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  1. Article ; Online: Treatment of spatial memory impairment in hamsters infected with West Nile virus using a humanized monoclonal antibody MGAWN1.

    Smeraski, Cynthia A / Siddharthan, Venkatraman / Morrey, John D

    Antiviral research

    2011  Volume 91, Issue 1, Page(s) 43–49

    Abstract: In addition to functional disorders of paresis, paralysis, and cardiopulmonary complications, subsets of West Nile virus (WNV) patients may also experience neurocognitive deficits and memory disturbances. A previous hamster study has also demonstrated ... ...

    Abstract In addition to functional disorders of paresis, paralysis, and cardiopulmonary complications, subsets of West Nile virus (WNV) patients may also experience neurocognitive deficits and memory disturbances. A previous hamster study has also demonstrated spatial memory impairment using the Morris water maze (MWM) paradigm. The discovery of an efficacious therapeutic antibody MGAWN1 from pre-clinical rodent studies raises the possibility of preventing or treating WNV-induced memory deficits. In the current study, hamsters were treated intraperitoneally (i.p.) with 32 mg/kg of MGAWN1 at 4.5 days after subcutaneously (s.c.) challenging with WNV. As expected, MGAWN1 prevented mortality, weight loss, and improved food consumption of WNV-infected hamsters. The criteria for entry of surviving hamsters into the study were that they needed to have normal motor function (forelimb grip strength, beam walking) and normal spatial reference memory in the MWM probe task. Twenty-eight days after the acute phase of the disease had passed, MGAWN1- and saline-treated infected hamsters were again trained in the MWM. Spatial memory was evaluated 48 h after this training in which the hamsters searched for the location where a submerged escape platform had been positioned. Only 56% of infected hamsters treated with saline spent more time in the correct quadrant than the other three quadrants, as compared to 92% of MGAWN1-treated hamsters (P⩽0.05). Overall these studies support the possibility that WNV can cause spatial memory impairment and that therapeutic intervention may be considered.
    MeSH term(s) Animals ; Antibodies, Monoclonal/administration & dosage ; Antibodies, Monoclonal/therapeutic use ; Antiviral Agents/therapeutic use ; Cricetinae ; Disease Models, Animal ; Hippocampus/virology ; Male ; Maze Learning ; Memory Disorders/drug therapy ; Memory Disorders/etiology ; Mesocricetus ; Treatment Outcome ; West Nile Fever/complications ; West Nile Fever/drug therapy ; West Nile Fever/mortality ; West Nile virus/drug effects ; West Nile virus/immunology
    Chemical Substances Antibodies, Monoclonal ; Antiviral Agents
    Language English
    Publishing date 2011-04-30
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 306628-9
    ISSN 1872-9096 ; 0166-3542
    ISSN (online) 1872-9096
    ISSN 0166-3542
    DOI 10.1016/j.antiviral.2011.04.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Towards a definition of recovery of function.

    Murray, Marion / Fischer, Itzhak / Smeraski, Cynthia / Tessler, Alan / Giszter, Simon

    Journal of neurotrauma

    2004  Volume 21, Issue 4, Page(s) 405–413

    Abstract: In this review we consider recovery of function after spinal cord injury, and, in particular, recovery improved following intraspinal cellular transplants. Some recovery occurs spontaneously and this can be especially dramatic in neonates, supporting the ...

