Wang Xiumin, Teng Da, Mao Ruoyu, Yang Na, Hao Ya, Wang Jianhua
Key Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, China.
Gene Engineering Laboratory, Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing, China.
Antimicrob Agents Chemother. 2016 Dec 27;61(1). doi: 10.1128/AAC.01056-16. Print 2017 Jan.
A marine arenicin-3 derivative, N4, displayed potent antibacterial activity against Gram-negative bacteria, but its antibacterial mode of action remains elusive. The mechanism of action of N4 against pathogenic Escherichia coli was first researched by combined cytological and transcriptomic techniques in this study. The N4 peptide permeabilized the outer membrane within 1 min, disrupted the plasma membrane after 0.5 h, and localized in the cytoplasm within 5 min. Gel retardation and circular dichroism (CD) spectrum analyses demonstrated that N4 bound specifically to DNA and disrupted the DNA conformation from the B type to the C type. N4 inhibited 21.1% of the DNA and 20.6% of the RNA synthesis within 15 min. Several hallmarks of apoptosis-like cell death were exhibited by N4-induced E. coli, such as cell cycle arrest in the replication (R) and division(D) phases, reactive oxygen species production, depolarization of the plasma membrane potential, and chromatin condensation within 0.5 h. Deformed cell morphology, disappearance of the plasma membrane, leakage of the contents, and ghost cell formation were demonstrated by transmission electron microscopy, and nearly 100% of the bacteria were killed by N4. A total of 428 to 663 differentially expressed genes are involved in the response to N4, which are associated mainly with membrane biogenesis (53.9% to 56.7%) and DNA binding (13.3% to 14.9%). N4-protected mice that were lethally challenged with lipopolysaccharide (LPS) exhibited reduced levels of interleukin-6 (IL-6), IL-1β, and tumor necrosis factor alpha (TNF-α) in serum and protected the lungs from LPS-induced injury. These data facilitate an enhanced understanding of the mechanisms of marine antimicrobial peptides (AMPs) against Gram-negative bacteria and provide guidelines in developing and applying novel multitarget AMPs in the field of unlimited marine resources as therapeutics.
一种海洋沙蚕毒素 -3 衍生物 N4 对革兰氏阴性菌显示出强大的抗菌活性,但其抗菌作用模式仍不清楚。本研究首次通过细胞学和转录组学技术相结合的方法研究了 N4 对致病性大肠杆菌的作用机制。N4 肽在 1 分钟内使外膜通透,0.5 小时后破坏质膜,并在 5 分钟内定位到细胞质中。凝胶阻滞和圆二色(CD)光谱分析表明,N4 特异性结合 DNA 并将 DNA 构象从 B 型转变为 C 型。N4 在 15 分钟内抑制了 21.1%的 DNA 和 20.6%的 RNA 合成。N4 诱导的大肠杆菌表现出几种凋亡样细胞死亡的特征,如在复制(R)和分裂(D)阶段的细胞周期停滞、活性氧产生、质膜电位去极化以及 0.5 小时内的染色质凝聚。透射电子显微镜显示细胞形态变形、质膜消失、内容物泄漏和空壳细胞形成,并且近 100%的细菌被 N4 杀死。共有 428 至 663 个差异表达基因参与对 N4 的反应,这些基因主要与膜生物合成(53.9%至 56.7%)和 DNA 结合(13.3%至 14.9%)相关。用脂多糖(LPS)进行致死性攻击的 N4 保护小鼠血清中白细胞介素 -6(IL -6)、IL -1β 和肿瘤坏死因子α(TNF -α)水平降低,并保护肺部免受 LPS 诱导的损伤。这些数据有助于加深对海洋抗菌肽(AMPs)抗革兰氏阴性菌机制的理解,并为在无限海洋资源领域开发和应用新型多靶点 AMPs 作为治疗药物提供指导。