Atherogenic Bacterium Porphyromonas gingivalis Evades Circulating Phagocytes by Adhering to Erythrocytes

• Published in: Infection and Immunity 2011-04, Vol.79 (4), p.1559-1565
• Main Authors: Belstrøm, Daniel, Holmstrup, Palle, Damgaard, Christian, Borch, Tanja S, Skjødt, Mikkel-Ole, Bendtzen, Klaus, Nielsen, Claus H
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Aged; Atherosclerosis - immunology; Atherosclerosis - microbiology; bacteria; Bacterial Adhesion - immunology; Biological and medical sciences; blood serum; Cell Adhesion; Cell Separation; Cellular Microbiology: Pathogen-Host Cell Molecular Interactions; complement; Complement Activation - immunology; Complement C3 - immunology; coronary disease; erythrocytes; Erythrocytes - cytology; Erythrocytes - metabolism; Erythrocytes - microbiology; Female; Flow Cytometry; Fundamental and applied biological sciences. Psychology; Humans; Male; Microbiology; Middle Aged; monocytes; neutrophils; Phagocytes - immunology; Porphyromonas gingivalis; Porphyromonas gingivalis - immunology; Young Adult
• ISSN: 0019-9567; 1098-5522
• DOI: 10.1128/IAI.01036-10

A relationship between periodontitis and coronary heart disease has been investigated intensively. A pathogenic role for the oral bacterium Porphyromonas gingivalis has been suggested for both diseases. We examined whether complement activation by P. gingivalis strain ATCC 33277 allows the bacterium to adhere to human red blood cells (RBCs) and thereby evade attack by circulating phagocytes. On incubation with normal human serum, the P. gingivalis strain efficiently fixed complement component 3 (C3). Incubation of bacteria with washed whole blood cells suspended in autologous serum resulted in a dose- and time-dependent adherence to RBCs. The adherence required functionally intact complement receptor 1 (CR1; also called CD35) on the RBCs and significantly inhibited the uptake of P. gingivalis by neutrophils and B cells within 1 min of incubation (by 64% and 51%, respectively) and that by monocytes after between 15 min and 30 min of incubation (by 66% and 53%, respectively). The attachment of C3b/iC3b to bacterium-bearing RBCs decreased progressively after 15 min, indicating that conversion of C3 fragments into C3dg occurred, decreasing the affinity for CR1 on RBCs. We propose that P. gingivalis exploits RBCs as a transport vehicle, rendering it inaccessible to attack by phagocytes, and by doing so plays a role in the development of systemic diseases.