Furukawa Takanori, van Rhijn Norman, Chown Harry, Rhodes Johanna, Alfuraiji Narjes, Fortune-Grant Rachael, Bignell Elaine, Fisher Matthew C, Bromley Michael
Manchester Fungal Infection Group, Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, CTF Building, 46 Grafton Street, Manchester M13 9NT, UK; Lydia Becker Institute of Immunology and Inflammation, Manchester Collaborative Centre for Inflammation Research, Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Fungal Genet Biol. 2022 Jul;161:103702. doi: 10.1016/j.fgb.2022.103702. Epub 2022 May 13.
Aspergillus fumigatus is the most important airborne fungal pathogen and allergen of humans causing high morbidity and mortality worldwide. The factors that govern pathogenicity of this organism are multi-factorial and are poorly understood. Molecular tools to dissect the mechanisms of pathogenicity in A. fumigatus have improved significantly over the last 20 years however many procedures have not been standardised for A. fumigatus. Here, we present a new genomic safe-haven locus at the site of an inactivated transposon, named SH-aft4, which can be used to insert DNA sequences in the genome of this fungus without impacting its phenotype. We show that we are able to effectively express a transgene construct from the SH-aft4 and that natural regulation of promoter function is conserved at this site. Furthermore, the SH-aft4 locus is highly conserved in the genome of a wide range of clinical and environmental isolates including the isolates commonly used by many laboratories CEA10, Af293 and ATCC46645, allowing a wide range of isolates to be manipulated. Our results show that the aft4 locus can serve as a site for integration of a wide range of genetic constructs to aid functional genomics studies of this important human fungal pathogen.
烟曲霉是人类最重要的空气传播真菌病原体和过敏原,在全球范围内导致高发病率和死亡率。决定这种生物体致病性的因素是多方面的,目前了解甚少。在过去20年里,用于剖析烟曲霉致病性机制的分子工具已有显著改进,然而许多程序尚未针对烟曲霉进行标准化。在此,我们在一个失活转座子位点上提出了一个新的基因组安全位点,命名为SH-aft4,它可用于在该真菌基因组中插入DNA序列而不影响其表型。我们表明能够从SH-aft4有效表达转基因构建体,并且启动子功能的自然调控在该位点得以保留。此外,SH-aft4位点在广泛的临床和环境分离株基因组中高度保守,包括许多实验室常用的分离株CEA10、Af293和ATCC46645,从而使多种分离株能够被操作。我们的结果表明,aft4位点可作为整合多种遗传构建体的位点,以辅助对这种重要的人类真菌病原体进行功能基因组学研究。