Bell T M, Shaia C I, Bunton T E, Robinson C G, Wilkinson E R, Hensley L E, Cashman K A
US Army Medical Research Institute of Infectious Diseases (USAMRIID), Frederick, MD, USA
Joint Pathology Center, Silver Spring, MD, USA.
Vet Pathol. 2015 Jan;52(1):26-37. doi: 10.1177/0300985814540544. Epub 2014 Jul 2.
Machupo virus, the causative agent of Bolivian hemorrhagic fever (BHF), is a highly lethal viral hemorrhagic fever of which little is known and for which no Food and Drug Administration-approved vaccines or therapeutics are available. This study evaluated the cynomolgus macaque as an animal model using the Machupo virus, Chicava strain, via intramuscular and aerosol challenge. The incubation period was 6 to 10 days with initial signs of depression, anorexia, diarrhea, mild fever, and a petechial skin rash. These were often followed by neurologic signs and death within an average of 18 days. Complete blood counts revealed leukopenia as well as marked thrombocytopenia. Serum chemistry values identified a decrease in total protein, marked increases in alanine aminotransferase and aspartate aminotransferase, and moderate increases in alkaline phosphatase. Gross pathology findings included a macular rash extending across the axillary and inguinal regions beginning at approximately 10 days postexposure as well as enlarged lymph nodes and spleen, enlarged and friable liver, and sporadic hemorrhages along the gastrointestinal mucosa and serosa. Histologic lesions consisted of foci of degeneration and necrosis/apoptosis in the haired skin, liver, pancreas, adrenal glands, lymph nodes, tongue, esophagus, salivary glands, stomach, small intestine, and large intestine. Lymphohistiocytic interstitial pneumonia was also present. Inflammation within the central nervous system (nonsuppurative encephalitis) was histologically apparent approximately 16 days postexposure and was generally progressive. This study provides insight into the course of Machupo virus infection in cynomolgus macaques and supports the usefulness of cynomolgus macaques as a viable model of human Machupo virus infection.
马丘波病毒是玻利维亚出血热(BHF)的病原体,是一种高度致命的病毒性出血热,人们对其了解甚少,且美国食品药品监督管理局未批准用于该病毒的疫苗或治疗药物。本研究通过肌肉注射和气溶胶攻击,评估了食蟹猴作为感染马丘波病毒奇卡瓦毒株的动物模型。潜伏期为6至10天,初期症状包括抑郁、厌食、腹泻、低热和瘀点性皮疹。随后常出现神经症状,平均18天内死亡。全血细胞计数显示白细胞减少以及明显的血小板减少。血清化学值显示总蛋白降低、丙氨酸转氨酶和天冬氨酸转氨酶显著升高、碱性磷酸酶中度升高。大体病理学发现包括暴露后约10天开始出现的遍布腋窝和腹股沟区域的斑疹,以及淋巴结和脾脏肿大、肝脏肿大且质脆、胃肠道黏膜和浆膜散在出血。组织学病变包括有毛皮肤、肝脏、胰腺、肾上腺、淋巴结、舌头、食管、唾液腺、胃、小肠和大肠的变性和坏死/凋亡灶。还存在淋巴细胞性间质性肺炎。暴露后约16天,中枢神经系统炎症(非化脓性脑炎)在组织学上明显可见,且通常呈进行性发展。本研究深入了解了食蟹猴感染马丘波病毒的病程,并支持食蟹猴作为人类感染马丘波病毒的可行模型的实用性。