Bell T M, Shaia C I, Bearss J J, Mattix M E, Koistinen K A, Honnold S P, Zeng X, Blancett C D, Donnelly G C, Shamblin J D, Wilkinson E R, Cashman K A
1 US Army Medical Research Institute of Infectious Diseases, Frederick, MD, USA.
2 Current address: Joint Pathology Center, Silver Spring, MD, USA.
Vet Pathol. 2017 May;54(3):549-562. doi: 10.1177/0300985816677153. Epub 2016 Jan 1.
Lassa virus (LASV) infection causes an acute, multisystemic viral hemorrhagic fever that annually infects an estimated 100 000 to 300 000 persons in West Africa. This pathogenesis study evaluated the temporal progression of disease in guinea pigs following aerosol and subcutaneous inoculation of the Josiah strain of LASV as well as the usefulness of Strain 13 guinea pigs as an animal model for Lassa fever. After experimental infection, guinea pigs ( Cavia porcellus; n = 67) were serially sampled to evaluate the temporal progression of infection, gross and histologic lesions, and serum chemistry and hematologic changes. Guinea pigs developed viremia on day 5 to 6 postexposure (PE), with clinical signs appearing by day 7 to 8 PE. Complete blood counts revealed lymphopenia and thrombocytopenia. Gross pathologic findings included skin lesions and congested lungs. Histologic lesions consisted of cortical lymphoid depletion by day 6 to 7 PE with lymphohistiocytic interstitial pneumonia at 7 to 8 days PE. Scattered hepatocellular degeneration and cell death were also noted in the liver and, to a lesser extent, in other tissues including the haired skin, lung, heart, adrenal gland, lymph nodes, thymus, and spleen. The first cell types to demonstrate staining for viral antigen were fibroblastic reticular cells and macrophages/dendritic cells in the lymph nodes on day 5 to 6 PE. This study demonstrates similarities between Lassa viral disease in human infections and experimental guinea pig infection. These shared pathologic characteristics support the utility of guinea pigs as an additional animal model for vaccine and therapeutic development under the Food and Drug Administration's Animal Rule.
拉沙病毒(LASV)感染会引发一种急性多系统病毒性出血热,在西非,每年估计有10万至30万人感染该病毒。本发病机制研究评估了豚鼠经气溶胶和皮下接种LASV约西亚株后疾病的时间进程,以及13号品系豚鼠作为拉沙热动物模型的实用性。实验感染后,对豚鼠(豚鼠;n = 67)进行连续采样,以评估感染的时间进程、大体和组织学病变以及血清化学和血液学变化。豚鼠在暴露后第5至6天出现病毒血症,在暴露后第7至8天出现临床症状。全血细胞计数显示淋巴细胞减少和血小板减少。大体病理表现包括皮肤病变和肺部充血。组织学病变包括在暴露后第6至7天出现皮质淋巴样细胞耗竭,在暴露后7至8天出现淋巴细胞组织细胞性间质性肺炎。在肝脏中也观察到散在的肝细胞变性和细胞死亡,在较小程度上,在包括有毛皮肤、肺、心脏、肾上腺、淋巴结、胸腺和脾脏在内的其他组织中也有发现。在暴露后第5至6天,淋巴结中最早显示病毒抗原染色的细胞类型是成纤维网状细胞和巨噬细胞/树突状细胞。本研究证明了人类感染中的拉沙病毒病与实验性豚鼠感染之间的相似性。这些共同的病理特征支持了豚鼠作为美国食品药品监督管理局动物规则下疫苗和治疗药物开发的额外动物模型的实用性。