    Abstract In this review we consider recovery of function after spinal cord injury, and, in particular, recovery improved following intraspinal cellular transplants. Some recovery occurs spontaneously and this can be especially dramatic in neonates, supporting the notion that developing and adult spinal cord respond differently to injury. Recovery can be improved in both neonates and adults by appropriate cellular transplants into the injury site. We describe several functional tests used in animals with spinal lesions and transplants. We compare the effects of transplants of fetal tissue and genetically modified fibroblasts into neonatal and adult injury sites on recovery of motor and sensorimotor function. Fetal tissue transplants support greater recovery and elicit more regeneration in neonates than in adults. Transplants of fibroblasts modified to produce neurotrophic factors however support both recovery and axonal growth even in adults. The contribution of the transplant to recovery is shown by the loss of function that follows a second lesion just rostral to the original lesion/transplant site. The effect of the re-lesion indicates that the recovery is mediated by the presence of the transplant but the way in which transplants act to promote recovery may include a number of mechanisms, including regeneration and sprouting, neuroprotection, and modifications of organization of spared CNS structures.
    MeSH term(s) Animals ; Brain Tissue Transplantation/standards ; Brain Tissue Transplantation/trends ; Fetal Tissue Transplantation/standards ; Fetal Tissue Transplantation/trends ; Fibroblasts/metabolism ; Fibroblasts/secretion ; Fibroblasts/transplantation ; Humans ; Nerve Growth Factors/metabolism ; Nerve Growth Factors/secretion ; Nerve Regeneration/physiology ; Neurologic Examination/standards ; Neuronal Plasticity/physiology ; Recovery of Function/physiology ; Spinal Cord Injuries/physiopathology ; Spinal Cord Injuries/therapy
    Chemical Substances Nerve Growth Factors
    Language English
    Publishing date 2004-04
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, U.S. Gov't, P.H.S. ; Review
    ZDB-ID 645092-1
    ISSN 1557-9042 ; 0897-7151
    ISSN (online) 1557-9042
    ISSN 0897-7151
    DOI 10.1089/089771504323004557
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: West Nile virus infection in American Robins: new insights on dose response.

    VanDalen, Kaci K / Hall, Jeffrey S / Clark, Larry / McLean, Robert G / Smeraski, Cynthia

    PloS one

    2013  Volume 8, Issue 7, Page(s) e68537

    Abstract: West Nile virus (WNV) is a vector-borne pathogen that was first detected in the United States in 1999. The natural transmission cycle of WNV involves mosquito vectors and avian hosts, which vary in their competency to transmit the virus. American robins ... ...

    Abstract West Nile virus (WNV) is a vector-borne pathogen that was first detected in the United States in 1999. The natural transmission cycle of WNV involves mosquito vectors and avian hosts, which vary in their competency to transmit the virus. American robins are an abundant backyard species in the United States and appear to have an important role in the amplification and dissemination of WNV. In this study we examine the response of American robins to infection with various WNV doses within the range of those administered by some natural mosquito vectors. Thirty American robins were assigned a WNV dosage treatment and needle inoculated with 10(0.95) PFU, 10(1.26) PFU, 10(2.15) PFU, or 10(3.15) PFU. Serum samples were tested for the presence of infectious WNV and/or antibodies, while oral swabs were tested for the presence of WNV RNA. Five of the 30 (17%) robins had neutralizing antibodies to WNV prior to the experiment and none developed viremia or shed WNV RNA. The proportion of WNV-seronegative birds that became viremic after WNV inoculation increased in a dose dependent manner. At the lowest dose, only 40% (2/5) of the inoculated birds developed productive infections while at the highest dose, 100% (7/7) of the birds became viremic. Oral shedding of WNV RNA followed a similar trend where robins inoculated with the lower two doses were less likely to shed viral RNA (25%) than robins inoculated with one of the higher doses (92%). Viremia titers and morbidity did not increase in a dose dependent manner; only two birds succumbed to infection and, interestingly, both were inoculated with the lowest dose of WNV. It is clear that the disease ecology of WNV is a complex interplay of hosts, vectors, and viral dose delivered.
    MeSH term(s) Animals ; Antibodies, Viral/blood ; Antigens, Viral/analysis ; Antigens, Viral/immunology ; Bird Diseases/blood ; Bird Diseases/transmission ; Bird Diseases/virology ; Culicidae/virology ; Enzyme-Linked Immunosorbent Assay ; Host-Pathogen Interactions ; Immunohistochemistry ; Insect Vectors/virology ; RNA, Viral/genetics ; RNA, Viral/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Songbirds/virology ; United States ; Viremia/blood ; Viremia/virology ; West Nile Fever/blood ; West Nile Fever/transmission ; West Nile Fever/virology ; West Nile virus/genetics ; West Nile virus/immunology ; West Nile virus/physiology
    Chemical Substances Antibodies, Viral ; Antigens, Viral ; RNA, Viral
    Language English
    Publishing date 2013-07-02
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0068537
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Suprachiasmatic nucleus input to autonomic circuits identified by retrograde transsynaptic transport of pseudorabies virus from the eye.

