Ryan Lisa K, Hise Amy G, Hossain Chowdhury Mobaswar, Ruddick William, Parveen Rezwana, Freeman Katie B, Weaver Damian G, Narra Hema P, Scott Richard W, Diamond Gill
Division of Infectious Disease and Global Medicine, Department of Medicine, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Department of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
J Fungi (Basel). 2020 Sep 30;6(4):197. doi: 10.3390/jof6040197.
Disseminated infection by species represents a common, often life-threatening condition. Increased resistance to current antifungal drugs has led to an urgent need to develop new antifungal drugs to treat this pathogen. However, in vivo screening of candidate antifungal compounds requires large numbers of animals and using immunosuppressive agents to allow for fungal dissemination. To increase the efficiency of screening, to use fewer mice, and to remove the need for immunosuppressive agents, which may interfere with the drug candidates, we tested the potential for a novel approach using in vivo imaging of a fluorescent strain of , in a mouse strain deficient in the host defense peptide, murine β-defensin 1 (mBD-1). We developed a strain of that expresses red fluorescent protein (RFP), which exhibits similar infectivity to the non-fluorescent parent strain. When this strain was injected into immunocompetent mBD-1-deficient mice, we observed a non-lethal disseminated infection. Further, we could quantify its dissemination in real time, and observe the activity of an antifungal peptide mimetic drug by in vivo imaging. This novel method will allow for the rapid in vivo screening of antifungal drugs, using fewer mice, and increase the efficiency of testing new antifungal agents.
该菌种的播散性感染是一种常见的、往往危及生命的病症。对当前抗真菌药物耐药性的增加导致迫切需要开发新的抗真菌药物来治疗这种病原体。然而,在体内筛选候选抗真菌化合物需要大量动物,并使用免疫抑制剂以实现真菌播散。为了提高筛选效率、减少小鼠使用数量,并消除对可能干扰候选药物的免疫抑制剂的需求,我们在缺乏宿主防御肽鼠β-防御素1(mBD-1)的小鼠品系中,测试了一种使用荧光菌株体内成像的新方法的潜力。我们构建了一种表达红色荧光蛋白(RFP)的菌株,其与非荧光亲本菌株表现出相似的感染性。当将该菌株注射到具有免疫活性的mBD-1缺陷小鼠中时,我们观察到了非致死性播散性感染。此外,我们可以实时量化其播散情况,并通过体内成像观察抗真菌肽模拟药物的活性。这种新方法将允许使用更少的小鼠在体内快速筛选抗真菌药物,并提高测试新型抗真菌剂的效率。