Important Considerations When Using AAVs

Posted by Guest Blogger on Jun 13, 2017 10:30:00 AM


This post was contributed by guest blogger Katrina Armstrong, a Neurophysiology Msc Student at the University of Manitoba.

  1. Location, Location, Location!
  2. Failure to Plan (for Storage) Is Planning to Fail
  3. Patience Is Bitter but Its Fruit Is Sweet
  4. The Future?

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I knew little about adeno-associated Viral Vectors (AAVs) before starting my graduate program at the University of Manitoba. Our lab has been utilizing chemogenetics (Designer Receptors Exclusively Activated By Designer Drugs, DREADDs) and optogenetics as tools to investigate the roles of certain cell types in locomotion. We have relied heavily upon AAV vectors to deliver chemogenetic/optogenetic constructs into our cells of interest. Although they have a small packaging capacity, AAV vectors were suitable for our needs for the following reasons:

  • Safety: Since AAVs are nonpathogenic, we are able to use AAV vectors without specific facilities (Biosafety Level-1). Other possible tools, lentiviruses for example, are not approved for use in vivo use at the University of Manitoba due to their Biosafety Level-2 or 2+.

    • Please Note: Despite the fact that AAVs themselves are not pathogenic, precautions should still be taken when using them. There are suspected cases of insertional mutagenesis in humans (1) and AAVs are non-enveloped viruses, so they are resistant to alcohol-based disinfectants. A 10% bleach solution should be used to clean AAVs from workspaces.
  • Speed: AAV transduction experiments are relatively quick. We have found that expression occurs quickly and results in long and stable expression (up to 9 months in mice [2]).

  • Low Immune Response: Compared to other viral vectors (e.g. Lentivirus, Adenovirus) AAVs cause the least amount of immune response. Any investigator who is using an in vivo animal model should consider the possible elicited immune response from viral infection. Animal safety is a top priority in our lab so we opted for AAV.

While these benefits make AAVs useful for a wide variety of experiments, care still needs to be taken when selecting which particular AAVs to use for your research. Below I’ll provide some tips that will help you think about how to get started with AAVs. Since my research is rooted in the CNS, my focus will be mostly on the brain, but many of these tips apply to all tissues.

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1. Location, Location, Location!

Triple AAV InfectionWhat do buying real estate and using AAVs have in common? The three most important items when looking for a house and choosing an AAV are… location, location, location! Just like this common real estate mantra, the choice of serotype (which determines which tissues and cells an AAV can infect) can influence an AAV’s value greatly. Applying this mantra to AAV selection, there are three important factors related to location.

  • Location (1): What tissue?
  • Location (2): Where in the tissue/which cell type?
  • Location (3): Traveling from the original location - Axonal Transport in the CNS
Location (1): What tissue?

What is commonly known is that different serotypes have different tropisms but, as you can see, AAVs of each serotype can transduce multiple tissues. So how do you choose the right serotype? Keep asking questions! 

Table 1: AAV Serotypes and Tropism

Experiment  Detection Method
CNS AAV1, AAV2, AAV4, AAV5, AAV8, AAV9
Heart AAV1, AAV8, AAV9
Kidney AAV2
Liver AAV7, AAV8, AAV9
Lung AAV4, AAV5, AAV6, AAV9
Pancreas AAV8
Photoreceptor Cells AAV2, AAV5, AAV8
RPE (Retinal Pigment Epithelium) AAV1, AAV2, AAV4, AAV5, AAV8
Skeletal Muscle AAV1, AAV6, AAV7, AAV8, AAV9

Adapted from https://www.addgene.org/viral-vectors/aav/aav-guide.

Location (2): Where in the tissue/what cell type?

In the CNS, for instance, there are marked differences among serotypes in their efficiency at transducing different brain regions. Although AAV2 can transduce many tissue types, it has low expression in several brain regions where other serotypes may perform better (3).

Brain Region  Optimal Serotype
Striatum AAV5>AAV9>AAV8>AAV1>AAV6>AAV2
Hippocampus AAV9>AAV5>AAV8>AAV1>AAV6>AAV2
Auditory Cortex AAV9>AAV8>AAV6>AAV5>AAV1>AAV2

This preferential tropism for different brain regions is largely due the ability of different serotypes to infect different cell types. In the CNS, it has been shown that there is variable transduction of oligodendrocytes, microglia, astrocytes, neurons, and inhibitory neurons. Your choice of AAV will depend upon which section you’re looking at (striatum, hippocampus and cortex) within the mouse brain (4). An example from the cortex is outlined in the table below.

