The Wor2 phenotypic switching regulator controls biofilm formation in Candida auris.

IF 11.4 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Weihong Liang, Shuyun Guan, Jian Bing, Han Du, Qiushi Zheng, Li Tao, Bing Li, Guanghua Huang, Haiqing Chu
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Abstract

The emerging fungal pathogen Candida auris is a serious global public health threat due to its ability to persist in healthcare environments and on human skin. Here, we report a prevalent cluster of clinical C. auris strains with enhanced biofilm formation, a contributor to environmental and skin persistence. Genomic analyses show that the clinical isolates with enhanced biofilm formation ability carry a loss-of-function mutation in the WOR2 locus, which encodes a white-opaque switching regulator in Candida species. Analysis of 13,314 published genomes revealed that 3104 strains (23.3%) harbor nonsense or frameshift mutations in WOR2, indicating frequent clinical occurrence. Deletion of WOR2 in a clinical strain markedly increased biofilm formation, whereas reintroduction of an intact WOR2 significantly attenuated biofilm development. Further analyses show that Wor2 inactivation upregulates GFC1, ALS4, and multiple biofilm-associated genes. Together, these findings reveal a key regulatory mechanism underlying biofilm development, environmental persistence, and transmission of C. auris.

Wor2表型开关调节因子控制耳念珠菌生物膜的形成。
新出现的真菌病原体耳念珠菌是一种严重的全球公共卫生威胁,因为它能够在卫生保健环境和人类皮肤上持续存在。在这里,我们报告了一个普遍的临床耳念珠菌群,其生物膜形成增强,这是环境和皮肤持久性的一个贡献者。基因组分析表明,具有增强生物膜形成能力的临床分离株携带WOR2位点的功能缺失突变,该位点编码念珠菌种中的白色不透明开关调节因子。对13,314个已发表基因组的分析显示,3104株(23.3%)在WOR2中存在无义或移码突变,表明临床频繁发生。临床菌株中WOR2的缺失显著增加了生物膜的形成,而重新引入完整的WOR2则显著减弱了生物膜的形成。进一步分析表明,Wor2失活上调GFC1、ALS4和多种生物膜相关基因。总之,这些发现揭示了金黄色葡萄球菌生物膜发育、环境持久性和传播的关键调控机制。
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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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