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棘白菌素耐药的耳念珠菌的种系特异性染色体重排和端粒黏附因子丢失。

Clade-specific chromosomal rearrangements and loss of subtelomeric adhesins in Candida auris.

机构信息

Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

Mycotic Diseases Branch, U.S. Department of Health and Human Services, Atlanta, GA, USA.

出版信息

Genetics. 2021 May 17;218(1). doi: 10.1093/genetics/iyab029.

Abstract

Candida auris is an emerging fungal pathogen of rising concern due to global spread, the ability to cause healthcare-associated outbreaks, and antifungal resistance. Genomic analyses revealed that early contemporaneously detected cases of C. auris were geographically stratified into four major clades. While Clades I, III, and IV are responsible for ongoing outbreaks of invasive and multidrug-resistant infections, Clade II, also termed the East Asian clade, consists primarily of cases of ear infection, is often susceptible to all antifungal drugs, and has not been associated with outbreaks. Here, we generate chromosome-level assemblies of twelve isolates representing the phylogenetic breadth of these four clades and the only isolate described to date from Clade V. This Clade V genome is highly syntenic with those of Clades I, III, and IV, although the sequence is highly divergent from the other clades. Clade II genomes appear highly rearranged, with translocations occurring near GC-poor regions, and large subtelomeric deletions in most chromosomes, resulting in a substantially different karyotype. Rearrangements and deletion lengths vary across Clade II isolates, including two from a single patient, supporting ongoing genome instability. Deleted subtelomeric regions are enriched in Hyr/Iff-like cell-surface proteins, novel candidate cell wall proteins, and an ALS-like adhesin. Cell wall proteins from these families and other drug-related genes show clade-specific signatures of selection in Clades I, III, and IV. Subtelomeric dynamics and the conservation of cell surface proteins in the clades responsible for global outbreaks causing invasive infections suggest an explanation for the different phenotypes observed between clades.

摘要

耳念珠菌是一种新兴的真菌病原体,由于其在全球范围内的传播、引起医疗保健相关暴发的能力以及抗真菌药物耐药性,引起了越来越多的关注。基因组分析表明,早期同时检测到的耳念珠菌病例在地理上分为四个主要分支。虽然分支 I、III 和 IV 负责正在发生的侵袭性和多药耐药感染的暴发,但分支 II,也称为东亚分支,主要由耳部感染病例组成,通常对所有抗真菌药物敏感,并且与暴发无关。在这里,我们生成了代表这四个分支以及迄今为止唯一描述的来自分支 V 的 12 个分离株的染色体水平组装。该分支 V 基因组与分支 I、III 和 IV 的基因组高度同源,尽管序列与其他分支高度不同。分支 II 基因组似乎高度重排,易位发生在 GC 贫乏区域附近,并且大多数染色体上都存在大片段的亚端粒缺失,导致染色体组型发生了很大的变化。分支 II 分离株之间的重排和缺失长度存在差异,包括来自同一患者的两个分离株,支持持续的基因组不稳定性。缺失的亚端粒区域富含 Hyr/Iff 样细胞表面蛋白、新型候选细胞壁蛋白和 ALS 样黏附素。这些家族的细胞壁蛋白和其他与药物相关的基因在分支 I、III 和 IV 中表现出特定的选择特征。亚端粒动力学和导致全球侵袭性感染暴发的分支中细胞表面蛋白的保守性,为观察到的不同表型提供了一个解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec35/8128392/116beb082873/iyab029f1.jpg

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