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首页> 外文期刊>The American Journal of Tropical Medicine and Hygiene >Pirital virus (Arenaviridae) infection in the syrian golden hamster, Mesocricetus auratus: a new animal model for arenaviral hemorrhagic fever.
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Pirital virus (Arenaviridae) infection in the syrian golden hamster, Mesocricetus auratus: a new animal model for arenaviral hemorrhagic fever.

机译:叙利亚金黄仓鼠中的胸膜炎病毒(Arenaviridae)感染:Mesocricetus auratus:一种新的动物模型,用于戊型肝炎出血热。

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Adult Syrian golden hamsters inoculated intraperitoneally with Pirital virus, a recently discovered member of the Tacaribe complex of New World arenaviruses, developed a progressively severe, fatal illness with many of the pathologic features observed in fatal human cases of Lassa fever and other arenaviral hemorrhagic fevers. Most of the animals became moribund by Day 5 and were dead by Day 7 after inoculation. The most consistent histopathologic changes included interstitial pneumonitis, splenic lymphoid depletion and necrosis, and multifocal hepatic necrosis without significant inflammatory cell infiltration. The liver changes ranged from single cell death by apoptosis to coagulative necrosis of clusters of hepatocytes. Immunohistochemical studies of the liver demonstrated the presence and accumulation ot Pirital virus antigen within hepatocytes as well as Kupffer cells. An in situ terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) assay showed progressively increasing apoptotic activity in the liver of infected hamsters. A human hepatoblastoma cell line (Hep G2/C3A) inoculated with Pirital virus also developed progressive cell destruction and accumulation of viral antigen, as demonstrated by immunofluorescence. Results of this pilot study suggest that the Pirital virus-hamster model is a very promising new small animal model for studying the pathogenesis of arenavirus infections, particularly, the mechanism of direct virus-induced hepatic injury. It may also be useful for testingantiviral agents for treatment of arenaviral hemorrhagic fevers.
机译:新发现的塔克拉里布病毒新近发现的新成员塔克拉里布病毒,腹膜内接种了成年的叙利亚金仓鼠腹膜炎病毒,这种病毒逐渐发展为致命性疾病,在致命的人类拉沙热和其他鼻病毒性出血热病例中观察到许多病理特征。大部分动物在接种后第5天就垂死,并在接种后第7天死亡。最一致的组织病理学改变包括间质性肺炎,脾淋巴样耗竭和坏死,以及多灶性肝坏死,而没有明显的炎症细胞浸润。肝脏变化的范围从凋亡引起的单细胞死亡到肝细胞簇的凝集性坏死。肝脏的免疫组织化学研究表明,肝炎病毒和库普弗细胞中存在和积累了胸膜炎病毒抗原。原位末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)分析显示感染的仓鼠肝脏中的凋亡活性逐渐增加。如免疫荧光所证实的,用Pirital病毒接种的人肝母细胞瘤细胞系(Hep G2 / C3A)也发生了渐进性细胞破坏和病毒抗原蓄积。这项初步研究的结果表明,Pirital病毒-仓鼠模型是一种非常有希望的新型小动物模型,用于研究类风疹病毒感染的发病机理,尤其是直接病毒诱发的肝损伤机制。它也可能用于测试抗病毒药物,以治疗晕厥病毒性出血热。

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