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本文引用的文献

1
Genomic Diversity across Candida auris Clinical Isolates Shapes Rapid Development of Antifungal Resistance and .Candida auris 临床分离株的基因组多样性导致抗真菌药物耐药性的快速发展。
mBio. 2022 Aug 30;13(4):e0084222. doi: 10.1128/mbio.00842-22. Epub 2022 Jul 5.
2
Evidence for the agricultural origin of resistance to multiple antimicrobials in Aspergillus fumigatus, a fungal pathogen of humans.证据表明,人类病原体烟曲霉对多种抗生素的耐药性起源于农业。
G3 (Bethesda). 2022 Feb 4;12(2). doi: 10.1093/g3journal/jkab427.
3
Forward and reverse genetic dissection of morphogenesis identifies filament-competent Candida auris strains.正向和反向遗传学解析形态发生,鉴定出有丝分裂能力的耳念珠菌菌株。
Nat Commun. 2021 Dec 10;12(1):7197. doi: 10.1038/s41467-021-27545-5.
4
Delineation of the Direct Contribution of Candida auris Mutations to Clinical Triazole Resistance.明确耳念珠菌突变对临床三唑类药物耐药性的直接贡献。
Microbiol Spectr. 2021 Dec 22;9(3):e0158521. doi: 10.1128/Spectrum.01585-21. Epub 2021 Dec 8.
5
Expandable and reversible copy number amplification drives rapid adaptation to antifungal drugs.可扩展和可逆的拷贝数扩增驱动快速适应抗真菌药物。
Elife. 2020 Jul 20;9:e58349. doi: 10.7554/eLife.58349.
6
Mutations in : a Novel Genetic Determinant of Clinical Fluconazole Resistance in Candida auris.C. auris 中 :一种新型的氟康唑临床耐药遗传决定因素的突变。
mBio. 2020 May 12;11(3):e00365-20. doi: 10.1128/mBio.00365-20.
7
A Zinc Cluster Transcription Factor Contributes to the Intrinsic Fluconazole Resistance of Candida auris.锌簇转录因子有助于耳念珠菌的固有氟康唑耐药性。
mSphere. 2020 Apr 22;5(2):e00279-20. doi: 10.1128/mSphere.00279-20.
8
Climate change brings the specter of new infectious diseases.气候变化带来了新传染病的幽灵。
J Clin Invest. 2020 Feb 3;130(2):553-555. doi: 10.1172/JCI135003.
9
On the Emergence of Candida auris: Climate Change, Azoles, Swamps, and Birds.关于耳念珠菌的出现:气候变化、唑类药物、沼泽和鸟类。
mBio. 2019 Jul 23;10(4):e01397-19. doi: 10.1128/mBio.01397-19.
10
Candida auris and multidrug resistance: Defining the new normal.耳念珠菌和多重耐药性:定义新常态。
Fungal Genet Biol. 2019 Oct;131:103243. doi: 10.1016/j.fgb.2019.103243. Epub 2019 Jun 20.

新兴人类真菌病原体的耐药性和可进化性。

Drug Resistance and Evolvability in an Emerging Human Fungal Pathogen.

机构信息

Stowers Institute for Medical Researchgrid.250820.d, Kansas City, Missouri, USA.

出版信息

mBio. 2022 Oct 26;13(5):e0187622. doi: 10.1128/mbio.01876-22. Epub 2022 Aug 18.

DOI:10.1128/mbio.01876-22
PMID:35980032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9600676/
Abstract

Over the past decade, Candida auris has emerged as a highly transmissible human fungal pathogen. Because of its ability to transmit between patients in hospitals and its ability to rapidly develop drug resistance, C. auris presents unique challenges. However, at a genetic and genomic level we still understand relatively little about how drug resistance develops in this pathogen. Burrack et al. use experimental evolution and whole-genome sequencing to identify mutations correlated with fluconazole resistance in C. auris. They identify interesting genomic features, including highly plastic subtelomeric regions and whole chromosomal and segmental aneuploidies. Excitingly, they also identify the first example of a hypermutator strain in C. auris. In comparison with the model human fungal pathogen Candida albicans, C. auris is more likely to undergo mutation and less likely to undergo copy number variation in response to drug selection, which may be linked to differences in base ploidy level.

摘要

在过去的十年中,耳念珠菌已成为一种具有高度传染性的人类真菌病原体。由于其能够在医院患者之间传播,并且能够迅速产生耐药性,因此耳念珠菌带来了独特的挑战。然而,在遗传和基因组水平上,我们对这种病原体的耐药性如何发展仍然知之甚少。Burrack 等人使用实验进化和全基因组测序来鉴定与耳念珠菌中氟康唑耐药性相关的突变。他们发现了有趣的基因组特征,包括高度可塑性的端粒外区域以及整条染色体和片段的非整倍性。令人兴奋的是,他们还鉴定出了耳念珠菌中首例超突变株。与模型人类真菌病原体白念珠菌相比,耳念珠菌更容易发生突变,而在药物选择下发生拷贝数变异的可能性较小,这可能与碱基倍性水平的差异有关。