Late biomaterial-centered infection is a major complication associated with the use of biomaterial implants. In this study biomaterials that had been implanted subcutaneously in rats were hematogenously challenged with bacteria 4 weeks after implantation. Bacteria were spread either by intravenous injection or by stimulation of bacterial translocation. It was found that none of the biomaterials was infected by hematogenous spread, whereas 5% of the implants were infected by perioperative contamination. We conclude that late hematogenous infection of subcutaneous biomaterials does not occur in the rat. For humans as well, there are growing doubts whether implants actually become infected through hematogenous routes; it is thought that late infections may be caused by delayed appearance of perioperatively introduced bacteria.A severe complication associated with the use of biomaterial implants is failure due to infection. About half of all biomaterial-centered infections occur months to years after deep tissue implantation. Controversy exists concerning the origin of the infecting microorganisms in these late infections. Either bacteria spread hematogenously from endogenous foci or they are inserted during implantation and stay clinically unnoticed for a long time; the latter are referred to as delayed infections (1).Most hematogenous infections are believed to arise from infected skin lesions producing relapsing bacteremia (2). This is supported by the fact that in most (56%) infections where hematogenous spreading is suspected, staphylococci, which are part of the normal skin flora, are involved. Dental or other surgical interventions, bacteriuria, intestinal surgery, and pneumonia have also been proposed as possible causes of hematogenous spreading of bacteria. Another possible mechanism for hematogenous spreading from the intestinal tract is bacterial translocation (BT) (24), i.e., the escape of mainly gram-negative rods through the intestinal wall (19).BT can be promoted by nutritional factors, such as total parenteral nutrition, fluid elemental nutrition, protein malnutrition (8), and vitamin A deficiency (25), hemorrhagic shock, extensive thermal injury, or endotoxins (10). Interestingly, intraperitoneal implants also promote BT (13,18).In animal studies on biomaterial-centered infections, human-derived bacteria are frequently used. In humans, however, biomaterial-centered infections are caused in most cases by the body's own commensal microflora, toward which the immune system is more tolerant than it is to foreign flora (3, 9). Since tolerated microorganisms probably survive longer in the circulatory system, it can be expected that their chances of causing biomaterial-centered infections are greater than those of nonimmunotolerated microorganisms.The aim of this study was to determine whether hematogenous spreading of bacteria, after healing of the implantation wound, infects subcutaneous (s.c.) implants in rats. To this end, rats were intravenously (i.v.) injected either with Staphylococcus aureus, Staph...