首页> 美国卫生研究院文献>Journal of Virology >The Cotton Rat (Sigmodon hispidus) Is a Permissive Small Animal Model of Human Metapneumovirus Infection Pathogenesis and Protective Immunity
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The Cotton Rat (Sigmodon hispidus) Is a Permissive Small Animal Model of Human Metapneumovirus Infection Pathogenesis and Protective Immunity

机译:棉鼠(Sigmodon hispidus)是人类间质肺炎病毒感染发病机制和保护性免疫的允许的小动物模型。

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摘要

Human metapneumovirus (hMPV) is a newly described paramyxovirus that is an important cause of acute respiratory tract disease. We undertook to develop a small animal model of hMPV infection, pathogenesis, and protection. Hamsters, guinea pigs, cotton rats, and nine inbred strains of mice were inoculated intranasally with hMPV. The animals were sacrificed, and nasal and lung tissue virus yields were determined by plaque titration. None of the animals exhibited respiratory symptoms. The quantity of virus present in the nasal tissue ranged from 4.6 × 102 PFU/gram tissue (C3H mice) to greater than 105 PFU/gram (hamster). The amount of virus in the lungs was considerably less than in nasal tissue in each species tested, ranging from undetectable (<5 PFU/g; guinea pigs) to 1.8 × 105 PFU/gram (cotton rat). The peak virus titer in cotton rat lungs occurred on day 4 postinfection. hMPV-infected cotton rat lungs examined on day 4 postinfection exhibited histopathological changes consisting of peribronchial inflammatory infiltrates. Immunohistochemical staining detected virus only at the luminal surfaces of respiratory epithelial cells throughout the respiratory tract. hMPV-infected cotton rats mounted virus-neutralizing antibody responses and were partially protected against virus shedding and lung pathology on subsequent rechallenge with hMPV. Viral antigen was undetectable in the lungs on challenge of previously infected animals. This study demonstrates that the cotton rat is a permissive small animal model of hMPV infection that exhibits lung histopathology associated with infection and that primary infection protected animals against subsequent infection. This model will allow further in vivo studies of hMPV pathogenesis and evaluation of vaccine candidates.
机译:人间质肺病毒(hMPV)是一种新近描述的副粘病毒,是急性呼吸道疾病的重要原因。我们承诺开发hMPV感染,发病机制和保护的小动物模型。仓鼠,豚鼠,棉鼠和9个自交系小鼠经鼻内接种hMPV。处死动物,并通过噬斑滴定确定鼻和肺组织病毒的产量。没有动物表现出呼吸道症状。鼻组织中存在的病毒数量范围为4.6×10 2 PFU /克组织(C3H小鼠)至大于10 5 PFU /克(仓鼠)。在每种测试的物种中,肺中的病毒数量明显少于鼻组织,范围从无法检测到(<5 PFU / g;豚鼠)到1.8×10 5 PFU /克(棉鼠) )。棉花大鼠肺部病毒滴度达到最高峰是在感染后第4天。感染后第4天检查的被hMPV感染的棉鼠肺表现出由支气管周炎性浸润组成的组织病理学变化。免疫组织化学染色仅在整个呼吸道的呼吸道上皮细胞腔表面检测到病毒。感染hMPV的棉鼠安装了病毒中和抗体反应,并在随后用hMPV再攻击时得到部分保护,以防止病毒脱落和肺部病理。在先前感染的动物攻击后,肺中无法检测到病毒抗原。这项研究表明,棉鼠是一种允许的hMPV感染小动物模型,具有与感染相关的肺组织病理学特征,并且原发性感染可以保护动物免受随后的感染。该模型将允许进一​​步进行hMPV发病机理的体内研究,并评估候选疫苗。

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