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      Rabies virus modifies host behaviour through a snake-toxin like region of its glycoprotein that inhibits neurotransmitter receptors in the CNS

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          Abstract

          Rabies virus induces drastic behaviour modifications in infected hosts. The mechanisms used to achieve these changes in the host are not known. The main finding of this study is that a region in the rabies virus glycoprotein, with homologies to snake toxins, has the ability to alter behaviour in animals through inhibition of nicotinic acetylcholine receptors present in the central nervous system. This finding provides a novel aspect to virus receptor interaction and host manipulation by pathogens in general. The neurotoxin-like region of the rabies virus glycoprotein inhibited acetylcholine responses of α4β2 nicotinic receptors in vitro, as did full length ectodomain of the rabies virus glycoprotein. The same peptides significantly altered a nicotinic receptor induced behaviour in C. elegans and increased locomotor activity levels when injected into the central nervous system of mice. These results provide a mechanistic explanation for the behavioural changes in hosts infected by rabies virus.

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          Most cited references36

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          Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences.

          We describe a dominant behavioral marker, rol-6(su-1006), and an efficient microinjection procedure which facilitate the recovery of Caenorhabditis elegans transformants. We use these tools to study the mechanism of C.elegans DNA transformation. By injecting mixtures of genetically marked DNA molecules, we show that large extrachromosomal arrays assemble directly from the injected molecules and that homologous recombination drives array assembly. Appropriately placed double-strand breaks stimulated homologous recombination during array formation. Our data indicate that the size of the assembled transgenic structures determines whether or not they will be maintained extrachromosomally or lost. We show that low copy number extrachromosomal transformation can be achieved by adjusting the relative concentration of DNA molecules in the injection mixture. Integration of the injected DNA, though relatively rare, was reproducibly achieved when single-stranded oligonucleotide was co-injected with the double-stranded DNA.
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            Quantitative ultrastructural analysis of hippocampal excitatory synapses.

            From three-dimensional reconstructions of CA1 excitatory synapses in the rodent hippocampus and in culture, we have estimated statistical distributions of active zone and postsynaptic density (PSD) sizes (average area approximately 0.04 micron2), the number of active zones per bouton (usually one), the number of docked vesicles per active zone (approximately 10), and the total number of vesicles per bouton (approximately 200), and we have determined relationships between these quantities, all of which vary from synapse to synapse but are highly correlated. These measurements have been related to synaptic physiology. In particular, we propose that the distribution of active zone areas can account for the distribution of synaptic release probabilities and that each active zone constitutes a release site as identified in the standard quantal theory attributable to Katz (1969).
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              Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences.

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                Author and article information

                Contributors
                khueffer@alaska.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                9 October 2017
                9 October 2017
                2017
                : 7
                : 12818
                Affiliations
                [1 ]ISNI 0000 0004 1936 981X, GRID grid.70738.3b, Department of Veterinary Medicine, University of Alaska Fairbanks, ; Fairbanks, Alaska United States of America
                [2 ]ISNI 0000 0000 8794 7643, GRID grid.267627.0, Department of Pharmaceutical Sciences, University of the Sciences, ; Philadelphia, Pennsylvania United States of America
                [3 ]ISNI 0000 0004 1936 981X, GRID grid.70738.3b, Department of Biology and Wildlife & Institute of arctic Biology, University of Alaska Fairbanks, ; Fairbanks, Alaska United States of America
                [4 ]ISNI 0000 0000 9093 6830, GRID grid.213902.b, Department of Biology, California State University Long Beach, ; Long Beach, California United States of America
                [5 ]ISNI 0000 0004 1936 8091, GRID grid.15276.37, Department of Pharmacology & Therapeutics University of Florida, ; Gainesville, Florida United States of America
                Article
                12726
                10.1038/s41598-017-12726-4
                5634495
                28993633
                6e5e84f8-49c2-433a-a629-989565e62dea
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 23 June 2017
                : 13 September 2017
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