Monosynaptic restriction of the anterograde herpes simplex virus strain H129 for neural circuit tracing

Author:

Fischer Kyle B.1,Collins Hannah K.1,Pang Yan1,Roy Dheeraj S.2,Zhang Ying3,Feng Guoping23,Li Shu‐Jing4,Kepecs Adam5,Callaway Edward M.1ORCID

Affiliation:

1. Systems Neurobiology Laboratories Salk Institute for Biological Studies La Jolla California USA

2. Stanley Center for Psychiatric Research Broad Institute of MIT and Harvard Cambridge Massachusetts USA

3. Department of Brain and Cognitive Sciences McGovern Institute for Brain Research at MIT Cambridge Massachusetts USA

4. Cold Spring Harbor Laboratory Cold Spring Harbor New York USA

5. Departments of Neuroscience and Psychiatry Washington University School of Medicine St. Louis Missouri USA

Abstract

AbstractIdentification of synaptic partners is a fundamental task for systems neuroscience. To date, few reliable techniques exist for whole brain labeling of downstream synaptic partners in a cell‐type‐dependent and monosynaptic manner. Herein, we describe a novel monosynaptic anterograde tracing system based on the deletion of the gene UL6 from the genome of a cre‐dependent version of the anterograde Herpes Simplex Virus 1 strain H129. Given that this knockout blocks viral genome packaging and thus viral spread, we reasoned that co‐infection of a HSV H129 ΔUL6 virus with a recombinant adeno‐associated virus expressing UL6 in a cre‐dependent manner would result in monosynaptic spread from target cre‐expressing neuronal populations. Application of this system to five nonreciprocal neural circuits resulted in labeling of neurons in expected projection areas. While some caveats may preclude certain applications, this system provides a reliable method to label postsynaptic partners in a brain‐wide fashion.

Funder

National Science Foundation

National Institutes of Health

Stanley Center for Psychiatric Research, Broad Institute

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

General Neuroscience

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