Abou-Donia H, Jennings R, Potter C W
J Med Virol. 1981;7(4):251-62. doi: 10.1002/jmv.1890070402.
The persistence and extrapulmonary spread of three strains of influenza virus, the mouse neuro-adapted A/NWS virus, the wild-type strain A/Victoria/75, and a recombinant virus RIT4050, bearing surface antigens derived from A/Victoria/75, were studied in both normal and cyclophosphamide-treated CBA mice following either intranasal or intracerebral inoculation. All three viruses showed increased lethality in mice in the presence of cyclophosphamide but exhibited distinctive patterns of replication and spread. The recombinant virus RIT4050 showed a reduced ability to replicate, persist, and spread in CBA mice compared to either A/NWS or A/Victoria/75 viruses, and in general, the A/NWS virus persisted to a greater extent than the A/Victoria/75 virus in both normal and treated mice. However, in the presence of cyclophosphamide, no extrapulmonary spread of A/NWS virus was observed. The reasons for the differences are discussed.
对三株流感病毒(小鼠神经适应型A/NWS病毒、野生型A/维多利亚/75病毒以及携带源自A/维多利亚/75表面抗原的重组病毒RIT4050)在正常和经环磷酰胺处理的CBA小鼠中经鼻内或脑内接种后的持续性和肺外传播情况进行了研究。在环磷酰胺存在的情况下,所有三种病毒在小鼠中的致死率均有所增加,但呈现出独特的复制和传播模式。与A/NWS或A/维多利亚/75病毒相比,重组病毒RIT4050在CBA小鼠中的复制、持续存在和传播能力降低,并且总体而言,在正常和处理过的小鼠中,A/NWS病毒比A/维多利亚/75病毒持续存在的程度更大。然而,在环磷酰胺存在的情况下,未观察到A/NWS病毒的肺外传播。文中讨论了这些差异的原因。