Brun-Pascaud M, Rajagopalan-Levasseur P, Chau F, Bertrand G, Garry L, Derouin F, Girard P M
Institut National de la Santé et de la Recherche Médicale Unité 13 Hôpital Bichat-Claude Bernard, Paris, France.
Antimicrob Agents Chemother. 1998 May;42(5):1068-72. doi: 10.1128/AAC.42.5.1068.
We present a new experimental model for the simultaneous evaluation of the activities of drugs against Pneumocystis carinii, Toxoplasma gondii, and Mycobacterium avium complex infections. Rats latently infected with P. carinii were challenged with the MO-1 strain of M. avium and then immunosuppressed with corticosteroids for 7 weeks. At week 5 the RH strain of T. gondii was intraperitoneally injected. Organs were examined for the three pathogens after death or killing of the animals at week 7. Without treatment, rats challenged with T. gondii died with pulmonary P. carinii infection and disseminated T. gondii and M. avium infections. In order to assess the value of the model for evaluation of the activities of drugs, we administered by oral gavage for 7 weeks drugs or combinations of drugs selected for their individual efficacies against at least one pathogen. We found that clarithromycin with sulfamethoxazole, clarithromycin with atovaquone, roxithromycin with sulfamethoxazole or dapsone, and rifabutin with atovaquone were effective against the three infections, whereas PS-15 with dapsone and trimethoprim with sulfamethoxazole were active against Toxoplasma and Pneumocystis infections only. This triple-infection rat model offers a new tool for the simultaneous evaluation of the activities of drugs against three of the major opportunistic infections occurring in immunosuppressed individuals.
我们提出了一种新的实验模型,用于同时评估药物抗卡氏肺孢子虫、刚地弓形虫和鸟分枝杆菌复合群感染的活性。将潜伏感染卡氏肺孢子虫的大鼠用鸟分枝杆菌MO-1菌株攻击,然后用皮质类固醇免疫抑制7周。在第5周时腹腔注射刚地弓形虫RH株。在第7周动物死亡或处死后检查各器官中的这三种病原体。未经治疗的情况下,受到刚地弓形虫攻击的大鼠死于肺部卡氏肺孢子虫感染以及播散性刚地弓形虫和鸟分枝杆菌感染。为了评估该模型在评价药物活性方面的价值,我们通过口服灌胃给药7周,使用了因对至少一种病原体具有单独疗效而选择的药物或药物组合。我们发现,克拉霉素与磺胺甲恶唑、克拉霉素与阿托伐醌、罗红霉素与磺胺甲恶唑或氨苯砜,以及利福布汀与阿托伐醌对这三种感染均有效,而PS-15与氨苯砜以及甲氧苄啶与磺胺甲恶唑仅对弓形虫和肺孢子虫感染有活性。这种三重感染大鼠模型为同时评估药物抗免疫抑制个体中发生的三种主要机会性感染的活性提供了一种新工具。