首页> 外文会议>Conference on multiphoton microscopy in the biomedical sciences >Spatially confined photoinactivation of bacteria: towards novel tools for detailed mechanistic studies
【24h】

Spatially confined photoinactivation of bacteria: towards novel tools for detailed mechanistic studies

机译:在空间上限制细菌的光灭活:寻求用于详细机理研究的新型工具

获取原文

摘要

Antimicrobial resistance is a serious global threat fueling an accelerated field of research aimed at developing novel antimicrobial therapies. A particular challenge is the treatment of microbial biofilms formed upon bacterial growth and often associated with chronic infections. Biofilms comprise bacteria that have adhered to a surface and formed 3D micro-colonies, and demonstrate significantly increased antimicrobial resistance compared to the planktonic counterpart. A challenge in developing novel strategies for fighting these chronic infections is a lack of mechanistic understanding of what primarily contributes to enhanced drug resistance. Tools for noninvasive study of live biofilms are necessary to begin to understand these mechanisms on both a single cell and 3D level. Herein, a method by which multiphoton microscopy is implemented to study a biofilm model of Staphylococcus epidermidis to noninvasively visualize and measure penetration of compounds in 3D biofilm structure and two photon excitation was exploited for spatially confined photoinactivation and microscopy optimized for evaluation of microbiological viability at a microscopic level. Future studies are aimed at future development of the proposed techniques for detailed studies of, e.g., quorum sensing and mechanisms contributing to antimicrobial resistance.
机译:抗菌素耐药性是严重的全球威胁,推动了旨在开发新型抗菌素疗法的加速研究领域。一个特殊的挑战是如何处理细菌生长时形成的微生物生物膜,通常与慢性感染有关。生物膜包含粘附在表面并形成3D微菌落的细菌,与浮游生物相比,细菌具有明显的抗微生物性。在开发对抗这些慢性感染的新颖策略中的挑战是,缺乏对主要是什么导致耐药性增强的机制的机械理解。要开始在单个细胞和3D水平上了解这些机制,必须使用非侵入性研究活生物膜的工具。本文中,采用多光子显微镜研究表皮葡萄球菌生物膜模型以无创地观察和测量化合物在3D生物膜结构中的渗透性的方法,并利用两个光子激发进行空间受限的光灭活,并优化了显微镜以评估微生物的生存力。微观层面。未来的研究旨在对所提出的技术进行进一步的发展,以便对例如群体感应和有助于抗药性的机制进行详细研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号