z-logo
Premium
Lectin‐Mediated, Nonopsonic Phagocytosis of Type 1 Escherichia coli by Human Peritoneal Macrophages of Uremic Patients Treated by Peritoneal Dialysis
Author(s) -
Boner Geoffrey,
Mhashilkar Abner Moses,
RodriguezOrtega Morella,
Sharon Nathan
Publication year - 1989
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1002/jlb.46.3.239
Subject(s) - escherichia coli , opsonin , phagocytosis , microbiology and biotechnology , peritoneal dialysis , macrophage , bacteria , antibody , biology , lectin , peritoneum , immunology , in vitro , medicine , biochemistry , genetics , anatomy , gene
Human peritoneal macrophages isolated from uremic patients undergoing peritoneal dialysis bind type 1 fimbriated Escherichia coli in the absence of opsonins. The number of bacteria bound per macrophage was 6.9, as determined by microscopic examination. Methyl α‐mannoside (0.1 mM) and p ‐nitrophenyl α‐mannoside (0.01 mM) inhibited this binding by about 66%. The ability of peritoneal macrophages to bind E . coli in a mannose‐specific manner was confirmed in further experiments using an enzyme‐linked immunosorbent assay (ELISA) with an antibacterial antibody, radiolabelled E. coli , and counts of colony‐forming units (CFU). The number of bacteria bound per macrophage was 7 to 12 in the ELISA and 5.5‐8.5 in the CFU assay. Methyl α‐mannoside caused 70% inhibition of binding In the ELISA and 84% in the CFU assay, whereas p ‐nitrophenyl α‐mannoside showed inhibition of 79% and 90%, respectively. Most bound bacteria (76‐80%) were subsequently killed. Nonfimbriated E . coli 827 bound poorly to the macrophages (~22%) as compared to that of the fimbriated bacteria. Although this binding was not inhibited by methyl α‐D‐mannoside or p ‐nitrophenyl α‐mannoside, the percentage of bacteria killed was similar to that of the fimbriated phenotype. The peritoneal macrophage is thus able to phagocytose E . coli in the absence of opsonins. This may explain the relative rarity of E . coli as an etiologic agent of peritoneal infections in the dialysed patient.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom