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小鼠巨细胞病毒肺炎:一种模型的描述及发病机制研究

Murine cytomegalovirus pneumonia. Description of a model and investigation of pathogenesis.

作者信息

Rose R M, Crumpacker C, Waner J L, Brain J D

出版信息

Am Rev Respir Dis. 1982 May;125(5):568-73. doi: 10.1164/arrd.1982.125.5.568.

Abstract

Pneumonitis was produced in CD-1 mice by intratracheal instillation of murine cytomegalovirus. Lethal pneumonia occurred after instillation of virus derived from partially purified salivary gland homogenates, whereas virus attenuated by serial passage in cell culture caused mild disease and no mortality, even though both virulent and attenuated strains achieved comparable peak titers in lung homogenates. Virulence was characterized by rapid association of virus with pulmonary macrophages and early spread of virus from macrophages to susceptible parenchymal cells. This resulted in enhanced viral growth and cellular destruction during the first 5 days of infection. Delay in the early growth of murine cytomegalovirus in pulmonary parenchyma may diminish the destructive effects of virus on the lung and prevent mortality.

摘要

通过气管内注入鼠巨细胞病毒在CD-1小鼠中诱发肺炎。注入来自部分纯化的唾液腺匀浆的病毒后发生致命性肺炎,而在细胞培养中连续传代减毒的病毒引起轻度疾病且无死亡,尽管强毒株和减毒株在肺匀浆中达到了相当的峰值滴度。毒力的特征是病毒与肺巨噬细胞快速结合以及病毒从巨噬细胞向易感实质细胞的早期传播。这导致感染的前5天病毒生长增强和细胞破坏。鼠巨细胞病毒在肺实质中的早期生长延迟可能会降低病毒对肺的破坏作用并预防死亡。

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