Tolbert M, Giron D J
Department of Microbiology and Immunology, Wright State University School of Science and Mathematics, Dayton, Ohio 45435.
Proc Soc Exp Biol Med. 1994 Feb;205(2):124-31. doi: 10.3181/00379727-205-43687.
The D variant of encephalomyocarditis virus (EMCV-D) is used in the murine model to study virus-induced, acute-onset diabetes mellitus (IDDM) and myocarditis. In this model, viral replication and disease occur within seven days post infection (p.i.), and by Day 10 p.i., no infectious virus is detectable. The present study examined the possibility that EMCV-D persists in ICR-Swiss mice after the acute infection is resolved. The data show that viral antigen is detected at 28 days p.i. within the pancreatic islets of 8/10 males and 13/14 females, and within the heart valves of all animals tested. Histologic examination of the organs at 28 days p.i. suggests the development of chronic obstructive pancreatitis, and shows almost fully healed lesions in the myocardium. These observations indicate that the murine model for the study of EMCV-D induced IDDM may be extended to investigate chronic pancreatitis and heart-valve disease.
脑心肌炎病毒D型(EMCV-D)被用于小鼠模型,以研究病毒诱导的急性发作型糖尿病(IDDM)和心肌炎。在该模型中,病毒复制和疾病在感染后七天内发生,到感染后第10天,检测不到传染性病毒。本研究检验了急性感染消退后EMCV-D在ICR-瑞士小鼠体内持续存在的可能性。数据显示,在感染后28天,在10只雄性小鼠中的8只和14只雌性小鼠中的13只的胰岛内以及所有受试动物的心脏瓣膜中检测到病毒抗原。对感染后28天的器官进行组织学检查表明出现了慢性阻塞性胰腺炎,且心肌中的病变几乎已完全愈合。这些观察结果表明,用于研究EMCV-D诱导的IDDM的小鼠模型可扩展用于研究慢性胰腺炎和心脏瓣膜疾病。