    Smeraski, Cynthia A / Sollars, Patricia J / Ogilvie, Malcolm D / Enquist, Lynn W / Pickard, Gary E

    The Journal of comparative neurology

    2004  Volume 471, Issue 3, Page(s) 298–313

    Abstract: Intraocular injection of the Bartha strain of pseudorabies virus (PRV Bartha) results in transsynaptic infection of the hypothalamic suprachiasmatic nucleus (SCN), a retinorecipient circadian oscillator. PRV Bartha infection of a limited number of ... ...

    Abstract Intraocular injection of the Bartha strain of pseudorabies virus (PRV Bartha) results in transsynaptic infection of the hypothalamic suprachiasmatic nucleus (SCN), a retinorecipient circadian oscillator. PRV Bartha infection of a limited number of retinorecipient structures, including the SCN, was initially interpreted as the differential infection of a subpopulation of rat retinal ganglion cells, followed by replication and anterograde transport via the optic nerve. A recent report that used a recombinant strain of PRV Bartha (PRV152) expressing enhanced green fluorescent protein demonstrated that SCN infection actually results from retrograde transneuronal transport of the virus via the autonomic innervation of the eye in the golden hamster. In the present study using the rat, the pattern of infection after intravitreal inoculation with PRV152 was examined to determine if infection of the rat SCN is also restricted to retrograde transsynaptic transport. It was observed that infection in preganglionic autonomic nuclei (i.e., Edinger-Westphal nucleus, superior salivatory nucleus, and intermediolateral nucleus) precedes infection in the SCN. Sympathetic superior cervical ganglionectomy did not abolish label in the SCN after intraocular infection, nor did lesions of parasympathetic preganglionic neurons in the Edinger-Westphal nucleus. However, combined Edinger-Westphal nucleus ablation and superior cervical ganglionectomy eliminated infection of the SCN. This observation allowed a detailed examination of the SCN contribution to descending autonomic circuits afferent to the eye. The results indicate that in the rat, as in the hamster, SCN infection after intraocular PRV152 inoculation is by retrograde transsynaptic transport via autonomic pathways to the eye.
    MeSH term(s) Animals ; Biological Transport/physiology ; Eye/chemistry ; Eye/innervation ; Eye/metabolism ; Eye/virology ; Herpesvirus 1, Suid/physiology ; Male ; Nerve Net/chemistry ; Nerve Net/metabolism ; Nerve Net/virology ; Pseudorabies/physiopathology ; Pseudorabies/virology ; Rats ; Rats, Sprague-Dawley ; Suprachiasmatic Nucleus/chemistry ; Suprachiasmatic Nucleus/metabolism ; Suprachiasmatic Nucleus/virology ; Swine ; Synapses/chemistry ; Synapses/metabolism ; Synapses/virology
    Language English
    Publishing date 2004-04-05
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 3086-7
    ISSN 1096-9861 ; 0021-9967 ; 0092-7317
    ISSN (online) 1096-9861
    ISSN 0021-9967 ; 0092-7317
    DOI 10.1002/cne.20030
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Melanopsin retinal ganglion cells receive bipolar and amacrine cell synapses.

    Belenky, Michael A / Smeraski, Cynthia A / Provencio, Ignacio / Sollars, Patricia J / Pickard, Gary E

    The Journal of comparative neurology

    2003  Volume 460, Issue 3, Page(s) 380–393

    Abstract: Melanopsin is a novel opsin synthesized in a small subset of retinal ganglion cells. Ganglion cells expressing melanopsin are capable of depolarizing in response to light in the absence of rod or cone input and are thus intrinsically light sensitive. ... ...