Cell Type Cortex Optimal Serotype
Oligodendrocytes AAV8 > AAV2 & AAV6
Microglia AAV9 > AAV2 & AAV6
Astrocytes AAV8 > AAV2 & AAV6

Modified from Aschauer et al. (2013)

What does this mean to us? Well, an AAV user must determine which serotype is most efficient at transducing the cell type under study. Many AAVs will show significant expression in a variety of cell types, but you should try to find the best AAV for your particular experiment!

Location (3): Traveling from the Original Location - Axonal Transport

It has been demonstrated that certain serotypes can undergo axoplasmic transport. These AAVs may move toward the cell bodies of neurons (retrograde transport) or towards the synapse (anterograde transport), which is a possible mechanism for the AAV to infect other cell types not within the vicinity of the injection.

Examining serotypes 1, 8 and 9, not only do they undergo retrograde and anterograde transport, but they also have similar transport characteristics (velocities of movement, distance traveled, etc.) (4). This has also been identified with AAV2 (5), AAV6 (6) and AAV5 at excitatory connections (3).

These facts beg the question: is axonal transport desirable or not desirable?

If diffuse gene expression is tolerated, then axonal transport is fine and a researcher should aim to inject a larger amount of vector using a serotype with strong CNS tropism (4).

If axonal transport is not desirable, transport can be reduced by injecting a smaller dose of AAV and using a serotype with weak CNS penetrance (such as AAV2) (4). Otherwise, using a specific system for controlling gene expression such as Cre-lox, may be sufficient to overcome the transport issues.

2. Failure to Plan (For Storage) Is Planning to Fail

Freeze/Thaw Cycles

Of course, one cannot truly predict the perfect titer, but one of the main recommendations when using AAVs is to avoid freezing and thawing. Although more stable than other viruses, multiple freeze thaw cycles can still reduce AAV titer. For long term storage, make > 25 μl aliquots in 0.5 ml tubes, snap freeze in liquid nitrogen or a dry ice/ethanol bath, and store at -80° C. Once thawed, the AAV aliquot should be used quickly.

3. Patience Is Bitter, but Its Fruit Is Sweet

Time

If you require a quick onset of expression, AAV may not be the best tool to use. However, we are starting to see that gene expression really does not take much time at all. Much of the previous literature using AAVs for DREADD delivery indicates ~7-21 days are required for the onset of gene expression. However, it has yet to be determined what gene expression looks like at 3 days vs 7 days vs 14 days etc. To decrease the time until expression, it is possible to use AAV constructs with self-complementing structure (scAAV) (7). As single stranded DNA viruses, AAVs normally require second strand synthesis before gene expression begins. ScAAV avoid this rate limiting step and can immediately undergo replication and transcription. However, with scAAV the effective genome size usable is shortened (from ~4.8 kB [8] to ~2.3 kB [9]).

4. The Future

What new types of research may be enabled by the use of AAVs?

1) Combined functional and anatomical mapping of circuits:

In our lab, we use AAV-DREADD complexes to study neural function. Often the reporter proteins associated with these complexes are so robustly expressed that anatomical assessments can be easily performed too. While I implied that axoplasmic transport of AAVs is a potential problem in many experiments, a group of researchers has identified this feature of AAVs as a new tool for neuroanatomical tracing (11). With the ability to produce neuron specific transfection using Cre-lox, this new method could allow for labeling of neurons showing a very specific phenotype. Previous neural tracing methods used viruses that were potentially toxic and would result in cell death. With several new constructs becoming available, AAVs could be much better tools for neural tracing in very specific cell populations.

Find Ready-to-Use Retrograde AAV Preps at Addgene

2) Comparison of genetically engineered receptors (i.e. chemogenetics vs. optogenetics):

I’m particularly interested in using chemogenetic and optogenetic AAV-based tools to study neural control. Surprisingly, little research has compared and contrasted optogenetic and chemogenetic receptors delivered by AAV within the same cell types. Not only can we compare these methods in specific applications, we may also be able to use these comparisons to enhance our understanding of receptor physiology and the effects of metabotropic and ionotropic influences on overall cell function. AAVs are the most appropriate vehicle for this type of research, as they are safe to use in vivo.

