Tara Gallagher, Simon Leemans, Alexander S. Dvornikov, Kumar Perinbam, Joshua Fong, Christina Kim, Joseph Kapcia, Miki Kagawa, Adam Grosvirt-Dramen, Allon I. Hochbaum, Michelle A. Digman, Enrico Gratton, Albert Siryaporn and Katrine Whiteson*,
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引用次数: 0
摘要
了解真实环境中的细菌生理需要非侵入性方法,这是有效治疗感染性疾病的一项具有挑战性但又必要的努力。细菌进化出耐受与感染相关的化学梯度的策略。DIVER (Deep Imaging Via Enhanced Recovery)显微镜可以通过高光学散射对整个样品的自身荧光和荧光寿命进行成像,从而可以研究整个完整生物膜中自然形成的化学梯度。使用DIVER,在低氧条件下,在铜绿假单胞菌生物膜表面和来自粘胶罗氏菌的发酵代谢物存在的低氧条件下,在铜绿假单胞菌感染的气道中共定殖,检测到与低氧下电子循环分子-还原性pyocyanin相关的长荧光寿命信号。这些发现强调了DIVER显微镜和荧光寿命在复杂环境中对细菌生理进行无创研究的实用性,这可以为管理慢性感染提供更有效的策略。
Fluorescence Lifetime Imaging Detects Long-Lifetime Signal Associated with Reduced Pyocyanin at the Surface of Pseudomonas aeruginosa Biofilms and in Cross-Feeding Conditions
Understanding bacterial physiology in real-world environments requires noninvasive approaches and is a challenging yet necessary endeavor to effectively treat infectious disease. Bacteria evolve strategies to tolerate chemical gradients associated with infections. The DIVER (Deep Imaging Via Enhanced Recovery) microscope can image autofluorescence and fluorescence lifetime throughout samples with high optical scattering, enabling the study of naturally formed chemical gradients throughout intact biofilms. Using the DIVER, a long fluorescent lifetime signal associated with reduced pyocyanin, a molecule for electron cycling in low oxygen, was detected in low-oxygen conditions at the surface of Pseudomonas aeruginosa biofilms and in the presence of fermentation metabolites from Rothia mucilaginosa, which cocolonizes infected airways with P. aeruginosa. These findings underscore the utility of the DIVER microscope and fluorescent lifetime for noninvasive studies of bacterial physiology within complex environments, which could inform on more effective strategies for managing chronic infection.
期刊介绍:
ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to:
* Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials.
* Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets.
* Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance.
* Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents.
* Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota.
* Small molecule vaccine adjuvants for infectious disease.
* Viral and bacterial biochemistry and molecular biology.