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小泛基因组反映出种内总体多样性较低。

Small pangenome of reflects overall low intraspecific diversity.

作者信息

Ryan Adam P, Bergin Sean, Scully Jillian, Zuniga-Soto Evelyn, Hession Conor, Barber Amelia E, Gómez-Molero Emilia, Bader Oliver, Morio Florent, Zhai Bing, Wolfe Kenneth H, Butler Geraldine

机构信息

School of Biomolecular and Biomedical Sciences, Conway Institute, University College Dublin, Dublin, Ireland.

Junior Research Group Fungal Informatics, Friedrich Schiller University, Jena, Germany.

出版信息

mBio. 2025 Aug 25:e0132025. doi: 10.1128/mbio.01320-25.

Abstract

is an opportunistic yeast pathogen that can cause life-threatening infections in immunocompromised humans. Whole-genome sequencing studies of the species have demonstrated remarkably low diversity, with strains typically differing by about 1.5 single nucleotide polymorphisms (SNPs) per 10 kb. However, SNP calling alone does not capture the full extent of genetic variation. Here, we define the pangenome of 372 . isolates to determine variation in gene content. The pangenome consists of 5,859 genes, of which 48 are not found in the genome of the reference strain. This includes 5,791 core genes (present in ≥99.5% of isolates). Four genes, including the allantoin permease gene , were present in all isolates but were truncated in some strains. The truncated was classified as a pseudogene in the reference strain CDC317. CRISPR-Cas9 gene editing showed that removing the early stop codon (producing the full-length Dal4 protein) is associated with improved use of allantoin as a sole nitrogen source. We find that the accessory genome of consists of 68 homologous clusters. This includes 38 previously annotated genes, 27 novel paralogs of previously annotated genes, and 3 uncharacterized open reading frames. Approximately one-third of the accessory genome (24/68 genes) is associated with gene fusions between tandem genes in the major facilitator superfamily. Additionally, we identified two highly divergent strains and found that, despite their increased phylogenetic distance (~30 SNPs per 10 kb), both strains have similar gene content to the other 372.IMPORTANCE is a human fungal pathogen listed in the high-priority group by the World Health Organization. It is an increasing cause of hospital-acquired and drug-resistant infections. Here, we studied the genetic diversity of 372 . isolates, the largest genomic surveillance of this species to date. We show that there is relatively little genetic variation. However, we identified two more distantly related isolates from Germany, suggesting that even more sampling may yield more diversity. We find that the pangenome (the cumulative gene content of all isolates) is surprisingly small, compared to other fungal species. Many of the non-core genes are involved in transport. We also find that variations in gene content are associated with nitrogen metabolism, which may contribute to the virulence characteristics of this species.

摘要

是一种机会性酵母病原体,可在免疫功能低下的人类中引起危及生命的感染。对该物种的全基因组测序研究表明其多样性极低,菌株之间通常每10 kb约有1.5个单核苷酸多态性(SNP)差异。然而,仅SNP检测并不能完全捕捉到遗传变异的全貌。在这里,我们定义了372株分离株的泛基因组,以确定基因含量的变异。泛基因组由5859个基因组成,其中48个在参考菌株的基因组中未发现。这包括5791个核心基因(在≥99.5%的分离株中存在)。四个基因,包括尿囊素通透酶基因,在所有分离株中都存在,但在一些菌株中被截断。在参考菌株CDC317中,截断的基因被归类为假基因。CRISPR-Cas9基因编辑表明,去除早期终止密码子(产生全长Dal4蛋白)与以尿囊素作为唯一氮源的利用改善有关。我们发现的附属基因组由68个同源簇组成。这包括38个先前注释的基因、27个先前注释基因的新旁系同源物和3个未表征的开放阅读框。附属基因组中约三分之一(24/68个基因)与主要转运体超家族中串联基因之间的基因融合有关。此外,我们鉴定出两个高度分化的菌株,发现尽管它们的系统发育距离增加(每10 kb约30个SNP),但这两个菌株与其他372个菌株具有相似的基因含量。重要性是世界卫生组织列入高优先级组的人类真菌病原体。它是医院获得性感染和耐药感染日益增加的原因。在这里,我们研究了372株分离株的遗传多样性,这是迄今为止对该物种最大规模的基因组监测。我们表明遗传变异相对较少。然而,我们从德国鉴定出另外两个亲缘关系较远的分离株,这表明更多的样本采集可能会产生更多的多样性。我们发现,与其他真菌物种相比,泛基因组(所有分离株的累积基因含量)出奇地小。许多非核心基因参与转运。我们还发现基因含量的变异与氮代谢有关,这可能有助于该物种的毒力特征。

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