So you’ve packaged your DNA into a virus and you’re ready to infect your cells!
But, how many viral particles are required for 100% infection?
In this video, we’ll explain the concept of Multiplicity of Infection or MOI and take
you through how to determine the best MOI for your experiment.
In a nutshell, MOI is the ratio of infectious agents to infection targets.
In many cases, it is the ratio of viral particles to target cells in a defined space, such as
a cell culture well.
For example, if you add 10 million viruses to 1 million cells, you’d have an MOI of
10 and an average probability of 10 viral particles infecting one cell.
Let’s do a quick example calculation!
Let’s say you’d like to achieve an MOI of 10.
If your virus titer is 1 x 10^6 infection units per ml and you are delivering to 1 x 10^5 cells,
what volume of virus will you need for your project?
You will need 1.0 ml of virus.
So, based on this simple definition of MOI, you would expect that if your MOI was one,
then each cell would be infected by one virus.
But the reality is not as simple!
Why?
Imagine yourself throwing 100 tennis balls into a room that has 100 buckets.
Theoretically, there is one ball for every bucket.
But in reality, the chance of every bucket getting 1 ball is very low!
There are other factors to consider, such as do the buckets have backboards that would
make it easier to make the shot?
Similarly, there are factors that can affect how easily viruses can infect their target
cells, such as the current state of your cell line – whether it is dividing or non-dividing,
the characteristics of the virus – whether it is a lentivirus or adenovirus, the transduction
efficiency, and your application – whether you are transducing a packaging cell line
for virus production or a stable cell line for protein production.
For example, if the cell is in a non-dividing state, a higher MOI may be needed to achieve
optimal transduction efficiency.
This is the case when infecting neuronal cells such as SH-SY5Y with lentiviruses for gene
delivery where a much higher MOI of 10-50 can be required.
On the other hand, when it comes to infecting insect cells such as Sf9 cells with baculovirus
for viral production, a low MOI of <1 is typically recommended.
This is because passaging baculoviruses at higher MOIs increases the possibility of transferring
large amounts of defective, non-infectious viruses.
AAV, in contrast, requires MOI ranges of 10,000 to 500,000.
Essentially, if the MOI is too high, it can cause cytotoxicity or other undesired effects.
If the MOI is too low, it will not achieve 100% infection.
So, how do you determine the optimal MOI for your experiment?
Simply perform a pilot experiment using a reporter virus on your target cell line!
For example, using a GFP Lentivirus, design a range of MOIs to use, let’s say, 6 conditions
ranging from MOIs 1, 2, 5, 10, 15, and 30.
It is typically better to test a lower MOI range to avoid cytotoxicity at the higher
MOIs.
A good starting point would be to reference commonly used MOI for cancer cells and devise
the range around the suggested MOI.
After you have infected your cells, allow the appropriate time to pass before evaluating
the fluorescence.
For lentiviruses, this is generally 48 -72 hours post infection.
Next, record the fluorescence at the various MOIs to determine your transduced cell percentage.
Select the minimum MOI at which all the cells are expressing the transgene.
Here is an example of how your results may look like.
In this case, a minimum MOI of 10 is required for 100% infection of the target cells.
If your cells are naturally harder to transduce, there are transduction enhancers such as polybrene
or our ViralMax Transduction Enhancers to increase infectivity performance.
We hope you found this video helpful in determining the optimal conditions for transduction of
your virus to your target cells.
At abm, we offer a ready-to-use collection of Lenti-, AAV, Adeno, and Retroviruses for
any human, mouse, and rat gene!
Browse our collection of tools and resources for gene expression today!