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首页> 外文期刊>Frontiers in Microbiology >Prophylactic Use of Ganoderma lucidum Extract May Inhibit Mycobacterium tuberculosis Replication in a New Mouse Model of Spontaneous Latent Tuberculosis Infection
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Prophylactic Use of Ganoderma lucidum Extract May Inhibit Mycobacterium tuberculosis Replication in a New Mouse Model of Spontaneous Latent Tuberculosis Infection

机译:灵芝提取物的预防性使用可抑制结核分枝杆菌在自发性潜伏性结核感染新小鼠模型中的复制

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A mouse model of spontaneous latent tuberculosis infection (LTBI) that mimics LTBI in humans is valuable for drug/vaccine development and the study of tuberculosis. However, most LTBI mouse models require interventions, and a spontaneous LTBI mouse model with a low bacterial load is difficult to establish. In this study, mice were IV-inoculated with 100 CFU Mycobacterium tuberculosis H37Rv, and a persistent LTBI was established with low bacterial loads (0.5~1.5log_(10)CFU in the lung; < 4log_(10)CFU in the spleen). Histopathological changes in the lung and spleen were mild during the first 20 weeks post-inoculation. The model was used to demonstrate the comparative effects of prophylactic and therapeutic administration of Ganoderma lucidum extract (spores and spores lipid) in preventing H37Rv replication in both lung and spleen. H37Rv was inhibited with prophylactic use of G. lucidum extract relative to that of the untreated control and therapy groups, and observed in the spleen and lung as early as post-inoculation week 3 and week 5 respectively. H37Rv infection in the therapy group was comparable to that of the untreated control mice. No significant mitigation of pathological changes was observed in either the prophylactic or therapeutic group. Our results suggest that this new LTBI mouse model is an efficient tool of testing anti-tuberculosis drug, the use of G. lucidum extract prior to M. tuberculosis infection may protect the host against bacterial replication to some extent.
机译:在人类中模仿LTBI的自发性潜伏性结核感染(LTBI)的小鼠模型对于药物/疫苗的开发和结核病的研究非常有价值。但是,大多数LTBI小鼠模型都需要干预,并且很难建立具有低细菌载量的自发LTBI小鼠模型。在这项研究中,小鼠接受了100 CFU结核分枝杆菌H37Rv的IV接种,并且建立了持久的LTBI,细菌载量低(肺中0.5〜1.5log_(10)CFU;脾中<4log_(10)CFU)。接种后的最初20周,肺和脾的组织病理学变化较轻。该模型用于证明灵芝提取物(孢子和孢子脂质)的预防性和治疗性给药在预防肺和脾中H37Rv复制中的比较作用。相对于未治疗的对照组和治疗组,预防性使用灵芝提取物可抑制H37Rv,并分别在接种后第3周和第5周在脾脏和肺中观察到H37Rv。治疗组中的H37Rv感染与未治疗的对照小鼠相当。在预防组或治疗组中均未观察到明显的病理变化缓解。我们的结果表明,这种新的LTBI小鼠模型是测试抗结核药的有效工具,在结核分枝杆菌感染之前使用灵芝提取物可以在一定程度上保护宿主免受细菌复制。

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