Le Mauff François, Sheppard Donald C
Infectious Disease and Immunity in Global Health Program, Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
McGill Interdisciplinary Initiative in Infection and Immunity, Montreal, Quebec, Canada.
Cell Surf. 2023 Jan 7;9:100095. doi: 10.1016/j.tcsw.2023.100095. eCollection 2023 Dec.
Half a century after their discovery, polymers of -acetylgalactosamine produced by the Aspergilli have garnered new interest as mediators of fungal virulence. Recent work has focused on the secreted and cell wall-associated heteropolymer, galactosaminogalactan (GAG). This polymer, composed of galactose (Gal) and partially deacetylated -acetylgalactosamine (GalNAc), plays a role in a variety of pathogenic processes including biofilm formation, immune modulation and evasion, and resistance to antifungals. Given its many potential contributions to fungal pathogenesis, GAG is a promising therapeutic target for novel antifungal strategies. As such, several studies have sought to elucidate the biosynthetic pathways required for GAG production and secretion. Herein we review the progress made in the understanding of the molecular mechanisms underlying GAG synthesis and identify several gaps in our understanding of this process.
在被发现半个世纪后,曲霉属真菌产生的β-乙酰半乳糖胺聚合物作为真菌毒力的介质重新引起了人们的关注。最近的研究工作集中在分泌型和细胞壁相关的杂聚物——半乳糖胺半乳聚糖(GAG)上。这种由半乳糖(Gal)和部分脱乙酰化的β-乙酰半乳糖胺(GalNAc)组成的聚合物,在包括生物膜形成、免疫调节与逃避以及抗真菌耐药性等多种致病过程中发挥作用。鉴于其对真菌致病机制的诸多潜在影响,GAG是新型抗真菌策略中一个有前景的治疗靶点。因此,多项研究试图阐明GAG产生和分泌所需的生物合成途径。在此,我们综述了在理解GAG合成的分子机制方面所取得的进展,并指出我们对这一过程理解中存在的若干空白。