scholarly journals A Minimal Genome Simian Foamy Virus Type 1 Vector System with Efficient Gene Transfer

Virology ◽  
2002 ◽  
Vol 302 (2) ◽  
pp. 236-244 ◽  
Author(s):  
Jeonghae Park ◽  
Peter E. Nadeau ◽  
Ayalew Mergia
1998 ◽  
Vol 72 (4) ◽  
pp. 3451-3454 ◽  
Author(s):  
Min Wu ◽  
Soumya Chari ◽  
Tina Yanchis ◽  
Ayalew Mergia

ABSTRACT We have constructed a series of vectors based on simian foamy virus type 1 (SFV-1) to define the minimum cis-acting elements required for gene transfer. To characterize these vectors, we inserted the coding sequence of the bacterial lacZ gene linked to the cytomegalovirus immediate-early gene promoter. Introduction of a deletion mutation in the leader region between the 5′ long terminal repeat and the start of the gag gene at position 1659 to 1694 completely abrogated gene transfer by the SFV-1 vector. Deletion of 39 nucleotides from position 1692 to 1731 in the leader region resulted in a significant reduction in the transducing-particle titer. Furthermore, we have identified a second cis-acting element located at the 3′ end of the pol gene between position 6486 and 6975 to be critical for SFV-1 vector transduction. These results identify the two important cis-acting elements required for SFV-1 vector construction, and the finding of a cis-acting element in the pol gene is unique among retroviruses.


1999 ◽  
Vol 73 (5) ◽  
pp. 4498-4501 ◽  
Author(s):  
Min Wu ◽  
Ayalew Mergia

ABSTRACT Foamy viruses are nonpathogenic retroviruses that offer several unique opportunities for gene transfer in various cell types from different species. We have previously demonstrated the utility of simian foamy virus type 1 (SFV-1) as a vector system by transient expression assay (M. Wu et al., J. Virol. 72:3451–3454, 1998). In this report, we describe the first stable packaging cell lines for foamy virus vectors based on SFV-1. We developed two packaging cell lines in which the helper DNA is placed under the control of either a constitutive cytomegalovirus (CMV) immediate-early gene or inducible tetracycline promoter for expression. Although the constitutive packaging expressing cell line had a higher copy number of packaging DNA, the inducible packaging cell line produced four times more vector particles. This result suggested that the structural gene products in the constitutively expressing packaging cell line were expressed at a level that is not toxic to the cells, and thus vector production was reduced. The SFV-1 vector in the presence of vesicular stomatitis virus envelope protein G (VSV-G) produced an insignificant level of transduction, indicating that foamy viruses could not be pseudotyped with VSV-G to generate high-titer vectors. The availability of stable packaging cell lines represents a step toward the use of an SFV-1 vector delivery system that will allow scaled-up production of vector stocks for gene therapy.


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

Gene ◽  
1991 ◽  
Vol 101 (2) ◽  
pp. 185-194 ◽  
Author(s):  
Jean-Jacques Kupiec ◽  
Alan Kay ◽  
Maud Hayat ◽  
Rodica Ravier ◽  
Jorge Périés ◽  
...  

1983 ◽  
Vol 47 (1) ◽  
pp. 249-252 ◽  
Author(s):  
A B Benzair ◽  
A Rhodes-Feuillette ◽  
R Emanoil-Ravicovitch ◽  
J Peries

1985 ◽  
Vol 66 (7) ◽  
pp. 1449-1455 ◽  
Author(s):  
A.-B. Benzair ◽  
A. Rhodes-Feuillette ◽  
J. Lasneret ◽  
R. Emanoil-Ravier ◽  
J. Peries

1998 ◽  
Vol 176 (5) ◽  
pp. 404-408 ◽  
Author(s):  
John F. Carew ◽  
Howard Federoff ◽  
Marc Halterman ◽  
Dennis H. Kraus ◽  
Howard Savage ◽  
...  

Virology ◽  
2000 ◽  
Vol 274 (1) ◽  
pp. 203-212 ◽  
Author(s):  
Jeonghae Park ◽  
Ayalew Mergia

1993 ◽  
Vol 67 (8) ◽  
pp. 4598-4604 ◽  
Author(s):  
A Mergia ◽  
L W Renshaw-Gegg ◽  
M W Stout ◽  
R Renne ◽  
O Herchenröeder

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