Re: Sorting Biohazards--second try

From: Dave Coder (dave@nucleus.immunol.washington.edu)
Date: Tue Nov 15 1994 - 14:43:31 EST


Although the normal mode of infection for T. cruzi is via a bug bite, the  
trypanasome will easily cross mucus membrane (infection via the conjunctiva  
is common). How much of an aerosol will sorting create? How many viable  
trypanasomes will be floating around? You should be able to have a well  
contained sorting area (negative pressure, properly shielded from the  
outside, etc.) BUT, there is no cure for T. cruzi infection: once infected  
you have a parasite for life.

So, do you need to sort with a flow cytometer? I'd look at the alternatives first.

Dave Coder
Univ. Washington
dcoder@u.washington.edu

Begin forwarded message:

X-Popmail-Charset: English
Date: Mon, 14 Nov 94 20:48:26 EST
From: (Steve G. Hilliard) <hilliard@zookeeper.zoo.uga.edu>
To: cytometry@flowcyt.cyto.purdue.edu
Subject: Sorting Biohazards--second try

I've had trouble "following my bouncing mail" (can't sing anyway ;-))
but I get the feeling my first attempt didn't make it.  To reiterate, I
have a user who wants me to SORT antibody-labelled, VIABLE _T. cruzi_.  I'd
appreciate anyone's thoughts--current regulations (if any), precautions,
"don't even consider it", etc.  Do we need to put our Elite in a P2 room,
or just forget it entirely?  Anyone?

Thanks,
Steve
++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++
Steve G. Hilliard, Cell Analysis Facility      |
University of Georgia                          | "Be good and you will
hilliard@zookeeper.zoo.uga.edu                 |      be lonesome..."
++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++


This archive was generated by hypermail 2.1.6 : Thu Jan 01 2004 - 17:27:08 EST