Vasconcelos Daphne, Barnewall Roy, Babin Michael, Hunt Robert, Estep James, Nielsen Carl, Carnes Robert, Carney John
Lab Invest. 2003 Aug;83(8):1201-9. doi: 10.1097/01.lab.0000080599.43791.01.
Anthrax is considered a serious biowarfare and bioterrorism threat because of its high lethality, especially by the inhalation route. Rhesus macaques (Macaca mulatta) are the most commonly used nonhuman primate model of human inhalation anthrax exposure. The nonavailability of rhesus macaques necessitated development of an alternate model for vaccine testing and immunologic studies. This report describes the median lethal dose (LD(50)) and pathology of inhalation anthrax in cynomolgus macaques (Macaca fascicularis). Gross and microscopic tissue changes were reviewed in 14 cynomolgus monkeys that died or were killed after aerosol exposure of spores of Bacillus anthracis (Ames strain). The LD(50) and 95% confidence intervals were 61800 (34000 to 110000) colony-forming units. The most common gross lesions were mild splenomegaly, lymph node enlargement, and hemorrhages in various organs, particularly involving the meninges and the lungs. Mediastinitis, manifested as hemorrhage or edema, affected 29% of the monkeys. Microscopically, lymphocytolysis occurred in the intrathoracic lymph nodes and spleens of all animals, and was particularly severe in the spleen and in germinal centers of lymph nodes. Hemorrhages were common in lungs, bronchial lymph nodes, meninges, gastrointestinal tract, and mediastinum. These results demonstrate that the Ames strain of B. anthracis is lethal by the inhalation route in the cynomolgus macaque. The LD(50) of the Ames strain of B. anthracis was within the expected experimental range of previously reported values in the rhesus monkey in an aerosol challenge. The gross and microscopic pathology of inhalation anthrax in the cynomolgus monkey is remarkably similar to that reported in rhesus monkeys and humans. The results of this study are important for the establishment of an alternative nonhuman primate model for evaluation of medical countermeasures against inhalational anthrax.
炭疽因其高致死率,尤其是通过吸入途径感染时的高致死率,被视为一种严重的生物战和生物恐怖主义威胁。恒河猴(猕猴)是人类吸入性炭疽暴露最常用的非人类灵长类动物模型。由于恒河猴难以获取,因此有必要开发一种替代模型用于疫苗测试和免疫学研究。本报告描述了食蟹猴吸入性炭疽的半数致死剂量(LD50)和病理学特征。对14只食蟹猴在暴露于炭疽芽孢杆菌(Ames菌株)孢子气溶胶后死亡或被处死的情况进行了大体和显微镜下组织变化的观察。LD50及其95%置信区间为61800(34000至110000)个菌落形成单位。最常见的大体病变为轻度脾肿大、淋巴结肿大以及各器官出血,尤其累及脑膜和肺部。表现为出血或水肿的纵隔炎影响了29%的猴子。显微镜下,所有动物的胸腔内淋巴结和脾脏均出现淋巴细胞溶解,脾脏和淋巴结生发中心尤为严重。肺部、支气管淋巴结、脑膜、胃肠道和纵隔出血很常见。这些结果表明,炭疽芽孢杆菌Ames菌株通过吸入途径对食蟹猴具有致死性。炭疽芽孢杆菌Ames菌株的LD50在先前报道的恒河猴气溶胶攻击实验预期范围内。食蟹猴吸入性炭疽的大体和显微镜下病理学与恒河猴和人类报道的情况非常相似。本研究结果对于建立一种替代非人类灵长类动物模型以评估针对吸入性炭疽的医学应对措施具有重要意义。