    Abstract Melanopsin is a novel opsin synthesized in a small subset of retinal ganglion cells. Ganglion cells expressing melanopsin are capable of depolarizing in response to light in the absence of rod or cone input and are thus intrinsically light sensitive. Melanopsin ganglion cells convey information regarding general levels of environmental illumination to the suprachiasmatic nucleus, the intergeniculate leaflet, and the pretectum. Typically, retinal ganglion cells communicate information to central visual structures by receiving input from retinal photoreceptors via bipolar and amacrine cells. Because melanopsin ganglion cells do not require synaptic input to generate light-induced signals, these cells need not receive synapses from other neurons in the retina. In this study, we examined the ultrastructure of melanopsin ganglion cells in the mouse retina to determine the type (if any) of synaptic input these cells receive. Melanopsin immunoreaction product was associated primarily with the plasma membrane of (1) perikarya in the ganglion cell layer, (2) dendritic processes in the inner plexiform layer (IPL), and (3) axons in the optic fiber layer. Melanopsin-immunoreactive dendrites in the inner (ON) region of the IPL were postsynaptic to bipolar and amacrine terminals, whereas melanopsin dendrites stratifying in the outer (OFF) region of the IPL received only amacrine terminals. These observations suggested that rod and/or cone signals may be capable of modifying the intrinsic light response in melanopsin-expressing retinal ganglion cells.
    MeSH term(s) Amacrine Cells/chemistry ; Amacrine Cells/physiology ; Amacrine Cells/ultrastructure ; Animals ; Male ; Mice ; Mice, Inbred C57BL ; Nerve Net/chemistry ; Nerve Net/physiology ; Nerve Net/ultrastructure ; Retinal Ganglion Cells/chemistry ; Retinal Ganglion Cells/physiology ; Retinal Ganglion Cells/ultrastructure ; Rod Opsins/analysis ; Rod Opsins/physiology ; Synapses/chemistry ; Synapses/physiology ; Synapses/ultrastructure
    Chemical Substances Rod Opsins ; melanopsin
    Language English
    Publishing date 2003-06-02
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 3086-7
    ISSN 1096-9861 ; 0021-9967 ; 0092-7317
    ISSN (online) 1096-9861
    ISSN 0021-9967 ; 0092-7317
    DOI 10.1002/cne.10652
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Susceptibility of greater sage-grouse to experimental infection with West Nile virus.

    Clark, Larry / Hall, Jeffrey / McLean, Robert / Dunbar, Michael / Klenk, Kaci / Bowen, Richard / Smeraski, Cynthia A

    Journal of wildlife diseases

    2006  Volume 42, Issue 1, Page(s) 14–22

    Abstract: Populations of greater sage-grouse (Centrocercus urophasianus) have declined 45-80% in North America since 1950. Although much of this decline has been attributed to habitat loss, recent field studies have indicated that West Nile virus (WNV) has had a ... ...

    Abstract Populations of greater sage-grouse (Centrocercus urophasianus) have declined 45-80% in North America since 1950. Although much of this decline has been attributed to habitat loss, recent field studies have indicated that West Nile virus (WNV) has had a significant negative impact on local populations of grouse. We confirm the susceptibility of greater sage-grouse to WNV infection in laboratory experimental studies. Grouse were challenged by subcutaneous injection of WNV (10(3.2) plaque-forming units [PFUs]). All grouse died within 6 days of infection. The Kaplan-Meier estimate for 50% survival was 4.5 days. Mean peak viremia for nonvaccinated birds was 10(6.4) PFUs/ml (+/-10(0.2) PFUs/ml, standard error of the mean [SEM]). Virus was shed cloacally and orally. Four of the five vaccinated grouse died, but survival time was increased (50% survival=9.5 days), with 1 grouse surviving to the end-point of the experiment (14 days) with no signs of illness. Mean peak viremia for the vaccinated birds was 10(2.3) PFUs/ml (+/-10(0.6) PFUs/ml, SEM). Two birds cleared the virus from their blood before death or euthanasia. These data emphasize the high susceptibility of greater sage-grouse to infection with WNV.
    MeSH term(s) Animals ; Animals, Wild/immunology ; Animals, Wild/virology ; Bird Diseases/immunology ; Bird Diseases/virology ; Disease Susceptibility/veterinary ; Enzyme-Linked Immunosorbent Assay/veterinary ; Galliformes ; Injections, Subcutaneous/veterinary ; Random Allocation ; Reverse Transcriptase Polymerase Chain Reaction/veterinary ; Survival Rate ; Time Factors ; Viral Vaccines/immunology ; Viremia/veterinary ; West Nile Fever/immunology ; West Nile Fever/mortality ; West Nile Fever/veterinary ; West Nile Fever/virology ; West Nile virus/pathogenicity
    Chemical Substances Viral Vaccines
    Language English
    Publishing date 2006-01
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 410709-3
    ISSN 1943-3700 ; 0090-3558
    ISSN (online) 1943-3700
    ISSN 0090-3558
    DOI 10.7589/0090-3558-42.1.14
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Melanopsin and non-melanopsin expressing retinal ganglion cells innervate the hypothalamic suprachiasmatic nucleus.

