Rachel Schowalter
Lab of Cellular Oncology, NCI, NIH
Primary reference:
Schowalter, R.M., D.V. Pastrana, and C.B. Buck, Glycosaminoglycans and sialylated glycans sequentially facilitate merkel cell polyomavirus infectious entry.PLoS Pathog, 2011. 7:e1002161
Vector release and re-ligationof MCV genomic DNA
- Add 4.5 ml of 7.5 M ammonium acetate (Sigma cat# A2706) and mix. Add 35 ml of 95%ethanol. Do not use absolute (100%) ethanol. Mix and incubate at 4ºC overnight.
-Bring the sample back to room temperature. Centrifuge at ~5,000 x g (room temp or 16ºC) for 60 minutes (e.g., Sorvall SH3000 swinging bucket rotor 4700 rpm).
- Wash pellet with 10 ml of 70% ethanol (incubate 10 min). Spin 10 min. Repeat. **I found this part the most difficult to get right. I think it’s important to treat the invisible pellet very delicately. Maintain the orientation of the tube in the bucket when you spin each time, and try not to jostle the tube a lot before you discard the supernatant. I prefer to pour the supernatant out, rather than aspirate. **
- Remove the second 70% ethanol wash. Spin residual ethanol off the walls of the tube. Remove residual ethanol, then allow pellet to air dry for several minutes.
- Add 100 µl of TE to the dried pellet. Allow the DNA to redissolve for at least 10 minutes (overnight is good). Transfer dissolved DNA to a microfuge tube. Rinse the walls and bottom of the 50 ml tube using an additional 100 µl of water. Expect a yield of about 35µg of DNA.
Transfection of 293TT cells, cell expansion and harvest:
I use VeriQuest SYBR Green qPCR Master Mix 2X (Affymetrix) and the primers I use are: GCTTGTTAAAGGAGGAGTGG and GATCTGGAGATGATCCCTTTG.
Native virion propagation and amplification using 293-4T cells:
The native MCV genome exhibits very little transcriptional activity and fails to replicate efficiently in all cell lines we have tested so far. This makes it difficult to titer the infectivity of native MCV virions. To overcome this problem, we developed a 293TT cell line, called 293-4T, that stably expresses the MCV Large T and small t antigens. The ectopically expressed T antigens drive replication of the MCV genome and this leads to the production of new virions, at least in a fraction of the infected cells. Thus, native MCV virion stocks produced by transient transfection (see above) can be amplified and serially propagated in 293-4T cells.
Propagation and amplification of MCV virions has not yet been carefully optimized. Pilot experiments used ~50 µl of native MCV virions (produced as described above) to infect a ~25% confluent T-75 flask of 293-4T cells for several days. The culture was then passaged continuously for several weeks. New MCV virions were produced essentially continuously during this period. No gross cytolytic effects were observed. However, the infected cultures reproducibly show a small percentage of cells that are much larger than normal. Immunofluorescence experiments seem consistent with the idea that cells expressing VP1 remain adherent but are visibly swollen (sometimes extremely swollen).
In the few experiments where we have propagated MCV in 293-4T cells, we adopted a strategy of subjecting ~10% of the culture to rapid freeze-thaw (without any cryo-protectants) during each passage. We then reintroduced the freeze-thawed lysate into the passaged culture. Our theory is that MCV does not promote active lysis and may need to be actively released (e.g. by freeze-thaw lysis). We have not carefully tested whether the freeze-thaw approach facilitates MCV propagation or is unnecessary.
A potential problem with serially passaging MCV in 293-4T cells is that the cell line continuously provides the virus with T antigens. Thus, mutant viruses that lose large segments of the MCV early region may have a fitness advantage (smaller genome size can mean faster replication and more efficient packaging into new virions). Similar effects are observed when polyomaviruses are propagated at high multiplicity of infection [5].
References:
1. Schowalter, R.M., D.V. Pastrana, K.A. Pumphrey, A.L. Moyer, and C.B. Buck, Merkel Cell Polyomavirus and Two Previously Unknown Polyomaviruses Are Chronically Shed From Human Skin.Cell Host Microbe, 2010. 7(6): p. 509-15.
http://www.ncbi.nlm.nih.gov/pubmed/20542254
2. Neumann, F., S. Borchert, C. Schmidt, R. Reimer, H. Hohenberg, N. Fischer, and A. Grundhoff, Replication, Gene Expression and Particle Production by a Consensus Merkel Cell Polyomavirus (MCPyV) Genome.PLoS One, 2011. 6(12): p. e29112.
http://www.ncbi.nlm.nih.gov/pubmed/22216177
3. Schowalter, R.M., D.V. Pastrana, and C.B. Buck, Glycosaminoglycans and sialylated glycans sequentially facilitate merkel cell polyomavirus infectious entry.PLoS Pathog, 2011. 7(7): p. e1002161.
http://www.ncbi.nlm.nih.gov/pubmed/21829355
4. Schowalter, R.M., W.C. Reinhold, and C.B. Buck, Entry tropism of BK and Merkel Cell Polyomaviruses in cell culture.PLoS One, 2012. 7(7): p. e42181.
http://www.ncbi.nlm.nih.gov/pubmed/22860078
5. Winocour, E., N. Frenkel, S. Lavi, M. Osenholts, and S. Rozenblatt, Host substitution in SV40 and polyoma DNA.Cold Spring Harb Symp Quant Biol, 1975. 39 Pt 1: p. 101-8.
http://www.ncbi.nlm.nih.gov/pubmed/169048