University of Wisconsin-Madison, Madison, WI, USA.
Methods Mol Biol. 2023;2658:225-238. doi: 10.1007/978-1-0716-3155-3_16.
Candida frequently produces three general disease states, including mucosal candidiasis, disseminated candidiasis, and biofilm infection (which can be present with either of the other disease states). Antifungal drug resistance is intrinsic to biofilm growth and has emerged in other disease states. Mechanistic studies have uncovered the genetic pathways governing resistance to a number of antifungal agents. However, analyzing the clinical relevance of distinct mechanisms is fundamental for broadening our knowledge of antifungal drug resistance and for delineating the potential impact of targeting these pathways medically. Also, as drug-resistant strains and biofilms represent important nosocomial problems, preclinical animal models to assess the activity of novel antifungals are of great interest. Here we describe two rodent models that mimic the most common biofilm device and disseminated candidiasis states in patients. The model systems incorporate the anatomical site, immune components, and antifungal exposures relevant for the study of antifungal resistance. The models can be used to analyze mutant strains, assess the extent of drug resistance, examine biofilm formation, test new antimicrobials, and help determine drug exposures that may be linked with clinical failure.
假丝酵母菌通常会引起三种常见疾病状态,包括黏膜假丝酵母菌病、播散性假丝酵母菌病和生物膜感染(可与其他任何一种疾病状态同时存在)。抗真菌药物耐药性是生物膜生长的固有特性,并且已经在其他疾病状态中出现。机制研究揭示了控制对多种抗真菌药物耐药性的遗传途径。然而,分析不同机制的临床相关性对于拓宽我们对抗真菌药物耐药性的认识以及阐明靶向这些途径的医学潜力至关重要。此外,由于耐药菌株和生物膜是重要的医院感染问题,评估新型抗真菌药物活性的临床前动物模型非常重要。在这里,我们描述了两种模拟患者中最常见生物膜装置和播散性假丝酵母菌病状态的啮齿动物模型。这些模型系统包含了与抗真菌耐药性研究相关的解剖部位、免疫成分和抗真菌暴露。这些模型可用于分析突变株、评估耐药程度、检查生物膜形成、测试新的抗菌药物,并有助于确定可能与临床失败相关的药物暴露。