    Sollars, Patricia J / Smeraski, Cynthia A / Kaufman, Jessica D / Ogilvie, Malcolm D / Provencio, Ignacio / Pickard, Gary E

    Visual neuroscience

    2004  Volume 20, Issue 6, Page(s) 601–610

    Abstract: Retinal input to the hypothalamic suprachiasmatic nucleus (SCN) synchronizes the SCN circadian oscillator to the external day/night cycle. Retinal ganglion cells that innervate the SCN via the retinohypothalamic tract are intrinsically light sensitive ... ...

    Abstract Retinal input to the hypothalamic suprachiasmatic nucleus (SCN) synchronizes the SCN circadian oscillator to the external day/night cycle. Retinal ganglion cells that innervate the SCN via the retinohypothalamic tract are intrinsically light sensitive and express melanopsin. In this study, we provide data indicating that not all SCN-projecting retinal ganglion cells express melanopsin. To determine the proportion of ganglion cells afferent to the SCN that express melanopsin, ganglion cells were labeled following transsynaptic retrograde transport of a recombinant of the Bartha strain of pseudorabies virus (PRV152) constructed to express the enhanced green fluorescent protein (EGFP). PRV152 injected into the anterior chamber of the eye retrogradely infects four retinorecipient nuclei in the brain via autonomic circuits to the eye, resulting in transneuronally labeled ganglion cells in the contralateral retina 96 h after intraocular infection. In animals with large bilateral lesions of the lateral geniculate body/optic tract, ganglion cells labeled with PRV152 are retrogradely infected from only the SCN. In these animals, most PRV152-infected ganglion cells were immunoreactive for melanopsin. However, a significant percentage (10-20%) of EGFP-labeled ganglion cells did not express melanopsin. These data suggest that in addition to the intrinsically light-sensitive melanopsin-expressing ganglion cells, conventional ganglion cells also innervate the SCN. Thus, it appears that the rod/cone system of photoreceptors may provide signals to the SCN circadian system independent of intrinsically light-sensitive melanopsin ganglion cells.
    MeSH term(s) Animals ; Biological Transport ; Circadian Rhythm ; Cricetinae ; Green Fluorescent Proteins ; Herpesvirus 1, Suid/physiology ; Luminescent Proteins/metabolism ; Male ; Mesocricetus ; Retinal Ganglion Cells/metabolism ; Rod Opsins/metabolism ; Suprachiasmatic Nucleus/metabolism ; Suprachiasmatic Nucleus/virology ; Visual Pathways/metabolism
    Chemical Substances Luminescent Proteins ; Rod Opsins ; melanopsin ; Green Fluorescent Proteins (147336-22-9)
    Language English
    Publishing date 2004-03-15
    Publishing country England
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 639436-x
    ISSN 1469-8714 ; 0952-5238
    ISSN (online) 1469-8714
    ISSN 0952-5238
    DOI 10.1017/s0952523803206027
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Intravitreal injection of the attenuated pseudorabies virus PRV Bartha results in infection of the hamster suprachiasmatic nucleus only by retrograde transsynaptic transport via autonomic circuits.

