Literature DB >> 16162477

Neuropathology associated with feline immunodeficiency virus infection highlights prominent lymphocyte trafficking through both the blood-brain and blood-choroid plexus barriers.

Gavin Ryan1, Terence Grimes, Brenda Brankin, Mohamad J E M F Mabruk, Margaret J Hosie, Oswald Jarrett, John J Callanan.   

Abstract

Feline immunodeficiency virus (FIV) infection in the cat is a well-evaluated model of human immunodeficiency virus (HIV)-1 infection in man with both viruses associated with significant neuropathology. Although studies in both HIV and FIV infections have shown that virus enters the brain in the acute stages of disease, little is known of the mechanisms of viral entry. The dissection of this stage is fundamental to the development of therapies that may prevent or modulate central nervous system (CNS) infection. The present study was designed to characterize the early sequential neuropathological changes following infection with FIV(GL8), a strain known to enter the CNS in acute infection. Cats were infected either by the intraperitoneal (n = 13) or intravenous (n = 12) route with 2000 cat infectious units of virus. Histopathological assessments following intraperitoneal infections were at 4 (n = 2), 5 (n = 1), 8 (n = 3), 10 (n = 1), 16 (n = 1), 32 (n = 2), 52 (n = 2), and 104 (n = 1) weeks post infection whereas animals infected intravenously were examined (n = 3) at 1, 4, 10, and 23 weeks post infection. The most significant lesions following both routes of infection were lymphocyte-rich perivascular infiltrates within cerebral and cerebellar meninges, in choroid plexus and spinal cord dura mater and within epineurium of the sciatic nerve. In addition, following intravenous infection perivascular infiltrations were noted in parenchymal blood vessels primarily of cerebral white matter. Infiltrates were composed of CD79+ B cells and CD3+ T cells. The latter population contained a mixture of CD4+ and CD8+ cells. The severity of lesions increased in intensity in the 8-to 16-week period following infection and then began to wane. The evaluation of this large group of cats at multiple time points revealed pathology comparable with that of early stage HIV-1-associated encephalitis. Moreover, in contrast to previous FIV neuropathology studies, transient meningeal, choroid plexus, and parenchymal vascular pathology were consistent significant findings suggesting that, as in HIV-1 infection, blood-brain barrier and choroid plexus brain barrier integrity are both compromised in early infection.

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Year:  2005        PMID: 16162477     DOI: 10.1080/13550280500186445

Source DB:  PubMed          Journal:  J Neurovirol        ISSN: 1355-0284            Impact factor:   2.643


  47 in total

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Journal:  J Virol       Date:  1998-11       Impact factor: 5.103

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Journal:  Immunology       Date:  1994-04       Impact factor: 7.397

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Journal:  Ann Neurol       Date:  1989-04       Impact factor: 10.422

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  16 in total

1.  Transmigration of macrophages across the choroid plexus epithelium in response to the feline immunodeficiency virus.

Authors:  Rick B Meeker; D C Bragg; Winona Poulton; Lola Hudson
Journal:  Cell Tissue Res       Date:  2012-01-27       Impact factor: 5.249

2.  Canine distemper virus uses both the anterograde and the hematogenous pathway for neuroinvasion.

Authors:  Penny A Rudd; Roberto Cattaneo; Veronika von Messling
Journal:  J Virol       Date:  2006-10       Impact factor: 5.103

3.  Cell trafficking through the choroid plexus.

Authors:  Rick B Meeker; Kimberly Williams; Deirdre A Killebrew; Lola C Hudson
Journal:  Cell Adh Migr       Date:  2012-08-20       Impact factor: 3.405

4.  Cerebrospinal fluid is an efficient route for establishing brain infection with feline immunodeficiency virus and transfering infectious virus to the periphery.

Authors:  Pinghuang Liu; Lola C Hudson; Mary B Tompkins; Thomas W Vahlenkamp; Brenda Colby; Cyndi Rundle; Rick B Meeker
Journal:  J Neurovirol       Date:  2006-08       Impact factor: 2.643

5.  Strain-specific viral distribution and neuropathology of feline immunodeficiency virus.

Authors:  Craig Miller; Helle Bielefeldt-Ohmann; Martha MacMillan; Salvador Huitron-Resendiz; Steven Henriksen; John Elder; Susan VandeWoude
Journal:  Vet Immunol Immunopathol       Date:  2011-06-12       Impact factor: 2.046

6.  Cell-to-cell contact facilitates HIV transmission from lymphocytes to astrocytes via CXCR4.

Authors:  Guan-Han Li; Caroline Anderson; Laura Jaeger; Thao Do; Eugene O Major; Avindra Nath
Journal:  AIDS       Date:  2015-04-24       Impact factor: 4.177

Review 7.  The neuropathogenesis of feline immunodeficiency virus infection: barriers to overcome.

Authors:  Nicola F Fletcher; Rick B Meeker; Lola C Hudson; John J Callanan
Journal:  Vet J       Date:  2010-04-24       Impact factor: 2.688

Review 8.  Feline immunodeficiency virus neuropathogenesis: from cats to calcium.

Authors:  Rick B Meeker
Journal:  J Neuroimmune Pharmacol       Date:  2006-11-28       Impact factor: 4.147

9.  Co-culture model consisting of human brain microvascular endothelial and peripheral blood mononuclear cells.

Authors:  Marianne Strazza; Monique E Maubert; Vanessa Pirrone; Brian Wigdahl; Michael R Nonnemacher
Journal:  J Neurosci Methods       Date:  2016-05-20       Impact factor: 2.390

10.  Ethanol suppression of peripheral blood mononuclear cell trafficking across brain endothelial cells in immunodeficiency virus infection.

Authors:  Lola C Hudson; Brenda A Colby; Rick B Meeker
Journal:  HIV AIDS (Auckl)       Date:  2010-01-28
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