RE: CFDA/SE for microbial analysis

From: Gerhard Nebe-von-Caron (Gerhard.Nebe-von-Caron@Unilever.com)
Date: Fri Jun 08 2001 - 06:07:03 EST


There are five things to remember when using CFDA-se or similar with bacteria:

pH 8 is a very good way to cleave the dye very rapidly, thus you should use
buffers below pH 7.3
Ensure that no free esterases are present in your system
Ensure you switch of the pumps that get the dye out of the bugs before it has a
chance to bind inside the cell
Unless you use di-chloro CFDA-SE the intracellular pH can seriously effect your
fluorescence readout.

Don't say you measure 'viability'!  Esterase activity only indicates metabolic
activity, not necessarily the ability of the cells to show reproductive growth
! You can also use CCFDA-SE to stain any type of vesicle you load with esterase
which will turn green but is definitively not viable. Assuming from your email
address that you work for a water company, this is particularly problematic if
you want to use it in the context of UV treated water where you will create
DNA, not membrane damage, thus leaving metabolism intact to some extend whilst
preventing reproductive growth.

regards
Gerhard




-----Original Message-----
From:	Daniel Hoefel [SMTP:daniel.hoefel@sawater.sa.gov.au]
Sent:	Thursday, June 07, 2001 1:58 AM
To:	Cytometry Mailing List
Subject:	CFDA/SE for microbial analysis


Dear List,

I would like to pose a question regarding the use of 5(6)-carboxy fluorescein
diacetate,
succinimidyl ester (5(6)CFDA/SE).  This question does not relate at all to the
current
CFSE discussion on the list.

I was planning to use CFDA/SE to enumerate viable bacteria from water samples by
flow cytometry, where viability is obviously based on the presence of active
internal
esterases that cleave the molecule into its fluorescent carboxy fluorescein
derivative.
I have made a stock solution of CFDA/SE (25mM) in high quality, fresh, anhydrous
DMSO (stock solution stored in a desiccator).	I have been trying to optimise
the
staining conditions by testing different buffers and varying pH (buffers
include PB,
PBS, MilliQ water and also seeing if the addition of EDTA facilitates
permeabilisation
of the cells for better staining).

However, after the addition of CFDA/SE (both 50 and 100uM final concentration)
to the bacterial suspensions at 35oC, I noticed that after about half an hour
the
solutions started to turn a bright yellow/green colour.  I thought that this
was due
to the bacteria taking up the molecule and cleaving it internally, and as a
result
some of the fluorescent product was leaking out of the cells into the
supernatant.
I examined the suspensions by epifluorescent microscopy (blue light excitation)
and I was nearly blinded by the intensity of the background (ie. the
supernatant was
fluorescent, tentatively indicating that the yellow/green colour of the
suspensions
was due to the cleaved fluorescent product of CFDA/SE).

Having seen this, I set up a series of negative controls, ie. all the different
buffers
without the addition of the bacteria.  I then added CFDA/SE at the same
concentrations as
before to the negative controls.  To my surprise, after half an hour at 35oC
incubation,
the negative controls started to turn the yellow/green colour.	To further
investigate
this, I set up the negative controls once again, this time in a real-time PCR
machine
set to detect fluorescein fluorescence.  After the addition of CFDA/SE to the
negative
controls, the real-time PCR maching started to detect fluorescence in the
phosphate
buffer [pH 8.0] negative controls within 30 seconds.  After 2 mins, all of the
buffers
were producing a fluorescent product and within 5 mins the PB solutions had
saturated
the fluorescent detector.  The fluorescent intensity and rate of fluorescent
product
production was proportional to pH of the buffers where the buffers at a pH of
8.0
produced the fluorescent product faster than buffers at 7.5 and 7.0.

Therefore, it seems clear to me that the addition of CFDA/SE to the aqueous
buffers is
causing the molecule to break down into its fluorescent derivative.  The
manufacturer
states that if CFDA/SE is stored in the presence of even minimal water, it will
break
down over time (therefore CFDA/SE is obviously not stable in an aqueous
medium). And even
when stored appropriatley, CFDA/SE is said to only be good for 6 months but
this isn't
an issue with my work because I am using new CFDA/SE and storing it in
anhydrous DMSO.
Therefore, it appears to me that the molecule is breaking down upon the
addition of
it to an aqueous solution such as the buffers.	If this is the case, obviously
I can't
use CFDA/SE for bacterial viability studies.

I have read many papers that use CFDA/SE for bacterial viability studies and I
am
basically following the same protocol as they report to be successful.	I was
therefore
wondering if anyone has seen this occur before or does anyone have any idea as
to why
this is happening or what infact is happening.

Have I just got a 'dud' batch of CFDA/SE from the manufacturer?

Any comments or suggestions would be appreciated.

Daniel Hoefel



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