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Transgenic mice carrying the human poliovirus receptor: new animal models for study of poliovirus neurovirulence.

机译:携带人类脊髓灰质炎病毒受体的转基因小鼠:用于研究脊髓灰质炎病毒神经毒性的新动物模型。

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摘要

Recombinant viruses between the virulent Mahoney and attenuated Sabin 1 strains of poliovirus type 1 were subjected to neurovirulence tests using a transgenic (Tg) mouse line, ICR-PVRTg1, that carried the human poliovirus receptor gene. The Tg mice were inoculated intracerebrally with these recombinant viruses and observed for clinical signs, histopathological lesions, and viral antigens as parameters of neurovirulence of the viruses. These parameters observed in the Tg mice were different for different inoculated viruses. Dose-dependent incidences of paralysis and of death were observed in the Tg mice inoculated with any viruses used. This indicates that values of 50% lethal dose are useful to score a wide range of neurovirulence of poliovirus. The neurovirulence of individual viruses estimated by the Tg mouse model had a strong correlation with those estimated by monkey model. Consequently, the mouse tests identified the neurovirulence determinants on the genome of poliovirus that had been identified by monkey tests. In addition, the mouse tests revealed new neurovirulence determinants, that is, different nucleotides between the two strains at positions 189 and 21 and/or 935 in the 5'-proximal 1,122 nucleotides. The Tg mice used in this study may be suitable for replacing monkeys for investigating poliovirus neurovirulence.
机译:使用携带人类脊髓灰质炎病毒受体基因的转基因(Tg)小鼠品系ICR-PVRTg1,对强毒Mahoney和减毒的Sabin 1型脊髓灰质炎病毒株之间的重组病毒进行神经毒力测试。用这些重组病毒在脑内接种Tg小鼠,并观察其临床体征,组织病理学损伤和病毒抗原作为病毒神经毒性的参数。对于不同的接种病毒,在Tg小鼠中观察到的这些参数是不同的。在接种了任何病毒的Tg小鼠中观察到了剂量依赖性麻痹和死亡的发生率。这表明50%致死剂量的值可用于对脊髓灰质炎病毒的广泛神经毒力进行评分。 Tg小鼠模型估计的单个病毒的神经毒力与猴子模型估计的神经毒力有很强的相关性。因此,小鼠试验确定了由猴试验确定的脊髓灰质炎病毒基因组上的神经毒性决定因素。另外,小鼠测试揭示了新的神经毒力决定因素,即两个毒株之间5'-近端的1,122个核苷酸中第189和21和/或935位的核苷酸不同。在这项研究中使用的Tg小鼠可能适合替代猴子以调查脊髓灰质炎病毒的神经毒性。

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