AAV11 permits efficient retrograde targeting of projection neurons

Author:

Han ZengpengORCID,Luo Nengsong,Kou Jiaxin,Li Lei,Ma Wenyu,Peng Siqi,Xu Zihong,Zhang Wen,Qiu Yuxiang,Wu Yang,Wang Jie,Ye Chaohui,Lin Kunzhang,Xu Fuqiang

Abstract

AbstractViral tracers that permit efficient retrograde targeting of projection neurons are powerful vehicles for structural and functional dissections of the neural circuit and for the treatment of brain diseases. Recombinant adeno-associated viruses (rAAVs) are the most potential candidates because they are low-toxic with high-level transgene expression and minimal host immune responses. Currently, some rAAVs based on capsid engineering for retrograde tracing have been widely used in the analysis and manipulation of neural circuits, but suffer from brain area selectivity and inefficient retrograde transduction in certain neural connections. Here, we discovered that the recombinant adeno-associated virus 11 (rAAV11) exhibits potent retrograde labeling of projection neurons with enhanced efficiency to rAAV2-retro in some neural connections. Combined with calcium recording technology, rAAV11 can be used to monitor neuronal activities by expressing Cre recombinase or calcium-sensitive functional probe. In addition, we further showed the suitability of rAAV11 for astrocyte targeting. These properties make rAAV11 a promising tool for the mapping and manipulation of neural circuits and gene therapy of some neurological and neurodegenerative disorders.HighlightsNaturally occurring AAV serotype capsid exhibits robust retrograde functionalityImproved distribution properties and retrograde transport efficiencyCan express Cre recombinase or calcium-sensitive functional probe for neural circuits monitoringCan specifically target astrocytes

Publisher

Cold Spring Harbor Laboratory

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