The CVS strain of rabies virus as transneuronal tracer in the olfactory system of mice
References (41)
Localization of acetylcholinesterase-positive neurons projecting to the mouse main olfactory bulb
Brain Res. Bull.
(1984)- et al.
Denervation in the primary olfactory pathway of mice. IV. Biochemical and morphological evidence for neuronal replacement following nerve section
Brain Res.
(1977) - et al.
Soybean agglutinin binding to the olfactory systems of the rat and mouse
Neurosci. Lett.
(1986) - et al.
Propagation of the CVS strain of rabies virus and of the avirulent mutant AvO1 along the olfactory pathways of the mouse after intranasal inoculation
Virology
(1991) - et al.
HSV (Type 1) infection of the trigeminal complex
Brain Res.
(1990) - et al.
Golgi-like, transneuronal retrograde labelling with CNS injections of Herpes simplex virus type 1
Brain Res. Bull.
(1989) A proposed relationship between increases in the number of olfactory receptor neurons, convergence ratio and sensitivity in the developing rat
Dev. Brain Res.
(1989)Membrane and synaptic properties of identified neurons in the olfactory bulb
Prog. Neurobiol.
(1987)- et al.
Interbulbar axonal collateralization and morphology of anterior olfactory nucleus neurons in the rat
Brain Res. Bull.
(1988) - et al.
Transneuronal labeling of spinal interneurons and sympathetic preganglionic neurons after pseudorabies virus injections in the rat medial gastrocnemius muscle
Brain Res.
(1992)
Laminar distributions of interneurons in the main olfactory bulb of the adult hamster
Brain Res. Bull.
The connections of the mouse olfactory bulb: A study using orthograde and retrograde transport of wheat germ agglutinin conjugated to horseradish peroxidase
Brain Res. Bull.
Parasympathetic influence on the nasal mucosa
Acta Otolaryngol.
Cellular expression of H and B antigens in the rat olfactory system during development
J. Comp. Neurol.
Olfactory neural pathway in mouse hepatitis virus nasoencephalitis
Acta Neuropathol.
Effects of sensory deprivation on the developing mouse olfactory system: a light and electron microscopic, morphometric analysis
J. Neurosci.
Invasion of the peripheral nervous systems of adult mice by the CVS strain of rabies virus and its avirulent derivative AVO1
J. Virol.
The afferent connections of the main and the accessory olfactory bulb formations in the rat: an experimental HRP-study
J. Comp. Neurol.
Essai sur la structure, le me´tabolisme et la fonction des neurones infecte´s par le virus herpes suis et celui de la rage
Rev. Inst. Pasteur (Lyon)
Axonal transport of rabies virus in the central nervous system of the rat
J. Neuropathol. Exp. Neurol.
Cited by (75)
Rhabdoviridae, Rabies Virus
2022, Encyclopedia of Infection and ImmunityGolgi staining-like retrograde labeling of brain circuits using rabies virus: Focus onto the striatonigral neurons
2020, Journal of Neuroscience MethodsCitation Excerpt :These fixed strains have been adapted from the street ones by repeated passages first in mice brains and then in cell cultures, leading to the selection of strains with stable properties. The first use of CVS-11 as neuronal tracer was reported by Astic and collaborators in the olfactory network (Astic et al., 1993), followed by a study from Ugolini (Ugolini, 1995) with injection in the hypoglossal nerve to reveal, by immunodetection of the viral nucleocapsids, the spread of the virus over time in the interconnected neurons. This latter study was a follow-up of series of experiments using the transsynaptic property of the herpes simplex virus type 1 or PRV to decipher neural networks (Aston-Jones and Card, 2000; Card et al., 1990; Card and Enquist, 2014; Ugolini et al., 1989).
Rabies virus
2020, Rabies: Scientific Basis of the Disease and Its Management, Fourth EditionThe phenotype of the RABV glycoprotein determines cellular and global virus load in the brain and is decisive for the pace of the disease
2017, VirologyCitation Excerpt :The two original virus strains SAD B19 (Vos et al., 1999) and DRV4 (Dietzschold et al., 2000) differ in their neuroinvasiveness after peripheral intramuscular (i.m.) inoculation, causing no (Faber et al., 2004) and 90% mortality (Preuss et al., 2009), respectively. Therefore, we used the intranasal route (i.n.) of infection (van Riel et al., 2015), which allowed both viruses to enter the brain as previously described for the challenge virus standard (CVS) strain (Astic et al., 1993; Lafay et al., 1991) without causing any iatrogenic injury. The recombinant RABV vector cSPBN was generated from a SAD B19 (GenBank accession no. M31046.1) cDNA clone as described previously (Morimoto et al., 2001; Schnell et al., 1994).