Busch N A, Zanzot E M, Loiselle P M, Carter E A, Allaire J E, Yarmush M L, Warren H S
Center for Engineering in Medicine and Surgical Services, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, USA.
Infect Immun. 2000 Jun;68(6):3349-51. doi: 10.1128/IAI.68.6.3349-3351.2000.
A difficulty that has emerged in the development and preclinical evaluation of adjuvant therapies for gram-negative sepsis is the lack of easily studied animal models that closely mimic human infection. An objective of this study was to adapt a previously described model of infection in burned mice to rats with a defined bacterial strain of Escherichia coli. Challenge with two colonies of live E. coli O18:K1:H7 bacteria into an 8% full-thickness burn of the dorsal skin surface of rats produced predictable bacteremia at 24 to 48 h and 80 to 100% mortality at 3 to 4 days. E. coli O18:K1:H7 was approximately 10-million-fold more virulent than several other gram-negative bacterial strains. The model should be a useful tool in studying the pathogenicity of burn wound infections and in evaluating the efficacy of novel adjuvant therapies for gram-negative sepsis.
革兰氏阴性菌败血症辅助治疗的研发及临床前评估中出现的一个难题是,缺乏能紧密模拟人类感染且易于研究的动物模型。本研究的一个目标是将先前描述的烧伤小鼠感染模型应用于感染特定大肠杆菌菌株的大鼠。向大鼠背部皮肤表面8%的全层烧伤处接种两菌落活的大肠杆菌O18:K1:H7细菌,在24至48小时产生了可预测的菌血症,3至4天的死亡率为80%至100%。大肠杆菌O18:K1:H7的毒性比其他几种革兰氏阴性菌菌株强约1000万倍。该模型应是研究烧伤创面感染致病性以及评估革兰氏阴性菌败血症新型辅助治疗疗效的有用工具。