TY - JOUR
T1 - Anterograde or retrograde transsynaptic circuit tracing in vertebrates with vesicular stomatitis virus vectors
AU - Beier, Kevin T.
AU - Mundell, Nathan A.
AU - Pan, Yu Chin Albert
AU - Cepko, Constance L.
N1 - Funding Information:
This work was supported by grants from the Howard Hughes Medical Institute (HHMI) U01 NS090449 (C.L.C.), and the National Institutes of Health (NIH) NS083848 (C.L.C.), EY023911 (N.A.M.), NS068012 (K.T.B.), and EY024844 (Y.A.P.). We thank Kathy DeLoach for assistance with mouse surgery images and Sylvain Lapan for assistance with chicken injection images.
Publisher Copyright:
© 2016 by John Wiley & Sons, Inc.
PY - 2016
Y1 - 2016
N2 - Viruses have been used as transsynaptic tracers, allowing one to map the inputs and outputs of neuronal populations, due to their ability to replicate in neurons and transmit in vivo only across synaptically connected cells. To date, their use has been largely restricted to mammals. In order to explore the use of such viruses in an expanded host range, we tested the transsynaptic tracing ability of recombinant vesicular stomatitis virus (rVSV) vectors in a variety of organisms. Successful infection and gene expression were achieved in a wide range of organisms, including vertebrate and invertebrate model organisms. Moreover, rVSV enabled transsynaptic tracing of neural circuitry in predictable directions dictated by the viral envelope glycoprotein (G), derived from either VSV or rabies virus (RABV). Anterograde and retrograde labeling, from initial infection and/or viral replication and transmission, was observed in Old and NewWorld monkeys, seahorses, jellyfish, zebrafish, chickens, and mice. These vectors are widely applicable for gene delivery, afferent tract tracing, and/or directional connectivity mapping. Here, we detail the use of these vectors and provide protocols for propagating virus, changing the surface glycoprotein, and infecting multiple organisms using several injection strategies.
AB - Viruses have been used as transsynaptic tracers, allowing one to map the inputs and outputs of neuronal populations, due to their ability to replicate in neurons and transmit in vivo only across synaptically connected cells. To date, their use has been largely restricted to mammals. In order to explore the use of such viruses in an expanded host range, we tested the transsynaptic tracing ability of recombinant vesicular stomatitis virus (rVSV) vectors in a variety of organisms. Successful infection and gene expression were achieved in a wide range of organisms, including vertebrate and invertebrate model organisms. Moreover, rVSV enabled transsynaptic tracing of neural circuitry in predictable directions dictated by the viral envelope glycoprotein (G), derived from either VSV or rabies virus (RABV). Anterograde and retrograde labeling, from initial infection and/or viral replication and transmission, was observed in Old and NewWorld monkeys, seahorses, jellyfish, zebrafish, chickens, and mice. These vectors are widely applicable for gene delivery, afferent tract tracing, and/or directional connectivity mapping. Here, we detail the use of these vectors and provide protocols for propagating virus, changing the surface glycoprotein, and infecting multiple organisms using several injection strategies.
KW - Axon tracing
KW - Gene delivery
KW - Neural circuitry
KW - Transsynaptic tracing
KW - VSV
UR - http://www.scopus.com/inward/record.url?scp=85014102538&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85014102538&partnerID=8YFLogxK
U2 - 10.1002/0471142301.ns0126s74
DO - 10.1002/0471142301.ns0126s74
M3 - Article
C2 - 26729030
AN - SCOPUS:85014102538
SN - 1934-8584
VL - 2016
SP - 1.26.1-1.26.27
JO - Current Protocols in Neuroscience
JF - Current Protocols in Neuroscience
ER -