Intra- and Intercellular Trafficking of the Foamy Virus Auxiliary Bet Protein

ABSTRACT The Bet protein of foamy viruses (FVs) is an auxiliary protein encoded by the 3′ end of the viral genome. Although its function during the viral replication cycle is still unknown, Bet seems to play a key role in the establishment and/or maintenance of viral persistence, representing the predominant viral protein detected during chronic infection. To clarify the function of this viral protein, the subcellular distribution of Bet from the prototypic human foamy virus (HFV) was examined. We report here that this protein is distributed in both the cytoplasm and the nucleus of HFV-infected or Bet-transfected cells. The nuclear targeting results from the presence of a bipartite nuclear localization signal at the C-terminal region, sufficient to direct heterologous reporter proteins to the nucleus. Since HFV Bet spreads between cells, we show here that the secreted protein targets the nuclei of recipient cells. HFV Bet follows an unconventional route to exit the cell since its secretion is not affected by brefeldin A, a drug which disrupts the trafficking between the endoplasmic reticulum and the Golgi complex. Finally, these inter- and intracellular movements were also observed for the equine foamy virus Bet protein, strongly suggesting that these remarkable features are conserved among FVs.

[1]  M. Löchelt,et al.  The bet gene of feline foamy virus is required for virus replication. , 2001, Virology.

[2]  M. Linial,et al.  Cell-Type-Specific Regulation of the Two Foamy Virus Promoters , 2001, Journal of Virology.

[3]  A. Saïb,et al.  Human Foamy Virus Capsid Formation Requires an Interaction Domain in the N Terminus of Gag , 2001, Journal of Virology.

[4]  M. Linial,et al.  Historical Perspective of Foamy Virus Epidemiology and Infection , 2001, Clinical Microbiology Reviews.

[5]  K. Hruska,et al.  Protein transduction: unrestricted delivery into all cells? , 2000, Trends in cell biology.

[6]  A. Saïb,et al.  Foamy viruses: between retroviruses and pararetroviruses. , 2000, Virology.

[7]  A. Saïb,et al.  Isolation and Characterization of an Equine Foamy Virus , 2000, Journal of Virology.

[8]  R. Hughes Secretion of the galectin family of mammalian carbohydrate-binding proteins. , 1999, Biochimica et biophysica acta.

[9]  W. Heneine,et al.  Persistent Zoonotic Infection of a Human with Simian Foamy Virus in the Absence of an Intact orf-2Accessory Gene , 1999, Journal of Virology.

[10]  T. Pietschmann,et al.  Foamy Virus Capsids Require the Cognate Envelope Protein for Particle Export , 1999, Journal of Virology.

[11]  D. Lindemann,et al.  Cells expressing the human foamy virus (HFV) accessory Bet protein are resistant to productive HFV superinfection. , 1998, Virology.

[12]  A. Saïb,et al.  An Evolutionarily Conserved Splice Generates a Secreted Env-Bet Fusion Protein during Human Foamy Virus Infection , 1998, Journal of Virology.

[13]  D. Lindemann,et al.  Characterization of a Human Foamy Virus 170-Kilodalton Env-Bet Fusion Protein Generated by Alternative Splicing , 1998, Journal of Virology.

[14]  D. Görlich,et al.  Nuclear protein import. , 1997, Current opinion in cell biology.

[15]  A. Saïb,et al.  Long-term persistent infection of domestic rabbits by the human foamy virus. , 1997, Virology.

[16]  A. Saïb,et al.  Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step , 1997, Journal of virology.

[17]  M. Giron,et al.  Expression and maturation of human foamy virus Gag precursor polypeptides , 1997, Journal of virology.

[18]  B. Cullen,et al.  The human foamy virus Bel-1 transcription factor is a sequence-specific DNA binding protein , 1996, Journal of virology.

[19]  S. Yu,et al.  Productive persistent infection of hematopoietic cells by human foamy virus , 1996, Journal of virology.

[20]  A. Saïb,et al.  Involvement of a spliced and defective human foamy virus in the establishment of chronic infection , 1995, Journal of virology.

[21]  A. Rethwilm,et al.  Nuclear localization of foamy virus Gag precursor protein , 1994, Journal of virology.

[22]  J. Chang,et al.  The Bel1 protein of human foamy virus contains one positive and two negative control regions which regulate a distinct activation domain of 30 amino acids , 1994, Journal of virology.

[23]  M. Löchelt,et al.  The human foamy virus internal promoter directs the expression of the functional Bel 1 transactivator and Bet protein early after infection , 1994, Journal of virology.

[24]  S. Yu,et al.  Analysis of the role of the bel and bet open reading frames of human foamy virus by using a new quantitative assay , 1993, Journal of virology.

[25]  A. Saïb,et al.  A defective human foamy provirus generated by pregenome splicing. , 1993, The EMBO journal.

[26]  G Baunach,et al.  Functional analysis of human foamy virus accessory reading frames , 1993, Journal of virology.

[27]  M. Löchelt,et al.  Human foamy virus genome possesses an internal, Bel-1-dependent and functional promoter. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[28]  G. Chinnadurai,et al.  The carboxy-terminal transcription enhancement region of the human spumaretrovirus transactivator contains discrete determinants of the activator function , 1993, Journal of virology.

[29]  M. Giron,et al.  Human foamy virus polypeptides: identification of env and bel gene products , 1993, Journal of virology.

[30]  B. Cullen,et al.  Functional organization of the Bel-1 trans activator of human foamy virus , 1993, Journal of virology.

[31]  J. Luzio,et al.  Ectocytosis caused by sublytic autologous complement attack on human neutrophils. The sorting of endogenous plasma-membrane proteins and lipids into shed vesicles. , 1991, The Biochemical journal.

[32]  N. Khanna,et al.  Purification and characterization of annexin proteins from bovine lung. , 1990, Biochemistry.

[33]  J. Lippincott-Schwartz,et al.  Microtubule-dependent retrograde transport of proteins into the ER in the presence of brefeldin a suggests an ER recycling pathway , 1990, Cell.

[34]  J. Hale,et al.  The mechanism of matrix vesicle formation. Studies on the composition of chondrocyte microvilli and on the effects of microfilament-perturbing agents on cellular vesiculation. , 1987, The Journal of biological chemistry.

[35]  A. Rethwilm,et al.  Regulation of foamy virus gene expression. , 1995, Current topics in microbiology and immunology.