    Pickard, Gary E / Smeraski, Cynthia A / Tomlinson, Christine C / Banfield, Bruce W / Kaufman, Jessica / Wilcox, Christine L / Enquist, Lynn W / Sollars, Patricia J

    The Journal of neuroscience : the official journal of the Society for Neuroscience

    2002  Volume 22, Issue 7, Page(s) 2701–2710

    Abstract: Intravitreal injection of the attenuated strain of pseudorabies virus (PRV Bartha) results in transneuronal spread of virus to a restricted set of central nuclei in the rat and mouse. We examined the pattern of central infection in the golden hamster ... ...

    Abstract Intravitreal injection of the attenuated strain of pseudorabies virus (PRV Bartha) results in transneuronal spread of virus to a restricted set of central nuclei in the rat and mouse. We examined the pattern of central infection in the golden hamster after intravitreal inoculation with a recombinant strain of PRV Bartha constructed to express enhanced green fluorescent protein (PRV 152). Neurons in a subset of retinorecipient nuclei [i.e., suprachiasmatic nucleus (SCN), intergeniculate leaflet, olivary pretectal nucleus (OPN), and lateral terminal nucleus] and autonomic nuclei [i.e., paraventricular hypothalamic nucleus and Edinger-Westphal nucleus (EW)] are labeled by late stages of infection. Infection of the EW precedes infection in retinorecipient structures, raising the possibility that the SCN becomes infected by retrograde transsynaptic infection via autonomic (i.e., EW) circuits. We tested this hypothesis in two ways: (1) by removing the infected eye 24 hr after PRV 152 inoculation, well before viral infection first appears in the SCN; and (2) by examining central infection after intravitreal PRV 152 injection in animals with ablation of the EW. The pattern and time course of central infection were unchanged after enucleation, whereas EW ablation before intravitreal inoculation eliminated viral infection in the SCN. The results of EW lesions along with known connections between EW, OPN, and SCN indicate that intravitreal injection of PRV Bartha produces a retrograde infection of the autonomic innervation of the eye, which subsequently labels a restricted set of retinorecipient nuclei via retrograde trans-synaptic infection. These results, taken together with other genetic data, indicate that the mutations in PRV Bartha render the virus incapable of anterograde transport. PRV Bartha is thus a retrograde transsynaptic marker in the CNS.
    MeSH term(s) Animals ; Autonomic Nervous System/pathology ; Autonomic Nervous System/virology ; Axonal Transport/physiology ; Biological Transport ; Cricetinae ; Disease Progression ; Eye Enucleation ; Genes, Reporter ; Herpesvirus 1, Suid/genetics ; Herpesvirus 1, Suid/growth & development ; Luminescent Proteins/genetics ; Mesocricetus ; Neurons/pathology ; Neurons/virology ; Pseudorabies/pathology ; Pseudorabies/virology ; Retinal Ganglion Cells/pathology ; Retinal Ganglion Cells/virology ; Suprachiasmatic Nucleus/pathology ; Suprachiasmatic Nucleus/virology ; Synapses/pathology ; Synapses/virology ; Visual Pathways/pathology ; Visual Pathways/virology ; Vitreous Body/virology
    Chemical Substances Luminescent Proteins
    Language English
    Publishing date 2002-04-01
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 604637-x
    ISSN 1529-2401 ; 0270-6474
    ISSN (online) 1529-2401
    ISSN 0270-6474
    DOI 20026174
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: West Nile virus infection in American Robins

    Kaci K VanDalen / Jeffrey S Hall / Larry Clark / Robert G McLean / Cynthia Smeraski

    PLoS ONE, Vol 8, Iss 7, p e

    new insights on dose response.

    2013  Volume 68537

    Abstract: West Nile virus (WNV) is a vector-borne pathogen that was first detected in the United States in 1999. The natural transmission cycle of WNV involves mosquito vectors and avian hosts, which vary in their competency to transmit the virus. American robins ... ...

