- Short paper
- Open Access
Relative persistence of AAV serotype 1 vector genomes in dystrophic muscle
Genetic Vaccines and Therapyvolume 6, Article number: 14 (2008)
The purpose of this study was to assess the behavior of pseudotyped recombinant adeno-associated virus type 1 (rAAV2/1) vector genomes in dystrophic skeletal muscle. A comparison was made between a therapeutic vector and a reporter vector by injecting the hindlimb in a mouse model of Limb Girdle Muscular Dystrophy Type 2D (LGMD-2D) prior to disease onset. We hypothesized that the therapeutic vector would establish long-term persistence through prevention of myofiber turnover. In contrast, the reporter vector genome copy number would diminish over time due to disease-associated muscle degradation.
One day old alpha sarcoglycan knockout mice (sgca-/-) were injected with 1 × 1011 vector genomes of rAAV2/1-tMCK-sgca in one hindlimb and the same dose of rAAV2/1-tMCK-LacZ in the contra lateral hindlimb. Newborn mice are tolerant of the foreign transgene allowing for long-term expression of both the marker and the therapeutic gene in the null background. At 2 time-points following vector administration, hindlimb muscles were harvested and analyzed for LacZ or sarcoglycan expression. Our data demonstrate prolonged vector genome persistence in skeletal muscle from the hindlimbs injected with the therapeutic transgene as compared to hindlimbs injected with the reporter gene. We observed loss of vector genomes in skeletal muscles that were there were not protected by the benefits of therapeutic gene transfer. In comparison, the therapeutic vector expressing sarcoglycan led to reduction or elimination of myofiber loss. Mitigating the membrane instability inherent in dystrophic muscle was able to prolong the life of individual myofibers.
Limb Girdle Muscular Dystrophy Type 2D (LGMD-2D) is an autosomal recessive disorder caused by mutations in the alpha sarcoglycan gene (sgca) and is the most prevalent of the sarcoglycanopathies; a class of dystrophies in which one of 6 transmembrane sarcoglycan proteins is deficient . LGMD-2D affects both genders equally with onset typically occurring in the first decade of life . The degree of severity in disease phenotype correlates with the amount of sgca protein present in the affected individual . Presently, there is no definitive treatment available for this disease and care is aimed at minimizing disease progression. A clinically applicable gene delivery technique for LGMD-2D is being pursued by various investigators as a method for halting the debilitating consequences of sarcoglycan deficiency and similar diseases [4, 5].
Adeno-associated virus (AAV) is a useful vehicle for gene transfer to skeletal muscle where it has been shown to persist as an episome [6, 7]. Here we sought to examine the persistence of AAV genomes in dystrophic muscle over time. To do so, we injected the skeletal muscles of 4 one-day old alpha-sarcoglycan knockout (sgca-/-) mouse hindlimbs with 1 × 1011 vector genomes of a vector we have previously shown to be therapeutic: rAAV2/1-tMCK-sgca . This vector contains the human alpha sarcoglycan (sgca) gene and a previously described truncated murine creatine kinase (tMCK) promoter . The skeletal muscles of the contra-lateral hindlimb were injected with 1 × 1011 vector genomes of a reporter-gene containing vector: rAAV2/1-tMCK-LacZ which contains the same promoter driving the beta galactosidase (LacZ) gene. Neonatal mice were anesthetized by induced hypothermia and a 29.5-G tuberculin syringe was used to perform single intra-muscular (IM) injections of each vector formulated in phosphate-buffered saline (total volume of 35 μL per injection). The bevel of the needle was inserted facing up near the tendons of the anterior compartment at the ankle and pointing up into the tibialis anterior along the tibia into the upper hindlimb area. The virus solution was injected while withdrawing the needle to maximize area over which the vector was distributed.
At either 4 or 12 months post-administration, muscles were harvested and vector genomes were quantified and compared. Genomic DNA was isolated from frozen tissue samples as previously described . The persistence of vector genomes was determined using the following PCR primer/probe set against the murine creatine kinase (tMCK) promoter. Forward Primer: 5'-GGCACCTATTGGTCTTACTGACA TC-3' Reverse Primer: 5'-GAGTGTCTCAGCCATGGTGGTA-3' Probe: 6FAM-CT CTCCACAGGTGTCCACTCCCAGTTCA-TAMRA.
Our results show that at both 4 and 12 months post virus administration there were a statistically significantly higher number of vector genomes present in those hindlimb muscles injected with rAAV2/1-tMCK-sgca than those injected with rAAV2/1-tMCK-LacZ (Figure 1A). At 2 months post administration differences in the number of transduced myofibers between each hindlimb (as demonstrated by immunohistochemistry and LacZ staining of frozen skeletal muscle cryosections to identify alpha sarcoglycan [green] and β-galactosidase [blue]) were subtle (Figure 1E–F) but increased over time (Figure 1G–J). Vector genome assessment of extensor digitorum longus (EDL), and the tibialis anterior (TA) were combined as they are both composed of predominately fast-twitch myofibers (Figure 1B). At 4 months post virus administration a significant difference in the ability of the two vectors to persist over time in dystrophic muscle became evident. This difference was still present but was not as profound at 12 months post injection since the total number of vector genomes in rAAV2/1-tMCK-sgca injected EDL, and TA muscles decreased over time.
