Department of Microbiology, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, New York 10029, USA.
J Virol. 2011 Dec;85(23):12825-9. doi: 10.1128/JVI.05930-11. Epub 2011 Sep 14.
We assessed the relative susceptibilities to disease of the DBA.2 and C57BL/6 mouse models upon infection with a range of influenza A and B viruses. DBA.2 mice were more susceptible to disease upon inoculation with human H1N1 influenza A virus strains, several swine influenza viruses, and influenza B viruses but were not overtly susceptible to infection with human seasonal H3N2 strains. Hemagglutination inhibition and immunoglobulin isotype profiling indicated that DBA.2 and C57BL/6 mice generate comparable humoral responses upon equivalent 50% mouse lethal dose (MLD(50)) challenges with influenza virus. Our data demonstrate the utility of DBA.2 mice for the elucidation of influenza virus pathogenicity determinants and the testing of influenza vaccines.
我们评估了 DBA.2 和 C57BL/6 两种小鼠模型在感染一系列甲型和乙型流感病毒时对疾病的相对易感性。在接种人源 H1N1 甲型流感病毒株、几种猪源流感病毒和乙型流感病毒后,DBA.2 小鼠更容易患病,但对人源季节性 H3N2 株的感染并不明显易感。血凝抑制和免疫球蛋白亚型分析表明,在接受相同的 50%致死剂量(MLD(50))的流感病毒挑战时,DBA.2 和 C57BL/6 小鼠产生相当的体液免疫反应。我们的数据表明 DBA.2 小鼠可用于阐明流感病毒致病性决定因素和测试流感疫苗。