bioRxiv · 10.64898/2026.05.04.722478
Adeno-Associated Virus Co-Precipitation with Extracellular Vesicles for Genome Editing in Rodent Embryo
Abstract
Adeno-associated virus purification by density-gradient ultracentrifugation is labor-intensive and often results in substantial titer loss due to particle aggregation. Here, we present a scalable co-isolation strategy in which AAV is precipitated together with extracellular vesicles secreted by the producer cell line, completely bypassing density-gradient separation. The resulting AAV-EV preparations comprise free AAV, free EVs, and EV-associated AAV. Functionally, AAV-EV vectors (AAV2/1 serotype) support efficient ex vivo genome editing across multiple independent loci in mouse and rat zygotes, achieving a mean targeting efficiency of approximately 26%. Compared with gradient-purified AAV administered at matched doses, AAV-EV formulations yielded 2.34-fold higher embryo viability while maintaining equivalent transgene copy numbers. By leveraging EVs as a biological matrix, this approach enables ultracentrifugation-free AAV isolation without compromising vector functionality. Overall, AAV-EV represents an accessible and embryo-tolerant platform for rodent genome engineering that aligns with the principles of Replacement, Reduction, and Refinement (3R) principles.
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Nickl, P., Barbiera, M., Zini, J., Nickl, T., Ushiki, A., Vaskovicova, M., Neburkova, J., Dolejs, V., Simova, M., Balounova, J., Vyletal, P., Zivna, M., Kmoch, S., Sumbalova-Koledova, Z., Filipp, D., Ballek, O., Neiderlova, V., Stepanek, O., Ahituv, N., Yliperttula, M., Sedlacek, R.. 2026-05-07. Adeno-Associated Virus Co-Precipitation with Extracellular Vesicles for Genome Editing in Rodent Embryo. https://doi.org/10.64898/2026.05.04.722478
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