ROGERS D E, MELLY M A
J Exp Med. 1957 Feb 1;105(2):113-24. doi: 10.1084/jem.105.2.113.
Large numbers of E. coli were rapidly removed from the blood stream of rabbits at rates which initially paralleled the removal of similar numbers of staphylococci. Splanchnic tissues removed approximately two-thirds of the circulating bacilli in transit through the liver and spleen. In contrast to the cessation of splanchnic trapping noted 20 to 40 minutes following the injection of staphylococci, splanchnic trapping of E. coli continued unchanged for 3 to 5 hours unless the splanchnic tissues were dearly reseeding the blood stream. This resulted in the continued disappearance of E. coli over a 60 to 90 minute period, and differed from the constant bacteriemia maintained beyond 20 minutes after the injection of staphylococci. Some of the differences in the initial clearance of these two microorganisms appeared to relate to differences in host leukocyte-bacterium relationships. In vitro studies indicated that E. coli were rapidly killed following ingestion by rabbit polymorphonuclear leukocytes. Staphylococci survive such ingestion. The injection of E. coli was followed by a prolonged granulocytopenia with evidence of sequestration of granulocytes within the pulmonary vascular bed. The injection of staphylococci was followed by a transient leukopenia, with rapid return of granulocytes to the circulation (15). It appears probable that E. coli ingested by sequestered leukocytes are destroyed within the cell, and that leukocytes do not reenter the circulation containing living E. coli. Such intraleukocytic residence in the blood stream has been shown to be of possible importance in the maintenance of staphylococcal bacteriemia (14). An increasing E. coli bacteriemia occurred rapidly after the initial clearance period, indicating that many sequestered bacilli remained viable. Increasing bacteriemia also occurs 3 to 5 hours after the injection of staphylococci. The bacterial or host cell mechanisms which allow this secondary resurgence of bacterial populations are currently under investigation.
大量大肠杆菌能从兔的血流中迅速清除,其清除速率最初与相似数量葡萄球菌的清除速率相当。内脏组织在大肠杆菌经肝脏和脾脏转运过程中清除了约三分之二的循环杆菌。与注射葡萄球菌后20至40分钟内脏捕获停止不同,大肠杆菌的内脏捕获持续3至5小时不变,除非内脏组织明显重新向血流中播散细菌。这导致大肠杆菌在60至90分钟内持续消失,与注射葡萄球菌后20分钟后维持的持续性菌血症不同。这两种微生物初始清除的一些差异似乎与宿主白细胞 - 细菌关系的差异有关。体外研究表明,兔多形核白细胞摄取大肠杆菌后,大肠杆菌会迅速被杀死。葡萄球菌在这种摄取后存活下来。注射大肠杆菌后会出现长时间的粒细胞减少,并有粒细胞在肺血管床内滞留的证据。注射葡萄球菌后会出现短暂的白细胞减少,粒细胞迅速返回循环(15)。似乎被滞留白细胞摄取的大肠杆菌在细胞内被破坏,并且白细胞不会重新进入含有活大肠杆菌的循环。这种在血流中的白细胞内驻留已被证明在维持葡萄球菌菌血症方面可能很重要(14)。在初始清除期后,大肠杆菌菌血症迅速增加,表明许多被滞留的杆菌仍然存活。注射葡萄球菌后3至5小时也会出现菌血症增加。目前正在研究允许细菌群体二次复苏的细菌或宿主细胞机制。