In contrast, vector genome assessment of muscles composed of either primarily slow-twitch or mixed amounts of each fiber type (gastrocnemius [Ga], soleus [So], and quadriceps [Qu]) showed a significant difference between the two vector's relative persistence at both time points (Figure 1C). Specifically, the number of vector genomes detected in the Ga muscles decreased only slightly and those detected in the So muscles of the same hindlimbs did not decrease over time.
The difference or spread in the numbers of detectable genomes in each muscle as compared to those in the same muscle of the contra lateral hindlimb revealed an interesting pattern. The mean number of genomes detected for each LacZ muscle at both time points was subtracted from the mean number of genomes detected for each sgca muscle at both time points to allow for a comparison of differences (or range in mean genome number) between individual muscles in hindlimbs over time. Of those muscles assessed in this study the So is composed of the highest percentage of slow twitch myofibers and it was the only muscle that demonstrated a larger spread between numbers of vector genomes at the 12 month time point than at the 4 month. The EDL however, is composed of predominately fast twitch myofibers. When compared to the other muscles in this study it showed the greatest decrease in spread between persistent vector genomes in muscles from each leg. Our results suggest a greater overall amount of muscle turnover in the EDL than in the other individual muscles we analyzed regardless of which vector was administered. This may suggest that fast-twitch (type II) fibers (of which the EDL is primarily composed of [≥ 97%]) have a tendency to turnover more rapidly than muscles composed of either a mixture of fiber types or of primarily slow twitch fibers (type I).
To our knowledge, an explanation for the random development of dystrophic lesions in both mouse models of muscular dystrophy as well as the humans suffering from this disease has not yet been presented. Our data provides further evidence that individual muscles in this disease model may not all have the same rate of myofiber turn-over leading to tissue fibrosis/necrosis.
The IM delivery method used in this study does not sufficiently deliver vector to every muscle fiber in an equal manner. Therefore, there are likely areas of protected muscle that do contain the therapeutic transgene as well as unprotected muscle areas that deteriorate over time and could eventually overwhelm the treated myofibers and could be another explanation for higher-level turnover in the EDL. Additionally, the sgca protein is membrane bound and not secreted, so transduction of one cell will not be a sufficient way to provide therapy to the surrounding area. Because our delivery method is simple and allows for a single injection to transduce multiple muscles to a high degree, it is a useful proof of concept technique. Use of alternative IV delivery methods could provide a more even biodistribution and may be more clinically applicable [5, 10].
Our data demonstrate the ability of a therapeutic vector to maintain the integrity of transduced muscle fibers, and thereby lead to improved myofiber survival. Our results derived from muscles transduced with a reporter gene vector serve as a model for determination of the amount of muscle fiber turnover between various muscles in this disease model. Future studies demonstrating protection of muscle from a degenerative disease could incorporate a cell proliferation assay such as that developed by Salic et al to further uncover the . While the body's natural muscle regeneration machinery attempts to restore damaged tissue, the non-therapeutic (reporter gene) AAV genomes that would persist in normal muscle as episomes are lost in proportion to the diseased myofiber number. The ability of the rAAV2/1-tMCK-sgca vector to prevent myofibers from membrane damage has the potential to serve as an important therapeutic strategy in the future. Further studies of the potential for this vector to promote repair in muscle with existing dystrophy will be needed.
extensor digitorum longus
limb girdle muscular dystrophy type 2D
polymerase chain reaction
truncated murine creatine kinase.
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We would like to express our gratitude to Dr. Kevin P. Campbell from the University of Iowa for providing the sgca-/- mouse model used in these studies. We would also like to acknowledge the University of Florida Powell Gene Therapy Center Toxicology staff for vector genome quantification and the Powell Gene Therapy Center Viral Vector Core for making the AAV used in these experiments. This work was supported in part by an American Heart Association Pre-doctoral Fellowship Award-Florida and Puerto Rico Affiliate (to CAP), the NIH National Heart, Lung, and Blood Institute grant PO1 HL59412; National Institute of Diabetes and Digestive and Kidney Diseases grant PO1 DK58327; AT-NHLBI-U01 HL69748; and the AHA National Center (to C.S.M.).
The Johns Hopkins University, the University of Florida, and B.J.B. could be entitled to patent royalties for inventions related to the findings in this article.
CAP participated in the design of the study, performed the injections, harvested the tissues, performed the immunohistochemistry analysis and drafted the manuscript. CSM participated in the design of the study and helped to draft the manuscript. TJC participated in the design of the study and performed vector genome analysis and helped to draft the manuscript. BJB participated in the design of the study. All authors read and approved the final manuscript.
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