Is it bacterial contamination

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sunandod sunandod
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Is it bacterial contamination

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Dear Confocal list users
   we are seeing a large number of small rod like staining in the dapi
channel in ATCC MDA-MB 231 cells. The media and the cells do not turn
turbid if incubated at 37Deg C for 48 Hrs.

We see more of these particles when the cells are grown in absence of
PS. In presence of PS, the number grows with passage of cells and actin
starts showing very thin needle like outward projections although the
cells grow (divide) normally.

What would be the possible contamination and what is the most probable
source and remedy?

Thank you in advance

Best
Sunando


Sunando Datta
Assistant Professor
Dept. of Biological Sciences
Indian Institute of Science Education and Research
Bhopal
India
Daniel Possin Daniel Possin
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Re: Is it bacterial contamination

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Mycoplasma?

Dan

On Oct 4, 2014, at 8:45 AM, Sunando <[hidden email]> wrote:

> *****
> To join, leave or search the confocal microscopy listserv, go to:
> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
> Post images on http://www.imgur.com and include the link in your posting.
> *****
>
> Dear Confocal list users
>  we are seeing a large number of small rod like staining in the dapi channel in ATCC MDA-MB 231 cells. The media and the cells do not turn turbid if incubated at 37Deg C for 48 Hrs.
>
> We see more of these particles when the cells are grown in absence of PS. In presence of PS, the number grows with passage of cells and actin starts showing very thin needle like outward projections although the cells grow (divide) normally.
>
> What would be the possible contamination and what is the most probable source and remedy?
>
> Thank you in advance
>
> Best
> Sunando
>
>
> Sunando Datta
> Assistant Professor
> Dept. of Biological Sciences
> Indian Institute of Science Education and Research
> Bhopal
> India
Farid Jalali Farid Jalali
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Re: Is it bacterial contamination

In reply to this post by sunandod
Hello Sunando, your description is suggestive of mycoplasm- media does not become turbid, but following fixation and DAPI staining you get positive signal for bacterial contamination inside the cells. Are you seeing a change in the doubling time/growth characteristics of the MDA cells as well? Mycoplasma will also do this, although more pronounced in normal cells vs. transformed.  There is a Hoechst 33258-based assay to ID mycoplasma, but it seems like your DAPI results provide the same data. There was a reagent you could add to media over many passages to remove the mycoplasma, the name escapes me now, but I recall that it was pretty effective. I'm sure you will find something online following a search for mycoplasma removal. Best to get to the bottom of this asap because it can spread. Good luck. Cheers. Farid.
Sent on the TELUS Mobility network with BlackBerry

-----Original Message-----
From: Sunando <[hidden email]>
Sender: Confocal Microscopy List <[hidden email]>
Date:         Sat, 4 Oct 2014 21:15:02
To: <[hidden email]>
Reply-To: Confocal Microscopy List <[hidden email]>
Subject: Is it bacterial contamination

*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
Post images on http://www.imgur.com and include the link in your posting.
*****

Dear Confocal list users
   we are seeing a large number of small rod like staining in the dapi
channel in ATCC MDA-MB 231 cells. The media and the cells do not turn
turbid if incubated at 37Deg C for 48 Hrs.

We see more of these particles when the cells are grown in absence of
PS. In presence of PS, the number grows with passage of cells and actin
starts showing very thin needle like outward projections although the
cells grow (divide) normally.

What would be the possible contamination and what is the most probable
source and remedy?

Thank you in advance

Best
Sunando


Sunando Datta
Assistant Professor
Dept. of Biological Sciences
Indian Institute of Science Education and Research
Bhopal
India