Viral Special Pathogens Branch, Division of High Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
PLoS Negl Trop Dis. 2012;6(8):e1801. doi: 10.1371/journal.pntd.0001801. Epub 2012 Aug 28.
Lujo virus (LUJV) is a novel member of the Arenaviridae family that was first identified in 2008 after an outbreak of severe hemorrhagic fever (HF). In what was a small but rapidly progressing outbreak, this previously unknown virus was transmitted from the critically ill index patient to 4 attending healthcare workers. Four persons died during this outbreak, for a total case fatality of 80% (4/5). The suspected rodent source of the initial exposure to LUJV remains a mystery. Because of the ease of transmission, high case fatality, and novel nature of LUJV, we sought to establish an animal model of LUJV HF. Initial attempts in mice failed, but infection of inbred strain 13/N guinea pigs resulted in lethal disease. A total of 41 adult strain 13/N guinea pigs were infected with either wild-type LUJV or a full-length recombinant LUJV. Results demonstrated that strain 13/N guinea pigs provide an excellent model of severe and lethal LUJV HF that closely resembles what is known of the human disease. All infected animals experienced consistent weight loss (3-5% per day) and clinical illness characterized by ocular discharge, ruffled fur, hunched posture, and lethargy. Uniform lethality occurred by 11-16 days post-infection. All animals developed disseminated LUJV infection in various organs (liver, spleen, lung, and kidney), and leukopenia, lymphopenia, thrombocytopenia, coagulopathy, and elevated transaminase levels. Serial euthanasia studies revealed a temporal pattern of virus dissemination and increasing severity of disease, primarily targeting the liver, spleen, lungs, and lower gastrointestinal tract. Establishing an animal LUJV model is an important first step towards understanding the high pathogenicity of LUJV and developing vaccines and antiviral therapeutic drugs for this highly transmissible and lethal emerging pathogen.
卢日病毒(LUJV)是一种新型沙粒病毒科成员,于 2008 年在一次严重出血热(HF)爆发后首次被鉴定。在这场规模虽小但迅速蔓延的爆发中,这种以前未知的病毒从病危的指数患者传播给 4 名医护人员。在这次爆发中,有 4 人死亡,总病死率为 80%(4/5)。LUJV 最初暴露的疑似啮齿动物来源仍然是个谜。由于 LUJV 易于传播、病死率高且性质新颖,我们试图建立 LUJV HF 的动物模型。最初在小鼠中的尝试失败了,但近交系 13/N 豚鼠的感染导致了致命的疾病。共有 41 只成年 13/N 豚鼠感染了野生型 LUJV 或全长重组 LUJV。结果表明,13/N 豚鼠为严重和致命的 LUJV HF 提供了一个极好的模型,非常类似于已知的人类疾病。所有感染动物均经历一致的体重减轻(每天 3-5%)和临床疾病特征,包括眼部分泌物、毛发蓬乱、蜷缩姿势和昏睡。感染后 11-16 天内,所有动物均出现均匀致死。所有动物在各种器官(肝脏、脾脏、肺和肾脏)中均发生弥散性 LUJV 感染,并伴有白细胞减少症、淋巴细胞减少症、血小板减少症、凝血功能障碍和转氨酶水平升高。连续安乐死研究揭示了病毒传播的时间模式和疾病严重程度的增加,主要针对肝脏、脾脏、肺部和下胃肠道。建立动物 LUJV 模型是了解 LUJV 高致病性并为这种高度传播和致命的新兴病原体开发疫苗和抗病毒治疗药物的重要第一步。