Anderson Tania M, Shammami Marcelio A, Taddei Steven M, Finkel Jonathan S
Department of Biology, College of Engineering and Science, University of Detroit Mercy, USA.
UJEMI. 2020;2:1-13. doi: 10.14288/ujemi.v2i.193711. Epub 2021 Jan 20.
With over 1 billion infections and the causative agents showing critical diseases such as pancreatic cancer, the study of pathogenic fungi has never been more critical. In 2017, the United States spent $7.2 billion on fungal diseases. $4.5 billion was allocated to 75,055 hospitalizations, while $2.6 billion went to 8,993,230 outpatient visits. For infections specifically, the cost was $1.4 billion. Currently, there are few classes of antifungals available, and resistance is growing. The identification of genes required for biofilm formation is essential for new antifungal development. This review details how to identify, verify, and characterize defective biofilm formation mutants in . This includes how to run an biofilm formation assay, how to create clean deletions using the modified CRISPR-Cas9 system, how to assay to identify the potential causes of the defect, and how to create complementation strains to confirm the mutant defect.
致病性真菌感染超过10亿例,其病原体引发诸如胰腺癌等严重疾病,因此对致病性真菌的研究从未如此关键。2017年,美国在真菌疾病上花费了72亿美元。其中45亿美元用于75055例住院治疗,26亿美元用于8993230例门诊就诊。仅感染方面的花费就达14亿美元。目前,可用的抗真菌药物种类很少,且耐药性正在增强。确定生物膜形成所需的基因对于新型抗真菌药物的开发至关重要。本综述详细介绍了如何鉴定、验证和表征酿酒酵母中生物膜形成缺陷突变体。这包括如何进行酿酒酵母生物膜形成测定,如何使用改良的CRISPR-Cas9系统创建无痕缺失,如何进行测定以确定缺陷的潜在原因,以及如何创建互补菌株以确认突变体缺陷。