGLE MICROSCOPIC SECTIONS , 1927 .