3) The use of AAVs in humans:

AAVs are already being used to treat disease in humans and additional improvements are being made to make them even more useful for therapeutic purposes. The University of Pennsylvania and the biotechnology firm Biogen have recently collaborated to develop “AAV 3.0”, vectors that will have substantially improved performance profiles and should be suitable for genome editing. These vectors can be used to improve targeted therapies for the eye, skeletal muscles, and the central nervous system.

Currently, AAVs are being used to deliver CRISPR/Cas9 but have the potential to deliver other therapeutic molecules such as microRNAs (miRNAs), short hairpin RNAs (shRNAs), antisense oligonucleotides (ASOs), zinc finger nucleases, and many others (12).

The most attractive potential of AAVs is their ability to be used with new exciting technologies (such as CRISPR/Cas9) as they allow for gene delivery in an efficient and non-pathogenic fashion. Work improving AAV tissue tropism, transduction efficiency, and safety profiles should strengthen its appeal for the scientific and medical communities.


Many thanks to our guest blogger Katrina Armstrong.

Katrina Armstrong Headshot.pngKatrina Armstrong is a Neurophysiology Msc Student at the University of Manitoba. Her project is examining the use of DREADDs (Designer Receptors Exclusively Activated By Designer Drugs) to determine the role of serotonin in movement. Follow her on twitter @katrinaboards.

 

References

1. Russell, David W. "AAV vectors, insertional mutagenesis, and cancer." Molecular Therapy 15.10 (2007): 1740-1743. PubMed PMID: 17882145.

2. Zincarelli, Carmela, et al. "Analysis of AAV serotypes 1–9 mediated gene expression and tropism in mice after systemic injection." Molecular Therapy 16.6 (2008): 1073-1080. PubMed PMID: 18414476.

3. Aschauer, Dominik F., Sebastian Kreuz, and Simon Rumpel. "Analysis of transduction efficiency, tropism and axonal transport of AAV serotypes 1, 2, 5, 6, 8 and 9 in the mouse brain." PloS one 8.9 (2013): e76310. PubMed PMID: 24086725. PubMed Central PMCID: PMC3785459.

4. Castle, Michael J., et al. "Adeno-associated virus serotypes 1, 8, and 9 share conserved mechanisms for anterograde and retrograde axonal transport." Human gene therapy 25.8 (2014): 705-720. PubMed PMID: 24694006. PubMed Central PMCID: PMC4137353.

5. Ciesielska, Agnieszka, et al. "Anterograde axonal transport of AAV2-GDNF in rat basal ganglia." Molecular Therapy 19.5 (2011): 922-927. PubMed PMID: 21102559. PubMed Central PMCID: PMC3098627.

6. Salegio, Ernesto A., et al. "Axonal transport of adeno-associated viral vectors is serotype-dependent." Gene therapy 20.3 (2013): 348-352. PubMed PMID: 22418061. PubMed Central PMCID: PMC3381869.

7. McCarty, D. M., Paul E. Monahan, and Richard J. Samulski. "Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis." Gene therapy 8.16 (2001): 1248. PubMed PMID: 11509958.

8. Ferrari, Forrest K., et al. "Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors." Journal of virology 70.5 (1996): 3227-3234. PubMed PMID: 8627803. PubMed Central PMCID: PMC190186.

9. Grieger, Joshua C., and Richard J. Samulski. "Packaging capacity of adeno-associated virus serotypes: impact of larger genomes on infectivity and postentry steps." Journal of virology 79.15 (2005): 9933-9944. PubMed PMID: 16014954. PubMed Central PMCID: PMC1181570.

10. Wu, Jianqing, et al. "Self-complementary recombinant adeno-associated viral vectors: packaging capacity and the role of rep proteins in vector purity." Human gene therapy 18.2 (2007): 171-182. PubMed PMID: 17328683.

11. Wouterlood, Floris G., et al. "A fourth generation of neuroanatomical tracing techniques: exploiting the offspring of genetic engineering." Journal of neuroscience methods 235 (2014): 331-348. PubMed PMID: 25107853.

12. Valdmanis, Paul, and Mark A. Kay. "Future of rAAV gene therapy: Platform for RNAi, Gene Editing and Beyond." Human Gene Therapy ja (2017). PubMed PMID: 28073291.

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