Literature DB >> 1665538

In situ amplification of visna virus DNA in tissue sections reveals a reservoir of latently infected cells.

K A Staskus1, L Couch, P Bitterman, E F Retzel, M Zupancic, J List, A T Haase.   

Abstract

Maedi and visna are, respectively, the pulmonary and neurological manifestations of slowly progressive infections of sheep caused by retroviruses of the lentivirus subfamily. Lentivirus infections are also persistent infections in which host defenses are generally not successful in eliminating the infectious agent because of restricted viral gene expression in many infected cells. In this report, we describe a method for amplifying and detecting viral DNA in tissue sections which has made it possible to verify experimentally the postulated existence of this reservoir of latently infected cells, as well as to estimate the actual number of cells which harbor viral genomes in infected tissues. In the discussion, we present a simple mathematical model that relates this number to the rate at which inflammatory lesions develop. This model can account for both the slow progression of natural infections and for the rapid accumulation of inflammatory foci in the high dosage experimental system analysed in our studies.

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Year:  1991        PMID: 1665538     DOI: 10.1016/0882-4010(91)90095-r

Source DB:  PubMed          Journal:  Microb Pathog        ISSN: 0882-4010            Impact factor:   3.738


  17 in total

1.  Infection of dendritic cells by the Maedi-Visna lentivirus.

Authors:  S Ryan; L Tiley; I McConnell; B Blacklaws
Journal:  J Virol       Date:  2000-11       Impact factor: 5.103

Review 2.  In cell amplification.

Authors:  V Uhlmann; I Silva; K Luttich; S Picton; J J O'Leary
Journal:  Mol Pathol       Date:  1998-06

3.  Functional murine leukemia virus vectors pseudotyped with the visna virus envelope show expanded visna virus cell tropism.

Authors:  L Bruett; J E Clements
Journal:  J Virol       Date:  2001-12       Impact factor: 5.103

4.  In situ polymerase chain reaction: toy or tool?

Authors:  H Höfler
Journal:  Histochemistry       Date:  1993-02

5.  PCR in situ: aspects which reduce amplification and generate false-positive results.

Authors:  I A Teo; S Shaunak
Journal:  Histochem J       Date:  1995-09

6.  Comparison of indirect and direct in-situ polymerase chain reaction in cell preparations and tissue sections. Detection of viral DNA, gene rearrangements and chromosomal translocations.

Authors:  A A Long; P Komminoth; E Lee; H J Wolfe
Journal:  Histochemistry       Date:  1993-02

7.  Widespread, restricted low-level measles virus infection of brain in a case of subacute sclerosing panencephalitis.

Authors:  S H Isaacson; D M Asher; M S Godec; C J Gibbs; D C Gajdusek
Journal:  Acta Neuropathol       Date:  1996       Impact factor: 17.088

8.  Detection of latent varicella zoster virus DNA and human gene sequences in human trigeminal ganglia by in situ amplification combined with in situ hybridization.

Authors:  A N Dueland; T Ranneberg-Nilsen; M Degré
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

9.  PCR-based analysis of herpes simplex virus type 1 latency in the rat trigeminal ganglion established with a ribonucleotide reductase-deficient mutant.

Authors:  R Ramakrishnan; M Levine; D J Fink
Journal:  J Virol       Date:  1994-11       Impact factor: 5.103

10.  Analysis of human immunodeficiency virus-infected tissues by amplification and in situ hybridization reveals latent and permissive infections at single-cell resolution.

Authors:  J Embretson; M Zupancic; J Beneke; M Till; S Wolinsky; J L Ribas; A Burke; A T Haase
Journal:  Proc Natl Acad Sci U S A       Date:  1993-01-01       Impact factor: 11.205

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