Andoh Masako, Naganawa Takashi, Hotta Akitoyo, Yamaguchi Tsuyoshi, Fukushi Hideto, Masegi Toshiaki, Hirai Katsuya
Department of Veterinary Microbiology, Faculty of Agriculture, Gifu University, 1-1 Yanagido, Gifu, Gifu 501-1193, Japan.
Infect Immun. 2003 Aug;71(8):4717-23. doi: 10.1128/IAI.71.8.4717-4723.2003.
Q fever, a worldwide zoonosis caused by Coxiella burnetii, has many manifestations in humans. Endocarditis is the most serious complication of Q fever. Animal models are limited to acute pulmonary or hepatic disease and reproductive disorders. An appropriate experimental animal model for Q fever endocarditis does not yet exist. In this study, severe combined immunodeficient (SCID) mice infected with C. burnetii showed persistent clinical symptoms and died, whereas immunocompetent mice similarly infected became asymptomatic and survived. The SCID mice examined in this study had severe chronic lesions in their primary organs: the heart, lung, spleen, liver, and kidney. The heart lesions of the SCID mice were similar to those in humans with chronic Q fever endocarditis: they had focal calcification and expanded macrophages containing C. burnetii. The 50% lethal dose of C. burnetii in SCID mice was at least 10(8) times less than that in immunocompetent mice. The SCID mouse is highly susceptible to C. burnetii, and the immunodeficiency of the host enhances the severity of Q fever. This animal model could provide a new tool for the study of chronic Q fever and Q fever in immunodeficient hosts.
Q热是一种由伯氏考克斯体引起的全球性人畜共患病,在人类中有多种表现形式。心内膜炎是Q热最严重的并发症。动物模型仅限于急性肺部或肝脏疾病以及生殖系统疾病。目前尚无适用于Q热心内膜炎的实验动物模型。在本研究中,感染伯氏考克斯体的严重联合免疫缺陷(SCID)小鼠出现持续的临床症状并死亡,而同样感染的免疫健全小鼠则无症状并存活。本研究中检测的SCID小鼠的主要器官(心脏、肺、脾脏、肝脏和肾脏)有严重的慢性病变。SCID小鼠的心脏病变与慢性Q热心内膜炎患者的相似:有局灶性钙化和含有伯氏考克斯体的扩大巨噬细胞。SCID小鼠中伯氏考克斯体的半数致死剂量比免疫健全小鼠至少低10^8倍。SCID小鼠对伯氏考克斯体高度易感,宿主的免疫缺陷会加重Q热的严重程度。这种动物模型可为研究免疫缺陷宿主中的慢性Q热和Q热提供一种新工具。