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首页> 外文期刊>MBio >Core N-Glycan Structures Are Critical for the Pathogenicity of Cryptococcus neoformans by Modulating Host Cell Death
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Core N-Glycan Structures Are Critical for the Pathogenicity of Cryptococcus neoformans by Modulating Host Cell Death

机译:核心<斜斜体> n -glycan结构对于<命名含量含量型=“属型”> Cryptococcus neoformans 的致病性至关重要

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摘要

Cryptococcus neoformans is a human-pathogenic fungal pathogen that causes life-threatening meningoencephalitis in immunocompromised individuals. To investigate the roles of N -glycan core structure in cryptococcal pathogenicity, we constructed mutant strains of C. neoformans with defects in the assembly of lipid-linked N -glycans in the luminal side of the endoplasmic reticulum (ER). Deletion of ALG3 ( alg3 Δ), which encodes dolichyl-phosphate-mannose (Dol-P-Man)-dependent α-1,3-mannosyltransferase, resulted in the production of truncated neutral N -glycans carrying five mannose residues as a major species. Despite moderate or nondetectable defects in virulence-associated phenotypes in vitro , the alg3 Δ mutant was avirulent in a mouse model of systemic cryptococcosis. Notably, the mutant did not show defects in early stages of host cell interaction during infection, including attachment to lung epithelial cells, opsonic/nonopsonic phagocytosis, and manipulation of phagosome acidification. However, the ability to drive macrophage cell death was greatly decreased in this mutant, without loss of cell wall remodeling capacity. Furthermore, deletion of ALG9 and ALG12 , encoding Dol-P-Man-dependent α-1,2-mannosyltransferases and α-1,6-mannosyltransferases, generating truncated core N -glycans with six and seven mannose residues, respectively, also displayed remarkably reduced macrophage cell death and in vivo virulence. However, secretion levels of interleukin-1β (IL-1β) were not reduced in the bone marrow-derived dendritic cells obtained from Asc - and Gsdmd -deficient mice infected with the alg3 Δ mutant strain, excluding the possibility that pyroptosis is a main host cell death pathway dependent on intact core N -glycans. Our results demonstrated N -glycan structures as a critical feature in modulating death of host cells, which is exploited by as a strategy for host cell escape for dissemination of C. neoformans .
机译:Cryptococcus Neoformans是一种人致病性真菌病原体,导致免疫功能性危及危及生命的脑膜炎。为了探讨N-Glycan核心结构在隐球菌致病性中的作用,我们构建了在内质网(ER)的腔侧含有脂质连接的N-Glycans组装中的突变体菌株C. neoformans的缺陷。缺失ALG3(ALG3δ),它们编码氯化物 - 磷酸甘露糖(DOL-P-MAN) - 依赖性α-1,3-甘露糖基氧基转移酶,导致截断中性N-Glycans的生产作为主要物种作为主要物种的5个甘露糖残基。尽管在体外毒力相关表型中的中等或不可缩小的缺陷,但ALG3δ突变体是在全身性密集菌病的小鼠模型中的无毒。值得注意的是,突变体未显示在感染期间宿主细胞相互作用的早期阶段的缺陷,包括对肺上皮细胞,Opsonic / Nonocsonic吞噬作用的附着和吞噬酸化的操纵。然而,在该突变体中促进巨噬细胞死亡的能力大大降低,而不会损失细胞壁重塑能力。此外,缺失ALG9和ALG12,编码DOL-P人依赖性α-1,2-甘露糖基酯酶和α-1,6-甘露糖基转移酶,分别产生具有六个和七个甘露糖残基的截短的核心N-甘露糖酶,也显着显示减少巨噬细胞死亡和体内毒力。然而,从ACC 3Δ突变菌株感染的ASC-和GSDMD -DEFICES小鼠获得的骨髓衍生的树突细胞中不降低白细胞介素-1β(IL-1β)的分泌水平,不包括糊化酶是主要宿主的可能性依赖于完整的核心N-glycans的细胞死亡途径。我们的结果证明了N-Glycan结构作为调节宿主细胞死亡的关键特征,这被作为宿主细胞逃逸的策略用于传播C. Neoformans的策略。

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