Giebink G S, Wright P F
Infect Immun. 1983 Sep;41(3):913-20. doi: 10.1128/iai.41.3.913-920.1983.
We have previously shown that chinchillas infected with a multiply passaged laboratory strain of influenza A/NWS/33 (H1N1) develop negative middle-ear pressure; polymorphonuclear leukocyte oxidative, bactericidal, and chemotactic dysfunction; and increased susceptibility to pneumococcal otitis media. Because influenza A virus strains show different virulence in humans, three such strains were compared in the chinchilla model. Negative middle-ear pressure and tympanic membrane inflammation developed significantly more often in chinchillas infected with wild-type H3N2 virus than with either wild-type H1N1 virus or an attenuated, cold-adapted H3N2 vaccine strain, CR29. Marked depression in polymorphonuclear leukocyte chemiluminescent activity also developed significantly more often in H3N2 infected animals than in H1N1- or CR29-infected animals. Intranasal challenge of influenza virus-infected animals with type 7 Streptococcus pneumoniae resulted in a significantly greater occurrence of pneumococcal otitis media in H3N2-infected animals than in H1N1-, CR29-, or non-influenza-infected control animals. Clearance of pneumococci from nasal washings of animals infected with wild-type H3N2 was significantly delayed in comparison with the other groups. Thus, the previously demonstrated increased susceptibility to otitis media among children infected with H3N2 influenza virus may relate to the capacity of this strain to induce negative middle-ear pressure, polymorphonuclear leukocyte dysfunction, and alteration in the mucosal clearance of pneumococci.
我们之前已经表明,感染多次传代的甲型流感病毒A/NWS/33(H1N1)实验室毒株的栗鼠会出现中耳负压、多形核白细胞氧化、杀菌和趋化功能障碍,以及对肺炎球菌性中耳炎易感性增加。由于甲型流感病毒毒株在人类中表现出不同的毒力,因此在栗鼠模型中比较了三种这样的毒株。感染野生型H3N2病毒的栗鼠比感染野生型H1N1病毒或减毒、冷适应的H3N2疫苗株CR29的栗鼠更常出现中耳负压和鼓膜炎症。多形核白细胞化学发光活性的显著降低在感染H3N2的动物中也比在感染H1N1或CR29的动物中更常出现。用7型肺炎链球菌对感染流感病毒的动物进行鼻内攻击,结果显示感染H3N2的动物比感染H1N1、CR29或未感染流感的对照动物更易发生肺炎球菌性中耳炎。与其他组相比,感染野生型H3N2的动物鼻洗液中肺炎球菌的清除明显延迟。因此,先前证明感染H3N2流感病毒的儿童对中耳炎易感性增加可能与该毒株诱导中耳负压、多形核白细胞功能障碍以及肺炎球菌黏膜清除改变的能力有关。