scholarly journals 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

Virology ◽  
1999 ◽  
Vol 257 (1) ◽  
pp. 7-14 ◽  
Author(s):  
Valeria Falcone ◽  
Jörg Leupold ◽  
Jörn Clotten ◽  
Enikö Urbanyi ◽  
Ottmar Herchenröder ◽  
...  
Epidemiologia ◽  
2021 ◽  
Vol 2 (1) ◽  
pp. 46-67
Author(s):  
Antoinette C. van der Kuyl

Old World monkeys (OWM), simians inhabiting Africa and Asia, are currently affected by at least four infectious retroviruses, namely, simian foamy virus (SFV), simian immunodeficiency virus (SIV), simian T-lymphotropic virus (STLV), and simian type D retrovirus (SRV). OWM also show chromosomal evidence of having been infected in the past with four more retroviral species, baboon endogenous virus (BaEV), Papio cynocephalus endogenous virus (PcEV), simian endogenous retrovirus (SERV), and Rhesus endogenous retrovirus-K (RhERV-K/SERV-K1). For some of the viruses, transmission to other primates still occurs, resulting, for instance, in the HIV pandemic. Retroviruses are intimately connected with their host as they are normally spread by close contact. In this review, an attempt to reconstruct the distribution and history of OWM retroviruses will be made. A literature overview of the species infected by any of the eight retroviruses as well as an age estimation of the pathogens will be given. In addition, primate genomes from databases have been re-analyzed for the presence of endogenous retrovirus integrations. Results suggest that some of the oldest retroviruses, SERV and PcEV, have travelled with their hosts to Asia during the Miocene, when a higher global temperature allowed simian expansions. In contrast, younger viruses, such as SIV and SRV, probably due to the lack of a primate continuum between the continents in later times, have been restricted to Africa and Asia, respectively.


Retrovirology ◽  
2010 ◽  
Vol 7 (1) ◽  
pp. 42 ◽  
Author(s):  
Thaidra Gaufin ◽  
Ruy M Ribeiro ◽  
Rajeev Gautam ◽  
Jason Dufour ◽  
Daniel Mandell ◽  
...  

2007 ◽  
Vol 13 (9) ◽  
pp. 1314-1320 ◽  
Author(s):  
Sara Calattini ◽  
Edouard B.A. Betsem ◽  
Alain Froment ◽  
Philippe Mauclère ◽  
Patricia Tortevoye ◽  
...  

Retrovirology ◽  
2011 ◽  
Vol 8 (S1) ◽  
Author(s):  
Jayashree S Nandi ◽  
Anil K Chhangani ◽  
Surendra M Mohnot

FEBS Open Bio ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 2137-2148
Author(s):  
Junshi Zhang ◽  
Chenchen Wang ◽  
Xiaopeng Tuo ◽  
Keli Chai ◽  
Yali Xu ◽  
...  

2001 ◽  
Vol 75 (15) ◽  
pp. 6857-6864 ◽  
Author(s):  
Scott W. Eastman ◽  
Maxine L. Linial

ABSTRACT In contrast to all retroviruses but similar to the hepatitis B virus, foamy viruses (FV) require expression of the envelope protein for budding of intracellular capsids from the cell, suggesting a specific interaction between the Gag and Env proteins. Capsid assembly occurs in the cytoplasm of infected cells in a manner similar to that for the B- and D-type viruses; however, in contrast to these retroviruses, FV Gag lacks an N-terminal myristylation signal and capsids are not targeted to the plasma membrane (PM). We have found that mutation of an absolutely conserved arginine (Arg) residue at position 50 to alanine (R50A) of the simian foamy virus SFV cpz(hu) inhibits proper capsid assembly and abolishes viral budding even in the presence of the envelope (Env) glycoproteins. Particle assembly and extracellular release of virus can be restored to this mutant with the addition of an N-terminal Src myristylation signal (Myr-R50A), presumably by providing an alternate site for assembly to occur at the PM. In addition, the strict requirement of Env expression for capsid budding can be bypassed by addition of a PM-targeting signal to Gag. These results suggest that intracellular capsid assembly may be mediated by a signal akin to the cytoplasmic targeting and retention signal CTRS found in Mason-Pfizer monkey virus and that FV Gag has the inherent ability to assemble capsids at multiple sites like conventional retroviruses. The necessity of Env expression for particle egress is most probably due to the lack of a membrane-targeting signal within FV Gag to direct capsids to the PM for release and indicates that Gag-Env interactions are essential to drive particle budding.


PLoS ONE ◽  
2016 ◽  
Vol 11 (6) ◽  
pp. e0157709 ◽  
Author(s):  
William M. Switzer ◽  
Shaohua Tang ◽  
HaoQiang Zheng ◽  
Anupama Shankar ◽  
Patrick S. Sprinkle ◽  
...  

Virology ◽  
2003 ◽  
Vol 309 (2) ◽  
pp. 248-257 ◽  
Author(s):  
Althaf I. Hussain ◽  
Vedapuri Shanmugam ◽  
Vinod B. Bhullar ◽  
Brigitte E. Beer ◽  
Dominique Vallet ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document