Almaarik Basmah M, Ali Rizwan, Cooper Paul R, Milward Michael R, Hirschfeld Josefine
Clinical Laboratory Science Department (CLS), College of Applied Medical Sciences (CAMS), King Saud University (KSU), Riyadh, Saudi Arabia.
Periodontal Research Group, Department of Dentistry, School of Health Sciences, College of Medicine and Health, University of Birmingham, Edgbaston, UK.
J Oral Microbiol. 2025 Jan 23;17(1):2453986. doi: 10.1080/20002297.2025.2453986. eCollection 2025.
is a commensal bacterium and an early biofilm coloniser found in the human oral cavity. One of the biofilm matrix constituents is bacterial extracellular DNA (eDNA). Neutrophils are innate immune cells that respond to biofilms, employing antimicrobial mechanisms such as neutrophil extracellular trap (NET) and reactive oxygen species (ROS) release. Here, bidirectional effects of neutrophils on biofilms were investigated.
Isolated neutrophils were introduced to biofilms at different stages of biofilm development. Biofilm quantity was assessed by crystal violet technique, confocal microscopy and CFU enumeration. Surface adhesion during shear stress was quantified by spectrophotometry. Bacterial and neutrophil extracellular DNA within biofilms and ROS production were analysed using fluorescence and luminescence assays, and neutrophil-eDNA interactions were investigated by flow cytometry and fluorescence microscopy.
Neutrophils decreased biofilm quantity transiently and reduced eDNA but did not affect biofilm surface adhesion. Unexpectedly, CFUs were increased by neutrophils. Bacterial DNA was found to co-localise with neutrophil membranes. Neutrophils produced elevated total and intracellular ROS, however, no NETs in response to biofilms.
Neutrophils are not excessively activated by biofilms but are able to reduce biofilm quantity in the short-term, possibly through interfering with eDNA.
[细菌名称]是一种共生菌,也是在人类口腔中发现的早期生物膜定植菌。生物膜基质成分之一是细菌细胞外DNA(eDNA)。中性粒细胞是对生物膜产生反应的先天性免疫细胞,采用中性粒细胞胞外诱捕网(NET)和活性氧(ROS)释放等抗菌机制。在此,研究了中性粒细胞对[细菌名称]生物膜的双向作用。
将分离的中性粒细胞引入生物膜发育的不同阶段。通过结晶紫技术、共聚焦显微镜和菌落形成单位(CFU)计数评估生物膜数量。通过分光光度法定量剪切应力下的表面粘附。使用荧光和发光测定法分析生物膜内的细菌和中性粒细胞细胞外DNA以及ROS产生,并通过流式细胞术和荧光显微镜研究中性粒细胞与eDNA的相互作用。
中性粒细胞短暂降低了生物膜数量并减少了eDNA,但不影响生物膜表面粘附。出乎意料的是,中性粒细胞增加了CFU。发现细菌DNA与中性粒细胞膜共定位。中性粒细胞产生的总ROS和细胞内ROS升高,然而,对生物膜无NETs反应。
中性粒细胞不会被[细菌名称]生物膜过度激活,但能够在短期内减少生物膜数量,可能是通过干扰eDNA实现的。