Hendricks A L, More K R, Devaraj A, Buzzo J R, Robledo-Avila F H, Partida-Sanchez S, Bakaletz L O, Goodman S D
Center for Microbe and Immunity Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Department of Pediatrics, College of Medicine, Ohio State University, Columbus, OH, USA.
NPJ Biofilms Microbiomes. 2025 Apr 15;11(1):58. doi: 10.1038/s41522-025-00691-0.
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.
细胞外DNA(eDNA)对于细菌生物膜的结构完整性至关重要,因为随着生物膜成熟,它们会从B-DNA转变为Z-DNA。这种向Z-DNA的转变增加了生物膜的刚性,并阻止包括核酸酶在内的典型B-DNA结合蛋白的结合。对抗细菌感染的主要防御机制之一是中性粒细胞胞外陷阱(NETs),其中中性粒细胞释放自身的eDNA来捕获和杀死细菌。在这里,我们表明H-NS是一种在生物膜形成过程中也会释放的细菌类核相关蛋白(NAP),它能够使NETs失活。事实上,当暴露于人类来源的中性粒细胞时,H-NS会阻止NETs的形成,并导致先前形成的NETs中的NET eDNA回缩。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物。本文讨论了生物膜释放H-NS和NET失活的模型。