Hi all,
From my timelapse imaging, I always observe my bacteria trap in late endosomal compartments, even after overnight. Although the bacteria look fairly intact from the morphology, I would like to know if the bacteria are still viable.
Do you know if there is any way I can check it?
I came across the Live/Dead Baclight staining kit from Molecular Probes, but not sure if this kit is going to stain the intracellular bacteria specifically, or it will stain up my cells simultaneously.
I also thought of lysing the cells to release the intracellular bacteria and plate them on agar plates. However, this approach will only work if the gentamicin work at 100% efficiency to kill of the extracellular bacteria. Normally, I still get 1 or 2 colonies on my agar plate when I plate the medium containing gentamicin at the end of the experiment.
Any idea from all the genius out there?????
Many thanks in advance.
Viability of intracellular bacteria
Started by virusfan, Nov 18 2010 04:16 AM
1 reply to this topic
#1
Posted 18 November 2010 - 04:16 AM
#2
Posted 22 November 2010 - 04:11 AM
I would lyse the cells and plate out serial dilutions to work out viable CFU/ml. Is it the standard method for measuring bacterial invasion. One or two 'background' colonies shouldn't alter your result too much. From my experience, 100ug/ml gentamicin for 2 hours was sufficient to kill extracelluar bacteria.
Edited by microRNAboy, 22 November 2010 - 04:11 AM.














