Trypanosoma cruzi Chagas (ATCC® PRA-376)

Organism: Trypanosoma cruzi Chagas  /  Depositor: DS Lindsay

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Strain Designations TcVT-1
Biosafety Level 2
Isolation Blood from chagasic dog, Virginia, USA
Product Format frozen
Storage Conditions Frozen: -70°C or colder
Freeze-Dried: 2°C to 8°C
Live Culture: See Protocols Section
Medium Medium 2222: Cell Cultivation Medium for Parasites
Growth Conditions Temperature: 35°C to 37°C
Atmosphere: 5% CO2
Cell Line: BS-C-1 monkey kidney epithelial cells (ATCC® CCL-26™), Hs27 human foreskin fibroblasts (ATCC® CRL-1634™), or BALB/3T3 mouse embryonic fibroblasts (ATCC® CCL-163™). Contact ATCC Sales to order.
Cryopreservation Harvest and Preservation
  1. Harvest Trypanosoma cultures when emergent parasites (trypomastigote stage) have reached or are near peak density in the liquid column. Gently invert the Trypanosoma culture flasks to suspend parasites in the liquid medium.
  2. Transfer the cell suspension (including parasites) to 15 mL plastic centrifuge tubes. Centrifuge at 1300 x g for 10 min.
  3. Remove all but 0.5 mL of the supernatant from each tube, resuspend the cell pellets, and pool them to a single tube.
  4. Adjust the parasite concentration to 2.0 - 4.0 x 107 cells/mL with fresh medium or PBS. NOTE: If the concentration of parasites is too low, centrifuge at 1300 x g for 10 min and resuspend in the volume of fresh medium or PBS required to yield the desired concentration.
  5. Prepare a cryoprotective solution containing 10% (v/v) DMSO in fresh medium or PBS.
  6. Mix the cell preparation and cryoprotective solution in equal portions. The final concentration will be 1.0 - 2.0 x 107 cells/mL and 5% DMSO. The time from the mixing of the cell preparation and cryoprotective solution to the start of the freezing process should be no less than 15 min and no more than 30 min. NOTE: To prevent culture contamination, penicillin-streptomycin solution (ATCC® 30-2300) may be added to a final concentration of 50 to 100 I.U./mL penicillin and 50 to 100 µg/mL streptomycin.
  7. Dispense in 0.5 mL aliquots to 1.0-2.0 mL sterile plastic screw-capped cryovials.
  8. Place cryovials in a controlled rate freezing unit. From room temperature cool at -1°C/min to -40°C. If freezing unit can compensate for the heat of fusion, maintain rate at -1°C/min through heat of fusion. At -40°C plunge ampules into liquid nitrogen. Alternatively, place the vials in a Nalgene 1°C freezing apparatus. Place the apparatus at -80°C for 1.5 to 2 hours and then plunge ampules into liquid nitrogen. (The cooling rate in this apparatus is approximately -1°C/min.)
  9. Store frozen ampules in either the vapor or liquid phase of a nitrogen refrigerator.
  10. To thaw a frozen ampule, place it in a 35-37°C water bath such that the lip of the ampule remains above the water line. Thawing time is approximately 2 to 3 minutes.  Do not agitate the ampule.  Do not leave ampule in water bath after thawed.
  11. Immediately after thawing, aseptically transfer contents to a T-25 tissue culture flask containing a fresh monolayer of the host cell line and 10 mL ATCC® 30-2002 with 10% (v/v) HIFBS.
  12. Outgas the flask for 10 seconds with a 95% air, 5% CO2 gas mixture.
  13. Incubate in a 35-37°C CO2 incubator with the cap screwed on tightly.
Name of Depositor DS Lindsay
References

Patel JM, et al. Isolation, mouse pathogenicity, and genotyping of Trypanosoma cruzi from an English Cocker Spaniel from Virginia, USA. Vet. Parasitol. 187(3-4): 394-398, 2012. PubMed: 22341614

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