    Abstract West Nile virus (WNV) is a vector-borne pathogen that was first detected in the United States in 1999. The natural transmission cycle of WNV involves mosquito vectors and avian hosts, which vary in their competency to transmit the virus. American robins are an abundant backyard species in the United States and appear to have an important role in the amplification and dissemination of WNV. In this study we examine the response of American robins to infection with various WNV doses within the range of those administered by some natural mosquito vectors. Thirty American robins were assigned a WNV dosage treatment and needle inoculated with 10(0.95) PFU, 10(1.26) PFU, 10(2.15) PFU, or 10(3.15) PFU. Serum samples were tested for the presence of infectious WNV and/or antibodies, while oral swabs were tested for the presence of WNV RNA. Five of the 30 (17%) robins had neutralizing antibodies to WNV prior to the experiment and none developed viremia or shed WNV RNA. The proportion of WNV-seronegative birds that became viremic after WNV inoculation increased in a dose dependent manner. At the lowest dose, only 40% (2/5) of the inoculated birds developed productive infections while at the highest dose, 100% (7/7) of the birds became viremic. Oral shedding of WNV RNA followed a similar trend where robins inoculated with the lower two doses were less likely to shed viral RNA (25%) than robins inoculated with one of the higher doses (92%). Viremia titers and morbidity did not increase in a dose dependent manner; only two birds succumbed to infection and, interestingly, both were inoculated with the lowest dose of WNV. It is clear that the disease ecology of WNV is a complex interplay of hosts, vectors, and viral dose delivered.
    Keywords Medicine ; R ; Science ; Q
    Subject code 630
    Language English
    Publishing date 2013-01-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article: West Nile Virus Infection in American Robins: New Insights on Dose Response

    VanDalen, Kaci K / Clark, Larry / Hall, Jeffrey S / McLean, Robert G / Smeraski, Cynthia / Wang, Tian

    PloS one. , v. 8, no. 7

    2013  

    Abstract: West Nile virus (WNV) is a vector-borne pathogen that was first detected in the United States in 1999. The natural transmission cycle of WNV involves mosquito vectors and avian hosts, which vary in their competency to transmit the virus. American robins ... ...

    Title variant American Robins and West Nile Virus Dose Response
    Abstract West Nile virus (WNV) is a vector-borne pathogen that was first detected in the United States in 1999. The natural transmission cycle of WNV involves mosquito vectors and avian hosts, which vary in their competency to transmit the virus. American robins are an abundant backyard species in the United States and appear to have an important role in the amplification and dissemination of WNV. In this study we examine the response of American robins to infection with various WNV doses within the range of those administered by some natural mosquito vectors. Thirty American robins were assigned a WNV dosage treatment and needle inoculated with 10 0.95 PFU, 10 1.26 PFU, 10 2.15 PFU, or 10 3.15 PFU. Serum samples were tested for the presence of infectious WNV and/or antibodies, while oral swabs were tested for the presence of WNV RNA. Five of the 30 (17%) robins had neutralizing antibodies to WNV prior to the experiment and none developed viremia or shed WNV RNA. The proportion of WNV-seronegative birds that became viremic after WNV inoculation increased in a dose dependent manner. At the lowest dose, only 40% (2/5) of the inoculated birds developed productive infections while at the highest dose, 100% (7/7) of the birds became viremic. Oral shedding of WNV RNA followed a similar trend where robins inoculated with the lower two doses were less likely to shed viral RNA (25%) than robins inoculated with one of the higher doses (92%). Viremia titers and morbidity did not increase in a dose dependent manner; only two birds succumbed to infection and, interestingly, both were inoculated with the lowest dose of WNV. It is clear that the disease ecology of WNV is a complex interplay of hosts, vectors, and viral dose delivered.
    Keywords birds ; blood serum ; dose response ; hosts ; insect vectors ; morbidity ; neutralizing antibodies ; pathogens ; RNA ; viremia ; viruses ; West Nile virus ; United States
    Language English
    Dates of publication 2013-0702
    Publishing place Public Library of Science
    Document type Article
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0068537
    Database NAL-Catalogue (AGRICOLA)

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