Molecular Minutes

What is Multiplicity of Infection (MOI)?

Posted by Applied Biological Materials (abm) on January 1, 2020

abm_homepage_MOI-video_blog-post_v2

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 blog post and 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.

What is multiplicity of infection?

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.

 

MOI = Infectious Agents = Viral Particles
Infection Targets Target Cells

 

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.

 

MOI = Viral Particles
Target Cells

 

MOI = 10 million viral particles
1 million cells

 

 MOI = 10

 

A simple sample calculation

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 106 IU/ml and you are delivering to 1 x 105 cells, what volume of virus will you need for your project?

We’ll use the following calculation:
 
MOI = Virus Titer X Virus Volume
Total Cell Number

 

10 = 1 x 106 IU/ml X ?
1 x 105 cells
 
 ? = 1 ml
 
So you will need 1.0 ml of virus to achieve an MOI of 10.
 

Factors that can affect your MOI

So, based on the 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: dividing or non-dividing
  • the characteristics of the virus: lentivirus, adenovirus, etc.
  • the transduction efficiency
  • your application: transducing a packaging cell line for virus production, generating a stable cell line for protein production, etc.

 

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.

Do a pilot experiment to find your optimal MOI
 

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!

General workflow:

Step 1: Select 6 MOI conditions to test

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.

Table-of-suggested-MOIs-for-cancer-cell-lines

Table 1: A general guide for Lentivirus MOIs of popular cell line models. Adapted from Molecular Therapy (2004) 9, S281
 
Step 2: Infect your target cells and record results
 
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.
 
Step 3: 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.

MOI-pilot-study-example
 

If your cells are naturally harder to transduce, there are transduction enhancers such as polybrene or our ViralMax Transduction Enhancers to increase infectivity performance.

 

Summary Video (Duration: 5 min)

 

We hope you found this blog post 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!

Additional Resources:

 

Topics: Viral Vectors, Multiplicity of Infection

Molecular Minutes

Educational resources for life scientists and interviews with scientists/science communicators in the field.

For more in-depth articles, check out our knowledge base, which covers topics such as CRISPR, Next Generation Sequencing, PCR, Cell Culture, and more.

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