首页> 外文期刊>Infection and immunity >Synergistic effect on mortality in mice with murine cytomegalovirus and Pseudomonas aeruginosa, Staphylococcus aureus, or Candida albicans infections.
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Synergistic effect on mortality in mice with murine cytomegalovirus and Pseudomonas aeruginosa, Staphylococcus aureus, or Candida albicans infections.

机译:对小鼠巨细胞病毒和铜绿假单胞菌,金黄色葡萄球菌或白色念珠菌感染的小鼠具有协同增效作用。

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A synergistic effect on mortality was demonstrated in a combined infection of mice with murine cytomegalovirus (MCMV) and Pseudomonas aeruginosa, Staphylococcus aureus, or Candida albicans. Mice infected intraperitoneally with a 0 to 20% lethal dose inoculum of MCMV 3 days prior to the intravenous injection of a 0 to 20% lethal dose inoculum of either the bacteria or fungus demonstrated a striking enhancement of mortality. MCMV-infected mice given Pseudomonas or Staphylococcus exhibited a 90 to 100% mortality within 24 to 48 h, whereas 80% of viral-infected animals injected with Candida died in 5 days. Injection of the bacteria or fungus at various times during the MCMV infection resulted in enhanced mortality on days 0,1,2, and 3 of the viral infection. Greatest synergism was observed on day 3, with a progressive decline in death rates thereafter. Immunization with MCMV abrogated the synergistic effect on mortality in all three combined infections. Immunization with Pseudomonas reduced mortality in the combined MCMV-Pseudomonas infection. These results indicate that mice exhibit a markedly enhanced susceptibility to bacterial and fungal infections during the course of the MCMV infection and suggest that the enhancement may be related to viral-induced alterations in host resistance.
机译:在小鼠巨细胞病毒(MCMV)和铜绿假单胞菌,金黄色葡萄球菌或白色念珠菌联合感染小鼠中,证实了对死亡率的协同作用。在静脉注射0至20%致死剂量的细菌或真菌接种前3天,腹腔内用0至20%致死剂量的MCMV接种的小鼠表现出惊人的死亡率增加。接种了假单胞菌或葡萄球菌的MCMV感染小鼠在24至48小时内表现出90至100%的死亡率,而注射念珠菌的病毒感染动物中有80%在5天内死亡。在MCMV感染期间的不同时间注射细菌或真菌会导致病毒感染第0、1、2和3天的死亡率增加。在第3天观察到最大的协同作用,此后死亡率逐渐下降。 MCMV免疫消除了所有三种合并感染对死亡率的协同作用。假单胞菌免疫降低了合并的MCMV-假单胞菌感染的死亡率。这些结果表明,小鼠在MCMV感染过程中对细菌和真菌感染的敏感性显着增强,并表明这种增强可能与病毒诱导的宿主抗性改变有关。

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