Nielsen Ole L, Iburg Tine, Aalbaek Bent, Leifsson Páll S, Agerholm Jørgen S, Heegaard Peter, Boye Mette, Simon Sofie, Jensen Kristine B, Christensen Sophie, Melsen Karin, Bak Anne K, Backman Elín R, Jørgensen Mia H, Groegler Désirée K, Jensen Asger L, Kjelgaard-Hansen Mads, Jensen Henrik E
Department of Veterinary Disease Biology, University of Copenhagen, Frederiksberg C, Denmark.
Acta Vet Scand. 2009 Mar 27;51(1):14. doi: 10.1186/1751-0147-51-14.
Sepsis caused by Staphylococcus aureus constitutes an important cause of morbidity and mortality in humans, and the incidence of this disease-entity is increasing. In this paper we describe the initial microbial dynamics and lesions in pigs experimentally infected with S. aureus, with the aim of mimicking human sepsis and pyemia.
The study was conducted in anaesthetized and intravenously inoculated pigs, and was based on bacteriological examination of blood and testing of blood for IL-6 and C-reactive protein. Following killing of the animals and necropsy bacteriological and histological examinations of different organs were performed 4, 5 or 6 h after inoculation.
Clearance of bacteria from the blood was completed within the first 2 h in some of the pigs and the highest bacterial load was recorded in the lungs as compared to the spleen, liver and bones. This probably was a consequence of both the intravenous route of inoculation and the presence of pulmonary intravascular macrophages. Inoculation of bacteria induced formation of acute microabscesses in the lungs, spleen and liver, but not in the kidneys or bones. No generalized inflammatory response was recorded, i.e. IL-6 was not detected in the blood and C-reactive protein did not increase, probably because of the short time course of the study.
This study demonstrates the successful induction of acute pyemia (microabscesses), and forms a basis for future experiments that should include inoculation with strains of S. aureus isolated from man and an extension of the timeframe aiming at inducing sepsis, severe sepsis and septic shock.
金黄色葡萄球菌引起的脓毒症是人类发病和死亡的重要原因,且该疾病实体的发病率正在上升。在本文中,我们描述了实验性感染金黄色葡萄球菌的猪的初始微生物动态和病变情况,旨在模拟人类脓毒症和脓血症。
该研究在麻醉并静脉接种的猪身上进行,基于血液的细菌学检查以及血液中白细胞介素-6和C反应蛋白的检测。在动物处死和尸检后,于接种后4、5或6小时对不同器官进行细菌学和组织学检查。
部分猪在最初2小时内血液中的细菌清除完毕,与脾脏、肝脏和骨骼相比,肺部的细菌载量最高。这可能是静脉接种途径以及肺血管内巨噬细胞存在的结果。接种细菌导致肺部、脾脏和肝脏形成急性微脓肿,但肾脏和骨骼未出现。未记录到全身性炎症反应,即血液中未检测到白细胞介素-6且C反应蛋白未增加,这可能是由于研究时间较短。
本研究证明成功诱导了急性脓血症(微脓肿),并为未来的实验奠定了基础,未来实验应包括接种从人类分离的金黄色葡萄球菌菌株,并延长时间框架以诱导脓毒症、严重脓毒症和感染性休克。