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Lethal murine infection model for human respiratory disease-associated Pteropine orthoreovirus

机译:人类呼吸系统疾病相关的pteropine Orthoreovirus的致死鼠感染模型

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摘要

Abstract Pteropine orthoreovirus (PRV) is an emerging bat-borne human pathogen causing severe respiratory illness. To date, however, the evaluation of PRV virulence has largely depended on the limited numbers of clinical cases owing to the lack of animal models. To develop an in vivo model of PRV infection, an inbred C3H mouse strain was infected intranasally with pathogenic PRV strain Miyazaki-Bali/2007. C3H mice suffered severe lung infection with significant body weight reduction and died within 7 days after intranasal infection. Infectious viruses were isolated mainly from the lungs and trachea. Histopathological examination revealed interstitial pneumonia with monocytes infiltration. Following repeated intranasal infection, mice developed antibodies to particular structural and non-structural proteins of PRV. The results of these immunological assays will help to develop laboratory protocols for sero-epidemiological studies. Our small rodent model of lethal respiratory infection will further allow investigation of the molecular mechanisms underlying the high pathogenicity of PRV. Highlights ? A lethal PRV strain Miyazaki-Bali/2007 murine infection model was established. ? Susceptibility of different mouse strains to PRV infection was investigated. ? Antibody responses to PRV proteins in C3H mice post intranasal infection were studied.
机译:摘要pteropine Orthoreovirus(PRV)是一种新兴的蝙蝠患者,导致严重的呼吸道疾病。然而,迄今为止,由于缺乏动物模型,PRV毒力的评估主要取决于有限的临床病例。为了开发PRV感染的体内模型,含有致病性PRV菌株Miyazaki-Bali / 2007的患有近交的C3H小鼠菌株。 C3h小鼠患有严重的肺部感染,体重显着减少,鼻内感染后7天内死亡。传染性病毒主要来自肺和气管。组织病理学检查揭示了单核细胞浸润的间质性肺炎。在重复鼻内感染之后,小鼠对PRV的特定结构和非结构蛋白产生抗体。这些免疫检测结果将有助于为血清流行病学研究制定实验室方案。我们的小啮齿动物致命呼吸道感染模型将进一步允许研究PRV的高致病性下面的分子机制。强调 ?建立了致死的PRV菌株Miyazaki-Bali / 2007鼠感染模型。还是研究了不同小鼠菌株与PRV感染的易感性。还是研究了对鼻内感染后C3H小鼠中PRV蛋白的抗体反应。

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