Time-lapse videos were made around the colony spreading of GFP-expressing F. johnsoniae strains using a BX50F microscope (Olympus). The culture plate was placed on a sample stage, and a cover glass was carefully placed over the colony. After the top surface of the dendrites formed was imaged using phase contrast microscopy, fluorescence signals in the same area were observed to track the cells using confocal laser scanning fluorescent microscopy (CLSM) with an objective lens of UPlanFl 100× (Olympus) and ANDOR iXon EMCCD camera (Oxford Instruments, Abingdon, UK) in combination with Andor iQ3 software (Oxford Instruments). Exposure time of each image was typically 100 ms (excitation light: 490–510 nm, emission light: 520–550 nm). Fluorescence images were taken every 3 s for 10 min, and movies were produced.
Visualizing Bacterial Colony Spreading
Time-lapse videos were made around the colony spreading of GFP-expressing F. johnsoniae strains using a BX50F microscope (Olympus). The culture plate was placed on a sample stage, and a cover glass was carefully placed over the colony. After the top surface of the dendrites formed was imaged using phase contrast microscopy, fluorescence signals in the same area were observed to track the cells using confocal laser scanning fluorescent microscopy (CLSM) with an objective lens of UPlanFl 100× (Olympus) and ANDOR iXon EMCCD camera (Oxford Instruments, Abingdon, UK) in combination with Andor iQ3 software (Oxford Instruments). Exposure time of each image was typically 100 ms (excitation light: 490–510 nm, emission light: 520–550 nm). Fluorescence images were taken every 3 s for 10 min, and movies were produced.
Corresponding Organization : Nagasaki University
Other organizations : Gifu Prefectural Research Institute for Fisheries and Aquatic Environments, University of Tsukuba, Aoyama Gakuin University, Nihon University
Variable analysis
- Presence of GFP-expressing F. johnsoniae strains
- Colony spreading
- Cell movement and behavior
- Microscope setup (phase contrast objective, CLSM with 100x objective lens)
- Imaging parameters (exposure time, excitation/emission wavelengths)
- Positive control: None mentioned
- Negative control: None mentioned
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