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鉴定近平滑念珠菌凝集素样序列(ALS)基因。

Characterization of the Candida orthopsilosis agglutinin-like sequence (ALS) genes.

机构信息

Department of Biology, University of Pisa, Pisa, Italy.

Roy J. Carver Biotechnology Center, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.

出版信息

PLoS One. 2019 Apr 24;14(4):e0215912. doi: 10.1371/journal.pone.0215912. eCollection 2019.

Abstract

Agglutinin like sequence (Als) cell-wall proteins play a key role in adhesion and virulence of Candida species. Compared to the well-characterized Candida albicans ALS genes, little is known about ALS genes in the Candida parapsilosis species complex. Three incomplete ALS genes were identified in the genome sequence for Candida orthopsilosis strain 90-125 (GenBank assembly ASM31587v1): CORT0C04210 (named CoALS4210), CORT0C04220 (CoALS4220) and CORT0B00800 (CoALS800). To complete the gene sequences, new data were derived from strain 90-125 using Illumina (short-read) and Oxford Nanopore (long-read) methods. Long-read sequencing analysis confirmed the presence of 3 ALS genes in C. orthopsilosis 90-125 and resolved the gaps located in repetitive regions of CoALS800 and CoALS4220. In the new genome assembly (GenBank PQBP00000000), the CoALS4210 sequence was slightly longer than in the original assembly. C. orthopsilosis Als proteins encoded features well-known in C. albicans Als proteins such as a secretory signal peptide, N-terminal domain with a peptide-binding cavity, amyloid-forming region, repeated sequences, and a C-terminal site for glycosylphosphatidylinositol anchor addition that, in yeast, suggest localization of the proteins in the cell wall. CoAls4210 and CoAls800 lacked the classic C. albicans Als tandem repeats, instead featuring short, imperfect repeats with consensus motifs such as SSSEPP and GSGN. Quantitative RT-PCR showed differential regulation of CoALS genes by growth stage in six genetically diverse C. orthopsilosis clinical isolates, which also exhibited length variation in the ALS alleles, and strain-specific gene expression patterns. Overall, long-read DNA sequencing methodology was instrumental in generating an accurate assembly of CoALS genes, thus revealing their unconventional features and first insights into their allelic variability within C. orthopsilosis clinical isolates.

摘要

凝集素样序列(Als)细胞壁蛋白在念珠菌属的粘附和毒力中发挥关键作用。与特征良好的白色念珠菌 ALS 基因相比,对近平滑念珠菌种复合物中的 ALS 基因知之甚少。在近平滑念珠菌菌株 90-125 的基因组序列中鉴定出三个不完整的 ALS 基因:CORT0C04210(命名为 CoALS4210)、CORT0C04220(CoALS4220)和 CORT0B00800(CoALS800)。为了完成基因序列,使用 Illumina(短读)和 Oxford Nanopore(长读)方法从菌株 90-125 中获得新数据。长读测序分析证实了 3 个 ALS 基因在 C. orthopsilosis 90-125 中的存在,并解决了 CoALS800 和 CoALS4220 重复区域中的间隙。在新的基因组组装(GenBank PQBP00000000)中,CoALS4210 序列比原始组装略长。C. orthopsilosis Als 蛋白编码的特征与白色念珠菌 Als 蛋白中的特征非常相似,例如分泌信号肽、具有肽结合腔的 N 端结构域、淀粉样形成区域、重复序列和 C 端用于糖基磷脂酰肌醇锚定添加的位点,在酵母中,这些特征表明蛋白质定位于细胞壁中。CoAls4210 和 CoAls800 缺乏经典的白色念珠菌 Als 串联重复序列,而是具有带有 SSSEPP 和 GSGN 等共识基序的短而不完美的重复序列。定量 RT-PCR 显示六个遗传多样化的 C. orthopsilosis 临床分离株中 CoALS 基因的生长阶段存在差异调节,这些分离株还表现出 ALS 等位基因的长度变异,以及菌株特异性基因表达模式。总体而言,长读 DNA 测序方法对于生成 CoALS 基因的准确组装至关重要,从而揭示了它们的非传统特征,并首次深入了解了 C. orthopsilosis 临床分离株中它们的等位基因变异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37cc/6481836/a7c70b1802fe/pone.0215912.g001.jpg

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