细菌生物膜衍生的H-NS蛋白作为对中性粒细胞胞外陷阱(NETs)的防御。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
A L Hendricks, K R More, A Devaraj, J R Buzzo, F H Robledo-Avila, S Partida-Sanchez, L O Bakaletz, S D Goodman
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引用次数: 0

摘要

细胞外DNA (eDNA)对细菌生物膜的结构完整性至关重要,因为它们随着生物膜的成熟而从B-DNA转化为Z-DNA。这种向Z-DNA的转变增加了生物膜的刚性,并阻止了典型的b - dna结合蛋白(包括核酸酶)的结合。抵御细菌感染的主要防御之一是中性粒细胞胞外陷阱(NETs),其中中性粒细胞释放自己的eDNA来捕获和杀死细菌。在这里,我们发现H-NS,一种细菌类核相关蛋白(NAP),也在生物膜发育过程中被释放,能够使NETs失能。事实上,当暴露于人源性中性粒细胞时,H-NS阻止了NETs的形成,并导致先前形成的NETs中的NET eDNA缩回。暴露于H-NS的NETs也失去了杀死自由生活细菌的能力,这使得H-NS成为控制与net相关的人类疾病的有吸引力的治疗候选者。讨论了H-NS从生物膜中释放和NET失能的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bacterial biofilm-derived H-NS protein acts as a defense against Neutrophil Extracellular Traps (NETs).

Extracellular DNA (eDNA) is crucial for the structural integrity of bacterial biofilms as they undergo transformation from B-DNA to Z-DNA as the biofilm matures. This transition to Z-DNA increases biofilm rigidity and prevents binding by canonical B-DNA-binding proteins, including nucleases. One of the primary defenses against bacterial infections are Neutrophil Extracellular Traps (NETs), wherein neutrophils release their own eDNA to trap and kill bacteria. Here we show that H-NS, a bacterial nucleoid associated protein (NAP) that is also released during biofilm development, is able to incapacitate NETs. Indeed, when exposed to human derived neutrophils, H-NS prevented the formation of NETs and lead to NET eDNA retraction in previously formed NETs. NETs that were exposed to H-NS also lost their ability to kill free-living bacteria which made H-NS an attractive therapeutic candidate for the control of NET-related human diseases. A model of H-NS release from biofilms and NET incapacitation is discussed.

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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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