Literature DB >> 10208915

Sites of simian foamy virus persistence in naturally infected African green monkeys: latent provirus is ubiquitous, whereas viral replication is restricted to the oral mucosa.

V Falcone1, J Leupold, J Clotten, E Urbanyi, O Herchenröder, W Spatz, B Volk, N Böhm, A Toniolo, D Neumann-Haefelin, M Schweizer.   

Abstract

Foamy viruses (FV), retroviruses of the genus Spumavirus, are able to infect a wide variety of animal species and replicate in nearly all types of cultured cells. To identify the cells targeted by FV in the natural host and define the sites of viral replication, multiple organs of four African green monkeys naturally infected with simian FV type 3 were investigated for the presence of FV proviral DNA and viral transcripts. All organs contained significant amounts of FV proviral DNA. In addition to proviruses containing the complete transactivator gene taf, proviral genomes carrying a specific 295-bp deletion in the taf gene were detected in all monkeys. As in the case of human foamy virus the deletion leads to the formation of the bet gene that is regarded to be instrumental in the regulation of viral persistence. FV RNA was detected by RT-PCR and in situ hybridization only in the oral mucosa of one monkey. No other samples contained detectable levels of viral transcripts. Histopathological changes were not observed in any of the tissue samples analyzed. Our results show that the natural history of FV is characterized by latent infection in all organs of the host and by minimal levels of harmless viral replication in the oral mucosa. The broad host cell range in vivo further encourages the development of FV-derived vectors for therapeutic gene delivery. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10208915     DOI: 10.1006/viro.1999.9634

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  53 in total

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3.  Systematic Review of Important Viral Diseases in Africa in Light of the 'One Health' Concept.

Authors:  Ravendra P Chauhan; Zelalem G Dessie; Ayman Noreddin; Mohamed E El Zowalaty
Journal:  Pathogens       Date:  2020-04-20

4.  Expanded tissue targets for foamy virus replication with simian immunodeficiency virus-induced immunosuppression.

Authors:  S M Murray; L J Picker; M K Axthelm; M L Linial
Journal:  J Virol       Date:  2006-01       Impact factor: 5.103

5.  Simian foamy virus infection of rhesus macaques in Bangladesh: relationship of latent proviruses and transcriptionally active viruses.

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Journal:  J Virol       Date:  2013-10-09       Impact factor: 5.103

6.  Constitutive release of IFNγ and IL2 from peripheral blood mononuclear cells of rhesus macaques (Macaca mulatta) infected with simian T-lymphotropic virus type 1.

Authors:  JoAnn L Yee; Nestor A Montiel; Amir Ardeshir; Amir Ardeshr; Nicholas W Lerche
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7.  Similar patterns of infection with bovine foamy virus in experimentally inoculated calves and sheep.

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Journal:  J Virol       Date:  2013-01-16       Impact factor: 5.103

8.  Genomic fossils calibrate the long-term evolution of hepadnaviruses.

Authors:  Clément Gilbert; Cédric Feschotte
Journal:  PLoS Biol       Date:  2010-09-28       Impact factor: 8.029

9.  Mother-offspring transmission and age-dependent accumulation of simian foamy virus in wild chimpanzees.

Authors:  Anja Blasse; Sébastien Calvignac-Spencer; Kevin Merkel; Adeelia S Goffe; Christophe Boesch; Roger Mundry; Fabian H Leendertz
Journal:  J Virol       Date:  2013-02-28       Impact factor: 5.103

10.  Simian foamy virus transmission from apes to humans, rural Cameroon.

Authors:  Sara Calattini; Edouard Betsem A Betsem; Alain Froment; Philippe Mauclère; Patricia Tortevoye; Christine Schmitt; Richard Njouom; Ali Saib; Antoine Gessain
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