Gregory S Miller1,2, Ryan M Parente1, Swadeshmukul Santra1,2,3,4, Andre J Gesquiere5,6,7,8. 1. NanoScience Technology Center, University of Central Florida, Orlando, FL, 32826, USA. 2. Department of Chemistry, University of Central Florida, Orlando, FL, 32826, USA. 3. Department of Materials Science and Engineering, University of Central Florida, Orlando, FL, 32826, USA. 4. Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL, 32826, USA. 5. NanoScience Technology Center, University of Central Florida, Orlando, FL, 32826, USA. andre@ucf.edu. 6. Department of Chemistry, University of Central Florida, Orlando, FL, 32826, USA. andre@ucf.edu. 7. Department of Materials Science and Engineering, University of Central Florida, Orlando, FL, 32826, USA. andre@ucf.edu. 8. The College of Optics and Photonics (CREOL), University of Central Florida, Orlando, FL, 32826, USA. andre@ucf.edu.
Abstract
MAIN CONCLUSION: Excited state lifetime-based separation of fluorophore-tagged antibiotic conjugate emission from the spectrally broad plant autofluorescence enables in planta tracking of the translocation of systemic cargo such as antibiotics via fluorescence lifetime imaging. The efficacy of antibiotic treatments in citrus crops is uncertain due to mixed results from in-field experiments and a lack of study on their systemic movement. As of yet there has been an inability to track treatments using traditional fluorescence microscopy due to treatments having little fluorescence characteristics, and signal convolution due to plant autofluorescence. In this study, we used streptomycin sulfate, a commercially available antibiotic, and conjugated it to a modified tris(bipyridine) ruthenium (II) chloride, a dye with an excited state lifetime magnitudes higher than other commonly used organic fluorescent probes. The resultant is a fluorescence lifetime imaging (FLIM) trackable antibiotic conjugate, covalently attached via an amide linkage that is uniquely distinguishable from plant autofluorescence. Characterization of the fluorescent antibiotic conjugate showed no mitigation of excited state lifetime, and a distinct IR peak not found in any synthetic components. Subsequent tracking using FLIM in citrus tissue was achieved, with identification of movement through citrus plant vasculature via tissue localization in xylem and phloem. Results indicated upwards systemic movement of the conjugate in both xylem and phloem after 48 h of incubation. However, the conjugate failed to move down towards the root system of the plant by 168 h. Mechanistically, it is likely that xylem contributes heavily in the translocation of the conjugate upwards; however, phloem led flow due to growth changes could act as a contributor. This proof-of-concept sets groundwork for subsequent studies regarding antibiotic localization and movement in citrus.
MAIN CONCLUSION: Excited state lifetime-based separation of fluorophore-tagged antibiotic conjugate emission from the spectrally broad plant autofluorescence enables in planta tracking of the translocation of systemic cargo such as antibiotics via fluorescence lifetime imaging. The efficacy of antibiotic treatments in citrus crops is uncertain due to mixed results from in-field experiments and a lack of study on their systemic movement. As of yet there has been an inability to track treatments using traditional fluorescence microscopy due to treatments having little fluorescence characteristics, and signal convolution due to plant autofluorescence. In this study, we used streptomycin sulfate, a commercially available antibiotic, and conjugated it to a modified tris(bipyridine) ruthenium (II) chloride, a dye with an excited state lifetime magnitudes higher than other commonly used organic fluorescent probes. The resultant is a fluorescence lifetime imaging (FLIM) trackable antibiotic conjugate, covalently attached via an amide linkage that is uniquely distinguishable from plant autofluorescence. Characterization of the fluorescent antibiotic conjugate showed no mitigation of excited state lifetime, and a distinct IR peak not found in any synthetic components. Subsequent tracking using FLIM in citrus tissue was achieved, with identification of movement through citrus plant vasculature via tissue localization in xylem and phloem. Results indicated upwards systemic movement of the conjugate in both xylem and phloem after 48 h of incubation. However, the conjugate failed to move down towards the root system of the plant by 168 h. Mechanistically, it is likely that xylem contributes heavily in the translocation of the conjugate upwards; however, phloem led flow due to growth changes could act as a contributor. This proof-of-concept sets groundwork for subsequent studies regarding antibiotic localization and movement in citrus.
Authors: Georg Mayerhofer; Irina Schwaiger-Nemirova; Thomas Kuhn; Leopold Girsch; Franz Allerberger Journal: J Antimicrob Chemother Date: 2009-02-24 Impact factor: 5.790
Authors: Christoph A Bücherl; Arjen Bader; Adrie H Westphal; Sergey P Laptenok; Jan Willem Borst Journal: Protoplasma Date: 2014-01-04 Impact factor: 3.356