Center for Microbial Pathogenesis, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH 43205, USA.
Department of Orthopedics, Ohio State University, Columbus, OH 43210, USA.
Cell. 2021 Nov 11;184(23):5740-5758.e17. doi: 10.1016/j.cell.2021.10.010. Epub 2021 Nov 3.
Biofilms are community architectures adopted by bacteria inclusive of a self-formed extracellular matrix that protects resident bacteria from diverse environmental stresses and, in many species, incorporates extracellular DNA (eDNA) and DNABII proteins for structural integrity throughout biofilm development. Here, we present evidence that this eDNA-based architecture relies on the rare Z-form. Z-form DNA accumulates as biofilms mature and, through stabilization by the DNABII proteins, confers structural integrity to the biofilm matrix. Indeed, substances known to drive B-DNA into Z-DNA promoted biofilm formation whereas those that drive Z-DNA into B-DNA disrupted extant biofilms. Importantly, we demonstrated that the universal bacterial DNABII family of proteins stabilizes both bacterial- and host-eDNA in the Z-form in situ. A model is proposed that incorporates the role of Z-DNA in biofilm pathogenesis, innate immune response, and immune evasion.
生物膜是细菌采用的群落结构,包括自我形成的细胞外基质,保护驻留细菌免受各种环境压力的影响,并且在许多物种中,包含细胞外 DNA(eDNA)和 DNABII 蛋白,以在整个生物膜发育过程中保持结构完整性。在这里,我们提供的证据表明,这种基于 eDNA 的结构依赖于罕见的 Z 型。Z 型 DNA 在生物膜成熟时积累,并通过 DNABII 蛋白的稳定作用赋予生物膜基质结构完整性。实际上,已知可将 B-DNA 驱动为 Z-DNA 的物质促进生物膜形成,而将 Z-DNA 驱动为 B-DNA 的物质则破坏现有的生物膜。重要的是,我们证明了普遍存在的细菌 DNABII 蛋白家族可稳定原位细菌和宿主 eDNA 的 Z 型。提出了一个模型,该模型将 Z-DNA 在生物膜发病机制、先天免疫反应和免疫逃避中的作用结合在一起。