Zhang Qingsong, Lu Menghan, Ou Richang, Lin Hong, Xuan Guanhua, Wang Xiudan, Xu Xiaofeng, Zhang Weiwei, Wang Guoqing
MOE Key Laboratory of Evolution & Marine Biodiversity and Institute of Evolution & Marine Biodiversity, Ocean University of China, 5 Yushan Road, Qingdao, 266003, China.
Laboratory for Marine Drugs and Bioproducts, Qingdao Marine Science and Technology Center, Qingdao, 266237, China.
Adv Sci (Weinh). 2025 Apr;12(13):e2415169. doi: 10.1002/advs.202415169. Epub 2025 Feb 14.
The complex and dynamic nature of aquatic ecosystems, particularly in marine environments, makes managing wound infections a significant challenge for individuals engaged in underwater activities and for aquatic organisms. Although antibiotics have played a critical role in safeguarding humans and aquatic health, their risk of drug resistance and environmental impact present substantial obstacles to long-term sustainability. Using fin rot disease in turbot (Scophthalmus maximus) caused by infection of Vibrio anguillarum (V. anguillarum) as a model, a new strategy is presented that employs a carbon dot (CD)-based antisense oligonucleotide (ASO) delivery system, combined with an adhesive hydrogel, to achieve targeted gene silencing of V. anguillarum for underwater healing. The CDs that cause enhanced cytoplasmic membrane permeability, efficiently deliver ASOs into V. anguillarum without requiring additional equipment or chemical facilitators. The specific design of the ASO sequence enables targeted silencing of empA, achieving efficiency as high as 71.2%. An adhesive hydrogel is applied to boost the local concentration of ASO/CDs at wound sites in seawater, effectively sealing the infected area and preventing fin rot disease in turbot. This study pioneer targeted bacterial gene regulation using CD-based delivery integrated with a hydrogel bandage, offering practical solutions for managing underwater bacterial diseases.
水生生态系统的复杂性和动态性,尤其是在海洋环境中,使得对于从事水下活动的个人和水生生物来说,处理伤口感染成为一项重大挑战。尽管抗生素在保护人类和水生生物健康方面发挥了关键作用,但其耐药性风险和环境影响对长期可持续性构成了重大障碍。以由鳗弧菌(Vibrio anguillarum,V. anguillarum)感染引起的大菱鲆(Scophthalmus maximus)鳍腐病为模型,提出了一种新策略,该策略采用基于碳点(CD)的反义寡核苷酸(ASO)递送系统,并结合粘性水凝胶,以实现对鳗弧菌的靶向基因沉默,用于水下伤口愈合。能够增强细胞质膜通透性的碳点无需额外设备或化学促进剂就能有效地将反义寡核苷酸递送至鳗弧菌中。反义寡核苷酸序列的特定设计能够实现对empA的靶向沉默,效率高达71.2%。应用粘性水凝胶可提高海水伤口部位反义寡核苷酸/碳点的局部浓度,有效封闭感染区域并预防大菱鲆鳍腐病。本研究率先利用基于碳点的递送与水凝胶绷带相结合实现了靶向细菌基因调控,为处理水下细菌疾病提供了切实可行的解决方案。