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      Vesicular stomatitis virus enables gene transfer and transsynaptic tracing in a wide range of organisms

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          Abstract

          Current limitations in technology have prevented an extensive analysis of the connections among neurons, particularly within nonmammalian organisms. We developed a transsynaptic viral tracer originally for use in mice, and then tested its utility in a broader range of organisms. By engineering the vesicular stomatitis virus (VSV) to encode a fluorophore and either the rabies virus glycoprotein (RABV‐G) or its own glycoprotein (VSV‐G), we created viruses that can transsynaptically label neuronal circuits in either the retrograde or anterograde direction, respectively. The vectors were investigated for their utility as polysynaptic tracers of chicken and zebrafish visual pathways. They showed patterns of connectivity consistent with previously characterized visual system connections, and revealed several potentially novel connections. Further, these vectors were shown to infect neurons in several other vertebrates, including Old and New World monkeys, seahorses, axolotls, and Xenopus. They were also shown to infect two invertebrates, Drosophila melanogaster, and the box jellyfish, Tripedalia cystophora, a species previously intractable for gene transfer, although no clear evidence of transsynaptic spread was observed in these species. These vectors provide a starting point for transsynaptic tracing in most vertebrates, and are also excellent candidates for gene transfer in organisms that have been refractory to other methods. J. Comp. Neurol. 523:1639–1663, 2015. © 2015 Wiley Periodicals, Inc.

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          Most cited references91

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          Characteristics of a human cell line transformed by DNA from human adenovirus type 5.

          Human embryonic kidney cells have been transformed by exposing cells to sheared fragments of adenovirus type 5 DNA. The transformed cells (designated 293 cells) exhibited many of the characteristics of transformation including the elaboration of a virus-specific tumour antigen. Analysis of the polypeptides synthesized in the 293 cells by labelling with 35S-methionine and SDS PAGE showed a variable pattern of synthesis, different in a number of respects from that seen in otheruman cells. On labelling the surface of cells by lactoperoxidase catalysed radio-iodination, the absence of a labelled polypeptide analogous to the 250 K (LETS) glycoprotein was noted. Hybridization of labelled cellular RNA with restriction fragments of adenovirus type 5 DNA indicated transcription of a portion of the adenovirus genome at the conventional left hand end.
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            Autophagy is an essential component of Drosophila immunity against vesicular stomatitis virus.

            Intrinsic innate immune mechanisms are the first line of defense against pathogens and exist to control infection autonomously in infected cells. Here, we showed that autophagy, an intrinsic mechanism that can degrade cytoplasmic components, played a direct antiviral role against the mammalian viral pathogen vesicular stomatitis virus (VSV) in the model organism Drosophila. We found that the surface glycoprotein, VSV-G, was likely the pathogen-associated molecular pattern (PAMP) that initiated this cell-autonomous response. Once activated, autophagy decreased viral replication, and repression of autophagy led to increased viral replication and pathogenesis in cells and animals. Lastly, we showed that the antiviral response was controlled by the phosphatidylinositol 3-kinase (PI3K)-Akt-signaling pathway, which normally regulates autophagy in response to nutrient availability. Altogether, these data uncover an intrinsic antiviral program that links viral recognition to the evolutionarily conserved nutrient-signaling and autophagy pathways.
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              The DF-1 chicken fibroblast cell line: transformation induced by diverse oncogenes and cell death resulting from infection by avian leukosis viruses.

              DF-1 is a continuous cell line of chicken embryo fibroblasts. The cells are free of endogenous sequences related to avian sarcoma and leukosis viruses and have normal fibroblastic morphology. DF-1 cells support the replication of avian retroviruses; diverse oncogenes induce foci of oncogenic transformation on monolayers of DF-1, and avian leukosis viruses of envelope subgroups B, D, and C induce cell death and form plaques. The new cell line will greatly facilitate studies on oncogenic transformation and cell killing by avian viruses. Copyright 1998 Academic Press.
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                Author and article information

                Journal
                J Comp Neurol
                J. Comp. Neurol
                10.1002/(ISSN)1096-9861
                CNE
                The Journal of Comparative Neurology
                John Wiley and Sons Inc. (Hoboken )
                0021-9967
                1096-9861
                01 August 2015
                02 April 2015
                : 523
                : 11 ( doiID: 10.1002/cne.v523.11 )
                : 1639-1663
                Affiliations
                [ 1 ] Department of GeneticsHarvard Medical School Boston Massachusetts 02115
                [ 2 ] Department of Ophthalmology, Howard Hughes Medical InstituteHarvard Medical School Boston Massachusetts 02115
                [ 3 ] Department of Molecular and Cellular Biology and Center for Brain ScienceHarvard University Cambridge Massachusetts 01238
                [ 4 ] Department of NeurobiologyHarvard Medical School Boston Massachusetts 02115
                [ 5 ] Department of Ecology, Evolution and Marine BiologyUniversity of California, Santa Barbara Santa Barbara California 93106
                [ 6 ]Present address: Department of Biology, 385 Serra MallStanford University Stanford CA 94305
                [ 7 ]Present address: Department of Neuroscience and Regenerative Medicine, Medical College of GeorgiaGeorgia Regents University Augusta GA 30912
                Author notes
                [*] [* ]Correspondence to: Constance L. Cepko, Department of Genetics, Department of Ophthalmology, Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115. E‐mail: cepko@ 123456genetics.med.harvard.edu
                Article
                CNE23761
                10.1002/cne.23761
                4458151
                25688551
                deec4bf7-224f-48c4-9b32-7c878f9d404d
                © 2015 Wiley Periodicals, Inc.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 02 December 2014
                : 03 February 2015
                : 10 February 2015
                Page count
                Pages: 26
                Funding
                Funded by: Howard Hughes Medical Institute (HHMI)
                Funded by: National Institutes of Health (NIH)
                Award ID: NS083848
                Award ID: EY7145 and EY023911
                Award ID: NS068012
                Award ID: EY024844
                Award ID: HD067140
                Award ID: EY12196 and EY11379 and AG041582
                Funded by: Lundbeckfonden
                Award ID: R125‐A10379
                Funded by: Danish Research Council
                Award ID: DFF132500146
                Funded by: Harvard/MIT Joint Research Grants Program in Basic Neuroscience
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                cne23761
                1 August 2015
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.4 mode:remove_FC converted:09.09.2016

                Neurology
                vsv,transsynaptic,polysynaptic,anterograde,retrograde,visual pathways,centrifugal,retina,in vivo,rrid: ab_10053281,ab_591819,ab_531908,ab_10562207,scires_000161

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